Zobrazeno 1 - 4
of 4
pro vyhledávání: '"M L Bustamante"'
Autor:
T Pérez, M L Bustamante, D Travisany, F Magne, C Hernandez-Rocha, M Alvarez-Lobos, M Orellana, G Ascui, L Azocar, A Espino, N Aguilar, P Baez, A Zazueta, R Estela, V Silva, S Escobar, A De la Vega, E Arriagada, J F Miquel, D Alvares
Publikováno v:
Journal of Crohn's and Colitis. 17:i1017-i1018
Background IBD has emerged as a worldwide disease with an increased incidence in newly industrialized countries such as Chile. This population has been underrepresented in genome-wide association studies (GWAS) because IBD genetics studies have focus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f24ec91c7e2f8726f8dd9c7f98f34256
https://doi.org/10.1093/ecco-jcc/jjac190.1034
https://doi.org/10.1093/ecco-jcc/jjac190.1034
Autor:
T Pérez, M L Bustamante, F Magne, D Travisany, M Alvarez-Lobos, C Hernandez-Rocha, L Azocar, N Aguilar, A Espino, R Estela, S Escobar, A Zazueta, P Baez, V Silva, E Arriagada, C Barahona, L Zollner, J F Miquel, J Lorenzo-Bermejo
Publikováno v:
Journal of Crohn's and Colitis. 17:i1015-i1016
Background Most genetic association studies rely on Caucasian, African and Asian individuals with inconsistent results depending on the population investigated, suggesting that genetic susceptibility to inflammatory bowel disease (IBD) may depend on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef2f3ef08e54eb2e3599e1c7c864679d
https://doi.org/10.1093/ecco-jcc/jjac190.1032
https://doi.org/10.1093/ecco-jcc/jjac190.1032
Autor:
T Pérez, M L Bustamante, F Magne, D Alvares, M Álvarez-Lobos, C Hernandez-Rocha, N Aguliar, L Azocar, P Baez, A Zazueta, R Estela, S Escobar, V Silva, A De la Vega, E Arriagada, A Espino, J F Miquel, D Travisany
Publikováno v:
Journal of Crohn's and Colitis. 17:i1019-i1019
Background Genome-wide association studies (GWAS) have identified hundreds of polymorphisms associated with an increased risk of developing IBD. Among risk genes identified by GWAS, CARD9, a gene encoding an adapter molecule involved in the innate im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d406dfa2f871234007c2c10dd49888e
https://doi.org/10.1093/ecco-jcc/jjac190.1036
https://doi.org/10.1093/ecco-jcc/jjac190.1036
Publikováno v:
Current Pharmaceutical Biotechnology. 13:1543-1548
Cognitive deficits are trait markers in schizophrenia and the improvement of these dysfunctions has been considered as a new frontier of treatment in this disease. A current model for the patophysiology of schizophrenia states that N-methyl-D-asparta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4eca643f49f18f0f92f6bcb4e117634b
https://doi.org/10.2174/138920112800784790
https://doi.org/10.2174/138920112800784790