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CHMP2B gene

Known as: VPS2 homolog B (S. cerevisiae), VACUOLAR PROTEIN SORTING 2, YEAST, HOMOLOG OF, B, DKFZP564O123 
National Institutes of Health

Related topics

Related topics

1 relation
FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Localization of CHMP2B in postnatal rd1 mouse retina
Retinitis pigmentosa is the most common form of inherited blindness in humans. A well-studied model of the disease is the rd1… 
2016
2016
Human Charged Multivesicular Body Protein 2B (CHMP2B) Causes Deficits in Morning Circadian Activity when Expressed in Drosophila Clock Neurons
2016
2016
Investigation of RNA Binding Protein Pumilio as a Genetic Modifier of Mutant CHMP2B in Frontotemporal Dementia (FTD): A Masters Thesis
Frontotemporal dementia (FTD) is the second most common early-onset dementia. A rare mutation in CHMP2B gene was found to be… 
2013
2013
Localization of CHMP2B‐immunoreactivity in the brainstem of Lewy body disease
Alpha‐synuclein (αS) is one of the major constituents of Lewy bodies (LBs). Several lines of evidence suggest that the autophagy… 
Review
2013
Review
2013
Genetic factors in frontotemporal dementia: A review
Frontotemporal dementia (FTD) is the second most common form of neurogenerative dementia, following Alzheimer’s disease (AD). FTD… 
2012
2012
Population-Specific Regulation of Chmp2b by Lbx1 during Onset of Synaptogenesis in Lateral Association Interneurons
Chmp2b is closely related to Vps2, a key component of the yeast protein complex that creates the intralumenal vesicles of… 
2009
2009
Presymptomatic Generalized Brain Atrophy in Frontotemporal Dementia Caused by CHMP2B Mutation
Background/Aims:CHMP2B mutations are a rare cause of familial frontotemporal dementia (FTD). The clinical syndrome is dominated… 
Highly Cited
2009
Highly Cited
2009
Absence of FUS-immunoreactive pathology in frontotemporal dementia linked to chromosome 3 (FTD-3) caused by mutation in the CHMP2B gene
Frontotemporal dementia linked to chromosome 3 (FTD-3) is a very rare disease described in a large Danish family [1] and also in… 
2008
2008
The role of CHMP 2 B in frontotemporal dementia
Mutations in the CHMP2B (charged multivesicular body protein 2B) gene that lead to C-terminal truncations of the protein can… 
2006
2006
A mutation in the endosomal gene CHMP2B in frontotemporal dementia.
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