Detalhe da pesquisa
1.
Role of epigenetic m6 A RNA methylation in vascular development: mettl3 regulates vascular development through PHLPP2/mTOR-AKT signaling.
FASEB J
; 35(5): e21465, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33788967
2.
Long noncoding RNA ANRIL regulates endothelial cell activities associated with coronary artery disease by up-regulating CLIP1, EZR, and LYVE1 genes.
J Biol Chem
; 294(11): 3881-3898, 2019 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30655286
3.
Splice variants of lncRNA RNA ANRIL exert opposing effects on endothelial cell activities associated with coronary artery disease.
RNA Biol
; 17(10): 1391-1401, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32602777
4.
Analysis of causal effect of APOA5 variants on premature coronary artery disease.
Ann Hum Genet
; 82(6): 437-447, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30024021
5.
Knockout of ush2a gene in zebrafish causes hearing impairment and late onset rod-cone dystrophy.
Hum Genet
; 137(10): 779-794, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30242501
6.
Whole exome sequencing identifies a novel NRL mutation in a Chinese family with autosomal dominant retinitis pigmentosa.
Mol Vis
; 22: 234-42, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27081294
7.
Correction: Long noncoding RNA ANRIL regulates endothelial cell activities associated with coronary artery disease by up-regulating CLIP1, EZR, and LYVE1 genes.
J Biol Chem
; 294(22): 8715, 2019 May 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-31152096
8.
Comparative gene expression analysis between coronary arteries and internal mammary arteries identifies a role for the TES gene in endothelial cell functions relevant to coronary artery disease.
Hum Mol Genet
; 21(6): 1364-73, 2012 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22156939
9.
HSF4 is involved in DNA damage repair through regulation of Rad51.
Biochim Biophys Acta
; 1822(8): 1308-15, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22587838
10.
Statistical and Functional Studies Identify Epistasis of Cardiovascular Risk Genomic Variants From Genome-Wide Association Studies.
J Am Heart Assoc
; 9(7): e014146, 2020 04 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32237974
11.
ADTRP regulates TFPI expression via transcription factor POU1F1 involved in coronary artery disease.
Gene
; 753: 144805, 2020 Aug 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-32445923
12.
Microarray analysis of cardiovascular diseases.
Methods Mol Med
; 129: 1-13, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-17085801
13.
Identification of three mutations in the MVK gene in six patients associated with disseminated superficial actinic porokeratosis.
Clin Chim Acta
; 454: 124-9, 2016 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26794421
14.
pVHL interacts with Ceramide kinase like (CERKL) protein and ubiquitinates it for oxygen dependent proteasomal degradation.
Cell Signal
; 27(11): 2314-23, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26296657
15.
Proteomic approach to coronary atherosclerosis shows ferritin light chain as a significant marker: evidence consistent with iron hypothesis in atherosclerosis.
Physiol Genomics
; 13(1): 25-30, 2003 Mar 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-12644631
16.
Identification of new genes differentially expressed in coronary artery disease by expression profiling.
Physiol Genomics
; 15(1): 65-74, 2003 Sep 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-12902549
17.
A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene.
Circ Cardiovasc Genet
; 7(4): 514-20, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24867879
18.
Mutations in ABCB6 cause dyschromatosis universalis hereditaria.
J Invest Dermatol
; 133(9): 2221-8, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23519333
19.
Mutation p.Leu354Pro in EDA causes severe hypohidrotic ectodermal dysplasia in a Chinese family.
Gene
; 491(2): 246-50, 2012 Jan 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-22008666
20.
A novel SCN1A missense mutation causes generalized epilepsy with febrile seizures plus in a Chinese family.
Neurosci Lett
; 503(1): 27-30, 2011 Sep 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-21843600