Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Víctor Martínez-Cruz"'
Autor:
Liliana Fernández-Hernández, Carmen Sánchez, Aidy González-Núñez, Ariadna González-del Angel, Miguel Angel Alcántara-Ortigoza, Iraís Sánchez-Verdiguel, Rosario Moreno-Rojas, Víctor Martínez-Cruz
Publikováno v:
Journal of Pediatric Genetics. :041-046
Congenital hypothyroidism (CH), attributable to thyroid dysgenesis (TD), has an unusually high prevalence in Mexican population but the causes are unknown. NKX2-1, as a candidate gene, was subjected to automated Sanger sequencing in 122 unrelated Mex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38e8783910f83488c085fbb203cdabf5
https://doi.org/10.1055/s-0038-1676644
https://doi.org/10.1055/s-0038-1676644
Autor:
Ariadna, González-Del Angel, Liliana, Fernández-Hernández, Iraís, Sánchez-Verdiguel, Aidy, González-Núñez, Víctor, Martínez-Cruz, Carmen, Sánchez, Rosario, Moreno-Rojas, Miguel Angel, Alcántara-Ortigoza
Publikováno v:
J Pediatr Genet
Congenital hypothyroidism (CH), attributable to thyroid dysgenesis (TD), has an unusually high prevalence in Mexican population but the causes are unknown. NKX2-1 , as a candidate gene, was subjected to automated Sanger sequencing in 122 unrelated Me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0c158aa71fe65c5ba090689890389c51
https://pubmed.ncbi.nlm.nih.gov/31061744
https://pubmed.ncbi.nlm.nih.gov/31061744
Autor:
Miguel Angel Alcántara-Ortigoza, Bernardette Estandia-Ortega, Diana Judith Gutiérrez-Tinajero, Astrid Rasmussen, Claudia Sofía Gómez-González, Ariadna González-del Angel, Víctor Martínez-Cruz
Publikováno v:
American journal of medical genetics. Part A. 170(12)
Muenke syndrome (MS) is an autosomal dominant coronal craniosynostosis syndrome with variable extracranial anomalies. We studied 56 unrelated patients with non-syndromic uni- or bicoronal craniosynostosi to identify the frequency and clinical charact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d4a1147bbcc1e87075e471d809c5e88
https://pubmed.ncbi.nlm.nih.gov/27568649
https://pubmed.ncbi.nlm.nih.gov/27568649
Autor:
Miguel Angel Alcántara-Ortigoza, Ariadna González-del Angel, Víctor Martínez-Cruz, Marcela Vela-Amieva, Carmen Sánchez-Pérez, Rosario Moreno-Rojas, Bernardette Estandía-Ortega, Nancy Hernández-Martínez
Publikováno v:
Clinical Endocrinology. 76:148-150
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::614f40f77802064a69d629944e65e059
https://doi.org/10.1111/j.1365-2265.2011.04153.x
https://doi.org/10.1111/j.1365-2265.2011.04153.x
Autor:
Miguel A, Alcántara-Ortigoza, Jesús, De Rubens-Figueroa, Miriam E, Reyna-Fabian, Bernardette, Estandía-Ortega, Ariadna, González-del Angel, Bertha, Molina-Álvarez, José A, Velázquez-Aragón, Sandra, Villagómez-Martínez, Gabriela I, Pereira-López, Víctor, Martínez-Cruz, Víctor, Cruz-Martínez, Rosa M, Álvarez-Gómez, Luisa, Díaz-García, Luisa, García-Díaz
Publikováno v:
Pediatric cardiology. 36(4)
Congenital heart defects (CHD) are found in ~50 % of Down syndrome (DS) patients. Genetic variants have been implicated, including CRELD1 mutations, but no previous study has examined the candidate genes, NKX2-5 and GATA4, in DS patients with secundu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a993627a54a2ac18950cf1cb14cd37a7
https://pubmed.ncbi.nlm.nih.gov/26205256
https://pubmed.ncbi.nlm.nih.gov/26205256
Autor:
Estefanía Contreras-Sanzón, Heriberto Prado-Garcia, Susana Romero-Garcia, David Nuñez-Corona, Blanca Ortiz-Quintero, Cesar Luna-Rivero, Victor Martínez-Cruz, Ángeles Carlos-Reyes
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
The acetylation status of histones located in both oncogenes and tumor suppressor genes modulate cancer hallmarks. In lung cancer, changes in the acetylation status are associated with increased cell proliferation, tumor growth, migration, invasion,
Externí odkaz:
https://doaj.org/article/06d32fad4a744af3b2c6494b6645b787
Autor:
Marcela Vela-Amieva, Víctor Martínez-Cruz, S. Monroy, C. Todd-Quiñones, A. González-del Angel, José A. Velázquez-Aragón, Miguel Angel Alcántara-Ortigoza
Publikováno v:
Journal of inherited metabolic disease. 31
Classical galactosaemia is an autosomal recessive disease of galactose metabolism caused by a deficiency of the enzyme galactose-1-phosphate uridyltransferase (GALT). Galactosaemia is not included in the neonatal screening programme in Mexico and it
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7006f340a149027ae9587cc51b2c4dca
https://pubmed.ncbi.nlm.nih.gov/18956253
https://pubmed.ncbi.nlm.nih.gov/18956253