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- Publications
- Influence
Single nucleotide polymorphisms of the FTO gene and cancer risk: an overview
- M. E. Hernández-Caballero, J. A. Sierra-Ramírez
- Biology, Medicine
- Molecular Biology Reports
- 1 March 2015
The FTO (fat mass and obesity-associated) gene has a strong linkage disequilibrium block, within which SNPs have been identified that are involved in the development of obesity. Recently some of… Expand
[Autosomal recessive limb-girdle muscular dystrophy].
- M. E. Hernández-Caballero, A. Miranda-Duarte, R. Escobar-Cedillo, H. Villegas-castrejon
- Medicine
- Revista de neurologia
- 16 October 2010
Muscular dystrophies are a heterogeneous group of hereditary diseases characterized by loss of muscle and weakness of non neurogenic origin. They are caused by mutations in one or more genes involved… Expand
Effects of luteectomy in early pregnancy on the maintenance of gestation and plasma progesterone concentrations in the viviparous temperate lizard Barisia imbricata imbricata
- M. Martínez-Torres, M. E. Hernández-Caballero, J. Luis-Díaz, Guadalupe Ortíz-López, Mario Cárdenas-León, L. Moreno-Fierros
- Biology, Medicine
- Reproductive biology and endocrinology : RB&E
- 25 February 2010
BackgroundSeveral studies have shown that the corpus luteum is the principal source of progesterone during the gravidity period in reptiles; however, its participation in the maintenance of gestation… Expand
Impact of D-bifunctional Protein Deficiency on Telomere Length and Gene Expression in a Child
- M. E. Hernández-Caballero, D. Arenas-Aranda, Raquel Chávez-Torres, J. A. Sierra-Ramírez, Calzada-Mendoza Claudia Camelia
- Biology
- 10 January 2013
Aim: To explore, in one patient, the possibility that D-bifunctional protein (D-BP) deficiency affects telomere length, and to determine the profile of genetic expression. Presentation of Case: Due… Expand
Methylation Analysis of PHF20L1 and DACT2 Gene Promoters in Women with Breast Cancer
- M. E. Hernández-Caballero, V. Borgonio-Cuadra, +4 authors Teresa Abad-Camacho
- Biology
- 8 December 2016
Distrofias musculares de cinturas autosómicas recesivas
Resumen. Las distrofias musculares son un grupo heterogeneo de enfermedades hereditarias, caracterizadas por debilidad y perdida muscular de origen no neurogenico. Son causadas por mutaciones de uno… Expand
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