Detalhe da pesquisa
1.
Genetic Regulation of SMC Gene Expression and Splicing Predict Causal CAD Genes.
Circ Res
; 132(3): 323-338, 2023 02 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36597873
2.
FHL5 Controls Vascular Disease-Associated Gene Programs in Smooth Muscle Cells.
Circ Res
; 132(9): 1144-1161, 2023 04 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37017084
3.
Polygenic Risk Score Associates With Atherosclerotic Plaque Characteristics at Autopsy.
Arterioscler Thromb Vasc Biol
; 44(1): 300-313, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37916415
4.
The HDAC9-associated risk locus promotes coronary artery disease by governing TWIST1.
PLoS Genet
; 18(6): e1010261, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35714152
5.
INKILN is a Novel Long Noncoding RNA Promoting Vascular Smooth Muscle Inflammation via Scaffolding MKL1 and USP10.
Circulation
; 148(1): 47-67, 2023 07 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37199168
6.
Mitochondria-localized AMPK responds to local energetics and contributes to exercise and energetic stress-induced mitophagy.
Proc Natl Acad Sci U S A
; 118(37)2021 09 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-34493662
7.
Cardiovascular utility of single cell RNA-Seq.
Curr Opin Cardiol
; 38(3): 193-200, 2023 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36728943
8.
Clonally expanding smooth muscle cells promote atherosclerosis by escaping efferocytosis and activating the complement cascade.
Proc Natl Acad Sci U S A
; 117(27): 15818-15826, 2020 07 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32541024
9.
Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle Cells.
Circ Res
; 127(12): 1552-1565, 2020 12 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33040646
10.
PCSK6 Is a Key Protease in the Control of Smooth Muscle Cell Function in Vascular Remodeling.
Circ Res
; 126(5): 571-585, 2020 02 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-31893970
11.
APOL1 Genetic Variants Are Associated With Increased Risk of Coronary Atherosclerotic Plaque Rupture in the Black Population.
Arterioscler Thromb Vasc Biol
; 41(7): 2201-2214, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34039022
12.
CD47-blocking antibodies restore phagocytosis and prevent atherosclerosis.
Nature
; 536(7614): 86-90, 2016 08 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27437576
13.
Genetic Regulatory Mechanisms of Smooth Muscle Cells Map to Coronary Artery Disease Risk Loci.
Am J Hum Genet
; 103(3): 377-388, 2018 09 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30146127
14.
Coronary artery disease genes SMAD3 and TCF21 promote opposing interactive genetic programs that regulate smooth muscle cell differentiation and disease risk.
PLoS Genet
; 14(10): e1007681, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30307970
15.
Functional regulatory mechanism of smooth muscle cell-restricted LMOD1 coronary artery disease locus.
PLoS Genet
; 14(11): e1007755, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30444878
16.
Inducible Pluripotent Stem Cell-Derived Cardiomyocytes Reveal Aberrant Extracellular Regulated Kinase 5 and Mitogen-Activated Protein Kinase Kinase 1/2 Signaling Concomitantly Promote Hypertrophic Cardiomyopathy in RAF1-Associated Noonan Syndrome.
Circulation
; 140(3): 207-224, 2019 07 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-31163979
17.
Genetic Insights Into Smooth Muscle Cell Contributions to Coronary Artery Disease.
Arterioscler Thromb Vasc Biol
; 39(6): 1006-1017, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31043074
18.
TCF21 and the environmental sensor aryl-hydrocarbon receptor cooperate to activate a pro-inflammatory gene expression program in coronary artery smooth muscle cells.
PLoS Genet
; 13(5): e1006750, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28481916
19.
The novel coronary artery disease risk gene JCAD/KIAA1462 promotes endothelial dysfunction and atherosclerosis.
Eur Heart J
; 40(29): 2398-2408, 2019 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31539914
20.
BART: a transcription factor prediction tool with query gene sets or epigenomic profiles.
Bioinformatics
; 34(16): 2867-2869, 2018 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29608647