Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Iris Torres Muñoz"'
Autor:
Viviana Maricela Gómez-Puente, José de Jesús Lugo-Trampe, Michelle de Jesús Zamudio-Osuna, S. Elisa Schaeffer, Braulio Hernán Velasco-Sepúlveda, Patricia Arredondo-Vázquez, Luis Daniel Campos-Acevedo, Jesús Zacarías Villarreal-Pérez, Iram P. Rodriguez-Sanchez, Laura Elia Martínez-de-Villarreal, Gloria García-Castañeda, Iris Torres-Muñoz, Marisol Ibarra-Ramírez
Publikováno v:
Genetic Testing and Molecular Biomarkers. 24:352-358
Aims: To explore the feasibility of detecting sex chromosome aneuploidies (SCAs) by means of gene copy number quantification of short stature homeobox (SHOX), vesicle-associated membrane protein 7 (VAMP7), and SRY in newborns. Materials and Methods:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b211651ec317d00cb0d36258a88c873
https://doi.org/10.1089/gtmb.2019.0226
https://doi.org/10.1089/gtmb.2019.0226
Autor:
Gloria Beatriz García Castañeda, Graciela Arelí López Uriarte, Laura Martínez de Villareal, Iris Torres Muñoz, Marco Antonio Ponce Camacho, Oralia Barboza Quintana, José de Jesús Lugo Trampe, Kiabeth Robles Espinoza, Guillermo Elizondo Riojas, Abel Guzmán López
Purpose Stillbirth is an important health problem in obstetrics practice. In Mexico, half of the stillbirths have an explainable cause. The aim of this study was to detect potential stillbirth risk factors and etiology by implementing a multidiscipli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25a4a57f6a3d1f9e2b3d6c66bdd495d7
https://doi.org/10.21203/rs.3.rs-647477/v1
https://doi.org/10.21203/rs.3.rs-647477/v1
Autor:
Marisol, Ibarra-Ramírez, José de Jesús, Lugo-Trampe, Luis Daniel, Campos-Acevedo, Michelle, Zamudio-Osuna, Iris, Torres-Muñoz, Viviana, Gómez-Puente, Gloria, García-Castañeda, Patricia, Arredondo-Vázquez, Irám Pablo, Rodríguez-Sánchez, S Elisa, Schaeffer, Braulio Hernán, Velasco-Sepúlveda, Jesús Zacarías, Villarreal-Pérez, Laura Elia, Martínez-de-Villarreal
Publikováno v:
Genetic testing and molecular biomarkers. 24(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4b62fd256090725c4aa88c781624e83b
https://pubmed.ncbi.nlm.nih.gov/32423256
https://pubmed.ncbi.nlm.nih.gov/32423256
Autor:
Iram P. Rodriguez-Sanchez, Michelle de Jesús Zamudio-Osuna, Laura Elia Martínez-de-Villarreal, Luz Rojas-Patlan, Ma Del Roble Velasco-Campos, Iris Torres-Muñoz, José de Jesús Lugo-Trampe, Luis Daniel Campos-Acevedo, Marisol Ibarra-Ramírez
Publikováno v:
Genetic Testing and Molecular Biomarkers. 20:786-790
In this study, we examined the doses of the stature homeobox (SHOX), vesicle-associated membrane protein 7 (VAMP7), and SRY genes to establish a protocol for using peripheral blood samples deposited on filter paper for the screening of sex chromosome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d386b488bdff80c8e7e58978476df110
https://doi.org/10.1089/gtmb.2016.0101
https://doi.org/10.1089/gtmb.2016.0101
Autor:
Ricardo M. Cerda-Flores, Silvina Contreras-Capetillo, José de Jesús Lugo-Trampe, Antonio Bravo-Oro, Hugo Leonid Gallardo‑Blanco, Carmen Esmer, Laura Ella Martínez De Villarreal, Iris Torres-Muñoz
Publikováno v:
Experimental and Therapeutic Medicine. 9:2053-2058
Individuals who suffer from spinal muscular atrophy (SMA) exhibit progressive muscle weakness that frequently results in mortality in the most severe forms of the disease. In 98% of cases, there is a homozygous deletion of the survival of motor neuro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::614ad8b8b0cedbd0fd92a8a1fc210050
https://doi.org/10.3892/etm.2015.2436
https://doi.org/10.3892/etm.2015.2436
Autor:
Silvina Noemi, Contreras-Capetillo, Hugo Leonid Gallardo, Blanco, Ricardo Martin, Cerda-Flores, José, Lugo-Trampe, Iris, Torres-Muñoz, Antonio, Bravo-Oro, Carmen, Esmer, Laura Ella Martínez, DE Villarreal
Publikováno v:
Experimental and therapeutic medicine. 9(6)
Individuals who suffer from spinal muscular atrophy (SMA) exhibit progressive muscle weakness that frequently results in mortality in the most severe forms of the disease. In 98% of cases, there is a homozygous deletion of the survival of motor neuro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::947e18af1528f545fbd46473807bcbe4
https://pubmed.ncbi.nlm.nih.gov/26136935
https://pubmed.ncbi.nlm.nih.gov/26136935