Zobrazeno 1 - 2
of 2
pro vyhledávání: '"E. Melissa Arvide"'
Autor:
Christopher S. Ward, Teng-Wei Huang, Jose A. Herrera, Rodney C. Samaco, Christopher M. McGraw, Diana E. Parra, E. Melissa Arvide, Aya Ito-Ishida, Xiangling Meng, Kerstin Ure, Huda Y. Zoghbi, Jeffrey L. Neul
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Rett Syndrome (RTT) is a neurodevelopmental disorder caused by loss of function of the transcriptional regulator Methyl-CpG-Binding Protein 2 (MeCP2). In addition to the characteristic loss of hand function and spoken language after the first year of
Externí odkaz:
https://doaj.org/article/068530e644a94a5095446b5ab905b4e5
Autor:
Christopher A. Chapleau, Andreas Hoeflich, Friedrich Metzger, Christopher S. Ward, Meagan R. Pitcher, Manaswini Sivaramakrishnan, Lucas Pozzo-Miller, E. Melissa Arvide, Jeffrey L. Neul, Stefanie Saenger
Publikováno v:
Human molecular genetics, 22(13): 2626-2633
Rett syndrome (RTT), an X-linked postnatal disorder, results from mutations in Methyl CpG-binding protein 2 (MECP2). Survival and breathing in Mecp2(NULL/Y) animals are improved by an N-terminal tripeptide of insulin-like growth factor I (IGF-I) trea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d75248733fff42a12eba08ff9ac9059a
https://academic.oup.com/hmg/article/22/13/2626/608693#85658339
https://academic.oup.com/hmg/article/22/13/2626/608693#85658339