GRID2 gene

Known as: GRID2, GLUTAMATE RECEPTOR, IONOTROPIC, DELTA 2, GluR-delta-2 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1979-2018
02419792018

Papers overview

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2016
2016
Autism is one of the most common subtypes of autism spectrum disorder (ASD). Recent studies suggested a relationship between… (More)
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2015
2015
Purpose:The aim of this study was to identify the genetic cause of early-onset autosomal recessive cerebellar ataxia associated… (More)
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2015
2015
OBJECTIVES In a large family of Algerian origin, we aimed to identify the genetic mutation segregating with simultaneous presence… (More)
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2014
2014
INTRODUCTION Complex forms of spastic paraplegia (SPG) are rare and genetically heterogeneous. In apparently sporadic cases… (More)
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2014
2014
Mevalonate kinase deficiency (MKD) is a rare autosomal disease caused by mutations in the mevalonate kinase gene (MVK). The… (More)
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2013
2013
GRID2 is a member of the ionotropic glutamate receptor family of excitatory neurotransmitter receptors. GRID2 encodes the… (More)
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2013
2013
OBJECTIVE To identify the genetic cause of a syndrome causing cerebellar ataxia and eye movement abnormalities. METHODS We… (More)
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2003
2003
Activity-driven delivery of AMPA receptors is proposed to mediate glutamatergic synaptic plasticity, both during development and… (More)
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2003
2003
The Lurcher mutation transforms the GRID2 receptor into a constitutively opened channel. In Lurcher heterozygous mice, cerebellar… (More)
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2003
2003
The orphan glutamate receptor delta2 is selectively expressed in Purkinje cells and plays a crucial role in cerebellar functions… (More)
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