메뉴 건너뛰기




Volumn 18, Issue 3, 1997, Pages 212-218

Characterization of a YAC contig containing the NBCCS locus and a novel kruppel-type zinc finger sequence on chromosome segment 9q22.3

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; CONTIG; ZINC FINGER PROTEIN;

EID: 0030891547     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2264(199703)18:3<212::AID-GCC7>3.0.CO;2-4     Document Type: Article
Times cited : (6)

References (25)
  • 1
    • 0027141519 scopus 로고
    • Number of CpG islands and genes in human and mouse
    • Antequera F, Bird A (1993) Number of CpG islands and genes in human and mouse. Proc Natl Acad Sci USA 90:11995-11999.
    • (1993) Proc Natl Acad Sci USA , vol.90 , pp. 11995-11999
    • Antequera, F.1    Bird, A.2
  • 2
    • 0342788462 scopus 로고
    • Analysis of the FACC and XPAC genes as candidate genes for the basal cell nevus syndrome
    • Program and Abstract
    • Bare JW, Xie J, Quinn AG, Epstein Jr EH (1995) Analysis of the FACC and XPAC genes as candidate genes for the basal cell nevus syndrome. Am J Hum Genet 57: Program and Abstract 312.
    • (1995) Am J Hum Genet , vol.57 , pp. 312
    • Bare, J.W.1    Xie, J.2    Quinn, A.G.3    Epstein E.H., Jr.4
  • 3
    • 0024393234 scopus 로고
    • The human genome contains hundreds of gene encoding zinc finger proteins of the Kruppel type
    • Bellefroid EJ, Lecocq PJ, Benhida A, Poncelet DA, Belayew A, Martial JA (1989) The human genome contains hundreds of gene encoding zinc finger proteins of the Kruppel type. DNA 8:377-387.
    • (1989) DNA , vol.8 , pp. 377-387
    • Bellefroid, E.J.1    Lecocq, P.J.2    Benhida, A.3    Poncelet, D.A.4    Belayew, A.5    Martial, J.A.6
  • 4
    • 0025920615 scopus 로고
    • The evolutionary conserved kruppel-associated box domain defines a subfamily of eukaryotic multifingered proteins
    • Bellefroid EJ, Poncelet DA, Lecocq, PJ, Revelant O, Martial JA (1991) The evolutionary conserved kruppel-associated box domain defines a subfamily of eukaryotic multifingered proteins. Proc Natl Acad Sci USA 88:3608-3612.
    • (1991) Proc Natl Acad Sci USA , vol.88 , pp. 3608-3612
    • Bellefroid, E.J.1    Poncelet, D.A.2    Lecocq, P.J.3    Revelant, O.4    Martial, J.A.5
  • 5
    • 0028219676 scopus 로고
    • Parental origin of chromosome 9q22.3-q31 lost in basal cell carcinomas from basal cell nevus syndrome patients
    • Bonifas JM, Bare JW, Kerschmann RL, Master SP, Epstein EH Jr (1994) Parental origin of chromosome 9q22.3-q31 lost in basal cell carcinomas from basal cell nevus syndrome patients. Hum Mol Genet 3:447-448.
    • (1994) Hum Mol Genet , vol.3 , pp. 447-448
    • Bonifas, J.M.1    Bare, J.W.2    Kerschmann, R.L.3    Master, S.P.4    Epstein E.H., Jr.5
  • 7
    • 0027436115 scopus 로고
    • Kurther localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: Linkage and loss of hererozygosity
    • Chenevix-Trench G, Wicking C, Berkman J, Sharpe H, Goldgar D, Searle J, Wainright B (1993) Kurther localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: Linkage and loss of hererozygosity. Am J Hum Genet 53:760-767.
    • (1993) Am J Hum Genet , vol.53 , pp. 760-767
    • Chenevix-Trench, G.1    Wicking, C.2    Berkman, J.3    Sharpe, H.4    Goldgar, D.5    Searle, J.6    Wainright, B.7
  • 9
    • 0021760092 scopus 로고
    • A comprehensive set of sequence analysis programs for the VAX
    • Devereaux J, Haberli P, Smithies O (1984) A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Res 12:387-395.
    • (1984) Nucleic Acids Res , vol.12 , pp. 387-395
    • Devereaux, J.1    Haberli, P.2    Smithies, O.3
  • 10
    • 0027968936 scopus 로고
    • Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anaemia Group C in a 2.6-cM interval and contributes to the fine map of 9q22.3
    • Farndon PA, Morris DJ, Hardy C, McConville CM, Weissenbach J, Kilpatrick MW, Reis A (1994) Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anaemia Group C in a 2.6-cM interval and contributes to the fine map of 9q22.3. Genomics 23:486-489.
    • (1994) Genomics , vol.23 , pp. 486-489
    • Farndon, P.A.1    Morris, D.J.2    Hardy, C.3    McConville, C.M.4    Weissenbach, J.5    Kilpatrick, M.W.6    Reis, A.7
  • 12
    • 0027269608 scopus 로고
    • Sun exposure and basal cell carcinomas in the nevoid basal cell carcinoma syndrome
    • Goldstein AM, Bale SJ, Peck GL, DiGiovanna JJ (1993) Sun exposure and basal cell carcinomas in the nevoid basal cell carcinoma syndrome. J Am Acad Dermatol 29:34-41.
    • (1993) J Am Acad Dermatol , vol.29 , pp. 34-41
    • Goldstein, A.M.1    Bale, S.J.2    Peck, G.L.3    DiGiovanna, J.J.4
  • 14
    • 0023222358 scopus 로고
    • Nevoid basal-cell carcinoma syndrome
    • Gorlin RJ (1987) Nevoid basal-cell carcinoma syndrome. Medicine 66:98-113.
    • (1987) Medicine , vol.66 , pp. 98-113
    • Gorlin, R.J.1
  • 18
    • 44049115577 scopus 로고
    • Choice of enzymes for mapping based on CpG islands in the human genome
    • Larsen F, Gundersen G, Prydz H (1992) Choice of enzymes for mapping based on CpG islands in the human genome. GATA 9:80-85.
    • (1992) GATA , vol.9 , pp. 80-85
    • Larsen, F.1    Gundersen, G.2    Prydz, H.3
  • 19
    • 0028049612 scopus 로고
    • A YAC contig spanning the nevoid basal cell carcinoma syndrome, Fanconi anaemia Group C, and xeroderma pigmentosum Group a loci on chromosome 9q
    • Morris DJ, Reis A (1994) A YAC contig spanning the nevoid basal cell carcinoma syndrome, Fanconi anaemia Group C, and xeroderma pigmentosum Group A loci on chromosome 9q. Genomics 23: 23-29.
    • (1994) Genomics , vol.23 , pp. 23-29
    • Morris, D.J.1    Reis, A.2
  • 21
    • 43949167467 scopus 로고
    • Methods for finding genes a major rate limiting step in positional cloning
    • Parrish JK, Nelson DL (1993) Methods for finding genes a major rate limiting step in positional cloning. GATA 10:29-11.
    • (1993) GATA , vol.10 , pp. 29-111
    • Parrish, J.K.1    Nelson, D.L.2
  • 22
    • 0028476207 scopus 로고
    • Report on the 3rd International Workshop on Chromosome 9
    • Report on the 3rd International Workshop on Chromosome 9 (1994) Ann Hum Genet 58:177-250.
    • (1994) Ann Hum Genet , vol.58 , pp. 177-250
  • 24
    • 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 (1995) 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) Genomics , vol.27 , pp. 259-264
    • Tommerup, N.1    Vissing, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.