Zobrazeno 1 - 6
of 6
pro vyhledávání: '"José J. Lugo-Trampe"'
Autor:
Víctor M. Salinas‐Torres, Hugo L. Gallardo‐Blanco, Rafael A. Salinas‐Torres, Ricardo M. Cerda‐Flores, José J. Lugo‐Trampe, Daniel Z. Villarreal‐Martínez, Marisol Ibarra‐Ramírez, Laura E. Martínez de Villarreal
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 5, Pp n/a-n/a (2020)
Abstract Background Genetic association studies for gastroschisis have highlighted several candidate variants. However, genetic basis in gastroschisis from noninvestigated heritable factors could provide new insights into the human biology for this b
Externí odkaz:
https://doaj.org/article/f518ab6c7deb4264b409418854d49862
Autor:
Sandra M. González-Peña, Geovana Calvo-Anguiano, Laura E. Martínez-de-Villarreal, Patricia R. Ancer-Rodríguez, José J. Lugo-Trampe, Donato Saldivar-Rodríguez, María D. Hernández-Almaguer, Melissa Calzada-Dávila, Ligia S. Guerrero-Orjuela, Luis D. Campos-Acevedo
Publikováno v:
Nutrients, Vol 13, Iss 6, p 2071 (2021)
Background: DNA methylation is the best epigenetic mechanism for explaining the interactions between nutrients and genes involved in intrauterine growth and development programming. A possible contributor of methylation abnormalities to congenital he
Externí odkaz:
https://doaj.org/article/f1f1ecb40db74669aec9fd799260da8e
Autor:
Víctor M. Salinas-Torres, Hugo L. Gallardo-Blanco, Rafael A. Salinas-Torres, Ricardo M. Cerda-Flores, José J. Lugo-Trampe, Daniel Z. Villarreal-Martínez, Laura E. Martínez de Villarreal
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 9, p 2295 (2019)
We investigated whether likely pathogenic variants co-segregating with gastroschisis through a family-based approach using bioinformatic analyses were implicated in body wall closure. Gene Ontology (GO)/Panther functional enrichment and protein-prote
Externí odkaz:
https://doaj.org/article/99df7a7337f447ad9afacf7bc9a272b6
Autor:
Melissa Calzada-Dávila, Geovana Calvo-Anguiano, Laura E. Martínez-de-Villarreal, José J. Lugo-Trampe, Sandra M. González-Peña, Patricia R. Ancer-Rodríguez, María D. Hernández-Almaguer, Luis D. Campos-Acevedo
Publikováno v:
Genes; Volume 13; Issue 11; Pages: 2115
(1) Background: The interaction between single nucleotide variants (SNVs) associated with congenital heart diseases (CHDs) and their gene methylation status has not been well researched. The aim of the present study was to determine if there is a rel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66c22317128beddeb7c819e7b84bf2e4
https://doi.org/10.3390/genes13112115
https://doi.org/10.3390/genes13112115
Autor:
Hernández-Almaguer MD; Facultad de Medicina Mexicali, Universidad Autónoma de Baja California, Mexicali, Mexico., Calvo-Anguiano G; Departamento de Genética, Hospital Universitario 'Dr. José E. González,' Universidad Autónoma de Nuevo León, Monterrey, Mexico., Cerda-Flores RM; Facultad de Enfermería, Universidad Autónoma de Nuevo León, Monterrey, Mexico., Salinas-Torres VM; Departamento de Genética, Hospital Universitario 'Dr. José E. González,' Universidad Autónoma de Nuevo León, Monterrey, Mexico., Orozco-Galicia F; Departamento de Genética, Hospital Universitario 'Dr. José E. González,' Universidad Autónoma de Nuevo León, Monterrey, Mexico., Glenn E; Facultad de Medicina Mexicali, Universidad Autónoma de Baja California, Mexicali, Mexico., García-Guerra J; Hospital Regional Materno Infantil, Monterrey, Mexico., Sánchez-Cortés G; Departamento de Pediatría, Hospital Universitario 'Dr. José E. González,' Universidad Autónoma de Nuevo León, Monterrey, Mexico., Lugo-Trampe J; Departamento de Genética, Hospital Universitario 'Dr. José E. González,' Universidad Autónoma de Nuevo León, Monterrey, Mexico., Martínez-Garza LE; Departamento de Genética, Hospital Universitario 'Dr. José E. González,' Universidad Autónoma de Nuevo León, Monterrey, Mexico.
Publikováno v:
Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2019 Sep; Vol. 23 (9), pp. 664-670.
Autor:
Contreras-Capetillo SN; Department of Genetics, Dr. Hideyo Noguchi Regional Research Center, Autonomous University of Yucatan, Mérida, Yucatán CP 97225, Mexico., Blanco HL; Department of Genetics, School of Medicine, Monterrey, Nuevo León CP 64460, Mexico., Cerda-Flores RM; School of Nursing, Autonomous University of Nuevo León, Monterrey, Nuevo León CP 64460, Mexico., Lugo-Trampe J; Department of Genetics, School of Medicine, Monterrey, Nuevo León CP 64460, Mexico., Torres-Muñoz I; Department of Genetics, School of Medicine, Monterrey, Nuevo León CP 64460, Mexico., Bravo-Oro A; Neuropediatrics, Central Hospital 'Dr. Ignacio Morones Prieto', San Luis Potosí CP 78240, Mexico., Esmer C; Department of Genetics, Central Hospital 'Dr. Ignacio Morones Prieto', San Luis Potosí CP 78240, Mexico., DE Villarreal LE; Department of Genetics, School of Medicine, Monterrey, Nuevo León CP 64460, Mexico.
Publikováno v:
Experimental and therapeutic medicine [Exp Ther Med] 2015 Jun; Vol. 9 (6), pp. 2053-2058. Date of Electronic Publication: 2015 Apr 20.