Detalhe da pesquisa
1.
Identification of the pathogenic effects of missense variants causing PRKAG2 cardiomyopathy.
Arch Biochem Biophys
; 727: 109340, 2022 09 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-35787834
2.
Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry.
Pediatr Blood Cancer
; 66(10): e27923, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31321910
3.
Identification of potential target genes of ROR-alpha in THP1 and HUVEC cell lines.
Exp Cell Res
; 353(1): 6-15, 2017 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28238834
4.
CYP19A1, MIF and ABCA1 genes are targets of the RORα in monocyte and endothelial cells.
Cell Biol Int
; 41(2): 163-176, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-27925372
5.
Ultrastructure of coarse granules in the perivitelline space and association with ovulation induction protocols.
JBRA Assist Reprod
; 2023 Aug 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-37579275
6.
Clinical, Cytogenetic and Molecular Cytogenetic Outcomes of Cell-Free DNA Testing for Rare Chromosomal Anomalies.
Genes (Basel)
; 13(12)2022 12 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36553656
7.
Higher follicular fluid glycodelin levels are negatively correlated with embryonic development in assisted reproduction.
JBRA Assist Reprod
; 22(4): 346-351, 2018 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30264946
8.
Role of simvastatin and RORα activity in the macrophage apoptotic pathway.
Anatol J Cardiol
; 17(5): 362-366, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28613211