-
1
-
-
34248145546
-
Premature ovarian failure
-
10.1186/1750-1172-1-9, 1502130, 16722528
-
Beck-Peccoz P, Persani L. Premature ovarian failure. Orphanet J Rare Dis 2006, 1:9. 10.1186/1750-1172-1-9, 1502130, 16722528.
-
(2006)
Orphanet J Rare Dis
, vol.1
, pp. 9
-
-
Beck-Peccoz, P.1
Persani, L.2
-
2
-
-
55749098336
-
Recent developments in identifying genetic determinants of premature ovarian failure
-
10.1159/000152039, 18987497
-
Skillern A, Rajkovic A. Recent developments in identifying genetic determinants of premature ovarian failure. Sex Dev 2008, 2(4-5):228-243. 10.1159/000152039, 18987497.
-
(2008)
Sex Dev
, vol.2
, Issue.4-5
, pp. 228-243
-
-
Skillern, A.1
Rajkovic, A.2
-
3
-
-
0028588919
-
Epithelial transformation of metanephric mesenchyme in the developing kidney regulated by Wnt-4
-
10.1038/372679a0, 7990960
-
Stark K, Vainio S, Vassileva G, McMahon AP. Epithelial transformation of metanephric mesenchyme in the developing kidney regulated by Wnt-4. Nature 1994, 372(6507):679-683. 10.1038/372679a0, 7990960.
-
(1994)
Nature
, vol.372
, Issue.6507
, pp. 679-683
-
-
Stark, K.1
Vainio, S.2
Vassileva, G.3
McMahon, A.P.4
-
4
-
-
0036827930
-
Wnt-4 deficiency alters mouse adrenal cortex function, reducing aldosterone production
-
10.1210/en.2002-220275, 12399432
-
Heikkila M, Peltoketo H, Leppaluoto J, Ilves M, Vuolteenaho O, Vainio S. Wnt-4 deficiency alters mouse adrenal cortex function, reducing aldosterone production. Endocrinology 2002, 143(11):4358-4365. 10.1210/en.2002-220275, 12399432.
-
(2002)
Endocrinology
, vol.143
, Issue.11
, pp. 4358-4365
-
-
Heikkila, M.1
Peltoketo, H.2
Leppaluoto, J.3
Ilves, M.4
Vuolteenaho, O.5
Vainio, S.6
-
5
-
-
0033521967
-
Female development in mammals is regulated by Wnt-4 signalling
-
10.1038/17068, 9989404
-
Vainio S, Heikkila M, Kispert A, Chin N, McMahon AP. Female development in mammals is regulated by Wnt-4 signalling. Nature 1999, 397(6718):405-409. 10.1038/17068, 9989404.
-
(1999)
Nature
, vol.397
, Issue.6718
, pp. 405-409
-
-
Vainio, S.1
Heikkila, M.2
Kispert, A.3
Chin, N.4
McMahon, A.P.5
-
6
-
-
23844544781
-
The partial female to male sex reversal in Wnt-4-deficient females involves induced expression of testosterone biosynthetic genes and testosterone production, and depends on androgen action
-
10.1210/en.2005-0463, 15932923
-
Heikkila M, Prunskaite R, Naillat F, Itaranta P, Vuoristo J, Leppaluoto J, Peltoketo H, Vainio S. The partial female to male sex reversal in Wnt-4-deficient females involves induced expression of testosterone biosynthetic genes and testosterone production, and depends on androgen action. Endocrinology 2005, 146(9):4016-4023. 10.1210/en.2005-0463, 15932923.
-
(2005)
Endocrinology
, vol.146
, Issue.9
, pp. 4016-4023
-
-
Heikkila, M.1
Prunskaite, R.2
Naillat, F.3
Itaranta, P.4
Vuoristo, J.5
Leppaluoto, J.6
Peltoketo, H.7
Vainio, S.8
-
7
-
-
35748965278
-
Loss of Wnt4 and Foxl2 leads to female-to-male sex reversal extending to germ cells
-
10.1093/hmg/ddm235, 17728319
-
Ottolenghi C, Pelosi E, Tran J, Colombino M, Douglass E, Nedorezov T, Cao A, Forabosco A, Schlessinger D. Loss of Wnt4 and Foxl2 leads to female-to-male sex reversal extending to germ cells. Hum Mol Genet 2007, 16(23):2795-2804. 10.1093/hmg/ddm235, 17728319.
-
(2007)
Hum Mol Genet
, vol.16
, Issue.23
, pp. 2795-2804
-
-
Ottolenghi, C.1
Pelosi, E.2
Tran, J.3
Colombino, M.4
Douglass, E.5
Nedorezov, T.6
Cao, A.7
Forabosco, A.8
Schlessinger, D.9
-
8
-
-
0035506747
-
Wnts and the female reproductive system
-
10.1002/jez.1112, 11748610
-
Heikkila M, Peltoketo H, Vainio S. Wnts and the female reproductive system. J Exp Zool 2001, 290(6):616-623. 10.1002/jez.1112, 11748610.
-
(2001)
J Exp Zool
, vol.290
, Issue.6
, pp. 616-623
-
-
Heikkila, M.1
Peltoketo, H.2
Vainio, S.3
-
9
-
-
2442715158
-
Follistatin operates downstream of Wnt4 in mammalian ovary organogenesis
-
10.1002/dvdy.20042, 15162500
-
Yao HH, Matzuk MM, Jorgez CJ, Menke DB, Page DC, Swain A, Capel B. Follistatin operates downstream of Wnt4 in mammalian ovary organogenesis. Dev Dyn 2004, 230(2):210-215. 10.1002/dvdy.20042, 15162500.
-
(2004)
Dev Dyn
, vol.230
, Issue.2
, pp. 210-215
-
-
Yao, H.H.1
Matzuk, M.M.2
Jorgez, C.J.3
Menke, D.B.4
Page, D.C.5
Swain, A.6
Capel, B.7
-
10
-
-
74749109906
-
WNT4 is expressed in human fetal and adult ovaries and its signaling contributes to ovarian cell survival
-
Jaaskelainen M, Prunskaite-Hyyrylainen R, Naillat F, Parviainen H, Anttonen M, Heikinheimo M, Liakka A, Ola R, Vainio S, Vaskivuo TE, et al. WNT4 is expressed in human fetal and adult ovaries and its signaling contributes to ovarian cell survival. Mol Cell Endocrinol 317(1-2):106-111.
-
Mol Cell Endocrinol
, vol.317
, Issue.1-2
, pp. 106-111
-
-
Jaaskelainen, M.1
Prunskaite-Hyyrylainen, R.2
Naillat, F.3
Parviainen, H.4
Anttonen, M.5
Heikinheimo, M.6
Liakka, A.7
Ola, R.8
Vainio, S.9
Vaskivuo, T.E.10
-
11
-
-
2642526849
-
Increased expression of the FIGLA transcription factor is associated with primordial follicle formation in the human fetal ovary
-
10.1093/molehr/gah056, 15044608
-
Bayne RA, Martins da Silva SJ, Anderson RA. Increased expression of the FIGLA transcription factor is associated with primordial follicle formation in the human fetal ovary. Mol Hum Reprod 2004, 10(6):373-381. 10.1093/molehr/gah056, 15044608.
-
(2004)
Mol Hum Reprod
, vol.10
, Issue.6
, pp. 373-381
-
-
Bayne, R.A.1
Martins da Silva, S.J.2
Anderson, R.A.3
-
12
-
-
34548288054
-
NOBOX homeobox mutation causes premature ovarian failure
-
10.1086/519496, 1950834, 17701902
-
Qin Y, Choi Y, Zhao H, Simpson JL, Chen ZJ, Rajkovic A. NOBOX homeobox mutation causes premature ovarian failure. Am J Hum Genet 2007, 81(3):576-581. 10.1086/519496, 1950834, 17701902.
-
(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
-
13
-
-
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, Schoenle E, Sultan C. 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 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
Pienkowski, C.4
Paris, F.5
Konrad, D.6
Schoenle, E.7
Sultan, C.8
-
14
-
-
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, Schoenle EJ. WNT4 deficiency--a 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
-
15
-
-
38749129178
-
SERKAL syndrome: an autosomal-recessive disorder caused by a loss-of-function mutation in WNT4
-
10.1016/j.ajhg.2007.08.005, 2253972, 18179883
-
Mandel H, Shemer R, Borochowitz ZU, Okopnik M, Knopf C, Indelman M, Drugan A, Tiosano D, Gershoni-Baruch R, Choder M, 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. 10.1016/j.ajhg.2007.08.005, 2253972, 18179883.
-
(2008)
Am J Hum Genet
, vol.82
, Issue.1
, pp. 39-47
-
-
Mandel, H.1
Shemer, R.2
Borochowitz, Z.U.3
Okopnik, M.4
Knopf, C.5
Indelman, M.6
Drugan, A.7
Tiosano, D.8
Gershoni-Baruch, R.9
Choder, M.10
|