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1.
The -514C>T polymorphism in the LIPC gene modifies type 2 diabetes risk through modulation of HDL-cholesterol levels in Mexicans.
J Endocrinol Invest
; 44(3): 557-565, 2021 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-32617858
2.
R230C but not - 565C/T variant of the ABCA1 gene is associated with type 2 diabetes in Mexicans through an effect on lowering HDL-cholesterol levels.
J Endocrinol Invest
; 43(8): 1061-1071, 2020 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-32016916
3.
A cis-acting element in the promoter of human ether à go-go 1 potassium channel gene mediates repression by calcitriol in human cervical cancer cells.
Biochem Cell Biol
; 93(1): 94-101, 2015 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-25495694
4.
Early-onset type 2 diabetes: metabolic and genetic characterization in the mexican population.
J Clin Endocrinol Metab
; 86(1): 220-6, 2001 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-11232004
5.
Mutation analysis in patients with congenital adrenal hyperplasia in the Spanish population: identification of putative novel steroid 21-hydroxylase deficiency alleles associated with the classic form of the disease.
Hum Hered
; 49(3): 169-75, 1999 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-10364682
6.
Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: evidence of different genetic mechanisms involved in the production of the disease.
J Med Genet
; 35(12): 1014-9, 1998 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-9863599
7.
Molecular genetic analysis of patients carrying steroid 21-hydroxylase deficiency in the Mexican population: identification of possible new mutations and high prevalence of apparent germ-line mutations.
Hum Genet
; 102(2): 170-7, 1998 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-9580109
8.
Low frequency of deletion alleles in patients with steroid 21-hydroxylase deficiency in a Mexican population.
Hum Genet
; 98(3): 376-9, 1996 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-8707311
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