메뉴 건너뛰기




Volumn 101, Issue 2, 1997, Pages 154-157

Gene structure and allelic expression assay of the human GLI3 gene

Author keywords

[No Author keywords available]

Indexed keywords

DNA; TRANSCRIPTION FACTOR; ZINC FINGER PROTEIN;

EID: 0031469311     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050605     Document Type: Article
Times cited : (18)

References (23)
  • 2
    • 0030035157 scopus 로고    scopus 로고
    • Syndrome of the month: Pallister - Hall syndrome
    • Biesecker LG, Graham JM Jr (1996) Syndrome of the month: Pallister - Hall syndrome. J Med Genet 33:585-589
    • (1996) J Med Genet , vol.33 , pp. 585-589
    • Biesecker, L.G.1    Graham Jr., J.M.2
  • 5
    • 1842297302 scopus 로고
    • Amplification of sequences from affected individuals
    • Dracopoli NC, Haines JL, Korf BR, Moir DT, Morton CC, Seidman CE, Seidman JG, Smith DR (eds). John Wiley and Sons, New York
    • Dracopoli NC, Haines JL, Korf BR, Moir DT, Morton CC, Seidman CE, Seidman JG, Smith DR (1994) Amplification of sequences from affected individuals. In: Dracopoli NC, Haines JL, Korf BR, Moir DT, Morton CC, Seidman CE, Seidman JG, Smith DR (eds) Current protocols in human genetics, vol 1. John Wiley and Sons, New York, pp 7.1.1-7.1.4
    • (1994) Current Protocols in Human Genetics , vol.1 , pp. 711-714
    • Dracopoli, N.C.1    Haines, J.L.2    Korf, B.R.3    Moir, D.T.4    Morton, C.C.5    Seidman, C.E.6    Seidman, J.G.7    Smith, D.R.8
  • 6
    • 0030446485 scopus 로고    scopus 로고
    • Molecular cytogenetic characterization and physical mapping of 12q13-15 amplification in human cancers
    • Elkahoun AG, Bittner M, Hoskins K, Gemmill R, Meltzer PS (1996) Molecular cytogenetic characterization and physical mapping of 12q13-15 amplification in human cancers. Genes Chromosom Cancer 17: 205-214
    • (1996) Genes Chromosom Cancer , vol.17 , pp. 205-214
    • Elkahoun, A.G.1    Bittner, M.2    Hoskins, K.3    Gemmill, R.4    Meltzer, P.S.5
  • 7
    • 0027346772 scopus 로고
    • Molecular linkage of the morphogenetic mutant add and the zinc finger gene GLI3
    • Hoeven F van der, Schimmang T, Vortkamp A, Rüther U (1993) Molecular linkage of the morphogenetic mutant add and the zinc finger gene GLI3. Mamm Genome 4: 276-277
    • (1993) Mamm Genome , vol.4 , pp. 276-277
    • Hoeven, F.V.D.1    Schimmang, T.2    Vortkamp, A.3    Rüther, U.4
  • 8
    • 0027478216 scopus 로고
    • A mouse model of Greig cephalopolysyndactyly syndrome: The extra-toes - Mutation contains an intragenic deletion of the GLI3 gene
    • Hui C-C, Joyner A (1993) A mouse model of Greig cephalopolysyndactyly syndrome: the extra-toes - mutation contains an intragenic deletion of the GLI3 gene. Nat Genet 3:241-246
    • (1993) Nat Genet , vol.3 , pp. 241-246
    • Hui, C.-C.1    Joyner, A.2
  • 10
    • 0031019090 scopus 로고    scopus 로고
    • GLI3 frameshift mutations cause autosomal dominant Pallister - Hall syndrome
    • Kang S, Graham JM Jr, Olney AH, Biesecker LG (1997b) GLI3 frameshift mutations cause autosomal dominant Pallister - Hall syndrome. Nat Genet 15: 266-268
    • (1997) Nat Genet , vol.15 , pp. 266-268
    • Kang, S.1    Graham Jr., J.M.2    Olney, A.H.3    Biesecker, L.G.4
  • 12
    • 0027473988 scopus 로고
    • Multiplex PCR of three dinucleotide repeats in the Prader - Willi/Angelman critical region (15q11-q13): Molecular diagnosis and mechanism of uniparental disomy
    • Mutirangura A, Greenberg F, Butler MG, Malcolm S, Nicholls RD, Chakravarti A, Ledbetter DH (1993) Multiplex PCR of three dinucleotide repeats in the Prader - Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy. Hum Mol Genet 2: 143-151
    • (1993) Hum Mol Genet , vol.2 , pp. 143-151
    • Mutirangura, A.1    Greenberg, F.2    Butler, M.G.3    Malcolm, S.4    Nicholls, R.D.5    Chakravarti, A.6    Ledbetter, D.H.7
  • 13
    • 0025605517 scopus 로고
    • Evidence for allelism of the recessive insertional mutation add and the dominant mouse mutation extra toes (Xt)
    • Pohl TP, Mattei M-G, Rüther U (1990) Evidence for allelism of the recessive insertional mutation add and the dominant mouse mutation extra toes (Xt). Development 110: 1153-1157
    • (1990) Development , vol.110 , pp. 1153-1157
    • Pohl, T.P.1    Mattei, M.-G.2    Rüther, U.3
  • 16
    • 0025172883 scopus 로고
    • GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity
    • Ruppert JM, Vogelstein B, Arheden K, Kinzler KW (1990) GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity. Mol Cell Biol 10: 5408-5415
    • (1990) Mol Cell Biol , vol.10 , pp. 5408-5415
    • Ruppert, J.M.1    Vogelstein, B.2    Arheden, K.3    Kinzler, K.W.4
  • 18
    • 0026445646 scopus 로고
    • Expression of the zinc finger gene GLI3 is affected in the morphogenetic mouse mutant extra-toes (Xt)
    • Schimmang T, Lemaistre M, Vortkamp A, Rüther U (1992) Expression of the zinc finger gene GLI3 is affected in the morphogenetic mouse mutant extra-toes (Xt). Development 116: 799-804
    • (1992) Development , vol.116 , pp. 799-804
    • Schimmang, T.1    Lemaistre, M.2    Vortkamp, A.3    Rüther, U.4
  • 19
    • 0027739603 scopus 로고
    • GLI3 expression is affected in the morphogenetic mouse mutants Add and Xt
    • Schimmang T, Hoeven F van der, Rüther U (1993) GLI3 expression is affected in the morphogenetic mouse mutants Add and Xt. Prog Clin Biol Res 53a: 153-161
    • (1993) Prog Clin Biol Res , vol.53 A , pp. 153-161
    • Schimmang, T.1    Hoeven, F.V.D.2    Rüther, U.3
  • 20
    • 0028446529 scopus 로고
    • The mouse mutant polydactyly Nagoya (Pdn) defines a novel allele of the zinc finger gene GLI3
    • Schimmang T, Oda SI, Rüther U (1994) The mouse mutant polydactyly Nagoya (Pdn) defines a novel allele of the zinc finger gene GLI3. Mamm Genome 5: 384-386
    • (1994) Mamm Genome , vol.5 , pp. 384-386
    • Schimmang, T.1    Oda, S.I.2    Rüther, U.3
  • 21
    • 0025812172 scopus 로고
    • GLI3 zinc finger gene interrupted by translocations in Greig syndrome families
    • Vortkamp A, Gessler M, Grzeschik K-H (1991) GLI3 zinc finger gene interrupted by translocations in Greig syndrome families. Nature 352: 539-540
    • (1991) Nature , vol.352 , pp. 539-540
    • Vortkamp, A.1    Gessler, M.2    Grzeschik, K.-H.3
  • 22
    • 0027981512 scopus 로고
    • Isolation of a yeast artificial chromosome contig spanning the Greig cephalopolysyndactyly (GCPS) gene region
    • Vortkamp A, Gessler M, Le Paslier D, Elaswarapu R, Smith S, Grezeschik K-H (1994) Isolation of a yeast artificial chromosome contig spanning the Greig cephalopolysyndactyly (GCPS) gene region. Genomics 22: 563-568
    • (1994) Genomics , vol.22 , pp. 563-568
    • Vortkamp, A.1    Gessler, M.2    Le Paslier, D.3    Elaswarapu, R.4    Smith, S.5    Grezeschik, K.-H.6
  • 23
    • 0028821386 scopus 로고
    • Isolation and characterization of a cosmid contig for the GCPS gene region
    • Vortkamp A, Heid C, Gessler M, Grzeschik K-H (1995) Isolation and characterization of a cosmid contig for the GCPS gene region. Hum Genet 95: 82-88
    • (1995) Hum Genet , vol.95 , pp. 82-88
    • Vortkamp, A.1    Heid, C.2    Gessler, M.3    Grzeschik, K.-H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.