The MBP0002 set of Samples

Overview
Publications

Brief Description: 50 µg DNA from each of 24 human/rodent somatic cell hybrids and 100 µg DNA from each of three parental cell lines.

Walker JA, Hedges DJ, Perodeau BP, Landry KE, Stoilova N, Laborde ME, Shewale J, Sinha SK, Batzer MA, Multiplex polymerase chain reaction for simultaneous quantitation of human nuclear, mitochondrial, and male Y-chromosome DNA: application in human identification. Anal Biochem337(1):89-97 2005

PubMed ID: 15649380

Otieno AC, Carter AB, Hedges DJ, Walker JA, Ray DA, Garber RK, Anders BA, Stoilova N, Laborde ME, Fowlkes JD, Huang CH, Perodeau B, Batzer MA, Analysis of the human Alu Ya-lineage. J Mol Biol342(1):109-18 2004

PubMed ID: 15313610

Bridgland L, Footz TK, Kardel MD, Riazi MA, McDermid HE, Three duplicons form a novel chimeric transcription unit in the pericentromeric region of chromosome 22q11. Hum Genet112(1):57-61 2003

PubMed ID: 12483300

Butler MP, Iida S, Capello D, Rossi D, Rao PH, Nallasivam P, Louie DC, Chaganti S, Au T, Gascoyne RD, Gaidano G, Chaganti RS, Dalla-Favera R, Alternative translocation breakpoint cluster region 5' to BCL-6 in B-cell non-Hodgkin's lymphoma. Cancer Res62(14):4089-94 2002

PubMed ID: 12124346

Marti, S.B., Cichon, S., Propping, P., and Nothen, M., Human metabotropic glutamate receptor 2 gene (GRM2): chromosomal sublocalization (3p21.1-p21.2) and genomic organization Am J Med Genet114(1):12-14 2002

PubMed ID: 11840499

Ormestad M, Blixt A, Churchill A, Martinsson T, Enerback S, Carlsson P, Foxe3 haploinsufficiency in mice: a model for Peters' anomaly. Invest Ophthalmol Vis Sci43(5):1350-7 2002

PubMed ID: 11980846

Delany NS, Hurle M, Facer P, Alnadaf T, Plumpton C, Kinghorn I, See CG, Costigan M, Anand P, Woolf CJ, Crowther D, Sanseau P, Tate SN, Identification and characterization of a novel human vanilloid receptor-like protein, VRL-2. Physiol Genomics4(3):165-74 2001

PubMed ID: 11160995

Ghosh AK, Majumder M, Steele R, White RA, Ray RB, A novel 16-kilodalton cellular protein physically interacts with and antagonizes the functional activity of c-myc promoter-binding protein 1. Mol Cell Biol21(2):655-62 2001

PubMed ID: 11134351

Watkins WS, Ricker CE, Bamshad MJ, Carroll ML, Nguyen SV, Batzer MA, Harpending HC, Rogers AR, Jorde LB, Patterns of ancestral human diversity: an analysis of Alu-insertion and restriction-site polymorphisms. Am J Hum Genet68(3):738-52 2001

PubMed ID: 11179020

Knight SJ, Lese CM, Precht KS, Kuc J, Ning Y, Lucas S, Regan R, Brenan M, Nicod A, Lawrie NM, Cardy DL, Nguyen H, Hudson TJ, Riethman HC, Ledbetter DH, Flint J, An optimized set of human telomere clones for studying telomere integrity and architecture. Am J Hum Genet67(2):320-32 2000

PubMed ID: 10869233

Provencio I, Rodriguez IR, Jiang G, Hayes WP, Moreira EF, Rollag MD, A novel human opsin in the inner retina. J Neurosci20(2):600-5 2000

PubMed ID: 10632589

Brass N, Racz A, Bauer C, Heckel D, Sybrecht G, Meese E, Role of amplified genes in the production of autoantibodies. Blood93(7):2158-66 1999

PubMed ID: 10090922

Franz T, Vingron M, Boehm T, Dear TN, Capn7: a highly divergent vertebrate calpain with a novel C-terminal domain. Mamm Genome10(3):318-21 1999

PubMed ID: 10051333

Kimura M, Matsuda Y, Yoshioka T, Okano Y, Cell cycle-dependent expression and centrosome localization of a third human aurora/Ipl1-related protein kinase, AIK3. J Biol Chem274(11):7334-40 1999

PubMed ID: 10066797

Lu R, Chan BS, Schuster VL, Cloning of the human kidney PAH transporter: narrow substrate specificity and regulation by protein kinase C. Am J Physiol276(2 Pt 2):F295-303 1999

PubMed ID: 9950961

Somia NV, Schmitt MJ, Vetter DE, Van Antwerp D, Heinemann SF, Verma IM, LFG: an anti-apoptotic gene that provides protection from Fas-mediated cell death. Proc Natl Acad Sci U S A96(22):12667-72 1999

PubMed ID: 10535980

Song YH, Naumova AK, Liebhaber SA, Cooke NE, Physical and meiotic mapping of the region of human chromosome 4q11-q13 encompassing the vitamin D binding protein DBP/Gc-globulin and albumin multigene cluster. Genome Res9(6):581-7 1999

PubMed ID: 10400926

Wong J, Blanco P, Affara NA, An exon map of the AZFc male infertility region of the human Y chromosome. Mamm Genome10(1):57-61 1999

PubMed ID: 9892735

Angrist M, Jing S, Bolk S, Bentley K, Nallasamy S, Halushka M, Fox GM, Chakravarti A, Human GFRA1: cloning, mapping, genomic structure, and evaluation as a candidate gene for Hirschsprung disease susceptibility. Genomics48:354-62 1998

PubMed ID: 9545641

Bernard M, Sanseau P, Henry C, Couturier A, Prigent C, Cloning of STK13, a third human protein kinase related to Drosophila aurora and budding yeast Ipl1 that maps on chromosome 19q13.3-ter. Genomics53:406-9 1998

PubMed ID: 9799611

Betz R, Gray SG, Ekstrom C, Larsson C, Ekstrom TJ, Human histone deacetylase 2, HDAC2 (Human RPD3), is localized to 6q21 by radiation hybrid mapping. Genomics52:245-6 1998

PubMed ID: 9782097

Bischoff JR, Anderson L, Zhu Y, Mossie K, Ng L, Souza B, Schryver B, Flanagan P, Clairvoyant F, Ginther C, Chan CS, Novotny M, Slamon DJ, Plowman GD, A homologue of Drosophila aurora kinase is oncogenic and amplified in human colorectal cancers. EMBO J17(11):3052-65 1998

PubMed ID: 9606188

Bonne S, van Hengel J, van Roy F, Chromosomal mapping of human armadillo genes belonging to the p120(ctn)/plakophilin subfamily. Genomics51:452-4 1998

PubMed ID: 9721216

Cao Y, Traer E, Zimmerman GA, McIntyre TM, Prescott SM, Cloning, expression, and chromosomal localization of human long-chain fatty acid-CoA ligase 4 (FACL4). Genomics49:327-30 1998

PubMed ID: 9598324

Chae YJ, Chung CE, Kim BJ, Lee MH, Lee H, The gene encoding guanidinoacetate methyltransferase (GAMT) maps to human chromosome 19 at band p13.3 and to mouse chromosome 10. Genomics49:162-4 1998

PubMed ID: 9570966

Chidambaram A, Gerrard B, Hanson M, Dean M, Chromosomal localization of the human and murine orthologues of the Drosophila smoothened gene. Genomics53:416-7 1998

PubMed ID: 9799615

Chou HH, Takematsu H, Diaz S, Iber J, Nickerson E, Wright KL, Muchmore EA, Nelson DL, Warren ST, Varki A, A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergence. Proc Natl Acad Sci U S A95(20):11751-6 1998

PubMed ID: 9751737

Ding H, Beckers MC, Plaisance S, Marynen P, Collen D, Belayew A, Characterization of a double homeodomain protein (DUX1) encoded by a cDNA homologous to 3.3 kb dispersed repeated elements. Hum Mol Genet7:1681-94 1998

PubMed ID: 9736770

Eki T, Okumura K, Abe M, Kagotani K, Taguchi H, Murakami Y, Pan ZQ, Hanaoka F, Mapping of the human genes encoding cyclin H (CCNH) and the CDK- activating kinase (CAK) assembly factor MAT1 (MNAT1) to chromosome bands 5q13.3-q14 and 14q23, respectively. Genomics47:115-20 1998

PubMed ID: 9465303

Garcia-Barcelo M, Tsui SKW, Chim SS, Fung KP, Lee CY, Waye MM, Mapping of the human cysteine-rich intestinal protein gene CRIP1 to the human chromosomal segment 7q11.23. Genomics47:419-22 1998

PubMed ID: 9480758

Gondo Y, Okada T, Matsuyama N, Saitoh Y, Yanagisawa Y, Ikeda JE, Human megasatellite DNA RS447: copy-number polymorphisms and interspecies conservation. Genomics54:39-49 1998

PubMed ID: 9806828

Hashida H, Goto J, Zhao N, Takahashi N, Hirai M, Kanazawa I, Sakaki Y, Cloning and mapping of ZNF231, a novel brain-specific gene encoding neuronal double zinc finger protein whose expression is enhanced in a neurodegenerative disorder, multiple system atrophy (MSA). Genomics54:50-8 1998

PubMed ID: 9806829

Her C, Doggett NA, Cloning, structural characterization, and chromosomal localization of the human orthologue of saccharomyces cerevisiae MSH5 gene [In Process Citation] Genomics52:50-61 1998

PubMed ID: 9740671

Her C, Wood TC, Eichler EE, Mohrenweiser HW, Ramagli LS, Siciliano MJ, Weinshilboum RM, Human hydroxysteroid sulfotransferase SULT2B1: two enzymes encoded by a single chromosome 19 gene. Genomics53:284-95 1998

PubMed ID: 9799594

Hirohata S, Seldin MF, Apte SS, Chromosomal assignment of two ADAM genes, TACE (ADAM17) and MLTNB (ADAM19), to human chromosomes 2 and 5, respectively, and of Mltnb to mouse chromosome 11. Genomics54:178-9 1998

PubMed ID: 9806848

Howe K, Williamson J, Boddy N, Sheer D, Freemont P, Solomon E, The ubiquitin-homology gene PIC1: characterization of mouse (Pic1) and human (UBL1) genes and pseudogenes. Genomics47:92-100 1998

PubMed ID: 9465300

Ishii H, Kim DH, Fujita T, Endo Y, Saeki S, Yamamoto TT, cDNA cloning of a new low-density lipoprotein receptor-related protein and mapping of its gene (LRP3) to chromosome bands 19q12-q13. 2. Genomics51:132-5 1998

PubMed ID: 9693042

Johnstone RW, Tommerup N, Hansen C, Vissing H, Shi Y, Mapping of the human PAWR (par-4) gene to chromosome 12q21. Genomics53:241-3 1998

PubMed ID: 9790775

Kishino T, Wagstaff J, Genomic organization of the UBE3A/E6-AP gene and related pseudogenes. Genomics47:101-7 1998

PubMed ID: 9465301

Kohno T, Kawanishi M, Inazawa J, Yokota J, Identification of CpG islands hypermethylated in human lung cancer by the arbitrarily primed-PCR method. Hum Genet102:258-64 1998

PubMed ID: 9544836

Kremmidiotis G, Baker E, Crawford J, Eyre HJ, Nahmias J, Callen DF, Localization of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosity. Genomics49:467-71 1998

PubMed ID: 9615235

Laurent AM, Puechberty J, Prades C, Roizes G, Localization of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosity. Genomics52:166-72 1998

PubMed ID: 9782082

Lin RY, Vera JC, Chaganti RS, Golde DW, Human monocarboxylate transporter 2 (MCT2) is a high affinity pyruvate transporter. J Biol Chem273:28959-65 1998

PubMed ID: 9786900

Lund EG, Kerr TA, Sakai J, Li WP, Russell DW, cDNA cloning of mouse and human cholesterol 25-hydroxylases, polytopic membrane proteins that synthesize a potent oxysterol regulator of lipid metabolism. J Biol Chem273(51):34316-27 1998

PubMed ID: 9852097

Malkhosyan S, Yasuda J, Soto JL, Sekiya T, Yokota J, Perucho M, Molecular karyotype (amplotype) of metastatic colorectal cancer by unbiased arbitrarily primed PCR DNA fingerprinting. Proc Natl Acad Sci U S A95:10170-5 1998

PubMed ID: 9707619

Matena K, Boehm T, Dear N, Genomic organization of mouse Capn5 and Capn6 genes confirms that they are a distinct calpain subfamily. Genomics48:117-20 1998

PubMed ID: 9503024

Nomiyama H, Amano K, Kusuda J, Imai T, Miura R, Yoshie O, Matsuda Y, The human CC chemokine TECK (SCYA25) maps to chromosome 19p13.2. Genomics51:311-2 1998

PubMed ID: 9722960

Nomiyama H, Osborne LR, Imai T, Kusuda J, Miura R, Tsui LC, Yoshie O, Assignment of the human CC chemokine MPIF-2/eotaxin-2 (SCYA24) to chromosome 7q11.23. Genomics49:339-40 1998

PubMed ID: 9598329

O'Keefe DS, Su SL, Bacich DJ, Horiguchi Y, Luo Y, Powell CT, Zandvliet D, Russell PJ, Molloy PL, Nowak NJ, Shows TB, Mullins C, Vonder Haar RA, Fair WR, Heston WDW, Mapping, genomic organization and promoter analysis of the human prostate-specific membrane antigen gene [In Process Citation] Biochim Biophys Acta1443:113-27 1998

PubMed ID: 9838072

Pelletier GJ, Brody SL, Liapis H, White RA, Hackett BP, A human forkhead/winged-helix transcription factor expressed in developing pulmonary and renal epithelium. Am J Physiol274:L351-9 1998

PubMed ID: 9530170

Peyrard M, Parveneh S, Lagercrantz S, Ekman M, Fransson I, Sahlen S, DumanskiJP, Cloning, expression pattern, and chromosomal assignment to 16q23 of the human gamma-adaptin gene (ADTG). Genomics50(2):275-80 1998

PubMed ID: 9653655

Porcellati F, Hlaing T, Togawa M, Stevens MJ, Larkin DD, Hosaka Y, Glover TW, Henry DN, Greene DA, Killen PD, Human Na(+)-myo-inositol cotransporter gene: alternate splicing generates diverse transcripts. Am J Physiol274(5 Pt 1):C1215-25 1998

PubMed ID: 9612208

Rouquier S, Friedman C, Delettre C, van den Engh G, Blancher A, Crouau-Roy B, Trask BJ, Giorgi D., A gene recently inactivated in human defines a new olfactory receptor family in mammals. Hum Mol Genet7(9):1337-45 1998

PubMed ID: 9700185

Saupe S, Roizes G, Peter M, Boyle S, Gardiner K, De Sario A, Molecular cloning of a human cDNA IGSF3 encoding an immunoglobulin-like membrane protein: expression and mapping to chromosome band 1p13. Genomics52:305-11 1998

PubMed ID: 9790749

Seifarth W, Baust C, Murr A, Skladny H, Krieg-Schneider F, Blusch J, Werner T, Hehlmann R, Leib-Mosch C, Proviral structure, chromosomal location, and expression of HERV-K-T47D, a novel human endogenous retrovirus derived from T47D particles. J Virol72(10):8384-91 1998

PubMed ID: 9733890

Shah ZH, Migliosi V, Miller SC, Wang A, Friedman TB, Jacobs HT, Chromosomal locations of three human nuclear genes (RPSM12, TUFM, and AFG3L1) specifying putative components of the mitochondrial gene expression apparatus. Genomics48:384-8 1998

PubMed ID: 9545647

Speel EJ, van der Ven PF, Albrechts JC, Ramaekers FC, Furst DO, Hopman AH, Assignment of the human gene for the sarcomeric M-band protein myomesin (MYOM1) to 18p11.31-p11.32. Genomics54:184-6 1998

PubMed ID: 9806852

Trask BJ, Massa H, Brand-Arpon V, Chan K, Friedman C, Nguyen OT, Eichler E, van den Engh G, Rouquier S, Shizuya H, Giorgi D, Large multi-chromosomal duplications encompass many members of the olfactory receptor gene family in the human genome. Hum Mol Genet7:2007-20 1998

PubMed ID: 9817916

Triepels R, van den Heuvel L, Loeffen J, Smeets R, Trijbels F, Smeitink J, The nuclear-encoded human NADH:ubiquinone oxidoreductase NDUFA8 subunit: cDNA cloning, chromosomal localization, tissue distribution, and mutation detection in complex-I-deficient patients. Hum Genet103:557-63 1998

PubMed ID: 9860297

Van Tine BA, Knops JF, Butler A, Deloukas P, Shaw GM, King PH, Localization of HuC (ELAVL3) to chromosome 19p13.2 by fluorescence in situ hybridization utilizing a novel tyramide labeling technique. Genomics53:296-9 1998

PubMed ID: 9799595

White KE, Econs MJ, Localization of PiUS, a stimulator of cellular phosphate uptake to human chromosome 3p21.3. Somat Cell Mol Genet24:71-4 1998

PubMed ID: 9776982

Winand NJ, Panzer JA, Kolodner RD, Cloning and characterization of the human and Caenorhabditis elegans homologs of the Saccharomyces cerevisiae MSH5 gene. Genomics53:69-80 1998

PubMed ID: 9787078

Xu WF, Andersen H, Whitmore TE, Presnell SR, Yee DP, Ching A, Gilbert T, Davie EW, Foster DC, Cloning and characterization of human protease-activated receptor 4. Proc Natl Acad Sci U S A95(12):6642-6 1998

PubMed ID: 9618465

Yamagoe S, Kameoka Y, Hashimoto K, Mizuno S, Suzuki K, Molecular cloning, structural characterization, and chromosomal mapping of the human LECT2 gene. Genomics48:324-9 1998

PubMed ID: 9545637

Yoshida K, Yoshitomo-Nakagawa K, Seki N, Sasaki M, Sugano S, Cloning, expression analysis, and chromosomal localization of BH- protocadherin (PCDH7), a novel member of the cadherin superfamily. Genomics49:458-61 1998

PubMed ID: 9615233

Albala JS, Thelen MP, Prange C, Fan W, Christensen M, Thompson LH, Lennon GG, Identification of a novel human RAD51 homolog, RAD51B [published erratum appears in Genomics 1998 Aug 1;51(3):480] Genomics46:476-9 1997

PubMed ID: 9441753

Bartuski AJ, Kamachi Y, Schick C, Overhauser J, Silverman GA, Cytoplasmic antiproteinase 2 (PI8) and bomapin (PI10) map to the serpin cluster at 18q21.3. Genomics43:321-8 1997

PubMed ID: 9268635

Bastians H, Krebber H, Hoheisel J, Ohl S, Lichter P, Ponstingl H, Joos S, Assignment of the human serine/threonine protein phosphatase 4 gene (PPP4C) to chromosome 16p11-p12 by fluorescence in situ hybridization. Genomics42:181-2 1997

PubMed ID: 9177794

Bergstein I, Eisenberg LM, Bhalerao J, Jenkins NA, Copeland NG, Osborne MP, Bowcock AM, Brown AM, Isolation of two novel WNT genes, WNT14 and WNT15, one of which (WNT15) is closely linked to WNT3 on human chromosome 17q21. Genomics46:450-8 1997

PubMed ID: 9441749

Budarf M, McDonald T, Sellinger B, Kozak C, Graham C, Wistow G, Localization of the human gene for macrophage migration inhibitory factor (MIF) to chromosome 22q11.2. Genomics39:235-6 1997

PubMed ID: 9027512

Chatterjee TK, Eapen A, Kanis AB, Fisher RA, Genomic organization, 5'-flanking region, and chromosomal localization of the human RGS3 gene. Genomics45:429-33 1997

PubMed ID: 9344672

Davies JP, Cotter PD, Ioannou YA, Cloning and mapping of human Rab7 and Rab9 cDNA sequences and identification of a Rab9 pseudogene. Genomics41:131-4 1997

PubMed ID: 9126495

Eichler EE, Budarf ML, Rocchi M, Deaven LL, Doggett NA, Baldini A, Nelson DL, Mohrenweiser HW, Interchromosomal duplications of the adrenoleukodystrophy locus: a phenomenon of pericentromeric plasticity. Hum Mol Genet6(7):991-1002 1997

PubMed ID: 9215666

Ernstsson S, Betz R, Lagercrantz S, Larsson C, Ericksson S, Cederberg A, Carlsson P, Enerbäck S, Cloning and Characterization of freac-9 (FKHL171), a Novel Kidney-Expressed Human Forkhead Gene That Maps to Chromosome 1p32-p34. Genomics46(1):78-85 1997

PubMed ID: 9405125

Ernstsson S, Betz R, Lagercrantz S, Larsson C, Ericksson S, Cederberg A, Carlsson P, Enerback S, Cloning and characterization of freac-9 (FKHL17), a novel kidney- expressed human forkhead gene that maps to chromosome 1p32-p34. Genomics46:78-85 1997

PubMed ID: 9403061

Fu GK, Lin D, Zhang MY, Bikle DD, Shackleton CH, Miller WL, Portale AA, Cloning of human 25-hydroxyvitamin D-1 alpha-hydroxylase and mutations causing vitamin D-dependent rickets type 1. Mol Endocrinol11:1961-70 1997

PubMed ID: 9415400

Godiska R, Chantry D, Raport CJ, Sozzani S, Allavena P, Leviten D, Mantovani A, Gray PW, Human macrophage-derived chemokine (MDC), a novel chemoattractant for monocytes, monocyte-derived dendritic cells, and natural killer cells. J Exp Med185(9):1595-604 1997

PubMed ID: 9151897

Haddad LA, Fuzikawa AK, Pena SD, Simultaneous detection of size and sequence polymorphisms in the transcribed trinucleotide repeat D2S196E (EST00493). Hum Genet99:796-800 1997

PubMed ID: 9187676

Harun RB, Smith KK, Leek JP, Markham AF, Norris A, Morrison JF, Characterization of human SHC p66 cDNA and its processed pseudogene mapping to Xq12-q13.1. Genomics42:349-52 1997

PubMed ID: 9192859

Her C, Kaur GP, Athwal RS, Weinshilboum RM, Human sulfotransferase SULT1C1: cDNA cloning, tissue-specific expression, and chromosomal localization. Genomics41:467-70 1997

PubMed ID: 9169148

Hieshima K, Imai T, Opdenakker G, Van Damme J, Kusuda J, Tei H, Sakaki Y, Takatsuki K, Miura R, Yoshie O, Nomiyama H, Molecular cloning of a novel human CC chemokine liver and activation-regulated chemokine (LARC) expressed in liver. Chemotactic activity for lymphocytes and gene localization on chromosome 2. J Biol Chem272(9):5846-53 1997

PubMed ID: 9038201

Howard TD, Paznekas WA, Green ED, Chiang LC, Ma N, Ortiz de Luna RI, Garcia Delgado C, Gonzalez-Ramos M, Kline AD, Jabs EW, Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome [see comments] Nat Genet15:36-41 1997

PubMed ID: 8988166

Huang X, Cheng A, Honkanen RE, Genomic organization of the human PP4 gene encoding a serine/threonine protein phosphatase (PP4) suggests a common ancestry with PP2A. Genomics44:336-43 1997

PubMed ID: 9325055

Ishiai M, Dean FB, Okumura K, Abe M, Moon KY, Amin AA, Kagotani K, Taguchi H, Murakami Y, Hanaoka F, O'Donnell M, Hurwitz J, Eki T, Isolation of human and fission yeast homologues of the budding yeast origin recognition complex subunit ORC5: human homologue (ORC5L) maps to 7q22. Genomics46:294-8 1997

PubMed ID: 9417919

Jones MH, Numata M, Shimane M, Identification and characterization of BRDT: A testis-specific gene related to the bromodomain genes RING3 and Drosophila fsh. Genomics45:529-34 1997

PubMed ID: 9367677

Jones MH, Zhang Y, Tirosvoutis KN, Davey PM, Webster AR, Walsh D, Spurr NK, Affara NA, Chromosomal assignment of 311 sequences transcribed in human adult testis. Genomics40:155-67 1997

PubMed ID: 9070934

Kastury K, Taylor WE, Gutierrez M, Ramirez L, Coucke PJ, Van Hauwe P, Van Camp G, Bhasin S, Chromosomal mapping of two members of the human dynein gene family to chromosome regions 7p15 and 11q13 near the deafness loci DFNA 5 and DFNA 11. Genomics44:362-4 1997

PubMed ID: 9325061

Kehrer-Sawatzki H, Haussler J, Krone W, Bode H, Jenne DE, Mehnert KU, Tummers U, Assum G, The second case of a t(17;22) in a family with neurofibromatosis type 1: sequence analysis of the breakpoint regions. Hum Genet99:237-47 1997

PubMed ID: 9048928

Kim DH, Magoori K, Inoue TR, Mao CC, Kim HJ, Suzuki H, Fujita T, Endo Y, Saeki S, Yamamoto TT, Exon/intron organization, chromosome localization, alternative splicing, and transcription units of the human apolipoprotein E receptor 2 gene. J Biol Chem272(13):8498-504 1997

PubMed ID: 9079678

Kowalski PE, Freeman JD, Nelson DT, Mager DL, Genomic structure and evolution of a novel gene (PLA2L) with duplicated phospholipase A2-like domains. Genomics39:38-46 1997

PubMed ID: 9027484

Kusuda J, Hirai M, Toyoda A, Hashimoto K, Localization of the human transaldolase gene (TALDO) to chromosome 1p33- p34.1 by fluorescence in situ hybridization and PCR analysis of somatic cell hybirds. Genomics40:378-81 1997

PubMed ID: 9119412

Lauer P, Meyer NC, Prass CE, Starnes SM, Wolff RK, Gnirke A, Clone-contig and STS maps of the hereditary hemochromatosis region on human chromosome 6p21.3-p22. Genome Res7(5):457-70 1997

PubMed ID: 9149942

Lench NJ, Macadam R, Markham AF, The human gene encoding FKBP-rapamycin associated protein (FRAP) maps to chromosomal band 1p36.2. Hum Genet99(4):547-9 1997

PubMed ID: 9099849

Li L, Wu Q, Barnoski BL, Cooper MD, High-resolution genetic map of the human glutamyl aminopeptidase gene (ENPEP). Genomics43:380-3 1997

PubMed ID: 9268642

Liang Y, Chen H, Asher JH Jr, Chang CC, Friedman TB, Human inner ear OCP2 cDNA maps to 5q22-5q35.2 with related sequences on chromosomes 4p16.2-4p14, 5p13-5q22, 7pter-q22, 10 and 12p13-12qter. Gene184:163-7 1997

PubMed ID: 9031623

Lutz CM, Richards JE, Scott KL, Sinha S, Yang-Feng TL, Frankel WN, Thompson DA, Neuropeptide Y receptor genes mapped in human and mouse: receptors with high affinity for pancreatic polypeptide are not clustered with receptors specific for neuropeptide Y and peptide YY. Genomics46:287-90 1997

PubMed ID: 9417917

Martinez de Arrieta C, Perez Jurado L, Bernal J, Coloma A, Structure, organization, and chromosomal mapping of the human neurogranin gene (NRGN). Genomics41:243-9 1997

PubMed ID: 9143500

Matthijs G, Schollen E, Pardon E, Veiga-Da-Cunha M, Jaeken J, Cassiman JJ, Van Schaftingen E, Mutations in PMMM2, a phosphomannomutase gene on chromosome 16p13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome) [published erratum appears in Nat Genet 1997 Jul;16(3):316] Nat Genet16:88-92 1997

PubMed ID: 9140401

Matthijs G, Schollen E, Pirard M, Budarf ML, Van Schaftingen E, Cassiman JJ, PMM (PMM1), the human homologue of SEC53 or yeast phosphomannomutase, is localized on chromosome 22q13. Genomics40:41-7 1997

PubMed ID: 9070917

Melkonyan HS, Chang WC, Shapiro JP, Mahadevappa M, Fitzpatrick PA, Kiefer MC, Tomei LD, Umansky SR, SARPs: a family of secreted apoptosis-related proteins. Proc Natl Acad Sci U S A94:13636-41 1997

PubMed ID: 9391078

Milon L, Rousseau-Merck MF, Munier A, Erent M, Lascu I, Capeau J, Lacombe ML, nm23-H4, a new member of the family of human nm23/nucleoside diphosphate kinase genes localised on chromosome 16p13. Hum Genet99:550-7 1997

PubMed ID: 9099850

Minekura H, Fujino T, Kang MJ, Fujita T, Endo Y, Yamamoto TT, Human acyl-coenzyme A synthetase 3 cDNA and localization of its gene (ACS3) to chromosome band 2q34-q35. Genomics42:180-1 1997

PubMed ID: 9177793

Morton SM, Veile RA, Helms C, Lee M, Kuo WL, Gray J, Donis-Keller H, Subregional localization of 21 chromosome 7-specific expressed sequence tags (ESTs) by FISH using newly identified YACs and P1s. Genomics46:491-4 1997

PubMed ID: 9441757

Nadal M, Moreno S, Pritchard M, Preciado MA, Estivill X, Ramos-Arroyo MA, Down syndrome: characterisation of a case with partial trisomy of chromosome 21 owing to a paternal balanced translocation (15;21) (q26;q22.1) by FISH. J Med Genet34(1):50-4 1997

PubMed ID: 9032650

Nagai M, Sakakibara J, Wakui K, Fukushima Y, Igarashi S, Tsuji S, Arakawa M, Ono T, Localization of the squalene epoxidase gene (SQLE) to human chromosome region 8q24.1. Genomics44:141-3 1997

PubMed ID: 9286711

Nakayama T, Fujiwara T, Miyazawa A, Asakawa S, Shimizu N, Shimizu Y, Mikoshiba K, Akagawa K, Mapping of the human HPC-1/syntaxin 1A gene (STX1A) to chromosome 7 band q11.2. Genomics42:173-6 1997

PubMed ID: 9177791

Odermatt A, Taschner PE, Scherer SW, Beatty B, Khanna VK, Cornblath DR, Chaudhry V, Yee WC, Schrank B, Karpati G, Breuning MH, Knoers N, MacLennan DH, Characterization of the gene encoding human sarcolipin (SLN), a proteolipid associated with SERCA1: absence of structural mutations in five patients with Brody disease. Genomics45:541-53 1997

PubMed ID: 9367679

Pangilinan F, Li Q, Weaver T, Lewis BC, Dang CV, Spencer F, Mammalian BUB1 protein kinases: map positions and in vivo expression. Genomics46:379-88 1997

PubMed ID: 9441741

Pichaud F, Delage-Mourroux R, Pidoux E, Jullienne A, Rousseau-Merck MF, Chromosomal localization of the type-I 15-PGDH gene to 4q34-q35. Hum Genet99(2):279-81 1997

PubMed ID: 9048936

Prinsen CF, de Bruijn DR, Merkx GF, Veerkamp JH, Assignment of the human adipocyte fatty acid-binding protein gene (FABP4) to chromosome 8q21 using somatic cell hybrid and fluorescence in situ hybridization techniques. Genomics40:207-9 1997

PubMed ID: 9070949

Reddy PH, Stockburger E, Gillevet P, Tagle DA, Mapping and characterization of novel (CAG)n repeat cDNAs from adult human brain derived by the oligo capture method. Genomics46:174-82 1997

PubMed ID: 9417904

Reddy UR, Phatak S, Allen C, Nycum LM, Sulman EP, White PS, Biegel JA, Localization of the human Ror1 gene (NTRKR1) to chromosome 1p31-p32 by fluorescence in situ hybridization and somatic cell hybrid analysis. Genomics41:283-5 1997

PubMed ID: 9143508

Seboun E, Barbaux S, Bourgeron T, Nishi S, Agulnik A, Egashira M, Nikkawa N, Bishop C, Fellous M, McElreavey K, Kasahara M, Algonik A$[corrected to Agulnik A], Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility gene [published erratum appears in Genomics 1997 Oct 15;45(2):477] Genomics41:227-35 1997

PubMed ID: 9143498

Sen S, Zhou H, Ripmaster T, Hittelman WN, Schimmel P, White RA, Expression of a gene encoding a tRNA synthetase-like protein is enhanced in tumorigenic human myeloid leukemia cells and is cell cycle stage- and differentiation-dependent. Proc Natl Acad Sci U S A94:6164-9 1997

PubMed ID: 9177188

Spicer AP, Seldin MF, Olsen AS, Brown N, Wells DE, Doggett NA, Itano N, Kimata K, Inazawa J, McDonald JA, Chromosomal localization of the human and mouse hyaluronan synthase genes. Genomics41:493-7 1997

PubMed ID: 9169154

Sun ZS, Albrecht U, Zhuchenko O, Bailey J, Eichele G, Lee CC, RIGUI, a putative mammalian ortholog of the Drosophila period gene. Cell90:1003-11 1997

PubMed ID: 9323128

Tamimi RM, Steingrimsson E, Montgomery-Dyer K, Copeland NG, Jenkins NA, Tapscott SJ, NEUROD2 and NEUROD3 genes map to human chromosomes 17q12 and 5q23-q31 and mouse chromosomes 11 and 13, respectively. Genomics40:355-7 1997

PubMed ID: 9119405

Tang XX, Pleasure DE, Ikegaki N, cDNA cloning, chromosomal localization, and expression pattern of EPLG8, a new member of the EPLG gene family encoding ligands of EPH- related protein-tyrosine kinase receptors. Genomics41:17-24 1997

PubMed ID: 9126477

Thiagalingam A, Lengauer C, Baylin SB, Nelkin BD, RREB1, a ras responsive element binding protein, maps to human chromosome 6p25. Genomics45:630-2 1997

PubMed ID: 9367691

Thiagalingam A, Lengauer C, Baylin SB, Nelkin BD, RREB1, a ras responsive element binding protein, maps to human chromosome 6p25. Genomics45(3):630-2 1997

PubMed ID: 98035890

Walker RL, Anziano P, Meltzer PS, A PAC containing the human mitochondrial DNA polymerase gamma gene (POLG) maps to chromosome 15q25. Genomics40:376-8 1997

PubMed ID: 9119411

White RA, Adkison LR, Dowler LL, Ray RB, Chromosomal localization of the human gene encoding c-myc promoter- binding protein (MPB1) to chromosome 1p35-pter. Genomics39:406-8 1997

PubMed ID: 9119380

Wickman K, Seldin MF, James MR, Gendler SJ, Clapham DE, Partial structure, chromosome localization, and expression of the mouse Icln gene. Genomics40:402-8 1997

PubMed ID: 9073507

Williams RS, Shohet RV, Stillman B., A human protein related to yeast Cdc6p. A human protein related to yeast Cdc6p. Proc Natl Acad Sci U S A94(1):142-7 1997

PubMed ID: 8990175

Yamada Y, Nezu J, Shimane M, Hirata Y, Molecular cloning of a novel vascular endothelial growth factor, VEGF-D. Genomics42:483-8 1997

PubMed ID: 9205122

Yoshida R, Imai T, Hieshima K, Kusuda J, Baba M, Kitaura M, Nishimura M, Kakizaki M, Nomiyama H, Yoshie O, Molecular cloning of a novel human CC chemokine EBI1-ligand chemokine that is a specific functional ligand for EBI1, CCR7. J Biol Chem272:13803-9 1997

PubMed ID: 9153236

Young AC, Chavez M, Giambernardi TA, Mattern V, McGill JR, Harris JM, Sarosdy MF, Patel P, Sakaguchi AY, Organization and expression of human telomere repeat binding factor genes. Somat Cell Mol Genet23:275-86 1997

PubMed ID: 9542529

Yu J, Nagarajan S, Knez JJ, Udenfriend S, Chen R, Medof ME, The affected gene underlying the class K glycosylphosphatidylinositol (GPI) surface protein defect codes for the GPI transamidase. Proc Natl Acad Sci U S A94:12580-5 1997

PubMed ID: 9356492

Albertsen HM, Smith SA, Melis R, Williams B, Holik P, Stevens J, White R, Sequence, genomic structure, and chromosomal assignment of human DOC-2. Genomics33:207-13 1996

PubMed ID: 8660969

Aman MJ, Tayebi N, Obiri NI, Puri RK, Modi WS, Leonard WJ, cDNA cloning and characterization of the human interleukin 13 receptor alpha chain. J Biol Chem271(46):29265-70 1996

PubMed ID: 8910586

Amann J, Valentine M, Kidd VJ, Lahti JM, Localization of chi1-related helicase genes to human chromosome regions 12p11 and 12p13: similarity between parts of these genes and conserved human telomeric-associated DNA. Genomics32:260-5 1996

PubMed ID: 8833153

Andersen SE, Lench NJ, Markham AF, YAC clones that extend the human chromosome 12cen-12q15 region contig map. Mamm Genome7(10):780-3 1996

PubMed ID: 8854870

Bergsagel PL, Chesi M, Nardini E, Brents LA, Kirby SL, Kuehl WM, Promiscuous translocations into immunoglobulin heavy chain switch regions in multiple myeloma. Proc Natl Acad Sci U S A93(24):13931-6 1996

PubMed ID: 8943038

Bosio A, Binczek E, Le Beau MM, Fernald AA, Stoffel W, The human gene CGT encoding the UDP-galactose ceramide galactosyl transferase (cerebroside synthase): cloning, characterization, and assignment to human chromosome 4, band q26. Genomics34:69-75 1996

PubMed ID: 8661025

Carrier A, Rosier MF, Guillemot F, Goguel AF, Pulcini F, Bernheim A, Auffray C, Devignes MD, Integrated physical, genetic, and genic map covering 3 Mb around the human NGF gene (NGFB) at 1p13. Genomics31:80-9 1996

PubMed ID: 8808283

Chen H, Gos A, Morris MA, Antonarakis SE, Localization of a human homolog of the mouse pericentrin gene (PCNT) to chromosome 21qter. Genomics35:620-4 1996

PubMed ID: 8812505

Chen H, Rossier C, Lalioti MD, Lynn A, Chakravarti A, Perrin G, Antonarakis SE, Cloning of the cDNA for a human homologue of the Drosophila white gene and mapping to chromosome 21q22.3. Am J Hum Genet59:66-75 1996

PubMed ID: 8659545

Chiang PW, Fogel E, Jackson CL, Lieuallen K, Lennon G, Qu X, Wang SQ, Kurnit DM, Isolation, sequencing, and mapping of the human homologue of the yeast transcription factor, SPT5. Genomics38:421-4 1996

PubMed ID: 8975720

Chiang PW, Wang SQ, Smithivas P, Song WJ, Crombez E, Akhtar A, Im R, Greenfield J, Ramamoorthy S, Van Keuren M, Blackburn CC, Tsai CH, Kurnit DM, Isolation and characterization of the human and mouse homologues (SUPT4H and Supt4h) of the yeast SPT4 gene. Genomics34:368-75 1996

PubMed ID: 8786137

Coon SL, Mazuruk K, Bernard M, Roseboom PH, Klein DC, Rodriguez IR, The human serotonin N-acetyltransferase (EC 2.3.1.87) gene (AANAT): structure, chromosomal localization, and tissue expression. Genomics34:76-84 1996

PubMed ID: 8661026

DiMarco SP, Glover TW, Miller DE, Reines D, Warren ST, Transcription elongation factor SII (TCEA) maps to human chromosome 3p22 --> p21.3. Genomics36:185-8 1996

PubMed ID: 8812434

Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A, Dormishian F, Domingo R Jr, Ellis MC, Fullan A, Hinton LM, Jones NL, Kimmel BE, Kronmal GS, Lauer P, Lee VK, Loeb DB, Mapa FA, McClelland E, Meyer NC, Mintier GA, Moeller N, Moore T, Morikang E, Wolff RK, et al, A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis [see comments] Nat Genet13:399-408 1996

PubMed ID: 8696333

Ferrer J, Aoki M, Behn P, Nestorowicz A, Riggs A, Permutt MA, Mitochondrial glycerol-3-phosphate dehydrogenase. Cloning of an alternatively spliced human islet-cell cDNA, tissue distribution, physical mapping, and identification of a polymorphic genetic marker. Diabetes45(2):262-6 1996

PubMed ID: 8549872

Gastier JM, Brody T, Pulido JC, Businga T, Sunden S, Hu X, Maitra S, Buetow KH, Murray JC, Sheffield VC, Boguski M, Duyk GM, Hudson TJ, Development of a screening set for new (CAG/CTG)n dynamic mutations. Genomics32:75-85 1996

PubMed ID: 8786123

Goldmuntz E, Wang Z, Roe BA, Budarf ML, Cloning, genomic organization, and chromosomal localization of human citrate transport protein to the DiGeorge/velocardiofacial syndrome minimal critical region. Genomics33:271-6 1996

PubMed ID: 8660975

Hahn SA, Hoque AT, Moskaluk CA, da Costa LT, Schutte M, Rozenblum E, Seymour AB, Weinstein CL, Yeo CJ, Hruban RH, Kern SE, Homozygous deletion map at 18q21.1 in pancreatic cancer. Cancer Res56:490-4 1996

PubMed ID: 8564959

Hanai R, Caron PR, Wang JC, Human TOP3: a single-copy gene encoding DNA topoisomerase III. Proc Natl Acad Sci U S A93:3653-7 1996

PubMed ID: 8622991

Hayward BE, Fantes JA, Warner JP, Intody S, Leek JP, Markham AF, Bonthron DT, Co-localization of the ketohexokinase and glucokinase regulator genes to a 500-kb region of chromosome 2p23. Mamm Genome7(6):454-8 1996

PubMed ID: 8662230

Her C, Raftogianis R, Weinshilboum RM, Human phenol sulfotransferase STP2 gene: molecular cloning, structural characterization, and chromosomal localization. Genomics33:409-20 1996

PubMed ID: 8661000

Hirai M, Kusuda J, Hashimoto K, Assignment of human ADP ribosylation factor (ARF) genes ARF1 and ARF3 to chromosomes 1q42 and 12q13, respectively. Genomics34(2):263-5 1996

PubMed ID: 8661066

Hu RJ, Lee MP, Johnson LA, Feinberg AP, A novel human homologue of yeast nucleosome assembly protein, 65 kb centromeric to the p57KIP2 gene, is biallelically expressed in fetal and adult tissues. Hum Mol Genet5(11):1743-8 1996

PubMed ID: 8923002

Ishizuka T, Ahmad I, Kita K, Sonoda T, Ishijima S, Sawa K, Suzuki N, Tatibana M, The human phosphoribosylpyrophosphate synthetase-associated protein 39 gene (PRPSAP1) is located in the chromosome region 17q24-q25. Genomics33:332-4 1996

PubMed ID: 8660991

Jones MH, Furlong RA, Burkin H, Chalmers IJ, Brown GM, Khwaja O, Affara NA, The Drosophila developmental gene fat facets has a human homologue in Xp11.4 which escapes X-inactivation and has related sequences on Yq11.2. Hum Mol Genet5(11):1695-701 1996

PubMed ID: 8922996

Junker S, Brondum-Nielsen K, Newell JW, Matthias P, Tommerup N, Assignment of the human gene for Oct-binding factor-1 (OBF1), a B-cell- specific coactivator of octamer-binding transcription factors 1 and 2, to 11q23.1 by somatic cell hybridization and in situ hybridization. Genomics33:143-5 1996

PubMed ID: 8617501

Kalz-Fuller B, Heidrich-Kaul C, Nothen M, Bause E, Schwanitz G, Localization of the human glucosidase I gene to chromosome 2p12-p13 by fluorescence in situ hybridization and PCR analysis of somatic cell hybrids. Genomics34:442-3 1996

PubMed ID: 8786151

Kekuda R, Prasad PD, Fei YJ, Torres-Zamorano V, Sinha S, Yang-Feng TL, Leibach FH, Ganapathy V, Cloning of the sodium-dependent, broad-scope, neutral amino acid transporter Bo from a human placental choriocarcinoma cell line. J Biol Chem271:18657-61 1996

PubMed ID: 8702519

Kokke FT, Elsawy T, Bengtsson U, Wasmuth JJ, Wang Jabs E, Tse CM, Donowitz M, Brant SR, A NHE3-related pseudogene is on human chromosome 10; the functional gene maps to 5p15.3. Mamm Genome7(3):235-6 1996

PubMed ID: 8833252

Kusuda J, Hidari N, Hirai M, Hashimoto K, Sequence analysis of the cDNA for the human casein kinase I delta (CSNK1D) gene and its chromosomal localization. Genomics32:140-3 1996

PubMed ID: 8786104

Lagercrantz J, Carson E, Larsson C, Nordenskjold M, Weber G, Isolation and characterization of a novel gene close to the human phosphoinositide-specific phospholipase C beta 3 gene on chromosomal region 11q13. Genomics31:380-4 1996

PubMed ID: 8838322

Leenders F, Prescher G, Dolez V, Begue A, de Launoit Y, Adamski J, Assignment of human 17 beta-hydroxysteroid dehydrogenase IV to chromosome 5q2 by fluorescence in situ hybridization. Genomics37:403-4 1996

PubMed ID: 8938456

Lench NJ, Telford EA, Andersen SE, Moynihan TP, Robinson PA, Markham AF, An EST and STS-based YAC contig map of human chromosome 9q22.3. Genomics38:199-205 1996

PubMed ID: 8954802

Li H, Lahti JM, Valentine M, Saito M, Reed SI, Look AT, Kidd VJ, Molecular cloning and chromosomal localization of the human cyclin C (CCNC) and cyclin E (CCNE) genes: deletion of the CCNC gene in human tumors. Genomics32:253-9 1996

PubMed ID: 8833152

Lomako J, Mazuruk K, Lomako WM, Alonso MD, Whelan WJ, Rodriguez IR, The human intron-containing gene for glycogenin maps to chromosome 3, band q24. Genomics33:519-22 1996

PubMed ID: 8661012

Ma T, Yang B, Kuo WL, Verkman AS, cDNA cloning and gene structure of a novel water channel expressed exclusively in human kidney: evidence for a gene cluster of aquaporins at chromosome locus 12q13. Genomics35:543-50 1996

PubMed ID: 8812490

Mao C, Baumgartner AP, Jha PK, Huang TH, Sarkar S, Assignment of the human fast skeletal troponin T gene (TNNT3) to chromosome 11p15.5: evidence for the presence of 11pter in a monochromosome 9 somatic cell hybrid in NIGMS mapping panel 2. Genomics31:385-8 1996

PubMed ID: 8838323

Margolis RL, Stine OC, McInnis MG, Ranen NG, Rubinsztein DC, Leggo J, Brando LV, Kidwai AS, Loev SJ, Breschel TS, Callahan C, Simpson SG, DePaulo JR, McMahon FJ, Jain S, Paykel ES, Walsh C, DeLisi LE, Crow TJ, Torrey EF, Ashworth RG, Macke JP, Nathans J, Ross CA, cDNA cloning of a human homologue of the Caenorhabditis elegans cell fate-determining gene mab-21: expression, chromosomal localization and analysis of a highly polymorphic (CAG)n trinucleotide repeat. Hum Mol Genet5:607-16 1996

PubMed ID: 8733127

Mattei MG, Borg JP, Rosnet O, Marme D, Birnbaum D, Assignment of vascular endothelial growth factor (VEGF) and placenta growth factor (PLGF) genes to human chromosome 6p12-p21 and 14q24-q31 regions, respectively. Genomics32:168-9 1996

PubMed ID: 8786112

Meese E, Gottert E, Zang KD, Sauter M, Schommer S, Mueller-Lantzsch N, Human endogenous retroviral element k10 (HERV-K10): chromosomal localization by somatic hybrid mapping and fluorescence in situ hybridization. Cytogenet Cell Genet72:40-2 1996

PubMed ID: 8565630

Miyagi Y, Yasumitsu H, Eki T, Miyata S, Kkawa N, Hirahara F, Aoki I, Misugi K, Miyazaki K, Assignment of the human PP5/TFPI-2 gene to 7q22 by FISH and PCR-based human/rodent cell hybrid mapping panel analysis. Genomics35:267-8 1996

PubMed ID: 8661135

Mock BA, Liu L, LePaslier D, Huang S, The B-lymphocyte maturation promoting transcription factor BLIMP1/PRDI- BF1 maps to D6S447 on human chromosome 6q21-q22.1 and the syntenic region of mouse chromosome 10. Genomics37:24-8 1996

PubMed ID: 8921366

Neri C, Albanese V, Lebre AS, Holbert S, Saada C, Bougueleret L, Meier-Ewert S, Le Gall I, Millasseau P, Bui H, Giudicelli C, Massart C, Guillou S, Gervy P, Poullier E, Rigault P, Weissenbach J, Lennon G, Chumakov I, Dausset J, Lehrach H, Cohen D, Cann HM, Survey of CAG/CTG repeats in human cDNAs representing new genes: candidates for inherited neurological disorders. Hum Mol Genet5:1001-9 1996

PubMed ID: 8817338

Nichols RC, Blinder J, Pai SI, Ge Q, Targoff IN, Plotz PH, Liu P, Assignment of two human autoantigen genes-isoleucyl-tRNA synthetase locates to 9q21 and lysyl-tRNA synthetase locates to 16q23-q24. Genomics36:210-3 1996

PubMed ID: 8812440

Riggins GJ, Thiagalingam S, Rozenblum E, Weinstein CL, Kern SE, Hamilton SR, Willson JK, Markowitz SD, Kinzler KW, Vogelstein B, Mad-related genes in the human. Nat Genet13:347-9 1996

PubMed ID: 8673135

Scherer SW, Duvoisin RM, Kuhn R, Heng HH, Belloni E, Tsui LC, Localization of two metabotropic glutamate receptor genes, GRM3 and GRM8, to human chromosome 7q. Genomics31:230-3 1996

PubMed ID: 8824806

Schultz D, Litt M, Smith L, Thayer M, McCormack K, Localization of two potassium channel beta subunit genes, KCNA1B and KCNA2B. Genomics31:389-91 1996

PubMed ID: 8838324

Simon A, Lagercrantz J, Bajalica-Lagercrantz S, Eriksson U, Primary structure of human 11-cis retinol dehydrogenase and organization and chromosomal localization of the corresponding gene. Genomics36:424-30 1996

PubMed ID: 8884265

Stafforini DM, Satoh K, Atkinson DL, Tjoelker LW, Eberhardt C, Yoshida H, Imaizumi T, Takamatsu S, Zimmerman GA, McIntyre TM, Gray PW, Prescott SM, Platelet-activating factor acetylhydrolase deficiency. A missense mutation near the active site of an anti-inflammatory phospholipase. J Clin Invest97(12):2784-91 1996

PubMed ID: 8675689

Stewart AF, Richard CW 3rd, Suzow J, Stephan D, Weremowicz S, Morton CC, Adra CN, Cloning of human RTEF-1, a transcriptional enhancer factor-1-related gene preferentially expressed in skeletal muscle: evidence for an ancient multigene family. Genomics37:68-76 1996

PubMed ID: 8921372

Sunden SL, Businga T, Beck J, McClain A, Gastier JM, Pulido JC, Yandava CN, Brody T, Ghazizadeh J, Weber JL, Duyk GM, Murray JC, Buetow KH, Sheffield VC, Chromosomal assignment of 2900 tri- and tetranucleotide repeat markers using NIGMS somatic cell hybrid panel 2. Genomics32:15-20 1996

PubMed ID: 8786107

Sunden SLF, Carr LL, Clements JL, Motto DG, Koretzky GA, Polymorphism in and localization of the gene LCP2 (SLP-76) to chromosome 5q33.1-qter. Genomics35:269-70 1996

PubMed ID: 8661136

Tamimi R, Steingrimsson E, Copeland NG, Dyer-Montgomery K, Lee JE, Hernandez R, Jenkins NA, Tapscott SJ, The NEUROD gene maps to human chromosome 2q32 and mouse chromosome 2. Genomics34:418-21 1996

PubMed ID: 8786144

Thibonnier M, Graves MK, Wagner MS, Auzan C, Clauser E, Willard HF, Structure, sequence, expression, and chromosomal localization of the human V1a vasopressin receptor gene. Genomics31:327-34 1996

PubMed ID: 8838314

Vocero-Akbani A, Helms C, Wang JC, Sanjurjo FJ, Korte-Sarfaty J, Veile RA, Liu L, Jauch A, Burgess AK, Hing AV, Holt MS, Ramachandra S, Whelan AJ, Anker R, Ahrent L, Chen M, Gavin MR, Iannantuoni K, Morton SM, Pandit SD, Read CM, Steinbrueck T, Warlick C, Smoller DA, Donis-Keller H, Mapping human telomere regions with YAC and P1 clones: chromosome- specific markers for 27 telomeres including 149 STSs and 24 polymorphisms for 14 proterminal regions. Genomics36:492-506 1996

PubMed ID: 8884273

Watson B Jr, Bergman SM, Myracle A, Callen DF, Acton RT, Warnock DG, Genetic association of 11 beta-hydroxysteroid dehydrogenase type 2 (HSD11B2) flanking microsatellites with essential hypertension in blacks. Hypertension28(3):478-82 1996

PubMed ID: 8794836

White RA, Hughes RT, Adkison LR, Bruns G, Zon LI, The gene encoding protein kinase SEK1 maps to mouse chromosome 11 and human chromosome 17. Genomics34:430-2 1996

PubMed ID: 8786147

Yasuda J, Navarro JM, Malkhosyan S, Velazquez A, Arribas R, Sekiya T, Perucho M, Chromosomal assignment of human DNA fingerprint sequences by simultaneous hybridization to arbitrarily primed PCR products from human/rodent monochromosome cell hybrids. Genomics34:1-8 1996

PubMed ID: 8661018

Yu F, Warburton D, Wellington S, Danziger RS, Assignment of GUCIA2, the gene coding for the alpha 2 subunit of soluble guanylyl cyclase, to position 11q21-q22 on human chromosome 11. Genomics33:334-6 1996

PubMed ID: 8660992

Angrist M, Wells DE, Chakravarti A, Pandey A, Chromosomal localization of the mouse Src-like adapter protein (Slap) gene and its putative human homolog SLA. Genomics30:623-5 1995

PubMed ID: 8825655

Avraham S, Jiang S, Ota S, Fu Y, Deng B, Dowler LL, White RA, Avraham H, Structural and functional studies of the intracellular tyrosine kinase MATK gene and its translated product. J Biol Chem270:1833-42 1995

PubMed ID: 7530249

Bailey A, Norris AL, Leek JP, Clissold PM, Carr IM, Ogilvie DJ, Morrison JF, Meredith DM, Markham AF, Yeast artificial chromosome cloning of the beta-catenin locus on human chromosome 3p21-22. Chromosome Res3:201-3 1995

PubMed ID: 7780664

Bloch KD, Wolfram JR, Brown DM, Roberts JD Jr, Zapol DG, Lepore JJ, Filippov G, Thomas JE, Jacob HJ, Bloch DB, Three members of the nitric oxide synthase II gene family (NOS2A, NOS2B, and NOS2C) colocalize to human chromosome 17. Genomics27:526-30 1995

PubMed ID: 7558036

Campion D, Martin C, Heilig R, Charbonnier F, Moreau V, Flaman JM, Petit JL, Hannequin D, Brice A, Frebourg T, The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer disease. Genomics26:254-7 1995

PubMed ID: 7601450

Chakravarti S, Stallings RL, SundarRaj N, Cornuet PK, Hassell JR, Primary structure of human lumican (keratan sulfate proteoglycan) and localization of the gene (LUM) to chromosome 12q21.3-q22. Genomics27:481-8 1995

PubMed ID: 7558030

Chen H, Leipprandt JR, Traviss CE, Sopher BL, Jones MZ, Cavanagh KT, Friderici KH, Molecular cloning and characterization of bovine beta-mannosidase. J Biol Chem270(8):3841-8 1995

PubMed ID: 7876128

Chiang PW, Dzida G, Grumet J, Cheng JF, Song WJ, Crombez E, Van Keuren ML, Kurnit DM, Expressed sequence tags from the long arm of human chromosome 21. Genomics29:383-9 1995

PubMed ID: 8666385

Chu W, Burns DK, Swerlick RA, Presky DH, Identification and characterization of a novel cytokine-inducible nuclear protein from human endothelial cells. J Biol Chem270(17):10236-45 1995

PubMed ID: 7730328

el-Maghrabi MR, Lange AJ, Jiang W, Yamagata K, Stoffel M, Takeda J, Fernald AA, Le Beau MM, Bell GI, Baker L, et al, Human fructose-1,6-bisphosphatase gene (FBP1): exon-intron organization, localization to chromosome bands 9q22.2-q22.3, and mutation screening in subjects with fructose-1,6-bisphosphatase deficiency. Genomics27:520-5 1995

PubMed ID: 7558035

Gastier JM, Pulido JC, Sunden S, Brody T, Buetow KH, Murray JC, Weber JL, Hudson TJ, Sheffield VC, Duyk GM, Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markers. Hum Mol Genet4:1829-36 1995

PubMed ID: 8595403

Gelernter J, Rao PA, Pauls DL, Hamblin MW, Sibley DR, Kidd KK, Assignment of the 5HT7 receptor gene (HTR7) to chromosome 10q and exclusion of genetic linkage with Tourette syndrome. Genomics26:207-9 1995

PubMed ID: 7601444

Gimbel W, Klein V, Brass N, Fischer U, Piontek K, Overmyer K, Gottert E, Zang KD, Meese E, Isolation and localization of transcribed sequences on human chromosome 22. Cytogenet Cell Genet71:81-5 1995

PubMed ID: 7606934

Henning KA, Li L, Iyer N, McDaniel LD, Reagan MS, Legerski R, Schultz RA, Stefanini M, Lehmann AR, Mayne LV, et al, The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH. Cell82:555-64 1995

PubMed ID: 7664335

Heppell-Parton A, Cahn A, Bench A, Lowe N, Lehrach H, Zehetner G, Rabbitts P, Thioredoxin, a mediator of growth inhibition, maps to 9q31. Genomics26:379-81 1995

PubMed ID: 7601465

Hunt CC, Eyre HJ, Akkari PA, Meredith C, Dorosz SM, Wilton SD, Callen DF, Laing NG, Baker E, Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation. Cytogenet Cell Genet71:94-5 1995

PubMed ID: 7606936

Johnson DW, Qumsiyeh M, Benkhalifa M, Marchuk DA, Assignment of human transforming growth factor-beta type I and type III receptor genes (TGFBR1 and TGFBR3) to 9q33-q34 and 1p32-p33, respectively. Genomics28:356-7 1995

PubMed ID: 8530052

Khanna M, Qin KN, Klisak I, Belkin S, Sparkes RS, Cheng KC, Localization of multiple human dihydrodiol dehydrogenase (DDH1 and DDH2) and chlordecone reductase (CHDR) genes in chromosome 10 by the polymerase chain reaction and fluorescence in situ hybridization. Genomics25:588-90 1995

PubMed ID: 7789999

Kiefer MC, Brauer MJ, Powers VC, Wu JJ, Umansky SR, Tomei LD, Barr PJ, Modulation of apoptosis by the widely distributed Bcl-2 homologue Bak. Nature374:736-9 1995

PubMed ID: 7715731

Klanke CA, Su YR, Callen DF, Wang Z, Meneton P, Baird N, Kandasamy RA, Orlowski J, Otterud BE, Leppert M, et al, Molecular cloning and physical and genetic mapping of a novel human Na+/H+ exchanger (NHE5/SLC9A5) to chromosome 16q22.1. Genomics25:615-22 1995

PubMed ID: 7759094

Koehler MR, Bosserhoff A, von Beust G, Bauer A, Blesch A, Buettner R, Schlegel J, Bogdahn U, Schmid M, Assignment of the human melanoma inhibitory activity gene (MIA) to 19q13.32-q13.33 by fluorescence in situ hybridization (FISH). Genomics35:265-7 1995

PubMed ID: 8661134

Kuo WL, Stafford DW, Cruces J, Gray J, Solera J, Chromosomal localization of the gamma-glutamyl carboxylase gene at 2p12. Genomics25:746-8 1995

PubMed ID: 7759116

Kusuda J, Tanuma R, Gotoh E, Toyoda A, Hashimoto K, Assignment of a human autoimmune antigen, p80-coilin gene to chromosome 17q21-q23 and of its possible pseudogene to chromosome 14. Hum Genet95:233-4 1995

PubMed ID: 7860074

Larsson C, Hellqvist M, Pierrou S, White I, Enerback S, Carlsson P, Chromosomal localization of six human forkhead genes, freac-1 (FKHL5), - 3 (FKHL7), -4 (FKHL8), -5 (FKHL9), -6 (FKHL10), and -8 (FKHL12). Genomics30:464-9 1995

PubMed ID: 8825632

Larsson C, Lardelli M, White I, Lendahl U, The human NOTCH1, 2, and 3 genes are located at chromosome positions 9q34, 1p13-p11, and 19p13.2-p13.1 in regions of neoplasia-associated translocation. Genomics24:253-8 1995

PubMed ID: 7698746

Larsson C, White I, Johansson C, Stark A, Meijer J, Localization of the human soluble epoxide hydrolase gene (EPHX2) to chromosomal region 8p21-p12. Hum Genet95:356-8 1995

PubMed ID: 7868134

Lee D, Szumlanski C, Houtman J, Honchel R, Rojas K, Overhauser J, Wieben ED, Weinshilboum RM, Thiopurine methyltransferase pharmacogenetics. Cloning of human liver cDNA and a processed pseudogene on human chromosome 18q21.1. Drug Metab Dispos23:398-405 1995

PubMed ID: 7628307

Li J, Ma J, Potter H, Identification and expression analysis of a potential familial Alzheimer disease gene on chromosome 1 related to AD3. Proc Natl Acad Sci U S A92:12180-4 1995

PubMed ID: 8618867

Liu J, Fujiwara TM, Buu NT, Sanchez FO, Cellier M, Paradis AJ, Frappier D, Skamene E, Gros P, Morgan K, et al, Identification of polymorphisms and sequence variants in the human homologue of the mouse natural resistance-associated macrophage protein gene. Am J Hum Genet56:845-53 1995

PubMed ID: 7717395

Marigo V, Roberts DJ, Lee SM, Tsukurov O, Levi T, Gastier JM, Epstein DJ, Gilbert DJ, Copeland NG, Seidman CE, et al, Cloning, expression, and chromosomal location of SHH and IHH: two human homologues of the Drosophila segment polarity gene hedgehog. Genomics28:44-51 1995

PubMed ID: 7590746

Moghrabi NN, Dawson DB, Bennett MJ, Assignment of the human peroxisomal palmitoyl-CoA oxidase gene to chromosome 17q23-qter by PCR technique. J Inherit Metab Dis18:705-9 1995

PubMed ID: 8750608

Monitto CL, Levitt RC, DiSilvestre D, Holroyd KJ, Localization of the A3 adenosine receptor gene (ADORA3) to human chromosome 1p. Genomics26:637-8 1995

PubMed ID: 7607699

Nichols RC, Pai SI, Ge Q, Targoff IN, Plotz PH, Liu P, Localization of two human autoantigen genes by PCR screening and in situ hybridization--glycyl-tRNA synthetase locates to 7p15 and alanyl- tRNA synthetase locates to 16q22. Genomics30:131-2 1995

PubMed ID: 8595897

Otterness DM, Mohrenweiser HW, Brandriff BF, Weinshilboum RM, Dehydroepiandrosterone sulfotransferase gene (STD): localization to human chromosome band 19q13.3. Cytogenet Cell Genet70:45-7 1995

PubMed ID: 7736787

Piontek K, Muller HW, Fischer U, Gottert E, Batzer MA, Meltzer PS, Trent JM, Meese E, Generation and characterization of a human chromosome 6-specific hncDNA library from a somatic cell hybrid. Cytogenet Cell Genet69:273-8 1995

PubMed ID: 7698027

Purandare SM, Huntsman Breidenbach H, Li Y, Zhu XL, Sawada S, Neil SM, Brothman A, White R, Cawthon R, Viskochil D, Identification of neurofibromatosis 1 (NF1) homologous loci by direct sequencing, fluorescence in situ hybridization, and PCR amplification of somatic cell hybrids. Genomics30:476-85 1995

PubMed ID: 8825634

Robinson PA, Leek JP, Thompson J, Carr IM, Bailey A, Moynihan TP, Coletta PL, Lench NJ, Markham AF, A human ubiquitin conjugating enzyme, L-UBC, maps in the Alzheimer's disease locus on chromosome 14q24.3. Mamm Genome6:725-31 1995

PubMed ID: 8563171

Sheffield VC, Weber JL, Buetow KH, Murray JC, Even DA, Wiles K, Gastier JM, Pulido JC, Yandava C, Sunden SL, et al, A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps. Hum Mol Genet4:1837-44 1995

PubMed ID: 8595404

Simmons CF Jr, Clancy TE, Quan R, Knoll JH, The oxytocin receptor gene (OXTR) localizes to human chromosome 3p25 by fluorescence in situ hybridization and PCR analysis of somatic cell hybrids. Genomics26:623-5 1995

PubMed ID: 7607693

Slaugenhaupt SA, Roca AL, Liebert CB, Altherr MR, Gusella JF, Reppert SM, Mapping of the gene for the Mel1a-melatonin receptor to human chromosome 4 (MTNR1A) and mouse chromosome 8 (Mtnr1a). Genomics27:355-7 1995

PubMed ID: 7558006

Starborg M, Brundell E, Gell K, Larsson C, White I, Daneholt B, Hoog C, A murine replication protein accumulates temporarily in the heterochromatic regions of nuclei prior to initiation of DNA replication. J Cell Sci108 ( Pt 3):927-34 1995

PubMed ID: 7622621

Steinkasserer A, Jones T, Sheer D, Koettnitz K, Hauber J, Bevec D, The eukaryotic cofactor for the human immunodeficiency virus type 1 (HIV-1) rev protein, eIF-5A, maps to chromosome 17p12-p13: three eIF-5A pseudogenes map to 10q23.3, 17q25, and 19q13.2. Genomics25:749-52 1995

PubMed ID: 7759117

Stirling B, Cox NJ, Bell GI, Hanis CL, Spielman RS, Concannon P, Identification of microsatellite markers near the human ob gene and linkage studies in NIDDM-affected sib pairs. Diabetes44(8):999-1001 1995

PubMed ID: 7622007

Stoffel M, Stein R, Wright CV, Espinosa R 3rd, Le Beau MM, Bell GI, Localization of human homeodomain transcription factor insulin promoter factor 1 (IPF1) to chromosome band 13q12.1. Genomics28:125-6 1995

PubMed ID: 7590740

Takeda J, Espinosa R 3rd, Eng S, Le Beau MM, Bell GI, Chromosomal assignment and tissue distribution of novel expressed sequence tags from a human pancreatic islet cDNA library. Genomics29:276-81 1995

PubMed ID: 8530086

Tan KL, Webb GC, Baker RT, Board PG, Molecular cloning of a cDNA and chromosomal localization of a human theta-class glutathione S-transferase gene (GSTT2) to chromosome 22. Genomics25:381-7 1995

PubMed ID: 7789971

Tirosvoutis KN, Divane A, Jones M, Affara NA, Characterization of a novel zinc finger gene (ZNF165) mapping to 6p21 that is expressed specifically in testis. Genomics28:485-90 1995

PubMed ID: 7490084

Tsaur ML, Menzel S, Lai FP, Espinosa R 3rd, Concannon P, Spielman RS, Hanis CL, Cox NJ, Le Beau MM, German MS, et al, Isolation of a cDNA clone encoding a KATP channel-like protein expressed in insulin-secreting cells, localization of the human gene to chromosome band 21q22.1, and linkage studies with NIDDM. Diabetes44(5):592-6 1995

PubMed ID: 7729621

Tucker SJ, James MR, Adelman JP, Assignment of KATP-1, the cardiac ATP-sensitive potassium channel gene (KCNJ5), to human chromosome 11q24. Genomics28:127-8 1995

PubMed ID: 7590741

Warner JP, Leek JP, Intody S, Markham AF, Bonthron DT, Human glucokinase regulatory protein (GCKR): cDNA and genomic cloning, complete primary structure, and chromosomal localization. Mamm Genome6:532-6 1995

PubMed ID: 8589523

Webb GC, Vaska VL, Gali RR, Ford JH, Board PG, The gene encoding human glutathione synthetase (GSS) maps to the long arm of chromosome 20 at band 11.2. Genomics30:617-9 1995

PubMed ID: 8825653

White RA, Angeloni SV, Pasztor LM, Chromosomal localization of the beta-adducin gene to mouse chromosome 6 and human chromosome 2. Mamm Genome6:741-3 1995

PubMed ID: 8563174

White RA, Dowler LL, Angeloni SV, Pasztor LM, MacArthur CA, Assignment of FGF8 to human chromosome 10q25-q26: mutations in FGF8 may be responsible for some types of acrocephalosyndactyly linked to this region. Genomics30:109-11 1995

PubMed ID: 8595889

White RA, Dowler LL, Pasztor LM, Gatson LL, Adkison LR, Angeloni SV, Wilson DB, Assignment of the transcription factor GATA4 gene to human chromosome 8 and mouse chromosome 14: Gata4 is a candidate gene for Ds (disorganization). Genomics27:20-6 1995

PubMed ID: 7665171

Whitmore TE, Day JR, Albers JJ, Localization of the human phospholipid transfer protein gene to chromosome 20q12-q13.1. Genomics28:599-600 1995

PubMed ID: 7490104

Willenbrink W, Halaschek J, Schuffenhauer S, Kunz J, Steinkasserer A, Cyclophilin A, the major intracellular receptor for the immunosuppressant cyclosporin A, maps to chromosome 7p11.2-p13: four pseudogenes map to chromosomes 3, 10, 14, and 18. Genomics28:101-4 1995

PubMed ID: 7590732

Yang B, Ma T, Verkman AS, cDNA cloning, gene organization, and chromosomal localization of a human mercurial insensitive water channel. Evidence for distinct transcriptional units. J Biol Chem270:22907-13 1995

PubMed ID: 7559426

Aksoy IA, Callen DF, Apostolou S, Her C, Weinshilboum RM, Thermolabile phenol sulfotransferase gene (STM): localization to human chromosome 16p11.2. Genomics23:275-7 1994

PubMed ID: 7829089

Allander SV, Larsson C, Ehrenborg E, Suwanichkul A, Weber G, Morris SL, Bajalica S, Kiefer MC, Luthman H, Powell DR, Characterization of the chromosomal gene and promoter for human insulin- like growth factor binding protein-5. J Biol Chem269:10891-8 1994

PubMed ID: 7511611

Blachly-Dyson E, Baldini A, Litt M, McCabe ER, Forte M, Human genes encoding the voltage-dependent anion channel (VDAC) of the outer mitochondrial membrane: mapping and identification of two new isoforms. Genomics20:62-7 1994

PubMed ID: 7517385

Bronner CE, Baker SM, Morrison PT, Warren G, Smith LG, Lescoe MK, Kane M, Earabino C, Lipford J, Lindblom A, et al, Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer. Nature368:258-61 1994

PubMed ID: 8145827

Brown A, Lemieux N, Rossant J, Kothary R, Human homolog of a mouse sequence from the dystonia musculorum locus is on chromosome 6p12. Mamm Genome5:434-7 1994

PubMed ID: 7919656

Chang MS, McNinch J, Basu R, Simonet S, Cloning and characterization of the human neutrophil-activating peptide (ENA-78) gene. J Biol Chem269:25277-82 1994

PubMed ID: 7929219

Day JR, Albers JJ, Gilbert TL, Whitmore TE, McConathy WJ, Wolfbauer G, Purification and molecular cloning of human apolipoprotein F. Biochem Biophys Res Commun203:1146-51 1994

PubMed ID: 8093033

Day JR, Albers JJ, Lofton-Day CE, Gilbert TL, Ching AF, Grant FJ, O'Hara PJ, Marcovina SM, Adolphson JL, Complete cDNA encoding human phospholipid transfer protein from human endothelial cells. J Biol Chem269:9388-91 1994

PubMed ID: 8132678

Engle LJ, Kennett RH, Cloning, analysis, and chromosomal localization of myoxin (MYH12), the human homologue to the mouse dilute gene. Genomics19:407-16 1994

PubMed ID: 8188282

Hanes J, von der Kammer H, Klaudiny J, Scheit KH, Characterization by cDNA cloning of two new human protein kinases. Evidence by sequence comparison of a new family of mammalian protein kinases. J Mol Biol244:665-72 1994

PubMed ID: 7990150

Hough MR, Rosten PM, Sexton TL, Kay R, Humphries RK, Mapping of CD24 and homologous sequences to multiple chromosomal loci. Genomics22:154-61 1994

PubMed ID: 7959762

Koppel DA, Wolfe SA, Fogelfeld LA, Merchant PS, Prouty L, Grimes SR, Primate testicular histone H1t genes are highly conserved and the human H1t gene is located on chromosome 6. J Cell Biochem54:219-30 1994

PubMed ID: 8175896

Kos CH, Tihy F, Econs MJ, Murer H, Lemieux N, Tenenhouse HS, Localization of a renal sodium-phosphate cotransporter gene to human chromosome 5q35. Genomics19:176-7 1994

PubMed ID: 8188224

Kuestner RE, Elrod RD, Grant FJ, Hagen FS, Kuijper JL, Matthewes SL, O'Hara PJ, Sheppard PO, Stroop SD, Thompson DL, et al, Cloning and characterization of an abundant subtype of the human calcitonin receptor. Mol Pharmacol46:246-55 1994

PubMed ID: 8078488

Kutty RK, Kutty G, Rodriguez IR, Chader GJ, Wiggert B, Chromosomal localization of the human heme oxygenase genes: heme oxygenase-1 (HMOX1) maps to chromosome 22q12 and heme oxygenase-2 (HMOX2) maps to chromosome 16p13.3. Genomics20:513-6 1994

PubMed ID: 8034330

Laliberte J, Momparler RL, Human cytidine deaminase: purification of enzyme, cloning, and expression of its complementary DNA. Cancer Res54:5401-7 1994

PubMed ID: 7923172

Leach RJ, Reus BE, Hundley JE, Johnson-Pais TL, Windle JJ, Confirmation of the assignment of the human tartrate-resistant acid phosphatase gene (ACP5) to chromosome 19. Genomics19:180-1 1994

PubMed ID: 8188227

MacCollin M, Peterfreund R, MacDonald M, Fink JS, Gusella J, Mapping of a human A2a adenosine receptor (ADORA2) to chromosome 22. Genomics20:332-3 1994

PubMed ID: 8020991

Macina RA, Negorev DG, Spais C, Ruthig LA, Hu XL, Riethman HC, Sequence organization of the human chromosome 2q telomere. Hum Mol Genet3:1847-53 1994

PubMed ID: 7545974

Malo MS, Srivastava K, Andresen JM, Chen XN, Korenberg JR, Ingram VM, Targeted gene walking by low stringency polymerase chain reaction: assignment of a putative human brain sodium channel gene (SCN3A) to chromosome 2q24-31. Proc Natl Acad Sci U S A91:2975-9 1994

PubMed ID: 8159690

McGregor LM, Baylin SB, Griffin CA, Hawkins AL, Nelkin BD, Molecular cloning of the cDNA for human TrkC (NTRK3), chromosomal assignment, and evidence for a splice variant. Genomics22:267-72 1994

PubMed ID: 7806211

McPherson JD, Morton RA, Ewing CM, Wasmuth JJ, Overhauser J, Nagafuchi A, Tsukita S, Isaacs WB, Assignment of the human alpha-catenin gene (CTNNA1) to chromosome 5q21- q22. Genomics19:188-90 1994

PubMed ID: 8188230

Negorev DG, Macina RA, Spais C, Ruthig LA, Hu XL, Riethman HC, Physical analysis of the terminal 270 kb of DNA from human chromosome 1q. Genomics22:569-78 1994

PubMed ID: 8001968

Nomura N, Miyajima N, Sazuka T, Tanaka A, Kawarabayasi Y, Sato S, Nagase T, Seki N, Ishikawa K, Tabata S, Prediction of the coding sequences of unidentified human genes. I. The coding sequences of 40 new genes (KIAA0001-KIAA0040) deduced by analysis of randomly sampled cDNA clones from human immature myeloid cell line KG-1 [published erratum appears in DNA Res 1995 Aug 31;2(4):211] DNA Res1:27-35 1994

PubMed ID: 7584026

Paschen W, Blackstone CD, Huganir RL, Ross CA, Human GluR6 kainate receptor (GRIK2): molecular cloning, expression, polymorphism, and chromosomal assignment. Genomics20:435-40 1994

PubMed ID: 8034316

Perfetti R, Hawkins AL, Griffin CA, Egan JM, Zenilman ME, Shuldiner AR, Assignment of the human pancreatic regenerating (REG) gene to chromosome 2p12. Genomics20:305-7 1994

PubMed ID: 8020983

Sakai J, Hoshino A, Takahashi S, Miura Y, Ishii H, Suzuki H, Kawarabayasi Y, Yamamoto T, Structure, chromosome location, and expression of the human very low density lipoprotein receptor gene. J Biol Chem269:2173-82 1994

PubMed ID: 8294473

Seki M, Miyazawa H, Tada S, Yanagisawa J, Yamaoka T, Hoshino S, Ozawa K, Eki T, Nogami M, Okumura K, et al, Molecular cloning of cDNA encoding human DNA helicase Q1 which has homology to Escherichia coli Rec Q helicase and localization of the gene at chromosome 12p12. Nucleic Acids Res22:4566-73 1994

PubMed ID: 7527136

Stoffel M, Espinosa R 3rd, Powell KL, Philipson LH, Le Beau MM, Bell GI, Human G-protein-coupled inwardly rectifying potassium channel (GIRK1) gene (KCNJ3): localization to chromosome 2 and identification of a simple tandem repeat polymorphism. Genomics21:254-6 1994

PubMed ID: 8088798

Su YR, Klanke CA, Houseal TW, Linn SC, Burk SE, Varvil TS, Otterud BE, Shull GE, Leppert MF, Menon AG, Molecular cloning and physical and genetic mapping of the human anion exchanger isoform 3 (SLC2C) gene to chromosome 2q36. Genomics22:605-9 1994

PubMed ID: 8001971

Tombran-Tink J, Pawar H, Swaroop A, Rodriguez I, Chader GJ, Localization of the gene for pigment epithelium-derived factor (PEDF) to chromosome 17p13.1 and expression in cultured human retinoblastoma cells. Genomics19:266-72 1994

PubMed ID: 8188257

Tomlinson IM, Cook GP, Carter NP, Elaswarapu R, Smith S, Walter G, Buluwela L, Rabbitts TH, Winter G, Human immunoglobulin VH and D segments on chromosomes 15q11.2 and 16p11.2. Hum Mol Genet3:853-60 1994

PubMed ID: 7951227

Uetz P, Abdelatty F, Villarroel A, Rappold G, Weiss B, Koenen M, Organisation of the murine 5-HT3 receptor gene and assignment to human chromosome 11. FEBS Lett339:302-6 1994

PubMed ID: 8112471

Vamvakopoulos NC, Kunz J, Olberding U, Scherer SW, Sioutopoulou TO, Schneider V, Durkin AS, Nierman WC, Mapping the human growth hormone-releasing hormone receptor (GHRHR) gene to the short arm of chromosome 7 (7p13-p21) near the epidermal growth factor receptor (EGFR) gene. Genomics20:338-40 1994

PubMed ID: 8020995

von der Kammer, The gene for the amyloid precursor-like protein APLP2 is assigned to human chromosome 11q23-q25. Genomics10:308 (1994):338-40 1994

PubMed ID: 8020995

Webb GC, Baker RT, Coggan M, Board PG, Localization of the human UBA52 ubiquitin fusion gene to chromosome band 19p13.1-p12. Genomics19:567-9 1994

PubMed ID: 8188300

Weber G, Friedman E, Grimmond S, Hayward NK, Phelan C, Skogseid B, Gobl A, Zedenius J, Sandelin K, Teh BT, et al, The phospholipase C beta 3 gene located in the MEN1 region shows loss of expression in endocrine tumours. Hum Mol Genet3:1775-81 1994

PubMed ID: 7849701

Yandava CN, Meyers V, Watkins H, Duyk G, A trinucleotide repeat polymorphism in XT00444 (D13S635E). Hum Mol Genet3:1209 1994

PubMed ID: 7981706

Yasuda K, Espinosa R 3rd, Takeda J, Le Beau MM, Bell GI, Localization of the kappa opioid receptor gene to human chromosome band 8q11.2. Genomics19:596-7 1994

PubMed ID: 8188308

Chen H, Kalaitsidaki M, Warren AC, Avramopoulos D, Antonarakis SE, A novel zinc finger cDNA with a polymorphic pentanucleotide repeat (ATTTT)n maps on human chromosome 19p. Genomics15:621-5 1993

PubMed ID: 8468057

Dixon B, Mansour M, Pohajdak B, Assignment of human B2-1 gene (D17S811E) to chromosome 17qter by PCR analysis of somatic cell hybrids and fluorescence in situ hybridization. Cytogenet Cell Genet63:42-4 1993

PubMed ID: 8449036

Drwinga HL, Toji LH, Kim CH, Greene AE, Mulivor RA, NIGMS human/rodent somatic cell hybrid mapping panels 1 and 2. Genomics16:311-4 1993

PubMed ID: 8314568

Dubois BL, Naylor SL, Characterization of NIGMS human/rodent somatic cell hybrid mapping panel 2 by PCR. Genomics16:315-9 1993

PubMed ID: 8314569

Durkin AS, Maglott DR, Vamvakopoulos NC, Zoghbi HY, Nierman WC, Assignment of an intron-containing human heat-shock protein gene (hsp90 beta, HSPCB) to chromosome 6 near TCTE1 (6p21) and two intronless pseudogenes to chromosomes 4 and 15 by polymerase chain reaction amplification from a panel of hybrid cell lines. Genomics18:452-4 1993

PubMed ID: 8288256

Fishel R, Lescoe MK, Rao MR, Copeland NG, Jenkins NA, Garber J, Kane M, Kolodner R, The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer [published erratum appears in Cell 1994 Apr 8;77(1):167] Cell75:1027-38 1993

PubMed ID: 8252616

Gregor P, Reeves RH, Jabs EW, Yang X, Dackowski W, Rochelle JM, Brown RH Jr, Haines JL, O'Hara BF, Uhl GR, et al, Chromosomal localization of glutamate receptor genes: relationship to familial amyotrophic lateral sclerosis and other neurological disorders of mice and humans. Proc Natl Acad Sci U S A90:3053-7 1993

PubMed ID: 8464923

Jabs EW, Muller U, Li X, Ma L, Luo W, Haworth IS, Klisak I, Sparkes R, Warman ML, Mulliken JB, et al, A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis. Cell75:443-50 1993

PubMed ID: 8106171

Lane SA, Baker E, Sutherland GR, Tonks I, Hayward N, Ellem K, The human cell cycle gene CDC25B is located at 20p13. Genomics15:693-4 1993

PubMed ID: 8468065

Li SH, McInnis MG, Margolis RL, Antonarakis SE, Ross CA, Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms. Genomics16:572-9 1993

PubMed ID: 8325628

McClatchey AI, Cannon SC, Slaugenhaupt SA, Gusella JF, The cloning and expression of a sodium channel beta 1-subunit cDNA from human brain. Hum Mol Genet2:745-9 1993

PubMed ID: 8394762

Myers JC, Sun MJ, D'Ippolito JA, Jabs EW, Neilson EG, Dion AS, Human cDNA clones transcribed from an unusually high-molecular-weight RNA encode a new collagen chain. Gene123:211-7 1993

PubMed ID: 7916703

Nagao Y, Platero JS, Waheed A, Sly WS, Human mitochondrial carbonic anhydrase: cDNA cloning, expression, subcellular localization, and mapping to chromosome 16. Proc Natl Acad Sci U S A90:7623-7 1993

PubMed ID: 8356065

Okuyama T, Batanian JR, Sly WS, Genomic organization and localization of gene for human carbonic anhydrase IV to chromosome 17q. Genomics16:678-84 1993

PubMed ID: 8325641

Puranam RS, Eubanks JH, Heinemann SF, McNamara JO, Chromosomal localization of gene for human glutamate receptor subunit-7. Somat Cell Mol Genet19:581-8 1993

PubMed ID: 8128318

Ramesh N, Ramesh V, Gusella JF, Geha R, Chromosomal localization of the gene for human B-cell antigen CD40. Somat Cell Mol Genet19:295-8 1993

PubMed ID: 7687385

Riethman HC, Spais C, Buckingham J, Grady D, Moyzis RK, Physical analysis of the terminal 240 kb of DNA from human chromosome 7q. Genomics17:25-32 1993

PubMed ID: 8406463

Shipley JM, Klinkenberg M, Wu BM, Bachinsky DR, Grubb JH, Sly WS, Mutational analysis of a patient with mucopolysaccharidosis type VII, and identification of pseudogenes. Am J Hum Genet52:517-26 1993

PubMed ID: 7680524

Surratt CK, Persico AM, Yang XD, Edgar SR, Bird GS, Hawkins AL, Griffin CA, Li X, Jabs EW, Uhl GR, A human synaptic vesicle monoamine transporter cDNA predicts posttranslational modifications, reveals chromosome 10 gene localization and identifies TaqI RFLPs. FEBS Lett318:325-30 1993

PubMed ID: 8095030

Talbot CC Jr, Warren AC, Avramopoulos D, Antonarakis SE, Polymorphic dinucleotide repeats at the D3S1417, D3S1418 and D12S271 loci. Hum Mol Genet2:1325 1993

PubMed ID: 8401519

Virtaneva KI, Angelisova P, Baumruker T, Horejsi V, Nevanlinna H, Schroder J, The genes for CD37, CD53, and R2, all members of a novel gene family, are located on different chromosomes. Immunogenetics37:461-5 1993

PubMed ID: 8436422

Westberg JA, Entler B, Prohaska R, Schroder JP, The gene coding for erythrocyte protein band 7.2b (EPB72) is located in band q34.1 of human chromosome 9. Cytogenet Cell Genet63:241-3 1993

PubMed ID: 8500356

Chen H, Phillips HA, Callen DF, Kim RY, Wistow GJ, Antonarakis SE, Localization of the human gene for mu-crystallin to chromosome 16p. Genomics14:1115-6 1992

PubMed ID: 1478656

Hudson TJ, Engelstein M, Lee MK, Ho EC, Rubenfield MJ, Adams CP, Housman DE, Dracopoli NC, Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms. Genomics13:622-9 1992

PubMed ID: 1639389

Peinado MA, Malkhosyan S, Velazquez A, Perucho M, Isolation and characterization of allelic losses and gains in colorectal tumors by arbitrarily primed polymerase chain reaction. Proc Natl Acad Sci U S A89:10065-9 1992

PubMed ID: 1359533

Tsai SP, Drayna D, The gene encoding human plasma carboxypeptidase B (CPB2) resides on chromosome 13. Genomics14:549-50 1992

PubMed ID: 1427879

Vandenbergh DJ, Persico AM, Hawkins AL, Griffin CA, Li X, Jabs EW, Uhl GR, Human dopamine transporter gene (DAT1) maps to chromosome 5p15.3 and displays a VNTR. Genomics14:1104-6 1992

PubMed ID: 1478653

Description: NIGMS HUMAN/RODENT SOMATIC CELL HYBRID MAPPING PANEL #2 DNA

Aliquot Size: 50 µg each