Detalhe da pesquisa
1.
Siblings with profound connective tissue disease: First report of biallelic TGFBR1-related Loeys-Dietz syndrome.
Am J Med Genet A
; 191(3): 786-793, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36584339
2.
Aortic Cellular Diversity and Quantitative Genome-Wide Association Study Trait Prioritization Through Single-Nuclear RNA Sequencing of the Aneurysmal Human Aorta.
Arterioscler Thromb Vasc Biol
; 42(11): 1355-1374, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36172868
3.
In Silico Analysis of Metabolites from Peruvian Native Plants as Potential Therapeutics against Alzheimer's Disease.
Molecules
; 27(3)2022 Jan 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35164183
4.
Hereditary Influence in Thoracic Aortic Aneurysm and Dissection.
Circulation
; 133(24): 2516-28, 2016 Jun 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-27297344
5.
miR-199a-5p Is upregulated during fibrogenic response to tissue injury and mediates TGFbeta-induced lung fibroblast activation by targeting caveolin-1.
PLoS Genet
; 9(2): e1003291, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23459460
6.
Co-occurring pathogenic variants in 6q27 associated with dementia spectrum disorders in a Peruvian family.
Front Mol Neurosci
; 16: 1104585, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36873109
7.
Arachidonic acid ω-hydroxylase CYP4A11: inter-ethnic variations in the 8590T>C loss-of-function variant.
Mol Biol Rep
; 39(2): 1503-8, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21617944
8.
Fibrillar Collagen Variants in Spontaneous Coronary Artery Dissection.
JAMA Cardiol
; 7(4): 396-406, 2022 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35234813
9.
Genetic polymorphisms of glycine N-acyltransferase (GLYAT) in a French Caucasian population.
Xenobiotica
; 40(12): 853-61, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20925583
10.
ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm.
Nat Genet
; 51(1): 42-50, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30455415
11.
A seed sequence variant in miR-145-5p causes multisystem smooth muscle dysfunction syndrome.
J Clin Invest
; 133(5)2023 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36649075
12.
Genetic polymorphism of CYP2U1, a cytochrome P450 involved in fatty acids hydroxylation.
Prostaglandins Leukot Essent Fatty Acids
; 83(2): 105-10, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20630735