Detalhe da pesquisa
1.
NR0B1 augments sorafenib resistance in hepatocellular carcinoma through promoting autophagy and inhibiting apoptosis.
Cancer Sci;
115(2): 465-476, 2024 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37991109
2.
A rare mutant of OFD1 gene responsible for Joubert syndrome with significant phenotype variation.
Mol Genet Genomics;
296(1): 33-40, 2021 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32944789
3.
Lipoprotein glomerulopathy induced by ApoE Kyoto mutation in ApoE-deficient mice.
J Transl Med;
19(1): 97, 2021 03 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33663537
4.
Clock1a affects mesoderm development and primitive hematopoiesis by regulating Nodal-Smad3 signaling in the zebrafish embryo.
J Biol Chem;
292(34): 14165-14175, 2017 08 25.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28687631
5.
[Identification and functional analysis of a testis-specific E3 ubiquitin ligase gene Rnf148 in mouse].
Sichuan Da Xue Xue Bao Yi Xue Ban;
45(1): 1-5, 2014 Jan.
Artigo
em Zh
| MEDLINE
| ID: mdl-24527571
6.
NR0B1 suppresses ferroptosis through upregulation of NRF2/c-JUN-CBS signaling pathway in lung cancer cells.
Am J Cancer Res;
13(11): 5174-5196, 2023.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38058844
7.
[Identification and expression analysis of Macaca mulatta piwil4 gene].
Yi Chuan;
33(4): 365-70, 2011 Apr.
Artigo
em Zh
| MEDLINE
| ID: mdl-21482527
8.
CLOCK and BMAL1 stabilize and activate RHOA to promote F-actin formation in cancer cells.
Exp Mol Med;
50(10): 1-15, 2018 10 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30287810
9.
[Clinical characteristics and spastin gene mutation analysis on an autosomal dominant kindred with hereditary spastic paraplegia].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi;
24(2): 224-6, 2007 Apr.
Artigo
em Zh
| MEDLINE
| ID: mdl-17407089
10.
Association of Sst I polymorphism in apolipoprotein C3 gene with hypertriglyceridaemia in coronary atherosclerotic heart disease and type II diabetes mellitus in Chinese population.
Yi Chuan Xue Bao;
32(1): 11-8, 2005 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15715433
11.
Common AZFc structure may possess the optimal spermatogenesis efficiency relative to the rearranged structures mediated by non-allele homologous recombination.
Sci Rep;
5: 10551, 2015 May 22.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26000765
12.
[Construction of recombinant ZNF230/GFP fused plasmids and their expression and cellular localization].
Yi Chuan;
26(4): 451-4, 2004 Jul.
Artigo
em Zh
| MEDLINE
| ID: mdl-15640038
13.
Human RING finger protein ZNF645 is a novel testis-specific E3 ubiquitin ligase.
Asian J Androl;
12(5): 658-66, 2010 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20657603
14.
c.822+126T>G/C: a novel triallelic polymorphism of the TSSK6 gene associated with spermatogenic impairment in a Chinese population.
Asian J Androl;
12(2): 234-9, 2010 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20037600