Oscar Hernández-Hernández
Oscar Hernández-Hernández
Instituto Nacional de Rehabilitación
Email confirmado em inr.gob.mx
Citado por
Citado por
Myotonic dystrophy CTG expansion affects synaptic vesicle proteins, neurotransmission and mouse behaviour
O Hernández-Hernández, C Guiraud-Dogan, G Sicot, A Huguet, S Luilier, ...
Brain 136 (3), 957-970, 2013
Histamine‐induced Ca2+ entry in human astrocytoma U373 MG cells: Evidence for involvement of store‐operated channels
M Barajas, A Andrade, O Hernandez‐Hernandez, R Felix, ...
Journal of neuroscience research 86 (15), 3456-3468, 2008
Identification of a disulfide bridge essential for structure and function of the voltage-gated Ca2+ channel α2δ-1 auxiliary subunit
A Calderón-Rivera, A Andrade, O Hernández-Hernández, ...
Cell calcium 51 (1), 22-30, 2012
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
Recombinant human ZP3-induced sperm acrosome reaction: evidence for the involvement of T-and L-type voltage-gated calcium channels
O José, O Hernández-Hernández, M Chirinos, ME González-González, ...
Biochemical and biophysical research communications 395 (4), 530-534, 2010
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 (1), 11-21, 2015
From traditional biochemical signals to molecular markers for detection of sepsis after burn injuries
B Muñoz, R Suárez-Sánchez, O Hernández-Hernández, ...
Burns 45 (1), 16-31, 2019
Nucleocytoplasmic shuttling of the Duchenne muscular dystrophy gene product dystrophin Dp71d is dependent on the importin α/β and CRM1 nuclear transporters and microtubule …
R Suárez-Sánchez, A Aguilar, KM Wagstaff, G Velez, PM Azuara-Medina, ...
Biochimica et Biophysica Acta (BBA)-Molecular Cell Research 1843 (5), 985-1001, 2014
Origin of the spinocerebellar ataxia type 7 gene mutation in Mexican population
JJ Magana, R Gomez, M Maldonado-Rodriguez, L Velazquez-Perez, ...
The Cerebellum 12 (6), 902-905, 2013
Myotonic dystrophy expanded CUG repeats disturb the expression and phosphorylation of τ in PC12 cells
O Hernández‐Hernández, M Bermúdez‐de‐León, P Gómez, ...
Journal of neuroscience research 84 (4), 841-851, 2006
Altered nuclear structure in myotonic dystrophy type 1-derived fibroblasts
R Rodríguez, O Hernández-Hernández, JJ Magana, R González-Ramírez, ...
Molecular biology reports 42 (2), 479-488, 2015
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 (3), 397-405, 2019
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 (5), 601-609, 2018
Voice alterations in patients with spinocerebellar ataxia type 7 (sca7): Clinical-genetic correlations
A Gómez-Coello, VM Valadez-Jiménez, B Cisneros, P Carrillo-Mora, ...
Journal of Voice 31 (1), 123. e1-123. e5, 2017
Synaptic protein dysregulation in myotonic dystrophy type 1: Disease neuropathogenesis beyond missplicing
O Hernández-Hernández, G Sicot, DM Dinca, A Huguet, A Nicole, L Buée, ...
Rare Diseases, 2013
Myotonic dystrophy CTG repeat expansion alters Ca2+ channel functional expression in PC12 cells
A Andrade, MB de León, O Hernández-Hernández, B Cisneros, R Felix
FEBS letters 581 (23), 4430-4438, 2007
Spinocerebellar ataxia type 7: a neurodegenerative disorder with peripheral neuropathy
J Salas-Vargas, J Mancera-Gervacio, L Velázquez-Pérez, ...
European neurology 73 (3-4), 173-178, 2015
Wide profiling of circulating MicroRNAs in spinocerebellar ataxia type 7
VM Borgonio-Cuadra, C Valdez-Vargas, S Romero-Córdoba, ...
Molecular neurobiology 56 (9), 6106-6120, 2019
Regulation of Ca v 3.1 channels by glucocorticoids
T Avila, O Hernández-Hernández, A Almanza, MB De León, M Urban, ...
Cellular and molecular neurobiology 29 (8), 1265-1273, 2009
A Complete Association of an intronic SNP rs6798742 with Origin of Spinocerebellar Ataxia Type 7‐CAG Expansion Loci in the Indian and Mexican Population
M Faruq, JJ Magaña, V Suroliya, A Narang, NM Murillo‐Melo, ...
Annals of human genetics 81 (5), 197-204, 2017
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