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Volumn 9, Issue 8, 1998, Pages 676-678

The Xt(J) allele generates a Gli3 fusion transcript

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ARTICLE; GENE DELETION; GENE FUSION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC TRANSCRIPTION; HETEROZYGOTE; MOUSE; NONHUMAN; PALLISTER HALL SYNDROME; POLYDACTYLY; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; ALLELE; AMINO ACID SEQUENCE; ANIMAL; BIOSYNTHESIS; CHEMISTRY; GENETICS; HUMAN; MOLECULAR GENETICS; MOUSE MUTANT; MULTIPLE MALFORMATION SYNDROME; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION;

EID: 0031595311     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003359900845     Document Type: Article
Times cited : (52)

References (17)
  • 1
    • 0030680207 scopus 로고    scopus 로고
    • Strike three for GLI3
    • Biesecker L (1997) Strike three for GLI3. Nat Genet 17, 259-260
    • (1997) Nat Genet , vol.17 , pp. 259-260
    • Biesecker, L.1
  • 2
    • 0040976312 scopus 로고    scopus 로고
    • Evidence for genetic control of Sonic hedgehog by Gli3 in mouse limb development
    • Büscher D, Bosse B, Heymer J, Rüther U (1997) Evidence for genetic control of Sonic hedgehog by Gli3 in mouse limb development. Mech Dev 62, 175-182
    • (1997) Mech Dev , vol.62 , pp. 175-182
    • Büscher, D.1    Bosse, B.2    Heymer, J.3    Rüther, U.4
  • 3
  • 4
    • 0027478216 scopus 로고
    • J mutation contains an intragenic deletion of the Gli3 gene
    • J 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
  • 5
    • 0014097059 scopus 로고
    • Extra-toes: A new mutant gene causing multiple abnormalities in the mouse
    • Johnson DR (1967) Extra-toes: a new mutant gene causing multiple abnormalities in the mouse. J Embryol Exp Morphol 17, 543-581
    • (1967) J Embryol Exp Morphol , vol.17 , pp. 543-581
    • Johnson, D.R.1
  • 6
    • 0031019090 scopus 로고    scopus 로고
    • GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome
    • Kang S, Graham J, Olney A, Biesecker L (1997) 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, J.2    Olney, A.3    Biesecker, L.4
  • 7
    • 0031080907 scopus 로고    scopus 로고
    • Multigenic control of the localization of the zone of polarizing activity in limb morphogenesis in the mouse
    • Masuya H, Sagai T, Moriwaki K, Shiroishi T (1997) Multigenic control of the localization of the zone of polarizing activity in limb morphogenesis in the mouse. Dev Biol 182, 42-51
    • (1997) Dev Biol , vol.182 , pp. 42-51
    • Masuya, H.1    Sagai, T.2    Moriwaki, K.3    Shiroishi, T.4
  • 8
    • 0027423758 scopus 로고
    • Crystal structure of a five-finger GLI-DNA complex: New perspectives on zinc fingers
    • Pavletich N, Pabo C (1993) Crystal structure of a five-finger GLI-DNA complex: new perspectives on zinc fingers. Science 261, 1701-1707
    • (1993) Science , vol.261 , pp. 1701-1707
    • Pavletich, N.1    Pabo, C.2
  • 9
    • 0025605517 scopus 로고
    • Evidence for allelism of the recessive insertional mutation add and the dominant mouse syndrome extra-toes (Xt)
    • Pohl T, Mattei M-G, Rüther U (1990) Evidence for allelism of the recessive insertional mutation add and the dominant mouse syndrome extra-toes (Xt). Development 110, 1153-1157
    • (1990) Development , vol.110 , pp. 1153-1157
    • Pohl, T.1    Mattei, M.-G.2    Rüther, U.3
  • 11
    • 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
  • 12
    • 0028446529 scopus 로고
    • The mouse mutant Polydactyly Nagoya (Pdn) defines a novel allele of the zinc finger gene Gli3
    • Schimmang T, Oda I, 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, I.2    Rüther, U.3
  • 13
    • 7344261975 scopus 로고    scopus 로고
    • The mouse syndrome Pdn is caused by the integration of a retrotransposon into the Gli3 gene
    • submitted
    • Thien H, Rüther U (1998) The mouse syndrome Pdn is caused by the integration of a retrotransposon into the Gli3 gene. J Biol Chem submitted.
    • (1998) J Biol Chem
    • Thien, H.1    Rüther, U.2
  • 14
    • 0030591489 scopus 로고    scopus 로고
    • Cloning and sequence analysis of the murine Gli3 cDNA
    • Thien H, Büscher D, Rüther U (1996) Cloning and sequence analysis of the murine Gli3 cDNA. Biochim Biophys Acta 1307, 267-269
    • (1996) Biochim Biophys Acta , vol.1307 , pp. 267-269
    • Thien, H.1    Büscher, D.2    Rüther, U.3
  • 15
    • 0027346772 scopus 로고
    • Molecular linkage of the morphogenetic mouse mutation add and the zinc finger gene Gli3
    • van der Hoeven F, Schimmang T, Vortkamp A, Rüther U (1993) Molecular linkage of the morphogenetic mouse mutation add and the zinc finger gene Gli3. Mamm Genome 4, 276-277
    • (1993) Mamm Genome , vol.4 , pp. 276-277
    • Van Der Hoeven, F.1    Schimmang, T.2    Vortkamp, A.3    Rüther, U.4
  • 16
    • 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
  • 17
    • 0026469401 scopus 로고
    • Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt)
    • Vortkamp A, Franz T, Gessler M, Grzeschik K-H (1992) Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt). Mamm Genome 3, 461-463
    • (1992) Mamm Genome , vol.3 , pp. 461-463
    • Vortkamp, A.1    Franz, T.2    Gessler, M.3    Grzeschik, K.-H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.