Detalhe da pesquisa
1.
In vivo versus in silico assessment of potentially pathogenic missense variants in human reproductive genes.
Proc Natl Acad Sci U S A
; 120(30): e2219925120, 2023 07 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37459509
2.
In vivo modeling of metastatic human high-grade serous ovarian cancer in mice.
PLoS Genet
; 16(6): e1008808, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32497036
3.
Variants in GCNA, X-linked germ-cell genome integrity gene, identified in men with primary spermatogenic failure.
Hum Genet
; 140(8): 1169-1182, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-33963445
4.
Familial Infertility (Azoospermia and Cryptozoospermia) in Two Brothers-Carriers of t(1;7) Complex Chromosomal Rearrangement (CCR): Molecular Cytogenetic Analysis.
Int J Mol Sci
; 21(12)2020 Jun 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-32604929
5.
Gene variants identified by whole-exome sequencing in 33 French women with premature ovarian insufficiency.
J Assist Reprod Genet
; 36(1): 39-45, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-30406445
6.
X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.
N Engl J Med
; 372(22): 2097-107, 2015 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-25970010
7.
Reproductive genetics and the aging male.
J Assist Reprod Genet
; 35(6): 933-941, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29524155
8.
Familial deletion of the HOXA gene cluster associated with Hand-Foot-Genital syndrome and phenotypic variability.
Am J Med Genet A
; 173(1): 221-224, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27649277
9.
High quality RNA in semen and sperm: isolation, analysis and potential application in clinical testing.
J Urol
; 193(1): 352-9, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25088949
10.
FISH and array CGH characterization of de novo derivative Y chromosome (Yq duplication and partial Yp deletion) in an azoospermic male.
Reprod Biomed Online
; 31(2): 217-24, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26096031
11.
Effects of Tcte1 knockout on energy chain transportation and spermatogenesis: implications for male infertility.
Hum Reprod Open
; 2024(2): hoae020, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38650655
12.
UBE2B mRNA alterations are associated with severe oligozoospermia in infertile men.
Mol Hum Reprod
; 19(6): 388-94, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23378580
13.
ESX1 gene as a potential candidate responsible for male infertility in nonobstructive azoospermia.
Sci Rep
; 13(1): 16563, 2023 10 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37783880
14.
Genomic study of TEX15 variants: prevalence and allelic heterogeneity in men with spermatogenic failure.
Front Genet
; 14: 1134849, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37234866
15.
Association of mutations in the zona pellucida binding protein 1 (ZPBP1) gene with abnormal sperm head morphology in infertile men.
Mol Hum Reprod
; 18(1): 14-21, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21911476
16.
Whole-genome sequencing identifies new candidate genes for nonobstructive azoospermia.
Andrology
; 10(8): 1605-1624, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36017582
17.
Comprehensive 5-year study of cytogenetic aberrations in 668 infertile men.
J Urol
; 183(4): 1636-42, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20172548
18.
GCNA Preserves Genome Integrity and Fertility Across Species.
Dev Cell
; 52(1): 38-52.e10, 2020 01 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31839537
19.
The impact of alicyclic substituents on the extraction ability of new family of 1,10-phenanthroline-2,9-diamides.
RSC Adv
; 10(44): 26022-26033, 2020 Jul 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35519740
20.
X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family.
Sci Rep
; 8(1): 16280, 2018 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30389958