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References


New Haven Conference (1973): First international workshop on human gene mapping. Cytogenet Cell Genet 13:1-2 (1974).

Abstracts of meeting presentations: Human gene mapping 7, Los Angeles Conference (1983), Seventh International Workshop on Human Gene Mapping. Cytogenet Cell Genet 37:399-616 (1984).

Adeyinka A, Kytola S, Mertens F, Pandis N, Larsson C: Spectral karyotyping and chromosome banding studies of primary breast carcinomas and their lymph node metastases. Int J Mol Med 5:235-240 (2000).

Amler LC, Bauer A, Corvi R, Dihlmann S, Praml C, Cavenee WK, Schwab M, Hampton GM: Identification and characterization of novel genes located at the t(1;15)(p36.2;q24) translocation breakpoint in the neuroblastoma cell line NGP. Genomics 64:195-202 (2000).

Workshop 2000
Introduction
Resources
Sanger Centre
Physical maps on 1p
Physical maps on 1q
Disease genes
Neoplasia
Participants
References

Abstracts

Andersen MK, Pedersen-Bjergaard J: Increased frequency of dicentric chromosomes in therapy-related MDS and AML compared to de novo disease is significantly related to previous treatment with alkylating agents and suggests a specific susceptibility to chromosome breakage at the centromere. Leukemia 14:105-111 (2000).

Aubele M, Mattis A, Zitzelsberger H, Walch A, Kremer M, Welzl G, Hofler H, Werner M: Extensive ductal carcinoma In situ with small foci of invasive ductal carcinoma: evidence of genetic resemblance by CGH. Int J Cancer 85:82-86 (2000a).

Aubele MM, Cummings MC, Mattis AE, Zitzelsberger HF, Walch AK, Kremer M, Hofler H, Werner M: Accumulation of chromosomal imbalances from intraductal proliferative lesions to adjacent in situ and invasive ductal breast cancer. Diagn Mol Pathol 9:14-19 (2000b).

Auranen M, Nieminen T, Majuri S, Vanhala R, Peltonen L, Jarvela I: Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families. Mol Psychiatry 5:320-322 (2000).

Baba Y, Matsushita M, Matsuda Y, Inazawa J, Yamadori T, Hashimoto S, Kishimoto T, Tsukada S: Assignment of SH3BP5/Sh3bp5 encoding sab, an SH3 domain-binding protein which preferentially associates with Bruton's tyrosine kinase, to human chromosome 1q43 and mouse chromosome 14B by in situ hybridization. Cytogenet Cell Genet 87:221-222 (1999).

Baek JY, Jun DY, Taub D, Kim YH: Assignment of human 3-phosphoglycerate dehydrogenase (PHGDH) to human chromosome band 1p12 by fluorescence in situ hybridization. Cytogenet Cell Genet 89:6-7 (2000).

Bastian BC, Wesselmann U, Pinkel D, Leboit PE: Molecular cytogenetic analysis of Spitz nevi shows clear differences to melanoma. J Invest Dermatol 113:1065-1069 (1999).

Beiraghi S, Miller-Chisholm A, Kimberling WJ, Sun CE, Wang YF, Russell LJ, Khoshnevisan M, Storm AL, Long RE, Jr., Witt PD, Mazaheri M, Diehl SR: Confirmation of linkage of Van der Woude syndrome to chromosome 1q32: evidence of association with STR alleles suggests possible unique origin of the disease mutation. J Craniofac Genet Dev Biol 19:128-134 (1999).

Bello MJ, de Campos JM, Vaquero J, Kusak ME, Sarasa JL, Rey JA: High-resolution analysis of chromosome arm 1p alterations in meningioma. Cancer Genet Cytogenet 120:30-36 (2000a).

Bello MJ, de Campos JM, Vaquero J, Ruiz-Barnes P, Kusak ME, Sarasa JL, Rey JA: hRAD54 gene and 1p high-resolution deletion-mapping analyses in oligodendrogliomas. Cancer Genet Cytogenet 116:142-147 (2000b).

Bergamo NA, Rogatto SR, Poli-Frederico RC, Reis PP, Kowalski LP, Zielenska M, Squire JA: Comparative genomic hybridization analysis detects frequent over- representation of DNA sequences at 3q, 7p, and 8q in head and neck carcinomas. Cancer Genet Cytogenet 119:48-55 (2000).

Bonne G, Di Barletta MR, Varnous S, Becane HM, Hammouda EH, Merlini L, Muntoni F, Greenberg CR, Gary F, Urtizberea JA, Duboc D, Fardeau M, et al: Mutations in the gene encoding lamin A/C cause autosomal dominant Emery- Dreifuss muscular dystrophy. Nat Genet 21:285-288 (1999).

Bouhouche A, Benomar A, Birouk N, Mularoni A, Meggouh F, Tassin J, Grid D, Vandenberghe A, Yahyaoui M, Chkili T, Brice A, LeGuern E: A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3. Am J Hum Genet 65:722-727 (1999).

Boute N, Gribouval O, Roselli S, Benessy F, Lee H, Fuchshuber A, Dahan K, Gubler MC, Niaudet P, Antignac C: NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome [published erratum appears in Nat Genet 2000 May;25(1):125]. Nat Genet 24:349-354 (2000).

Brouillard P, Olsen BR, Vikkula M: High-resolution physical and transcript map of the locus for venous malformations with glomus cells (VMGLOM) on chromosome 1p21-p22 [In Process Citation]. Genomics 67:96-101 (2000).

Brzustowicz LM, Hodgkinson KA, Chow EW, Honer WG, Bassett AS: Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22. Science 288:678-682 (2000).

Buerger H, Simon R, Schafer KL, Diallo R, Littmann R, Poremba C, van Diest PJ, Dockhorn-Dworniczak B, Bocker W: Genetic relation of lobular carcinoma in situ, ductal carcinoma in situ, and associated invasive carcinoma of the breast. Mol Pathol 53:118-121 (2000).

Bulfone A, Menguzzato E, Broccoli V, Marchitiello A, Gattuso C, Mariani M, Consalez GG, Martinez S, Ballabio A, Banfi S: Barhl1, a gene belonging to a new subfamily of mammalian homeobox genes, is expressed in migrating neurons of the CNS. Hum Mol Genet 9:1443-1452 (2000).

Capon F, Dallapiccola B, Novelli G: Advances in the search for psoriasis susceptibility genes [In Process Citation]. Mol Genet Metab 71:250-255 (2000).

Carling T, Imanishi Y, Gaz RD, Arnold A: Analysis of the RAD54 gene on chromosome 1p as a potential tumor-suppressor gene in parathyroid adenomas. Int J Cancer 83:80-82 (1999).

Carpten JD, Makalowska I, Robbins CM, Scott N, Sood R, Connors TD, Bonner TI, Smith JR, Faruque MU, Stephan DA, Pinkett H, Morgenbesser SD, et al: A 6-Mb high-resolution physical and transcription map encompassing the hereditary prostate cancer 1 (HPC1) region. Genomics 64:1-14 (2000).

Chadwick RB, Jiang GL, Bennington GA, Yuan B, Johnson CK, Stevens MW, Niemann TH, Peltomaki P, Huang S, de la Chapelle A: Candidate tumor suppressor RIZ is frequently involved in colorectal carcinogenesis. Proc Natl Acad Sci U S A 97:2662-2667 (2000).

Chelsea DM, Roberts T, Cowell JK: A new region of synteny between human chromosome 1p22 and mouse chromosome 5. Int J Mol Med 5:553-556 (2000).

Clifford R, Edmonson M, Hu Y, Nguyen C, Scherpbier T, Buetow KH: Expression-based genetic/physical maps of single-nucleotide polymorphisms identified by the cancer genome anatomy project. Genome Res 10:1259-1265 (2000).

Coon H, Myers RH, Borecki IB, Arnett DK, Hunt SC, Province MA, Djousse L, Leppert MF: Replication of linkage of familial combined hyperlipidemia to chromosome 1q with additional heterogeneous effect of apolipoprotein A- I/C-III/A-IV locus : the NHLBI family heart study [In Process Citation]. Arterioscler Thromb Vasc Biol 20:2275-2280 (2000).

Cormand B, Avela K, Pihko H, Santavuori P, Talim B, Topaloglu H, de la Chapelle A, Lehesjoki AE: Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mapping. Am J Hum Genet 64:126-135 (1999).

Cox PR, Zoghbi HY: Sequencing, expression analysis, and mapping of three unique human tropomodulin genes and their mouse orthologs. Genomics 63:97-107 (2000).

Dai KZ, Vergnaud G, Ando A, Inoko H, Spurkland A: The SH2D2A gene encoding the T-cell-specific adapter protein (TSAd) is localized centromeric to the CD1 gene cluster on human Chromosome 1. Immunogenetics 51:179-185 (2000).

Dannenberg H, Speel EJ, Zhao J, Saremaslani P, van Der Harst E, Roth J, Heitz PU, Bonjer HJ, Dinjens WN, Mooi WJ, Komminoth P, de Krijger RR: Losses of chromosomes 1p and 3q are early genetic events in the development of sporadic pheochromocytomas. Am J Pathol 157:353-359 (2000).

Donahue RP, Bias WB, Renwick JH, McKusick VA: Probable assignment of the Duffy blood group locus to chromosome 1 in man. Proc Natl Acad Sci U S A 61:949-955 (1968).

Dwight T, Twigg S, Delbridge L, Wong FK, Farnebo F, Richardson AL, Nelson A, Zedenius J, Philips J, Larsson C, Teh BT, Robinson B: Loss of heterozygosity in sporadic parathyroid tumours: involvement of chromosome 1 and the MEN1 gene locus in 11q13. Clin Endocrinol (Oxf) 53:85-92 (2000).

Edstrom E, Mahlamaki E, Nord B, Kjellman M, Karhu R, Hoog A, Goncharov N, Teh BT, Backdahl M, Larsson C: Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology. Am J Pathol 156:651-659 (2000).

El-Rifai W, Kamel D, Larramendy ML, Shoman S, Gad Y, Baithun S, El-Awady M, Eissa S, Khaled H, Soloneski S, Sheaff M, Knuutila S: DNA copy number changes in Schistosoma-associated and non-Schistosoma- associated bladder cancer. Am J Pathol 156:871-878 (2000a).

El-Rifai W, Sarlomo-Rikala M, Andersson LC, Knuutila S, Miettinen M: DNA sequence copy number changes in gastrointestinal stromal tumors: tumor progression and prognostic significance. Cancer Res 60:3899-3903 (2000b).

Fan CS, Wong N, Leung SF, To KF, Lo KW, Lee SW, Mok TS, Johnson PJ, Huang DP: Frequent c-myc and Int-2 overrepresentations in nasopharyngeal carcinoma. Hum Pathol 31:169-178 (2000).

Farr M, Strube J, Geppert H, Kocourek A, Mahne M, Tschesche H: Pregnancy-associated plasma protein-E (PAPP-E)(1). Biochim Biophys Acta 1493:356-362 (2000).

Fitzgerald LR, Dytko GM, Sarau HM, Mannan IJ, Ellis C, Lane PA, Tan KB, Murdock PR, Wilson S, Bergsma DJ, Ames RS, Foley JJ, et al: Identification of an EDG7 variant, HOFNH30, a G-protein-coupled receptor for lysophosphatidic acid. Biochem Biophys Res Commun 273:805-810 (2000).

Flanigan KM, Kerr L, Bromberg MB, Leonard C, Tsuruda J, Zhang P, Gonzalez-Gomez I, Cohn R, Campbell KP, Leppert M: Congenital muscular dystrophy with rigid spine syndrome: a clinical, pathological, radiological, and genetic study [see comments]. Ann Neurol 47:152-161 (2000).

Forozan F, Mahlamaki EH, Monni O, Chen Y, Veldman R, Jiang Y, Gooden GC, Ethier SP, Kallioniemi A, Kallioniemi OP: Comparative genomic hybridization analysis of 38 breast cancer cell lines: a basis for interpreting complementary DNA microarray data. Cancer Res 60:4519-4525 (2000).

Frank D, Mendelsohn CL, Ciccone E, Svensson K, Ohlsson R, Tycko B: A novel pleckstrin homology-related gene family defined by Ipl/Tssc3, TDAG51, and Tih1: tissue-specific expression, chromosomal location, and parental imprinting. Mamm Genome 10:1150-1159 (1999).

Girard L, Zochbauer-Muller S, Virmani AK, Gazdar AF, Minna JD: Genome-wide allelotyping of lung cancer identifies new regions of allelic loss, differences between small cell lung cancer and non-small cell lung cancer, and loci clustering [In Process Citation]. Cancer Res 60:4894-4906 (2000).

Gregory SG, Vaudin M, Wooster R, Coleman M, Mischke D, Porter C, Schutte BC, White P, Vance JM: Report of the fourth international workshop on human chromosome 1 mapping 1998. Cytogenet Cell Genet 83:147-175 (1998).

Gruber AD, Pauli BU: Clustering of the human CLCA gene family on the short arm of chromosome 1 (1p22-31). Genome 42:1030-1032 (1999).

Guan XY, Fang Y, Sham JS, Kwong DL, Zhang Y, Liang Q, Li H, Zhou H, Trent JM: Recurrent chromosome alterations in hepatocellular carcinoma detected by comparative genomic hybridization [In Process Citation]. Genes Chromosomes Chromosom Cancer 29:110-116 (2000).

Haven CJ, Wong FK, van Dam EW, van der Juijt R, van Asperen C, Jansen J, Rosenberg C, de Wit M, Roijers J, Hoppener J, Lips CJ, Larsson C, et al: A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome. J Clin Endocrinol Metab 85:1449-1454 (2000).

Hobby P, Wyatt MK, Gan W, Bernstein S, Tomarev S, Slingsby C, Wistow G: Cloning, modeling, and chromosomal localization for a small leucine- rich repeat proteoglycan (SLRP) family member expressed in human eye. Mol Vis 6:72-78 (2000).

Horvath JE, Schwartz S, Eichler EE: The mosaic structure of human pericentromeric DNA: a strategy for characterizing complex regions of the human genome. Genome Res 10:839-852 (2000).

Houdayer C, Soupre V, Rosenberg-Bourgin M, Martinez H, Tredano M, Feldmann D, Feingold J, Aymard P, Munnich A, Le Bouc Y, Vazquez MP, Bahuau M: Linkage analysis of 5 novel van der Woude syndrome kindreds to 1q32-q41 markers further supports locus homogeneity of the disease trait. Ann Genet 42:69-74 (1999).

Huang LW, Garrett AP, Schorge JO, Muto MG, Bell DA, Welch WR, Berkowitz RS, Mok SC: Distinct allelic loss patterns in papillary serous carcinoma of the peritoneum. Am J Clin Pathol 114:93-99 (2000).

Huiping C, Sigurgeirsdottir JR, Jonasson JG, Eiriksdottir G, Johannsdottir JT, Egilsson V, Ingvarsson S: Chromosome alterations and E-cadherin gene mutations in human lobular breast cancer. Br J Cancer 81:1103-1110 (1999).

Imyanitov EN, Togo AV, Suspitsin EN, Grigoriev MY, Pozharisski KM, Turkevich EA, Hanson KP, Hayward NK, Chenevix-Trench G, Theillet C, Lavin MF: Evidence for microsatellite instability in bilateral breast carcinomas. Cancer Lett 154:9-17 (2000).

Ino Y, Zlatescu MC, Sasaki H, Macdonald DR, Stemmer-Rachamimov AO, Jhung S, Ramsay DA, von Deimling A, Louis DN, Cairncross JG: Long survival and therapeutic responses in patients with histologically disparate high-grade gliomas demonstrating chromosome 1p loss [see comments]. J Neurosurg 92:983-990 (2000).

Jarvis A, Sharma P, Watson N, Smith A: Two children with acute lymphoblastic leukemia and "jumping""jumping" translocations: both involve 1q23 as the donor breakpoint. Cancer Genet Cytogenet 114:112-116 (1999).

Jin Y, Martins C, Jin C, Salemark L, Jonsson N, Persson B, Roque L, Fonseca I, Wennerberg J: Nonrandom karyotypic features in squamous cell carcinomas of the skin. Genes Chromosomes Chromosom Cancer 26:295-303 (1999).

Jogi A, Abel F, Sjoberg RM, Toftgard R, Zaphiropoulos PG, Pahlman S, Martinsson T, Axelson H: Patched 2, located in 1p32-34, is not mutated in high stage neuroblastoma tumors. Int J Oncol 16:943-949 (2000).

Kang YK, Kim YI, Kim WH: Allelotype analysis of intrahepatic cholangiocarcinoma. Mod Pathol 13:627-631 (2000).

Karkkainen I, Karhu R, Huovila AP: Assignment of the ADAM15 gene to human chromosome band 1q21.3 by in situ hybridization. Cytogenet Cell Genet 88:206-207 (2000).

Kashuba V, Protopopov A, Podowski R, Gizatullin R, Li J, Klein G, Wahlestedt C, Zabarovsky E: Isolation and chromosomal localization of a new human retinoblastoma binding protein 2 homologue 1a (RBBP2H1A) [In Process Citation]. Eur J Hum Genet 8:407-413 (2000).

Kiechle M, Hinrichs M, Jacobsen A, Luttges J, Pfisterer J, Kommoss F, Arnold N: Genetic imbalances in precursor lesions of endometrial cancer detected by comparative genomic hybridization. Am J Pathol 156:1827-1833 (2000).

Kitamura Y, Shimizu K, Tanaka S, Ito K, Emi M: Allelotyping of anaplastic thyroid carcinoma: frequent allelic losses on 1q, 9p, 11, 17, 19p, and 22q. Genes Chromosomes Chromosom Cancer 27:244-251 (2000a).

Kitamura Y, Shimizu K, Tanaka S, Ito K, Emi M: Association of allelic loss on 1q, 4p, 7q, 9p, 9q, and 16q with postoperative death in papillary thyroid carcinoma. Clin Cancer Res 6:1819-1825 (2000b).

Knight SJ, Lese CM, Precht KS, Kuc J, Ning Y, Lucas S, Regan R, Brenan M, Nicod A, Lawrie NM, Cardy DL, Nguyen H, et al: An optimized set of human telomere clones for studying telomere integrity and architecture. Am J Hum Genet 67:320-332 (2000).

Korenberg JR, Chen XN, Sun Z, Shi ZY, Ma S, Vataru E, Yimlamai D, Weissenbach JS, Shizuya H, Simon MI, Gerety SS, Nguyen H, et al: Human genome anatomy: BACs integrating the genetic and cytogenetic maps for bridging genome and biomedicine. Genome Res 9:994-1001 (1999).

Kornak U, Bosl MR, Kubisch C: Complete genomic structure of the CLCN6 and CLCN7 putative chloride channel genes(1). Biochim Biophys Acta 1447:100-106 (1999).

Kraggerud SM, Szymanska J, Abeler VM, Kaern J, Eknaes M, Heim S, Teixeira MR, Trope CG, Peltomaki P, Lothe RA: DNA copy number changes in malignant ovarian germ cell tumors. Cancer Res 60:3025-3030 (2000).

Kytola S, Farnebo F, Obara T, Isola J, Grimelius L, Farnebo LO, Sandelin K, Larsson C: Patterns of chromosomal imbalances in parathyroid carcinomas. Am J Pathol 157:579-586 (2000).

Lamlum H, Papadopoulou A, Ilyas M, Rowan A, Gillet C, Hanby A, Talbot I, Bodmer W, Tomlinson I: APC mutations are sufficient for the growth of early colorectal adenomas. Proc Natl Acad Sci U S A 97:2225-2228 (2000).

Lamszus K, Vahldiek F, Mautner VF, Schichor C, Tonn J, Stavrou D, Fillbrandt R, Westphal M, Kluwe L: Allelic losses in neurofibromatosis 2-associated meningiomas. J Neuropathol Exp Neurol 59:504-512 (2000).

Larramendy ML, Lushnikova T, Bjorkqvist A, Wistuba II, Virmani AK, Shivapurkar N, Gazdar AF, Knuutila S: Comparative genomic hybridization reveals complex genetic changes in primary breast cancer tumors and their cell lines [In Process Citation]. Cancer Genet Cytogenet 119:132-138 (2000).

Lee CG, Eki T, Okumura K, Nogami M, Soares VC, Murakami Y, Hanaoka F, Hurwitz J: The human RNA helicase A (DDX9) gene maps to the prostate cancer susceptibility locus at chromosome band 1q25 and its pseudogene (DDX9P) to 13q22, respectively. Somat Cell Mol Genet 25:33-39 (1999).

Lepretre S, Buchonnet G, Stamatoullas A, Lenain P, Duval C, d'Anjou J, Callat MP, Tilly H, Bastard C: Chromosome abnormalities in peripheral T-cell lymphoma. Cancer Genet Cytogenet 117:71-79 (2000).

Levy B, Mukherjee T, Hirschhorn K: Molecular cytogenetic analysis of uterine leiomyoma and leiomyosarcoma by comparative genomic hybridization. Cancer Genet Cytogenet 121:1-8 (2000).

Lo KW, Teo PM, Hui AB, To KF, Tsang YS, Chan SY, Mak KF, Lee JC, Huang DP: High resolution allelotype of microdissected primary nasopharyngeal carcinoma. Cancer Res 60:3348-3353 (2000).

Looijenga LH, Rosenberg C, van Gurp RJ, Geelen E, van Echten-Arends J, de Jong B, Mostert M, Wolter Oosterhuis J: Comparative genomic hybridization of microdissected samples from different stages in the development of a seminoma and a non-seminoma. J Pathol 191:187-192 (2000).

Loveday RL, Greenman J, Simcox DL, Speirs V, Drew PJ, Monson JR, Kerin MJ: Genetic changes in breast cancer detected by comparative genomic hybridisation. Int J Cancer 86:494-500 (2000).

Lu Y, Brush J, Stewart TA: NSP1 defines a novel family of adaptor proteins linking integrin and tyrosine kinase receptors to the c-Jun N-terminal kinase/stress- activated protein kinase signaling pathway. J Biol Chem 274:10047-10052 (1999).

Mairal A, Pinglier E, Gilbert E, Peter M, Validire P, Desjardins L, Doz F, Aurias A, Couturier J: Detection of chromosome imbalances in retinoblastoma by parallel karyotype and CGH analyses. Genes Chromosomes Chromosom Cancer 28:370-379 (2000).

Malamou-Mitsi VD, Syrrou M, Georgiou I, Pagoulatos G, Agnantis NJ: Analysis of chromosomal aberrations in breast cancer by comparative genomic hybridization (CGH). Correlation with histoprognostic variables and c-erbB-2 immunoexpression. J Exp Clin Cancer Res 18:357-361 (1999).

Mandahl N, Fletcher CD, Dal Cin P, De Wever I, Mertens F, Mitelman F, Rosai J, Rydholm A, Sciot R, Tallini G, Van Den Berghe H, Vanni R, et al: Comparative cytogenetic study of spindle cell and pleomorphic leiomyosarcomas of soft tissues: a report from the CHAMP Study Group. Cancer Genet Cytogenet 116:66-73 (2000).

Marcelino J, Carpten JD, Suwairi WM, Gutierrez OM, Schwartz S, Robbins C, Sood R, Makalowska I, Baxevanis A, Johnstone B, Laxer RM, Zemel L, et al: CACP, encoding a secreted proteoglycan, is mutated in camptodactyly- arthropathy-coxa vara-pericarditis syndrome. Nat Genet 23:319-322 (1999).

Marchio A, Pineau P, Meddeb M, Terris B, Tiollais P, Bernheim A, Dejean A: Distinct chromosomal abnormality pattern in primary liver cancer of non- B, non-C patients. Oncogene 19:3733-3738 (2000).

Marra MA, Kucaba TA, Dietrich NL, Green ED, Brownstein B, Wilson RK, McDonald KM, Hillier LW, McPherson JD, Waterston RH: High throughput fingerprint analysis of large-insert clones. Genome Res 7:1072-1084 (1997).

Matthews CP, Shera KA, McDougall JK: Genomic changes and HPV type in cervical carcinoma. Proc Soc Exp Biol Med 223:316-321 (2000).

Mayama T, Fukushige S, Shineha R, Nishihira T, Satomi S, Horii A: Frequent loss of copy number on the long arm of chromosome 21 in human esophageal squamous cell carcinoma. Int J Oncol 17:245-252 (2000).

Meissner B, Purmann S, Schurmann M, Zuhlke C, Lencer R, Arolt V, Muller-Myhsok B, Morris-Rosendahl DJ, Schwinger E: hSKCa3: a candidate gene for schizophrenia? Psychiatr Genet 9:91-96 (1999).

Michelland S, Gazzeri S, Brambilla E, Robert-Nicoud M: Comparison of chromosomal imbalances in neuroendocrine and non-small-cell lung carcinomas. Cancer Genet Cytogenet 114:22-30 (1999).

Mizushima K, Miyamoto Y, Tsukahara F, Hirai M, Sakaki Y, Ito T: A novel G-protein-coupled receptor gene expressed in striatum. Genomics 69:314-321 (2000).

Muller P, Henn W, Niedermayer I, Ketter R, Feiden W, Steudel WI, Zang KD, Steilen-Gimbel H: Deletion of chromosome 1p and loss of expression of alkaline phosphatase indicate progression of meningiomas. Clin Cancer Res 5:3569-3577 (1999).

Murthy SS, Tosolini A, Taguchi T, Testa JR: Mapping of AKT3, encoding a member of the Akt/protein kinase B family, to human and rodent chromosomes by fluorescence in situ hybridization. Cytogenet Cell Genet 88:38-40 (2000).

Muscheck M, Abol-Enein H, Chew K, Moore D, 2nd, Bhargava V, Ghoneim MA, Carroll PR, Waldman FM: Comparison of genetic changes in schistosome-related transitional and squamous bladder cancers using comparative genomic hybridization. Carcinogenesis 21:1721-1726 (2000).

Nagai M, Ichimiya S, Ozaki T, Seki N, Mihara M, Furuta S, Ohira M, Tomioka N, Nomura N, Sakiyama S, Kubo O, Takakura K, et al: Identification of the full-length KIAA0591 gene encoding a novel kinesin-related protein which is mapped to the neuroblastoma suppressor gene locus at 1p36.2. Int J Oncol 16:907-916 (2000).

Nagata T, Mugishima H, Shichino H, Suzuki T, Chin M, Koshinaga S, Inoue M, Harada K: Karyotypic analyses of hepatoblastoma. Report of two cases and review of the literature suggesting chromosomal loci responsible for the pathogenesis of this disease. Cancer Genet Cytogenet 114:42-50 (1999).

Nakaji T, Kataoka TR, Watabe K, Nishiyama K, Nojima H, Shimada Y, Sato F, Matsushima H, Endo Y, Kuroda Y, Kitamura Y, Ito A, et al: A new member of the GTPase superfamily that is upregulated in highly metastatic cells. Cancer Lett 147:139-147 (1999).

Nakamura M, Yang F, Fujisawa H, Yonekawa Y, Kleihues P, Ohgaki H: Loss of heterozygosity on chromosome 19 in secondary glioblastomas. J Neuropathol Exp Neurol 59:539-543 (2000).

Nomiyama H, Fukuda S, Iio M, Tanase S, Miura R, Yoshie O: Organization of the chemokine gene cluster on human chromosome 17q11.2 containing the genes for CC chemokine MPIF-1, HCC-2, HCC-1, LEC, and RANTES. J Interferon Cytokine Res 19:227-234 (1999).

Nomoto S, Haruki N, Tatematsu Y, Konishi H, Mitsudomi T, Takahashi T: Frequent allelic imbalance suggests involvement of a tumor suppressor gene at 1p36 in the pathogenesis of human lung cancers. Genes Chromosomes Chromosom Cancer 28:342-346 (2000).

Ogawa S, Saito T, Matsuda Y, Seki N, Hayashi A, Orimo A, Hosoi T, Ouchi Y, Muramatsu M, Hori T, Inoue S: Chromosome mapping of RNF16 and rnf16, human, mouse and rat genes coding for testis RING finger protein (terf), a member of the RING finger family. Cytogenet Cell Genet 89:56-58 (2000).

Ohira M, Kageyama H, Mihara M, Furuta S, Machida T, Shishikura T, Takayasu H, Islam A, Nakamura Y, Takahashi M, Tomioka N, Sakiyama S, et al: Identification and characterization of a 500-kb homozygously deleted region at 1p36.2-p36.3 in a neuroblastoma cell line [In Process Citation]. Oncogene 19:4302-4307 (2000).

Parada LA, Limon J, Iliszko M, Czauderna P, Gisselsson D, Hoglund M, Kullendorff CM, Wiebe T, Mertens F, Johansson B: Cytogenetics of hepatoblastoma: further characterization of 1q rearrangements by fluorescence in situ hybridization: an international collaborative study. Med Pediatr Oncol 34:165-170 (2000).

Pedersen B, Norgaard JM, Pedersen BB, Clausen N, Rasmussen IH, Thorling K: Many unbalanced translocations show duplication of a translocation participant. Clinical and cytogenetic implications in myeloid hematologic malignancies. Am J Hematol 64:161-169 (2000).

Pei W, Baron H, Muller-Myhsok B, Knoblauch H, Al-Yahyaee SA, Hui R, Wu X, Liu L, Busjahn A, Luft FC, Schuster H: Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families. Clin Genet 57:29-34 (2000).

Perlman EJ, Hu J, Ho D, Cushing B, Lauer S, Castleberry RP: Genetic analysis of childhood endodermal sinus tumors by comparative genomic hybridization. J Pediatr Hematol Oncol 22:100-105 (2000).

Poetsch M, Woenckhaus C, Dittberner T, Pambor M, Lorenz G, Herrmann FH: Significance of the small subtelomeric area of chromosome 1 (1p36.3) in the progression of malignant melanoma: FISH deletion screening with YAC DNA probes. Virchows Arch 435:105-111 (1999).

Postma AV, Bezzina CR, de Vries JF, Wilde AA, Moorman AF, Mannens MM: Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3. Hum Genet 106:614-619 (2000).

Prescott NJ, Lees MM, Winter RM, Malcolm S: Identification of susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a two stage genome scan of affected sib- pairs. Hum Genet 106:345-350 (2000).

Racevskis J, Dill A, Sparano JA, Ruan H: Molecular cloning of LMO41, a new human LIM domain gene. Biochim Biophys Acta 1445:148-153 (1999).

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