AMYOTROPHIC LATERAL SCLEROSIS 8 (disorder)

Known as: ALS8, Amyotrophic Lateral Sclerosis 8 
 
National Institutes of Health

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Topic mentions per year

1969-2017
012319692017

Papers overview

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2014
2014
A familial form of Amyotrophic lateral sclerosis (ALS8) is caused by a point mutation (P56S) in the vesicle-associated membrane… (More)
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2013
2013
The mutations P56S and T46I in the gene encoding vesicle-associated membrane protein-associated protein B/C (VAPB) cause ALS8, a… (More)
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2013
2013
The Vesicle-associated membrane protein (VAMP)-Associated Protein B (VAPB) is the causative gene of amyotrophic lateral sclerosis… (More)
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2013
2013
The substitution of Proline with Serine at residue 56 (P56S) of vesicle-associated membrane protein-associated protein B (VAPB… (More)
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2013
2013
BACKGROUND Protein aggregation and the formation of intracellular inclusions are a central feature of many neurodegenerative… (More)
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Highly Cited
2011
Highly Cited
2011
Amyotrophic lateral sclerosis (ALS) is an incurable neuromuscular disease that leads to a profound loss of life quality and… (More)
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2008
2008
ALS8 is caused by a dominant mutation in an evolutionarily conserved protein, VAPB (vesicle-associated membrane protein (VAMP… (More)
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2008
2008
The VAMP-associated proteins termed VAP are a small gene family of proteins characterised by the presence of an N-terminal major… (More)
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Highly Cited
2004
Highly Cited
2004
Motor neuron diseases (MNDs) are a group of neurodegenerative disorders with involvement of upper and/or lower motor neurons… (More)
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Highly Cited
2004
Highly Cited
2004
The ALS (agglutinin-like sequence) gene family of Candida albicans encodes eight cell-surface glycoproteins, some of which are… (More)
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