Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Judith Villa-Morales"'
Autor:
Salvador Atilano-Miguel, Lourdes Barbosa-Cortés, Rocío Ortiz-Muñiz, Jorge Maldonado-Hernández, Jorge A. Martin-Trejo, Maricela Rodríguez-Cruz, Lourdes Balcázar-Hernández, Karina A. Solís-Labastida, Benito A. Bautista-Martínez, Azalia Juárez-Moya, Zayra Hernández-Piñón, Raeline A. Galindo-Rodríguez, Adriana Chávez-Anaya, Rosa E. Valdez-Avilez, Juan M. Domínguez-Salgado, Judith Villa-Morales, María E. Rodríguez-Palacios
Publikováno v:
Cancers, Vol 16, Iss 16, p 2811 (2024)
Background: The receptor activator of the nuclear factor-kB (RANK)/RANK ligand (RANKL)/osteoprotegerin (OPG) pathway is a determining pathway in the balance between bone formation and resorption, and disruptions in this complex can affect bone metabo
Externí odkaz:
https://doaj.org/article/e4dfcf686bd44bd1a398e5abed9f9d5b
Autor:
Tomas Almeida-Becerril, Maricela Rodríguez-Cruz, Judith Villa-Morales, Christian Ricardo Sánchez-Mendoza, Jose Emilio Galeazzi-Aguilar
Publikováno v:
Antioxidants, Vol 12, Iss 4, p 871 (2023)
Oxidative stress (OS) plays an essential role in the pathophysiology of Duchenne muscular dystrophy (DMD). However, the actors that regulate OS need to be better studied. We aimed to evaluate whether NFE2-like bZIP transcription factor 2 (Nrf2), glut
Externí odkaz:
https://doaj.org/article/04336dd83aaf49a5b4b888806a771201
Autor:
Pilar A. Badillo-Suárez, Maricela Rodríguez-Cruz, Mariela Bernabe-García, Judith Villa-Morales, Ricardo Iglesias-Rodríguez, Samuel Canizales-Quinteros, Fairt V. Carmona-Sierra
Publikováno v:
Journal of Human Lactation. 38:619-632
Background: Insulin, insulin-like Growth Factor-1 (IGF-1), and obestatin in human milk originate from the circulation. There is also limited knowledge about the influence of body fat on the levels of these hormones in human milk. Research Aim: To det
Autor:
Alan Cárdenas-Conejo, Tomas Almeida-Becerril, René Cárdenas-Vázquez, Juan Raúl Sánchez-González, Judith Villa-Morales, Maricela Rodríguez-Cruz, Marco Antonio Villaldama-Soriano, Salvador Atilano-Miguel
Publikováno v:
Braindevelopment. 43(1)
A small number of studies have confirmed the presence of oxidative damage in patients with Duchenne muscular dystrophy (DMD). Nevertheless, it is unknown if there a relationship of circulating markers of oxidative stress with a muscle injury.We evalu
Autor:
Laura Gómez-Laguna, Alejandra Del Pilar Reyes-de la Rosa, Judith Villa-Morales, Verónica Fabiola Morán-Barroso, Alicia Cervantes, Ariadna Berenice Morales-Jiménez, Constanza García-Delgado, Alejandro Martínez-Herrera, Fernando Fernández-Ramírez, Tania Yanet Valderrama-Atayupanqui, Susana Kofman, Karem Nieto-Martínez
Publikováno v:
Ophthalmic Genetics. 39:56-62
The Nance-Horan syndrome is an X-linked disorder characterized by congenital cataract, facial features, microcornea, microphthalmia, and dental anomalies; most of the cases are due to NHS gene mutations on Xp22.13. Heterozygous carrier females genera
Autor:
Amilcar Polanco-Ortiz, Leovigildo Mateos-Sánchez, Eunice López-Muñoz, Judith Villa-Morales, Adelina Hernández-Zarco
Publikováno v:
Journal of Pediatric Urology. 9:e12-e18
Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) was first described in 1976. A rare congenital autosomal recessive alteration that predominantly affects females (4:1 ratio), it is characterized by the presence of distended bladder (
Autor:
Susana Kofman, Verónica Fabiola Morán-Barroso, Karem Nieto-Martínez, Jaime Berumen, Ariadna Berenice Morales-Jiménez, Mónica Quintana-Palma, Fernando Fernández-Ramírez, Carolina Isabel Galaz-Montoya, Judith Villa-Morales, Alicia Cervantes, Laura Gómez-Laguna, Constanza García-Delgado
Publikováno v:
BMC Medical Genomics
Background Trisomy 1q and monosomy 3p deriving from a t(1;3) is an infrequent event. The clinical characteristics of trisomy 1q41-qter have been described but there is not a delineation of the syndrome. The 3p25.3-pter monosomy syndrome (MIM 613792)