Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jorge Luis Guerrero-Camacho"'
Autor:
Sandra Romero-Hidalgo, José Flores-Rivera, Verónica Rivas-Alonso, Rodrigo Barquera, María Teresa Villarreal-Molina, Bárbara Antuna-Puente, Luis Rodrigo Macias-Kauffer, Marisela Villalobos-Comparán, Jair Ortiz-Maldonado, Neng Yu, Tatiana V. Lebedeva, Sharon M. Alosco, Juan Daniel García-Rodríguez, Carolina González-Torres, Sandra Rosas-Madrigal, Graciela Ordoñez, Jorge Luis Guerrero-Camacho, Irene Treviño-Frenk, Monica Escamilla-Tilch, Maricela García-Lechuga, Víctor Hugo Tovar-Méndez, Hanna Pacheco-Ubaldo, Victor Acuña-Alonzo, Maria-Cátira Bortolini, Carla Gallo, Gabriel Bedoya, Francisco Rothhammer, Rolando González-Jose, Andrés Ruiz-Linares, Samuel Canizales-Quinteros, Edmond Yunis, Julio Granados, Teresa Corona
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-11 (2020)
Abstract Neuromyelitis Optica (NMO) is an autoimmune disease with a higher prevalence in non-European populations. Because the Mexican population resulted from the admixture between mainly Native American and European populations, we used genome-wide
Externí odkaz:
https://doaj.org/article/e39fd4e23a1a453796fed8b8df762e41
Autor:
Adriana Ochoa-Morales, Ana Fresan-Orellana, Miguel Ángel Ramírez-García, Horacio Márquez-González, Iris E. Martínez-Juárez, Mayra López-Uribe, Carol Zuniga-García, Aurelio Jara-Prado, Jorge Luis Guerrero-Camacho, David José Dávila-Ortiz de Montellano
Publikováno v:
Epilepsy & Behavior. 144:109268
Autor:
Maricela García-Lechuga, Carla Gallo, Monica Escamilla-Tilch, José Flores-Rivera, Víctor Hugo Tovar-Méndez, María Teresa Villarreal-Molina, Bárbara Antuna-Puente, Verónica Rivas-Alonso, Sandra Romero-Hidalgo, Maria Cátira Bortolini, Tatiana Lebedeva, Juan Daniel García-Rodríguez, Jorge Luis Guerrero-Camacho, Francisco Rothhammer, Hanna Pacheco-Ubaldo, Samuel Canizales-Quinteros, Gabriel Bedoya, Edmond J. Yunis, S. M. Alosco, Victor Acuña-Alonzo, Graciela Ordoñez, Rodrigo Barquera, Luis Macías-Kauffer, Carolina Gonzalez-Torres, Marisela Villalobos-Comparán, Rolando González-José, Julio Granados, Teresa Corona, Sandra Rosas-Madrigal, Neng Yu, Irene Treviño-Frenk, Jair Fernando Ortiz-Maldonado, Andres Ruiz-Linares
Publikováno v:
Scientific Reports
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Scientific Reports, Vol 10, Iss 1, Pp 1-11 (2020)
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Scientific Reports, Vol 10, Iss 1, Pp 1-11 (2020)
Neuromyelitis Optica (NMO) is an autoimmune disease with a higher prevalence in non-European populations. Because the Mexican population resulted from the admixture between mainly Native American and European populations, we used genome-wide microarr
Autor:
Marie Catherine Boll-Woehrlen, Nancy Monroy-Jaramillo, Jorge Luis Guerrero-Camacho, Petra Yescas-Gómez, Mayela Rodríguez-Violante, Marisol López-López, María Elisa Alonso-Vilatela
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 165:235-244
Mutations in PARK2, PINK1, and DJ-1 have been associated with autosomal recessive early-onset Parkinson's disease. Here, we report the prevalence of sequence and structural mutations in these three main recessive genes in Mexican Mestizo patients. Th
Autor:
Nancy Monroy Jaramillo, Mayela De jesus Rodriguez Violante, Marisol López, Jorge Luis Guerrero Camacho, Catherine Boll Woehrlen, Ma Elisa Alonso Vilatela, Petra Yescas Gómez
Publikováno v:
Movement Disorders. 27:1047-1051
Background: Parkin mutations in patients with early-onset Parkinson's disease (EOPD) are estimated to occur in 49% of familial cases and 18% of sporadic cases. Methods: We analyzed the entire sequence-coding region and dosage mutations of parkin in 6
Autor:
Jorge Luis, Guerrero Camacho, Nancy, Monroy Jaramillo, Petra, Yescas Gómez, Mayela, Rodríguez Violante, Catherine, Boll Woehrlen, Ma Elisa, Alonso Vilatela, Marisol, López López
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 27(8)
Parkin mutations in patients with early-onset Parkinson's disease (EOPD) are estimated to occur in 49% of familial cases and 18% of sporadic cases.We analyzed the entire sequence-coding region and dosage mutations of parkin in 63 Mexican-mestizo EOPD
Autor:
Roberto Alfonso, Suástegui Román, Petra, Yescas Gómez, Jorge Luis, Guerrero Camacho, Adriana, Ochoa Morales, Julio, Granados, Aurelio, Jara Prado, Oscar Alejandro, López-Caro, Ma Elisa, Alonso Vilatela
Publikováno v:
Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion. 54(5)
The presence of different ethnic groups in Mexico may give rise to genetic diversity between the native Indian population and the Mestizos. It is therefore of medical and anthropological interest to analyze the genotypes of disease-associated loci, s
Autor:
T. Corona-Vázquez, Marisol López-López, Helgi Jung-Cook, María Elisa Alonso-Vilatela, I. M. Familiar-López, Jorge Luis Guerrero-Camacho
Publikováno v:
Revista de Neurología. 39:1063
Objetivo. Los pacientes presentan una gran variabilidad en la forma en que responden a los medicamentos. Las diferencias individuales en la respuesta a los farmacos dependen de factores ambientales, asi como de determinantes geneticos. En particular,