Detalhe da pesquisa
1.
Chromatin Accessibility of Human Mitral Valves and Functional Assessment of MVP Risk Loci.
Circ Res
; 128(5): e84-e101, 2021 03 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33508947
2.
Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse.
Eur Heart J
; 43(17): 1668-1680, 2022 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35245370
3.
The complex genetic basis of fibromuscular dysplasia, a systemic arteriopathy associated with multiple forms of cardiovascular disease.
Clin Sci (Lond)
; 136(16): 1241-1255, 2022 08 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-36043395
4.
Functional interplay between Mediator and RNA polymerase II in Rad2/XPG loading to the chromatin.
Nucleic Acids Res
; 47(17): 8988-9004, 2019 09 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-31299084
5.
Genomics of Fibromuscular Dysplasia.
Int J Mol Sci
; 19(5)2018 May 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-29883369
6.
Transcription factors: specific DNA binding and specific gene regulation.
Trends Genet
; 30(6): 211-9, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24774859
7.
Discovery of novel protein partners of the transcription factor FOXL2 provides insights into its physiopathological roles.
Hum Mol Genet
; 21(14): 3264-74, 2012 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22544055
8.
Transcription factor FOXL2 protects granulosa cells from stress and delays cell cycle: role of its regulation by the SIRT1 deacetylase.
Hum Mol Genet
; 20(9): 1673-86, 2011 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21289058
9.
Mutational probing of the forkhead domain of the transcription factor FOXL2 provides insights into the pathogenicity of naturally occurring mutations.
Hum Mol Genet
; 20(17): 3376-85, 2011 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21632871
10.
Genomic, Transcriptomic, and Proteomic Depiction of Induced Pluripotent Stem Cells-Derived Smooth Muscle Cells As Emerging Cellular Models for Arterial Diseases.
Hypertension
; 80(4): 740-753, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36655574
11.
Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation.
Nat Genet
; 55(6): 964-972, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37248441
12.
Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease.
JCI Insight
; 7(3)2022 02 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35132965
13.
Generic binding sites, generic DNA-binding domains: where does specific promoter recognition come from?
FASEB J
; 24(2): 346-56, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19762556
14.
Kinesin's cover-neck bundle folds forward to generate force.
Proc Natl Acad Sci U S A
; 105(49): 19247-52, 2008 Dec 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-19047639
15.
Plasma and genetic determinants of soluble TREM-1 and major adverse cardiovascular events in a prospective cohort of acute myocardial infarction patients. Results from the FAST-MI 2010 study.
Int J Cardiol
; 344: 213-219, 2021 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34534607
16.
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases.
Nat Commun
; 12(1): 6031, 2021 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34654805
17.
Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia.
Cardiovasc Res
; 117(4): 1154-1165, 2021 03 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32531060
18.
Transcriptome Analysis of lncRNAs in Pheochromocytomas and Paragangliomas.
J Clin Endocrinol Metab
; 105(3)2020 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31678991
19.
A plasma proteogenomic signature for fibromuscular dysplasia.
Cardiovasc Res
; 116(1): 63-77, 2020 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31424497
20.
Pooled Genetic Screenings to Identify Likely Pathogenic Variants in Hypertrophic Cardiomyopathy.
Circ Genom Precis Med
; 17(2): e004599, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38497213