Detalhe da pesquisa
1.
A novel homozygous CYP17A1 mutation causes partial 17 α-hydroxylase/17,20-lyase deficiency in 46,XX: a case report and literature review.
Blood Press
; 32(1): 2195008, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37088984
2.
New Insights into Radio-Resistance Mechanism Revealed by (Phospho)Proteome Analysis of Deinococcus Radiodurans after Heavy Ion Irradiation.
Int J Mol Sci
; 24(19)2023 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37834265
3.
Identification of a novel SDHB c.563 T > C mutation responsible for Paraganglioma syndrome and genetic analysis of the SDHB gene in China: a case report.
BMC Med Genet
; 21(1): 116, 2020 05 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-32460727
4.
Circ_0104652 Promotes the Proliferation and Migration of ox-LDL-Stimulated Vascular Smooth Muscle Cells via Stabilizing ADAMTS7 and HMGB1.
Am J Hypertens
; 37(7): 465-476, 2024 Jun 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38536049
5.
Glp-1 Receptor Agonists Regulate the Progression of Diabetes Mellitus Complicated with Fatty Liver by Down-regulating the Expression of Genes Related to Lipid Metabolism.
Appl Biochem Biotechnol
; 195(8): 5238-5251, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37140780