Detalhe da pesquisa
1.
Changes in environmental exposures over decades may influence the genetic architecture of severe spermatogenic failure.
Hum Reprod
; 39(3): 612-622, 2024 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38305414
2.
Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility.
Andrology
; 10(7): 1339-1350, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35752927
3.
Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome.
J Pers Med
; 12(6)2022 Jun 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35743717
4.
Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia.
Front Cell Dev Biol
; 10: 1089782, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36589743
5.
Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility.
Commun Biol
; 5(1): 1220, 2022 11 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36357561
6.
Sex-specific association of SELL gene polymorphisms with pattern hair loss in the Thai population: A candidate gene association study and in silico functional characterization.
J Dermatol Sci
; 109(2): 102-105, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36828746