TGM5 gene

Known as: TGX, TRANSGLUTAMINASE X, TGM5 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1995-2017
01219952017

Papers overview

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2017
2017
Adult polyglucosan body disease (APBD) is a neurological disorder characterized by adult-onset neurogenic bladder, spasticity… (More)
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2016
2016
BACKGROUND Rare gene variants are important sources of schizophrenia vulnerability that likely interact with polygenic… (More)
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2015
2015
Schizophrenia is a debilitating syndrome with high heritability. Genomic studies reveal more than a hundred genetic variants… (More)
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2015
2015
Acral peeling skin syndrome (APSS, MIM #609796) is a rare autosomal recessive disorder characterized by superficial exfoliation… (More)
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2013
2013
The acral peeling skin syndrome (APSS) is a rare autosomal recessive disorder clinically characterized by asymptomatic… (More)
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2004
2004
Screenhouse studies were conducted to investigate the effects of Fusarium oxysporum f. sp. glycines and Sclerotium rolfsii on the… (More)
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1998
1998
We developed a method using a single set of degenerate oligonucleotide primers for amplification of the conserved active site of… (More)
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1998
1998
Severe permanent cobalamin (Cbl) deficiency was induced in rats either by total gastrectomy (TG) or through prolonged dietary Cbl… (More)
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1997
1997
The totally gastrectomized (TGX) rat is a new experimental model for studying the pathogenesis of cobalamin (Cbl)-deficient… (More)
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1995
1995
BACKGROUND The totally gastrectomized (TGX) rat is a new experimental model with which to produce widespread spongy vacuolation… (More)
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