Detalhe da pesquisa
1.
Deficiency of primate-specific SSX1 induced asthenoteratozoospermia in infertile men and cynomolgus monkey and tree shrew models.
Am J Hum Genet
; 110(3): 516-530, 2023 03 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36796361
2.
Temporal transcriptomic landscape of postnatal mouse ovaries reveals dynamic gene signatures associated with ovarian aging.
Hum Mol Genet
; 30(21): 1941-1954, 2021 10 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-34137841
3.
Haploinsufficiency in non-homologous end joining factor 1 induces ovarian dysfunction in humans and mice.
J Med Genet
; 59(6): 579-588, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33888552
4.
A heterozygous hypomorphic mutation of Fanca causes impaired follicle development and subfertility in female mice.
Mol Genet Genomics
; 296(1): 103-112, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-33025164
5.
Rare variants in FANCA induce premature ovarian insufficiency.
Hum Genet
; 138(11-12): 1227-1236, 2019 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-31535215
6.
Whole exome sequencing identified a rare WT1 loss-of-function variant in a non-syndromic POI patient.
Mol Genet Genomic Med
; 10(1): e1820, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34845858
7.
Rare variants in FANCJ induce premature ovarian insufficiency in humans and mice.
J Genet Genomics
; 51(2): 252-255, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37062450