-
1
-
-
0001358982
-
A syndrome characterized by primary ovarian insufficiency and decreased stature: Report of 11 cases with a digression on hormonal control of axillary and pubic hair
-
Albright F, Smith PH, Fraser R. A syndrome characterized by primary ovarian insufficiency and decreased stature: report of 11 cases with a digression on hormonal control of axillary and pubic hair. Am J Med Sci 1942 ; 204 : 625-648
-
(1942)
Am J Med Sci
, vol.204
, pp. 625-648
-
-
Albright, F.1
Smith, P.H.2
Fraser, R.3
-
2
-
-
40749100654
-
Primary ovarian insufficiency: A more accurate term for premature ovarian failure
-
Welt CK. Primary ovarian insufficiency: a more accurate term for premature ovarian failure. Clin Endocrinol (Oxf) 2008 ; 68 : 499-509.
-
(2008)
Clin Endocrinol (Oxf)
, vol.68
, pp. 499-509
-
-
Welt, C.K.1
-
3
-
-
0034815279
-
The role of genetic factors in age at natural menopause
-
De Bruin JP, Bovenhuis H, van Noord PA, et al. The role of genetic factors in age at natural menopause. Hum Reprod 2001 ; 16 : 2014-2018 (Pubitemid 32916239)
-
(2001)
Human Reproduction
, vol.16
, Issue.9
, pp. 2014-2018
-
-
De Bruin, J.P.1
Bovenhuis, H.2
Van Noord, P.A.H.3
Pearson, P.L.4
Van Arendonk, J.A.M.5
Te Velde, E.R.6
Kuurman, W.W.7
Dorland, M.8
-
5
-
-
0032845866
-
Familial idiopathic premature ovarian failure: An overrated and underestimated genetic disease?
-
Van Kasteren YM, Hundscheid RD, Smits AP, et al. Familial idiopathic premature ovarian failure: an overrated and underestimated genetic disease? Hum Reprod 1999 ; 14 : 2455-2459
-
(1999)
Hum Reprod
, vol.14
, pp. 2455-2459
-
-
Van Kasteren, Y.M.1
Hundscheid, R.D.2
Smits, A.P.3
-
6
-
-
0037248189
-
Premature menopause in a multi-ethnic population study of the menopause transition
-
DOI 10.1093/humrep/deg005
-
Luborsky JL, Meyer P, Sowers MF, et al. Premature menopause in a multiethnic population study of the menopause transition. Hum Reprod 2003 ; 18 : 199-206. (Pubitemid 36138877)
-
(2003)
Human Reproduction
, vol.18
, Issue.1
, pp. 199-206
-
-
Luborsky, J.L.1
Meyer, P.2
Sowers, M.F.3
Gold, E.B.4
Santoro, N.5
-
8
-
-
0029127258
-
Family history as a predictor of early menopause
-
Cramer DW, Xu H, Harlow BL. Family history as a predictor of early menopause. Fertil Steril 1995 ; 64 : 740-745
-
(1995)
Fertil Steril
, vol.64
, pp. 740-745
-
-
Cramer, D.W.1
Xu, H.2
Harlow, B.L.3
-
10
-
-
33745285019
-
Disruption of POF1B binding to nonmuscle actin filaments is associated with premature ovarian failure
-
DOI 10.1086/505406
-
Lacombe A, Lee H, Zahed L, et al. Disruption of POF1B binding to nonmuscle actin filaments is associated with premature ovarian failure. Am J Hum Genet 2006 ; 79 : 113-119 (Pubitemid 43927381)
-
(2006)
American Journal of Human Genetics
, vol.79
, Issue.1
, pp. 113-119
-
-
Lacombe, A.1
Lee, H.2
Zahed, L.3
Choucair, M.4
Muller, J.-M.5
Nelson, S.F.6
Salameh, W.7
Vilain, E.8
-
11
-
-
0034065580
-
Mapping of the POF1 locus and identification of putative genes for premature ovarian failure
-
Davison RM, Fox M, Conway GS. Mapping of the POF1 locus and identification of putative genes for premature ovarian failure. Mol Hum Reprod 2000 ; 6 : 314-318 (Pubitemid 30171517)
-
(2000)
Molecular Human Reproduction
, vol.6
, Issue.4
, pp. 314-318
-
-
Davison, R.M.1
Fox, M.2
Conway, G.S.3
-
12
-
-
39149108084
-
Recent advances in the study of genes involved in non-syndromic premature ovarian failure
-
Laissue P, Vinci G, Veitia RA, et al. Recent advances in the study of genes involved in non-syndromic premature ovarian failure. Mol Cell Endocrinol 2008 ; 282 : 101-111
-
(2008)
Mol Cell Endocrinol
, vol.282
, pp. 101-111
-
-
Laissue, P.1
Vinci, G.2
Veitia, R.A.3
-
13
-
-
45549088147
-
Genetic and phenotypic heterogeneity in ovarian failure: Overview of selected candidate genes
-
Simpson JL. Genetic and phenotypic heterogeneity in ovarian failure: overview of selected candidate genes. Ann NY Acad Sci 2008 ; 1135 : 146-154
-
(2008)
Ann NY Acad Sci
, vol.1135
, pp. 146-154
-
-
Simpson, J.L.1
-
14
-
-
34548288054
-
NOBOX homeobox mutation causes premature ovarian failure
-
DOI 10.1086/519496
-
Qin Y, Choi Y, Zhao H, et al. NOBOX homeobox mutation causes premature ovarian failure. Am J Hum Genet 2007 ; 81 : 576-581 (Pubitemid 47330215)
-
(2007)
American Journal of Human Genetics
, 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
-
15
-
-
55749088979
-
Steroidogenic factor-1 (SF-1, Ad4BP, NR5A1) and disorders of testis development
-
Lin L, Achermann JC. Steroidogenic factor-1 (SF-1, Ad4BP, NR5A1) and disorders of testis development. Sex Dev 2008 ; 2 : 200-209
-
(2008)
Sex Dev
, vol.2
, pp. 200-209
-
-
Lin, L.1
Achermann, J.C.2
-
16
-
-
0028303959
-
A cell-specific nuclear receptor is essential for adrenal and gonadal development and sexual differentiation
-
DOI 10.1016/0092-8674(94)90211-9
-
Luo X, Ikeda Y, Parker KL. A cell-specific nuclear receptor is essential for adrenal and gonadal development and sexual differentiation. Cell 1994 ; 77 : 481-490 (Pubitemid 24153989)
-
(1994)
Cell
, vol.77
, Issue.4
, pp. 481-490
-
-
Luo, X.1
Ikeda, Y.2
Parker, K.L.3
-
17
-
-
34548413647
-
Mechanisms in the regulation of aromatase in developing ovary and placenta
-
DOI 10.1016/j.jsbmb.2007.05.001, PII S0960076007001112, Proceedings of the VIII International Aromatase Conference 'Aromastase 2006' (Baltimore, Maryland USA, 18-20 September, 2006)
-
Mendelson CR, Kamat A. Mechanisms in the regulation of aromatase in developing ovary and placenta. J Steroid Biochem Mol Biol 2007 ; 106 : 62-70. (Pubitemid 47362643)
-
(2007)
Journal of Steroid Biochemistry and Molecular Biology
, vol.106
, Issue.1-5
, pp. 62-70
-
-
Mendelson, C.R.1
Kamat, A.2
-
18
-
-
3042755053
-
Cell-specific knockout of steriodogenic factor 1 reveals its essential roles in gonadal function
-
DOI 10.1210/me.2003-0404
-
Jeyasuria P, Ikeda Y, Jamin SP, et al. Cell-specific knockout of steroidogenic factor 1 reveals its essential roles in gonadal function. Mol Endocrinol 2004 ; 18 : 1610-1619 (Pubitemid 38859570)
-
(2004)
Molecular Endocrinology
, vol.18
, Issue.7
, pp. 1610-1619
-
-
Jeyasuria, P.1
Ikeda, Y.2
Jamin, S.P.3
Zhao, L.4
De Rooij, D.G.5
Themmen, A.P.N.6
Behringer, R.R.7
Parker, K.L.8
-
19
-
-
0032990419
-
A mutation in the gene encoding steroidogenic factor-1 causes XY sex reversal and adrenal failure in humans [1]
-
DOI 10.1038/9629
-
Achermann JC, Ito M, Ito M, et al. A mutation in the gene encoding steroidogenic factor-1 causes XY sex reversal and adrenal failure in humans. Nat Genet 1999 ; 22 : 125-126 (Pubitemid 29264799)
-
(1999)
Nature Genetics
, vol.22
, Issue.2
, pp. 125-126
-
-
Achermann, J.C.1
Ito, M.2
Ito, M.3
Hindmarsh, P.C.4
Jameson, J.L.5
-
20
-
-
0033623571
-
Apparently normal ovarian differentiation in a prepubertal girl with transcriptionally inactive steroidogenic factor 1 (NR5A1/SF-1) and adrenocortical insufficiency
-
Biason-Lauber A, Schoenle EJ. Apparently normal ovarian differentiation in a prepubertal girl with transcriptionally inactive steroidogenic factor 1 (NR5A1/SF-1) and adrenocortical insufficiency. Am J Hum Genet 2000 ; 67 : 1563-1568
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1563-1568
-
-
Biason-Lauber, A.1
Schoenle, E.J.2
-
21
-
-
0036277895
-
Gonadal determination and adrenal development are regulated by the orphan nuclear receptor steroidogenic factor-1, in a dose-dependent manner
-
DOI 10.1210/jc.87.4.1829
-
Achermann JC, Ozisik G, Ito M, et al. Gonadal determination and adrenal development are regulated by the orphan nuclear receptor steroidogenic factor-1, in a dose-dependent manner. J Clin Endocrinol Metab 2002 ; 87 : 1829-1833 (Pubitemid 34615276)
-
(2002)
Journal of Clinical Endocrinology and Metabolism
, vol.87
, Issue.4
, pp. 1829-1833
-
-
Achermann, J.C.1
Ozisik, G.2
Ito, M.3
Orun, U.A.4
Harmanci, K.5
Gurakan, B.6
Larry Jameson, J.7
-
22
-
-
62749102793
-
Mutations in NR5A1 associated with ovarian insufficiency
-
Lourenço D, Brauner R, Lin L et al. Mutations in NR5A1 associated with ovarian insufficiency. N Engl J Med 2009 ; 360 : 1200-1210
-
(2009)
N Engl J Med
, vol.360
, pp. 1200-1210
-
-
Lourenço, D.1
Brauner, R.2
Lin, L.3
|