Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Juan Carlos Fernández-López"'
Autor:
Enrique Ambrocio-Ortiz, Gloria Pérez-Rubio, Alejandra Ramírez-Venegas, Rafael de Jesús Hernández-Zenteno, Juan Carlos Fernández-López, María Elena Ramírez-Díaz, Filiberto Cruz-Vicente, María de Lourdes Martínez-Gómez, Raúl Sansores, Julia Pérez-Ramos, Ramcés Falfán-Valencia
Publikováno v:
Current Issues in Molecular Biology, Vol 45, Iss 2, Pp 799-819 (2023)
Chronic obstructive pulmonary disease (COPD) is the third leading cause of death worldwide; the main risk factors associated with the suffering are tobacco smoking (TS) and chronic exposure to biomass-burning smoke (BBS). Different biological pathway
Externí odkaz:
https://doaj.org/article/b3958effa7c246bba04eb47799c80d1c
Autor:
Karol J. Nava-Quiroz, Jorge Rojas-Serrano, Gloria Pérez-Rubio, Ivette Buendia-Roldan, Mayra Mejía, Juan Carlos Fernández-López, Espiridión Ramos-Martínez, Luis A. López-Flores, Alma D. Del Ángel-Pablo, Ramcés Falfán-Valencia
Publikováno v:
Data, Vol 9, Iss 1, p 5 (2023)
Rheumatoid arthritis (RA) is an autoimmune disease mainly characterized by joint inflammation. It presents extra-articular manifestations, with the lungs being one of the affected areas. Among these, damage to the pulmonary interstitium (Interstitial
Externí odkaz:
https://doaj.org/article/1ffbf325db4740fea1759e76f4198a20
Autor:
Karol J. Nava-Quiroz, Jorge Rojas-Serrano, Gloria Pérez-Rubio, Ivette Buendia-Roldan, Mayra Mejía, Juan Carlos Fernández-López, Pedro Rodríguez-Henríquez, Noé Ayala-Alcantar, Espiridión Ramos-Martínez, Luis Alberto López-Flores, Alma D. Del Ángel-Pablo, Ramcés Falfán-Valencia
Publikováno v:
Cells, Vol 12, Iss 18, p 2235 (2023)
Around 50% of rheumatoid arthritis (RA) patients show some extra-articular manifestation, with the lung a usually affected organ; in addition, the presence of anti-citrullinated protein antibodies (ACPA) is a common feature, which is caused by protei
Externí odkaz:
https://doaj.org/article/e4e4ffe1a0bd462d9d83fee963d70276
Autor:
Israel Aguilar-Ordoñez, Fernando Pérez-Villatoro, Humberto García-Ortiz, Francisco Barajas-Olmos, Judith Ballesteros-Villascán, Ram González-Buenfil, Cristobal Fresno, Alejandro Garcíarrubio, Juan Carlos Fernández-López, Hugo Tovar, Enrique Hernández-Lemus, Lorena Orozco, Xavier Soberón, Enrique Morett
Publikováno v:
PLoS ONE, Vol 17, Iss 5, p e0269217 (2022)
[This corrects the article DOI: 10.1371/journal.pone.0249773.].
Externí odkaz:
https://doaj.org/article/0b76975c41fd4da3840c619209cf1122
Autor:
Alicia Huerta-Chagoya, Hortensia Moreno-Macías, Juan Carlos Fernández-López, María Luisa Ordóñez-Sánchez, Rosario Rodríguez-Guillén, Alejandra Contreras, Alfredo Hidalgo-Miranda, Luis Alberto Alfaro-Ruíz, Edgar Pavel Salazar-Fernandez, Andrés Moreno-Estrada, Carlos Alberto Aguilar-Salinas, Teresa Tusié-Luna
Publikováno v:
BMC Genetics, Vol 20, Iss 1, Pp 1-11 (2019)
Abstract Background Association studies are useful to unravel the genetic basis of common human diseases. However, the presence of undetected population structure can lead to both false positive results and failures to detect genuine associations. Ev
Externí odkaz:
https://doaj.org/article/ba897d81a80f47dd95f13ef840a8f202
Autor:
Israel Aguilar-Ordoñez, Fernando Pérez-Villatoro, Humberto García-Ortiz, Francisco Barajas-Olmos, Judith Ballesteros-Villascán, Ram González-Buenfil, Cristobal Fresno, Alejandro Garcíarrubio, Juan Carlos Fernández-López, Hugo Tovar, Enrique Hernández-Lemus, Lorena Orozco, Xavier Soberón, Enrique Morett
Publikováno v:
PLoS ONE, Vol 16, Iss 4, p e0249773 (2021)
There has been limited study of Native American whole genome diversity to date, which impairs effective implementation of personalized medicine and a detailed description of its demographic history. Here we report high coverage whole genome sequencin
Externí odkaz:
https://doaj.org/article/62a98caa338e49a4b8d333acaeb1af8e
Autor:
Aurora Medina-Sanson, Juan Carlos Núñez-Enríquez, Eduardo Hurtado-Cordova, María Luisa Pérez-Saldivar, Anayeli Martínez-García, Elva Jiménez-Hernández, Juan Carlos Fernández-López, Jorge Alfonso Martín-Trejo, Héctor Pérez-Lorenzana, Janet Flores-Lujano, Raquel Amador-Sánchez, Felix Gustavo Mora-Ríos, José Gabriel Peñaloza-González, David Aldebarán Duarte-Rodríguez, José Refugio Torres-Nava, Juan Eduardo Flores-Bautista, Rosa Martha Espinosa-Elizondo, Pedro Francisco Román-Zepeda, Luz Victoria Flores-Villegas, Juana Esther González-Ulivarri, Sofía Irene Martínez-Silva, Gilberto Espinoza-Anrubio, Carolina Almeida-Hernández, Rosario Ramírez-Colorado, Luis Hernández-Mora, Luis Ramiro García-López, Gabriela Adriana Cruz-Ojeda, Arturo Emilio Godoy-Esquivel, Iris Contreras-Hernández, Abraham Medina-Hernández, María Guadalupe López-Caballero, Norma Angélica Hernández-Pineda, Jorge Granados-Kraulles, María Adriana Rodríguez-Vázquez, Delfino Torres-Valle, Carlos Cortés-Reyes, Francisco Medrano-López, Jessica Arleet Pérez-Gómez, Annel Martínez-Ríos, Antonio Aguilar-De los Santos, Berenice Serafin-Díaz, Vilma Carolina Bekker-Méndez, Minerva Mata-Rocha, Blanca Angélica Morales-Castillo, Omar Alejandro Sepúlveda-Robles, Julián Ramírez-Bello, Haydeé Rosas-Vargas, Alfredo Hidalgo-Miranda, Juan Manuel Mejía-Aranguré, Silvia Jiménez-Morales
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
Background: Acute lymphoblastic leukemia (ALL) is the main type of cancer in children. In Mexico and other Hispanic populations, the incidence of this neoplasm is one of the highest reported worldwide. Functional polymorphisms of various enzymes invo
Externí odkaz:
https://doaj.org/article/212c864e3d6e45fb8d39f602a1c63e61
Autor:
Sandra Romero-Hidalgo, Adrián Ochoa-Leyva, Alejandro Garcíarrubio, Victor Acuña-Alonzo, Erika Antúnez-Argüelles, Martha Balcazar-Quintero, Rodrigo Barquera-Lozano, Alessandra Carnevale, Fernanda Cornejo-Granados, Juan Carlos Fernández-López, Rodrigo García-Herrera, Humberto García-Ortíz, Ángeles Granados-Silvestre, Julio Granados, Fernando Guerrero-Romero, Enrique Hernández-Lemus, Paola León-Mimila, Gastón Macín-Pérez, Angélica Martínez-Hernández, Marta Menjivar, Enrique Morett, Lorena Orozco, Guadalupe Ortíz-López, Fernando Pérez-Villatoro, Javier Rivera-Morales, Fernando Riveros-McKay, Marisela Villalobos-Comparán, Hugo Villamil-Ramírez, Teresa Villarreal-Molina, Samuel Canizales-Quinteros, Xavier Soberón
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-8 (2017)
People of Mexico have diverse historical and genetic background. Here, Romero-Hidalgo and colleagues sequence whole genomes of Native Americans of Mexico, and show demographic history and genetic variation shared among subgroups of Native Americans.
Externí odkaz:
https://doaj.org/article/05f1d6a41af94d978a388605d8eb5bf1
Autor:
Gloria Pérez-Rubio, Ramcés Falfán-Valencia, Juan Carlos Fernández-López, Alejandra Ramírez-Venegas, Rafael de Jesús Hernández-Zenteno, Fernando Flores-Trujillo, Irma Silva-Zolezzi
Publikováno v:
Diagnostics, Vol 11, Iss 4, p 599 (2021)
Genetic variability influences the susceptibility to and severity of complex diseases; there is a lower risk of COPD in Hispanics than in non-Hispanic Caucasians. In this study, we included 830 Mexican-Mestizo subjects; 299 were patients with COPD se
Externí odkaz:
https://doaj.org/article/313123d312154490884b8355c68117d9
Autor:
Cecilia Contreras-Cubas, Beatríz E Sánchez-Hernández, Humberto García-Ortiz, Angélica Martínez-Hernández, Francisco Barajas-Olmos, Miguel Cid, Elvia C Mendoza-Caamal, Federico Centeno-Cruz, Gabriela Ortiz-Cruz, José Concepción Jiménez-López, Emilio J Córdova, Eva Gabriela Salas-Bautista, Yolanda Saldaña-Alvarez, Juan Carlos Fernández-López, Osvaldo M Mutchinick, Lorena Orozco
Publikováno v:
PLoS ONE, Vol 11, Iss 9, p e0163248 (2016)
Methylenetetrahydrofolate reductase (MTHFR) is a key enzyme in folate metabolism. Folate deficiency has been related to several conditions, including neural tube defects (NTDs) and cardiovascular diseases. Hence, MTHFR genetic variants have been stud
Externí odkaz:
https://doaj.org/article/ddcf348243e04641a19a0812ff1f6f1b