-
2
-
-
22544447060
-
Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome
-
doi:10.1086/432083
-
Beysen D, Raes J, Leroy BP, Lucassen A, Yates JR, Clayton-Smith J, Ilyina H, Brooks SS, Christin-Maitre S, Fellous M et al. 2005 Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome. American Journal of Human Genetics 77 205-218. (doi:10.1086/432083)
-
(2005)
American Journal of Human Genetics
, vol.77
, pp. 205-218
-
-
Beysen, D.1
Raes, J.2
Leroy, B.P.3
Lucassen, A.4
Yates, J.R.5
Clayton-Smith, J.6
Ilyina, H.7
Brooks, S.S.8
Christin-Maitre, S.9
Fellous, M.10
-
3
-
-
59749101082
-
FOXL2 mutations and genomic rearrangements in BPES
-
doi:10.1002/humu.20807
-
Beysen D, De Paepe A & De Baere E 2009 FOXL2 mutations and genomic rearrangements in BPES. Human Mutation 30 158-169. (doi:10.1002/humu.20807)
-
(2009)
Human Mutation
, vol.30
, pp. 158-169
-
-
Beysen, D.1
De Paepe, A.2
De Baere, E.3
-
4
-
-
3042762359
-
One tissue, two fates: Molecular genetic events that underlie testis versus ovary development
-
doi:10.1038/nrg1381
-
Brennan J & Capel B 2004 One tissue, two fates: molecular genetic events that underlie testis versus ovary development. Nature Reviews. Genetics 5 509-521. (doi:10.1038/nrg1381)
-
(2004)
Nature Reviews. Genetics
, vol.5
, pp. 509-521
-
-
Brennan, J.1
Capel, B.2
-
5
-
-
77952525001
-
FOXO transcription factors: From cell fate decisions to regulation of human female reproduction
-
Brosens JJ, Wilson MS & Lam EW 2009 FOXO transcription factors: from cell fate decisions to regulation of human female reproduction. Advances in Experimental Medicine and Biology 665 227-241.
-
(2009)
Advances in Experimental Medicine and Biology
, vol.665
, pp. 227-241
-
-
Brosens, J.J.1
Wilson, M.S.2
Lam, E.W.3
-
6
-
-
0347418199
-
Alanine tracts: The expanding story of human illness and trinucleotide repeats
-
doi:10.1016/j.tig.2003.11.002
-
Brown LY & Brown SA 2004 Alanine tracts: the expanding story of human illness and trinucleotide repeats. Trends in Genetics 20 51-58. (doi:10.1016/j.tig.2003.11.002)
-
(2004)
Trends in Genetics
, vol.20
, pp. 51-58
-
-
Brown, L.Y.1
Brown, S.A.2
-
7
-
-
33750486857
-
R-spondin1 tips the balance in sex determination
-
doi:10.1038/ng1106-1233
-
Capel B 2006 R-spondin1 tips the balance in sex determination. Nature Genetics 38 1233-1234. (doi:10.1038/ng1106-1233)
-
(2006)
Nature Genetics
, vol.38
, pp. 1233-1234
-
-
Capel, B.1
-
8
-
-
0038152845
-
Suppression of ovarian follicle activation in mice by the transcription factor Foxo3a
-
doi:10.1126/science.1086336
-
Castrillon DH, Miao L, Kollipara R, Horner JW & DePinho RA 2003 Suppression of ovarian follicle activation in mice by the transcription factor Foxo3a. Science 301 215-218. (doi:10.1126/science.1086336)
-
(2003)
Science
, vol.301
, pp. 215-218
-
-
Castrillon, D.H.1
Miao, L.2
Kollipara, R.3
Horner, J.W.4
DePinho, R.A.5
-
9
-
-
33645083718
-
Genetics of early mammalian folliculogenesis
-
doi:10.1007/s00018-005-5394-7
-
Choi Y & Rajkovic A 2006 Genetics of early mammalian folliculogenesis. Cellular and Molecular Life Sciences 63 579-590. (doi:10.1007/s00018-005-5394-7)
-
(2006)
Cellular and Molecular Life Sciences
, vol.63
, pp. 579-590
-
-
Choi, Y.1
Rajkovic, A.2
-
10
-
-
0035131812
-
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome
-
doi:10.1038/84781
-
Crisponi L, Deiana M, Loi A, Chiappe F, Uda M, Amati P, Bisceglia L, Zelante L, Nagaraja R, Porcu S et al. 2001 The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome. Nature Genetics 27 159-166. (doi:10.1038/84781)
-
(2001)
Nature Genetics
, vol.27
, pp. 159-166
-
-
Crisponi, L.1
Deiana, M.2
Loi, A.3
Chiappe, F.4
Uda, M.5
Amati, P.6
Bisceglia, L.7
Zelante, L.8
Nagaraja, R.9
Porcu, S.10
-
11
-
-
1842665188
-
FOXL2 inactivation by a translocation 171 kb away: Analysis of 500 kb of chromosome 3 for candidate long-range regulatory sequences
-
doi:10.1016/j.ygeno.2003.11.010
-
Crisponi L, Uda M, Deiana M, Loi A, Nagaraja R, Chiappe F, Schlessinger D, Cao A & Pilia G 2004 FOXL2 inactivation by a translocation 171 kb away: analysis of 500 kb of chromosome 3 for candidate long-range regulatory sequences. Genomics 83 757-764. (doi:10.1016/j.ygeno.2003.11.010)
-
(2004)
Genomics
, vol.83
, pp. 757-764
-
-
Crisponi, L.1
Uda, M.2
Deiana, M.3
Loi, A.4
Nagaraja, R.5
Chiappe, F.6
Schlessinger, D.7
Cao, A.8
Pilia, G.9
-
12
-
-
0035878536
-
Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation
-
doi:10.1093/hmg/10.15.1591
-
De Baere E, Dixon MJ, Small KW, Jabs EW, Leroy BP, Devriendt K, Gillerot Y, Mortier G, Meire F, Van Maldergem L et al. 2001 Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation. Human Molecular Genetics 10 1591-1600. (doi:10.1093/hmg/10.15.1591)
-
(2001)
Human Molecular Genetics
, vol.10
, pp. 1591-1600
-
-
De Baere, E.1
Dixon, M.J.2
Small, K.W.3
Jabs, E.W.4
Leroy, B.P.5
Devriendt, K.6
Gillerot, Y.7
Mortier, G.8
Meire, F.9
Van Maldergem, L.10
-
13
-
-
0037318857
-
FOXL2 and BPES: Mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation
-
doi:10.1086/346118
-
De Baere E, Beysen D, Oley C, Lorenz B, Cocquet J, De Sutter P, Devriendt K, Dixon M, Fellous M, Fryns JP et al. 2003 FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation. American Journal of Human Genetics 72 478-487. (doi:10.1086/346118)
-
(2003)
American Journal of Human Genetics
, vol.72
, pp. 478-487
-
-
De Baere, E.1
Beysen, D.2
Oley, C.3
Lorenz, B.4
Cocquet, J.5
De Sutter, P.6
Devriendt, K.7
Dixon, M.8
Fellous, M.9
Fryns, J.P.10
-
14
-
-
75949092042
-
The transcription factor FOXL2 in ovarian function and dysfunction
-
doi:10.2478/v10042-009-0062-7
-
De Baere E, Fellous M & Veitia RA 2009 The transcription factor FOXL2 in ovarian function and dysfunction. Folia Histochemica et Cytobiologica 47 S43-S49. (doi:10.2478/v10042-009-0062-7)
-
(2009)
Folia Histochemica et Cytobiologica
, vol.47
-
-
De Baere, E.1
Fellous, M.2
Veitia, R.A.3
-
15
-
-
17144451343
-
Role of growth factors in ovary organogenesis
-
doi:10.1016/S1071-5576(00)00098-8
-
Erickson GF 2001 Role of growth factors in ovary organogenesis. Journal of the Society for Gynecologic Investigation 8 (1 Suppl Proceedings) S13-S16. (doi:10.1016/S1071-5576(00)00098-8)
-
(2001)
Journal of the Society for Gynecologic Investigation
, vol.8
, Issue.1 SUPPL. PROCEEDINGS
-
-
Erickson, G.F.1
-
16
-
-
40549128694
-
Sequence variation at the human FOXO3 locus: A study of premature ovarian failure and primary amenorrhea
-
doi:10.1093/humrep/dem255
-
Gallardo TD, John GB, Bradshaw K, Welt C, Reijo-Pera R, Vogt PH, Touraine P, Bione S, Toniolo D, Nelson LM et al. 2008 Sequence variation at the human FOXO3 locus: a study of premature ovarian failure and primary amenorrhea. Human Reproduction 23 216-221. (doi:10.1093/humrep/dem255)
-
(2008)
Human Reproduction
, vol.23
, pp. 216-221
-
-
Gallardo, T.D.1
John, G.B.2
Bradshaw, K.3
Welt, C.4
Reijo-Pera, R.5
Vogt, P.H.6
Touraine, P.7
Bione, S.8
Toniolo, D.9
Nelson, L.M.10
-
17
-
-
38749095854
-
Prolactin signaling through the short form of its receptor represses forkhead transcription factor FOXO3 and its target gene galt causing a severe ovarian defect
-
doi:10.1210/me.2007-0399
-
Halperin J, Devi SY, Elizur S, Stocco C, Shehu A, Rebourcet D, Unterman TG, Leslie ND, Le J, Binart N et al. 2008 Prolactin signaling through the short form of its receptor represses forkhead transcription factor FOXO3 and its target gene galt causing a severe ovarian defect. Molecular Endocrinology 22 513-522. (doi:10.1210/me.2007-0399)
-
(2008)
Molecular Endocrinology
, vol.22
, pp. 513-522
-
-
Halperin, J.1
Devi, S.Y.2
Elizur, S.3
Stocco, C.4
Shehu, A.5
Rebourcet, D.6
Unterman, T.G.7
Leslie, N.D.8
Le, J.9
Binart, N.10
-
18
-
-
62549108593
-
The evolution of Fox genes and their role in development and disease
-
doi:10.1038/nrg2523
-
Hannenhalli S & Kaestner KH 2009 The evolution of Fox genes and their role in development and disease. Nature Reviews. Genetics 10 233-240. (doi:10.1038/nrg2523)
-
(2009)
Nature Reviews. Genetics
, vol.10
, pp. 233-240
-
-
Hannenhalli, S.1
Kaestner, K.H.2
-
19
-
-
70349469577
-
The cunning little vixen: Foxo and the cycle of life and death
-
doi:10.1038/ni.1784
-
Hedrick SM 2009 The cunning little vixen: Foxo and the cycle of life and death. Nature Immunology 10 1057-1063. (doi:10.1038/ni.1784)
-
(2009)
Nature Immunology
, vol.10
, pp. 1057-1063
-
-
Hedrick, S.M.1
-
20
-
-
1542267804
-
Disruption of forkhead transcription factor (FOXO) family members in mice reveals their functional diversification
-
doi:10.1073/pnas.0400093101
-
Hosaka T, Biggs WH III, Tieu D, Boyer AD, Varki NM, Cavenee WK & Arden KC 2004 Disruption of forkhead transcription factor (FOXO) family members in mice reveals their functional diversification. PNAS 101 2975-2980. (doi:10.1073/pnas.0400093101)
-
(2004)
PNAS
, vol.101
, pp. 2975-2980
-
-
Hosaka, T.1
Biggs III, W.H.2
Tieu, D.3
Boyer, A.D.4
Varki, N.M.5
Cavenee, W.K.6
Arden, K.C.7
-
21
-
-
0041508536
-
Endothelial and steroidogenic cell migration are regulated by WNT4 in the developing mammalian gonad
-
doi:10.1242/dev.00591
-
Jeays-Ward K, Hoyle C, Brennan J, Dandonneau M, Alldus G, Capel B & Swain A 2003 Endothelial and steroidogenic cell migration are regulated by WNT4 in the developing mammalian gonad. Development 130 3663-3670. (doi:10.1242/dev.00591)
-
(2003)
Development
, vol.130
, pp. 3663-3670
-
-
Jeays-Ward, K.1
Hoyle, C.2
Brennan, J.3
Dandonneau, M.4
Alldus, G.5
Capel, B.6
Swain, A.7
-
22
-
-
49049116473
-
Foxo3 is a PI3K-dependent molecular switch controlling the initiation of oocyte growth
-
doi:10.1016/j.ydbio.2008.06.017
-
John GB, Gallardo TD, Shirley LJ & Castrillon DH 2008 Foxo3 is a PI3K-dependent molecular switch controlling the initiation of oocyte growth. Developmental Biology 321 197-204. (doi:10.1016/j.ydbio.2008.06.017)
-
(2008)
Developmental Biology
, vol.321
, pp. 197-204
-
-
John, G.B.1
Gallardo, T.D.2
Shirley, L.J.3
Castrillon, D.H.4
-
23
-
-
78650840062
-
FOXL2 and BMP2 act cooperatively to regulate follistatin gene expression during ovarian development
-
doi:10.1210/en.2010-0636
-
Kashimada K, Pelosi E, Chen H, Schlessinger D, Wilhelm D & Koopman P 2011 FOXL2 and BMP2 act cooperatively to regulate follistatin gene expression during ovarian development. Endocrinology 152 272-280. (doi:10.1210/en.2010- 0636)
-
(2011)
Endocrinology
, vol.152
, pp. 272-280
-
-
Kashimada, K.1
Pelosi, E.2
Chen, H.3
Schlessinger, D.4
Wilhelm, D.5
Koopman, P.6
-
24
-
-
33748313401
-
Balancing the bipotential gonad between alternative organ fates: A new perspective on an old problem
-
doi:10.1002/dvdy.20894
-
Kim Y & Capel B 2006 Balancing the bipotential gonad between alternative organ fates: a new perspective on an old problem. Developmental Dynamics 235 2292-2300. (doi:10.1002/dvdy.20894)
-
(2006)
Developmental Dynamics
, vol.235
, pp. 2292-2300
-
-
Kim, Y.1
Capel, B.2
-
25
-
-
70349783734
-
Sumoylation of forkhead L2 by Ubc9 is required for its activity as a transcriptional repressor of the steroidogenic acute regulatory gene
-
doi:10.1016/j.cellsig.2009.09.001
-
Kuo FT, Bentsi-Barnes IK, Barlow GM, Bae J & Pisarska MD 2009 Sumoylation of forkhead L2 by Ubc9 is required for its activity as a transcriptional repressor of the steroidogenic acute regulatory gene. Cellular Signalling 21 1935-1944. (doi:10.1016/j.cellsig.2009.09.001)
-
(2009)
Cellular Signalling
, vol.21
, pp. 1935-1944
-
-
Kuo, F.T.1
Bentsi-Barnes, I.K.2
Barlow, G.M.3
Bae, J.4
Pisarska, M.D.5
-
26
-
-
0037866671
-
Fox's in development and disease
-
doi:10.1016/S0168-9525(03)00111-2
-
Lehmann OJ, Sowden JC, Carlsson P, Jordan T & Bhattacharya SS 2003 Fox's in development and disease. Trends in Genetics 19 339-344. (doi:10.1016/S0168-9525(03)00111-2)
-
(2003)
Trends in Genetics
, vol.19
, pp. 339-344
-
-
Lehmann, O.J.1
Sowden, J.C.2
Carlsson, P.3
Jordan, T.4
Bhattacharya, S.S.5
-
27
-
-
33846538095
-
Infertility caused by retardation of follicular development in mice with oocyte-specific expression of Foxo3a
-
doi:10.1242/dev.02667
-
Liu L, Rajareddy S, Reddy P, Du C, Jagarlamudi K, Shen Y, Gunnarsson D, Selstam G, Boman K & Liu K 2007 Infertility caused by retardation of follicular development in mice with oocyte-specific expression of Foxo3a. Development 134 199-209. (doi:10.1242/dev.02667)
-
(2007)
Development
, vol.134
, pp. 199-209
-
-
Liu, L.1
Rajareddy, S.2
Reddy, P.3
Du, C.4
Jagarlamudi, K.5
Shen, Y.6
Gunnarsson, D.7
Selstam, G.8
Boman, K.9
Liu, K.10
-
28
-
-
66649095347
-
FSH and FOXO1 regulate genes in the sterol/steroid and lipid biosynthetic pathways in granulosa cells
-
doi:10.1210/me.2008-0412
-
Liu Z, Rudd MD, Hernandez-Gonzalez I, Gonzalez-Robayna I, Fan HY, Zeleznik AJ & Richards JS 2009 FSH and FOXO1 regulate genes in the sterol/steroid and lipid biosynthetic pathways in granulosa cells. Molecular Endocrinology 23 649-661. (doi:10.1210/me.2008-0412)
-
(2009)
Molecular Endocrinology
, vol.23
, pp. 649-661
-
-
Liu, Z.1
Rudd, M.D.2
Hernandez-Gonzalez, I.3
Gonzalez-Robayna, I.4
Fan, H.Y.5
Zeleznik, A.J.6
Richards, J.S.7
-
29
-
-
66149163230
-
A "FOXO" in sight: Targeting Foxo proteins from conception to cancer
-
doi:10.1002/med.20139
-
Maiese K, Chong ZZ, Shang YC & Hou J 2009 A "FOXO" in sight: targeting Foxo proteins from conception to cancer. Medicinal Research Reviews 29 395-418. (doi:10.1002/med.20139)
-
(2009)
Medicinal Research Reviews
, vol.29
, pp. 395-418
-
-
Maiese, K.1
Chong, Z.Z.2
Shang, Y.C.3
Hou, J.4
-
30
-
-
31544432542
-
The mouse forkhead gene Foxc1 is required for primordial germ cell migration and antral follicle development
-
doi:10.1016/j.ydbio.2005.12.007
-
Mattiske D, Kume T & Hogan BL 2006 The mouse forkhead gene Foxc1 is required for primordial germ cell migration and antral follicle development. Developmental Biology 290 447-458. (doi:10.1016/j.ydbio.2005.12.007)
-
(2006)
Developmental Biology
, vol.290
, pp. 447-458
-
-
Mattiske, D.1
Kume, T.2
Hogan, B.L.3
-
31
-
-
0036798824
-
Genetic dissection of mammalian fertility pathways
-
Matzuk MM & Lamb DJ 2002 Genetic dissection of mammalian fertility pathways. Nature Cell Biology 4 (Supplement) s41-s49. (Pubitemid 35175933)
-
(2002)
Nature Medicine
, vol.8
, Issue.10 SUPPL.
-
-
Matzuk, M.M.1
Lamb, D.J.2
-
32
-
-
55549115368
-
The biology of infertility: Research advances and clinical challenges
-
doi:10.1038/nm.f.1895
-
Matzuk MM & Lamb DJ 2008 The biology of infertility: research advances and clinical challenges. Nature Medicine 14 1197-1213. (doi:10.1038/nm.f.1895)
-
(2008)
Nature Medicine
, vol.14
, pp. 1197-1213
-
-
Matzuk, M.M.1
Lamb, D.J.2
-
33
-
-
0037150650
-
Intercellular communication in the mammalian ovary: Oocytes carry the conversation
-
doi:10.1126/science.1071965
-
Matzuk MM, Burns KH, Viveiros MM & Eppig JJ 2002 Intercellular communication in the mammalian ovary: oocytes carry the conversation. Science 296 2178-2180. (doi:10.1126/science.1071965)
-
(2002)
Science
, vol.296
, pp. 2178-2180
-
-
Matzuk, M.M.1
Burns, K.H.2
Viveiros, M.M.3
Eppig, J.J.4
-
34
-
-
39149117672
-
The mutations and potential targets of the forkhead transcription factor FOXL2
-
doi:10.1016/j.mce.2007.11.006
-
Moumne L, Batista F, Benayoun BA, Nallathambi J, Fellous M, Sundaresan P & Veitia RA 2008 The mutations and potential targets of the forkhead transcription factor FOXL2. Molecular and Cellular Endocrinology 282 2-11. (doi:10.1016/j.mce.2007.11.006)
-
(2008)
Molecular and Cellular Endocrinology
, vol.282
, pp. 2-11
-
-
Moumne, L.1
Batista, F.2
Benayoun, B.A.3
Nallathambi, J.4
Fellous, M.5
Sundaresan, P.6
Veitia, R.A.7
-
35
-
-
26444511733
-
Foxl2 is required for commitment to ovary differentiation
-
doi:10.1093/hmg/ddi210
-
Ottolenghi C, Omari S, Garcia-Ortiz JE, Uda M, Crisponi L, Forabosco A, Pilia G & Schlessinger D 2005 Foxl2 is required for commitment to ovary differentiation. Human Molecular Genetics 14 2053-2062. (doi:10.1093/hmg/ddi210)
-
(2005)
Human Molecular Genetics
, vol.14
, pp. 2053-2062
-
-
Ottolenghi, C.1
Omari, S.2
Garcia-Ortiz, J.E.3
Uda, M.4
Crisponi, L.5
Forabosco, A.6
Pilia, G.7
Schlessinger, D.8
-
36
-
-
33846295218
-
FoxOs are lineage-restricted redundant tumor suppressors and regulate endothelial cell homeostasis
-
doi:10.1016/j.cell.2006.12.029
-
Paik JH, Kollipara R, Chu G, Ji H, Xiao Y, Ding Z, Miao L, Tothova Z, Horner JW, Carrasco DR et al. 2007 FoxOs are lineage-restricted redundant tumor suppressors and regulate endothelial cell homeostasis. Cell 128 309-323. (doi:10.1016/j.cell.2006.12.029)
-
(2007)
Cell
, vol.128
, pp. 309-323
-
-
Paik, J.H.1
Kollipara, R.2
Chu, G.3
Ji, H.4
Xiao, Y.5
Ding, Z.6
Miao, L.7
Tothova, Z.8
Horner, J.W.9
Carrasco, D.R.10
-
37
-
-
0035733723
-
A 11.7-kb deletion triggers intersexuality and polledness in goats
-
doi:10.1038/ng769
-
Pailhoux E, Vigier B, Chaffaux S, Servel N, Taourit S, Furet JP, Fellous M, Grosclaude F, Cribiu EP, Cotinot C et al. 2001 A 11.7-kb deletion triggers intersexuality and polledness in goats. Nature Genetics 29 453-458. (doi:10.1038/ng769)
-
(2001)
Nature Genetics
, vol.29
, pp. 453-458
-
-
Pailhoux, E.1
Vigier, B.2
Chaffaux, S.3
Servel, N.4
Taourit, S.5
Furet, J.P.6
Fellous, M.7
Grosclaude, F.8
Cribiu, E.P.9
Cotinot, C.10
-
38
-
-
33750489078
-
R-spondin1 is essential in sex determination, skin differentiation and malignancy
-
doi:10.1038/ng1907
-
Parma P, Radi O, Vidal V, Chaboissier MC, Dellambra E, Valentini S, Guerra L, Schedl A & Camerino G 2006 R-spondin1 is essential in sex determination, skin differentiation and malignancy. Nature Genetics 38 1304-1309. (doi:10.1038/ng1907)
-
(2006)
Nature Genetics
, vol.38
, pp. 1304-1309
-
-
Parma, P.1
Radi, O.2
Vidal, V.3
Chaboissier, M.C.4
Dellambra, E.5
Valentini, S.6
Guerra, L.7
Schedl, A.8
Camerino, G.9
-
39
-
-
77951175531
-
The ovary: Basic biology and clinical implications
-
doi:10.1172/JCI41350
-
Richards JS & Pangas SA 2010 The ovary: basic biology and clinical implications. Journal of Clinical Investigation 120 963-972. (doi:10.1172/JCI41350)
-
(2010)
Journal of Clinical Investigation
, vol.120
, pp. 963-972
-
-
Richards, J.S.1
Pangas, S.A.2
-
40
-
-
0036191716
-
Expression of FKHR, FKHRL1, and AFX genes in the rodent ovary: Evidence for regulation by IGF-I, estrogen, and the gonadotropins
-
doi:10.1210/me.16.3.580
-
Richards JS, Sharma SC, Falender AE & Lo YH 2002 Expression of FKHR, FKHRL1, and AFX genes in the rodent ovary: evidence for regulation by IGF-I, estrogen, and the gonadotropins. Molecular Endocrinology 16 580-599. (doi:10.1210/me.16.3.580)
-
(2002)
Molecular Endocrinology
, vol.16
, pp. 580-599
-
-
Richards, J.S.1
Sharma, S.C.2
Falender, A.E.3
Lo, Y.H.4
-
41
-
-
41549135942
-
FoxO transcription factors in the maintenance of cellular homeostasis during aging
-
doi:10.1016/j.ceb.2008.02.005
-
Salih DA & Brunet A 2008 FoxO transcription factors in the maintenance of cellular homeostasis during aging. Current Opinion in Cell Biology 20 126-136. (doi:10.1016/j.ceb.2008.02.005)
-
(2008)
Current Opinion in Cell Biology
, vol.20
, pp. 126-136
-
-
Salih, D.A.1
Brunet, A.2
-
42
-
-
1342327343
-
The murine winged-helix transcription factor Foxl2 is required for granulosa cell differentiation and ovary maintenance
-
doi:10.1242/dev.00969
-
Schmidt D, Ovitt CE, Anlag K, Fehsenfeld S, Gredsted L, Treier AC & Treier M 2004 The murine winged-helix transcription factor Foxl2 is required for granulosa cell differentiation and ovary maintenance. Development 131 933-942. (doi:10.1242/dev.00969)
-
(2004)
Development
, vol.131
, pp. 933-942
-
-
Schmidt, D.1
Ovitt, C.E.2
Anlag, K.3
Fehsenfeld, S.4
Gredsted, L.5
Treier, A.C.6
Treier, M.7
-
43
-
-
67649406102
-
Mutation of FOXL2 in granulosa-cell tumors of the ovary
-
doi:10.1056/NEJMoa0902542
-
Shah SP, Köbel M, Senz J, Morin RD, Clarke BA, Wiegand KC, Leung G, Zayed A, Mehl E, Kalloger SE et al. 2009 Mutation of FOXL2 in granulosa-cell tumors of the ovary. New England Journal of Medicine 360 2719-2729. (doi:10.1056/NEJMoa0902542)
-
(2009)
New England Journal of Medicine
, vol.360
, pp. 2719-2729
-
-
Shah, S.P.1
Köbel, M.2
Senz, J.3
Morin, R.D.4
Clarke, B.A.5
Wiegand, K.C.6
Leung, G.7
Zayed, A.8
Mehl, E.9
Kalloger, S.E.10
-
44
-
-
71149084102
-
Females battle to suppress their inner male
-
doi:10.1016/j.cell.2009.11.036
-
Sinclair A & Smith C 2009 Females battle to suppress their inner male. Cell 139 1051-1053. (doi:10.1016/j.cell.2009.11.036)
-
(2009)
Cell
, vol.139
, pp. 1051-1053
-
-
Sinclair, A.1
Smith, C.2
-
45
-
-
70549088923
-
Axenfeld-Rieger syndrome and spectrum of PITX2 and FOXC1 mutations
-
doi:10.1038/ejhg.2009.93
-
Tumer Z & Bach-Holm D 2009 Axenfeld-Rieger syndrome and spectrum of PITX2 and FOXC1 mutations. European Journal of Human Genetics 17 1527-1539. (doi:10.1038/ejhg.2009.93)
-
(2009)
European Journal of Human Genetics
, vol.17
, pp. 1527-1539
-
-
Tumer, Z.1
Bach-Holm, D.2
-
46
-
-
2942750361
-
Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development
-
doi:10.1093/hmg/ddh124
-
Uda M, Ottolenghi C, Crisponi L, Garcia JE, Deiana M, Kimber W, Forabosco A, Cao A, Schlessinger D & Pilia G 2004 Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development. Human Molecular Genetics 13 1171-1181. (doi:10.1093/hmg/ddh124)
-
(2004)
Human Molecular Genetics
, vol.13
, pp. 1171-1181
-
-
Uda, M.1
Ottolenghi, C.2
Crisponi, L.3
Garcia, J.E.4
Deiana, M.5
Kimber, W.6
Forabosco, A.7
Cao, A.8
Schlessinger, D.9
Pilia, G.10
-
47
-
-
33745505572
-
Foxl2 function in ovarian development
-
doi:10.1016/j.ymgme.2006.03.005
-
Uhlenhaut NH & Treier M 2006 Foxl2 function in ovarian development. Molecular Genetics and Metabolism 88 225-234. (doi:10.1016/j.ymgme.2006.03.005)
-
(2006)
Molecular Genetics and Metabolism
, vol.88
, pp. 225-234
-
-
Uhlenhaut, N.H.1
Treier, M.2
-
48
-
-
71149095052
-
Somatic sex reprogramming of adult ovaries to testes by FOXL2 ablation
-
doi:10.1016/j.cell.2009.11.021
-
Uhlenhaut NH, Jakob S, Anlag K, Eisenberger T, Sekido R, Kress J, Treier AC, Klugmann C, Klasen C, Holter NI et al. 2009 Somatic sex reprogramming of adult ovaries to testes by FOXL2 ablation. Cell 139 1130-1142. (doi:10.1016/j.cell.2009.11.021)
-
(2009)
Cell
, vol.139
, pp. 1130-1142
-
-
Uhlenhaut, N.H.1
Jakob, S.2
Anlag, K.3
Eisenberger, T.4
Sekido, R.5
Kress, J.6
Treier, A.C.7
Klugmann, C.8
Klasen, C.9
Holter, N.I.10
-
49
-
-
33750152602
-
Mutational screening of FOXO3A and FOXO1A in women with premature ovarian failure
-
doi:10.1016/j.fertnstert.2006.03.054
-
Watkins WJ, Umbers AJ, Woad KJ, Harris SE, Winship IM, Gersak K & Shelling AN 2006 Mutational screening of FOXO3A and FOXO1A in women with premature ovarian failure. Fertility and Sterility 86 1518-1521. (doi:10.1016/j.fertnstert.2006.03.054)
-
(2006)
Fertility and Sterility
, vol.86
, pp. 1518-1521
-
-
Watkins, W.J.1
Umbers, A.J.2
Woad, K.J.3
Harris, S.E.4
Winship, I.M.5
Gersak, K.6
Shelling, A.N.7
-
50
-
-
0025029381
-
The fork head domain: A novel DNA binding motif of eukaryotic transcription factors?
-
doi:10.1016/0092-8674(90)90439-L
-
Weigel D & Jäckle H 1990 The fork head domain: a novel DNA binding motif of eukaryotic transcription factors? Cell 63 455-456. (doi:10.1016/0092-8674(90)90439-L)
-
(1990)
Cell
, vol.63
, pp. 455-456
-
-
Weigel, D.1
Jäckle, H.2
-
51
-
-
0024973841
-
The homeotic gene fork head encodes a nuclear protein and is expressed in the terminal regions of the Drosophila embryo
-
doi:10.1016/0092-8674(89)90133-5
-
Weigel D, Jürgens G, Küttner F, Seifert E & Jäckle H 1989 The homeotic gene fork head encodes a nuclear protein and is expressed in the terminal regions of the Drosophila embryo. Cell 57 645-658. (doi:10.1016/0092-8674(89)90133-5)
-
(1989)
Cell
, vol.57
, pp. 645-658
-
-
Weigel, D.1
Jürgens, G.2
Küttner, F.3
Seifert, E.4
Jäckle, H.5
|