Zobrazeno 1 - 10
of 26
pro vyhledávání: '"María Teresa Villarreal Molina"'
Autor:
Leda Torres, Pedro Reyes, Benilde García-de Teresa, María Teresa Villarreal Molina, Ulises Juárez, Angélica Solis, Moises Fiesco-Roa, Fernando Pérez Villatoro, Bertha Molina, Alfredo Rodríguez, Alessandra Carnevale, Sara Frías
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101564- (2024)
Externí odkaz:
https://doaj.org/article/812ed95c8673480fb911c62bcbf97dca
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:
Sandra Rosas-Madrigal, María Teresa Villarreal-Molina, José Flores-Rivera, Verónica Rivas-Alonso, Luis Rodrigo Macias-Kauffer, Graciela Ordoñez, María del Carmen Chima-Galán, Víctor Acuña-Alonzo, Gastón Macín-Pérez, Rodrigo Barquera, Julio Granados, Ricardo Valle-Rios, Teresa Corona, Alessandra Carnevale, Sandra Romero-Hidalgo
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Neuromyelitis Optica Spectrum Disorder (NMOSD) is a demyelinating autoimmune disease of the central nervous system, more prevalent in individuals of non-European ancestry. Few studies have analyzed genetic risk factors in NMOSD, and HLA class II gene
Externí odkaz:
https://doaj.org/article/aebb55ac4b2e498c8c34592a56d7fbfb
Autor:
Alessandra Carnevale, Sandra Rosas‐Madrigal, Rigoberto Rosendo‐Gutiérrez, Enrique López‐Mora, Sandra Romero‐Hidalgo, Nydia Avila‐Vazzini, Leonor Jacobo‐Albavera, Mayra Domínguez‐Pérez, Gilberto Vargas‐Alarcón, Fernando Pérez‐Villatoro, Juana Inés Navarrete‐Martínez, María Teresa Villarreal–Molina
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 11, Pp n/a-n/a (2020)
Abstract Background Dilated cardiomyopathy (DCM) is a major cause of nonischemic heart failure and death in young adults. Next generation sequencing (NGS) has become part of the diagnostic workup in idiopathic and familial DCM. More than 50 DCM genes
Externí odkaz:
https://doaj.org/article/599d186982a54fa1bc443a52769359ef
Autor:
Marisela Villalobos-Comparán, Bárbara Antuna-Puente, María Teresa Villarreal-Molina, Samuel Canizales-Quinteros, Rafael Velázquez-Cruz, Paola León-Mimila, Hugo Villamil-Ramírez, Juan Antonio González-Barrios, José Luis Merino-García, María Rocío Thompson-Bonilla, Diego Jarquin, Osvaldo Erik Sánchez-Hernández, Martha Eunice Rodríguez-Arellano, Carlos Posadas-Romero, Gilberto Vargas-Alarcón, Francisco Campos-Pérez, Manuel Quiterio, Jorge Salmerón-Castro, Alessandra Carnevale, Sandra Romero-Hidalgo
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-6 (2017)
Abstract Background The aim of this study was to explore whether interactions between FTO rs9939609 and ABCA1 rs9282541 affect BMI and waist circumference (WC), and could explain previously reported population differences in FTO-obesity and FTO-BMI a
Externí odkaz:
https://doaj.org/article/c2f9f236a14b4b749effc0fbcec7d347
Autor:
Berenice Otero-Díaz, Marcela Rodríguez-Flores, Verónica Sánchez-Muñoz, Fernando Monraz-Preciado, Samuel Ordoñez-Ortega, Vicente Becerril-Elias, Guillermina Baay-Guzmán, Rodolfo Obando-Monge, Eduardo García-García, Berenice Palacios-González, María Teresa Villarreal-Molina, Mauricio Sierra-Salazar, Barbara Antuna-Puente
Publikováno v:
Frontiers in Physiology, Vol 9 (2018)
While the effect of exercise on white adipose tissue browning and metabolic improvement in rodents is clear, there are few studies in humans with inconclusive results. Thus, the aim of the study was to assess whether an exercise intervention promotes
Externí odkaz:
https://doaj.org/article/8bebd4f536124352a2b35ea0516dabac
Autor:
Antonia, González-Garrido, Sandra, Rosas-Madrigal, Arturo, Rojo-Domínguez, Jaime, Arellanes-Robledo, Enrique, López-Mora, Alessandra, Carnevale, Leticia, Arregui, Rigoberto, Rosendo-Gutiérrez, Sandra, Romero-Hidalgo, María Teresa, Villarreal-Molina
Publikováno v:
International journal of molecular sciences. 23(21)
The clinical phenotype of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c7bbdeb7c091850612032162bdfa2be0
https://pubmed.ncbi.nlm.nih.gov/36362411
https://pubmed.ncbi.nlm.nih.gov/36362411
Autor:
Pedro Reyes, Benilde García-de Teresa, Ulises Juárez, Fernando Pérez-Villatoro, Moisés O. Fiesco-Roa, Alfredo Rodríguez, Bertha Molina, María Teresa Villarreal-Molina, Jorge Meléndez-Zajgla, Alessandra Carnevale, Leda Torres, Sara Frias
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 4; Pages: 2334
Fanconi anemia (FA) is a rare genetic disorder caused by pathogenic variants (PV) in at least 22 genes, which cooperate in the Fanconi anemia/Breast Cancer (FA/BRCA) pathway to maintain genome stability. PV in FANCA, FANCC, and FANCG account for most
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be937e4af9a3ccaac899ca888e7021b2
Autor:
Victor Acuña-Alonzo, Alessandra Carnevale, Ricardo Valle-Rios, Verónica Rivas-Alonso, Rodrigo Barquera, Julio Granados, Sandra Rosas-Madrigal, Gastón Macín-Pérez, María del Carmen Chima-Galán, Luis Macías-Kauffer, Sandra Romero-Hidalgo, José Flores-Rivera, Teresa Corona, Graciela Ordoñez, María Teresa Villarreal-Molina
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 12 (2021)
Frontiers in Genetics, Vol 12 (2021)
Neuromyelitis Optica Spectrum Disorder (NMOSD) is a demyelinating autoimmune disease of the central nervous system, more prevalent in individuals of non-European ancestry. Few studies have analyzed genetic risk factors in NMOSD, and HLA class II gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8aa3b78732463f36f25a258e744b05a0
https://doi.org/10.3389/fgene.2021.647343
https://doi.org/10.3389/fgene.2021.647343
Autor:
Enrique López-Mora, Hugo Rodríguez-Zanella, Rigoberto Rosendo-Gutiérrez, Ana L. Calderón-Avila, Alessandra Carnevale, Sandra Romero-Hidalgo, Sandra Rosas-Madrigal, María Teresa Villarreal-Molina
Publikováno v:
Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion. 73(5)
espanolAntecedentes: la distrofia muscular congenita de Fukuyama (FCMD) es la forma mas comun de un grupo de trastornos autosomicos recesivos caracterizados por una glicosilacion alterada de a-distroglicanos y causada por mutaciones del gen FKTN. Sin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b850d95383a62c6a0a3690b801394f9
https://pubmed.ncbi.nlm.nih.gov/33048919
https://pubmed.ncbi.nlm.nih.gov/33048919