Publications by authors named "Maria E Alonso"

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Sticholysins, pore-forming proteins from a marine anemone can induce maturation of dendritic cells through a TLR4 dependent-pathway.
Rady J Laborde, Mayari E Ishimura, Lianne Abreu-Butin, Catarina V Nogueira, Daniel Grubaugh, María E Alonso

Mol Immunol· March 2021

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Variant Intestinal-Cell Kinase in Juvenile Myoclonic Epilepsy.
Julia N Bailey, Laurence de Nijs, Dongsheng Bai, Toshimitsu Suzuki, Hiroyuki Miyamoto, María E Alonso

N Engl J Med· March 2018

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Novel Adjuvant Based on the Pore-Forming Protein Sticholysin II Encapsulated into Liposomes Effectively Enhances the Antigen-Specific CTL-Mediated Immune Response.
Rady J Laborde, Oraly Sanchez-Ferras, María C Luzardo, Yoelys Cruz-Leal, Audry Fernández, María E Alonso

J Immunol· April 2017

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EFHC1 variants in juvenile myoclonic epilepsy: reanalysis according to NHGRI and ACMG guidelines for assigning disease causality.
Julia N Bailey, Christopher Patterson, Laurence de Nijs, Reyna M Durón, Viet-Huong Nguyen, María E Alonso

Genet Med· February 2017

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Late onset Lafora disease and novel EPM2A mutations: breaking paradigms.
Aurelio Jara-Prado, Adriana Ochoa, María Elisa Alonso, Gabriel A Lima Villeda, Francisca Fernández-Valverde

Epilepsy Res· November 2014

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Role of B-1 cells in the immune response against an antigen encapsulated into phosphatidylcholine-containing liposomes.
Yoelys Cruz-Leal, Yoan Machado, Alejandro López-Requena, Liem Canet, Rady Laborde, María E Alonso

Int Immunol· August 2014

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Liposomes of phosphatidylcholine and cholesterol induce an M2-like macrophage phenotype reprogrammable to M1 pattern with the involvement of B-1 cells.
Yoelys Cruz-Leal, María Fernanda Lucatelli Laurindo, Lika Osugui, María Del Carmen Luzardo, Alejandro López-Requena, María Eugenia Alonso

Immunobiology· June 2014

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Interethnic differences in UGT1A4 genetic polymorphisms between Mexican Mestizo and Spanish populations.
Marisol López, Pedro Dorado, Alberto Ortega, Eva Peñas-Lledó, Nancy Monroy, María Elisa Alonso

Mol Biol Rep· April 2013

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Novel Myoclonin1/EFHC1 mutations in Mexican patients with juvenile myoclonic epilepsy.
Aurelio Jara-Prado, Iris E Martínez-Juárez, Adriana Ochoa, Víctor M González, María Del Carmen Fernández-González-Aragón, María Elisa Alonso

Seizure· September 2012

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Pharmacogenetics of the antiepileptic drugs phenytoin and lamotrigine.
Marisol López, Pedro Dorado, Nancy Monroy, María Elisa Alonso, Helgi Jung-Cook

Drug Metabol Drug Interact· August 2012

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Oral administration of an enzymatic protein hydrolysate from the green microalga Chlorella vulgaris enhances the nutritional recovery of malnourished mice.
Humberto J Morris, Olimpia V Carrillo, María E Alonso, Rosa C Bermúdez, Ángel Almarales

J Med Food· December 2011

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Effect of starvation and refeeding on biochemical and immunological status of Balb/c mice: an experimental model of malnutrition.
Humberto J Morris, Olimpia V Carrillo, Gabriel Llauradó, María E Alonso, Rosa C Bermúdez

Immunopharmacol Immunotoxicol· September 2011

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Low frequency of common LRRK2 mutations in Mexican patients with Parkinson's disease.
Petra Yescas, Marisol López, Nancy Monroy, Marie-Catherine Boll, Mayela Rodríguez-Violante, María Elisa Alonso

Neurosci Lett· November 2010

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Presymptomatic diagnosis in Huntington's disease: the Mexican experience.
Maria Elisa Alonso, Adriana Ochoa, Ana Luisa Sosa, Yaneth Rodríguez, Mireya Chávez

Genet Test Mol Biomarkers· December 2009

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p73 plays a role in erythroid differentiation through GATA1 induction.
Fernando Marqués-García, Nuria Ferrandiz, Rosalía Fernández-Alonso, Laura González-Cano, Marta Herreros-Villanueva, María Eugenia Alonso

J Biol Chem· August 2009

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DNA variants in coding region of EFHC1: SNPs do not associate with juvenile myoclonic epilepsy.
Dongsheng Bai, Julia N Bailey, Reyna M Durón, María E Alonso, Marco T Medina

Epilepsia· May 2009

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Hyperglycosylation and reduced GABA currents of mutated GABRB3 polypeptide in remitting childhood absence epilepsy.
Miyabi Tanaka, Richard W Olsen, Marco T Medina, Emily Schwartz, Maria Elisa Alonso

Am J Hum Genet· June 2008

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Anticipation and intergenerational repeat instability in spinocerebellar ataxia type 17.
Astrid Rasmussen, Irene De Biase, Marcela Fragoso-Benítez, Marco Antonio Macías-Flores, Petra Yescas, María Elisa Alonso

Ann Neurol· June 2007

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Mutational analysis of CACNA1G in idiopathic generalized epilepsy. Mutation in brief #962. Online.
Baljinder Singh, Arnaud Monteil, Isabelle Bidaud, Yoshihisa Sugimoto, Toshimitsu Suzuki, Maria E Alonso

Hum Mutat· May 2007

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Apolipoprotein E epsilon4 allele is associated with Parkinson disease risk in a Mexican Mestizo population.
Marisol López, Jorge Guerrero, Petra Yescas, Marie-Catherine Boll, Itziar Familiar, María Elisa Alonso

Mov Disord· February 2007

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Olfaction and neurodegeneration in HD.
Fernando A Barrios, Leopoldo Gonzalez, Rafael Favila, Maria E Alonso, Perla M Salgado

Neuroreport· January 2007

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Mutation analyses of genes on 6p12-p11 in patients with juvenile myoclonic epilepsy.
Toshimitsu Suzuki, Antonio V Delgado-Escueta, Maria E Alonso, Ryoji Morita, Nami Okamura

Neurosci Lett· September 2006

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Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer's disease in Mexican families.
Petra Yescas, Adriana Huertas-Vazquez, María Teresa Villarreal-Molina, Astrid Rasmussen, María Teresa Tusié-Luna, María Elisa Alonso

Neurogenetics· July 2006

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Juvenile myoclonic epilepsy subsyndromes: family studies and long-term follow-up.
Iris E Martínez-Juárez, María Elisa Alonso, Marco T Medina, Reyna M Durón, Julia N Bailey

Brain· May 2006

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