메뉴 건너뛰기




Volumn 6, Issue 4, 1997, Pages 583-586

Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young (MODY3)

Author keywords

[No Author keywords available]

Indexed keywords

NUCLEAR FACTOR I; TRANSCRIPTION FACTOR;

EID: 8244219694     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/6.4.583     Document Type: Article
Times cited : (122)

References (23)
  • 2
    • 0026754672 scopus 로고
    • Primary pancreatic beta-cell secretory defect caused by mutations in the glucokinase in kindreds of maturity onset diabetes of the young
    • Velho, G., Froguel, P., Clment, K., Pueyo, M.E., Rakotoambinina, B., Zouali, H., Passa, P., Cohen, D. and Robert, J.J. (1992) Primary pancreatic beta-cell secretory defect caused by mutations in the glucokinase in kindreds of maturity onset diabetes of the young. Lancet 340, 444-448.
    • (1992) Lancet , vol.340 , pp. 444-448
    • Velho, G.1    Froguel, P.2    Clment, K.3    Pueyo, M.E.4    Rakotoambinina, B.5    Zouali, H.6    Passa, P.7    Cohen, D.8    Robert, J.J.9
  • 4
    • 0028087153 scopus 로고
    • Abnormal insulin secretion, not insulin resistance, is the genetic or primary defect of MODY in the RW pedigree
    • Herman, W.H., Fajans, S.S., Ortiz, F.J., Smith, M.J., Sturis, J., Bell, G.I., Polonsky, K.S. and Halter, J.B. (1994) Abnormal insulin secretion, not insulin resistance, is the genetic or primary defect of MODY in the RW pedigree. Diabetes 43, 40-46.
    • (1994) Diabetes , vol.43 , pp. 40-46
    • Herman, W.H.1    Fajans, S.S.2    Ortiz, F.J.3    Smith, M.J.4    Sturis, J.5    Bell, G.I.6    Polonsky, K.S.7    Halter, J.B.8
  • 7
    • 0025874033 scopus 로고
    • Strategies for the collection sibling-pair data for genetic studies in type 2 (non insulin-dependent) diabetes mellitus
    • Froguel, P., Velho, G., Cohen, D. and Passa, P. (1991) Strategies for the collection sibling-pair data for genetic studies in type 2 (non insulin-dependent) diabetes mellitus. Diabetologia 34, 685.
    • (1991) Diabetologia , vol.34 , pp. 685
    • Froguel, P.1    Velho, G.2    Cohen, D.3    Passa, P.4
  • 8
    • 0026032055 scopus 로고
    • Gene for non insulin dependent diabetes mellitus (maturity onset diabetes of the young subtype) is linked to DNA polymorphism on chromosome 20q
    • Bell, G.I., Xiang, K.S., Newman, M.V., Wu, S.H., Wright, L.G., Fajans, S.S. and Cox, N.J. (1991) Gene for non insulin dependent diabetes mellitus (maturity onset diabetes of the young subtype) is linked to DNA polymorphism on chromosome 20q. Proc. Natl. Acad. Sci. USA 88, 1484-1488.
    • (1991) Proc. Natl. Acad. Sci. USA , vol.88 , pp. 1484-1488
    • Bell, G.I.1    Xiang, K.S.2    Newman, M.V.3    Wu, S.H.4    Wright, L.G.5    Fajans, S.S.6    Cox, N.J.7
  • 13
    • 0029762068 scopus 로고    scopus 로고
    • Diabetes complications in NIDDM kindreds linked to the MODY-3 locus on chromosome 12q
    • Velho, G., Vaxillaire, M., Boccio, V., Charpentier, G. and Froguel, P. (1996) Diabetes complications in NIDDM kindreds linked to the MODY-3 locus on chromosome 12q. Diabetes Care 19, 915-919.
    • (1996) Diabetes Care , vol.19 , pp. 915-919
    • Velho, G.1    Vaxillaire, M.2    Boccio, V.3    Charpentier, G.4    Froguel, P.5
  • 15
    • 0026928723 scopus 로고
    • HNF1, a homeoprotein member of the hepatic transcription regulatory network
    • Tronche, F. and Yaniv, M. (1992) HNF1, a homeoprotein member of the hepatic transcription regulatory network. Bioessays 14, 579-587.
    • (1992) Bioessays , vol.14 , pp. 579-587
    • Tronche, F.1    Yaniv, M.2
  • 17
    • 0025775278 scopus 로고
    • vHNF1 is a homeoprotein that activates transcription and forms heterodimers with HNF1
    • Rey-Campos, J., Chouard, T., Yaniv, M. and Cereghini, S. (1991) vHNF1 is a homeoprotein that activates transcription and forms heterodimers with HNF1. EMBO J. 10, 1445-1457.
    • (1991) EMBO J. , vol.10 , pp. 1445-1457
    • Rey-Campos, J.1    Chouard, T.2    Yaniv, M.3    Cereghini, S.4
  • 18
    • 0030031453 scopus 로고    scopus 로고
    • Hepatocyte Nuclear Factor 1 inactivation results in hepatic dysfunction, phenylketonuria, and renal Fanconi syndrome
    • Pontoglio, M., Barra, J., Hadchouel, M., Doyen, A., Kress, C., Poggi Bach, J., Babinet, C. and Yaniv, M. (1996) Hepatocyte Nuclear Factor 1 inactivation results in hepatic dysfunction, phenylketonuria, and renal Fanconi syndrome. Cell 84, 572-585.
    • (1996) Cell , vol.84 , pp. 572-585
    • Pontoglio, M.1    Barra, J.2    Hadchouel, M.3    Doyen, A.4    Kress, C.5    Poggi Bach, J.6    Babinet, C.7    Yaniv, M.8
  • 20
    • 0026670321 scopus 로고
    • Trans-dominant inhibition of transcription activator LFB1
    • Nicosia, A., Tafi, R. and Monaci, P. (1992) Trans-dominant inhibition of transcription activator LFB1. Nucleic Acids Res. 20, 5321-5328.
    • (1992) Nucleic Acids Res. , vol.20 , pp. 5321-5328
    • Nicosia, A.1    Tafi, R.2    Monaci, P.3
  • 23
    • 0025892211 scopus 로고
    • HNF-1α and HNF-1β (vHNF-1) share dimerization and homeo domains, but not activation domains, and form heterodimers in vitro
    • Mendel, D.B., Hausen, L.P., Graves, M.K., Conley, B.P. and Crabtree, G.R. (1991) HNF-1α and HNF-1β (vHNF-1) share dimerization and homeo domains, but not activation domains, and form heterodimers in vitro. Genes Dev. 5, 1042-1056.
    • (1991) Genes Dev. , vol.5 , pp. 1042-1056
    • Mendel, D.B.1    Hausen, L.P.2    Graves, M.K.3    Conley, B.P.4    Crabtree, G.R.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.