-
1
-
-
63449129199
-
Programme de Recherches sur les Aplasies Müllériennes. Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome
-
Morcel K., Camborieux L., and Guerrier D. Programme de Recherches sur les Aplasies Müllériennes. Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome. Orphanet J Rare Dis 14 (2007) 2-13
-
(2007)
Orphanet J Rare Dis
, vol.14
, pp. 2-13
-
-
Morcel, K.1
Camborieux, L.2
Guerrier, D.3
-
2
-
-
33845599605
-
WNT4 deficiency-a 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., and Schoenle E.J. WNT4 deficiency-a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report. Hum Reprod 22 (2007) 224-229
-
(2007)
Hum Reprod
, vol.22
, pp. 224-229
-
-
Biason-Lauber, A.1
De Filippo, G.2
Konrad, D.3
Scarano, G.4
Nazzaro, A.5
Schoenle, E.J.6
-
3
-
-
33847019563
-
Multiplicity of the interactions of Wnt proteins and their receptors
-
Kikuchi A., Yamamoto H., and Kishida S. Multiplicity of the interactions of Wnt proteins and their receptors. Cell Signal 19 (2007) 659-671
-
(2007)
Cell Signal
, vol.19
, pp. 659-671
-
-
Kikuchi, A.1
Yamamoto, H.2
Kishida, S.3
-
4
-
-
0033521967
-
Female development in mammals is regulated by Wnt-4 signaling
-
Vainio S., Heikkila M., Kispert A., Chin N., and McMahon A.P. Female development in mammals is regulated by Wnt-4 signaling. Nature 397 (1999) 405-409
-
(1999)
Nature
, vol.397
, pp. 405-409
-
-
Vainio, S.1
Heikkila, M.2
Kispert, A.3
Chin, N.4
McMahon, A.P.5
-
5
-
-
4143139955
-
A WNT4 mutation associated with müllerian-duct regression and virilization in a 46,XX woman
-
Biason-Lauber A., Konrad D., Navratil F., and Schoenle E.J. A WNT4 mutation associated with müllerian-duct regression and virilization in a 46,XX woman. N Engl J Med 351 (2004) 792-798
-
(2004)
N Engl J Med
, vol.351
, pp. 792-798
-
-
Biason-Lauber, A.1
Konrad, D.2
Navratil, F.3
Schoenle, E.J.4
-
6
-
-
40849126622
-
Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and mullerian duct abnormalities: a French collaborative study
-
Philibert P., Biason-Lauber A., Rouzier R., Pienkowski C., Paris F., Konrad D., et al. Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and mullerian duct abnormalities: a French collaborative study. J Clin Endocrinol Metab 93 (2008) 895-900
-
(2008)
J Clin Endocrinol Metab
, vol.93
, pp. 895-900
-
-
Philibert, P.1
Biason-Lauber, A.2
Rouzier, R.3
Pienkowski, C.4
Paris, F.5
Konrad, D.6
-
7
-
-
9644281006
-
Abnormal gene expression profiles in human ovaries from polycystic ovary syndrome patients
-
Jansen E., Laven J.S., Dommerholt H.B., Polman J., van Rijt C., van den Hurk C., et al. Abnormal gene expression profiles in human ovaries from polycystic ovary syndrome patients. Mol Endocrinol 18 (2004) 3050-3063
-
(2004)
Mol Endocrinol
, vol.18
, pp. 3050-3063
-
-
Jansen, E.1
Laven, J.S.2
Dommerholt, H.B.3
Polman, J.4
van Rijt, C.5
van den Hurk, C.6
-
8
-
-
2542557308
-
Wnt5a is required for proper epithelial-mesenchymal interactions in the uterus
-
Mericskay M., Kitajewski J., and Sassoon D. Wnt5a is required for proper epithelial-mesenchymal interactions in the uterus. Development 131 (2004) 2061-2072
-
(2004)
Development
, vol.131
, pp. 2061-2072
-
-
Mericskay, M.1
Kitajewski, J.2
Sassoon, D.3
-
9
-
-
36549025433
-
Wnt5a is required for proper mammary gland development and TGF-beta-mediated inhibition of ductal growth
-
Roarty K., and Serra R. Wnt5a is required for proper mammary gland development and TGF-beta-mediated inhibition of ductal growth. Development 134 (2007) 3929-3939
-
(2007)
Development
, vol.134
, pp. 3929-3939
-
-
Roarty, K.1
Serra, R.2
-
10
-
-
23344437794
-
Exclusion of WNT4 as a major gene in Rokitansky-Küster-Hauser anomaly
-
Clément-Ziza M., Khen N., Gonzales J., Crétolle-Vastel C., Picard J.Y., Tullio-Pelet A., et al. Exclusion of WNT4 as a major gene in Rokitansky-Küster-Hauser anomaly. Am J Med Genet A 137 (2005) 98-99
-
(2005)
Am J Med Genet A
, vol.137
, pp. 98-99
-
-
Clément-Ziza, M.1
Khen, N.2
Gonzales, J.3
Crétolle-Vastel, C.4
Picard, J.Y.5
Tullio-Pelet, A.6
-
11
-
-
51449120560
-
Molecular analysis of the WNT4 gene in 6 patients with Mayer-Rokitansky-Küster-Hauser syndrome
-
Drummond J., Reis F., Boson W., Silveira L., Bicalho M., and De Marco L. Molecular analysis of the WNT4 gene in 6 patients with Mayer-Rokitansky-Küster-Hauser syndrome. Fertil Steril 90 (2008) 857-859
-
(2008)
Fertil Steril
, vol.90
, pp. 857-859
-
-
Drummond, J.1
Reis, F.2
Boson, W.3
Silveira, L.4
Bicalho, M.5
De Marco, L.6
-
12
-
-
0031791874
-
Fetal exposure to DES results in de-regulation of Wnt7a during uterine morphogenesis
-
Miller C., Degenhardt K., and Sassoon D.A. Fetal exposure to DES results in de-regulation of Wnt7a during uterine morphogenesis. Nat Genet 20 (1998) 228-230
-
(1998)
Nat Genet
, vol.20
, pp. 228-230
-
-
Miller, C.1
Degenhardt, K.2
Sassoon, D.A.3
-
13
-
-
33746555937
-
Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome
-
Woods C.G., Stricker S., Seemann P., Stern R., Cox J., Sherridan E., et al. Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome. Am J Hum Genet 79 (2006) 402-408
-
(2006)
Am J Hum Genet
, vol.79
, pp. 402-408
-
-
Woods, C.G.1
Stricker, S.2
Seemann, P.3
Stern, R.4
Cox, J.5
Sherridan, E.6
-
14
-
-
0032531820
-
Sexually dimorphic development of the mammalian reproductive tract requires Wnt-7a
-
Parr B.A., and McMahon A.P. Sexually dimorphic development of the mammalian reproductive tract requires Wnt-7a. Nature 395 (1998) 707-710
-
(1998)
Nature
, vol.395
, pp. 707-710
-
-
Parr, B.A.1
McMahon, A.P.2
-
16
-
-
0031690260
-
Wnt-7a maintains appropriate uterine patterning during the development of the mouse female reproductive tract
-
Miller C., and Sassoon D.A. Wnt-7a maintains appropriate uterine patterning during the development of the mouse female reproductive tract. Development 125 (1998) 3201-3211
-
(1998)
Development
, vol.125
, pp. 3201-3211
-
-
Miller, C.1
Sassoon, D.A.2
-
17
-
-
22944463010
-
Wnt9b plays a central role in the regulation of mesenchymal to epithelial transitions underlying organogenesis of the mammalian urogenital system
-
Carroll T.J., Park J.S., Hayashi S., Majumdar A., and McMahon A.P. Wnt9b plays a central role in the regulation of mesenchymal to epithelial transitions underlying organogenesis of the mammalian urogenital system. Dev Cell 9 (2005) 283-292
-
(2005)
Dev Cell
, vol.9
, pp. 283-292
-
-
Carroll, T.J.1
Park, J.S.2
Hayashi, S.3
Majumdar, A.4
McMahon, A.P.5
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