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33篇 您的检索式:作者名="Dode C"
    题名 作者 年代 出处 被引量
1The complex genetics of Kallmann syndrome: KAL1, FGFR1, FGF8, ROKR2, PROK2, et al 显示文摘HARDELIN JP DODE C 2008Sex Dev2008,2,8:1
2显示文摘Samain D Descoins C A short stereo - selective synthesis of E E - 8 10 -dode cadien - 1 - ol the sex pheromone of the codling moth Laspeyresia pomoneUa L 1978Synthesis1978,,5:1
3PROKR2 missense muta- tions associated with Kallmann syndrome impair receptor sig- nalling activity显示文摘Monnier C Dode C Fabre L 2009Hum Mol Genet2009,18,1:1
4The complex genetics of Kallmann syndrome KALl, FCFRI , FCF8, PROKR2, PROK2 显示文摘HARDELIN J P DODE C 2008Sex Dev2008,2,45:1
5The effect of sperm preparation and co-incubation time onin vitrofertilization ofBos indicus oocytes显示文摘Dode M A Rodovalho N C Ueno V G Fernandes C E 0,,:1
6Involvement of steroid hormones on in vitro maturation of pig oocyte 显示文摘Dode M Careia C 2002Theriogenology2002,57,2:1
7Loss of function mutations in FGFR1 cause autosomal dominant Kallmann syndrome显示文摘DODE C LEVILLIERS J DUPONT J M 2001Proc Natl Acad Sci2001,98,13:1
8Involvement of steroid hormones on in vitro maturation of pig oocytes显示文摘Dode M A Graves C 2002Theriogenology2002,57,:1
9The enlarging clinical,genetical,and population spectrum of tumor necrosis factor receptor-associated periodic syndrome显示文摘Dode C Andre M Bienvenu I 2002Arthritis Rheum2002,48,6:1
10Effects of freeze-drying on cytology, ultrastructure, DNA fragmentation, and fertilizing ability of bovine sperm 显示文摘Martins C F Bao S N Dode M N 2007Theriogenology2007,67,:1
11Loss of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome显示文摘DODE C LEVILLIERS J DUPON J 2003NatGenet2003,33,4:1
12The Complex genetics of Kallmann syndrome: KAL1 ,FGFR1 ,FGF8 ,PROKR2, PROK2 显示文摘Hardelin JP Dode C 2008Sex Dev2008,2,45:1
13Effects of freeze-dr-ying on cytology,ultrastructure,DNA fragmentation,and fertilizing a-bility of bovine sperm显示文摘MARTINS C F BAO S N DODE M N 2007Theriogenology2007,67,8:1
14Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome显示文摘Dode C Levilliers J Dupont JM 2003Nat Genet2003,33,4:1
15Kallmann syndrome显示文摘Dode C Hardelin JP 2009Eur J Hum Genet2009,17,2:1
16Kallmann syndrome : mutations in the genes encoding prokineticin-2 and prokineticin receptor-2 显示文摘Dode C Teixeira L Levilliers J 2006Plos Genet2006,2,10:1
17Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome显示文摘Dode C Levilliers J Dupont J M 2003Nat Genet2003,33,4:1
18Kallmann syndrome:mutations in the genes encoding prokineticin-2 and prokineticin receptor-2显示文摘Dode C Teixeira L Levilliers J 2006PLo S Genet2006,2,10:1
19Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome显示文摘 Levilliers J Dupont JM 2003Nat Genet2003,33,4:1
20PROKR2 missense mutations associated with Kallmann syndrome impair receptor signalling activity显示文摘Monnier C Dode C Fabre L 2009Hum Mol Genet2009,18,1:1
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