-
1
-
-
0033118412
-
Mammalian sex determination: A molecular drama
-
Swain A and Lovell-Badge R (1999) Mammalian sex determination: A molecular drama. Genes Dev 13: 755-767
-
(1999)
Genes Dev
, vol.13
, pp. 755-767
-
-
Swain, A.1
Lovell-Badge, R.2
-
3
-
-
3042762359
-
One tissue, two fates: Molecular genetic events that underlie testis versus ovary development
-
Brennan J and Capel B (2004) One tissue, two fates: Molecular genetic events that underlie testis versus ovary development. Nat Rev Genet 5: 509-521
-
(2004)
Nat Rev Genet
, vol.5
, pp. 509-521
-
-
Brennan, J.1
Capel, B.2
-
4
-
-
12344333666
-
The pathway to femaleness: Current knowledge on embryonic development of the ovary
-
Yao HH (2005) The pathway to femaleness: Current knowledge on embryonic development of the ovary. Mol Cell Endocrinol 230: 87-93
-
(2005)
Mol Cell Endocrinol
, vol.230
, pp. 87-93
-
-
Yao, H.H.1
-
5
-
-
0026145804
-
Development of the mammalian gonad: The fate of the supporting cell lineage
-
McLaren A (1991) Development of the mammalian gonad: The fate of the supporting cell lineage. Bioessays 13: 151-156
-
(1991)
Bioessays
, vol.13
, pp. 151-156
-
-
McLaren, A.1
-
6
-
-
1942477149
-
SF-1 a key player in the development and differentiation of steroidogenic tissues
-
Val P et al. (2003) SF-1 a key player in the development and differentiation of steroidogenic tissues. Nucl Recept 1:8
-
(2003)
Nucl Recept
, vol.1
, pp. 8
-
-
Val, P.1
-
7
-
-
0028303959
-
A cell-specific nuclear receptor is essential for adrenal and gonadal development and sexual differentiation
-
Luo X et al. (1994) A cell-specific nuclear receptor is essential for adrenal and gonadal development and sexual differentiation. Cell 77: 481-490
-
(1994)
Cell
, vol.77
, pp. 481-490
-
-
Luo, X.1
-
8
-
-
1842530978
-
Differential requirement for steroidogenic factor-1 gene dosage in adrenal development versus endocrine function
-
Bland ML et al. (2004) Differential requirement for steroidogenic factor-1 gene dosage in adrenal development versus endocrine function. Mol Endocrinol 18: 941-952
-
(2004)
Mol Endocrinol
, vol.18
, pp. 941-952
-
-
Bland, M.L.1
-
9
-
-
6344258377
-
Gonadal dysgenesis without adrenal insufficiency in a 46,XY patient heterozygous for the nonsense C16X mutation: A case of SF1 haploinsufficiency
-
Mallet D et al. (2004) Gonadal dysgenesis without adrenal insufficiency in a 46,XY patient heterozygous for the nonsense C16X mutation: A case of SF1 haploinsufficiency. J Clin Endocrinol Metab 89: 4829-4832
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 4829-4832
-
-
Mallet, D.1
-
10
-
-
10344264981
-
Testicular dysgenesis without adrenal insufficiency in a 46,XY patient with a heterozygous inactive mutation of steroidogenic factor-1
-
Hasegawa T et al. (2004) Testicular dysgenesis without adrenal insufficiency in a 46,XY patient with a heterozygous inactive mutation of steroidogenic factor-1. J Clin Endocrinol Metab 89: 5930-5935
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 5930-5935
-
-
Hasegawa, T.1
-
11
-
-
0034687721
-
Haploinsufficiency of steroidogenic factor-1 in mice disrupts adrenal development leading to an impaired stress response
-
Bland ML et al. (2000) Haploinsufficiency of steroidogenic factor-1 in mice disrupts adrenal development leading to an impaired stress response. Proc Natl Acad Sci USA 97: 14488-14493
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 14488-14493
-
-
Bland, M.L.1
-
12
-
-
0035943454
-
Life, sex, and WT1 isoforms - Three amino acids can make all the difference
-
Hastie ND (2001) Life, sex, and WT1 isoforms - three amino acids can make all the difference. Cell 106: 391-394
-
(2001)
Cell
, vol.106
, pp. 391-394
-
-
Hastie, N.D.1
-
13
-
-
0029941043
-
The WT1 Wilms' tumor suppressor gene: How much do we really know?
-
Reddy JC and Licht JD (1996) The WT1 Wilms' tumor suppressor gene: How much do we really know? Biochim Biophys Acta 1287: 1-28
-
(1996)
Biochim Biophys Acta
, vol.1287
, pp. 1-28
-
-
Reddy, J.C.1
Licht, J.D.2
-
14
-
-
0035839099
-
Two splice variants of the Wilms' tumor 1 gene have distinct functions during sex determination and nephron formation
-
Hammes A et al. (2001) Two splice variants of the Wilms' tumor 1 gene have distinct functions during sex determination and nephron formation. Cell 106: 319-329
-
(2001)
Cell
, vol.106
, pp. 319-329
-
-
Hammes, A.1
-
15
-
-
3042852257
-
Gonad development in Drash and Frasier syndromes depends on WT1 mutations
-
Jaubert F et al. (2003) Gonad development in Drash and Frasier syndromes depends on WT1 mutations. Arkh Patol 65: 40-44
-
(2003)
Arkh Patol
, vol.65
, pp. 40-44
-
-
Jaubert, F.1
-
16
-
-
0032543560
-
Male-to-female sex reversal in M33 mutant mice
-
Katoh-Fukui Y et al. (1998) Male-to-female sex reversal in M33 mutant mice. Nature 393: 688-692
-
(1998)
Nature
, vol.393
, pp. 688-692
-
-
Katoh-Fukui, Y.1
-
17
-
-
0030997340
-
Defects of urogenital development in mice lacking Emx2
-
Miyamoto N et al. (1997) Defects of urogenital development in mice lacking Emx2. Development 124: 1653-1664
-
(1997)
Development
, vol.124
, pp. 1653-1664
-
-
Miyamoto, N.1
-
18
-
-
0343340431
-
The LIM homeobox gene Lhx9 is essential for mouse gonad formation
-
Birk OS et al. (2000) The LIM homeobox gene Lhx9 is essential for mouse gonad formation. Nature 403: 909-913
-
(2000)
Nature
, vol.403
, pp. 909-913
-
-
Birk, O.S.1
-
19
-
-
0031942619
-
Regulation of sexual dimorphism in mammals
-
Haqq CM and Donahoe PK (1998) Regulation of sexual dimorphism in mammals. Physiol Rev 78: 1-33
-
(1998)
Physiol Rev
, vol.78
, pp. 1-33
-
-
Haqq, C.M.1
Donahoe, P.K.2
-
20
-
-
0031922880
-
Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms
-
Klamt B et al. (1998) Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms. Hum Mol Genet 7: 709-714
-
(1998)
Hum Mol Genet
, vol.7
, pp. 709-714
-
-
Klamt, B.1
-
21
-
-
0031876652
-
Transcription factor GATA-4 is expressed in a sexually dimorphic pattern during mouse gonadal development and is a potent activator of the müllerian inhibiting substance promoter
-
Viger RS et al. (1998) Transcription factor GATA-4 is expressed in a sexually dimorphic pattern during mouse gonadal development and is a potent activator of the müllerian inhibiting substance promoter. Development 125: 2665-2675
-
(1998)
Development
, vol.125
, pp. 2665-2675
-
-
Viger, R.S.1
-
22
-
-
0036796863
-
Gonadal differentiation, sex determination and normal Sry expression in mice require direct interaction between transcription partners GATA4 and FOG2
-
Tevosian SG et al. (2002) Gonadal differentiation, sex determination and normal Sry expression in mice require direct interaction between transcription partners GATA4 and FOG2. Development 129: 4627-4634
-
(2002)
Development
, vol.129
, pp. 4627-4634
-
-
Tevosian, S.G.1
-
23
-
-
0033305667
-
Transcription factor GATA-4 enhances müllerian inhibiting substance gene transcription through a direct interaction with the nuclear receptor SF-1
-
Tremblay JJ and Viger RS (1999) Transcription factor GATA-4 enhances müllerian inhibiting substance gene transcription through a direct interaction with the nuclear receptor SF-1. Mol Endocrinol 13: 1388-1401
-
(1999)
Mol Endocrinol
, vol.13
, pp. 1388-1401
-
-
Tremblay, J.J.1
Viger, R.S.2
-
24
-
-
0035089769
-
GATA factors differentially activate multiple gonadal promoters through conserved GATA regulatory elements
-
Tremblay JJ and Viger RS (2001) GATA factors differentially activate multiple gonadal promoters through conserved GATA regulatory elements. Endocrinology 142: 977-986
-
(2001)
Endocrinology
, vol.142
, pp. 977-986
-
-
Tremblay, J.J.1
Viger, R.S.2
-
25
-
-
0036498971
-
Sry and sex determination: How lazy can it be?
-
Canning CA and Lovell-Badge R (2002) Sry and sex determination: How lazy can it be? Trends Genet 18: 111-113
-
(2002)
Trends Genet
, vol.18
, pp. 111-113
-
-
Canning, C.A.1
Lovell-Badge, R.2
-
26
-
-
0029033699
-
A clinical and genetic study of campomelic dysplasia
-
Mansour S et al. (1995) A clinical and genetic study of campomelic dysplasia. J Med Genet 32: 415-420
-
(1995)
J Med Genet
, vol.32
, pp. 415-420
-
-
Mansour, S.1
-
27
-
-
0032725866
-
Autosomal XX sex reversal caused by duplication of SOX9
-
Huang BL et al. (1999) Autosomal XX sex reversal caused by duplication of SOX9. Am J Med Genet 87: 349-353
-
(1999)
Am J Med Genet
, vol.87
, pp. 349-353
-
-
Huang, B.L.1
-
28
-
-
0033662409
-
A transgenic insertion upstream of sox9 is associated with dominant XX sex reversal in the mouse
-
Bishop CE et al. (2000) A transgenic insertion upstream of sox9 is associated with dominant XX sex reversal in the mouse. Nat Genet 26: 490-494
-
(2000)
Nat Genet
, vol.26
, pp. 490-494
-
-
Bishop, C.E.1
-
29
-
-
0034931871
-
Sox9 induces testis development in XX transgenic mice
-
Vidal V et al. (2001) Sox9 induces testis development in XX transgenic mice. Nat Genet 28: 216-217
-
(2001)
Nat Genet
, vol.28
, pp. 216-217
-
-
Vidal, V.1
-
30
-
-
2542514539
-
Functional analysis of Sox8 and Sox9 during sex determination in the mouse
-
Chaboissier MC et al. (2004) Functional analysis of Sox8 and Sox9 during sex determination in the mouse. Development 131: 1891-1901
-
(2004)
Development
, vol.131
, pp. 1891-1901
-
-
Chaboissier, M.C.1
-
31
-
-
0032705186
-
Targeted mutagenesis of the endogenous mouse Mis gene promoter: In vivo definition of genetic pathways of vertebrate sexual development
-
Arango NA et al. (1999) Targeted mutagenesis of the endogenous mouse Mis gene promoter: In vivo definition of genetic pathways of vertebrate sexual development. Cell 99: 409-419
-
(1999)
Cell
, vol.99
, pp. 409-419
-
-
Arango, N.A.1
-
32
-
-
0038206950
-
Cell proliferation is necessary for the determination of male fate in the gonad
-
Schmahl J and Capel B (2003) Cell proliferation is necessary for the determination of male fate in the gonad. Dev Biol 258: 264-276
-
(2003)
Dev Biol
, vol.258
, pp. 264-276
-
-
Schmahl, J.1
Capel, B.2
-
33
-
-
0035937405
-
Male-to-female sex reversal in mice lacking fibroblast growth factor 9
-
Colvin JS et al. (2001) Male-to-female sex reversal in mice lacking fibroblast growth factor 9. Cell 104: 875-889
-
(2001)
Cell
, vol.104
, pp. 875-889
-
-
Colvin, J.S.1
-
34
-
-
0344875027
-
Testis determination requires insulin receptor family function in mice
-
Nef S et al. (2003) Testis determination requires insulin receptor family function in mice. Nature 426: 291-295
-
(2003)
Nature
, vol.426
, pp. 291-295
-
-
Nef, S.1
-
35
-
-
0032076964
-
Wilms' tumor 1 and Dax-1 modulate the orphan nuclear receptor SF-1 in sex-specific gene expression
-
Nachtigal MW et al. (1998) Wilms' tumor 1 and Dax-1 modulate the orphan nuclear receptor SF-1 in sex-specific gene expression. Cell 93: 445-454
-
(1998)
Cell
, vol.93
, pp. 445-454
-
-
Nachtigal, M.W.1
-
36
-
-
0028558750
-
An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita
-
Zanaria E et al. (1994) An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita. Nature 372: 635-641
-
(1994)
Nature
, vol.372
, pp. 635-641
-
-
Zanaria, E.1
-
37
-
-
0028598360
-
Mutations in the DAX1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism
-
Muscatelli F et al. (1994) Mutations in the DAX1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism. Nature 372: 672-676
-
(1994)
Nature
, vol.372
, pp. 672-676
-
-
Muscatelli, F.1
-
38
-
-
0027957103
-
A dosage-sensitive locus at chromosome Xp21 is involved in male to female sex reversal
-
Bardoni B et al. (1994) A dosage-sensitive locus at chromosome Xp21 is involved in male to female sex reversal. Nat Genet 7: 497-501
-
(1994)
Nat Genet
, vol.7
, pp. 497-501
-
-
Bardoni, B.1
-
39
-
-
0032546009
-
Dax1 antagonizes Sry action in mammalian sex determination
-
Swain A et al. (1998) Dax1 antagonizes Sry action in mammalian sex determination. Nature 391: 761-767
-
(1998)
Nature
, vol.391
, pp. 761-767
-
-
Swain, A.1
-
40
-
-
23144455957
-
Gonadal sex reversal in mutant Dax1 XY mice: A failure to upregulate Sox9 in pre-Sertoli cells
-
Bouma GJ et al. (2005) Gonadal sex reversal in mutant Dax1 XY mice: A failure to upregulate Sox9 in pre-Sertoli cells. Development 132: 3045-3054
-
(2005)
Development
, vol.132
, pp. 3045-3054
-
-
Bouma, G.J.1
-
41
-
-
0037994140
-
Dax1 is required for testis determination
-
Meeks JJ et al. (2003) Dax1 is required for testis determination. Nat Genet 34: 32-33
-
(2003)
Nat Genet
, vol.34
, pp. 32-33
-
-
Meeks, J.J.1
-
42
-
-
0043268895
-
DAX1, an unusual orphan receptor at the crossroads of steroidogenic function and sexual differentiation
-
Lalli E and Sassone-Corsi P (2003) DAX1, an unusual orphan receptor at the crossroads of steroidogenic function and sexual differentiation. Mol Endocrinol 17: 1445-1453
-
(2003)
Mol Endocrinol
, vol.17
, pp. 1445-1453
-
-
Lalli, E.1
Sassone-Corsi, P.2
-
43
-
-
0035924060
-
Phenotypic spectrum of mutations in DAX1 and SF-1
-
Achermann JC et al. (2001) Phenotypic spectrum of mutations in DAX1 and SF-1. Mol Cell Endocrinol 185: 17-25
-
(2001)
Mol Cell Endocrinol
, vol.185
, pp. 17-25
-
-
Achermann, J.C.1
-
44
-
-
0033960595
-
A novel mutation in DAX1 causes delayed-onset adrenal insufficiency and incomplete hypogonadotropic hypogonadism
-
Tabarin A et al. (2000) A novel mutation in DAX1 causes delayed-onset adrenal insufficiency and incomplete hypogonadotropic hypogonadism. J Clin Invest 105: 321-328
-
(2000)
J Clin Invest
, vol.105
, pp. 321-328
-
-
Tabarin, A.1
-
45
-
-
0037238501
-
An alternate translation initiation site circumvents an amino-terminal DAX1 nonsense mutation leading to a mild form of X-linked adrenal hypoplasia congenita
-
Ozisik G et al. (2003) An alternate translation initiation site circumvents an amino-terminal DAX1 nonsense mutation leading to a mild form of X-linked adrenal hypoplasia congenita. J Clin Endocrinol Metab 88: 417-423
-
(2003)
J Clin Endocrinol Metab
, vol.88
, pp. 417-423
-
-
Ozisik, G.1
-
46
-
-
0036606827
-
Desert hedgehog/patched 1 signaling specifies fetal Leydig cell fate in testis organogenesis
-
Yao HH et al. (2002) Desert hedgehog/patched 1 signaling specifies fetal Leydig cell fate in testis organogenesis. Genes Dev 16: 1433-1440
-
(2002)
Genes Dev
, vol.16
, pp. 1433-1440
-
-
Yao, H.H.1
-
47
-
-
0033709190
-
Desert hedgehog (Dhh) gene is required in the mouse for formation of adult-type Leydig cells and normal development of peritubular cells and seminiferous tubules
-
Clark AM et al. (2000) Desert hedgehog (Dhh) gene is required in the mouse for formation of adult-type Leydig cells and normal development of peritubular cells and seminiferous tubules. Biol Reprod 63: 1825-1838
-
(2000)
Biol Reprod
, vol.63
, pp. 1825-1838
-
-
Clark, A.M.1
-
48
-
-
0033754159
-
A novel mutation of desert hedgehog in a patient with 46,XY partial gonadal dysgenesis accompanied by minifascicular neuropathy
-
Umehara F et al. (2000) A novel mutation of desert hedgehog in a patient with 46,XY partial gonadal dysgenesis accompanied by minifascicular neuropathy. Am J Hum Genet 67: 1302-1305
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1302-1305
-
-
Umehara, F.1
-
49
-
-
0345700294
-
Pdgfr-a mediates testis cord organization and fetal Leydig cell development in the XY gonad
-
Brennan J et al. (2003) Pdgfr-a mediates testis cord organization and fetal Leydig cell development in the XY gonad. Genes Dev 17: 800-810
-
(2003)
Genes Dev
, vol.17
, pp. 800-810
-
-
Brennan, J.1
-
50
-
-
0036844387
-
Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans
-
Kitamura K et al. (2002) Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans. Nat Genet 32: 359-369
-
(2002)
Nat Genet
, vol.32
, pp. 359-369
-
-
Kitamura, K.1
-
51
-
-
3042755053
-
Cell-specific knockout of steroidogenic factor 1 reveals its essential roles in gonadal function
-
Jeyasuria P et al. (2004) Cell-specific knockout of steroidogenic factor 1 reveals its essential roles in gonadal function. Mol Endocrinol 18: 1610-1619
-
(2004)
Mol Endocrinol
, vol.18
, pp. 1610-1619
-
-
Jeyasuria, P.1
-
52
-
-
0035062734
-
Pod-1/capsulin shows a sex- and stage-dependent expression pattern in the mouse gonad development and represses expression of Ad4BP/SF-1
-
Tamura M et al. (2001) Pod-1/capsulin shows a sex- and stage-dependent expression pattern in the mouse gonad development and represses expression of Ad4BP/SF-1. Mech Dev 102: 135-144
-
(2001)
Mech Dev
, vol.102
, pp. 135-144
-
-
Tamura, M.1
-
53
-
-
4544227743
-
Disrupted gonadogenesis and male-to-female sex reversal in Pod1 knockout mice
-
Cui S et al. (2004) Disrupted gonadogenesis and male-to-female sex reversal in Pod1 knockout mice. Development 131: 4095-4105
-
(2004)
Development
, vol.131
, pp. 4095-4105
-
-
Cui, S.1
-
54
-
-
0035131812
-
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus/inversus syndrome
-
Crisponi L et al. (2001) The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus/inversus syndrome. Nat Genet 27: 159-166
-
(2001)
Nat Genet
, vol.27
, pp. 159-166
-
-
Crisponi, L.1
-
55
-
-
1842665188
-
FOXL2 inactivation by a translocation 171 kb away: Analysis of 500 kb of chromosome 3 for candidate long-range regulatory sequences
-
Crisponi L et al. (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
-
(2004)
Genomics
, vol.83
, pp. 757-764
-
-
Crisponi, L.1
-
56
-
-
2942750361
-
Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development
-
Uda M et al. (2004) Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development. Hum Mol Genet 13: 1171-1181
-
(2004)
Hum Mol Genet
, vol.13
, pp. 1171-1181
-
-
Uda, M.1
-
57
-
-
1342327343
-
The murine winged-helix transcription factor Foxl2 is required for granulosa cell differentiation and ovary maintenance
-
Schmidt D et al. (2004) The murine winged-helix transcription factor Foxl2 is required for granulosa cell differentiation and ovary maintenance. Development 131: 933-942
-
(2004)
Development
, vol.131
, pp. 933-942
-
-
Schmidt, D.1
-
58
-
-
0035733723
-
A 11.7-kb deletion triggers intersexuality and polledness in goats
-
Pailhoux E et al. (2001) A 11.7-kb deletion triggers intersexuality and polledness in goats. Nat Genet 29: 453-458
-
(2001)
Nat Genet
, vol.29
, pp. 453-458
-
-
Pailhoux, E.1
-
59
-
-
18844437228
-
Ovarian-specific expression of a new gene regulated by the goat PIS region and transcribed by a FOXL2 bidirectional promoter
-
Pannetier M et al. (2005) Ovarian-specific expression of a new gene regulated by the goat PIS region and transcribed by a FOXL2 bidirectional promoter. Genomics 85: 715-726
-
(2005)
Genomics
, vol.85
, pp. 715-726
-
-
Pannetier, M.1
-
60
-
-
0036234843
-
Ontogenesis of female-to-male sex-reversal in XX polled goats
-
Pailhoux E et al. (2002) Ontogenesis of female-to-male sex-reversal in XX polled goats. Dev Dyn 224: 39-50
-
(2002)
Dev Dyn
, vol.224
, pp. 39-50
-
-
Pailhoux, E.1
-
61
-
-
0033521967
-
Female development in mammals is regulated by Wnt-4 signalling
-
Vainio S et al. (1999) Female development in mammals is regulated by Wnt-4 signalling. Nature 397: 405-409
-
(1999)
Nature
, vol.397
, pp. 405-409
-
-
Vainio, S.1
-
62
-
-
0041508536
-
Endothelial and steroidogenic cell migration are regulated by WNT4 in the developing mammalian gonad
-
Jeays-Ward C et al. (2003) Endothelial and steroidogenic cell migration are regulated by WNT4 in the developing mammalian gonad. Development 130: 3663-3670
-
(2003)
Development
, vol.130
, pp. 3663-3670
-
-
Jeays-Ward, C.1
-
63
-
-
4143139955
-
A WNT4 mutation associated with müllerian duct regression and virilization in a 46,XX woman
-
Biason-Lauber A et al. (2004) A WNT4 mutation associated with müllerian duct regression and virilization in a 46,XX woman. N Engl J Med 351: 792-798
-
(2004)
N Engl J Med
, vol.351
, pp. 792-798
-
-
Biason-Lauber, A.1
-
64
-
-
10044235047
-
Wnt4 is required for proper male as well as female sexual development
-
Jeays-Ward C et al. (2004) Wnt4 is required for proper male as well as female sexual development. Dev Biol 276: 431-440
-
(2004)
Dev Biol
, vol.276
, pp. 431-440
-
-
Jeays-Ward, C.1
-
65
-
-
0035002512
-
Up-regulation of WNT-4 signaling and dosage-sensitive sex reversal in humans
-
Jordan BK et al. (2001) Up-regulation of WNT-4 signaling and dosage-sensitive sex reversal in humans. Am J Hum Genet 68: 1102-1109
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1102-1109
-
-
Jordan, B.K.1
-
66
-
-
0141591505
-
Wnt4 overexpression disrupts normal testicular vasculature and inhibits testosterone synthesis by repressing steroidogenic factor 1/b-catenin synergy
-
Jordan BK et al. (2003) Wnt4 overexpression disrupts normal testicular vasculature and inhibits testosterone synthesis by repressing steroidogenic factor 1/b-catenin synergy. Proc Natl Acad Sci USA 100: 10866-10871
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 10866-10871
-
-
Jordan, B.K.1
-
67
-
-
2442715158
-
Follistatin operates downstream of Wnt4 in mammalian ovary organogenesis
-
Yao HH et al. (2004) Follistatin operates downstream of Wnt4 in mammalian ovary organogenesis. Dev Dyn 230: 210-215
-
(2004)
Dev Dyn
, vol.230
, pp. 210-215
-
-
Yao, H.H.1
-
68
-
-
0034977110
-
Absence of mutations involving the LIM homeobox domain gene LHX9 in 46,XY gonadal agenesis and dysgenesis
-
Ottolenghi C et al. (2001) Absence of mutations involving the LIM homeobox domain gene LHX9 in 46,XY gonadal agenesis and dysgenesis. J Clin Endocrinol Metab 86: 2465-2469
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 2465-2469
-
-
Ottolenghi, C.1
|