Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Juan P. Meza-Espinoza"'
Autor:
Valeria Peralta-Leal, Evelia Leal-Ugarte, Juan P. Meza-Espinoza, Ingrid P. Dávalos-Rodríguez, Anabel Bocanegra-Alonso, Rosa I. Acosta-González, Enrique Gonzales, Saraswathy Nair, Jorge Durán-González
Publikováno v:
Genetics and Molecular Biology, Vol 35, Iss 3, Pp 589-593 (2012)
The serotonergic system has been hypothesized to contribute to the biological susceptibility to type 2 diabetes mellitus (T2DM) and body-mass index (BMI) categories. We investigate a possible association of 5-HTTLPR polymorphism (L and S alleles) in
Externí odkaz:
https://doaj.org/article/d344bf945f1f4079934b5402142db90f
Autor:
Juan Pablo Meza-Espinoza, Juan Ramón González-García, Nayeli Nieto-Marín, Liliana Itzel Patrón-Baro, Rosa María González-Arreola, Eliakym Arámbula-Meraz, Julio Benítez-Pascual, Alberto Kousuke De la Herrán-Arita, Claudia Desireé Norzagaray-Valenzuela, Marco Antonio Valdez-Flores, Tomás Adrián Carrillo-Cázares, Verónica Judith Picos-Cárdenas
Publikováno v:
Molecular Cytogenetics, Vol 17, Iss 1, Pp 1-9 (2024)
Abstract Background Ring chromosome 14 syndrome is a rare disorder primarily marked by early-onset epilepsy, microcephaly, distinctive craniofacial features, hypotonia, intellectual disability, and delay in both development and language acquisition.
Externí odkaz:
https://doaj.org/article/e33d5175759a4250aeb0dc1cd2918616
Autor:
Juan Pablo Meza-Espinoza, Valeria Peralta-Leal, Jorge Durán-González, Nelly Macías-Gómez, Anabel Bocanegra-Alonso, Evelia Leal-Ugarte
Publikováno v:
Genetics Research, Vol 2023 (2023)
Colorectal cancer (CRC) is one of the most common cancers worldwide. Its etiopathogenesis is complex, mainly influenced by genetic instability caused by the accumulation of mutations. The XRCC1 gene, which is involved in DNA repair, has been associat
Externí odkaz:
https://doaj.org/article/2d973d6bbbd946cf8577be13442f5e1e
Autor:
Juan Pablo Meza-Espinoza, José Alfredo Contreras-Gutiérrez, Eliakym Arámbula-Meraz, Juan Ramón González-García, Ma. Guadalupe Domínguez-Quezada, Noemí García-Magallanes, Jesús Madueña-Molina, Julio Benítez-Pascual, Miriam Partida-Pérez, Verónica Judith Picos-Cárdenas
Publikováno v:
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-8 (2021)
Abstract Background 4q deletion syndrome is a rare chromosomal disorder that mostly arises de novo. The syndrome is characterized by craniofacial dysmorphism, digital abnormalities, skeletal alterations, heart malformations, developmental delay, grow
Externí odkaz:
https://doaj.org/article/58e75f044b6d4ba493f7a36db8751beb
Publikováno v:
The Turkish Journal of Gastroenterology, Vol 34, Iss 7, Pp 779-779 (2023)
Externí odkaz:
https://doaj.org/article/773c696a1dbd4667a92b3b4372a63109
Autor:
Juan Pablo Meza-Espinoza, Enrique Sáinz González, Christian J. N. León-León, Eliakym Arámbula-Meraz, José Alfredo Contreras-Gutiérrez, Noemí García-Magallanes, Jesús Madueña-Molina, Fred Luque-Ortega, Salvador Cervín-Serrano, Verónica Judith Picos-Cárdenas
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-7 (2020)
Abstract Background Concomitant trisomy 2q3 and monosomy 4q3 have been rarely reported. Pure trisomy 2q3 has been associated with microcephaly, hypertelorism, low-set ears, micrognathia, visceral abnormalities, and growth retardation. Monosomy 4q3 in
Externí odkaz:
https://doaj.org/article/982862c5d1c441fab377338617081324