Detalles de la búsqueda
1.
KCNQ1 p.D446E Variant as a Risk Allele for Arrhythmogenic Phenotypes: Electrophysiological Characterization Reveals a Complex Phenotype Affecting the Slow Delayed Rectifier Potassium Current (IKs) Voltage Dependence by Causing a Hyperpolarizing Shift and a Lack of Response to Protein Kinase A Activation.
Int J Mol Sci
; 25(2)2024 Jan 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-38256028
2.
Genome-Wide Association Study Identifies a Functional SIDT2 Variant Associated With HDL-C (High-Density Lipoprotein Cholesterol) Levels and Premature Coronary Artery Disease.
Arterioscler Thromb Vasc Biol
; 41(9): 2494-2508, 2021 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-34233476
3.
Inflammasome genes polymorphisms and susceptibility to gout. Is there a link?
Rev Invest Clin
; 74(3): 147-155, 2022 05 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-35313392
4.
The Role of the ATP-Binding Cassette A1 (ABCA1) in Human Disease.
Int J Mol Sci
; 22(4)2021 Feb 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-33562440
5.
Endothelial Dysfunction, Inflammation and Coronary Artery Disease: Potential Biomarkers and Promising Therapeutical Approaches.
Int J Mol Sci
; 22(8)2021 Apr 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-33917744
6.
A functional ABCA1 gene variant is associated with low HDL-cholesterol levels and shows evidence of positive selection in Native Americans.
Hum Mol Genet
; 19(14): 2877-85, 2010 Jul 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-20418488
7.
Effect of the Melanocortin 4-Receptor Ile269Asn Mutation on Weight Loss Response to Dietary, Phentermine and Bariatric Surgery Interventions.
Genes (Basel)
; 13(12)2022 12 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-36553534
8.
Clinical Spectrum of SCN5A Channelopathy in Children with Primary Electrical Disease and Structurally Normal Hearts.
Genes (Basel)
; 13(1)2021 12 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-35052356
9.
Compound Heterozygous KCNQ1 Mutations Causing Recessive Romano-Ward Syndrome: Functional Characterization by Mutant Co-expression.
Front Cardiovasc Med
; 8: 625449, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-33693037
10.
Genomic study of dilated cardiomyopathy in a group of Mexican patients using site-directed next generation sequencing.
Mol Genet Genomic Med
; 8(11): e1504, 2020 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-32969603
11.
Impact of cadmium toxicity on cartilage loss in a 3D in vitro model.
Environ Toxicol Pharmacol
; 74: 103307, 2020 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-31830724
12.
Genetic contributors to serum uric acid levels in Mexicans and their effect on premature coronary artery disease.
Int J Cardiol
; 279: 168-173, 2019 Mar 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-30305239
13.
Compound heterozygous KCNQ1 mutations (A300T/P535T) in a child with sudden unexplained death: Insights into possible molecular mechanisms based on protein modeling.
Gene
; 627: 40-48, 2017 Sep 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-28600177
14.
A novel approach for human whole transcriptome analysis based on absolute gene expression of microarray data.
PeerJ
; 5: e4133, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-29230367
15.
Inflammasome Genes Polymorphisms and Susceptibility to Gout. Is There a Link?
Rev. invest. clín
; 74(3): 147-155, May.-Jun. 2022. tab
Artículo
en Inglés
|
LILACS-Express
| ID: biblio-1409573
16.
Dietary fat and carbohydrate modulate the effect of the ATP-binding cassette A1 (ABCA1) R230C variant on metabolic risk parameters in premenopausal women from the Genetics of Atherosclerotic Disease (GEA) Study.
Nutr Metab (Lond)
; 12: 45, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26579206
17.
Contribution of common genetic variants to obesity and obesity-related traits in mexican children and adults.
PLoS One
; 8(8): e70640, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-23950976
18.
Association of the I148M/PNPLA3 variant with elevated alanine transaminase levels in normal-weight and overweight/obese Mexican children.
Gene
; 520(2): 185-8, 2013 May 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-23510779
19.
PCSK1 rs6232 is associated with childhood and adult class III obesity in the Mexican population.
PLoS One
; 7(6): e39037, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-22737226
20.
VNN1 gene expression levels and the G-137T polymorphism are associated with HDL-C levels in Mexican prepubertal children.
PLoS One
; 7(11): e49818, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-23185446