Detalhe da pesquisa
1.
Combined loss of CDH1 and downstream regulatory sequences drive early-onset diffuse gastric cancer and increase penetrance of hereditary diffuse gastric cancer.
Gastric Cancer
; 26(5): 653-666, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37249750
2.
Familial hypertriglyceridemia: an entity with distinguishable features from other causes of hypertriglyceridemia.
Lipids Health Dis
; 20(1): 14, 2021 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33588820
3.
A panel of 32 AIMs suitable for population stratification correction and global ancestry estimation in Mexican mestizos.
BMC Genet
; 20(1): 5, 2019 01 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30621578
4.
Molecular Characterization of the Lipid Genome-Wide Association Study Signal on Chromosome 18q11.2 Implicates HNF4A-Mediated Regulation of the TMEM241 Gene.
Arterioscler Thromb Vasc Biol
; 36(7): 1350-5, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27199446
5.
Genome-wide association study of colorectal cancer in Hispanics.
Carcinogenesis
; 37(6): 547-556, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27207650
6.
Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.
J Med Genet
; 50(5): 298-308, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23505323
7.
Implication of myddosome complex genetic variants in outcome severity of COVID-19 patients.
J Microbiol Immunol Infect
; 56(5): 939-950, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37365052
8.
Primary amenorrhea in two sisters: description of a Mexican family with 17α hydroxylase-17 lyase deficiency caused by arginine - stop mutation.
Gynecol Endocrinol
; 28(9): 733-5, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22309630
9.
Familial hypobetalipoproteinemia in a hospital survey: genetics, metabolism and non-alcoholic fatty liver disease.
Ann Hepatol
; 10(2): 155-64, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21502677
10.
[Familial homozygous hypercholesterolemia due to the c2271delT mutation in the LDL receptor gene, detected exclusively in Mexicans]. / Hipercolesterolemia familiar homocigota por la mutación c2271delT del gen del receptor LDL, detectada únicamente en mexicanos.
Gac Med Mex
; 147(5): 394-8, 2011.
Artigo
em Espanhol
| MEDLINE | ID: mdl-22089669
11.
Contribution of genetic, biochemical and environmental factors on insulin resistance and obesity in Mexican young adults.
Obes Res Clin Pract
; 13(6): 533-540, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31796261
12.
Mexican Carriers of the HNF1A p.E508K Variant Do Not Experience an Enhanced Response to Sulfonylureas.
Diabetes Care
; 41(8): 1726-1731, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29844095
13.
A Loss-of-Function Splice Acceptor Variant in IGF2 Is Protective for Type 2 Diabetes.
Diabetes
; 66(11): 2903-2914, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28838971
14.
The R230C variant of the ATP binding cassette protein A1 (ABCA1) gene is associated with a decreased response to glyburide therapy in patients with type 2 diabetes mellitus.
Metabolism
; 62(5): 638-41, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23273975
15.
Contribution of common genetic variation to the risk of type 2 diabetes in the Mexican Mestizo population.
Diabetes
; 61(12): 3314-21, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22923468
16.
The non-synonymous Arg230Cys variant (R230C) of the ATP-binding cassette transporter A1 is associated with low HDL cholesterol concentrations in Mexican adults: a population based nation wide study.
Atherosclerosis
; 216(1): 146-50, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21315358
17.
The N342S MYLIP polymorphism is associated with high total cholesterol and increased LDL receptor degradation in humans.
J Clin Invest
; 121(8): 3062-71, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21765216
18.
Apolipoprotein E epsilon4, Alzheimer's disease, and cognitive performance in elderly Mexican Mestizos.
J Am Geriatr Soc
; 56(4): 677-82, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18205760