Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Laura Elia Martínez-de Villarreal"'
Prevalencia del polimorfismo 677T del gen MTHFR en una muestra de la población de Nuevo León, México
Autor:
Ana Alejandra Aguirre-Rodríguez, Laura Elia Martínez-de Villarreal, María del Roble Velazco-Campos, Ernestina Sampallo-Hernández, María del Carmen Esmer-Sánchez
Publikováno v:
Salud Pública de México, Vol 50, Iss 1, Pp 5-6 (2008)
Externí odkaz:
https://doaj.org/article/f43cfb33c79c4fdf8545d7537f4f6cbb
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
Autor:
Erika del Carmen Ochoa-Correa, Pedro Alberto García-Hernández, Jesús Zacarías Villarreal-Pérez, Consuelo Treviño-Garza, Isaías Rodríguez-Balderrama, Laura Elia Martínez-de Villarreal, Carlos Alberto Zapata-Castilleja
Publikováno v:
Gaceta Médica de México. 153
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83596e2a5dec9325c4ba90ac21d15b95
https://doi.org/10.24875/gmm.m18000043
https://doi.org/10.24875/gmm.m18000043
Autor:
María Marisela Sánchez-Chaparro, Idalia Garza-Veloz, Omar Alejandro Zayas-Villanueva, Margarita L. Martinez-Fierro, Iván Delgado-Enciso, Mayra Alejandra Gomez-Govea, Laura Elia Martínez-de-Villarreal, Diana Reséndez-Pérez, Iram Pablo Rodríguez-Sánchez
Publikováno v:
Diagnostics, Vol 10, Iss 5, p 298 (2020)
Hereditary breast and ovarian cancer (HBOC) syndrome is mainly caused by mutations in the BRCA1 and BRCA2 genes. The 3’UTR region allows for the binding of microRNAs, which are involved in genetic tune regulation. We aimed to identify allelic varia
Externí odkaz:
https://doaj.org/article/6b0f63b3f48c40fbbd1fb24d0f78c87a
Autor:
Graciela Arelí López-Uriarte, Ana Cecilia Ortiz-Figueroa, Geovana Calvo-Anguiano, Alejandra Sánchez-Peña, María del Rosario Torres-Sepúlveda, José de Jesús Lugo-Trampe, Laura Elia Martínez-de Villarreal
Publikováno v:
Revista Mexicana de Pediatría. 88:143-148
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c2e272f3d5781771eed3c0a7815aade
https://doi.org/10.35366/102778
https://doi.org/10.35366/102778
Autor:
Rodolfo Amador Salazar-Ybarra, Santos Guzmán-López, Víctor Torres-de-la-Cruz, Guillermo Jacobo-Baca, Rodrigo Enrique Elizondo-Omaña, Abel Guzmán-López, Laura Elia Martínez-de-Villarreal, Miguel Ángel Vázquez-Barragán
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 35:3446-3452
Preeclampsia (PE) is a leading cause of pregnancy-associated maternal and neonatal morbidity and mortality. Detection of patients at risk before the clinical onset of PE is a priority. Proteomics have become a valuable tool for the discovery of new b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbd0812bef3e5bec51a4278e70f96306
https://doi.org/10.1080/14767058.2020.1820980
https://doi.org/10.1080/14767058.2020.1820980
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)
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
https://doaj.org/article/9ef4831d8d774443994ce2e6bb432e32
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:
David Tucker, Miriam Gatt, Barry Borman, Wendy N. Nembhard, A. J. Agopian, Jorieke E. H. Bergman, Giovanna Tagliabue, Margery Morgan, Karin Kallen, Natasha Nassar, M. Aaurora Canessa, Wei Luo, Pierpaolo Mastroiacovo, Eva Bermejo-Sánchez, Rosa Gajardo, Xiao Yu, Elena Szabova, Mark A. Canfield, Carol Bower, Juan Andrés León, Jocelyn Rouleau, Antonin Sipek, R. Brian Lowry, Charlotte A. Hobbs, Melinda Csáky-Szunyogh, Boris Groisman, Ignacio Zarante, Hermien E. K. de Walle, Janet D. Cragan, Sonja Kiuru-Kuhlefelt, Amy Nance, Annukka Ritvanen, Anke Rissmann, Emmanuelle Amar, Anna Pierini, Osvaldo M. Mutchinick, Nicolás Fernández, Saeed Dastgiri, Paolo Contiero, Dorit Goetz, Fabrizio Bianchi, Gareth Baynam, Adriana Benavides, Laura Elia Martínez-de-Villarreal
Publikováno v:
European Urology, 76(4), 482-490. ELSEVIER SCIENCE BV
Background: Hypospadias is a common male birth defect that has shown widespread variation in reported prevalence estimates. Many countries have reported increasing trends over recent decades.Objective: To analyze the prevalence and trends of hypospad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::727c15f6cf0dff6aff7a07e5af8efc56
https://doi.org/10.1016/j.eururo.2019.06.027
https://doi.org/10.1016/j.eururo.2019.06.027
Autor:
Maria Dolores Hernández-Almaguer, Laura Elia Martínez-de-Villarreal, Donato Saldívar-Rodríguez, Luis Daniel Campos-Acevedo, Patricia R. Ancer-Rodríguez, Sandra M. González-Peña, Geovana Calvo-Anguiano, Melissa Calzada-Dávila, José de Jesús Lugo-Trampe, Ligia S Guerrero-Orjuela
Publikováno v:
Nutrients, Vol 13, Iss 2071, p 2071 (2021)
Nutrients
Volume 13
Issue 6
Nutrients
Volume 13
Issue 6
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d1713ab163096c819c907ffc7a34a33
https://pubmed.ncbi.nlm.nih.gov/34204335
https://pubmed.ncbi.nlm.nih.gov/34204335