Zobrazeno 1 - 10
of 20
pro vyhledávání: '"M. T. Tusié-Luna"'
Autor:
A, Ochoa-Guzmán, D, Guillén-Quintero, L, Muñoz-Hernández, A, García, E, Díaz-Díaz, O, Pérez-Méndez, R, Rodríguez-Guillén, I B, Mitre-Aguilar, A, Zentella-Dehesa, C A, Aguilar-Salinas, M T, Tusié-Luna
Publikováno v:
Journal of endocrinological investigation. 44(9)
High-density lipoprotein (HDL) is considered a complex plasma-circulating particle with subfractions that vary in function, size, and chemical composition. We sought to test the effects of HDL, and HDL subfractions on insulin secretion and cholestero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7b4883ff2f08ecef8e5f2c5eb1ec0afb
https://pubmed.ncbi.nlm.nih.gov/33486704
https://pubmed.ncbi.nlm.nih.gov/33486704
Autor:
M T, Guerra-García, H, Moreno-Macías, A, Ochoa-Guzmán, M L, Ordoñez-Sánchez, R, Rodríguez-Guillen, P, Vázquez-Cárdenas, V M, Ortíz-Ortega, M, Peimbert-Torres, C A, Aguilar-Salinas, M T, Tusié-Luna
Publikováno v:
Journal of endocrinological investigation. 44(3)
Both type 2 diabetes (T2D) and low levels of high-density lipoprotein cholesterol (HDL-C) are very prevalent conditions among Mexicans. Genetic variants in the LIPC gene have been associated with both conditions. This study aimed to evaluate the asso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6450d6f575dcbbf7dd0146d32359fdda
https://pubmed.ncbi.nlm.nih.gov/32617858
https://pubmed.ncbi.nlm.nih.gov/32617858
Autor:
Laura Riba, Salvador Ramírez-Jiménez, M T Tusié-Luna, A U López-Gutiérrez, M Cerrillo-Hinojosa, María Luisa Ordóñez-Sánchez
Publikováno v:
Journal of Medical Genetics. 35:1014-1019
Congenital adrenal hyperplasia (CAH) is an inherited recessive disorder of adrenal steroidogenesis caused by mutations in the steroid 21-hydroxylase gene (CYP21) in more than 90% of affected patients. The CYP21 gene is located within the HLA complex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c28111d3a43aa2dd461b22635f86436
https://doi.org/10.1136/jmg.35.12.1014
https://doi.org/10.1136/jmg.35.12.1014
Akademický článek
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Autor:
J. C. Florez, A. L. Price, D. Campbell, L. Riba, M. V. Parra, F. Yu, C. Duque, R. Saxena, N. Gallego, M. Tello-Ruiz, L. Franco, M. Rodríguez-Torres, A. Villegas, G. Bedoya, C. A. Aguilar-Salinas, M. T. Tusié-Luna, A. Ruiz-Linares, D. Reich
Publikováno v:
Racial Identities, Genetic Ancestry, and Health in South America ISBN: 9781349293056
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::131f56b93ad2faacbdbc9952dd76e09a
https://doi.org/10.1057/9781137001702_7
https://doi.org/10.1057/9781137001702_7
Autor:
E, García-García, M, De la Llata-Romero, M, Kaufer-Horwitz, M T, Tusié-Luna, R, Calzada-León, V, Vázquez-Velázquez, S, Barquera-Cervera, A J, Caballero-Romo, L, Orozco, D, Velásquez-Fernández, M, Rosas-Peralta, A, Barriguete-Meléndez, R, Zacarías-Castillo, J, Sotelo-Morales
Publikováno v:
Archivos de cardiologia de Mexico. 78(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::517d063acf3900a62ed624fe27673393
https://pubmed.ncbi.nlm.nih.gov/19039443
https://pubmed.ncbi.nlm.nih.gov/19039443
Autor:
A, Huertas-Vázquez, J P, del Rincón, S, Canizales-Quinteros, L, Riba, G, Vega-Hernández, S, Ramírez-Jiménez, M, Aurón-Gómez, F J, Gómez-Pérez, C A, Aguilar-Salinas, M T, Tusié-Luna
Publikováno v:
Annals of human genetics. 68(Pt 5)
Familial combined hyperlipidemia (FCHL) is the most common familial dyslipidemia, with a prevalence of 1-2% in the general population. A major locus for FCHL has been mapped to chromosome 1q21-q23 in Finnish, Chinese, German and US families. We studi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::55aaf216c4ff8f7c01f2c05585e94d8c
https://pubmed.ncbi.nlm.nih.gov/15469419
https://pubmed.ncbi.nlm.nih.gov/15469419
Autor:
M T, Tusié Luna
Publikováno v:
Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion. 53(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::47daa1d8fb3be19311f84fb53a1ccd3d
https://pubmed.ncbi.nlm.nih.gov/11599476
https://pubmed.ncbi.nlm.nih.gov/11599476
Publikováno v:
Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion. 52(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6b25b785e2b9b75f0ce7eff1f0143198
https://pubmed.ncbi.nlm.nih.gov/10953615
https://pubmed.ncbi.nlm.nih.gov/10953615
Autor:
M T, Tusié Luna
Publikováno v:
Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion. 52(3)
Non-insulin dependent type 2 diabetes (NIDDM) is a chronic and degenerative disease characterized by elevated glucose serum and the predisposition to the development of vascular complications. In Mexico the incidence of the disease reaches 8%, where
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ed4af2653b5bdc1743a3108828232f5b
https://pubmed.ncbi.nlm.nih.gov/10953613
https://pubmed.ncbi.nlm.nih.gov/10953613