Zobrazeno 1 - 10 of 25 pro vyhledávání: '"Marisol Ibarra-Ramírez"'
1
Akademický článek
Expression profile of microRNAs in the testes of patients with Klinefelter syndrome
Autor: Marisol Ibarra-Ramírez, Geovana Calvo-Anguiano, José de Jesús Lugo-Trampe, Laura Elia Martínez-de-Villarreal, David Rodríguez-Torres, Manuel Nistal, Pilar González-Peramato
Publikováno v: Scientific Reports, Vol 10, Iss 1, Pp 1-11 (2020)
Abstract Klinefelter syndrome (KS) is the most common sex chromosome aneuploidy. A distinctive characteristic of KS is oligozoospermia. Despite multiple studies that have described the natural history of the degenerative process of germ cells in pati
Externí odkaz: https://doaj.org/article/9ef4831d8d774443994ce2e6bb432e32
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2
Akademický článek
Whole exome sequencing identifies multiple novel candidate genes in familial gastroschisis
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
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3
The Latin American network for congenital malformation surveillance: ReLAMC
Autor: Lucas Gabriel Gimenez, Marta Ascurra, Paula Hurtado-Villa, Jorge S. Lopez-Camelo, Maria Aurora Canessa‐Tapia, Dania Maria Pastora, Flávia Martinez de Carvalho, Daniel Mattos Correa, Iêda M. Orioli, Adriana Benavides-Lara, Boris Groisman, Flávia Schneider Soares, Giovanny Vinícius Araújo de França, Marisol Ibarra-Ramírez, Mariana Piola, Rosa Pardo, Helen Dolk, Ignacio Zarante, Eliana de Aquino Bonilha
Publikováno v: American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 184:1078-1091
The early detection of congenital anomaly epidemics occurs when comparing current with previous frequencies in the same population. The success of epidemiologic surveillance depends on numerous factors, including the accuracy of the rates available i
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26b277a7c232a409c943ffd94f340b68
https://doi.org/10.1002/ajmg.c.31872
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4
Expression profile of microRNAs in the testes of patients with Klinefelter syndrome
Autor: Geovana Calvo-Anguiano, Manuel Nistal, Laura Elia Martínez-de-Villarreal, David Rodríguez-Torres, José de Jesús Lugo-Trampe, Marisol Ibarra-Ramírez, Pilar González-Peramato
Publikováno v: Scientific Reports, Vol 10, Iss 1, Pp 1-11 (2020)
Scientific Reports
Biblos-e Archivo: Repositorio Institucional de la UAM
Universidad Autónoma de Madrid
Biblos-e Archivo. Repositorio Institucional de la UAM
Consejo Superior de Investigaciones Científicas (CSIC)
Klinefelter syndrome (KS) is the most common sex chromosome aneuploidy. A distinctive characteristic of KS is oligozoospermia. Despite multiple studies that have described the natural history of the degenerative process of germ cells in patients with
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d89306e3da076bfc85b33b946daa861
https://doaj.org/article/9ef4831d8d774443994ce2e6bb432e32
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6
Gene expression in peripheral blood in treatment-free major depression
Autor: Antonio Costilla-Esquivel, Jorge A. Sánchez-Ruiz, José Lugo, Iram P. Rodriguez-Sanchez, Geovana Calvo, Marisol Ibarra-Ramírez, Laura Martinez, Sarai Rodríguez González, Alfredo B. Cuellar-Barboza
Publikováno v: Acta Neuropsychiatrica. 32:135-144
Background:Peripheral gene expression of several molecular pathways has been studied in major depressive disorder (MDD) with promising results. We sought to investigate some of these genes in a treatment-free Latino sample of Mexican descent.Material
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fd7079061f10b81bcf85572cbb4cc5f
https://doi.org/10.1017/neu.2020.5
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7
How Does Comprehensive Care Impact Life of Pediatric Patients With Hemophilia? Results From a Center in a Developing Country
Autor: Laura Villarreal-Martínez, Marcela Cantú-Moreno, José A Garza, Marbely Quiroga-Treviño, Ileana Velasco-Ruiz, Sulia E Pope-Salazar, Domingo Garay-Mendoza, Atenas Meléndez-Aguirre, Marisol Ibarra-Ramírez
Publikováno v: Journal of Pediatric Hematology/Oncology. 41:601-605
BACKGROUND Quality of life (QoL) has been included as a marker of treatment effectiveness in pediatric patients with chronic diseases. We believe that frequent multidisciplinary interventions and patient education could lead to an improvement in QoL.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbf1752cf7d88947b6c545ff0342b9ae
https://doi.org/10.1097/mph.0000000000001575
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