Cargando…
N-terminal Huntingtin Knock-In Mice: Implications of Removing the N-terminal Region of Huntingtin for Therapy
The Huntington’s disease (HD) protein, huntingtin (HTT), is a large protein consisting of 3144 amino acids and has conserved N-terminal sequences that are followed by a polyglutamine (polyQ) repeat. Loss of Htt is known to cause embryonic lethality in mice, whereas polyQ expansion leads to adult neu...
Autores principales: | Liu, Xudong, Wang, Chuan-En, Hong, Yan, Zhao, Ting, Wang, Guohao, Gaertig, Marta A., Sun, Miao, Li, Shihua, Li, Xiao-Jiang |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4874551/ https://www.ncbi.nlm.nih.gov/pubmed/27203582 http://dx.doi.org/10.1371/journal.pgen.1006083 |
Ejemplares similares
-
Emerging Therapies for Huntington’s Disease – Focus on N-Terminal Huntingtin and Huntingtin Exon 1
por: van der Bent, M Leontien, et al.
Publicado: (2022) -
Synaptic mutant huntingtin inhibits synapsin-1 phosphorylation and causes neurological symptoms
por: Xu, Qiaoqiao, et al.
Publicado: (2013) -
Truncation of mutant huntingtin in knock-in mice demonstrates exon1 huntingtin is a key pathogenic form
por: Yang, Huiming, et al.
Publicado: (2020) -
Promoters Are Differentially Sensitive to N-Terminal Mutant Huntingtin-Mediated Transcriptional Repression
por: Hogel, Matthew, et al.
Publicado: (2012) -
Selection and characterization of llama single domain antibodies against N-terminal huntingtin
por: Schut, Menno H., et al.
Publicado: (2014)