-
1
-
-
0027466437
-
A regulatory cascade hypothesis for mammalian sex determination: SRY represses a negative regulator of male development
-
McElreavey K., Vilain E., Abbas N., Herskowitz I., Fellous M. A regulatory cascade hypothesis for mammalian sex determination: SRY represses a negative regulator of male development. Proc Natl Acad Sci USA: 1993; 90 8 3368 3372
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, Issue.8
, pp. 3368-3372
-
-
McElreavey, K.1
Vilain, E.2
Abbas, N.3
Herskowitz, I.4
Fellous, M.5
-
2
-
-
2342430345
-
LDL receptor-related proteins 5 and 6 in Wnt/beta-catenin signaling: Arrows point the way
-
He X., Semenov M., Tamai K., Zeng X. LDL receptor-related proteins 5 and 6 in Wnt/beta-catenin signaling: arrows point the way. Development: 2004; 131 8 1663 1677
-
(2004)
Development
, vol.131
, Issue.8
, pp. 1663-1677
-
-
He, X.1
Semenov, M.2
Tamai, K.3
Zeng, X.4
-
3
-
-
0344464720
-
Wnts and Hedgehogs: Lipid-modified proteins and similarities in signaling mechanisms at the cell surface
-
Nusse R. Wnts and Hedgehogs: lipid-modified proteins and similarities in signaling mechanisms at the cell surface. Development: 2003; 130 22 5297 5305
-
(2003)
Development
, vol.130
, Issue.22
, pp. 5297-5305
-
-
Nusse, R.1
-
4
-
-
0037043688
-
Wnt-11 activation of a non-canonical Wnt signalling pathway is required for cardiogenesis
-
Pandur P., Läsche M., Eisenberg L. M., Kühl M. Wnt-11 activation of a non-canonical Wnt signalling pathway is required for cardiogenesis. Nature: 2002; 418 6898 636 641
-
(2002)
Nature
, vol.418
, Issue.6898
, pp. 636-641
-
-
Pandur, P.1
Läsche, M.2
Eisenberg, L.M.3
Kühl, M.4
-
5
-
-
74749109906
-
WNT4 is expressed in human fetal and adult ovaries and its signaling contributes to ovarian cell survival
-
et al.
-
Jääskeläinen M., Prunskaite-Hyyryläinen R., Naillat F., et al. WNT4 is expressed in human fetal and adult ovaries and its signaling contributes to ovarian cell survival. Mol Cell Endocrinol: 2010; 317 12 106 111
-
(2010)
Mol Cell Endocrinol
, vol.317
, Issue.12
, pp. 106-111
-
-
Jääskeläinen, M.1
Prunskaite-Hyyryläinen, R.2
Naillat, F.3
-
6
-
-
0035002512
-
Up-regulation of WNT-4 signaling and dosage-sensitive sex reversal in humans
-
et al.
-
Jordan B. K., Mohammed M., Ching S. T., et al. Up-regulation of WNT-4 signaling and dosage-sensitive sex reversal in humans. Am J Hum Genet: 2001; 68 5 1102 1109
-
(2001)
Am J Hum Genet
, vol.68
, Issue.5
, pp. 1102-1109
-
-
Jordan, B.K.1
Mohammed, M.2
Ching, S.T.3
-
7
-
-
0033521967
-
Female development in mammals is regulated by Wnt-4 signalling
-
Vainio S., Heikkilä M., Kispert A., Chin N., McMahon A. P. Female development in mammals is regulated by Wnt-4 signalling. Nature: 1999; 397 6718 405 409
-
(1999)
Nature
, vol.397
, Issue.6718
, pp. 405-409
-
-
Vainio, S.1
Heikkilä, M.2
Kispert, A.3
Chin, N.4
McMahon, A.P.5
-
8
-
-
2442715158
-
Follistatin operates downstream of Wnt4 in mammalian ovary organogenesis
-
et al.
-
Yao H. H., Matzuk M. M., Jorgez C. J., et al. Follistatin operates downstream of Wnt4 in mammalian ovary organogenesis. Dev Dyn: 2004; 230 2 210 215
-
(2004)
Dev Dyn
, vol.230
, Issue.2
, pp. 210-215
-
-
Yao, H.H.1
Matzuk, M.M.2
Jorgez, C.J.3
-
9
-
-
0016593481
-
Rat gonadal and ovarioan organogenesis with and without germ cells. An ultrastructural study
-
Merchant H. Rat gonadal and ovarioan organogenesis with and without germ cells. An ultrastructural study. Dev Biol: 1975; 44 1 1 21
-
(1975)
Dev Biol
, vol.44
, Issue.1
, pp. 1-21
-
-
Merchant, H.1
-
10
-
-
0021657916
-
Meiosis and differentiation of mouse germ cells
-
McLaren A. Meiosis and differentiation of mouse germ cells. Symp Soc Exp Biol: 1984; 38 7 23
-
(1984)
Symp Soc Exp Biol
, vol.38
, pp. 7-23
-
-
McLaren, A.1
-
11
-
-
77952317137
-
Wnt4/5a signalling coordinates cell adhesion and entry into meiosis during presumptive ovarian follicle development
-
et al.
-
Naillat F., Prunskaite-Hyyryläinen R., Pietilä I., et al. Wnt4/5a signalling coordinates cell adhesion and entry into meiosis during presumptive ovarian follicle development. Hum Mol Genet: 2010; 19 8 1539 1550
-
(2010)
Hum Mol Genet
, vol.19
, Issue.8
, pp. 1539-1550
-
-
Naillat, F.1
Prunskaite-Hyyryläinen, R.2
Pietilä, I.3
-
12
-
-
35748965278
-
Loss of Wnt4 and Foxl2 leads to female-to-male sex reversal extending to germ cells
-
et al.
-
Ottolenghi C., Pelosi E., Tran J., et al. Loss of Wnt4 and Foxl2 leads to female-to-male sex reversal extending to germ cells. Hum Mol Genet: 2007; 16 23 2795 2804
-
(2007)
Hum Mol Genet
, vol.16
, Issue.23
, pp. 2795-2804
-
-
Ottolenghi, C.1
Pelosi, E.2
Tran, J.3
-
13
-
-
38749129178
-
SERKAL syndrome: An autosomal-recessive disorder caused by a loss-of-function mutation in WNT4
-
et al.
-
Mandel H., Shemer R., Borochowitz Z. U., et al. SERKAL syndrome: an autosomal-recessive disorder caused by a loss-of-function mutation in WNT4. Am J Hum Genet: 2008; 82 1 39 47
-
(2008)
Am J Hum Genet
, vol.82
, Issue.1
, pp. 39-47
-
-
Mandel, H.1
Shemer, R.2
Borochowitz, Z.U.3
-
14
-
-
1242352080
-
Mutations in the SRY, DAX1, SF1 and WNT4 genes in Brazilian sex-reversed patients
-
et al.
-
Domenice S., Corrêa R. V., Costa E. M., et al. Mutations in the SRY, DAX1, SF1 and WNT4 genes in Brazilian sex-reversed patients. Braz J Med Biol Res: 2004; 37 1 145 150
-
(2004)
Braz J Med Biol Res
, vol.37
, Issue.1
, pp. 145-150
-
-
Domenice, S.1
Corrêa, R.V.2
Costa, E.M.3
-
15
-
-
4143139955
-
A WNT4 mutation associated with Müllerian-duct regression and virilization in a 46,XX woman
-
Biason-Lauber A., Konrad D., Navratil F., Schoenle E. JA. A WNT4 mutation associated with Müllerian-duct regression and virilization in a 46,XX woman. N Engl J Med: 2004; 351 8 792 798
-
(2004)
N Engl J Med
, vol.351
, Issue.8
, pp. 792-798
-
-
Biason-Lauber, A.1
Konrad, D.2
Navratil, F.3
Schoenle, E.J.4
-
16
-
-
33845599605
-
WNT4 deficiencya 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 E. J. WNT4 deficiencya 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
-
17
-
-
40849126622
-
Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and müllerian duct abnormalities: A French collaborative study
-
et al.
-
Philibert P., Biason-Lauber A., Rouzier R., et al. Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and müllerian 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
-
18
-
-
79959720658
-
Molecular analysis of WNT4 gene in four adolescent girls with mullerian duct abnormality and hyperandrogenism (atypical Mayer-Rokitansky-Küster- Hauser syndrome)
-
et al.
-
Philibert P., Biason-Lauber A., Gueorguieva I., et al. Molecular analysis of WNT4 gene in four adolescent girls with mullerian duct abnormality and hyperandrogenism (atypical Mayer-Rokitansky-Küster-Hauser syndrome). Fertil Steril: 2011; 95 8 2683 2686
-
(2011)
Fertil Steril
, vol.95
, Issue.8
, pp. 2683-2686
-
-
Philibert, P.1
Biason-Lauber, A.2
Gueorguieva, I.3
-
19
-
-
1642300426
-
R-spondin, a novel gene with thrombospondin type 1 domain, was expressed in the dorsal neural tube and affected in Wnts mutants
-
Kamata T., Katsube K., Michikawa M., Yamada M., Takada S., Mizusawa H. R-spondin, a novel gene with thrombospondin type 1 domain, was expressed in the dorsal neural tube and affected in Wnts mutants. Biochim Biophys Acta: 2004; 1676 1 51 62
-
(2004)
Biochim Biophys Acta
, vol.1676
, Issue.1
, pp. 51-62
-
-
Kamata, T.1
Katsube, K.2
Michikawa, M.3
Yamada, M.4
Takada, S.5
Mizusawa, H.6
-
20
-
-
23844455584
-
Mitogenic influence of human R-spondin1 on the intestinal epithelium
-
et al.
-
Kim K. A., Kakitani M., Zhao J., et al. Mitogenic influence of human R-spondin1 on the intestinal epithelium. Science: 2005; 309 5738 1256 1259
-
(2005)
Science
, vol.309
, Issue.5738
, pp. 1256-1259
-
-
Kim, K.A.1
Kakitani, M.2
Zhao, J.3
-
21
-
-
55749098807
-
Genetics of ovarian differentiation: Rspo1, a major player
-
Chassot A. A., Gregoire E. P., Magliano M., Lavery R., Chaboissier M. C. Genetics of ovarian differentiation: Rspo1, a major player. Sex Dev: 2008; 2 45 219 227
-
(2008)
Sex Dev
, vol.2
, Issue.45
, pp. 219-227
-
-
Chassot, A.A.1
Gregoire, E.P.2
Magliano, M.3
Lavery, R.4
Chaboissier, M.C.5
-
22
-
-
42449095964
-
Activation of beta-catenin signaling by Rspo1 controls differentiation of the mammalian ovary
-
et al.
-
Chassot A. A., Ranc F., Gregoire E. P., et al. Activation of beta-catenin signaling by Rspo1 controls differentiation of the mammalian ovary. Hum Mol Genet: 2008; 17 9 1264 1277
-
(2008)
Hum Mol Genet
, vol.17
, Issue.9
, pp. 1264-1277
-
-
Chassot, A.A.1
Ranc, F.2
Gregoire, E.P.3
-
23
-
-
33750489078
-
R-spondin1 is essential in sex determination, skin differentiation and malignancy
-
et al.
-
Parma P., Radi O., Vidal V., et al. R-spondin1 is essential in sex determination, skin differentiation and malignancy. Nat Genet: 2006; 38 11 1304 1309
-
(2006)
Nat Genet
, vol.38
, Issue.11
, pp. 1304-1309
-
-
Parma, P.1
Radi, O.2
Vidal, V.3
-
24
-
-
38949110809
-
Syndromic true hermaphroditism due to an R-spondin1 (RSPO1) homozygous mutation
-
et al.
-
Tomaselli S., Megiorni F., De Bernardo C., et al. Syndromic true hermaphroditism due to an R-spondin1 (RSPO1) homozygous mutation. Hum Mutat: 2008; 29 2 220 226
-
(2008)
Hum Mutat
, vol.29
, Issue.2
, pp. 220-226
-
-
Tomaselli, S.1
Megiorni, F.2
De Bernardo, C.3
-
25
-
-
0035131812
-
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome
-
et al.
-
Crisponi L., Deiana M., Loi A., et al. The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome. Nat Genet: 2001; 27 2 159 166
-
(2001)
Nat Genet
, vol.27
, Issue.2
, pp. 159-166
-
-
Crisponi, L.1
Deiana, M.2
Loi, A.3
-
26
-
-
0036913692
-
Evolution and expression of FOXL2
-
et al.
-
Cocquet J., Pailhoux E., Jaubert F., et al. Evolution and expression of FOXL2. J Med Genet: 2002; 39 12 916 921
-
(2002)
J Med Genet
, vol.39
, Issue.12
, pp. 916-921
-
-
Cocquet, J.1
Pailhoux, E.2
Jaubert, F.3
-
27
-
-
3042554114
-
Forkhead l2 is expressed in the ovary and represses the promoter activity of the steroidogenic acute regulatory gene
-
Pisarska M. D., Bae J., Klein C., Hsueh A. J. Forkhead l2 is expressed in the ovary and represses the promoter activity of the steroidogenic acute regulatory gene. Endocrinology: 2004; 145 7 3424 3433
-
(2004)
Endocrinology
, vol.145
, Issue.7
, pp. 3424-3433
-
-
Pisarska, M.D.1
Bae, J.2
Klein, C.3
Hsueh, A.J.4
-
28
-
-
33745186041
-
FOXL2 activates P450 aromatase gene transcription: Towards a better characterization of the early steps of mammalian ovarian development
-
et al.
-
Pannetier M., Fabre S., Batista F., et al. FOXL2 activates P450 aromatase gene transcription: towards a better characterization of the early steps of mammalian ovarian development. J Mol Endocrinol: 2006; 36 3 399 413
-
(2006)
J Mol Endocrinol
, vol.36
, Issue.3
, pp. 399-413
-
-
Pannetier, M.1
Fabre, S.2
Batista, F.3
-
29
-
-
33751528497
-
FOXL2 in the pituitary: Molecular, genetic, and developmental analysis
-
et al.
-
Ellsworth B. S., Egashira N., Haller J. L., et al. FOXL2 in the pituitary: molecular, genetic, and developmental analysis. Mol Endocrinol: 2006; 20 11 2796 2805
-
(2006)
Mol Endocrinol
, vol.20
, Issue.11
, pp. 2796-2805
-
-
Ellsworth, B.S.1
Egashira, N.2
Haller, J.L.3
-
30
-
-
18844437228
-
Ovarian-specific expression of a new gene regulated by the goat PIS region and transcribed by a FOXL2 bidirectional promoter
-
Pannetier M., Renault L., Jolivet G., Cotinot C., Pailhoux E. Ovarian-specific expression of a new gene regulated by the goat PIS region and transcribed by a FOXL2 bidirectional promoter. Genomics: 2005; 85 6 715 726
-
(2005)
Genomics
, vol.85
, Issue.6
, pp. 715-726
-
-
Pannetier, M.1
Renault, L.2
Jolivet, G.3
Cotinot, C.4
Pailhoux, E.5
-
31
-
-
39149117672
-
The mutations and potential targets of the forkhead transcription factor FOXL2
-
et al.
-
Moumné L., Batista F., Benayoun B. A., et al. The mutations and potential targets of the forkhead transcription factor FOXL2. Mol Cell Endocrinol: 2008; 282 12 2 11
-
(2008)
Mol Cell Endocrinol
, vol.282
, Issue.12
, pp. 2-11
-
-
Moumné, L.1
Batista, F.2
Benayoun, B.A.3
-
32
-
-
0035846604
-
Daf-16 integrates developmental and environmental inputs to mediate aging in the nematode Caenorhabditis elegans
-
Henderson S. T., Johnson T. E. daf-16 integrates developmental and environmental inputs to mediate aging in the nematode Caenorhabditis elegans. Curr Biol: 2001; 11 24 1975 1980
-
(2001)
Curr Biol
, vol.11
, Issue.24
, pp. 1975-1980
-
-
Henderson, S.T.1
Johnson, T.E.2
-
33
-
-
33847666428
-
Potential targets of FOXL2, a transcription factor involved in craniofacial and follicular development, identified by transcriptomics
-
Batista F., Vaiman D., Dausset J., Fellous M., Veitia R. A. Potential targets of FOXL2, a transcription factor involved in craniofacial and follicular development, identified by transcriptomics. Proc Natl Acad Sci U S A: 2007; 104 9 3330 3335
-
(2007)
Proc Natl Acad Sci U S A
, vol.104
, Issue.9
, pp. 3330-3335
-
-
Batista, F.1
Vaiman, D.2
Dausset, J.3
Fellous, M.4
Veitia, R.A.5
-
34
-
-
0029975669
-
Prostaglandin endoperoxide H synthases-1 and -2
-
Smith W. L., Dewitt D. L. Prostaglandin endoperoxide H synthases-1 and -2. Adv Immunol: 1996; 62 167 215
-
(1996)
Adv Immunol
, vol.62
, pp. 167-215
-
-
Smith, W.L.1
Dewitt, D.L.2
-
35
-
-
71149095052
-
Somatic sex reprogramming of adult ovaries to testes by FOXL2 ablation
-
et al.
-
Uhlenhaut N. H., Jakob S., Anlag K., et al. Somatic sex reprogramming of adult ovaries to testes by FOXL2 ablation. Cell: 2009; 139 6 1130 1142
-
(2009)
Cell
, vol.139
, Issue.6
, pp. 1130-1142
-
-
Uhlenhaut, N.H.1
Jakob, S.2
Anlag, K.3
-
36
-
-
67649406102
-
Mutation of FOXL2 in granulosa-cell tumors of the ovary
-
et al.
-
Shah S. P., Köbel M., Senz J., et al. Mutation of FOXL2 in granulosa-cell tumors of the ovary. N Engl J Med: 2009; 360 26 2719 2729
-
(2009)
N Engl J Med
, vol.360
, Issue.26
, pp. 2719-2729
-
-
Shah, S.P.1
Köbel, M.2
Senz, J.3
-
37
-
-
28744431913
-
Deletions in the polyAlanine-containing transcription factor FOXL2 lead to intranuclear aggregation
-
Moumné L., Fellous M., Veitia R. A. Deletions in the polyAlanine-containing transcription factor FOXL2 lead to intranuclear aggregation. Hum Mol Genet: 2005; 14 23 3557 3564
-
(2005)
Hum Mol Genet
, vol.14
, Issue.23
, pp. 3557-3564
-
-
Moumné, L.1
Fellous, M.2
Veitia, R.A.3
-
38
-
-
41149124043
-
Differential aggregation and functional impairment induced by polyalanine expansions in FOXL2, a transcription factor involved in cranio-facial and ovarian development
-
et al.
-
Moumné L., Dipietromaria A., Batista F., et al. Differential aggregation and functional impairment induced by polyalanine expansions in FOXL2, a transcription factor involved in cranio-facial and ovarian development. Hum Mol Genet: 2008; 17 7 1010 1019
-
(2008)
Hum Mol Genet
, vol.17
, Issue.7
, pp. 1010-1019
-
-
Moumné, L.1
Dipietromaria, A.2
Batista, F.3
-
39
-
-
68749103447
-
Towards a functional classification of pathogenic FOXL2 mutations using transactivation reporter systems
-
Dipietromaria A., Benayoun B. A., Todeschini A. L., Rivals I., Bazin C., Veitia R. A. Towards a functional classification of pathogenic FOXL2 mutations using transactivation reporter systems. Hum Mol Genet: 2009; 18 17 3324 3333
-
(2009)
Hum Mol Genet
, vol.18
, Issue.17
, pp. 3324-3333
-
-
Dipietromaria, A.1
Benayoun, B.A.2
Todeschini, A.L.3
Rivals, I.4
Bazin, C.5
Veitia, R.A.6
-
40
-
-
79954545155
-
Transcription factor FOXL2 protects granulosa cells from stress and delays cell cycle: Role of its regulation by the SIRT1 deacetylase
-
et al.
-
Benayoun B. A., Georges A. B., L'Hôte D., et al. Transcription factor FOXL2 protects granulosa cells from stress and delays cell cycle: role of its regulation by the SIRT1 deacetylase. Hum Mol Genet: 2011; 20 9 1673 1686
-
(2011)
Hum Mol Genet
, vol.20
, Issue.9
, pp. 1673-1686
-
-
Benayoun, B.A.1
Georges, A.B.2
L'Hôte, D.3
-
41
-
-
0031283061
-
FIGalpha, a germ cell specific transcription factor involved in the coordinate expression of the zona pellucida genes
-
Liang L., Soyal S. M., Dean J. FIGalpha, a germ cell specific transcription factor involved in the coordinate expression of the zona pellucida genes. Development: 1997; 124 24 4939 4947
-
(1997)
Development
, vol.124
, Issue.24
, pp. 4939-4947
-
-
Liang, L.1
Soyal, S.M.2
Dean, J.3
-
42
-
-
4143068997
-
NOBOX deficiency disrupts early folliculogenesis and oocyte-specific gene expression
-
Rajkovic A., Pangas S. A., Ballow D., Suzumori N., Matzuk M. M. NOBOX deficiency disrupts early folliculogenesis and oocyte-specific gene expression. Science: 2004; 305 5687 1157 1159
-
(2004)
Science
, vol.305
, Issue.5687
, pp. 1157-1159
-
-
Rajkovic, A.1
Pangas, S.A.2
Ballow, D.3
Suzumori, N.4
Matzuk, M.M.5
-
43
-
-
0033623183
-
FIGalpha, a germ cell-specific transcription factor required for ovarian follicle formation
-
Soyal S. M., Amleh A., Dean J. FIGalpha, a germ cell-specific transcription factor required for ovarian follicle formation. Development: 2000; 127 21 4645 4654
-
(2000)
Development
, vol.127
, Issue.21
, pp. 4645-4654
-
-
Soyal, S.M.1
Amleh, A.2
Dean, J.3
-
44
-
-
41549153923
-
Fbxw15/Fbxo12J is an F-box protein-encoding gene selectively expressed in oocytes of the mouse ovary
-
De La Chesnaye E., Kerr B., Paredes A., Merchant-Larios H., Méndez J. P., Ojeda S. R. Fbxw15/Fbxo12J is an F-box protein-encoding gene selectively expressed in oocytes of the mouse ovary. Biol Reprod: 2008; 78 4 714 725
-
(2008)
Biol Reprod
, vol.78
, Issue.4
, pp. 714-725
-
-
De La Chesnaye, E.1
Kerr, B.2
Paredes, A.3
Merchant-Larios, H.4
Méndez, J.P.5
Ojeda, S.R.6
-
45
-
-
38849162128
-
Oocyte regulation of metabolic cooperativity between mouse cumulus cells and oocytes: BMP15 and GDF9 control cholesterol biosynthesis in cumulus cells
-
et al.
-
Su Y. Q., Sugiura K., Wigglesworth K., et al. Oocyte regulation of metabolic cooperativity between mouse cumulus cells and oocytes: BMP15 and GDF9 control cholesterol biosynthesis in cumulus cells. Development: 2008; 135 1 111 121
-
(2008)
Development
, vol.135
, Issue.1
, pp. 111-121
-
-
Su, Y.Q.1
Sugiura, K.2
Wigglesworth, K.3
-
46
-
-
33646389819
-
Identification of new variants of human BMP15 gene in a large cohort of women with premature ovarian failure
-
et al.
-
Di Pasquale E., Rossetti R., Marozzi A., et al. Identification of new variants of human BMP15 gene in a large cohort of women with premature ovarian failure. J Clin Endocrinol Metab: 2006; 91 5 1976 1979
-
(2006)
J Clin Endocrinol Metab
, vol.91
, Issue.5
, pp. 1976-1979
-
-
Di Pasquale, E.1
Rossetti, R.2
Marozzi, A.3
-
47
-
-
33645750342
-
Missense mutations in the BMP15 gene are associated with ovarian failure
-
et al.
-
Dixit H., Rao L. K., Padmalatha V. V., et al. Missense mutations in the BMP15 gene are associated with ovarian failure. Hum Genet: 2006; 119 4 408 415
-
(2006)
Hum Genet
, vol.119
, Issue.4
, pp. 408-415
-
-
Dixit, H.1
Rao, L.K.2
Padmalatha, V.V.3
-
48
-
-
34548288054
-
NOBOX homeobox mutation causes premature ovarian failure
-
Qin Y., Choi Y., Zhao H., Simpson J. L., Chen Z. J., Rajkovic A. NOBOX homeobox mutation causes premature ovarian failure. Am J Hum Genet: 2007; 81 3 576 581
-
(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
-
49
-
-
33751512498
-
Novel variants in growth differentiation factor 9 in mothers of dizygotic twins
-
et al.
-
Palmer J. S., Zhao Z. Z., Hoekstra C., et al. Novel variants in growth differentiation factor 9 in mothers of dizygotic twins. J Clin Endocrinol Metab: 2006; 91 11 4713 4716
-
(2006)
J Clin Endocrinol Metab
, vol.91
, Issue.11
, pp. 4713-4716
-
-
Palmer, J.S.1
Zhao, Z.Z.2
Hoekstra, C.3
-
50
-
-
33749246535
-
Mutational analysis of BMP15 and GDF9 as candidate genes for premature ovarian failure
-
Chand A. L., Ponnampalam A. P., Harris S. E., Winship I. M., Shelling A. N. Mutational analysis of BMP15 and GDF9 as candidate genes for premature ovarian failure. Fertil Steril: 2006; 86 4 1009 1012
-
(2006)
Fertil Steril
, vol.86
, Issue.4
, pp. 1009-1012
-
-
Chand, A.L.1
Ponnampalam, A.P.2
Harris, S.E.3
Winship, I.M.4
Shelling, A.N.5
-
51
-
-
33845728499
-
Growth differentiating factor-9 mutations may be associated with premature ovarian failure
-
Kovanci E., Rohozinski J., Simpson J. L., Heard M. J., Bishop C. E., Carson S. A. Growth differentiating factor-9 mutations may be associated with premature ovarian failure. Fertil Steril: 2007; 87 1 143 146
-
(2007)
Fertil Steril
, vol.87
, Issue.1
, pp. 143-146
-
-
Kovanci, E.1
Rohozinski, J.2
Simpson, J.L.3
Heard, M.J.4
Bishop, C.E.5
Carson, S.A.6
-
52
-
-
0036061053
-
Identification of novel mutations in FOXL2 associated with premature ovarian failure
-
Harris S. E., Chand A. L., Winship I. M., Gersak K., Aittomäki K., Shelling A. N. Identification of novel mutations in FOXL2 associated with premature ovarian failure. Mol Hum Reprod: 2002; 8 8 729 733
-
(2002)
Mol Hum Reprod
, vol.8
, Issue.8
, pp. 729-733
-
-
Harris, S.E.1
Chand, A.L.2
Winship, I.M.3
Gersak, K.4
Aittomäki, K.5
Shelling, A.N.6
-
53
-
-
0038627542
-
Regulation of the phenotype of ovarian somatic cells by estrogen
-
Britt K. L., Findlay J. K. Regulation of the phenotype of ovarian somatic cells by estrogen. Mol Cell Endocrinol: 2003; 202 12 11 17
-
(2003)
Mol Cell Endocrinol
, vol.202
, Issue.12
, pp. 11-17
-
-
Britt, K.L.1
Findlay, J.K.2
-
54
-
-
0342445418
-
Postnatal sex reversal of the ovaries in mice lacking estrogen receptors alpha and beta
-
et al.
-
Couse J. F., Hewitt S. C., Bunch D. O., et al. Postnatal sex reversal of the ovaries in mice lacking estrogen receptors alpha and beta. Science: 1999; 286 5448 2328 2331
-
(1999)
Science
, vol.286
, Issue.5448
, pp. 2328-2331
-
-
Couse, J.F.1
Hewitt, S.C.2
Bunch, D.O.3
-
55
-
-
0033767836
-
Effect of single and compound knockouts of estrogen receptors alpha (ERalpha) and beta (ERbeta) on mouse reproductive phenotypes
-
Dupont S., Krust A., Gansmuller A., Dierich A., Chambon P., Mark M. Effect of single and compound knockouts of estrogen receptors alpha (ERalpha) and beta (ERbeta) on mouse reproductive phenotypes. Development: 2000; 127 19 4277 4291
-
(2000)
Development
, vol.127
, Issue.19
, pp. 4277-4291
-
-
Dupont, S.1
Krust, A.2
Gansmuller, A.3
Dierich, A.4
Chambon, P.5
Mark, M.6
-
56
-
-
55749088979
-
Steroidogenic factor-1 (SF-1, Ad4BP, NR5A1) and disorders of testis development
-
Lin L., Achermann J. C. Steroidogenic factor-1 (SF-1, Ad4BP, NR5A1) and disorders of testis development. Sex Dev: 2008; 2 45 200 209
-
(2008)
Sex Dev
, vol.2
, Issue.45
, pp. 200-209
-
-
Lin, L.1
Achermann, J.C.2
-
57
-
-
0032844814
-
Expression of steroidogenic factor 1 and Wilms' tumour 1 during early human gonadal development and sex determination
-
et al.
-
Hanley N. A., Ball S. G., Clement-Jones M., et al. Expression of steroidogenic factor 1 and Wilms' tumour 1 during early human gonadal development and sex determination. Mech Dev: 1999; 87 12 175 180
-
(1999)
Mech Dev
, vol.87
, Issue.12
, pp. 175-180
-
-
Hanley, N.A.1
Ball, S.G.2
Clement-Jones, M.3
-
58
-
-
45449085418
-
Involvement of Ad4BP/SF-1, DAX-1, and COUP-TFII transcription factor on steroid production and luteinization in ovarian theca cells
-
Murayama C., Miyazaki H., Miyamoto A., Shimizu T. Involvement of Ad4BP/SF-1, DAX-1, and COUP-TFII transcription factor on steroid production and luteinization in ovarian theca cells. Mol Cell Biochem: 2008; 314 12 51 58
-
(2008)
Mol Cell Biochem
, vol.314
, Issue.12
, pp. 51-58
-
-
Murayama, C.1
Miyazaki, H.2
Miyamoto, A.3
Shimizu, T.4
-
59
-
-
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 E. J. 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 6 1563 1568
-
(2000)
Am J Hum Genet
, vol.67
, Issue.6
, pp. 1563-1568
-
-
Biason-Lauber, A.1
Schoenle, E.J.2
-
60
-
-
62749102793
-
Mutations in NR5A1 associated with ovarian insufficiency
-
et al.
-
Lourenço D., Brauner R., Lin L., et al. Mutations in NR5A1 associated with ovarian insufficiency. N Engl J Med: 2009; 360 12 1200 1210
-
(2009)
N Engl J Med
, vol.360
, Issue.12
, pp. 1200-1210
-
-
Lourenço, D.1
Brauner, R.2
Lin, L.3
-
61
-
-
0041508536
-
Endothelial and steroidogenic cell migration are regulated by WNT4 in the developing mammalian gonad
-
et al.
-
Jeays-Ward K., Hoyle C., Brennan J., et al. Endothelial and steroidogenic cell migration are regulated by WNT4 in the developing mammalian gonad. Development: 2003; 130 16 3663 3670
-
(2003)
Development
, vol.130
, Issue.16
, pp. 3663-3670
-
-
Jeays-Ward, K.1
Hoyle, C.2
Brennan, J.3
-
62
-
-
63449124841
-
Germ cell sex determination in mammals
-
Kocer A., Reichmann J., Best D., Adams I. R. Germ cell sex determination in mammals. Mol Hum Reprod: 2009; 15 4 205 213
-
(2009)
Mol Hum Reprod
, vol.15
, Issue.4
, pp. 205-213
-
-
Kocer, A.1
Reichmann, J.2
Best, D.3
Adams, I.R.4
-
63
-
-
77950541207
-
Gonadal defects in Cited2-mutant mice indicate a role for SF1 in both testis and ovary differentiation
-
et al.
-
Combes A. N., Spiller C. M., Harley V. R., et al. Gonadal defects in Cited2-mutant mice indicate a role for SF1 in both testis and ovary differentiation. Int J Dev Biol: 2010; 54 4 683 689
-
(2010)
Int J Dev Biol
, vol.54
, Issue.4
, pp. 683-689
-
-
Combes, A.N.1
Spiller, C.M.2
Harley, V.R.3
-
64
-
-
42449158088
-
R-spondin1 plays an essential role in ovarian development through positively regulating Wnt-4 signaling
-
et al.
-
Tomizuka K., Horikoshi K., Kitada R., et al. R-spondin1 plays an essential role in ovarian development through positively regulating Wnt-4 signaling. Hum Mol Genet: 2008; 17 9 1278 1291
-
(2008)
Hum Mol Genet
, vol.17
, Issue.9
, pp. 1278-1291
-
-
Tomizuka, K.1
Horikoshi, K.2
Kitada, R.3
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