Výsledky vyhledávání - "Xochitl Helga Castro Martínez"

Akademický článek

Differential DNA Methylation from Autistic Children Enriches Evidence for Genes Associated with ASD and New Candidate Genes

Autor: Mirna Edith Morales-Marín, Xochitl Helga Castro Martínez, Federico Centeno Cruz, Francisco Barajas-Olmos, Omar Náfate López, Amalia Guadalupe Gómez Cotero, Lorena Orozco, Humberto Nicolini Sánchez

Publikováno v: Brain Sciences, Vol 13, Iss 10, p 1420 (2023)

The etiology of Autism Spectrum Disorders (ASD) is a result of the interaction between genes and the environment. The study of epigenetic factors that affect gene expression, such as DNA methylation, has become an important area of research in ASD. I

Externí odkaz: https://doaj.org/article/90a490f9c0304012a44790f05b59a676

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FOXP2 expression and gray matter density in the male brains of patients with schizophrenia

Autor: J. Javier Meana, Gracián García-Martí, Noelia Sebastiá-Ortega, María Dolores Moltó, Julio Sanjuán, Javier Gilabert-Juan, Josep Maria Haro, Luis Martí-Bonmatí, Javier González-Fernández, Roberto Sanz-Requena, Juan Nacher, Xochitl Helga Castro-Martínez

Publikováno v: Brain Imaging and Behavior
Addi: Archivo Digital para la Docencia y la Investigación
Universidad del País Vasco
Sanjuán Arias, Julio Castro-Martínez, Xochitl Helga García Martí, Gracián González-Fernández, Javier Sanz-Requena, Roberto Haro, Josep María Meana, J. Javier Martí Bonmatí, Luis Nácher Roselló, Juan Salvador Sebastiá Ortega, Noelia Gilabert Juan, Javier Moltó Ruiz, María Dolores 2020 FOXP2 expression and gray matter density in the male brains of patients with schizophrenia Brain Imaging And Behavior
RODERIC. Repositorio Institucional de la Universitat de Valéncia
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Addi. Archivo Digital para la Docencia y la Investigación
RODERIC: Repositorio Institucional de la Universitat de Valéncia

Common genetic variants ofFOXP2may contribute to schizophrenia vulnerability, but controversial results have been reported for this proposal. Here we evaluated the potential impact of the commonFOXP2rs2396753 polymorphism in schizophrenia. It was pre

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d94f0b3353bbf60c560017bf8697f80a
https://doi.org/10.1007/s11682-020-00339-x

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FOXP2 and language alterations in psychiatric pathology

Autor: José Humberto Nicolini Sánchez, Xochitl Helga Castro Martínez, Mirna Edith Morales Marin, María Dolores Moltó Ruiz, Julio César Flores Lázaro, Nora Andrea Gutiérrez Najera, Javier González Fernández, Daniel Eduardo Alvarez Amado

Publikováno v: Salud mental. 42:299-308

Background. From the first reports of the linguist Noam Chomsky it has become clear that the development of language has an important genetic component. Several reports in families have shown the relationship between language disorders and genetic po

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9ed2f4932cc09c86413bcea3fad04e65
https://doi.org/10.17711/sm.0185-3325.2019.039

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Metabolic and genetic markers’ associations with elevated levels of alanine aminotransferase in adolescents

Autor: Francisco Mendoza-Carrera, Jorge Salmerón, Victoria Valles-Sánchez, Segundo Morán-Villota, Xochitl Helga Castro-Martínez, Guadalupe Ramírez-López, Eliseo Portilla-de Buen, José Sánchez-Corona

Publikováno v: Journal of Pediatric Endocrinology and Metabolism. 31:407-414

Background: Non-alcoholic fatty liver disease (NAFLD), the most common chronic liver disease in adolescents, is a feature of metabolic syndrome (MetS). Obesity and insulin resistance (IR) are risk factors for NAFLD, as well as inflammation-related ge

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdb0de57a90b2d08b09f7ca292045dab
https://doi.org/10.1515/jpem-2017-0217

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No association of HLA-DRB1 and TNF alleles in Mexican patients with autoimmune hepatitis

Autor: María Inmaculada Concepción Arellano-Olivera, Caridad Leal-Cortés, Francisco Mendoza-Carrera, Xochitl Helga Castro-Martínez, Jesús Ramírez-García, Luis Eduardo Hernández-Ramos, Carlos Dávalos-Cobián, Miguel Ángel Gastélum-Meza

Publikováno v: Genes and immunity. 20(8)

HLA–DRB1 alleles has been found implicated in susceptibility to autoimmune hepatitis (AIH) in populations from different genetic backgrounds. In Mexicans, HLA–DRB1*04:04 is recognized as a risk allele for AIH but, to date, there is no high-resolu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1e5fe30ea8cb11be4bf12a0356fedf7
https://pubmed.ncbi.nlm.nih.gov/31570816

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CYP2C9 and CYP2C19 Allele and Haplotype Distributions in Four Mestizo Populations from Western Mexico: An Interethnic Comparative Study

Autor: Xochitl Helga Castro-Martínez, María Cristina Morán-Moguel, Lilia Carolina León-Moreno, Ana Miriam Saldaña-Cruz, Daniel Alejandro Márquez-de Santiago, José Sánchez-Corona, Alejandra Guadalupe García-Zapién, Francisco Mendoza-Carrera, Silvia Esperanza Flores-Martínez

Publikováno v: Genetic Testing and Molecular Biomarkers. 20:702-709

Polymorphisms in the CYP2C9 and CYP2C19 genes confer potential risk for specific adverse drug reactions and therapeutic effect failure. Their frequencies differ among ethnic groups. This study was aimed to describe the distribution of CYP2C9 and CYP2

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f807836193dadf72b53d24d80e4ff122
https://doi.org/10.1089/gtmb.2016.0115

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Interleukin-1 Alpha Polymorphisms Are Associated With Body Mass Index in Male But Not in Female Adolescents

Autor: Silvia Esperanza Flores-Martínez, Francisco Mendoza-Carrera, Andrés López-Quintero, Eliseo Portilla-de-Buen, Guadalupe Ramírez-López, Anna Gabriela Castro Martínez, Caridad Leal-Cortés, José Sánchez-Corona, Xochitl Helga Castro-Martínez, Luis Eduardo Hernández-Ramos

Publikováno v: Archives of medical research. 50(3)

The Interleukin (IL)-1 family of cytokines plays a key role in the inflammatory response. Genes coding for IL-1α, IL-1β, and IL-1Ra are located together as a block gene known as the IL-1 cluster. This genomic region shows wide nucleotide variabilit

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2bff09e4e76b7b4b08c72477362a578
https://pubmed.ncbi.nlm.nih.gov/31495392

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Behavioral addictions in early-onset Parkinson disease are associated with DRD3 variants

Autor: Francesc Palau, Lydia Vela, Juan Carlos Martínez-Castrillo, Pedro J. Garcia-Ruiz, Carlos Martínez-García, Marina Mata, Janet Hoenicka, Cici Feliz-Feliz, Xochitl Helga Castro-Martínez, Irene Martinez-Torres

Publikováno v: PARKINSONISM & RELATED DISORDERS
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
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r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
r-CIPF: Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
Centro de Investigación Principe Felipe (CIPF)

Background: Impulse control disorders (ICDs) comprise abnormal behaviors frequently found in patients with Parkinson's disease (PD) receiving antiparkinsonian medication. ICDs in PD would develop when dopaminergic treatment overstimulates the dopamin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f49368dbced059e0ac43496d18267d82
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=13507

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Analysis of cytokine gene polymorphisms in Mestizo and native populations from Mexico

Autor: Irene A Gómez-Espinel, Francisco Mendoza-Carrera, Eliseo Portilla-de Buen, Blanca G. Baez-Duarte, Jorge Guillermo Sánchez-Zazueta, Irma Zamora-Ginez, Guadalupe Ramírez-López, Xochitl Helga Castro-Martínez, José Sánchez-Corona, Alejandra Guadalupe García-Zapién, Silvia Esperanza Flores-Martínez, Caridad Leal, Jesús Salvador Velarde-Félix

Publikováno v: American journal of human biology : the official journal of the Human Biology Council. 29(1)

Objectives To determine whether the well-known genetic structure of the Mexican population observed with other multiallelic markers can be detected by analyzing functional polymorphisms of cytokine and other inflammatory-response-related genes. Metho

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfb6bc51ab085da4afe59ecd92d47770
https://pubmed.ncbi.nlm.nih.gov/27482861

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