Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Maria Laura Bertoldi"'
Autor:
Maria Laura Bertoldi, Maria Ines Zalosnik, Maria Carolina Fabio, Susan Aja, German A. Roth, Gabriele V. Ronnett, Alicia L. Degano
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 13 (2019)
Methyl cytosine binding protein 2 (MeCP2) is a structural chromosomal protein involved in the regulation of gene expression. Mutations in the gene encoding MeCP2 result in Rett Syndrome (RTT), a pervasive neurodevelopmental disorder. RTT is one of fe
Externí odkaz:
https://doaj.org/article/3ce058f8452c4971817d47ec3cb81a1f
Autor:
Alicia L. Degano, Maria Laura Bertoldi, María Carolina Fabio, M. I. Zalosnik, Clara Nicole Castanares
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
Scientific Reports
Scientific Reports
Rett syndrome is a severe and progressive neurological disorder linked to mutations in the MeCP2 gene. It has been suggested that immune alterations may play an active role in the generation and/or maintenance of RTT phenotypes. However, there is no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02d3d4c988f772984c78287452d84ecc
https://doaj.org/article/e167572fef6d48aba42e87b6f968b708
https://doaj.org/article/e167572fef6d48aba42e87b6f968b708
Autor:
Maria Laura Bertoldi, Alicia L. Degano, Clara Nicole Castanares, M. I. Zalosnik, María Carolina Fabio
BackgroundRett syndrome is a severe and progressive neurological disorder linked to mutations in the MeCP2 gene located on the X chromosome. So far it has not been established how the presence of a mutant form of MeCP2 can maintain essential regulati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::969143309b01f8e5e7693e1993fa6f64
https://doi.org/10.1101/2020.08.05.238683
https://doi.org/10.1101/2020.08.05.238683
