Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Veluma Calassara"'
Autor:
Cíntia B. Santos-Rebouças, Raquel Boy, Evelyn Q. Vianna, Andressa P. Gonçalves, Rafael M. Piergiorge, Bianca B. Abdala, Jussara M. dos Santos, Veluma Calassara, Filipe B. Machado, Enrique Medina-Acosta, Márcia M. G. Pimentel
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
In mammalian females, X-chromosome inactivation (XCI) acts as a dosage compensation mechanism that equalizes X-linked genes expression between homo- and heterogametic sexes. However, approximately 12–23% of X-linked genes escape from XCI, being bi-
Externí odkaz:
https://doaj.org/article/e9a6c946e30e4850a681b8dd0dda85b6
Autor:
Márcia Mattos Gonçalves Pimentel, Jussara Mendonça dos Santos, Rafael Mina Piergiorge, Raquel Tavares Boy da Silva, Enrique Medina-Acosta, Carla Rosenberg, Veluma Calassara, Suely Rodrigues dos Santos, Márcia Gonçalves Ribeiro, Filipe Brum Machado, Ana Cristina Victorino Krepischi, Cíntia Barros Santos-Rebouças, Andressa Pereira Gonçalves, Evelyn Quintanilha Vianna
Publikováno v:
Molecular neurobiology. 57(9)
Intellectual disability (ID) affects 30% more males than females. This sex bias can be attributed to the enrichment of genes on the X chromosome playing essential roles in the central nervous system and their hemizygous state on males. Moreover, as a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e8f08116042ec0c3021aba88a1bec26
https://pubmed.ncbi.nlm.nih.gov/32564284
https://pubmed.ncbi.nlm.nih.gov/32564284
Autor:
Veluma Calassara, Marcus V. Della Coletta, Marco Antonio Araujo Leite, Debora Valença, Camilla P. da Silva, Ana Lúcia Zuma de Rosso, Delson José da Silva, C. Martins, Pedro H. Cabello Acero, João Santos Pereira, Cíntia Barros Santos-Rebouças, Jussara Mendonça dos Santos, Márcia Mattos Gonçalves Pimentel, Caroline M. Nascimento, Sarah R. de A. Ramos, Denise Hack Nicaretta, Danielle Dutra Voigt, Luiz Felipe Rocha Vasconcellos, Andressa Pereira Gonçalves, Mário Campos, Gabriella de Medeiros Abreu
Publikováno v:
Journal of the neurological sciences. 381
Background Parkinson's disease (PD) is a neurodegenerative disorder characterized by remarkable phenotypic variability. Accumulated evidence points that the manifestation of PD clinical signs might be differentially modified by genetic factors, as mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10afb5f538a980d344e59daa4b55561f
https://pubmed.ncbi.nlm.nih.gov/28991672
https://pubmed.ncbi.nlm.nih.gov/28991672
Autor:
Camilla P. da Silva, Marcus V. Della Coletta, Andressa Pereira Gonçalves, Delson José da Silva, Veluma Calassara, Denise Hack Nicaretta, Cíntia Barros Santos-Rebouças, Ritiele B. de Souza, João Santos Pereira, Jussara Mendonça dos Santos, Danielle Dutra Voigt, Márcia Mattos Gonçalves Pimentel, Pedro H. Cabello Acero, Mario Campos Junior, Ana Lúcia Zuma de Rosso, Luiz Felipe Rocha Vasconcellos, Caroline M. Nascimento, Marco Antonio Araujo Leite
Publikováno v:
Neurobiology of Aging. 74:236.e7-236.e8
Robust evidence on the involvement of genetic factors in the etiology of Parkinson's disease (PD) expands our knowledge about monogenic causes that contribute for this important neurodegenerative disorder. Mutations in the CHCHD2 gene have been linke
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5efba7261e1e7e404d77cf030501e321
https://doi.org/10.1016/j.neurobiolaging.2018.09.026
https://doi.org/10.1016/j.neurobiolaging.2018.09.026