메뉴 건너뛰기




Volumn 9, Issue , 2011, Pages

Mutation analysis of the WNT4 gene in Han Chinese women with premature ovarian failure

Author keywords

[No Author keywords available]

Indexed keywords

WNT4 PROTEIN; FOLLITROPIN; LUTEINIZING HORMONE; WNT PROTEIN;

EID: 79957568900     PISSN: None     EISSN: 14777827     Source Type: Journal    
DOI: 10.1186/1477-7827-9-75     Document Type: Article
Times cited : (11)

References (15)
  • 1
    • 34248145546 scopus 로고    scopus 로고
    • Premature ovarian failure
    • 10.1186/1750-1172-1-9, 1502130, 16722528
    • Beck-Peccoz P, Persani L. Premature ovarian failure. Orphanet J Rare Dis 2006, 1:9. 10.1186/1750-1172-1-9, 1502130, 16722528.
    • (2006) Orphanet J Rare Dis , vol.1 , pp. 9
    • Beck-Peccoz, P.1    Persani, L.2
  • 2
    • 55749098336 scopus 로고    scopus 로고
    • Recent developments in identifying genetic determinants of premature ovarian failure
    • 10.1159/000152039, 18987497
    • Skillern A, Rajkovic A. Recent developments in identifying genetic determinants of premature ovarian failure. Sex Dev 2008, 2(4-5):228-243. 10.1159/000152039, 18987497.
    • (2008) Sex Dev , vol.2 , Issue.4-5 , pp. 228-243
    • Skillern, A.1    Rajkovic, A.2
  • 3
    • 0028588919 scopus 로고
    • Epithelial transformation of metanephric mesenchyme in the developing kidney regulated by Wnt-4
    • 10.1038/372679a0, 7990960
    • Stark K, Vainio S, Vassileva G, McMahon AP. Epithelial transformation of metanephric mesenchyme in the developing kidney regulated by Wnt-4. Nature 1994, 372(6507):679-683. 10.1038/372679a0, 7990960.
    • (1994) Nature , vol.372 , Issue.6507 , pp. 679-683
    • Stark, K.1    Vainio, S.2    Vassileva, G.3    McMahon, A.P.4
  • 4
    • 0036827930 scopus 로고    scopus 로고
    • Wnt-4 deficiency alters mouse adrenal cortex function, reducing aldosterone production
    • 10.1210/en.2002-220275, 12399432
    • Heikkila M, Peltoketo H, Leppaluoto J, Ilves M, Vuolteenaho O, Vainio S. Wnt-4 deficiency alters mouse adrenal cortex function, reducing aldosterone production. Endocrinology 2002, 143(11):4358-4365. 10.1210/en.2002-220275, 12399432.
    • (2002) Endocrinology , vol.143 , Issue.11 , pp. 4358-4365
    • Heikkila, M.1    Peltoketo, H.2    Leppaluoto, J.3    Ilves, M.4    Vuolteenaho, O.5    Vainio, S.6
  • 5
    • 0033521967 scopus 로고    scopus 로고
    • Female development in mammals is regulated by Wnt-4 signalling
    • 10.1038/17068, 9989404
    • Vainio S, Heikkila M, Kispert A, Chin N, McMahon AP. Female development in mammals is regulated by Wnt-4 signalling. Nature 1999, 397(6718):405-409. 10.1038/17068, 9989404.
    • (1999) Nature , vol.397 , Issue.6718 , pp. 405-409
    • Vainio, S.1    Heikkila, M.2    Kispert, A.3    Chin, N.4    McMahon, A.P.5
  • 6
    • 23844544781 scopus 로고    scopus 로고
    • The partial female to male sex reversal in Wnt-4-deficient females involves induced expression of testosterone biosynthetic genes and testosterone production, and depends on androgen action
    • 10.1210/en.2005-0463, 15932923
    • Heikkila M, Prunskaite R, Naillat F, Itaranta P, Vuoristo J, Leppaluoto J, Peltoketo H, Vainio S. The partial female to male sex reversal in Wnt-4-deficient females involves induced expression of testosterone biosynthetic genes and testosterone production, and depends on androgen action. Endocrinology 2005, 146(9):4016-4023. 10.1210/en.2005-0463, 15932923.
    • (2005) Endocrinology , vol.146 , Issue.9 , pp. 4016-4023
    • Heikkila, M.1    Prunskaite, R.2    Naillat, F.3    Itaranta, P.4    Vuoristo, J.5    Leppaluoto, J.6    Peltoketo, H.7    Vainio, S.8
  • 8
    • 0035506747 scopus 로고    scopus 로고
    • Wnts and the female reproductive system
    • 10.1002/jez.1112, 11748610
    • Heikkila M, Peltoketo H, Vainio S. Wnts and the female reproductive system. J Exp Zool 2001, 290(6):616-623. 10.1002/jez.1112, 11748610.
    • (2001) J Exp Zool , vol.290 , Issue.6 , pp. 616-623
    • Heikkila, M.1    Peltoketo, H.2    Vainio, S.3
  • 9
    • 2442715158 scopus 로고    scopus 로고
    • Follistatin operates downstream of Wnt4 in mammalian ovary organogenesis
    • 10.1002/dvdy.20042, 15162500
    • Yao HH, Matzuk MM, Jorgez CJ, Menke DB, Page DC, Swain A, Capel B. Follistatin operates downstream of Wnt4 in mammalian ovary organogenesis. Dev Dyn 2004, 230(2):210-215. 10.1002/dvdy.20042, 15162500.
    • (2004) Dev Dyn , vol.230 , Issue.2 , pp. 210-215
    • Yao, H.H.1    Matzuk, M.M.2    Jorgez, C.J.3    Menke, D.B.4    Page, D.C.5    Swain, A.6    Capel, B.7
  • 11
    • 2642526849 scopus 로고    scopus 로고
    • Increased expression of the FIGLA transcription factor is associated with primordial follicle formation in the human fetal ovary
    • 10.1093/molehr/gah056, 15044608
    • Bayne RA, Martins da Silva SJ, Anderson RA. Increased expression of the FIGLA transcription factor is associated with primordial follicle formation in the human fetal ovary. Mol Hum Reprod 2004, 10(6):373-381. 10.1093/molehr/gah056, 15044608.
    • (2004) Mol Hum Reprod , vol.10 , Issue.6 , pp. 373-381
    • Bayne, R.A.1    Martins da Silva, S.J.2    Anderson, R.A.3
  • 12
    • 34548288054 scopus 로고    scopus 로고
    • NOBOX homeobox mutation causes premature ovarian failure
    • 10.1086/519496, 1950834, 17701902
    • Qin Y, Choi Y, Zhao H, Simpson JL, Chen ZJ, Rajkovic A. NOBOX homeobox mutation causes premature ovarian failure. Am J Hum Genet 2007, 81(3):576-581. 10.1086/519496, 1950834, 17701902.
    • (2007) Am J Hum Genet , vol.81 , Issue.3 , pp. 576-581
    • Qin, Y.1    Choi, Y.2    Zhao, H.3    Simpson, J.L.4    Chen, Z.J.5    Rajkovic, A.6
  • 13
    • 40849126622 scopus 로고    scopus 로고
    • Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and mullerian duct abnormalities: a French collaborative study
    • Philibert P, Biason-Lauber A, Rouzier R, Pienkowski C, Paris F, Konrad D, Schoenle E, Sultan C. Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and mullerian duct abnormalities: a French collaborative study. J Clin Endocrinol Metab 2008, 93(3):895-900.
    • (2008) J Clin Endocrinol Metab , vol.93 , Issue.3 , pp. 895-900
    • Philibert, P.1    Biason-Lauber, A.2    Rouzier, R.3    Pienkowski, C.4    Paris, F.5    Konrad, D.6    Schoenle, E.7    Sultan, C.8
  • 14
    • 33845599605 scopus 로고    scopus 로고
    • WNT4 deficiency--a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report
    • Biason-Lauber A, De Filippo G, Konrad D, Scarano G, Nazzaro A, Schoenle EJ. WNT4 deficiency--a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report. Hum Reprod 2007, 22(1):224-229.
    • (2007) Hum Reprod , vol.22 , Issue.1 , pp. 224-229
    • Biason-Lauber, A.1    De Filippo, G.2    Konrad, D.3    Scarano, G.4    Nazzaro, A.5    Schoenle, E.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.