C9orf72 is differentially expressed in the central nervous system and myeloid cells and consistently reduced in C9orf72, MAPT and GRN mutation carriers

A non-coding hexanucleotide repeat expansion (HRE) in C9orf72 is a common cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) acting through a loss of function mechanism due to haploinsufficiency of C9orf72 or a gain of function mediated by aggregates of bidirectionally tr...

Full description

Saved in:

Bibliographic Details
Published in:	Acta neuropathologica communications Vol. 4; no. 1; p. 37
Main Authors:	Rizzu, Patrizia, Blauwendraat, Cornelis, Heetveld, Sasja, Lynes, Emily M., Castillo-Lizardo, Melissa, Dhingra, Ashutosh, Pyz, Elwira, Hobert, Markus, Synofzik, Matthis, Simón-Sánchez, Javier, Francescatto, Margherita, Heutink, Peter
Format:	Journal Article
Language:	English
Published:	London BioMed Central 14.04.2016 BioMed Central Ltd
Subjects:	Amyotrophic Lateral Sclerosis - metabolism Animals Biomedical and Life Sciences Biomedicine C9orf72 Protein Central Nervous System - metabolism Databases, Factual - standards Databases, Factual - statistics & numerical data Degeneration Frontotemporal Dementia - metabolism Gene expression Gene Expression Regulation Gene mutations Genetic aspects Health aspects Humans Identification and classification Intercellular Signaling Peptides and Proteins - genetics Lipopolysaccharide Receptors - metabolism Mutation - genetics Myeloid Cells - metabolism Nervous system Neurology Neurosciences Open reading frames Pathology Properties Proteins - genetics Proteins - metabolism tau Proteins - genetics Frontotemporal dementia Neurodegeneration C9orf72 risk haplotype Hexanucleotide repeat expansion
ISSN:	2051-5960, 2051-5960
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!

Be the first to leave a comment!