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Volumn 88, Issue 3-4, 2000, Pages 225-229

Expression map of human chromosome region 17p13.3, spanning the RP13 dominant retinitis pigmentosa locus, the Miller-Dieker lissencephaly syndrome (MDLS) region, and a putative tumour suppressor locus

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 17P; EXPRESSED SEQUENCE TAG; GENE EXPRESSION; GENE MAPPING; GENETIC MARKER; HETEROZYGOSITY LOSS; HUMAN; LUNG CANCER; MILLER DIEKER SYNDROME; PRIORITY JOURNAL; RETINITIS PIGMENTOSA; SEQUENCE TAGGED SITE; TUMOR SUPPRESSOR GENE; YEAST ARTIFICIAL CHROMOSOME;

EID: 0034068019     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: 10.1159/000015556     Document Type: Article
Times cited : (7)

References (19)
  • 2
    • 0030827255 scopus 로고    scopus 로고
    • Loss of heterozygosity of a locus on 17p13.3, independent of p53, is associated with higher grades of astrocytic tumours
    • Chattopadhyay P, Rathore A, Mathur M, Sarkar C, Mahapatra AK, Sinha S: Loss of heterozygosity of a locus on 17p13.3, independent of p53, is associated with higher grades of astrocytic tumours. Oncogene 15:871-874 (1997).
    • (1997) Oncogene , vol.15 , pp. 871-874
    • Chattopadhyay, P.1    Rathore, A.2    Mathur, M.3    Sarkar, C.4    Mahapatra, A.K.5    Sinha, S.6
  • 4
    • 0027723477 scopus 로고
    • A 1st-generation physical map of the human genome
    • Cohen D, Chumakov I, Weissenbach J. A 1st-generation physical map of the human genome. Nature 366:698-701 (1993).
    • (1993) Nature , vol.366 , pp. 698-701
    • Cohen, D.1    Chumakov, I.2    Weissenbach, J.3
  • 5
    • 0027486966 scopus 로고
    • Lissencephaly - A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13
    • Dobyns WB, Reiner O, Carrozzo R, Ledbetter DH: Lissencephaly - a human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13. JAMA 270:2838-2842 (1993).
    • (1993) JAMA , vol.270 , pp. 2838-2842
    • Dobyns, W.B.1    Reiner, O.2    Carrozzo, R.3    Ledbetter, D.H.4
  • 8
    • 0031869359 scopus 로고    scopus 로고
    • Fine localisation of the gene for central areolar choroidal dystrophy on chromosome 17p
    • Hughes AE, Lotery AJ, Silvestri G: Fine localisation of the gene for central areolar choroidal dystrophy on chromosome 17p. J med Genet 35:770-772 (1998).
    • (1998) J Med Genet , vol.35 , pp. 770-772
    • Hughes, A.E.1    Lotery, A.J.2    Silvestri, G.3
  • 9
    • 0031133261 scopus 로고    scopus 로고
    • Intelligent linkage analysis using gene density estimates
    • Inglehearn CF: Intelligent linkage analysis using gene density estimates. Nature Genet 16:15 (1997).
    • (1997) Nature Genet , vol.16 , pp. 15
    • Inglehearn, C.F.1
  • 16
    • 0342799615 scopus 로고    scopus 로고
    • Human aryl-hydrocarbon interacting protein-like 1 gene (AIPL1), a candidate for inherited retinal disorders mapping to 17p13: Characterisation and mutation testing
    • Sohocki MM, Blackshaw S, Cepko CL, Sullivan LS, Daiger SP: Human aryl-hydrocarbon interacting protein-like 1 gene (AIPL1), a candidate for inherited retinal disorders mapping to 17p13: characterisation and mutation testing. Am J hum Genet 65(Suppl):569 (1999).
    • (1999) Am J Hum Genet , vol.65 , Issue.SUPPL. , pp. 569
    • Sohocki, M.M.1    Blackshaw, S.2    Cepko, C.L.3    Sullivan, L.S.4    Daiger, S.P.5
  • 18
    • 0026669469 scopus 로고
    • p53 function and dysfunction
    • Vogelstein B, Kinzler KW: p53 Function and dysfunction. Cell 70:523-526 (1992).
    • (1992) Cell , vol.70 , pp. 523-526
    • Vogelstein, B.1    Kinzler, K.W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.