Detalhe da pesquisa
1.
The FES Gene at the 15q26 Coronary-Artery-Disease Locus Inhibits Atherosclerosis.
Circ Res
; 131(12): 1004-1017, 2022 12 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36321446
2.
Effects of Coronary Artery Disease-Associated Variants on Vascular Smooth Muscle Cells.
Circulation
; 146(12): 917-929, 2022 09 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-35735005
3.
Novel LOX Variants in Five Families with Aortic/Arterial Aneurysm and Dissection with Variable Connective Tissue Findings.
Int J Mol Sci
; 22(13)2021 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34281165
4.
HHIPL1, a Gene at the 14q32 Coronary Artery Disease Locus, Positively Regulates Hedgehog Signaling and Promotes Atherosclerosis.
Circulation
; 140(6): 500-513, 2019 08 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31163988
5.
Functional investigation of the coronary artery disease gene SVEP1.
Basic Res Cardiol
; 115(6): 67, 2020 11 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-33185739
6.
The Atherosclerosis Risk Variant rs2107595 Mediates Allele-Specific Transcriptional Regulation of HDAC9 via E2F3 and Rb1.
Stroke
; 50(10): 2651-2660, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31500558
7.
Influence of a Coronary Artery Disease-Associated Genetic Variant on FURIN Expression and Effect of Furin on Macrophage Behavior.
Arterioscler Thromb Vasc Biol
; 38(8): 1837-1844, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29976768
8.
JCAD, a Gene at the 10p11 Coronary Artery Disease Locus, Regulates Hippo Signaling in Endothelial Cells.
Arterioscler Thromb Vasc Biol
; 38(8): 1711-1722, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29794114
9.
Coronary Artery Disease-Associated LIPA Coding Variant rs1051338 Reduces Lysosomal Acid Lipase Levels and Activity in Lysosomes.
Arterioscler Thromb Vasc Biol
; 37(6): 1050-1057, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28279971
10.
The Coronary Artery Disease-associated Coding Variant in Zinc Finger C3HC-type Containing 1 (ZC3HC1) Affects Cell Cycle Regulation.
J Biol Chem
; 291(31): 16318-27, 2016 07 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-27226629
11.
Enrichment of Rare Variants in Loeys-Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia.
Circulation
; 142(10): 1021-1024, 2020 09 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32897753
12.
X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment development.
Am J Hum Genet
; 90(2): 247-59, 2012 Feb 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-22284829
13.
Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23).
Hum Mol Genet
; 21(16): 3647-54, 2012 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22619378
14.
Referee Abuse, Intention to Quit, and Well-Being.
Res Q Exerc Sport
; 95(1): 207-217, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-37039732
15.
X-linked cone dystrophy caused by mutation of the red and green cone opsins.
Am J Hum Genet
; 87(1): 26-39, 2010 Jul 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-20579627
16.
Examining the mental health status of referees in the turkish professional football league.
Sci Med Footb
; 7(3): 272-278, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35621335
17.
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
18.
What is macroecology?
Biol Lett
; 8(6): 904-6, 2012 Dec 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-22915630
19.
MRAP and MRAP2 are bidirectional regulators of the melanocortin receptor family.
Proc Natl Acad Sci U S A
; 106(15): 6146-51, 2009 Apr 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-19329486
20.
Abuse is not a zero-sum game! The case for zero tolerance of match official physical and verbal abuse.
Eur J Sport Sci
; 22(3): 417-424, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33504289