Detalles de la búsqueda
1.
Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse.
Am J Hum Genet
; 102(4): 636-648, 2018 04 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-29606301
2.
A Homozygous Ancestral SVA-Insertion-Mediated Deletion in WDR66 Induces Multiple Morphological Abnormalities of the Sperm Flagellum and Male Infertility.
Am J Hum Genet
; 103(3): 400-412, 2018 09 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-30122540
3.
Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWP.
Hum Mol Genet
; 25(5): 878-91, 2016 Mar 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-26721930
4.
Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella.
Hum Reprod
; 33(10): 1973-1984, 2018 10 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30137358
5.
Progesterone-induced Acrosome Exocytosis Requires Sequential Involvement of Calcium-independent Phospholipase A2ß (iPLA2ß) and Group X Secreted Phospholipase A2 (sPLA2).
J Biol Chem
; 291(6): 3076-89, 2016 Feb 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-26655718
6.
Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella.
Am J Hum Genet
; 94(1): 95-104, 2014 Jan 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-24360805
7.
Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations.
Hum Reprod
; 31(12): 2872-2880, 2016 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-27798045
8.
Fine characterisation of a recombination hotspot at the DPY19L2 locus and resolution of the paradoxical excess of duplications over deletions in the general population.
PLoS Genet
; 9(3): e1003363, 2013 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-23555282
9.
Dpy19l2-deficient globozoospermic sperm display altered genome packaging and DNA damage that compromises the initiation of embryo development.
Mol Hum Reprod
; 21(2): 169-85, 2015 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-25354700
10.
Subcellular localization of phospholipase Cζ in human sperm and its absence in DPY19L2-deficient sperm are consistent with its role in oocyte activation.
Mol Hum Reprod
; 21(2): 157-68, 2015 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-25354701
11.
PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice.
EMBO Mol Med
; 10(5)2018 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-29661911
12.
Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human.
Nat Commun
; 9(1): 686, 2018 02 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-29449551
13.
SPINK2 deficiency causes infertility by inducing sperm defects in heterozygotes and azoospermia in homozygotes.
EMBO Mol Med
; 9(8): 1132-1149, 2017 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-28554943
14.
Dynamics of Sun5 localization during spermatogenesis in wild type and Dpy19l2 knock-out mice indicates that Sun5 is not involved in acrosome attachment to the nuclear envelope.
PLoS One
; 10(3): e0118698, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-25775128
15.
Comparative testicular transcriptome of wild type and globozoospermic Dpy19l2 knock out mice.
Basic Clin Androl
; 23: 7, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-25780569
Resultados
1 -
15
de 15
1
Próxima >
>>