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pro vyhledávání: '"C, Vidales"'
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Autor:
Francisco Cammarata-Scalisi, M.A. Lacruz-Rengel, Andrea Avendaño, D. Araque, Michele Callea, F. Stock, Andrea Diociaiuti, Emanuele Bellacchio, C. Vidales Moreno
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 32:e243-e245
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::981c1c13bb0288c98bf7818db0478790
https://doi.org/10.1111/jdv.14765
https://doi.org/10.1111/jdv.14765
Autor:
F.J. Murcia García, C. Vidales Moreno, S. Llamas Velasco, A. Camacho Salas, R.M. Ceballos Rodríguez, R. Simón de la Heras
Publikováno v:
Anales de Pediatría, Vol 79, Iss 1, Pp 42-45 (2013)
Resumen: El gen TSC2, responsable de la esclerosis tuberosa, se encuentra en el cromosoma 16p13.3, adyacente al gen de la poliquistosis renal autosómica dominante PKD1. Una deleción de gran tamaño puede afectar a ambos genes produciendo el llamado
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ac9be6973618b455d6921b9f95d5e8c
https://doi.org/10.1016/j.anpedi.2012.12.004
https://doi.org/10.1016/j.anpedi.2012.12.004
Autor:
Miguel A. Alfonso-Sánchez, José A. Peña, C. Vidales, D. Arroyo, Susana García-Obregón, A.M. Pérez-Miranda
Publikováno v:
American Journal of Human Biology. 18:187-195
In this work, eight human-specific Alu insertion polymorphisms (ACE, TPA25, PV92, APO, FXIIIB, D1, A25, and B65) were typed in 106 unrelated healthy individuals born in the province of Valencia (Spain), with the aim of analyzing the genetic relations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8813df5a4646db26609109d41c914466
https://doi.org/10.1002/ajhb.20487
https://doi.org/10.1002/ajhb.20487
Genetic polymorphism and linkage disequilibrium of the HLA-DP region in Basques from Navarre (Spain)
Publikováno v:
Tissue Antigens. 64:264-275
In this work, a sample of 116 individuals from an autochthonous Basque population (northern Navarre, Spain) was typed at the DNA level for HLA-DPA1 and HLA-DPB1 loci, with the aim of analysing the genetic polymorphism andthe linkage disequilibrium (L
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8df07cf62c9dca360314ce3eac4b55c
https://doi.org/10.1111/j.1399-0039.2004.00284.x
https://doi.org/10.1111/j.1399-0039.2004.00284.x
Autor:
JF García Castro, C Vidales
Publikováno v:
La discusión social sobre la democratización de los medios en México
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31ae770aaf79fbaf6c48bc0d7e4f091e
https://doi.org/10.4185/cac73
https://doi.org/10.4185/cac73
Autor:
B. Crouau-Roy, Rosario Calderón, Jean-Michel Dugoujon, C. Vidales, M. Carrion, José A. Peña, A.M. Pérez-Miranda
Publikováno v:
Annals of Human Biology. 29:176-191
The extent of the genetic polymorphism of the HLA complex is becoming well characterized in Basque population and their subpopulations. This level of knowledge mainly concerns HLA class I loci. However, Basque population surveys dealing with HLA clas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::798a11c3ee3fe87b2a5811092ed979a7
https://doi.org/10.1080/03014460110075675
https://doi.org/10.1080/03014460110075675
Publikováno v:
Revista mexicana de tuberculosis y enfermedades del aparato respiratorio. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::faef0e53f9415dc3810c7c2082ad6c1a
https://pubmed.ncbi.nlm.nih.gov/24545764
https://pubmed.ncbi.nlm.nih.gov/24545764
Autor:
S, Llamas Velasco, A, Camacho Salas, C, Vidales Moreno, R M, Ceballos Rodríguez, F J, Murcia García, R, Simón de la Heras
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 79(1)
The TSC2 gene responsible for Tuberous Sclerosis, is located in chromosome 16p 13.3, adjacent to the gene for autosomal dominant polycystic kidney disease. A large deletion can involve both genes, causing the so-called TSC2/PKD1 contiguous gene syndr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::02093fa719f491944591b7ae7d13654e
https://pubmed.ncbi.nlm.nih.gov/23402778
https://pubmed.ncbi.nlm.nih.gov/23402778
Autor:
Karina Maxzud, Oscar Garcia, Marta Espinoza, I. Aragón, A. Hernández, M.F. Pinheiro, R. Ortiz, I. Salgado, José Pestano, I. Miguel, G. Arrieta, Lourdes Prieto, Daniel Corach, Sandra Silva, I. Atmetlla, David Comas, D. Manzanares, Iñaki Yurrebaso, Nidia M. Modesti, Fernando Rendo, Leonor Gusmão, Beatriz Martínez, Antonio Gonzalez, M. R. Espinheira, R. Campos, Ulises Toscanini, María Cecilia Bobillo, Iva Gomes, Célia Alves, M Carvalho, C. Vidales, P. Lozano, Regina Maria Barretto Cicarelli, A. I. Zubillaga, Angel Carracedo, Marcelo Malaghini, M. C. Villalobos, B. Arce, Javier Riancho, C. Baeza, M. B. Rodríguez, Cláudia Vieira da Silva, Laura M. Cainé, María T. Zarrabeitia, Joyce Aparecida Martins, Paula Sánchez-Diz, Eugenia Carvalho, M. Hidalgo, Juan J. Sanchez, Carlos Vullo, Eduardo Raimondi, M. Montesino, Luis Caraballo, M. A. Abovich, Eduardo Arroyo, António Amorim, N. Salgueiro
A collaborative work was carried out by the Spanish and Portuguese ISFG Working Group with a PCR multiplex for X chromosome STRs. Markers were selected among those described as polymorphic in humans and that have been used by some laboratories in for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d62064267e86e0766427d7ec0c7909f4
https://hdl.handle.net/10400.26/44657
https://hdl.handle.net/10400.26/44657