Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Timothy D. Ruff"'
Autor:
Fernardo A. Poletta, Alexandre R. Vieira, Merve Bayram, Thelma Lopes da Silva, Jessica Briseño-Ruiz, Aline de Lima Leite, Piper M. Dizak, Juan C. Mereb, Iêda M. Orioli, Zerrin Abbasoglu, Marília Afonso Rabelo Buzalaf, Asli Patir, Eduardo E. Castilla, Figen Seymen, Kai Liu, Margaret E. Cooper, Ida Anjomshoaa, Kathleen Deeley, Priscila A. T. M. Barreta, Timothy D. Ruff, Ilknur Tanboga, Priscila Ladeira Casado, Mine Koruyucu, Erika Calvano Küchler, Charles Sfeir, José Mauro Granjeiro, Andrew Brown, Mary L. Marazita, Samer H. Zaky, Hongjiao Owyang
Publikováno v:
PLoS ONE, Vol 10, Iss 12, p e0143068 (2015)
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
PLoS ONE
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
PLoS ONE
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Aquaporins (AQP) are water channel proteins and the genes coding for AQP2, AQP5, and AQP6 are clustered in 12q13. Since AQP5 is expressed in serous acinar cells of salivary glands, we investigated its involvement in caries. DNA samples from 1,383 ind
Autor:
Michael Hummel, Thottala Jayaraman, Eduardo E. Castilla, Juan C. Mereb, Dana T. Brožková, Timothy D. Ruff, Alexandre R. Vieira, José Mauro Granjeiro, Jessica Briseño-Ruiz, Hong Yuan Hsin, Mary L. Marazita, Jessalyn Forella, Marcelo de Castro Costa, Leonardo Santos Antunes, Shankar Revu, Merve Bayram, Regina C. Sencak, Erika Calvano Küchler, Megan L. Weber, Kathleen Deeley, Lívia Azeredo Alves Antunes, Vanessa M. Trombetta, Fernando A. Poletta, Hongjiao Ouyang, Patricia Nivoloni Tannure, Fernanda Volpe de Abreu, Iêda M. Orioli, Figen Seymen, Mine Koruyucu, Ersan Kalay, Takehiko Shimizu, Asli Patir
Publikováno v:
BMC Medical Genetics
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
BACKGROUND: Congenital forms of hearing impairment can be caused by mutations in the estrogen related receptor beta (ESRRB) gene. Our initial linkage studies suggested the ESRRB locus is linked to high caries experience in humans. METHODS: We tested
Autor:
Carla A. Brandon, Juan C. Mereb, Eduardo E. Castilla, Fernando A. Poletta, Giovana Daniela Pecharki, Mary L. Marazita, Judith M. Resick, Ariadne Letra, Alexandre R. Vieira, Takehiko Shimizu, Thays Cristine dos Santos Vieira, Jessica Briseño-Ruiz, Margaret E. Cooper, Italo M. Faraco, Asli Patir, Kathleen Deeley, Marcelo de Castro Costa, Piper M. Dizak, Timothy D. Ruff, Erika Calvano Küchler, Iêda M. Orioli, Patricia Nivoloni Tannure, Andrea Lips, João Armando Brancher, Mine Koruyucu, Figen Seymen, Paula Cristina Trevilatto, Renato Menezes Silva, José Mauro Granjeiro
Caries is the most common chronic, multifactorial disease in the world today; and little is still known about the genetic factors influencing susceptibility. Our previous genome-wide linkage scan has identified five loci related to caries susceptibil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aff6735bd337d328ac0a4bd748a44cc2
https://hdl.handle.net/20.500.12511/2624
https://hdl.handle.net/20.500.12511/2624