-
1
-
-
33645793459
-
An SNP in protamine 1: A possible genetic cause of male infertility?
-
Iguchi N, Yang S, Lamb DJ, Hecht NB. An SNP in protamine 1: a possible genetic cause of male infertility? J Med Genet 2006;43:382-4.
-
(2006)
J Med Genet
, vol.43
, pp. 382-384
-
-
Iguchi, N.1
Yang, S.2
Lamb, D.J.3
Hecht, N.B.4
-
2
-
-
34447330695
-
Mutations in the protamine 1 gene associated with male infertility
-
Ravel C, Chantot-Bastaraud S, El Houate B, Berthaut I, Verstraete L, De Larouziere V, Lourenco D, Dumaine A, Antoine JM, Mandelbaum J, Siffroi JP, McElreavey K. Mutations in the protamine 1 gene associated with male infertility. Mol Hum Reprod 2007;13:461-4.
-
(2007)
Mol Hum Reprod
, vol.13
, pp. 461-464
-
-
Ravel, C.1
Chantot-Bastaraud, S.2
El Houate, B.3
Berthaut, I.4
Verstraete, L.5
De Larouziere, V.6
Lourenco, D.7
Dumaine, A.8
Antoine, J.M.9
Mandelbaum, J.10
Siffroi, J.P.11
McElreavey, K.12
-
3
-
-
0035030318
-
Haploinsufficiency of protamine-1 or -2 causes infertility in mice
-
Cho C, Willis WD, Goulding EH, Jung-Ha H, Choi YC, Hecht NB, Eddy EM. Haploinsufficiency of protamine-1 or -2 causes infertility in mice. Nat Genet 2001;28:82-6.
-
(2001)
Nat Genet
, vol.28
, pp. 82-86
-
-
Cho, C.1
Willis, W.D.2
Goulding, E.H.3
Jung-Ha, H.4
Choi, Y.C.5
Hecht, N.B.6
Eddy, E.M.7
-
4
-
-
33750168480
-
Identification of novel polymorphisms in the nuclear protein genes and their relationship with human sperm protamine deficiency and severe male infertility
-
Aoki VW, Christensen GL, Atkins JF, Carrell DT. Identification of novel polymorphisms in the nuclear protein genes and their relationship with human sperm protamine deficiency and severe male infertility. Fertil Steril 2006;86:1416-22.
-
(2006)
Fertil Steril
, vol.86
, pp. 1416-1422
-
-
Aoki, V.W.1
Christensen, G.L.2
Atkins, J.F.3
Carrell, D.T.4
-
5
-
-
8744291701
-
Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility
-
Machev N, Saut N, Longepied G, Terriou P, Navarro A, Levy N, Guichaoua M, Metzler-Guillemain C, Collignon P, Frances A-M, Belougne J, Clemente E, Chiaroni J, Chevillard C, Durand C, Ducourneau A, Pech N, McElreavey K, Mattei M-G, Mitchell MJ. Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility. J Med Genet 2004;41:814-25.
-
(2004)
J Med Genet
, vol.41
, pp. 814-825
-
-
Machev, N.1
Saut, N.2
Longepied, G.3
Terriou, P.4
Navarro, A.5
Levy, N.6
Guichaoua, M.7
Metzler-Guillemain, C.8
Collignon, P.9
Frances, A.-M.10
Belougne, J.11
Clemente, E.12
Chiaroni, J.13
Chevillard, C.14
Durand, C.15
Ducourneau, A.16
Pech, N.17
McElreavey, K.18
Mattei, M.-G.19
Mitchell, M.J.20
more..
-
6
-
-
33751294089
-
Alterations of the USP26 gene in Caucasian men
-
Stouffs K, Lissens W, Tournaye H, Van Steirteghem A, Liebaers I. Alterations of the USP26 gene in Caucasian men. Int J Androl 2006;29:614-17.
-
(2006)
Int J Androl
, vol.29
, pp. 614-617
-
-
Stouffs, K.1
Lissens, W.2
Tournaye, H.3
Van Steirteghem, A.4
Liebaers, I.5
-
7
-
-
33750216646
-
Haplotypes, mutations and male fertility: The story of the testis-specific ubiquitin protease USP26
-
Ravel C, El Houate B, Chantot S, Lourenco D, Dumaine A, Rouba H, Bandyopadahyay A, Radhakrishna U, Das B, Sengupta S, Mandelbaum J, Siffroi JP, McElreavey K. Haplotypes, mutations and male fertility: the story of the testis-specific ubiquitin protease USP26. Mol Hum Reprod 2006;12:643-646.
-
(2006)
Mol Hum Reprod
, vol.12
, pp. 643-646
-
-
Ravel, C.1
El Houate, B.2
Chantot, S.3
Lourenco, D.4
Dumaine, A.5
Rouba, H.6
Bandyopadahyay, A.7
Radhakrishna, U.8
Das, B.9
Sengupta, S.10
Mandelbaum, J.11
Siffroi, J.P.12
McElreavey, K.13
-
8
-
-
8044219672
-
Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: Lack of genotype/phenotype correlations
-
Meyer J, Sudbeck P, Held M, Wagner T, Schmitz ML, Bricarelli FD, Eggermont E, Friedrich U, Haas OA, Kobelt A, Leroy JG, Van Maldergem L, Michel E, Mitulla B, Pfeiffer RA, Schinzel A, Schmidt H, Scherer G. Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: lack of genotype/phenotype correlations. Hum Mol Genet 1997;6:91-8.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 91-98
-
-
Meyer, J.1
Sudbeck, P.2
Held, M.3
Wagner, T.4
Schmitz, M.L.5
Bricarelli, F.D.6
Eggermont, E.7
Friedrich, U.8
Haas, O.A.9
Kobelt, A.10
Leroy, J.G.11
Van Maldergem, L.12
Michel, E.13
Mitulla, B.14
Pfeiffer, R.A.15
Schinzel, A.16
Schmidt, H.17
Scherer, G.18
|