-
1
-
-
0000009634
-
Problems of fetal endocrinology: The gonadal and hypophyseal hormones
-
Jost A. Problems of fetal endocrinology: the gonadal and hypophyseal hormones. Recent Prog Horm Res. 1953;8:379-418.
-
(1953)
Recent Prog Horm Res
, vol.8
, pp. 379-418
-
-
Jost, A.1
-
2
-
-
84873276494
-
Persistent Müllerian duct syndrome: Lessons learned from managing a series of eight patients over a 10-year period and review of literature regarding malignant risk from the Mullerian remnants
-
Epub 2012 Apr 30
-
Farikullah J, Ehtisham S, Nappo S, Patel L, Hennayake S. Persistent Müllerian duct syndrome: lessons learned from managing a series of eight patients over a 10-year period and review of literature regarding malignant risk from the Mullerian remnants. BJU Int. 2012; Epub 2012 Apr 30.
-
(2012)
BJU Int
-
-
Farikullah, J.1
Ehtisham, S.2
Nappo, S.3
Patel, L.4
Hennayake, S.5
-
3
-
-
84872369598
-
Síndrome de Persistência dos Ductos de Müller
-
In: Guerra ATM, Guerra Júnior G, editors, 2. ed. Rubio
-
Rey R, Picard JY, Josso N. Síndrome de Persistência dos Ductos de Müller. In: Guerra ATM, Guerra Júnior G, editors. Menino ou Menina? Distúrbios da Diferenciação do Sexo. 2. ed. Rubio; 2010. p. 279-95.
-
(2010)
Menino ou Menina? Distúrbios da Diferenciação do Sexo
, pp. 279-295
-
-
Rey, R.1
Picard, J.Y.2
Josso, N.3
-
4
-
-
0028116696
-
Failure of gubernacular development in the persistent Müllerian duct syndrome allows herniation of the testes
-
Hutson JM, Davidson PM, Reece LA, Baker M, Zhou B. Failure of gubernacular development in the persistent Müllerian duct syndrome allows herniation of the testes. Pediatr Surg Int. 1994;9:544-6.
-
(1994)
Pediatr Surg Int
, vol.9
, pp. 544-546
-
-
Hutson, J.M.1
Davidson, P.M.2
Reece, L.A.3
Baker, M.4
Zhou, B.5
-
5
-
-
84863322633
-
Mutations of the AMH Type II receptor in two extended families with persistent Müllerian duct syndrome: Lack of phenotype/genotype correlation
-
Abduljabbar M, Taheini K, Picard JY, Cate RL, Josso N. Mutations of the AMH Type II receptor in two extended families with persistent Müllerian duct syndrome: lack of phenotype/genotype correlation. Horm Res Paediatr. 2012;77(5):291-7.
-
(2012)
Horm Res Paediatr
, vol.77
, Issue.5
, pp. 291-297
-
-
Abduljabbar, M.1
Taheini, K.2
Picard, J.Y.3
Cate, R.L.4
Josso, N.5
-
6
-
-
0028972867
-
Insensitivity to anti-Müllerian hormone due to a mutation in the human anti-Müllerian hormone receptor
-
Imbeaud S, Faure E, Lamarre I, Mattei MG, di Clemente N, Tizard R, et al. Insensitivity to anti-Müllerian hormone due to a mutation in the human anti-Müllerian hormone receptor. Nat Genet. 1995;11(4):382-8.
-
(1995)
Nat Genet
, vol.11
, Issue.4
, pp. 382-388
-
-
Imbeaud, S.1
Faure, E.2
Lamarre, I.3
Mattei, M.G.4
Di Clemente, N.5
Tizard, R.6
-
7
-
-
0022499726
-
Isolation of the bovine and human genes for Müllerian inhibiting substance and expression of the human gene in animal cells
-
Cate RL, Mattaliano RJ, Hession C, Tizard R, Farber NM, Cheung A, et al. Isolation of the bovine and human genes for Müllerian inhibiting substance and expression of the human gene in animal cells. Cell. 1986;45(5):685-98.
-
(1986)
Cell
, vol.45
, Issue.5
, pp. 685-698
-
-
Cate, R.L.1
Mattaliano, R.J.2
Hession, C.3
Tizard, R.4
Farber, N.M.5
Cheung, A.6
-
8
-
-
0033176536
-
TGF-beta family members and gonadal development
-
Josso N, di Clemente N. TGF-beta family members and gonadal development. Trends Endocrinol Metab. 1999;10(6):216-22.
-
(1999)
Trends Endocrinol Metab
, vol.10
, Issue.6
, pp. 216-222
-
-
Josso, N.1
Di Clemente, N.2
-
9
-
-
21244498141
-
AMH and AMH receptor defects in persistent Müllerian duct syndrome
-
Josso N, Belville C, di Clemente N, Picard JY. AMH and AMH receptor defects in persistent Müllerian duct syndrome. Hum Reprod Update. 2005;11(4):351-6.
-
(2005)
Hum Reprod Update
, vol.11
, Issue.4
, pp. 351-356
-
-
Josso, N.1
Belville, C.2
Di Clemente, N.3
Picard, J.Y.4
-
10
-
-
54449099496
-
Three novel AMH gene mutations in a patient with persistent Müllerian duct syndrome and normal AMH serum dosage
-
Menabo S, Balsamo A, Nicoletti A, Gennari M, Pirazzoli P, Cicognani A, et al. Three novel AMH gene mutations in a patient with persistent Müllerian duct syndrome and normal AMH serum dosage. Horm Res. 2008;70(2):124-8.
-
(2008)
Horm Res
, vol.70
, Issue.2
, pp. 124-128
-
-
Menabo, S.1
Balsamo, A.2
Nicoletti, A.3
Gennari, M.4
Pirazzoli, P.5
Cicognani, A.6
-
11
-
-
84870834403
-
A novel AMH missense mutation in a patient with persistent Müllerian duct syndrome
-
Epub 2012 Jul 11
-
van der Zwan YG, Bruggenwirth HT, Drop SL, Wolffenbuttel KP, Madern GC, Looijenga LH, et al. A novel AMH missense mutation in a patient with persistent Müllerian duct syndrome. Sex Dev. 2012; Epub 2012 Jul 11.
-
(2012)
Sex Dev
-
-
van der Zwan, Y.G.1
Bruggenwirth, H.T.2
Drop, S.L.3
Wolffenbuttel, K.P.4
Madern, G.C.5
Looijenga, L.H.6
-
12
-
-
0027953410
-
A novel member of the transmembrane serine/threonine kinase receptor family is specifically expressed in the gonads and in mesenchymal cells adjacent to the Müllerian duct
-
Baarends WM, van Helmond MJ, Post M, van der Schoot PJ, Hoogerbrugge JW, de Winter JP, et al. A novel member of the transmembrane serine/threonine kinase receptor family is specifically expressed in the gonads and in mesenchymal cells adjacent to the Müllerian duct. Development. 1994;120(1):189-97.
-
(1994)
Development
, vol.120
, Issue.1
, pp. 189-197
-
-
Baarends, W.M.1
van Helmond, M.J.2
Post, M.3
van der Schoot, P.J.4
Hoogerbrugge, J.W.5
de Winter, J.P.6
-
13
-
-
0028106201
-
Cloning, expression, and alternative splicing of the receptor for anti-Müllerian hormone
-
di Clemente N, Wilson C, Faure E, Boussin L, Carmillo P, Tizard R, et al. Cloning, expression, and alternative splicing of the receptor for anti-Müllerian hormone. Mol Endocrinol. 1994;8(8):1006-20.
-
(1994)
Mol Endocrinol
, vol.8
, Issue.8
, pp. 1006-1020
-
-
Di Clemente, N.1
Wilson, C.2
Faure, E.3
Boussin, L.4
Carmillo, P.5
Tizard, R.6
-
14
-
-
68049088937
-
Natural mutations of the anti-Müllerian hormone type II receptor found in persistent Müllerian duct syndrome affect ligand binding, signal transduction and cellular transport
-
Belville C, Marechal JD, Pennetier S, Carmillo P, Masgrau L, Messika-Zeitoun L, et al. Natural mutations of the anti-Müllerian hormone type II receptor found in persistent Müllerian duct syndrome affect ligand binding, signal transduction and cellular transport. Hum Mol Genet. 2009;18(16):3002-13.
-
(2009)
Hum Mol Genet
, vol.18
, Issue.16
, pp. 3002-3013
-
-
Belville, C.1
Marechal, J.D.2
Pennetier, S.3
Carmillo, P.4
Masgrau, L.5
Messika-Zeitoun, L.6
-
15
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 1988;16(3):1215.
-
(1988)
Nucleic Acids Res
, vol.16
, Issue.3
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
16
-
-
0028118823
-
Molecular genetics of the persistent Müllerian duct syndrome: A study of 19 families
-
Imbeaud S, Carre-Eusebe D, Rey R, Belville C, Josso N, Picard JY. Molecular genetics of the persistent Müllerian duct syndrome: a study of 19 families. Hum Mol Genet. 1994;3(1):125-31.
-
(1994)
Hum Mol Genet
, vol.3
, Issue.1
, pp. 125-131
-
-
Imbeaud, S.1
Carre-Eusebe, D.2
Rey, R.3
Belville, C.4
Josso, N.5
Picard, J.Y.6
-
17
-
-
33745751952
-
Testicular anti-Müllerian hormone: History, genetics, regulation and clinical applications
-
Josso N, Picard JY, Rey R, di Clemente N. Testicular anti-Müllerian hormone: history, genetics, regulation and clinical applications. Pediatr Endocrinol Rev. 2006;3(4):347-58.
-
(2006)
Pediatr Endocrinol Rev
, vol.3
, Issue.4
, pp. 347-358
-
-
Josso, N.1
Picard, J.Y.2
Rey, R.3
Di Clemente, N.4
-
18
-
-
27744583396
-
Low risk of impaired testicular Sertoli and Leydig cell functions in boys with isolated hypospadias
-
Rey RA, Codner E, Iniguez G, Bedecarras P, Trigo R, Okuma C, et al. Low risk of impaired testicular Sertoli and Leydig cell functions in boys with isolated hypospadias. J Clin Endocrinol Metab. 2005;90(11):6035-40.
-
(2005)
J Clin Endocrinol Metab
, vol.90
, Issue.11
, pp. 6035-6040
-
-
Rey, R.A.1
Codner, E.2
Iniguez, G.3
Bedecarras, P.4
Trigo, R.5
Okuma, C.6
-
19
-
-
0029811588
-
A 27 base-pair deletion of the anti-Müllerian type II receptor gene is the most common cause of the persistent Müllerian duct syndrome
-
Imbeaud S, Belville C, Messika-Zeitoun L, Rey R, di Clemente N, Josso N, et al. A 27 base-pair deletion of the anti-Müllerian type II receptor gene is the most common cause of the persistent Müllerian duct syndrome. Hum Mol Genet. 1996;5(9):1269-77.
-
(1996)
Hum Mol Genet
, vol.5
, Issue.9
, pp. 1269-1277
-
-
Imbeaud, S.1
Belville, C.2
Messika-Zeitoun, L.3
Rey, R.4
Di Clemente, N.5
Josso, N.6
|