O Lekarev, Y Morel… - Hormonal and Genetic Basis of …, 2011 - books.google.com Chapter 29 Atypical Presentation and Novel StAR Protein Gene Mutation in a 46, XY Female with Lipoid Congenital Adrenal Hyperplasia Oksana Lekarev, Yves Morel, and Maria I. New Introduction Congenital lipoid adrenal hyperplasia is a severe disorder of adrenal and gonadal ... All 2 versions
T Sahakitrungruang, MK Tee… - Journal of Clinical …, 2011 - Endocrine Soc Context: The cholesterol side-chain cleavage enzyme (P450scc), encoded by the CYP11A1 gene, converts cholesterol to pregnenolone to initiate steroidogenesis. Genetic defects in P450scc cause a rare autosomal recessive disorder that is clinically indistinguishable from ... Cited by 1 - Related articles - All 4 versions
JM Kim, JH Choi, JH Lee, GH Kim, BH Lee… - European Journal of …, 2011 - EFES ... mutation in the StAR gene in Korean patients with congenital lipoidadrenalhyperplasia Running title: Functional analysis of a novel StAR mutation Authors: ... Abbreviations: CLAH, congenital lipoid adrenalhyperplasia; StAR, steroidogenic acute regulatory protein ...
HY Jin, JH Choi, BH Lee, GH Kim… - European journal of …, 2011 - Springer Abstract Congenital lipoid adrenal hyperplasia (CLAH) is the most severe form of congenital adrenal hyperplasia, characterized by lack of synthesis of all gonadal and adrenal steroid hormones. Ovarian cysts can develop as complications of CLAH. However, the precise ... Cited by 1 - Related articles - All 4 versions
[HTML] from plos.orgCE Flück, AV Pandey, B Dick, N Camats… - PloS one, 2011 - dx.plos.org Steroidogenic acute regulatory protein (StAR) is crucial for transport of cholesterol to mitochondria where biosynthesis of steroids is initiated. Loss of StAR function causes lipoid congenital adrenal hyperplasia (LCAH). ... StAR gene mutations causing partial loss of function manifest ... Related articles - Cached - All 3 versions
O Lekarev, Y Morel… - Hormonal and Genetic Basis of …, 2011 - books.google.com Chapter 29 Atypical Presentation and Novel StAR Protein Gene Mutation in a 46, XY Female with Lipoid Congenital Adrenal Hyperplasia Oksana Lekarev, Yves Morel, and Maria I. New Introduction Congenital lipoid adrenal hyperplasia is a severe disorder of adrenal and gonadal ... All 2 versions
T Sahakitrungruang, MK Tee… - Journal of Clinical …, 2011 - Endocrine Soc Context: The cholesterol side-chain cleavage enzyme (P450scc), encoded by the CYP11A1 gene, converts cholesterol to pregnenolone to initiate steroidogenesis. Genetic defects in P450scc cause a rare autosomal recessive disorder that is clinically indistinguishable from ... Cited by 1 - Related articles - All 4 versions
JM Kim, JH Choi, JH Lee, GH Kim, BH Lee… - European Journal of …, 2011 - EFES ... mutation in the StAR gene in Korean patients with congenital lipoidadrenalhyperplasia Running title: Functional analysis of a novel StAR mutation Authors: ... Abbreviations: CLAH, congenital lipoid adrenalhyperplasia; StAR, steroidogenic acute regulatory protein ...
HY Jin, JH Choi, BH Lee, GH Kim… - European journal of …, 2011 - Springer Abstract Congenital lipoid adrenal hyperplasia (CLAH) is the most severe form of congenital adrenal hyperplasia, characterized by lack of synthesis of all gonadal and adrenal steroid hormones. Ovarian cysts can develop as complications of CLAH. However, the precise ... Cited by 1 - Related articles - All 4 versions
[HTML] from plos.orgCE Flück, AV Pandey, B Dick, N Camats… - PloS one, 2011 - dx.plos.org Steroidogenic acute regulatory protein (StAR) is crucial for transport of cholesterol to mitochondria where biosynthesis of steroids is initiated. Loss of StAR function causes lipoid congenital adrenal hyperplasia (LCAH). ... StAR gene mutations causing partial loss of function manifest ... Related articles - Cached - All 3 versions
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