
|
Aalto Y, Nordling S, Kivioja AH, Karaharju E, Elomaa I, Knuutila S: Among numerous DNA copy number changes, losses of chromosome 13 are highly recurrent in plasmacytoma. Genes Chromosom Cancer 25:104-107 (1999). Agarwal SK, Schrock E, Kester MB, Burns AL, Heffess CS, Ried T, Marx SJ: Comparative genomic hybridization analysis of human parathyroid tumors. Cancer Genet Cytogenet 106:30-36 (1998). Arlt MF, Li M, Herzog TJ, Goodfellow PJ: A 1-Mb bacterial clone contig spanning the endometrial cancer deletion region at 1p32-p33. Genomics 57:62-69 (1999). Aubele M, Zitzelsberger H, Schenck U, Walch A, Hofler H, Werner M: Distinct cytogenetic alterations in squamous intraepithelial lesions of the cervix revealed by laser-assisted microdissection and comparative genomic hybridization. Cancer 84:375-379 (1998). Balsara BR, Bell DW, Sonoda G, De Rienzo A, du Manoir S, Jhanwar SC, Testa JR: Comparative genomic hybridization and loss of heterozygosity analyses identify a common region of deletion at 15q11.1-15 in human malignant mesothelioma. Cancer Res 59:450-454 (1999). Banikazemi M, Diaz GA, Vossough P, Jalali M, Desnick RJ, Gelb BD: Localization of the thiamine-responsive megaloblastic anemia syndrome locus to a 1.4-cM region of 1q23. Mol Genet Metab 66:193-198 (1999). Bauer MF, Gempel K, Reichert AS, Rappold GA, Lichtner P, Gerbitz KD, Neupert W, Brunner M, Hofmann S: Genetic and structural characterization of the human mitochondrial inner membrane translocase. J Mol Biol 289:69-82 (1999). |
|
|||||||||||||
|
Bea S, Ribas M, Hernandez JM, Bosch F, Pinyol M, Hernandez L, Garcia JL, Flores T, Gonzalez M, Lopez-Guillermo A, Piris MA, Cardesa A, et al.: Increased number of chromosomal imbalances and high-level DNA amplifications in mantle cell lymphoma are associated with blastoid variants. Blood 93:4365-4374 (1999). Beck S, Sterk P: Genome-scale DNA sequencing: where are we? Curr Opin Biotechnol 9:116-121 (1998). Berthon P, Valeri A, Cohen-Akenine A, Drelon E, Paiss T, Wohr G, Latil A, Millasseau P, Mellah I, Cohen N, Blanche H, Bellane-Chantelot C, et al.: Predisposing gene for early-onset prostate cancer, localized on chromosome 1q42.2-43. Am J Hum Genet 62:1416-1424 (1998). Betz R, Lagercrantz J, Kedra D, Dumanski JP, Nordenskjold A: Genomic structure, 5' flanking sequences, and precise localization in 1P31.1 of the human prostaglandin F receptor gene. Biochem Biophys Res Commun 254:413-416 (1999). Bieche I, Khodja A, Lidereau R: Deletion mapping of chromosomal region 1p32-pter in primary breast cancer. Genes Chromosom Cancer 24:255-263 (1999). Bigner SH, Matthews MR, Rasheed BK, Wiltshire RN, Friedman HS, Friedman AH, Stenzel TT, Dawes DM, McLendon RE, Bigner DD: Molecular genetic aspects of oligodendrogliomas including analysis by comparative genomic hybridization. Am J Pathol 155:375-386 (1999). Boguski MS, Schuler GD: ESTablishing a human transcript map. Nat Genet 10:369-371 (1995). Boon LM, Mulliken JB, Vikkula M, Watkins H, Seidman J, Olsen BR, Warman ML: Assignment of a locus for dominantly inherited venous malformations to chromosome 9p. Hum Mol Genet 3:1583-1587 (1994). Bown N, Cotterill S, Lastowska M, O'Neill S, Pearson AD, Plantaz D, Meddeb M, Danglot G, Brinkschmidt C, Christiansen H, Laureys G, Speleman F: Gain of chromosome arm 17q and adverse outcome in patients with neuroblastoma. N Engl J Med 340:1954-1961 (1999). Bradley JF, Rothberg PG: Processed pseudogene from the von Hippel-Lindau disease gene is located on human chromosome 1. Diagn Mol Pathol 8:101-106 (1999). Buerger H, Otterbach F, Simon R, Poremba C, Diallo R, Decker T, Riethdorf L, Brinkschmidt C, Dockhorn-Dworniczak B, Boecker W: Comparative genomic hybridization of ductal carcinoma in situ of the breast-evidence of multiple genetic pathways. J Pathol 187:396-402 (1999). Buetow KH, Edmonson MN, Cassidy AB: Reliable identification of large numbers of candidate SNPs from public EST data. Nat Genet 21:323-325 (1999). Bulfone A, Gattuso C, Marchitiello A, Pardini C, Boncinelli E, Borsani G, Banfi S, Ballabio A: The embryonic expression pattern of 40 murine cDNAs homologous to Drosophila mutant genes (Dres): a comparative and topographic approach to predict gene function. Hum Mol Genet 7:1997-2006 (1998). Bussey KJ, Lawce HJ, Olson SB, Arthur DC, Kalousek DK, Krailo M, Giller R, Heifetz S, Womer R, Magenis RE: Chromosome abnormalities of eighty-one pediatric germ cell tumors: sex-, age-, site-, and histopathology-related differences&emdash;a Children's Cancer Group study. Genes Chromosom Cancer 25:134-146 (1999). Carpenter D, Stone DM, Brush J, Ryan A, Armanini M, Frantz G, Rosenthal A, de Sauvage FJ: Characterization of two patched receptors for the vertebrate hedgehog protein family. Proc Natl Acad Sci USA 95:13630-13634 (1998). Cerretti DP, DuBose RF, Black RA, Nelson N: Isolation of two novel metalloproteinase-disintegrin (ADAM) cDNAs that show testis-specific gene expression. Biochem Biophys Res Commun 263:810-815 (1999). Chalifa-Caspi V, Prilusky J, Lancet D: The Unified Database. Weizmann Institute of Science, Bioinformatics Unit and Genome Center (Rehovot, Israel). World Wide Web URL: http://bioinformatics.weizmann.ac.il/udb (1998). Charbonneau A, Luu-The V: Assignment of steroid 5-beta-reductase (SRD5B1) and its pseudogene (SRD5BP1) to human chromosome bands 7q32-q33 and 1q23-q25, respectively, by in situ hybridization. Cytogenet Cell Genet 84:105-106 (1999). Chen YJ, Ko JY, Chen PJ, Shu CH, Hsu MT, Tsai SF, Lin CH: Chromosomal aberrations in nasopharyngeal carcinoma analyzed by comparative genomic hybridization. Genes Chromosom Cancer 25:169-175 (1999a). Chen F, Zhang Q, McDonald T, Davidoff MJ, Bailey W, Bai C, Liu Q, Caskey CT: Identification of two hERR2-related novel nuclear receptors utilizing bioinformatics and inverse PCR. Gene 228:101-109 (1999b). Cigudosa JC, Parsa NZ, Louie DC, Filippa DA, Jhanwar SC, Johansson B, Mitelman F, Chaganti RS: Cytogenetic analysis of 363 consecutively ascertained diffuse large B- cell lymphomas. Genes Chromosom Cancer 25:123-133 (1999). Claudio JO, Liew CC, Ma J, Heng HH, Stewart AK, Hawley RG: Cloning and expression analysis of a novel WD repeat gene, WDR3, mapping to 1p12-p13. Genomics 59:85-89 (1999). Cohen S, Dadi H, Shaoul E, Sharfe N, Roifman CM: Cloning and characterization of a lymphoid-specific, inducible human protein tyrosine phosphatase, Lyp. Blood 93:2013-2024 (1999). Collins A, Frezal J, Teague J, Morton NE: A metric map of humans: 23,500 loci in 850 bands. Proc Natl Acad Sci USA 93:14771-14775 (1996). Conklin D, Lofton-Day CE, Haldeman BA, Ching A, Whitmore TE, Lok S, Jaspers S: Identification of INSL5, a new member of the insulin superfamily. Genomics 60:50-56 (1999). Deloukas P, Schuler GD, Gyapay G, Beasley EM, Soderlund C, Rodriguez-Tomé P, Hui L, Matise TC, McKusick KB, Beckmann JS, Benolila S, Bihoreau M-T, et al.: A physical map of 30,000 human genes. Science 282:744-746 (1998). Diaz GA, Banikazemi M, Oishi K, Desnick RJ, Gelb BD: Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndrome. Nat Genet 22:309-312 (1999a). Diaz GA, Gelb BD, Ali F, Sakati N, Sanjad S, Meyer BF, Kambouris M: Autosomal recessive Kenny-Caffey syndromes are allelic: Evidence for an ancestral founder mutation and locus refinement. Am J Med Genet 85:48-52 (1999b). Dorkeld F, Bernheim A, Dessen P, Huret JL: A database on cytogenetics in haematology and oncology. Nucleic Acids Res 27:353-354 (1999). Dror V, Shamir E, Ghanshani S, Kimhi R, Swartz M, Barak Y, Weizman R, Avivi L, Litmanovitch T, Fantino E, Kalman K, Jones EG, et al.: hKCa3/KCNN3 potassium channel gene: association of longer CAG repeats with schizophrenia in Israeli Ashkenazi Jews, expression in human tissues and localization to chromosome 1q21. Mol Psychiatry 4:254-260 (1999). Du Plessis L, Dietzsch E, Van Gele M, Van Roy N, Van Helden P, Parker MI, Mugwanya DK, De Groot M, Marx MP, Kotze MJ, Speleman F: Mapping of novel regions of DNA gain and loss by comparative genomic hybridization in esophageal carcinoma in the Black and Colored populations of South Africa. Cancer Res 59:1877-1883 (1999). Dunsmuir WD, Edwards SM, Lakhani SR, Young M, Corbishley C, Kirby RS, Dearnaley DP, Dowe A, Ardern-Jones A, Kelly J, Eeles RA: Allelic imbalance in familial and sporadic prostate cancer at the putative human prostate cancer susceptibility locus, HPC1. CRC/BPG UK Familial Prostate Cancer Study Collaborators. Cancer Research Campaign/British Prostate Group. Br J Cancer 78:1430-1433 (1998). Durbin R, Thierry Mieg J: A C. elegans database. Documentation, code and data available from anonymous FTP servers at lirmm.lirmm.fr, cele.mrc-lmb.cam.ac.uk and ncbi.nlm.nih.gov (1991). Eddleston J, Murdoch JN, Copp AJ, Stanier P: Physical and transcriptional map of a 3-Mb region of mouse chromosome 1 containing the gene for the neural tube defect mutant loop-tail (Lp). Genomics 56:149-159 (1999). Ejeskar K, Sjoberg RM, Kogner P, Martinsson T: Variable expression and absence of mutations in p73 in primary neuroblastoma tumors argues against a role in neuroblastoma development. Int J Mol Med 3:585-589 (1999). El-Rifai W, Sarlomo-Rikala M, Knuutila S, Miettinen M: DNA copy number changes in development and progression in leiomyosarcomas of soft tissues. Am J Pathol 153:985-990 (1998). Elbehti-Green A, Au HC, Mascarello JT, Ream-Robinson D, Scheffler IE: Characterization of the human SDHC gene encoding of the integral membrane proteins of succinate-quinone oxidoreductase in mitochondria. Gene 213:133-140 (1998). Emahazion T, Beskow A, Gyllensten U, Brookes AJ: Intron based radiation hybrid mapping of 15 complex I genes of the human electron transport chain. Cytogenet Cell Genet 82:115-119 (1998). Erdel M, Weiskirchen R: Assignment of CSRP1 encoding the LIM domain protein CRP1, to human chromosome 1q32 by fluorescence in situ hybridization. Cytogenet Cell Genet 83:10-11 (1998). Ericsson J, Greene JM, Carter KC, Shell BK, Duan DR, Florence C, Edwards PA: Human geranylgeranyl diphosphate synthase: isolation of the cDNA, chromosomal mapping and tissue expression. J Lipid Res 39:1731-1739 (1998). Farza H, Townsend PJ, Carrier L, Barton PJ, Mesnard L, Bahrend E, Forissier JF, Fiszman M, Yacoub MH, Schwartz K: Genomic organisation, alternative splicing and polymorphisms of the human cardiac troponin T gene. J Mol Cell Cardiol 30:1247-1253 (1998). Figueiredo BC, Stratakis CA, Sandrini R, DeLacerda L, Pianovsky MA, Giatzakis C, Young HM, Haddad BR: Comparative genomic hybridization analysis of adrenocortical tumors of childhood. J Clin Endocrinol Metab 84:1116-1121 (1999). Flagiello D, Gerbault-Seureau M, Sastre-Garau X, Padoy E, Vielh P, Dutrillaux B: Highly recurrent der(1;16)(q10;p10) and other 16q arm alterations in lobular breast cancer. Genes Chromosom Cancer 23:300-306 (1998). Fletcher CD, Dal Cin P, de Wever I, Mandahl N, Mertens F, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, van den Berghe H, Vanni R, et al.: Correlation between clinicopathological features and karyotype in spindle cell sarcomas. A report of 130 cases from the CHAMP study group. Am J Pathol 154:1841-1847 (1999). Forus A, Berner J-M, Meza-Zepeda LA, Saeter G, Mischke D, Fodstad Ø, Myklebost O: Molecular characterisation of a novel amplicon at 1q21-q22 frequently observed in human sarcomas. Br J Cancer 78:495-503 (1998). Freije JM, Blay P, Pendas AM, Cadinanos J, Crespo P, Lopez-Otin C: Identification and chromosomal location of two human genes encoding enzymes potentially involved in proteolytic maturation of farnesylated proteins. Genomics 58:270-280 (1999). Fujii J, Hamaoka R, Matsumoto A, Fujii T, Yamaguchi Y, Egashira M, Miyoshi O, Niikawa N, Taniguchi N: The structural organization of the human aldehyde reductase gene, AKR1A1, and mapping to chromosome 1p33-p32. Cytogenet Cell Genet 84:230-232 (1999). Fujiwara T, Saito A, Suzuki M, Shinomiya H, Suzuki T, Takahashi E, Tanigami A, Ichiyama A, Chung CH, Nakamura Y, Tanaka K: Identification and chromosomal assignment of USP1, a novel gene encoding a human ubiquitin-specific protease. Genomics 54:155-158 (1998). Gailani MR, Stahle-Backdahl M, Leffell DJ, Glynn M, Zaphiropoulos PG, Pressman C, Unden AB, Dean M, Brash DE, Bale AE, Toftgard R: The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas. Nat Genet 14:78-81 (1996). Galarneau L, Drouin R, Belanger L: Assignment of the fetoprotein transcription factor gene (FTF) to human chromosome band 1q32.11 by in situ hybridization. Cytogenet Cell Genet 82:269-270 (1998). Gallego S, Parareda A, Munell F, Sanchez de Toledo J, Reventos J: Clinical relevance of molecular markers in neuroblastoma: results from a single institution. Oncol Rep 6:891-896 (1999). Gates MA, Kim L, Egan ES, Cardozo T, Sirotkin HI, Dougan ST, Lashkari D, Abagyan R, Schier AF, Talbot WS: A genetic linkage map for zebrafish: comparative analysis and localization of genes and expressed sequences. Genome Res 9:334-347 (1999). Gauguier D, Kaisaki PJ, Rouard M, Wallis RH, Browne J, Rapp JP, Bihoreau MT: A gene map of the rat derived from linkage analysis and related regions in the mouse and human genomes. Mamm Genome 10:675-686 (1999). Gerull B, Osterziel KJ, Witt C, Dietz R, Thierfelder L: A rapid protocol for cardiac troponin T gene mutation detection in familial hypertrophic cardiomyopathy. Hum Mutat 11:179-182 (1998). Getman ME, Houseal TW, Miller GA, Grundy PE, Cowell JK, Landes GM: Comparative genomic hybridization and its application to Wilms' tumorigenesis. Cytogenet Cell Genet 82:284-290 (1998). Gibbs M, Stanford JL, McIndoe RA, Jarvik GP, Kolb S, Goode EL, Chakrabarti L, Schuster EF, Buckley VA, Miller EL, Brandzel S, Li S, et al.: Evidence for a rare prostate cancer-susceptibility locus at chromosome 1p36. Am J Hum Genet 64:776-787 (1999a). Gibbs M, Chakrabarti L, Stanford JL, Goode EL, Kolb S, Schuster EF, Buckley VA, Shook M, Hood L, Jarvik GP, Ostrander EA: Analysis of chromosome 1q42.2-43 in 152 families with high risk of prostate cancer. Am J Hum Genet 64:1087-1095 (1999b). Gladyshev VN, Jeang KT, Wootton JC, Hatfield DL: A new human selenium-containing protein. Purification, characterization, and cDNA sequence. J Biol Chem 273:8910-8915 (1998). Graphodatsky AS, Vorobieva NV, Filipenko ML, Voronina EV, Frengen E, Prydz H: Assignment of the L11 ribosomal protein gene (RPL11) to human chromosome 1p36.1-p35 by in situ hybridization. Cytogenet Cell Genet 84:97-98 (1999). Gregory SG, Vaudin M, Wooster R, Mischke D, Coleman M, Porter C, Schutte BC, White P, Vance JM: Report of the Fourth International Workshop on Human Chromosome 1 Mapping. Cytogenet Cell Genet 78:154-182 (1998). Gronberg H, Smith J, Emanuelsson M, Jonsson BA, Bergh A, Carpten J, Isaacs W, Xu J, Meyers D, Trent J, Damber JE: In Swedish families with hereditary prostate cancer, linkage to the HPC1 locus on chromosome 1q24-25 is restricted to families with early-onset prostate cancer. Am J Hum Genet 65:134-140 (1999). Gruber AD, Elble RC, Ji HL, Schreur KD, Fuller CM, Pauli BU: Genomic cloning, molecular characterization, and functional analysis of human CLCA1, the first human member of the family of Ca2+-activated Cl- channel proteins. Genomics 54:200-214 (1998). Gurney AL, Marsters SA, Huang RM, Pitti RM, Mark DT, Baldwin DT, Gray AM, Dowd AD, Brush AD, Heldens AD, Schow AD, Goddard AD, et al.: Identification of a new member of the tumor necrosis factor family and its receptor, a human ortholog of mouse GITR. Curr Biol 9:215-218 (1999). Gururajan R, Lahti JM, Grenet J, Easton J, Gruber I, Ambros PF, Kidd VJ: Duplication of a genomic region containing the Cdc2L1-2 and MMP21-22 genes on human chromosome 1p36.3 and their linkage to D1Z2. Genome Res 8:929-939 (1998a). Gururajan R, Grenet J, Lahti JM, Kidd VJ: Isolation and characterization of two novel metalloproteinase genes linked to the Cdc2L locus on human chromosome 1p36.3. Genomics 52:101-106 (1998b). Hadano S, Nasir J, Nichol K, Rasper DM, Vaillancourt JP, Sherer SW, Beatty BG, Ikeda JE, Nicholson DW, Hayden MR: Genomic organization of the human caspase-9 gene on chromosome 1p36. 1-p36.3. Mamm Genome 10:757-760 (1999). Haeseleer F, Huang J, Lebioda L, Saari JC, Palczewski K: Molecular characterization of a novel short-chain dehydrogenase/reductase that reduces all-trans-retinal. J Biol Chem 273:21790-21799 (1998). Hahn H, Wicking C, Zaphiropoulous PG, Gailani MR, Shanley S, Chidambaram A, Vorechovsky I, Holmberg E, Unden AB, Gillies S, Negus K, Smyth I, et al.: Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome. Cell 85:841-851 (1996). Harte PJ, Wu W, Carrasquillo MM, Matera AG: Assignment of a novel bifurcated SET domain gene, SETDB1, to human chromosome band 1q21 by in situ hybridization and radiation hybrids. Cytogenet Cell Genet 84:83-86 (1999). Hartsfield Jr JK, Sutcliffe MJ, Everett ET, Hassett C, Omiecinski CJ, Saari JA: Assignment1 of microsomal epoxide hydrolase (EPHX1) to human chromosome 1q42.1 by in situ hybridization. Cytogenet Cell Genet 83:44-45 (1998). Hasuike S, Miura K, Miyoshi O, Miyamoto T, Niikawa N, Jinno Y, Ishikawa M: Isolation and localization of an IDDMK1,2-22-related human endogenous retroviral gene, and identification of a CA repeat marker at its locus. J Hum Genet 44:343-347 (1999). Hatakeyama S, Osawa M, Omine M, Ishikawa F: JTB: a novel membrane protein gene at 1q21 rearranged in a jumping translocation. Oncogene 18:2085-2090 (1999). Hemmer S, Wasenius VM, Knuutila S, Joensuu H, Franssila K: Comparison of benign and malignant follicular thyroid tumours by comparative genomic hybridization. Br J Cancer 78:1012-1017 (1998). Hermsen MA, Baak JP, Meijer GA, Weiss JM, Walboomers JW, Snijders PJ, van Diest PJ: Genetic analysis of 53 lymph node-negative breast carcinomas by CGH and relation to clinical, pathological, morphometric, and DNA cytometric prognostic factors. J Pathol 186:356-362 (1998). Herrnstadt C, Clevenger W, Ghosh SS, Anderson C, Fahy E, Miller S, Howell N, Davis RE: A novel mitochondrial DNA-like sequence in the human nuclear genome. Genomics 60:67-77 (1999). Hilgers W, Tang DJ, Sugar AY, Shekher MC, Hruban RH, Kern SE: High-resolution deletion mapping of chromosome arm 1p in pancreatic cancer identifies a major consensus region at 1p35. Genes Chromosom Cancer 24:351-355 (1999). Hirai M, Yoshida S, Kashiwagi H, Kawamura T, Ishikawa T, Kaneko M, Ohkawa H, Nakagawara A, Miwa M, Uchida K: 1q23 gain is associated with progressive neuroblastoma resistant to aggressive treatment. Genes Chromosom Cancer 25:261-269 (1999). Hobbs MR, Pole AR, Pidwirny GN, Rosen IB, Zarbo RJ, Coon H, Heath 3rd H, Leppert M, Jackson CE: Hyperparathyroidism-jaw tumor syndrome: the HRPT2 locus is within a 0.7-cM region on chromosome 1q. Am J Hum Genet 64:518-525 (1999). Hui AB, Lo KW, Leung SF, Teo P, Fung MK, To KF, Wong N, Choi PH, Lee JC, Huang DP: Detection of recurrent chromosomal gains and losses in primary nasopharyngeal carcinoma by comparative genomic hybridisation. Int J Cancer 82:498-503 (1999). Inglehearn CF, Tarttelin EE, Keen TJ, Bhattacharya SS, Moore AT, Taylor R, Bird AC: A new dominant retinitis pigmentosa family mapping to the RP18 locus on chromosome 1q11-21. J Med Genet 35:788-789 (1998). Iolascon A, Lo Cunsolo C, Giordani L, Cusano R, Mazzocco K, Boumgartner M, Ghisellini P, Faienza MF, Boni L, De Bernardi B, Conte M, Romeo G, et al.: Interstitial and large chromosome 1p deletion occurs in localized and disseminated neuroblastomas and predicts an unfavourable outcome. Cancer Lett 130:83-92 (1998). Jang W, Chen HC, Sicotte H, Schuler GD: Making effective use of human genomic sequence data. Trends Genet 15:284-286 (1999). Jerkeman M, Johansson B, Akerman M, Cavallin-Stahl E, Kristoffersson U, Mitelman F: Prognostic implications of cytogenetic aberrations in diffuse large B- cell lymphomas. Eur J Haematol 62:184-190 (1999). Jeuken JW, Sprenger SH, Wesseling P, Macville MV, von Deimling A, Teepen HL, van Overbeeke JJ, Boerman RH: Identification of subgroups of high-grade oligodendroglial tumors by comparative genomic hybridization. J Neuropathol Exp Neurol 58:606-612 (1999). Jiang F, Richter J, Schraml P, Bubendorf L, Gasser T, Sauter G, Mihatsch MJ, Moch H: Chromosomal imbalances in papillary renal cell carcinoma: genetic differences between histological subtypes. Am J Pathol 153:1467-1473 (1998). Jin Y, Jin C, Wennerberg J, Mertens F, Hoglund M: Cytogenetic and fluorescence in situ hybridization characterization of chromosome 1 rearrangements in head and neck carcinomas delineate a target region for deletions within 1p11-1p13. Cancer Res 58:5859-5865 (1998). Katsanis N, Fitzgibbon J, Fisher EMC: Paralogy mapping: identification of a region in the human MHC triplicated onto human chromosomes 1 and 9 allows the prediction and isolation of novel PBX and NOTCH loci. Genomics 35:101-108 (1996). Kim IF, Mohammadi E, Huang RC: Isolation and characterization of IPP, a novel human gene encoding an actin-binding, kelch-like protein. Gene 228:73-83 (1999). Kim JO, Nau MM, Allikian KA, Makela TP, Alitalo K, Johnson BE, Kelley MJ: Co-amplification of a novel cyclophilin-like gene (PPIE) with L-myc in small cell lung cancer cell lines. Oncogene 17:1019-1026 (1998). Kingsmore SF, Watson ML, Howard TA, Seldin MF: A 6000 kb segment of chromosome 1 is conserved in human and mouse. EMBO J 8:4073-4080 (1989). Kirchhoff M, Gerdes T, Rose H, Maahr J, Ottesen AM, Lundsteen C: Detection of chromosomal gains and losses in comparative genomic hybridisation analysis based on standard reference intervals. Cytometry 31:163-173 (1998). Kocher O, Comella N, Gilchrist A, Pal R, Tognazzi K, Brown LF, Knoll JH: PDZK1, a novel PDZ domain-containing protein up-regulated in carcinomas and mapped to chromosome 1q21, interacts with cMOAT (MRP2), the multidrug resistance-associated protein. Lab Invest 79:1161-1170 (1999). Komuro H, Valentine MB, Rowe ST, Kidd VJ, Makino S, Brodeur GM, Cohn SL, Look AT: Fluorescence in situ hybridization analysis of chromosome 1p36 deletions in human MYCN amplified neuroblastoma. J Pediatr Surg 33:1695-1698 (1998). Kong W, Po S, Yamagishi T, Ashen MD, Stetten G, Tomaselli GF: Isolation and characterization of the human gene encoding Ito: further diversity by alternative mRNA splicing. Am J Physiol 275:1963-1970 (1998). Koo SH, Kwon KC, Ihm CH, Jeon YM, Park JW, Sul CK: Detection of genetic alterations in bladder tumors by comparative genomic hybridization and cytogenetic analysis. Cancer Genet Cytogenet 110:87-93 (1999). Korn WM, Yasutake T, Kuo WL, Warren RS, Collins C, Tomita M, Gray J, Waldman FM: Chromosome arm 20q gains and other genomic alterations in colorectal cancer metastatic to liver, as analyzed by comparative genomic hybridization and fluorescence in situ hybridization. Genes Chromosom Cancer 25:82-90 (1999). Kosaki K, Bassi MT, Kosaki R, Lewin M, Belmont J, Schauer G, Casey B: Characterization and mutation analysis of human LEFTY A and LEFTY B, homologues of murine genes implicated in left-right axis development. Am J Hum Genet 64:712-721 (1999). Kusano N, Shiraishi K, Kubo K, Oga A, Okita K, Sasaki K: Genetic aberrations detected by comparative genomic hybridization in hepatocellular carcinomas: their relationship to clinicopathological features. Hepatology 29:1858-1862 (1999). Labay V, Raz T, Baron D, Mandel H, Williams H, Barrett T, Szargel R, McDonald L, Shalata A, Nosaka K, Gregory S, Cohen N: Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness. Nat Genet 22:300-304 (1999). Lamant L, Dastugue N, Pulford K, Delsol G, Mariame B: A new fusion gene TPM3-ALK in anaplastic large cell lymphoma created by a (1;2)(q25;p23) translocation. Blood 93:3088-3095 (1999). Lambert de Rouvroit C, Goffinet AM: Cloning of human DAB1 and mapping to chromosome 1p31-p32. Genomics 53:246-247 (1998). Larramendy ML, El-Rifai W, Kokkola A, Puolakkainen P, Monni O, Salovaara R, Aarnio M, Knuutila S: Comparative genomic hybridization reveals difference in DNA copy number changes between sporadic gastric carcinomas and gastric carcinomas from patients with hereditary nonpolyposis colorectal cancer. Cancer Genet Cytogenet 106:62-65 (1998). Larramendy ML, Huhta T, Vettenranta K, El-Rifai W, Lundin J, Pakkala S, Saarinen-Pihkala UM, Knuutila S: Comparative genomic hybridization in childhood acute lymphoblastic leukemia. Leukemia 12:1638-1644 (1998). Law DJ, Du M, Law GL, Merchant JL: ZBP-99 defines a conserved family of transcription factors and regulates ornithine decarboxylase gene expression. Biochem Biophys Res Commun 262:113-120 (1999). Lee HK, Lee YK, Park SH, Kim YS, Lee JW, Kwon HB, Soh J, Moore DD, Choi HS: Structure and expression of the orphan nuclear receptor SHP gene. J Biol Chem 273:14398-14402 (1998a). Lee SM, Tsui SK, Chan KK, Kotaka M, Li HY, Chim SS, Waye MM, Fung KP, Lee CY: Chromosomal mapping of a skeletal muscle specific LIM-only protein FHL3 to the distal end of the short arm of human chromosome 1. Somat Cell Mol Genet 24:197-202 (1998b). Leone PE, Bello MJ, de Campos JM, Vaquero J, Sarasa JL, Pestana A, Rey JA: NF2 gene mutations and allelic status of 1p, 14q and 22q in sporadic meningiomas. Oncogene 18:2231-2239 (1999). Li WH: Evolutionary changes in duplicate genes, in Rattazzi MC, Scandalios JG, Whitt GS (eds): Isozymes: Current topics in biological and medical research, pp 55-92 (A. R. Liss, New York 1982). Loeffen J, Smeets R, Smeitink J, Triepels R, Sengers R, Trijbels F, van den Heuvel L: The human NADH: ubiquinone oxidoreductase NDUFS5 (15 kDa) subunit: cDNA cloning, chromosomal localization, tissue distribution and the absence of mutations in isolated complex I-deficient patients. J Inherit Metab Dis 22:19-28 (1999). Lu YJ, Osin P, Lakhani SR, Di Palma S, Gusterson BA, Shipley JM: Comparative genomic hybridization analysis of lobular carcinoma in situ and atypical lobular hyperplasia and potential roles for gains and losses of genetic material in breast neoplasia. Cancer Res 58:4721-4727 (1998). Lueders KK, Elliott RW, Marenholz I, Mischke D, DuPree M, Hamer D: Genomic organization and mapping of the human and mouse neuronal beta 2-nicotinic acetylcholine receptor genes. Mamm Genome 10:900-905 (1999). Lundin LG: Evolution of the vertebrate genome as reflected in paralogous chromosomal regions in man and the house mouse. Genomics 16:1-19 (1993). Magert HJ, Reinecke M, David I, Raab HR, Adermann K, Zucht HD, Hill O, Hess R, Forssmann WG: Uroguanylin: gene structure, expression, processing as a peptide hormone, and co-storage with somatostatin in gastrointestinal D-cells. Regul Pept 73:165-176 (1998). Mairal A, Terrier P, Chibon F, Sastre X, Lecesne A, Aurias A: Loss of chromosome 13 is the most frequent genomic imbalance in malignant fibrous histiocytomas. A comparative genomic hybridization analysis of a series of 30 cases. Cancer Genet Cytogenet 111:134-138 (1999). Martinez-Dominguez MT, Justesen J, Kruse TA, Hansen LL: Assignment of the human mitochondrial tryptophanyl-tRNA synthetase (WARS2) to 1p13.3-p13.1 by radiation hybrid mapping. Cytogenet Cell Genet 83:249-250 (1998). Maruno M, Yoshimine T, Muhammad AK, Ninomiya H, Hayakawa T: Chromosomal losses and gains in meningiomas: comparative genomic hybridization (CGH) study of the whole genome. Neurol Res 20:612-616 (1998). Masaki T, Sakai E, Furuta Y, Kobayashi M, Takamatsu K: Genomic structure and chromosomal mapping of the human and mouse hippocalcin genes. Gene 225:117-124 (1998). Mason PJ, Stevens D, Diez A, Knight SW, Scopes DA, Vulliamy TJ: Human hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) encoded at 1p36: coding sequence and expression. Blood Cells Mol Dis 25:30-37 (1999). Masure S, Haefner B, Wesselink JJ, Hoefnagel E, Mortier E, Verhasselt P, Tuytelaars A, Gordon R, Richardson A: Molecular cloning, expression and characterization of the human serine/threonine kinase Akt-3. Eur J Biochem 265:353-360 (1999). Matsumoto N, Ledbetter DH: Molecular cloning and characterization of the human NUDC gene. Hum Genet 104:498-504 (1999). Matsuzaki M, Nagase S, Abe T, Miura K, Shiiba K, Sunamura M, Horii A: Detailed deletion mapping on chromosome 1p32-p36 in human colorectal cancer: identification of three distinct regions of common allelic loss. Int J Oncol 13:1229-1233 (1998). Mechtersheimer G, Otano-Joos M, Ohl S, Benner A, Lehnert T, Willeke F, Moller P, Otto HF, Lichter P, Joos S: Analysis of chromosomal imbalances in sporadic and NF1-associated peripheral nerve sheath tumors by comparative genomic hybridization. Genes Chromosom Cancer 25:362-369 (1999). Millikan RC, Ingles SA, Diep AT, Xue S, Zhou N, Florentine BD, Sparkes RS, Haile RW: Linkage analysis and loss of heterozygosity for chromosome arm 1p in familial breast cancer. Genes Chromosom Cancer 25:354-361 (1999). Mogensen J, Kruse TA, Borglum AD: Assignment of the human skeletal muscle a-actin gene (ACTA1) to chromosome 1q42.13-q42.2 by radiation hybrid mapping. Cytogenet Cell Genet 83:224-225 (1998). Morgan MJ, Madgwick AJ: The LIM proteins FHL1 and FHL3 are expressed differently in skeletal muscle. Biochem Biophys Res Commun 255:245-250 (1999). Mori N, Morosetti R, Spira S, Lee S, Ben-Yehuda D, Schiller G, Landolfi R, Mizoguchi H, Koeffler HP: Chromosome band 1p36 contains a putative tumor suppressor gene important in the evolution of chronic myelocytic leukemia. Blood 92:3405-3409 (1998). Muda M, Manning ER, Orth K, Dixon JE: Identification of the human YVH1 protein-tyrosine phosphatase orthologue reveals a novel zinc binding domain essential for in vivo function. J Biol Chem 274:23991-23995 (1999). Mukae N, Enari M, Sakahira H, Fukuda Y, Inazawa J, Toh H, Nagata S: Molecular cloning and characterization of human caspase-activated DNase. Proc Natl Acad Sci USA 95:9123-9128 (1998). Mural RJ, Parang M, Shah M, Snoddy J, Uberbacher EC: The Genome Channel: a browser to a uniform first-pass annotation of genomic DNA. Trends Genet 15:38-39 (1999). Nagasaki K, Maass N, Manabe T, Hanzawa H, Tsukada T, Kikuchi K, Yamaguchi K: Identification of a novel gene, DAM1, amplified at chromosome 1p13.3-21 region in human breast cancer cell lines. Cancer Lett 140:219-226 (1999). Nakatani K, Thompson DA, Barthel A, Sakaue H, Liu W, Weigel RJ, Roth RA: Up-regulation of Akt3 in estrogen receptor-deficient breast cancers and androgen-independent prostate cancer lines. J Biol Chem 274:21528-21532 (1999). Neufeld EJ, Mandel H, Raz T, Szargel R, Yandava CN, Stagg A, Faure S, Barrett T, Buist N, Cohen N: Localization of the gene for thiamine-responsive megaloblastic anemia syndrome, on the long arm of chromosome 1, by homozygosity mapping. Am J Hum Genet 61:1335-1341 (1997). Nicole S, White PS, Topaloglu H, Beigthon P, Salih M, Hentati F, Fontaine B: The human CDC42 gene: genomic organization, evidence for the existence of a putative pseudogene and exclusion as a SJS1 candidate gene. Hum Genet 105:98-103 (1999). Nishigori H, Yamada S, Tomura H, Fernald AA, Le Beau MM, Takeuchi T, Takeda J: Identification and characterization of the gene encoding a second proteolipid subunit of human vacuolar H(+)-ATPase (ATP6F). Genomics 50:222-228 (1998). Olivier LM, Chambliss KL, Gibson KM, Krisans SK: Characterization of phosphomevalonate kinase: chromosomal localization, regulation, and subcellular targeting. J Lipid Res 40:672-679 (1999). Pack SD, Karkera JD, Zhuang Z, Pak ED, Balan KV, Hwu P, Park WS, Pham T, Ault DO, Glaser M, Liotta L, Detera-Wadleigh SD, et al.: Molecular cytogenetic fingerprinting of esophageal squamous cell carcinoma by comparative genomic hybridization reveals a consistent pattern of chromosomal alterations. Genes Chromosom Cancer 25:160-168 (1999). Patskovsky YV, Huang MQ, Takayama T, Listowsky I, Pearson WR: Distinctive structure of the human GSTM3 gene-inverted orientation relative to the mu class glutathione transferase gene cluster. Arch Biochem Biophys 361:85-93 (1999). Pedeutour F, Forus A, Coindre JM, Berner JM, Nicolo G, Michiels JF, Terrier P, Ranchere-Vince D, Collin F, Myklebost O, Turc-Carel C: Structure of the supernumerary ring and giant rod chromosomes in adipose tissue tumors. Genes Chromosom Cancer 24:30-41 (1999). Pere H, Tapper J, Seppala M, Knuutila S, Butzow R: Genomic alterations in fallopian tube carcinoma: comparison to serous uterine and ovarian carcinomas reveals similarity suggesting likeness in molecular pathogenesis. Cancer Res 58:4274-4276 (1998). Perri P, Praml C, Savelyeva L, Pillmann A, Schwab M: Fine mapping of distal 1p loci reveals TP73 at D1S468. Cytogenet Cell Genet 84:111-114 (1999). Praml C, Savelyeva L, Perri P, Schwab M: Cloning of the human aflatoxin B1-aldehyde reductase gene at 1p35-1p36.1 in a region frequently altered in human tumor cells. Cancer Res 58:5014-5018 (1998). Ragnarsson G, Eiriksdottir G, Johannsdottir JT, Jonasson JG, Egilsson V, Ingvarsson S: Loss of heterozygosity at chromosome 1p in different solid human tumours: association with survival. Br J Cancer 79:1468-1474 (1999). Raich N, Mattei MG, Romeo PH, Beaupain D: PHTF, a novel atypical homeobox gene on chromosome 1p13, is evolutionarily conserved. Genomics 59:108-109 (1999). Rao PR, Houldsworth J, Palanisamy N, Murty VVVS, Reuter VE, Motzer RJ, Bosl GJ, Chaganti RSK: Chromosomal amplification is associated with cisplatin resistance of human male germ cell tumors. Cancer Res 58:4260-4263 (1998). Rasheed BK, Wiltshire RN, Bigner SH, Bigner DD: Molecular pathogenesis of malignant gliomas. Curr Opin Oncol 11:162-167 (1999). Raymond MH, Schutte BC, Torner JC, Burns TL, Willing MC: Osteocalcin: Genetic and physical mapping of the human gene BGLAP and its potential role in postmenopausal osteoporosis. Genomics 60:210-217 (1999). Raz T, Barrett T, Szargel R, Mandel H, Neufeld EJ, Nosaka K, Viana MB, Cohen N: Refined mapping of the gene for thiamine-responsive megaloblastic anemia syndrome and evidence for genetic homogeneity. Hum Genet 103:455-461 (1998). Richard G, Smith LE, Bailey RA, Itin P, Hohl D, Epstein Jr EH, DiGiovanna JJ, Compton JG, Bale SJ: Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis. Nat Genet 20:366-369 (1998). Richter J, Beffa L, Wagner U, Schraml P, Gasser TC, Moch H, Mihatsch MJ, Sauter G: Patterns of chromosomal imbalances in advanced urinary bladder cancer detected by comparative genomic hybridization. Am J Pathol 153:1615-1621 (1998). Riegert P, Wanner V, Bahram S: Genomics, isoforms, expression, and phylogeny of the MHC class I- related MR1 gene. J Immunol 161:4066-4077 (1998). Roberts T, Chernova O, Cowell JK: NB4S, a member of the TBC1 domain family of genes, is truncated as a result of a constitutional t(1;10)(p22;q21) chromosome translocation in a patient with stage 4S neuroblastoma. Hum Mol Genet 7:1169-1178 (1998). Rosenwald A, Ott G, Katzenberger T, Siebert R, Kalla J, Kuse R, Ott MM, Muller-Hermelink HK, Schlegelberger B: Jumping translocation of 1q as the sole aberration in a case of follicular lymphoma. Cancer Genet Cytogenet 108:53-56 (1999). Rozet JM, Gerber S, Perrault I, Calvas P, Souied E, Chatelin S, Viegas P, Molina-Gomez D, Munnich A, Kaplan J: Structure and refinement of the physical mapping of the gamma-glutamylcysteine ligase regulatory subunit (GLCLR) gene to chromosome 1p22.1 within the critically deleted region of human malignant mesothelioma. Cytogenet Cell Genet 82:91-94 (1998). 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. Genomics 52:305-311 (1998). Sawzdargo M, Nguyen T, Lee DK, Lynch KR, Cheng R, Heng HH, George SR, O'Dowd BF: Identification and cloning of three novel human G protein-coupled receptor genes GPR52, PsiGPR53 and GPR55: GPR55 is extensively expressed in human brain. Brain Res Mol Brain Res 64:193-198 (1999). Schaffler A, Orso E, Palitzsch KD, Buchler C, Drobnik W, Furst A, Scholmerich J, Schmitz G: The human apM-1, an adipocyte-specific gene linked to the family of TNF's and to genes expressed in activated T cells, is mapped to chromosome 1q21.3-q23, a susceptibility locus identified for familial combined hyperlipidaemia (FCH). Biochem Biophys Res Commun 260:416-425 (1999). Schibler L, Vaiman D, Oustry A, Giraud-Delville C, Cribiu EP: Comparative gene mapping: a fine-scale survey of chromosome rearrangements between ruminants and humans. Genome Res 8:901-915 (1998). Schmidt A, Langbein L, Pratzel S, Rode M, Rackwitz HR, Franke WW: Plakophilin 3&emdash;a novel cell-type-specific desmosomal plaque protein. Differentiation 64:291-306 (1999). Schultz DC, Balasara BR, Testa JR, Godwin AK: Cloning and localization of a human diphthamide biosynthesis-like protein-2 gene, DPH2L2. Genomics 52:186-191 (1998). Schwendel A, Richard F, Langreck H, Kaufmann O, Lage H, Winzer KJ, Petersen I, Dietel M: Chromosome alterations in breast carcinomas: frequent involvement of DNA losses including chromosomes 4q and 21q. Br J Cancer 78:806-811 (1998). Sciot R, Rosai J, Dal Cin P, de Wever I, Fletcher CD, Mandahl N, Mertens F, Mitelman F, Rydholm A, Tallini G, van den Berghe H, Vanni R, et al.: Analysis of 35 cases of localized and diffuse tenosynovial giant cell tumor: a report from the Chromosomes and Morphology (CHAMP) study group. Mod Pathol 12:576-579 (1999). Seki N, Sugano S, Suzuki Y, Nakagawara A, Ohira M, Muramatsu M, Saito T, Hori T: Isolation, tissue expression, and chromosomal assignment of human RGS5, a novel G-protein signaling regulator gene. J Hum Genet 43:202-205 (1998). Semprini S, Capon F, Bovolenta S, Bruscia E, Pizzuti A, Fabrizi G, Schietroma C, Zambruno G, Dallapiccola B, Novelli G: Genomic structure, promoter characterisation and mutational analysis of the S100A7 gene: exclusion of a candidate for familial psoriasis susceptibility. Hum Genet 104:130-134 (1999). Simon R, Burger H, Brinkschmidt C, Bocker W, Hertle L, Terpe HJ: Chromosomal aberrations associated with invasion in papillary superficial bladder cancer. J Pathol 185:345-351 (1998). Smith JS, Alderete B, Minn Y, Borell TJ, Perry A, Mohapatra G, Hosek SM, Kimmel D, O'Fallon J, Yates A, Feuerstein BG, Burger PC, et al.: Localization of common deletion regions on 1p and 19q in human gliomas and their association with histological subtype. Oncogene 18:4144-4152 (1999). Smolarek TA, Blough RI, Foster RS, Ulbright TM, Palmer CG, Heerema NA: Cytogenetic analyses of 85 testicular germ cell tumors: comparison of postchemotherapy and untreated tumors. Cancer Genet Cytogenet 108:57-69 (1999). Smyth I, Narang MA, Evans T, Heimann C, Nakamura Y, Chenevix-Trench G, Pietsch T, Wicking C, Wainwright BJ: Isolation and characterization of human patched 2 (PTCH2), a putative tumour suppressor gene in basal cell carcinoma and medulloblastoma on chromosome 1p32. Hum Mol Genet 8:291-297 (1999). South AP, Cabral A, Ives JH, James CH, Mirza G, Marenholz I, Mischke D, Backendorf C, Ragoussis J, Nizetic D: Human epidermal differentiation complex in a single 2.5 Mbp long continuum of overlapping DNA cloned in bacteria integrating physical and transcript maps. J Invest Dermatol 112:910-918 (1999). Spieker N, Beitsma M, van Sluis P, Roobeek I, den Dunnen J, Speleman F, Caron H, Versteeg R: An integrated 5 Mb physical, genetic and radiation hybrid map of a 1p36.1 region implicated in neuroblastoma pathogenesis. Genes Chromosom Cancer (in press). Stanier P, Abu-Hayyeh S, Murdoch JN, Eddleston J, Copp AJ: Paralogous sm22alpha (Tagln) genes map to mouse chromosomes 1 and 9: further evidence for a paralogous relationship. Genomics 51:144-147 (1998). Stephan DA, Hoffman EP: Physical mapping of the rippling muscle disease locus. Genomics 55:268-274 (1999). Stover CM, Schwaeble WJ, Lynch NJ, Thiel S, Speicher MR: Assignment of the gene encoding mannan-binding lectin-associated serine protease 2 (MASP2) to human chromosome 1p36.3-p36.2 by in situ hybridization and somatic cell hybrid analysis. Cytogenet Cell Genet 84:148-149 (1999). Stumpo DJ, Eddy Jr. RL, Haley LL, Sait S, Shows TB, Lai WS, Young 3rd WS, Speer MC, Dehejia A, Polymeropoulos M, Blackshear PJ: Promoter sequence, expression, and fine chromosomal mapping of the human gene (MLP) encoding the MARCKS-like protein: identification of neighboring and linked polymorphic loci for MLP and MACS and use in the evaluation of human neural tube defects. Genomics 49:253-264 (1998). Su G, Roberts T, Cowell JK: TTC4, a novel human gene containing the tetratricopeptide repeat and mapping to the region of chromosome 1p31 that is frequently deleted in sporadic breast cancer. Genomics 55:157-163 (1999). Sulman EP, Dumanski JP, White PS, Zhao H, Maris JM, Mathiesen T, Bruder C, Cnaan A, Brodeur GM: Identification of a consistent region of allelic loss on 1p32-34 in meningiomas: correlation with increased morbidity. Cancer Res 58:3226-3230 (1998). Taetle R, Aickin M, Panda L, Emerson J, Roe D, Thompson F, Davis J, Trent J, Alberts D: Chromosome abnormalities in ovarian adenocarcinoma: II. Prognostic impact of nonrandom chromosome abnormalities in 244 cases. Genes Chromosom Cancer 25:46-52 (1999a). Taetle R, Aickin M, Yang JM, Panda L, Emerson J, Roe D, Adair L, Thompson F, Liu Y, Wisner L, Davis JR, Trent J, et al.: Chromosome abnormalities in ovarian adenocarcinoma: I. Nonrandom chromosome abnormalities from 244 cases. Genes Chromosom Cancer 25:290-300 (1999b). Taira T, Maeda J, Onishi T, Kitaura H, Yoshida S, Kato H, Ikeda M, Tamai K, Iguchi-Ariga SM, Ariga H: AMY-1, a novel C-MYC binding protein that stimulates transcription activity of C-MYC. Genes Cells 3:549-565 (1998). Talmadge CB, Finkernagel S, Sumegi J, Sciorra L, Rabinow L: Chromosomal mapping of three human LAMMER protein-kinase-encoding genes. Hum Genet 103:523-524 (1998). Tarkkanen M, Huuhtanen R, Virolainen M, Wiklund T, Asko-Seljavaara S, Tukiainen E, Lepantalo M, Elomaa I, Knuutila S: Comparison of genetic changes in primary sarcomas and their pulmonary metastases. Genes Chromosom Cancer 25:323-331 (1999a). Tarkkanen M, Elomaa I, Blomqvist C, Kivioja AH, Kellokumpu-Lehtinen P, Bohling T, Valle J, Knuutila S: DNA sequence copy number increase at 8q: a potential new prognostic marker in high-grade osteosarcoma. Int J Cancer 84:114-121 (1999b). Tirado CA, Sandberg AA, Stone JF: Identification of a novel amplicon at 1q31 in pancreatic cancer cell lines. Cancer Genet Cytogenet 113:110-114 (1999). Tsukamoto K, Yoshimoto M, Kasumi F, Akiyama F, Sakamoto G, Nakamura Y, Emi M: Frequent multiplication of chromosome 1q in non-invasive and papillotubular carcinoma of the breast. Cancer Lett 141:21-28 (1999). Ueki N, Seki N, Yano K, Saito T, Masuho Y, Muramatsu M: Isolation and chromosomal assignment of a human gene encoding protein inhibitor of activated STAT3 (PIAS3). J Hum Genet 44:193-196 (1999). Van Rompay AR, Johansson M, Karlsson A: Phosphorylation of deoxycytidine analog monophosphates by UMP-CMP kinase: molecular characterization of the human enzyme. Mol Pharmacol 56:562-569 (1999a). Van Rompay AR, Johansson M, Karlsson A: Identification of a novel human adenylate kinase. cDNA cloning, expression analysis, chromosome localization and characterization of the recombinant protein. Eur J Biochem 261:509-517 (1999b). van Soest S, van Rossem MJ, Heckenlively JR, van den Born LI, de Meulemeester TM, Vliex S, de Jong PT, Bleeker-Wagemakers EM, Westerveld A, Bergen AA: Integrated genetic and physical map of the 1q31-q32.1 region, encompassing the RP12 locus, the F13B and HF1 genes, and the EEF1AL11 and RPL30 pseudogenes. Cytogenet Cell Genet 84:22-27 (1999). Vance JM, Matise TC, Wooster R, Schutte BC, Bruns GAP, Van Roy N, Brodeur GM, Tao YX, Gregory S, Weith A, Vaudin M, White P: Report of the Third International Workshop on Human Chromosome 1 Mapping 1997. Cytogenet Cell Genet 78:153-182 (1997). Velasco G, Pendas AM, Fueyo A, Knauper V, Murphy G, Lopez-Otin C: Cloning and characterization of human MMP-23, a new matrix metalloproteinase predominantly expressed in reproductive tissues and lacking conserved domains in other family members. J Biol Chem 274:4570-4576 (1999). Verma RS, Manikal M, Conte RA, Godec CJ: Chromosomal basis of adenocarcinoma of the prostate. Cancer Invest 17:441-447 (1999). Vikkula M, Boon LM, Carraway 3rd KL, Calvert JT, Diamonti AJ, Goumnerov B, Pasyk KA, Marchuk DA, Warman ML, Cantley LC, Mulliken JB, Olsen BR: Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2. Cell 87:1181-1190 (1996). Wan M, Cravatt BF, Ring HZ, Zhang X, Francke U: Conserved chromosomal location and genomic structure of human and mouse fatty-acid amide hydrolase genes and evaluation of clasper as a candidate neurological mutation. Genomics 54:408-414 (1998). Wang Y, Devereux W, Stewart TM, Casero Jr. RA: Cloning and characterization of human polyamine-modulated factor-1, a transcriptional cofactor that regulates the transcription of the spermidine/spermine N(1)-acetyltransferase gene. J Biol Chem 274:22095-22101 (1999). West A, Vojta PJ, Welch DR, Weissman BE: Chromosome localization and genomic structure of the KiSS-1 metastasis suppressor gene (KISS1). Genomics 54:145-148 (1998). White PS, Sulman EP, Porter CJ, Matise TC: A comprehensive view of human chromosome 1. Genome Research 9:978-988 (1999). Wilson 3rd DM, Carney JP, Coleman MA, Adamson AW, Christensen M, Lamerdin JE: Hex1: a new human Rad2 nuclease family member with homology to yeast exonuclease 1. Nucleic Acids Res 26:3762-3768 (1998). Wong AK, Chen Y, Lian L, Ha PC, Petersen K, Laity K, Carillo A, Emerson M, Heichman K, Gupte J, Tavtigian SV, Teng DH: Genomic structure, chromosomal location, and mutation analysis of the human CDC14A gene. Genomics 59:248-251 (1999a). Wong N, Lai P, Lee SW, Fan S, Pang E, Liew CT, Sheng Z, Lau JW, Johnson PJ: Assessment of genetic changes in hepatocellular carcinoma by comparative genomic hybridization analysis: relationship to disease stage, tumor size, and cirrhosis. Am J Pathol 154:37-43 (1999b). Wu YQ, Heilstedt HA, Bedell JA, May KM, Starkey DE, McPherson JD, Shapira SK, Shaffer LG: Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletions. Hum Mol Genet 8:313-321 (1999). Xiao W, Lechler T, Chow BL, Fontanie T, Agustus M, Carter KC, Wei YF: Identification, chromosomal mapping and tissue-specific expression of hREV3 encoding a putative human DNA polymerase zeta. Carcinogenesis 19:945-949 (1998). Xu SY, Rosenberg T, Gal A: Refined genetic mapping of autosomal dominant retinitis pigmentosa locus RP18 reduces the critical region to 2 cM between D1S442 and D1S2858 on chromosome 1q. Hum Genet 102:493-494 (1998). Yi CH, Terrett JA, Li QY, Ellington K, Packham EA, Armstrong-Buisseret L, McClure P, Slingsby T, Brook JD: Identification, mapping, and phylogenomic analysis of four new human members of the T-box gene family: EOMES, TBX6, TBX18, and TBX19. Genomics 55:10-20 (1999). Yu Y, Xu F, Peng H, Fang X, Zhao S, Li Y, Cuevas B, Kuo WL, Gray JW, Siciliano M, Mills GB, Bast RC, Jr.: NOEY2 (ARHI), an imprinted putative tumor suppressor gene in ovarian and breast carcinomas. Proc Natl Acad Sci USA 96:214-219 (1999). Zborovskaya I, Gasparian A, Karseladze A, Elcheva I, Trofimova E, Driouch K, Trassard M, Tatosyan A, Lidereau R: Somatic genetic alterations (LOH) in benign, borderline and invasive ovarian tumours: intratumoral molecular heterogeneity. Int J Cancer 82:822-826 (1999). Zhang J, Shen-Ong G, Ostell J: "KARIBIN," an information resource for obtaining genomic information in a cytogenetic band. Genome Res 9:91-98 (1999). Zhao XF, Colaizzo-Anas T, Nowak NJ, Shows TB, Elliott RW, Aplan PD: The mammalian homologue of mago nashi encodes a serum-inducible protein. Genomics 47:319-322 (1998). Zimonjic DB, Keck CL, Thorgeirsson SS, Popescu NC: Novel recurrent genetic imbalances in human hepatocellular carcinoma cell lines identified by comparative genomic hybridization. Hepatology 29:1208-1214 (1999). |
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