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Norberto Leyva García
Norberto Leyva García
Jefe de Servicio de Génética y Genómica
Dirección de correo verificada de inr.gob.mx
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Citado por
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Año
Nanoparticle technology for treatment of Parkinson's disease: the role of surface phenomena in reaching the brain
G Leyva-Gomez, H Cortes, JJ Magana, N Leyva-García, ...
Drug discovery today 20 (7), 824-837, 2015
1022015
Analysis of CAG repeats in five SCA loci in Mexican population: epidemiological evidence of a SCA7 founder effect
JJ Magaña, YS Tapia‐Guerrero, L Velázquez‐Pérez, ...
Clinical genetics 85 (2), 159-165, 2014
472014
A comprehensive clinical and genetic study of a large Mexican population with spinocerebellar ataxia type 7
L Velázquez-Pérez, CM Cerecedo-Zapata, O Hernández-Hernández, ...
Neurogenetics 16, 11-21, 2015
332015
Origin of the spinocerebellar ataxia type 7 gene mutation in Mexican population
JJ Magaña, R Gómez, M Maldonado-Rodríguez, L Velázquez-Pérez, ...
The Cerebellum 12, 902-905, 2013
312013
Oxidative stress in spinocerebellar ataxia type 7 is associated with disease severity
Y Torres-Ramos, A Montoya-Estrada, B Cisneros, K Tercero-Pérez, ...
The Cerebellum 17, 601-609, 2018
302018
The relationship among IL-13, GSTP1, and CYP1A1 polymorphisms and environmental tobacco smoke in a population of children with asthma in Northern Mexico
B Muñoz, JJ Magaña, I Romero-Toledo, E Juárez-Pérez, A López-Moya, ...
Environmental toxicology and pharmacology 33 (2), 226-232, 2012
292012
Effects of physical rehabilitation in patients with spinocerebellar ataxia type 7
K Tercero-Pérez, H Cortés, Y Torres-Ramos, R Rodríguez-Labrada, ...
The Cerebellum 18, 397-405, 2019
282019
Distribution of CTG repeats at the DMPK gene in myotonic distrophy patients and healthy individuals from the Mexican population
JJ Magaña, P Cortés-Reynosa, R Escobar-Cedillo, R Gómez, ...
Molecular biology reports 38, 1341-1346, 2011
222011
Congenital heart defect and conductive hypoacusia in a patient with the KBG syndrome.
MR Rivera-Vega, SA Cuevas-Covarrubias, SH Kofman-Alfaro
Clinical genetics 50 (4), 278-279, 1996
171996
Pathogenesis of myotonic dystrophy type 1
JJ Magana, N Leyva-Garcia, B Cisneros
Gaceta Medica de Mexico 145 (4), 331-337, 2009
152009
Transcriptome analysis reveals altered inflammatory pathway in an inducible glial cell model of myotonic dystrophy type 1
CN Azotla-Vilchis, D Sanchez-Celis, LE Agonizantes-Juárez, ...
Biomolecules 11 (2), 159, 2021
132021
High prevalence of autosomal recessive congenital ichthyosis in a Mexican population caused by a new mutation in the TGM1 gene: epidemiological evidence of a …
M González‐Del Carmen, S Montaño, OD Reyes‐Hernández, ...
International Journal of Dermatology 59 (8), 969-977, 2020
92020
Association of TLR4 gene polymorphisms with sepsis after a burn injury: findings of the functional role of rs2737190 SNP
CA Colín-Castro, R Franco-Cendejas, HI Rocha-González, ...
Genes & Immunity 22 (1), 24-34, 2021
82021
Severity of dyskinesia and D3R signaling changes induced by L-DOPA treatment of hemiparkinsonian rats are features inherent to the treated subjects
S Albarrán-Bravo, JA Ávalos-Fuentes, H Cortés, M Rodriguez-Sánchez, ...
Biomolecules 9 (9), 431, 2019
82019
Ataxia espinocerebelosa tipo 2 (parte A): epidemiología y características clínicas y genéticas
L Velázquez-Pérez, O Hernández-Hernández, N Leyva-García, H Cortés, ...
Investigación en Discapacidad 3 (3), 114-122, 2014
72014
Non-invasive methods for evaluation of skin manifestations in patients with ichthyosis
H Cortés, G Figueroa-González, OD Reyes-Hernández, JJ Magaña, ...
Archives of Dermatological Research 312, 231-236, 2020
62020
Strategies for clinical and molecular diagnosis of Charcot-Marie-Tooth 1A among Mexican patients
E Hernández-Zamora, RE Escobar-Cedillo, NC González-Huerta, ...
Gaceta Medica de Mexico 143 (5), 383-389, 2007
62007
Myotonic Dystrophy Protein Kinase: Structure, Function and Its Possible Role in the Pathogenesis of Myotonic Dystrophy Type 1
JJ Magaña, R Suárez-Sánchez, N Leyva-García, B Cisneros, ...
Advances in Protein Kinases, 213-42, 2012
32012
The Molecular Role of Polyamines in Age-Related Diseases: An Update
GE Jimenez Gutierrez, FV Borbolla Jiménez, LG Muñoz, ...
International Journal of Molecular Sciences 24 (22), 16469, 2023
22023
Genetic distribution of five spinocerebellar ataxia microsatellite loci in mexican native american populations and its impact on contemporary mestizo populations
R Gómez, YS Tapia-Guerrero, B Cisneros, L Orozco, C Cerecedo-Zapata, ...
Genes 13 (1), 157, 2022
22022
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