Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Víctor M. Salinas-Torres"'
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:
Víctor M. Salinas-Torres, Hugo L. Gallardo-Blanco, Rafael A. Salinas-Torres, Laura E. Martínez de Villarreal
Publikováno v:
Data, Vol 4, Iss 3, p 97 (2019)
Gastroschisis is one of the most prevalent human birth defects concerning the ventral body wall development. Recent research has given a better understanding of gastroschisis pathogenesis through the identification of multiple novel pathogenetic path
Externí odkaz:
https://doaj.org/article/d0a803a393b44ccb92faf55cc1d2154d
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:
Maria Dolores, Hernández-Almaguer, Geovana, Calvo-Anguiano, Ricardo M, Cerda-Flores, Víctor M, Salinas-Torres, Francisco, Orozco-Galicia, Eva, Glenn, Jaime, García-Guerra, Gerardo, Sánchez-Cortés, José, Lugo-Trampe, Laura E, Martínez-Garza
Publikováno v:
Genetic testing and molecular biomarkers. 23(9)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::762c72b44bc6b2aed3dc0c6e5c18f499
https://pubmed.ncbi.nlm.nih.gov/31524541
https://pubmed.ncbi.nlm.nih.gov/31524541
Autor:
Víctor M, Salinas-Torres, Martha E, Ramos-Márquez, Leticia, Serra-Ruiz, Eusebio, Angulo-Castellanos
Publikováno v:
Archivos argentinos de pediatria. 110(4)
VACTERL-H syndrome is a complex disorder of congenital malformations that implies vertebrae, anus, heart, trachea, esophagus, kidneys, limbs and hydrocephalus. Its etiology has been identified in a fraction of patients largely due to their sporadic n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6a307c2977b7213b82a4bce4b389b79a
https://pubmed.ncbi.nlm.nih.gov/22859335
https://pubmed.ncbi.nlm.nih.gov/22859335