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Volumn 72, Issue 2-3, 1996, Pages 113-154

Report of the second international workshop on human chromosome 1 mapping 1995

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 1; CHROMOSOME MAP; CONFERENCE PAPER; GENETICS; HUMAN; GENE ASSIGNMENT; GENE LOCATION; GENE LOCUS; GENE MAPPING; GENETIC DISORDER; PRIORITY JOURNAL; WORKSHOP;

EID: 0030333738     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: 10.1159/000134173     Document Type: Article
Times cited : (85)

References (233)
  • 1
    • 0029012428 scopus 로고
    • Lysosomal chitobiase (CTB) and the G-protein gamma-5 (GNG5) genes colocalize to human chromosome 1p22
    • Ahmad W, Li S, Chen H, Tuck-Muller CM, Pittler SJ, Aronson NN: Lysosomal chitobiase (CTB) and the G-protein gamma-5 (GNG5) genes colocalize to human chromosome 1p22. Cytogenet Cell Genet 71:44-46 (1995).
    • (1995) Cytogenet Cell Genet , vol.71 , pp. 44-46
    • Ahmad, W.1    Li, S.2    Chen, H.3    Tuck-Muller, C.M.4    Pittler, S.J.5    Aronson, N.N.6
  • 3
    • 0025368589 scopus 로고
    • Construction and characterization of a yeast artificial chromosome library containing seven haploid genome equivalents
    • Albertsen HM, Abderrahim H, Cann HC, Dausset J, LePaslier D, Cohen D: Construction and characterization of a yeast artificial chromosome library containing seven haploid genome equivalents. Proc natl Acad Sci, USA 87:4256-4260 (1990).
    • (1990) Proc Natl Acad Sci, USA , vol.87 , pp. 4256-4260
    • Albertsen, H.M.1    Abderrahim, H.2    Cann, H.C.3    Dausset, J.4    LePaslier, D.5    Cohen, D.6
  • 4
    • 3042958258 scopus 로고
    • The adenovirus 12 modification site. 1p (A12M2) is also a site of preferential viral integration in human cells transfected with the hybrid recombinant virus Adenovirus 5/SV40
    • Alhadeff B, Purello M, Romani M, Szabo P, Gluzman Y, Siniscalco M: The adenovirus 12 modification site. 1p (A12M2) is also a site of preferential viral integration in human cells transfected with the hybrid recombinant virus Adenovirus 5/SV40. Cytogenet Cell Genet 46:569 (1987).
    • (1987) Cytogenet Cell Genet , vol.46 , pp. 569
    • Alhadeff, B.1    Purello, M.2    Romani, M.3    Szabo, P.4    Gluzman, Y.5    Siniscalco, M.6
  • 6
    • 0025369509 scopus 로고
    • A 3.5 genome equivalent multi access YAC library: Construction, characterization, screening and storage
    • Anand R, Riley JH, Butler R, Smith JC, Markham AF: A 3.5 genome equivalent multi access YAC library: construction, characterization, screening and storage. Nucl Acids Res 18:1951-1956 (1990).
    • (1990) Nucl Acids Res , vol.18 , pp. 1951-1956
    • Anand, R.1    Riley, J.H.2    Butler, R.3    Smith, J.C.4    Markham, A.F.5
  • 7
    • 0028938043 scopus 로고
    • Localizalion of the human B-type natriuretic peptide precursor (NPPB) gene to chromosome 1p36
    • Arden KC, Viars CS, Weiss S, Argentin S, Nemer M: Localizalion of the human B-type natriuretic peptide precursor (NPPB) gene to chromosome 1p36. Genomics 26:385-389 (1995).
    • (1995) Genomics , vol.26 , pp. 385-389
    • Arden, K.C.1    Viars, C.S.2    Weiss, S.3    Argentin, S.4    Nemer, M.5
  • 8
    • 0028936363 scopus 로고
    • High-resolution cytogenetic mapping of the short arm of chromosome 1 with newly isolated 411 cosmid markers by fluorescence in situ hybridization: The precise order of 18 markers on 1p36.1 on prophase chromosomes and "stretched" DNAs
    • Ariyama T, Inazawa J, Ezaki T, Nakamura Y, Horii A, Abe T: High-resolution cytogenetic mapping of the short arm of chromosome 1 with newly isolated 411 cosmid markers by fluorescence in situ hybridization: the precise order of 18 markers on 1p36.1 on prophase chromosomes and "stretched" DNAs. Genomics 25:114-123 (1995).
    • (1995) Genomics , vol.25 , pp. 114-123
    • Ariyama, T.1    Inazawa, J.2    Ezaki, T.3    Nakamura, Y.4    Horii, A.5    Abe, T.6
  • 9
    • 0022573439 scopus 로고
    • Chromosome 1 aberrations in cancer
    • Atkin NB: Chromosome 1 aberrations in cancer. Cancer Genet Cytogenet 21:279-285 (1986).
    • (1986) Cancer Genet Cytogenet , vol.21 , pp. 279-285
    • Atkin, N.B.1
  • 11
    • 0027157843 scopus 로고
    • Deletion of 1p36 as primary chromosomal aberration in intestinal tumorigenesis
    • Bardi G, Pandis N, Fenger C, Kronborg O, Bomme L, Heim, S: Deletion of 1p36 as primary chromosomal aberration in intestinal tumorigenesis. Cancer Res 53:1895-1898 (1993).
    • (1993) Cancer Res , vol.53 , pp. 1895-1898
    • Bardi, G.1    Pandis, N.2    Fenger, C.3    Kronborg, O.4    Bomme, L.5    Heim, S.6
  • 12
    • 0028181661 scopus 로고
    • Chromosomal localization of the delta opioid receptor gene to human 1p34.3→p36.1 and mouse 4D bands by in situ hybridization
    • Befort K, Mattei MG, Roeckel N, Kieffer B: Chromosomal localization of the delta opioid receptor gene to human 1p34.3→p36.1 and mouse 4D bands by in situ hybridization. Genomics 20:143-145 (1994).
    • (1994) Genomics , vol.20 , pp. 143-145
    • Befort, K.1    Mattei, M.G.2    Roeckel, N.3    Kieffer, B.4
  • 18
    • 0028215338 scopus 로고
    • A novel gene, AF-1p, fused to HRX in t(1;11)(p32;q23), is not related to AF-4, AF-9 nor ENL
    • Bernard OA, Mauchauffe M, Mecucci C, Van Den Berghe H, Berger R: A novel gene, AF-1p, fused to HRX in t(1;11)(p32;q23), is not related to AF-4, AF-9 nor ENL. Oncogene 9:1039-1045 (1994).
    • (1994) Oncogene , vol.9 , pp. 1039-1045
    • Bernard, O.A.1    Mauchauffe, M.2    Mecucci, C.3    Van Den Berghe, H.4    Berger, R.5
  • 20
    • 0028920875 scopus 로고
    • Loss and gain of distinct regions of chromosome 1q in primary breast cancer
    • Bieche I, Champeme M-H, Lidereau R: Loss and gain of distinct regions of chromosome 1q in primary breast cancer. Clin Cancer Res 1:123-127 (1995).
    • (1995) Clin Cancer Res , vol.1 , pp. 123-127
    • Bieche, I.1    Champeme, M.-H.2    Lidereau, R.3
  • 22
    • 0028208520 scopus 로고
    • Human genes encoding the voltage-dependent anion channel (VDAC) of the outer mitochondrial membrane: Mapping and identification of two new isoforms
    • Blachly-Dyson E, Baldini A, Litt M, McCabe ERB, Forte M: Human genes encoding the voltage-dependent anion channel (VDAC) of the outer mitochondrial membrane: mapping and identification of two new isoforms. Genomics 20:62-67 (1994).
    • (1994) Genomics , vol.20 , pp. 62-67
    • Blachly-Dyson, E.1    Baldini, A.2    Litt, M.3    McCabe, E.R.B.4    Forte, M.5
  • 23
    • 0022409280 scopus 로고
    • T(1;3)(p36;q21) in acute nonlymphocytic leukemia: A new cytogenetic-clinicopathologic association
    • Bloomfield CD, Garson OM, Voilin L, Knuutila S, de la Chapelle A: t(1;3)(p36;q21) in acute nonlymphocytic leukemia: A new cytogenetic-clinicopathologic association. Blood 66:1409-1413 (1985).
    • (1985) Blood , vol.66 , pp. 1409-1413
    • Bloomfield, C.D.1    Garson, O.M.2    Voilin, L.3    Knuutila, S.4    De la Chapelle, A.5
  • 24
    • 0029355897 scopus 로고
    • ESTablishing a human transcript map
    • Boguski MS, Schuler GD: ESTablishing a human transcript map. Nature Genet 10:369-371 (1995).
    • (1995) Nature Genet , vol.10 , pp. 369-371
    • Boguski, M.S.1    Schuler, G.D.2
  • 25
    • 0028053823 scopus 로고
    • Human mitochondrial HMG CoA Synthase: Liver cDNA and partial genomic cloning, chromosome mapping to 1p12→p13, and possible role in vertebrate evolution
    • Boukaftane Y, Duncan A, Wang S, Labuda D, Robert M, Sarrazin J, Schappert K, Mitchell GA: Human mitochondrial HMG CoA Synthase: liver cDNA and partial genomic cloning, chromosome mapping to 1p12→p13, and possible role in vertebrate evolution. Genonucs 23:552-559 (1994).
    • (1994) Genonucs , vol.23 , pp. 552-559
    • Boukaftane, Y.1    Duncan, A.2    Wang, S.3    Labuda, D.4    Robert, M.5    Sarrazin, J.6    Schappert, K.7    Mitchell, G.A.8
  • 27
    • 0019819011 scopus 로고
    • Break points in chromosome number 1. Abnormalities of 218 human neoplasms
    • Brito-Babapulle V, Alkin NB: Break points in chromosome number 1. Abnormalities of 218 human neoplasms. Cancer Genet Cytogenet 4:215-225 (1981).
    • (1981) Cancer Genet Cytogenet , vol.4 , pp. 215-225
    • Brito-Babapulle, V.1    Alkin, N.B.2
  • 30
    • 0023349389 scopus 로고
    • Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors
    • Burke DT, Carle GF, Olson Mv: Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors. Science 236:806-812 (1987).
    • (1987) Science , vol.236 , pp. 806-812
    • Burke, D.T.1    Carle, G.F.2    Olson, Mv.3
  • 31
    • 0029020759 scopus 로고
    • The retinoblastoma protein binds to RIZ, a zinc-finger protein that shares an epitope with the adenovirus E1A protein
    • Buyse IM, Shao G, Huang S. The retinoblastoma protein binds to RIZ, a zinc-finger protein that shares an epitope with the adenovirus E1A protein. Proc natl Acad Sci, USA 92:4467-4471 (1995).
    • (1995) Proc Natl Acad Sci, USA , vol.92 , pp. 4467-4471
    • Buyse, I.M.1    Shao, G.2    Huang, S.3
  • 37
  • 38
    • 0027965692 scopus 로고
    • Human 60-kDa SS-A/Ro ribonucleoprotein autoantigen gene (SSA2) localized to 1q31 by fluorescence in situ hybridization
    • Chan EKL, Tan EM, Ward DC, Matera AG: Human 60-kDa SS-A/Ro ribonucleoprotein autoantigen gene (SSA2) localized to 1q31 by fluorescence in situ hybridization. Genomics 23:298-300 (1994).
    • (1994) Genomics , vol.23 , pp. 298-300
    • Chan, E.K.L.1    Tan, E.M.2    Ward, D.C.3    Matera, A.G.4
  • 40
    • 0024447257 scopus 로고
    • Loss of heterozygosity on chromosome 1q in human breast cancer
    • Chen LC, Dollbaum C, Smith HS: Loss of heterozygosity on chromosome 1q in human breast cancer. Proc natl Acad Sci, USA 86:7204-7207 (1989).
    • (1989) Proc Natl Acad Sci, USA , vol.86 , pp. 7204-7207
    • Chen, L.C.1    Dollbaum, C.2    Smith, H.S.3
  • 42
    • 0028815356 scopus 로고
    • Deletion mapping in neuroblastoma cell lines suggests two distinct tumor suppressor genes in the 1p35→p36 region, only one of which is associated with N-myc amplification
    • Cheng NC, van Roy N, Chan A, Beitsma M, Westerveld A, Speleman F, Versteeg R: Deletion mapping in neuroblastoma cell lines suggests two distinct tumor suppressor genes in the 1p35→p36 region, only one of which is associated with N-myc amplification. Oncogens 10:291-297 (1995).
    • (1995) Oncogens , vol.10 , pp. 291-297
    • Cheng, N.C.1    Van Roy, N.2    Chan, A.3    Beitsma, M.4    Westerveld, A.5    Speleman, F.6    Versteeg, R.7
  • 43
    • 0029039368 scopus 로고
    • Isolation and mapping of the human beta-signal sequence receptor gene (SSR2)
    • Chinen K, Sudo K, Takahashi E, Nakamura Y: Isolation and mapping of the human beta-signal sequence receptor gene (SSR2). Cytogenet Cell Genet 70:215-217 (1995).
    • (1995) Cytogenet Cell Genet , vol.70 , pp. 215-217
    • Chinen, K.1    Sudo, K.2    Takahashi, E.3    Nakamura, Y.4
  • 44
    • 0027723477 scopus 로고
    • A first generation physical map of the human genome
    • Cohen D, Cumakov I, Weissenbach JF: A first generation physical map of the human genome. Nature 366:698-701 (1993).
    • (1993) Nature , vol.366 , pp. 698-701
    • Cohen, D.1    Cumakov, I.2    Weissenbach, J.F.3
  • 47
    • 0027957089 scopus 로고
    • Human and mouse chromosomal mapping of the myeloid cell leukemia-1 gene: MLC1 maps to human chromosome 1q21, a region that is frequently altered in preneoplasic and neoplastic disease
    • Craig RW, Jabs EW, Zhou P, Kozopas KM, Hawkins AL, Rochelle JM, Seldin MF, Griffin CA: Human and mouse chromosomal mapping of the myeloid cell leukemia-1 gene: MLC1 maps to human chromosome 1q21, a region that is frequently altered in preneoplasic and neoplastic disease. Genomics 23:457-463 (1994).
    • (1994) Genomics , vol.23 , pp. 457-463
    • Craig, R.W.1    Jabs, E.W.2    Zhou, P.3    Kozopas, K.M.4    Hawkins, A.L.5    Rochelle, J.M.6    Seldin, M.F.7    Griffin, C.A.8
  • 49
    • 0028908735 scopus 로고
    • The closely linked genes encoding the myeloid nuclear differentiation antigen (MNDA) and IFI16 exhibit contrasting haemopoietic expression
    • Dawson MJ, Trapani JA, Briggs RC, Nicholl JK, Sutherland GR, Baker E: The closely linked genes encoding the myeloid nuclear differentiation antigen (MNDA) and IFI16 exhibit contrasting haemopoietic expression. Immunogenetics 41:40-43 (1995).
    • (1995) Immunogenetics , vol.41 , pp. 40-43
    • Dawson, M.J.1    Trapani, J.A.2    Briggs, R.C.3    Nicholl, J.K.4    Sutherland, G.R.5    Baker, E.6
  • 50
    • 0028364374 scopus 로고
    • Fusion of PAX7 to FKHR by the variant t(1;13)(p36;q14) translocation in alveolar rhabdomyosarcoma
    • Davis RJ, D'Cruz CM, Lovell MA, Biegel JA, Barr FG. Fusion of PAX7 to FKHR by the variant t(1;13)(p36;q14) translocation in alveolar rhabdomyosarcoma. Cancer Res 54:2869-2872 (1994).
    • (1994) Cancer Res , vol.54 , pp. 2869-2872
    • Davis, R.J.1    D'Cruz, C.M.2    Lovell, M.A.3    Biegel, J.A.4    Barr, F.G.5
  • 51
    • 0028464353 scopus 로고
    • Mapping of the human tuftelin (TUFT1) gene to chromosome 1 by fluorescence in situ hybridization
    • Deutsch D, Palmon A, Young MF, Selig S, Kearns WG, Fisher LW: Mapping of the human tuftelin (TUFT1) gene to chromosome 1 by fluorescence in situ hybridization. Mammal Genome 5(7):461-462 (1994).
    • (1994) Mammal Genome , vol.5 , Issue.7 , pp. 461-462
    • Deutsch, D.1    Palmon, A.2    Young, M.F.3    Selig, S.4    Kearns, W.G.5    Fisher, L.W.6
  • 52
    • 0027363063 scopus 로고
    • Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse
    • Dietrich WF, Lander ES; Smith JS, Moser AR, Gould KA, Luongo C, Borenstein N, Dove W: Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse. Cell 75:631-639 (1993).
    • (1993) Cell , vol.75 , pp. 631-639
    • Dietrich, W.F.1    Lander, E.S.2    Smith, J.S.3    Moser, A.R.4    Gould, K.A.5    Luongo, C.6    Borenstein, N.7    Dove, W.8
  • 53
    • 0029589675 scopus 로고
    • Chromosomal localization of the human genes alpha 1A, alpha 1B and alpha 1E voltage-dependent Ca channel subunits
    • in press
    • Diriong S, Lory P, Williams ME, Ellis SB, Narpold MM, Taviaux S: Chromosomal localization of the human genes alpha 1A, alpha 1B and alpha 1E voltage-dependent Ca channel subunits. Genomics (in press, 1995).
    • (1995) Genomics
    • Diriong, S.1    Lory, P.2    Williams, M.E.3    Ellis, S.B.4    Narpold, M.M.5    Taviaux, S.6
  • 60
    • 0028985577 scopus 로고
    • Mapping of the receptor protein-tyrosine kinase 10 to human chromosome 1q21→q23 and mouse chromosome 1H1-5 by fluorescence in situ hybridization
    • Edelhoff S, Lai C, Disteche CM: Mapping of the receptor protein-tyrosine kinase 10 to human chromosome 1q21→q23 and mouse chromosome 1H1-5 by fluorescence in situ hybridization. Genomics 25:337-339 (1995).
    • (1995) Genomics , vol.25 , pp. 337-339
    • Edelhoff, S.1    Lai, C.2    Disteche, C.M.3
  • 61
    • 0029002373 scopus 로고
    • Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36
    • Eiberg H, Lund AM, Warburg M, Rosenberg T. Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36. Hum Genet 96:33-38 (1995).
    • (1995) Hum Genet , vol.96 , pp. 33-38
    • Eiberg, H.1    Lund, A.M.2    Warburg, M.3    Rosenberg, T.4
  • 63
    • 0028904634 scopus 로고
    • Characterization of the human gene for microfibril-associated glycoprotein (MFAP2), assignment to chromosome 1p36.1→p35, and linkage to D1S170
    • Faraco J, Bashir M, Rosenbloom J, Francke U: Characterization of the human gene for microfibril-associated glycoprotein (MFAP2), assignment to chromosome 1p36.1→p35, and linkage to D1S170. Genomics 25:630-637 (1995).
    • (1995) Genomics , vol.25 , pp. 630-637
    • Faraco, J.1    Bashir, M.2    Rosenbloom, J.3    Francke, U.4
  • 64
    • 0027980940 scopus 로고
    • Confirmation of the assignment of the gene encoding Kv1.3, a voltage-gated potassium channel (KCNA3) to the proximal short arm of human chromosome 1
    • Folander K, Douglass J, Swanson R: Confirmation of the assignment of the gene encoding Kv1.3, a voltage-gated potassium channel (KCNA3) to the proximal short arm of human chromosome 1. Genomics 23:295-296 (1994).
    • (1994) Genomics , vol.23 , pp. 295-296
    • Folander, K.1    Douglass, J.2    Swanson, R.3
  • 67
    • 0029097446 scopus 로고
    • Comparative genomic hybridization analysis of human sarcomas: I. Occurrence of genomic imbalances and identification of a novel major amplicon at 1q21→q22 in soft tissue sarcomas
    • Forus A, Weghuis DO, Smeets D, Fodstad O, Myklebost O, van Kessel AG: Comparative genomic hybridization analysis of human sarcomas: I. Occurrence of genomic imbalances and identification of a novel major amplicon at 1q21→q22 in soft tissue sarcomas. Genes Chrom Cancer 14:8-14 (1995a).
    • (1995) Genes Chrom Cancer , vol.14 , pp. 8-14
    • Forus, A.1    Weghuis, D.O.2    Smeets, D.3    Fodstad, O.4    Myklebost, O.5    Van Kessel, A.G.6
  • 68
    • 0029157147 scopus 로고
    • Comparative genomic hybridization analysis of human sarcomas: II. Identification of novel amplicons at 6p and 17p in osteosarcomas
    • Forus A, Weghuis DO, Smeets D, Fodstad O, Myklebost O, van Kessel AG: Comparative genomic hybridization analysis of human sarcomas: II. Identification of novel amplicons at 6p and 17p in osteosarcomas. Genes Chrom Cancer 14:15-21 (1995b).
    • (1995) Genes Chrom Cancer , vol.14 , pp. 15-21
    • Forus, A.1    Weghuis, D.O.2    Smeets, D.3    Fodstad, O.4    Myklebost, O.5    Van Kessel, A.G.6
  • 69
    • 43949152437 scopus 로고
    • Construction and preliminary analysis of the ICRF human P1 library
    • Francis F, Zehetner G, Hoglund M, Lehrach H: Construction and preliminary analysis of the ICRF human P1 library. Genet Anal Tech Appl 11:148-157 (1994).
    • (1994) Genet Anal Tech Appl , vol.11 , pp. 148-157
    • Francis, F.1    Zehetner, G.2    Hoglund, M.3    Lehrach, H.4
  • 70
    • 0027939545 scopus 로고
    • CDNA cloning of the human monocarboxylate transporter 1 and chromosomal localization of the SLC16A1 locus to 1p13.2→p12
    • Garcia CK, Li X, Luna J, Francke U: cDNA cloning of the human monocarboxylate transporter 1 and chromosomal localization of the SLC16A1 locus to 1p13.2→p12. Genomics 23:500-503 (1994).
    • (1994) Genomics , vol.23 , pp. 500-503
    • Garcia, C.K.1    Li, X.2    Luna, J.3    Francke, U.4
  • 71
    • 0023181195 scopus 로고
    • Novel non-isotopic in situ hybridization technique detects small (1 kb) unique sequences in routinely G-banded human chromosomes: Fine mapping of N-myc and β-NGF genes
    • Garson JA, van den Berghe JA, Kemshead JT: Novel non-isotopic in situ hybridization technique detects small (1 kb) unique sequences in routinely G-banded human chromosomes: fine mapping of N-myc and β-NGF genes. Nucl Acids Res 15:4761-4770 (1987).
    • (1987) Nucl Acids Res , vol.15 , pp. 4761-4770
    • Garson, J.A.1    Van den Berghe, J.A.2    Kemshead, J.T.3
  • 75
    • 0028609163 scopus 로고
    • Localization of the genes encoding two transcription factors, LMX1 and CDX3, regulating insulin gene expression to human chromosomes 1 and 13
    • German MS, Wang J, Fernald AA, Espinosa R III, Le Beau MM, Bell GI: Localization of the genes encoding two transcription factors, LMX1 and CDX3, regulating insulin gene expression to human chromosomes 1 and 13. Genomics 24:403-404 (1994).
    • (1994) Genomics , vol.24 , pp. 403-404
    • German, M.S.1    Wang, J.2    Fernald, A.A.3    Espinosa III, R.4    Le Beau, M.M.5    Bell, G.I.6
  • 76
    • 0028211586 scopus 로고
    • Deletion of chromosome arm 1p in a Merkel cell carcinoma (MCC)
    • Gibas Z, Weil S, Chen S-T, McCue PA: Deletion of chromosome arm 1p in a Merkel cell carcinoma (MCC). Genes Chrom Cancer 9:216-220 (1994).
    • (1994) Genes Chrom Cancer , vol.9 , pp. 216-220
    • Gibas, Z.1    Weil, S.2    Chen, S.-T.3    McCue, P.A.4
  • 79
    • 0021717846 scopus 로고
    • Evolution of the human sarcomeric actin genes: Evidence for units of selection within the 3′ untranslated regions of the mRNAs
    • Gunning P, Mohun T, Ng SY, Ponte P, Kedes L: Evolution of the human sarcomeric actin genes: evidence for units of selection within the 3′ untranslated regions of the mRNAs. J mol Evol 20:202-214 (1984).
    • (1984) J Mol Evol , vol.20 , pp. 202-214
    • Gunning, P.1    Mohun, T.2    Ng, S.Y.3    Ponte, P.4    Kedes, L.5
  • 80
    • 0028272994 scopus 로고
    • The gene for the retinal pigment epithelium-specific protein RPE65 is localized to human 1p31 and mouse 3
    • Hamel CP, Jenkins NA, Gilbert DJ, Copeland NG, Redmond TM: The gene for the retinal pigment epithelium-specific protein RPE65 is localized to human 1p31 and mouse 3. Genomics 20:509-512 (1994).
    • (1994) Genomics , vol.20 , pp. 509-512
    • Hamel, C.P.1    Jenkins, N.A.2    Gilbert, D.J.3    Copeland, N.G.4    Redmond, T.M.5
  • 81
    • 0011918814 scopus 로고
    • Physical linkage of CRABP-II and calcyclin on chromosome 1q21 by yeast artificial chromosome cloning. (abstr.)
    • Hardas BD, Elder JT: Physical linkage of CRABP-II and calcyclin on chromosome 1q21 by yeast artificial chromosome cloning. (abstr.) J Invest Dermatol 98:569 (1992).
    • (1992) J Invest Dermatol , vol.98 , pp. 569
    • Hardas, B.D.1    Elder, J.T.2
  • 82
    • 0028357269 scopus 로고
    • Direct evidence for homologous sequences on the paracentric regions of human chromosome 1
    • Hardas BD, Zhang J, Trent JM, Elder JT: Direct evidence for homologous sequences on the paracentric regions of human chromosome 1. Genomics 21(2)359-63 (1994).
    • (1994) Genomics , vol.21 , Issue.2 , pp. 359-363
    • Hardas, B.D.1    Zhang, J.2    Trent, J.M.3    Elder, J.T.4
  • 83
    • 0025870449 scopus 로고
    • Loss of allelic heterozygosity on distal chromosome 1p in Merkel cell carcinoma: A marker of neural crest origins?
    • Harnett PR, Kearsley JH, Hayward NK, Dracopoli NC, Kefford RF: Loss of allelic heterozygosity on distal chromosome 1p in Merkel cell carcinoma: A marker of neural crest origins? Cancer Genet Cytogenet 54:109-113 (1991).
    • (1991) Cancer Genet Cytogenet , vol.54 , pp. 109-113
    • Harnett, P.R.1    Kearsley, J.H.2    Hayward, N.K.3    Dracopoli, N.C.4    Kefford, R.F.5
  • 87
    • 0028098186 scopus 로고
    • Genes encoding general initiation factors for RNA polymerase II transcription are dispersed in the human genome
    • Heng HHQ, Xiao H, Shi XM, Greenblatt J, Tsui L-C: Genes encoding general initiation factors for RNA polymerase II transcription are dispersed in the human genome. Hum mol Genet 3.61-64 (1994).
    • (1994) Hum Mol Genet , vol.3 , pp. 61-64
    • Heng, H.H.Q.1    Xiao, H.2    Shi, X.M.3    Greenblatt, J.4    Tsui, L.-C.5
  • 88
    • 0028817596 scopus 로고
    • Translocation (1;16) identified by chromosome painting, and PRimed in Situ-labeling (PRINS). Report of two cases and review of the cytogenetic literature
    • Hindkjaer J, Hammoudah SA, Hansen KB, Jensen PD, Koch J, Pedersen B. Translocation (1;16) identified by chromosome painting, and PRimed IN Situ-labeling (PRINS). Report of two cases and review of the cytogenetic literature. Cancer Genet Cytogenet 79:15-20 (1995).
    • (1995) Cancer Genet Cytogenet , vol.79 , pp. 15-20
    • Hindkjaer, J.1    Hammoudah, S.A.2    Hansen, K.B.3    Jensen, P.D.4    Koch, J.5    Pedersen, B.6
  • 89
    • 0028917961 scopus 로고
    • Sequence of human FEN-1, a structure-specific endonuclease, and chromosomal localization of the gene (FEN1) in mouse and human
    • Hiraoka LR, Hanington JJ, Gerhard DS, Lieber MR, Hsieh C-L, Sequence of human FEN-1, a structure-specific endonuclease, and chromosomal localization of the gene (FEN1) in mouse and human. Genomics 25:220-225 (1995).
    • (1995) Genomics , vol.25 , pp. 220-225
    • Hiraoka, L.R.1    Hanington, J.J.2    Gerhard, D.S.3    Lieber, M.R.4    Hsieh, C.-L.5
  • 90
    • 0028819584 scopus 로고
    • Allelic imbalance on chromosome 1 in human breast cancer. II. Microsatellite repeat analysis
    • Hoggard N, Brintnell B, Howell A, Weissenbach J, Varley J: Allelic imbalance on chromosome 1 in human breast cancer. II. Microsatellite repeat analysis. Genes Chrom Cancer 12:24-31 (1995).
    • (1995) Genes Chrom Cancer , vol.12 , pp. 24-31
    • Hoggard, N.1    Brintnell, B.2    Howell, A.3    Weissenbach, J.4    Varley, J.5
  • 91
    • 0027993504 scopus 로고
    • Mapping of CD24 and homologous sequences to multiple chromosomal loci
    • Hough MR, Rosten PM, Sexton TL, Kay R, Humphries RK: Mapping of CD24 and homologous sequences to multiple chromosomal loci. Genomics 22:154-161 (1994).
    • (1994) Genomics , vol.22 , pp. 154-161
    • Hough, M.R.1    Rosten, P.M.2    Sexton, T.L.3    Kay, R.4    Humphries, R.K.5
  • 93
    • 0025361962 scopus 로고
    • The gene for the ubiquitous octamer-binding protein Oct-1 is on human chromosome 1 region cen→q32 and near Ly-22 and Ltw-4 on mouse chromosome 1
    • Hsieh CL, Sturm R, Herr W, Francke U: The gene for the ubiquitous octamer-binding protein Oct-1 is on human chromosome 1 region cen→q32 and near Ly-22 and Ltw-4 on mouse chromosome 1. Genomics 6:666-672 (1990).
    • (1990) Genomics , vol.6 , pp. 666-672
    • Hsieh, C.L.1    Sturm, R.2    Herr, W.3    Francke, U.4
  • 95
    • 0028595976 scopus 로고
    • Isolation and chromosomal localization of a novel human G- Protein-coupled receptor (GPR3) expressed predominantly in the central nervous system
    • Iismaa TP, Kieffer J, Liu ML, Baker E, Sutherland GR, Shine J: Isolation and chromosomal localization of a novel human G- protein-coupled receptor (GPR3) expressed predominantly in the central nervous system. Genomics 24:391-394 (1994).
    • (1994) Genomics , vol.24 , pp. 391-394
    • Iismaa, T.P.1    Kieffer, J.2    Liu, M.L.3    Baker, E.4    Sutherland, G.R.5    Shine, J.6
  • 96
    • 0028195084 scopus 로고
    • Refined localization of the alphal-subunit of the skeletal muscle L-type voltage-dependent calcium channel (CACNL1A3) to human chromosome 1q32 by in situ hybridization
    • Iles DE, Segers B, Olde Weghuis D, Mikala G, Schwartz A, Wieringa B: Refined localization of the alphal-subunit of the skeletal muscle L-type voltage-dependent calcium channel (CACNL1A3) to human chromosome 1q32 by in situ hybridization. Genomics 19:561-563 (1994).
    • (1994) Genomics , vol.19 , pp. 561-563
    • Iles, D.E.1    Segers, B.2    Olde Weghuis, D.3    Mikala, G.4    Schwartz, A.5    Wieringa, B.6
  • 98
    • 0029015445 scopus 로고
    • Cloning and chromosomal localization of the human A2b adenosine receptor gene (ADORA2B) and its pseudogene
    • Jacobson MA, Johnson RG, Luneau CJ, Salvatore CA: Cloning and chromosomal localization of the human A2b adenosine receptor gene (ADORA2B) and its pseudogene. Genomics 27:374-376 (1995).
    • (1995) Genomics , vol.27 , pp. 374-376
    • Jacobson, M.A.1    Johnson, R.G.2    Luneau, C.J.3    Salvatore, C.A.4
  • 100
    • 0029112736 scopus 로고
    • Assignment of human transforming growth factor-beta type I and type III receptor genes (TGFBR1 and TGFBR3) to 9q33→q34 and 1p32→p33, respectively
    • 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. Genomics 28:356-357 (1995).
    • (1995) Genomics , vol.28 , pp. 356-357
    • Johnson, D.W.1    Qumsiyeh, M.2    Benkhalifa, M.3    Marchuk, D.A.4
  • 101
    • 0029257482 scopus 로고
    • Synaptotagmin genes on mouse chromosomes 1, 7, and 10 and human chromosome 19
    • Jones JM, Popma SJ, Mizuta M, Seino S, Meisler MH: Synaptotagmin genes on mouse chromosomes 1, 7, and 10 and human chromosome 19. Mammal Genome 6:212-213 (1995).
    • (1995) Mammal Genome , vol.6 , pp. 212-213
    • Jones, J.M.1    Popma, S.J.2    Mizuta, M.3    Seino, S.4    Meisler, M.H.5
  • 103
    • 0027958169 scopus 로고
    • The human EPRS Locus (formerly the QARS locus): A gene encoding a class 1 and a class II aminoacyl-tRNA synthetase
    • Kaiser E, Hu B, Becher S, Eberhard D, Schray B, Baack M, Hameister H, Knippers R: The human EPRS Locus (formerly the QARS locus): a gene encoding a class 1 and a class II aminoacyl-tRNA synthetase. Genomics 19:280-290 (1994).
    • (1994) Genomics , vol.19 , pp. 280-290
    • Kaiser, E.1    Hu, B.2    Becher, S.3    Eberhard, D.4    Schray, B.5    Baack, M.6    Hameister, H.7    Knippers, R.8
  • 104
    • 0025137176 scopus 로고
    • A new homeobox gene contributes the DNA binding domain of the t(1;19) translocation protein in pre-B ALL
    • Kamps MP, Murre C, Sun X-h, Baltimore D: A new homeobox gene contributes the DNA binding domain of the t(1;19) translocation protein in pre-B ALL. Cell 60:547-555 (1990).
    • (1990) Cell , vol.60 , pp. 547-555
    • Kamps, M.P.1    Murre, C.2    Sun, X.-H.3    Baltimore, D.4
  • 107
    • 0028350579 scopus 로고
    • PE-1, a novel ETS oncogene family member, localizes to chromosome 1q21→q23
    • Klemsz M, Hromas R, Raskind W, Bruno E, Hoffinan R: PE-1, a novel ETS oncogene family member, localizes to chromosome 1q21→q23. Genomics 20:291-294 (1994).
    • (1994) Genomics , vol.20 , pp. 291-294
    • Klemsz, M.1    Hromas, R.2    Raskind, W.3    Bruno, E.4    Hoffinan, R.5
  • 108
    • 0018143429 scopus 로고
    • Abnormalities of chromosome No. 1 in human solid tumours
    • Kovacs G: Abnormalities of chromosome No. 1 in human solid tumours. Intl J Cancer 21:688-694 (1978).
    • (1978) Intl J Cancer , vol.21 , pp. 688-694
    • Kovacs, G.1
  • 110
    • 0025145162 scopus 로고
    • The human QARS locus: Assignment of the human gene for glutaminyl-tRNA synthetase to chromosome 1q32→q43
    • Kunze N, Bitter E, Fett R, Schray B, Hameister H, Wiedorn KH, Knippers R: The human QARS locus: Assignment of the human gene for glutaminyl-tRNA synthetase to chromosome 1q32→q43. Hum Genet 85:527-530 (1990).
    • (1990) Hum Genet , vol.85 , pp. 527-530
    • Kunze, N.1    Bitter, E.2    Fett, R.3    Schray, B.4    Hameister, H.5    Wiedorn, K.H.6    Knippers, R.7
  • 114
    • 0029003579 scopus 로고
    • Molecular characterisation and refined genomic localization of three human potassium ion channel genes
    • Landes GM, Curran ME, Keating MT: Molecular characterisation and refined genomic localization of three human potassium ion channel genes. Cytogenet Cell Genet 70:280-284 (1995).
    • (1995) Cytogenet Cell Genet , vol.70 , pp. 280-284
    • Landes, G.M.1    Curran, M.E.2    Keating, M.T.3
  • 115
    • 0025897085 scopus 로고
    • Yeast artificial chromosome libraries containing large insert fragments from mouse and human DNA
    • Larin Z, Monaco AP, Lehrach H: Yeast artificial chromosome libraries containing large insert fragments from mouse and human DNA. Proc natl Acad Sci, USA 88:4123-4127 (1991).
    • (1991) Proc Natl Acad Sci, USA , vol.88 , pp. 4123-4127
    • Larin, Z.1    Monaco, A.P.2    Lehrach, H.3
  • 116
    • 0028605515 scopus 로고
    • The human NOTCH 1, 2, and 3 genes are located at chromosome positions 9q34, 1p13«p11, and 19p13.2→p13.1 in regions of neoplasia-associaled translocation
    • Larsson C, Lardelli M, White I, Lendahl U. The human NOTCH 1, 2, and 3 genes are located at chromosome positions 9q34, 1p13«p11, and 19p13.2→p13.1 in regions of neoplasia-associaled translocation. Genomics 24:253-258 (1994).
    • (1994) Genomics , vol.24 , pp. 253-258
    • Larsson, C.1    Lardelli, M.2    White, I.3    Lendahl, U.4
  • 118
    • 0025049957 scopus 로고
    • Constitutional translocation t(1;17)(p36;q12-21) in a patient with neuroblastoma
    • Laureys G, Speleman F, Opdenakker G, Leroy J: Constitutional translocation t(1;17)(p36;q12-21) in a patient with neuroblastoma. Genes Chrom Cancer 2:252-254 (1990).
    • (1990) Genes Chrom Cancer , vol.2 , pp. 252-254
    • Laureys, G.1    Speleman, F.2    Opdenakker, G.3    Leroy, J.4
  • 120
    • 43949151776 scopus 로고
    • Large scale isolation of human 1p36 specific P1 clones and their use for fluorescence in situ hybridization
    • Lengauer C, Henn T, Onyango P, Francis F, Lehrach H, Weith A: Large scale isolation of human 1p36 specific P1 clones and their use for fluorescence in situ hybridization. Genet Anal Tech Appl 11:140-147 (1994).
    • (1994) Genet Anal Tech Appl , vol.11 , pp. 140-147
    • Lengauer, C.1    Henn, T.2    Onyango, P.3    Francis, F.4    Lehrach, H.5    Weith, A.6
  • 124
    • 0026213889 scopus 로고
    • Chromosomal mapping of A1 and A2 adenosine receptors, VIP receptor, and a new subtype of serotonin receptor
    • Libert F, Passage E, Parmentier M, Simons MJ, Vassart G, Mattei MG: Chromosomal mapping of A1 and A2 adenosine receptors, VIP receptor, and a new subtype of serotonin receptor. Genornics 11:225-227 (1991).
    • (1991) Genornics , vol.11 , pp. 225-227
    • Libert, F.1    Passage, E.2    Parmentier, M.3    Simons, M.J.4    Vassart, G.5    Mattei, M.G.6
  • 125
    • 0028853419 scopus 로고
    • Allelic imbalance on chromosome 1 in human breast cancer. I. Minisatellite and RELP analysis
    • Loupart ML, Armour J, Walker R, Adams S, Brammar W, Varley J: Allelic imbalance on chromosome 1 in human breast cancer. I. Minisatellite and RELP analysis. Genes Chrom Cancer 12:16-23 (1995).
    • (1995) Genes Chrom Cancer , vol.12 , pp. 16-23
    • Loupart, M.L.1    Armour, J.2    Walker, R.3    Adams, S.4    Brammar, W.5    Varley, J.6
  • 127
    • 0028912570 scopus 로고
    • Mapping of the human cone transducin alpha-subunit (GNAT2) gene to 1p13 and negative mutation analysis in patients with Stargardt disease
    • Magovcevic I, Weremowicz S, Morton CC, Fong S, Berson EL, Dryja TP: Mapping of the human cone transducin alpha-subunit (GNAT2) gene to 1p13 and negative mutation analysis in patients with Stargardt disease. Genomics 25:288-290 (1995).
    • (1995) Genomics , vol.25 , pp. 288-290
    • Magovcevic, I.1    Weremowicz, S.2    Morton, C.C.3    Fong, S.4    Berson, E.L.5    Dryja, T.P.6
  • 128
    • 0025800588 scopus 로고
    • Intrachromosomal rearrangements fusing L-myc and rlf in small-cell lung cancer
    • Makela TP, Kere J, Winqvist R, Alitalo K: Intrachromosomal rearrangements fusing L-myc and rlf in small-cell lung cancer. Mol cell Biol 11:4015-4021 (1991).
    • (1991) Mol Cell Biol , vol.11 , pp. 4015-4021
    • Makela, T.P.1    Kere, J.2    Winqvist, R.3    Alitalo, K.4
  • 131
    • 0006616576 scopus 로고
    • Localization of a lymphocyte-specific protein tyrosine kinase gene (lck) at a site of frequent chromosomal abnormalities in human lymphomas
    • Marth JD, Disteche C, Pratcheva D, Ruddle F, Krebs EG, Perlmuer RM: Localization of a lymphocyte-specific protein tyrosine kinase gene (lck) at a site of frequent chromosomal abnormalities in human lymphomas. Proc natl Acad Sci, USA 83:7400-7404 (1986).
    • (1986) Proc Natl Acad Sci, USA , vol.83 , pp. 7400-7404
    • Marth, J.D.1    Disteche, C.2    Pratcheva, D.3    Ruddle, F.4    Krebs, E.G.5    Perlmuer, R.M.6
  • 132
    • 3042961065 scopus 로고
    • Analysis of 1p deletions in neuroblastoma tumors: Delimitation of the critical region with genetically mapped short tandem repeat polymorphisms
    • in press
    • Martinsson T, Sjoberg RM, Hallstensson K, Hedborg F, Kogner P: Analysis of 1p deletions in neuroblastoma tumors: delimitation of the critical region with genetically mapped short tandem repeat polymorphisms. Cancer Res 55: (in press, 1995).
    • (1995) Cancer Res , vol.55
    • Martinsson, T.1    Sjoberg, R.M.2    Hallstensson, K.3    Hedborg, F.4    Kogner, P.5
  • 134
    • 0028310324 scopus 로고
    • Confirmation of Duffy blood group antigen locus (FY) at 1q22→q23 by fluorescence in situ hybridization
    • Mathew S, Chaudhuri A, Murty VVVS, Pogo AO: Confirmation of Duffy blood group antigen locus (FY) at 1q22→q23 by fluorescence in situ hybridization. Cytogenel Cell Genet 67:68 (1994).
    • (1994) Cytogenel Cell Genet , vol.67 , pp. 68
    • Mathew, S.1    Chaudhuri, A.2    Murty, V.3    Pogo, A.O.4
  • 135
  • 136
    • 0028020524 scopus 로고
    • Localization of the human gene for carnitine palmitoyltransferase to 1p13-p11 by nonradioactive in situ hybridization
    • Minoletti F, Colombo I, Martin AL, Di Donato S, Taroni F, Finocchiaro G, Pandolfo M: Localization of the human gene for carnitine palmitoyltransferase to 1p13-p11 by nonradioactive in situ hybridization. Genomics 24:198 (1994a).
    • (1994) Genomics , vol.24 , pp. 198
    • Minoletti, F.1    Colombo, I.2    Martin, A.L.3    Di Donato, S.4    Taroni, F.5    Finocchiaro, G.6    Pandolfo, M.7
  • 139
    • 0029038821 scopus 로고
    • Determination of the gene order of the three loci CD2, NGFB, and NRAS at human chromosome band 1p13 and refinement of their localization at the subband level by FISH
    • Mitchell ELD, Jones D, White GRM, Varley JM, Santibanez Koref MF: Determination of the gene order of the three loci CD2, NGFB, and NRAS at human chromosome band 1p13 and refinement of their localization at the subband level by FISH. Cytogenet Cell Genet 70:183-185 (1995).
    • (1995) Cytogenet Cell Genet , vol.70 , pp. 183-185
    • Mitchell, E.L.D.1    Jones, D.2    White, G.R.M.3    Varley, J.M.4    Santibanez Koref, M.F.5
  • 141
    • 0028986734 scopus 로고
    • Confirmed assignment of a novel human tyrosine kinase gene (JAK1A) to 1p32.3→p31.3 by nonisotopic in situ hybridization
    • Modi WS, Farrar WL, Howard OMZ: Confirmed assignment of a novel human tyrosine kinase gene (JAK1A) to 1p32.3→p31.3 by nonisotopic in situ hybridization. Cytogenet Cell Genet 69:232-234 (1995).
    • (1995) Cytogenet Cell Genet , vol.69 , pp. 232-234
    • Modi, W.S.1    Farrar, W.L.2    Howard, O.M.Z.3
  • 144
    • 0028988730 scopus 로고
    • Localization of the A3 adenosine receptor gene (ADORA3) to human chromosome 1p
    • Monitto CL, Levitt RC, DiSilvestre D, Holroyd KJ: Localization of the A3 adenosine receptor gene (ADORA3) to human chromosome 1p. Genomics 26:637-638 (1995).
    • (1995) Genomics , vol.26 , pp. 637-638
    • Monitto, C.L.1    Levitt, R.C.2    Disilvestre, D.3    Holroyd, K.J.4
  • 145
    • 0025912929 scopus 로고
    • Localization of the trk protooncogene to human chromosome bands 1q23→q24
    • Morris CM, Hao QL, Heisterkamp N, Fitzgerald PH, Groffen J: Localization of the trk protooncogene to human chromosome bands 1q23→q24. Oncogene 6:1093-1095 (1991).
    • (1991) Oncogene , vol.6 , pp. 1093-1095
    • Morris, C.M.1    Hao, Q.L.2    Heisterkamp, N.3    Fitzgerald, P.H.4    Groffen, J.5
  • 147
    • 0023785269 scopus 로고
    • Chromosomes in Ewing sarcoma: II. Nonrandom additional changes, trisomy 8 and der(16)t(1;16)
    • Mugneret F, Lizard S, Aurias A, Turc-Carel C: Chromosomes in Ewing sarcoma: II. Nonrandom additional changes, trisomy 8 and der(16)t(1;16). Cancer Genet Cytogenet 32:239-245 (1988).
    • (1988) Cancer Genet Cytogenet , vol.32 , pp. 239-245
    • Mugneret, F.1    Lizard, S.2    Aurias, A.3    Turc-Carel, C.4
  • 148
    • 0027410857 scopus 로고
    • Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2
    • Mulligan LM, Gardner E, Smith BA, Mathew CG, Ponder BA: Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2. Genes Chrom Cancer 6:166-177 (1993).
    • (1993) Genes Chrom Cancer , vol.6 , pp. 166-177
    • Mulligan, L.M.1    Gardner, E.2    Smith, B.A.3    Mathew, C.G.4    Ponder, B.A.5
  • 149
    • 3042992808 scopus 로고
    • In situ hybridization of NGF-beta and NRAS probes to t(1;11)(p22.1;p13) translocation chromosomes allow sub-band mapping
    • Munke M, Cowan J, Carroll AJ, Prchal J, Francke U: In situ hybridization of NGF-beta and NRAS probes to t(1;11)(p22.1;p13) translocation chromosomes allow sub-band mapping. Cytogenet Cell Genet 40:705-706 (1985).
    • (1985) Cytogenet Cell Genet , vol.40 , pp. 705-706
    • Munke, M.1    Cowan, J.2    Carroll, A.J.3    Prchal, J.4    Francke, U.5
  • 150
    • 0027144483 scopus 로고
    • Mapping of the gene coding for a paraneoplastic encephalomyelitis antigen (HuD) to human chromosome site 1p34
    • Muresu R, Baldini A, Cress T, Posner JB, Furneaux HM, Siniscalco M: Mapping of the gene coding for a paraneoplastic encephalomyelitis antigen (HuD) to human chromosome site 1p34. Cytogenet Cell Genet 65:177-178 (1994).
    • (1994) Cytogenet Cell Genet , vol.65 , pp. 177-178
    • Muresu, R.1    Baldini, A.2    Cress, T.3    Posner, J.B.4    Furneaux, H.M.5    Siniscalco, M.6
  • 153
    • 0027488049 scopus 로고
    • A B cell specific immediate early human gene is located on chromosome band 1q31 and encodes an alpha helical basic phosphoprotein
    • Newton JS, Deed RW, Mitchell ELD, Murphy JJ, Norton JD. A B cell specific immediate early human gene is located on chromosome band 1q31 and encodes an alpha helical basic phosphoprotein. Biochim Biophys Acta 1216:314-316 (1993).
    • (1993) Biochim Biophys Acta , vol.1216 , pp. 314-316
    • Newton, J.S.1    Deed, R.W.2    Mitchell, E.L.D.3    Murphy, J.J.4    Norton, J.D.5
  • 155
    • 0028172972 scopus 로고
    • The human CHC1 gene encoding RCC1 (Regulator of Chromosome Condensation) (CHC1) is located to human chromosome 1p36.1
    • Nishimoto T, Seino H, Seki N, Hori TA: The human CHC1 gene encoding RCC1
    • (1994) Genomics , vol.23 , pp. 719-721
    • Nishimoto, T.1    Seino, H.2    Seki, N.3    Hori, T.A.4
  • 156
    • 0028675056 scopus 로고
    • Construction of cosmid libraries from flow-sorted human chromosomes 1, 6, 7, 11, 13, and 18 for reference library resources
    • Nizetic D, Monard S, Young B, Cotter F, Zehetner G, Lehrach H: Construction of cosmid libraries from flow-sorted human chromosomes 1, 6, 7, 11, 13, and 18 for reference library resources. Mammal Genome 5:801-802 (1994).
    • (1994) Mammal Genome , vol.5 , pp. 801-802
    • Nizetic, D.1    Monard, S.2    Young, B.3    Cotter, F.4    Zehetner, G.5    Lehrach, H.6
  • 157
    • 0025064238 scopus 로고
    • Chromosomal translocation t(1;19) results in synthesis of a homeobox fusion mRNA that codes for a potential chimeric transcription factor
    • Nourse J, Mellentin JD, Galili N, Wilkinson J, Stanbridge E, Smith SD, Cleary ML: Chromosomal translocation t(1;19) results in synthesis of a homeobox fusion mRNA that codes for a potential chimeric transcription factor. Cell 60:535-545 (1990).
    • (1990) Cell , vol.60 , pp. 535-545
    • Nourse, J.1    Mellentin, J.D.2    Galili, N.3    Wilkinson, J.4    Stanbridge, E.5    Smith, S.D.6    Cleary, M.L.7
  • 160
    • 0028246372 scopus 로고
    • Cloning of genomic loci and chromosomal localization of the human PCTAIRE-1 and -3 protein kinase genes
    • Okuda T, Valentine VA, Shapiro DN, Downing JR: Cloning of genomic loci and chromosomal localization of the human PCTAIRE-1 and -3 protein kinase genes. Genomics 21:217-221 (1994).
    • (1994) Genomics , vol.21 , pp. 217-221
    • Okuda, T.1    Valentine, V.A.2    Shapiro, D.N.3    Downing, J.R.4
  • 161
    • 0024801447 scopus 로고
    • Abnormalities of chromosome 1 in relation to human malignant diseases
    • Olah E, Balogh E, Kovacs I, Kiss A: Abnormalities of chromosome 1 in relation to human malignant diseases. Cancer Genet Cytogenet 43:179-194 (1989).
    • (1989) Cancer Genet Cytogenet , vol.43 , pp. 179-194
    • Olah, E.1    Balogh, E.2    Kovacs, I.3    Kiss, A.4
  • 162
    • 0017255478 scopus 로고
    • Trisomy of the long arm of chromosome number 1 in human leukemia
    • Oshimura M, Sonta S-i, Sandberg AA: Trisomy of the long arm of chromosome number 1 in human leukemia. J natl Cancer Inst 56:183-184 (1976).
    • (1976) J Natl Cancer Inst , vol.56 , pp. 183-184
    • Oshimura, M.1    Sonta, S.-I.2    Sandberg, A.A.3
  • 163
    • 0028815487 scopus 로고
    • C4BPAL2: A second duplication of the C4BPA gene in the human RCA gene cluster
    • Pardo-Manuel-de-Villena F, Rodriguez-de-Cordoba S: C4BPAL2: a second duplication of the C4BPA gene in the human RCA gene cluster. Immunogenetics 41:139-143 (1995).
    • (1995) Immunogenetics , vol.41 , pp. 139-143
    • Pardo-Manuel-de-Villena, F.1    Rodriguez-de-Cordoba, S.2
  • 164
    • 0027392932 scopus 로고
    • Molecular cloning of the human alpha2(IX) collagen cDNA and assignment of the human COL9A2 gene to chromosome 1
    • Perälä M, Hanninen M, Hastabacka J, Elima K, Vuorio E: Molecular cloning of the human alpha2(IX) collagen cDNA and assignment of the human COL9A2 gene to chromosome 1. FEBS Lett 319:177-180 (1993).
    • (1993) FEBS Lett , vol.319 , pp. 177-180
    • Perälä, M.1    Hanninen, M.2    Hastabacka, J.3    Elima, K.4    Vuorio, E.5
  • 169
    • 0029122059 scopus 로고
    • Chromosomal localization of the four genes (NFIA, B, C and X) for the human transcription factor nuclear factor I by FISH
    • Qian F, Kruse U, Lichter P, Sippel A: Chromosomal localization of the four genes (NFIA, B, C and X) for the human transcription factor nuclear factor I by FISH. Genomics 28:66-73 (1995).
    • (1995) Genomics , vol.28 , pp. 66-73
    • Qian, F.1    Kruse, U.2    Lichter, P.3    Sippel, A.4
  • 171
    • 0028362748 scopus 로고
    • Concurrent mapping of an adenovirus 5/SV40 integration site and the U1 snRNA Cluster (RNU 1) within 400 kb of the chromosome region 1p36.1
    • Romani M, Baldini A, Volpi EV, Casciano I, Nobile C, Murescu R, Siniscalco M: Concurrent mapping of an adenovirus 5/SV40 integration site and the U1 snRNA Cluster (RNU 1) within 400 kb of the chromosome region 1p36.1. Cytogenet Cell Genet 67:37-40 (1994).
    • (1994) Cytogenet Cell Genet , vol.67 , pp. 37-40
    • Romani, M.1    Baldini, A.2    Volpi, E.V.3    Casciano, I.4    Nobile, C.5    Murescu, R.6    Siniscalco, M.7
  • 172
    • 0017735005 scopus 로고
    • Mapping of the human chromosomal regions related to neoplasia: Evidence from chromosomes 1 and 17
    • Rowley JD: Mapping of the human chromosomal regions related to neoplasia: Evidence from chromosomes 1 and 17. Proc natl Acad Sci, USA 74:5729-5733 (1977).
    • (1977) Proc Natl Acad Sci, USA , vol.74 , pp. 5729-5733
    • Rowley, J.D.1
  • 173
    • 0028068830 scopus 로고
    • Assignment of the human cytidine deaminase (CDA) gene to chromosome 1 band p35→p36.2
    • Saccone S, Besati C, Andreozzi L, Della Valle G, Garattini E, Terao M: Assignment of the human cytidine deaminase (CDA) gene to chromosome 1 band p35→p36.2. Genomics 22:661-662 (1994).
    • (1994) Genomics , vol.22 , pp. 661-662
    • Saccone, S.1    Besati, C.2    Andreozzi, L.3    Della Valle, G.4    Garattini, E.5    Terao, M.6
  • 174
    • 0029064774 scopus 로고
    • Molecular cloning of a human protein that binds to the retinoblastoma protein and chromosomal mapping
    • Saijo M, Sakai Y, Kishino T, Niikawa N, Matsuura Y, Merino K, Tamai K, Taya Y: Molecular cloning of a human protein that binds to the retinoblastoma protein and chromosomal mapping. Genomics 27:511-519 (1995).
    • (1995) Genomics , vol.27 , pp. 511-519
    • Saijo, M.1    Sakai, Y.2    Kishino, T.3    Niikawa, N.4    Matsuura, Y.5    Merino, K.6    Tamai, K.7    Taya, Y.8
  • 176
    • 0022350404 scopus 로고
    • Translocation (1;7)(p11;p11): A new myeloproliferative hematologic entity
    • Sandberg AA, Morgan R, Hecht BK, Hecht F: Translocation (1;7)(p11;p11): A new myeloproliferative hematologic entity. Cancer Genet Cytogenet 18:199-206 (1985).
    • (1985) Cancer Genet Cytogenet , vol.18 , pp. 199-206
    • Sandberg, A.A.1    Morgan, R.2    Hecht, B.K.3    Hecht, F.4
  • 177
    • 0027981831 scopus 로고
    • The glycerol kinase gene family: Structure of the Xp gene, and related intronless retroposons
    • Sargent CA, Young C, Marsch S, Ferguson-Smith MA, Affara NA: The glycerol kinase gene family: structure of the Xp gene, and related intronless retroposons. Hum mol Genet 3:1317-1324 (1994).
    • (1994) Hum Mol Genet , vol.3 , pp. 1317-1324
    • Sargent, C.A.1    Young, C.2    Marsch, S.3    Ferguson-Smith, M.A.4    Affara, N.A.5
  • 178
    • 0028987554 scopus 로고
    • Isolation of a YAC clone covering a cluster of nine S100 genes on human chromosome 1q21: Rationale for a new nomenclature of the S100 calcium-binding protein family
    • Schaefer BW, Wicki R, Engelkamp D, Mattei MG, Heizmann CW: Isolation of a YAC clone covering a cluster of nine S100 genes on human chromosome 1q21: rationale for a new nomenclature of the S100 calcium-binding protein family. Genomics 25:638-643 (1995).
    • (1995) Genomics , vol.25 , pp. 638-643
    • Schaefer, B.W.1    Wicki, R.2    Engelkamp, D.3    Mattei, M.G.4    Heizmann, C.W.5
  • 181
    • 0028237891 scopus 로고
    • Characterization of the human gene encoding LBR, an integral protein of the nuclear envelope inner membrane
    • Schuler E, Lin F, Worman HJ: Characterization of the human gene encoding LBR, an integral protein of the nuclear envelope inner membrane. J biol Chem 269:11312-11317 (1994).
    • (1994) J Biol Chem , vol.269 , pp. 11312-11317
    • Schuler, E.1    Lin, F.2    Worman, H.J.3
  • 183
    • 3042915895 scopus 로고
    • Mouse chromosome 1
    • in press
    • Seldin MF: Mouse chromosome 1: Mammal Genome (in press, 1995)
    • (1995) Mammal Genome
    • Seldin, M.F.1
  • 184
    • 0028064986 scopus 로고
    • Assignment of the human homologue of the mTRIC-P5 gene (TRIG5) to band 1q23 by fluorescence in situ hybridization
    • Sévigny G, Joly EC, Bibor-Hardy V, Lemieux N: Assignment of the human homologue of the mTRIC-P5 gene (TRIG5) to band 1q23 by fluorescence in situ hybridization. Genomics 22:634-636 (1994).
    • (1994) Genomics , vol.22 , pp. 634-636
    • Sévigny, G.1    Joly, E.C.2    Bibor-Hardy, V.3    Lemieux, N.4
  • 186
    • 0027960986 scopus 로고
    • Mapping of the human SAP1 (SRF accessory protein 1) gene and SAP2, a gene encoding a related protein, to chromosomal bands 1q32 and 12q23, respectively
    • Shipley J, Sheer D, Dalton S, Treisman R, Patel K: Mapping of the human SAP1 (SRF accessory protein 1) gene and SAP2, a gene encoding a related protein, to chromosomal bands 1q32 and 12q23, respectively. Genomics 23:710-711 (1994).
    • (1994) Genomics , vol.23 , pp. 710-711
    • Shipley, J.1    Sheer, D.2    Dalton, S.3    Treisman, R.4    Patel, K.5
  • 187
    • 0029155882 scopus 로고
    • Assignment of the 499-kDa (PRIM1) and 58-kDa (PRIM2A and PRTM2B) subunit genes of the human DNA primase to chromosome bands 1q44 and 6p11.1→p12
    • Shiratori A, Okumura K, Nogami M, Taguchi H, Onozaki T, Inoue T, Ando T, Shibata T et al.: Assignment of the 499-kDa (PRIM1) and 58-kDa (PRIM2A and PRTM2B) subunit genes of the human DNA primase to chromosome bands 1q44 and 6p11.1→p12. Genomics 28:350-353 (1995).
    • (1995) Genomics , vol.28 , pp. 350-353
    • Shiratori, A.1    Okumura, K.2    Nogami, M.3    Taguchi, H.4    Onozaki, T.5    Inoue, T.6    Ando, T.7    Shibata, T.8
  • 188
    • 0026703169 scopus 로고
    • Cloning and stable maintenance of 300 kilobase pair fragments of human DNA in Escherichia Coli using an F-factor based vector
    • Shizuya H, Birren B, Kim UJ, Mancino V, Slepak T, Tachiri Y, Simon M: Cloning and stable maintenance of 300 kilobase pair fragments of human DNA in Escherichia Coli using an F-factor based vector. Proc natl Acad Sci, USA 89:8794-8797 (1992).
    • (1992) Proc Natl Acad Sci, USA , vol.89 , pp. 8794-8797
    • Shizuya, H.1    Birren, B.2    Kim, U.J.3    Mancino, V.4    Slepak, T.5    Tachiri, Y.6    Simon, M.7
  • 189
    • 0028109139 scopus 로고
    • A human gene encoding a putative basic helix-loop-helix phosphoprotein whose mRNA increases rapidly in cycloheximide-treated blood mononuclear cells
    • Siderovski DP, Heximer SP, Forsdyke DR: A human gene encoding a putative basic helix-loop-helix phosphoprotein whose mRNA increases rapidly in cycloheximide-treated blood mononuclear cells. DNA Cell Biol 13:125-147 (1994).
    • (1994) DNA Cell Biol , vol.13 , pp. 125-147
    • Siderovski, D.P.1    Heximer, S.P.2    Forsdyke, D.R.3
  • 190
    • 0025801654 scopus 로고
    • Abnormalities of chromosome 1 and loss of heterozygosity on 1p in primary hepatomas
    • Simon D, Knowles BB, Weith A: Abnormalities of chromosome 1 and loss of heterozygosity on 1p in primary hepatomas. Oncogens 6:765-770 (1991).
    • (1991) Oncogens , vol.6 , pp. 765-770
    • Simon, D.1    Knowles, B.B.2    Weith, A.3
  • 193
    • 0029100828 scopus 로고
    • Molecular cloning and chromosomal localization of human genes encoding three closely related G protein-coupled receptors
    • Song Z-H, Modi W, Bonner TI: Molecular cloning and chromosomal localization of human genes encoding three closely related G protein-coupled receptors. Genomics 28:347-349 (1995).
    • (1995) Genomics , vol.28 , pp. 347-349
    • Song, Z.-H.1    Modi, W.2    Bonner, T.I.3
  • 196
    • 0026518431 scopus 로고
    • Cloning high molecular weight DNA fragments by the bacteriophage P1 system
    • Sternberg NL: Cloning high molecular weight DNA fragments by the bacteriophage P1 system. Trends in Genet 8:11-16 (1992).
    • (1992) Trends in Genet , vol.8 , pp. 11-16
    • Sternberg, N.L.1
  • 197
    • 0028108499 scopus 로고
    • Detection of numerical and structural chromosome abnormalities in pediatric germ cell tumors by means of interphase cytogenetics
    • Stock C, Ambros IM, Lion T, Haas OA, Zoubek A, Gadner H, Ambros PF: Detection of numerical and structural chromosome abnormalities in pediatric germ cell tumors by means of interphase cytogenetics. Genes Chrom Cancer 11:40-50 (1994).
    • (1994) Genes Chrom Cancer , vol.11 , pp. 40-50
    • Stock, C.1    Ambros, I.M.2    Lion, T.3    Haas, O.A.4    Zoubek, A.5    Gadner, H.6    Ambros, P.F.7
  • 198
    • 0028917759 scopus 로고
    • The human OTF1 locus which overlaps the CD3Z gene is located at 1q22→q23
    • Sturm RA, Eyre HJ, Baker E, Sutherland GR: The human OTF1 locus which overlaps the CD3Z gene is located at 1q22→q23. Cytogenet Cell Genet 68:231-232 (1995).
    • (1995) Cytogenet Cell Genet , vol.68 , pp. 231-232
    • Sturm, R.A.1    Eyre, H.J.2    Baker, E.3    Sutherland, G.R.4
  • 200
    • 0027853058 scopus 로고
    • Recurrent deletions of specific chromosomal sites in 1p, 3p, 6q, and 9p in human malignant mesothelioma
    • Taguchi T, Jhanwar SC, Siegfried JM, Keller SM, Testa JR: Recurrent deletions of specific chromosomal sites in 1p, 3p, 6q, and 9p in human malignant mesothelioma. Cancer Res 53:4349-4355 (1993).
    • (1993) Cancer Res , vol.53 , pp. 4349-4355
    • Taguchi, T.1    Jhanwar, S.C.2    Siegfried, J.M.3    Keller, S.M.4    Testa, J.R.5
  • 201
    • 0028053599 scopus 로고
    • Human Fas ligand: Gene structure, chromosomal location and species specificity
    • Takahashi T, Tanaka M, Inazawa J, Abe T, Suda T, Nagata S: Human Fas ligand: gene structure, chromosomal location and species specificity. Int Immunol 6:1567-1574 (1994).
    • (1994) Int Immunol , vol.6 , pp. 1567-1574
    • Takahashi, T.1    Tanaka, M.2    Inazawa, J.3    Abe, T.4    Suda, T.5    Nagata, S.6
  • 202
    • 0028564702 scopus 로고
    • Assignment of the human dihydropyrimidine dehydrogenase gene (DPYD) to chromosome region 1p22 by fluorescence in situ hybridization
    • Takai S, Fernandez-Salguero P, Kimura S, Gonzalez FJ, Yamada K: Assignment of the human dihydropyrimidine dehydrogenase gene (DPYD) to chromosome region 1p22 by fluorescence in situ hybridization. Genomics 24:613-614 (1994a).
    • (1994) Genomics , vol.24 , pp. 613-614
    • Takai, S.1    Fernandez-Salguero, P.2    Kimura, S.3    Gonzalez, F.J.4    Yamada, K.5
  • 203
    • 0028176111 scopus 로고
    • Human high-affinity FcganimaRI (CD64) gene mapped to chromosome 1q21.2→q21.3 by fluorescence in situ hybridization
    • Takai S, Kasama M, Yamada K, Kai N, Hirayama N, Namiki H, Taniyama T: Human high-affinity FcganimaRI (CD64) gene mapped to chromosome 1q21.2→q21.3 by fluorescence in situ hybridization. Hum Genet 93:13-15 (1994b).
    • (1994) Hum Genet , vol.93 , pp. 13-15
    • Takai, S.1    Kasama, M.2    Yamada, K.3    Kai, N.4    Hirayama, N.5    Namiki, H.6    Taniyama, T.7
  • 204
    • 0028258815 scopus 로고
    • There may be two tumor suppressor genes on chromosome arm 1p closely associated with biologically distinct subtypes of neuroblastoma
    • Takeda O, Homma C, Maseki N, Sakurai M, Kanda N, Schwab M, Nakamura Y, Kaneko Y: There may be two tumor suppressor genes on chromosome arm 1p closely associated with biologically distinct subtypes of neuroblastoma. Genes Chrom Cancer 1030-39 (1994).
    • (1994) Genes Chrom Cancer , pp. 1030-1039
    • Takeda, O.1    Homma, C.2    Maseki, N.3    Sakurai, M.4    Kanda, N.5    Schwab, M.6    Nakamura, Y.7    Kaneko, Y.8
  • 205
    • 0027944170 scopus 로고
    • Assignment of the human prostaglandin-endoperoxide synthase 2 (PTGS2) gene to 1q25 by fluorescence in situ hybridization
    • Tay A, Squire JA, Goldberg H, Skorecki K: Assignment of the human prostaglandin-endoperoxide synthase 2 (PTGS2) gene to 1q25 by fluorescence in situ hybridization. Genomics 23:718-719 (1994).
    • (1994) Genomics , vol.23 , pp. 718-719
    • Tay, A.1    Squire, J.A.2    Goldberg, H.3    Skorecki, K.4
  • 206
    • 0027945510 scopus 로고
    • Chromosomal localization of the genes encoding the kinetochore proteins CENPE and CENPF to human chromosomes 4q24→q25 and 1q32→q41, respectively, by fluorescence in situ hybridization
    • Testa JR, Zhou J, Bell DW, Yen TJ: Chromosomal localization of the genes encoding the kinetochore proteins CENPE and CENPF to human chromosomes 4q24→q25 and 1q32→q41, respectively, by fluorescence in situ hybridization. Genomics 23:691-693 (1994).
    • (1994) Genomics , vol.23 , pp. 691-693
    • Testa, J.R.1    Zhou, J.2    Bell, D.W.3    Yen, T.J.4
  • 207
    • 0029010375 scopus 로고
    • Isolation and fine mapping of 16 novel human zinc finger-encoding cDNAs identify putative candidate genes for developmental and malignant disorders
    • Tommerup N, Vissing H: Isolation and fine mapping of 16 novel human zinc finger-encoding cDNAs identify putative candidate genes for developmental and malignant disorders. Genomics 27:259-264 (1995).
    • (1995) Genomics , vol.27 , pp. 259-264
    • Tommerup, N.1    Vissing, H.2
  • 208
    • 0029017436 scopus 로고
    • Renal cell carcinoma with translocation (X;1). Further evidence for a cytogenetically defined subtype
    • Tonk V, Wilson KS, Timmons CF, Schneider NR, Tomlinson GE: Renal cell carcinoma with translocation (X;1). Further evidence for a cytogenetically defined subtype. Cancer Genet Cytogenet 81:72-75 (1995).
    • (1995) Cancer Genet Cytogenet , vol.81 , pp. 72-75
    • Tonk, V.1    Wilson, K.S.2    Timmons, C.F.3    Schneider, N.R.4    Tomlinson, G.E.5
  • 209
    • 0029107505 scopus 로고
    • Localization of the adenosine Al receptor subtype gene (ADORA1) to chromosome 1q32.1
    • Townsend-Nicholson A, Baker E, Schofield PR, Sutherland GR: Localization of the adenosine Al receptor subtype gene (ADORA1) to chromosome 1q32.1. Genomics 26:423-425 (1995).
    • (1995) Genomics , vol.26 , pp. 423-425
    • Townsend-Nicholson, A.1    Baker, E.2    Schofield, P.R.3    Sutherland, G.R.4
  • 210
    • 0027456335 scopus 로고
    • Cloning, overexpression and genomic mapping of the 14-kDa subunit of human replication protein A
    • Umbricht C, Erdile LP, Wang-Jabs E, Kelly TJ: Cloning, overexpression and genomic mapping of the 14-kDa subunit of human replication protein A. J biol Chem 268:6131-6138 (1993).
    • (1993) J Biol Chem , vol.268 , pp. 6131-6138
    • Umbricht, C.1    Erdile, L.P.2    Wang-Jabs, E.3    Kelly, T.J.4
  • 212
    • 0028201054 scopus 로고
    • The genes for nicein/kalinin 125- And 100 kDa subunits, candidates for junctional epidermolysis bullosa, map to chromosomes 1q32 and 1q25→q31
    • Vailly J, Szepetowski P, Mattei MG, Pedeutour F, Burgeson R, Ortonne JP, Meneguzzi G: The genes for nicein/kalinin 125- and 100 kDa subunits, candidates for junctional epidermolysis bullosa, map to chromosomes 1q32 and 1q25→q31. Genomics 21:286-288 (1994).
    • (1994) Genomics , vol.21 , pp. 286-288
    • Vailly, J.1    Szepetowski, P.2    Mattei, M.G.3    Pedeutour, F.4    Burgeson, R.5    Ortonne, J.P.6    Meneguzzi, G.7
  • 214
    • 0025048741 scopus 로고
    • Is the chromosome band 1p36 another hot-spot for rearrangements in uterine leiomyoma?
    • Vanni R, Dal Cin P, Van Den Berghe H: Is the chromosome band 1p36 another hot-spot for rearrangements in uterine leiomyoma? Genes Chrom Cancer 2:255-256 (1990).
    • (1990) Genes Chrom Cancer , vol.2 , pp. 255-256
    • Vanni, R.1    Dal Cin, P.2    Van Den Berghe, H.3
  • 215
    • 0028902409 scopus 로고
    • Subregional localization of 14 yeast artificial chromosomes to human chromosome region 1p by fluorescence in situ hybridization
    • Vernole P, Caporossi D, Tedeschi B, Nicoletti B, Van Ommen GJ: Subregional localization of 14 yeast artificial chromosomes to human chromosome region 1p by fluorescence in situ hybridization. Cytogenet Cell Genet 70:23-25 (1995).
    • (1995) Cytogenet Cell Genet , vol.70 , pp. 23-25
    • Vernole, P.1    Caporossi, D.2    Tedeschi, B.3    Nicoletti, B.4    Van Ommen, G.J.5
  • 217
    • 0022655767 scopus 로고
    • Three cases of preleukemic myelodysplastic disorders with the same translocation t(1;3)
    • Viguie F, Marie J-P, Poler F, Bernadou A: Three cases of preleukemic myelodysplastic disorders with the same translocation t(1;3). Cancer Genet Cytogenet 19:213-218 (1986).
    • (1986) Cancer Genet Cytogenet , vol.19 , pp. 213-218
    • Viguie, F.1    Marie, J.-P.2    Poler, F.3    Bernadou, A.4
  • 218
    • 0028146446 scopus 로고
    • Subregional mapping of the human lymphocyte-specific protein tyrosine kinasa gene (LCK) to 1p35→p34.3 and its position relative to the 1p marker D1S57
    • Volpi EV, Romani M, Siniscalco M: Subregional mapping of the human lymphocyte-specific protein tyrosine kinasa gene (LCK) to 1p35→p34.3 and its position relative to the 1p marker D1S57. Cytogenet Cell Genet 67:187-189 (1994).
    • (1994) Cytogenet Cell Genet , vol.67 , pp. 187-189
    • Volpi, E.V.1    Romani, M.2    Siniscalco, M.3
  • 221
    • 0028942724 scopus 로고
    • Rapid physical mapping of the human trk protooncogene (NTRK1) to human chromosome 1q21→q22 by P1 clone selection, fluorescence in situ hybridization (FISH) and computer-assisted microscopy
    • Weier H, Rhein AP, Shadravan F, Collins C, Polikoff D: Rapid physical mapping of the human trk protooncogene (NTRK1) to human chromosome 1q21→q22 by P1 clone selection, fluorescence in situ hybridization (FISH) and computer-assisted microscopy. Genomics 26:390-393 (1995).
    • (1995) Genomics , vol.26 , pp. 390-393
    • Weier, H.1    Rhein, A.P.2    Shadravan, F.3    Collins, C.4    Polikoff, D.5
  • 224
    • 0027151846 scopus 로고
    • Use of the single-strand conformation polymorphisms technique to detect loss of heterozygosity in neuroblastoma
    • White PS, Kaufman BA, Marshall HN, Brodeur GM: Use of the single-strand conformation polymorphisms technique to detect loss of heterozygosity in neuroblastoma. Genes Chrom Cancer 7:102-108 (1993).
    • (1993) Genes Chrom Cancer , vol.7 , pp. 102-108
    • White, P.S.1    Kaufman, B.A.2    Marshall, H.N.3    Brodeur, G.M.4
  • 226
    • 0028332417 scopus 로고
    • Genetic linkage of autosomal dominant juvenile glaucoma to 1q21→q31 in three affected pedigrees
    • Wiggs JL, Haines JL, Paglinauan C, Fine A, Sporn C, Lou D: Genetic linkage of autosomal dominant juvenile glaucoma to 1q21→q31 in three affected pedigrees. Genomics 21:299-303 (1994).
    • (1994) Genomics , vol.21 , pp. 299-303
    • Wiggs, J.L.1    Haines, J.L.2    Paglinauan, C.3    Fine, A.4    Sporn, C.5    Lou, D.6
  • 227
    • 0029071338 scopus 로고
    • Identification of a new murine runt domain-containing gene, Cbfa3, and localization of the human homolog, CBFA3, to chromosome 1p35→pter
    • Wijmenga C, Speck NA, Dracopoli NC, Hofker MH, Liu P, Collins FS: Identification of a new murine runt domain-containing gene, Cbfa3, and localization of the human homolog, CBFA3, to chromosome 1p35→pter. Genomics 26:611-614 (1995).
    • (1995) Genomics , vol.26 , pp. 611-614
    • Wijmenga, C.1    Speck, N.A.2    Dracopoli, N.C.3    Hofker, M.H.4    Liu, P.5    Collins, F.S.6
  • 229
    • 0025293056 scopus 로고
    • Structure, expression and genetic linkage of the mouse BcmI (OX45 of Blast1) antigen: Evidence for genetic duplication giving rise to the BCM1 region of mouse chromosome 1, and the CD2/LFA3 region on mouse chromosome 3
    • Vong YW, AF Williams, SF Kingsmore, MF Seldin: Structure, expression and genetic linkage of the mouse BcmI (OX45 of Blast1) antigen: evidence for genetic duplication giving rise to the BCM1 region of mouse chromosome 1, and the CD2/LFA3 region on mouse chromosome 3. J Exp Med 171:2115-2130 (1990).
    • (1990) J Exp Med , vol.171 , pp. 2115-2130
    • Vong, Y.W.1    Williams, A.F.2    Kingsmore, S.F.3    Seldin, M.F.4
  • 231
    • 0028027180 scopus 로고
    • CDNA cloning and chromosome mapping of human dihydropyrimidine dehydrogenase, an enzyme associated with 5-fluorouracil toxicity and congenital thymine uraciluria
    • Yokota H, Fernandez-Salguero P, Furuya H, Lin K, McBride OW, Podschun B, Schnackerz KD, Gonzalez FJ: CDNA cloning and chromosome mapping of human dihydropyrimidine dehydrogenase, an enzyme associated with 5-fluorouracil toxicity and congenital thymine uraciluria. J biol Chemistry 269:23192-23196 (1994).
    • (1994) J Biol Chemistry , vol.269 , pp. 23192-23196
    • Yokota, H.1    Fernandez-Salguero, P.2    Furuya, H.3    Lin, K.4    McBride, O.W.5    Podschun, B.6    Schnackerz, K.D.7    Gonzalez, F.J.8
  • 232
    • 0029019617 scopus 로고
    • A human SHC-related sequence maps to chromosome 17, the SHC gene maps to chromosome 1
    • Yulug IG, Egan SE, CG See, Fisher EMC: A human SHC-related sequence maps to chromosome 17, the SHC gene maps to chromosome 1. Hum Genet 96:245-248 (1995).
    • (1995) Hum Genet , vol.96 , pp. 245-248
    • Yulug, I.G.1    Egan, S.E.2    See, C.G.3    Fisher, E.M.C.4
  • 233
    • 0028762437 scopus 로고
    • The reference library system - Sharing biological material and experimental data
    • Zehetner G, Lehrach H: The reference library system - sharing biological material and experimental data. Nature 367:489-491 (1994).
    • (1994) Nature , vol.367 , pp. 489-491
    • Zehetner, G.1    Lehrach, H.2


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