FAQ

TGM5 gene

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

Topic mentions per year

Topic mentions per year

1995-2017
01219952017

Related topics

Related topics

3 relations
Peeling skin syndrome, acral typeTGM6 genetransglutaminase 5

Related mentions per year

Related mentions per year

1968-2018
1960198020002020
TGM5 gene
TGM6 gene
Peeling skin syndrome, acral type
transglutaminase 5

Papers overview

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2017
2017
Triacylglycerol mimetics regulate membrane interactions of glycogen branching enzyme: implications for therapy.
Adult polyglucosan body disease (APBD) is a neurological disorder characterized by adult-onset neurogenic bladder, spasticity… (More)
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2016
2016
Phenotypically distinct subtypes of psychosis accompany novel or rare variants in four different signaling genes.
BACKGROUND Rare gene variants are important sources of schizophrenia vulnerability that likely interact with polygenic… (More)
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2015
2015
De novo mutations from sporadic schizophrenia cases highlight important signaling genes in an independent sample.
Schizophrenia is a debilitating syndrome with high heritability. Genomic studies reveal more than a hundred genetic variants… (More)
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2015
2015
Novel TGM5 mutations in acral peeling skin syndrome.
Acral peeling skin syndrome (APSS, MIM #609796) is a rare autosomal recessive disorder characterized by superficial exfoliation… (More)
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2013
2013
Acral Peeling Skin Syndrome Resembling Epidermolysis Bullosa Simplex in a 10-Month-Old Boy
The acral peeling skin syndrome (APSS) is a rare autosomal recessive disorder clinically characterized by asymptomatic… (More)
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2004
2004
Effect of Fusarium oxysporum f. sp. glycines and Sclerotium rolfsii on the pathogenicity of Meloidogyne incognita race 2 to soybean
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
Isolation of a cDNA encoding a novel member of the transglutaminase gene family from human keratinocytes. Detection and identification of transglutaminase gene products based on reverse transcription…
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
Subacute combined degeneration in totally gastrectomized rats: an ultrastructural study.
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
Enhanced levels of biochemical markers for cobalamin deficiency in totally gastrectomized rats: uncoupling of the enhancement from the severity of spongy vacuolation in spinal cord.
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
Subacute combined degeneration in the spinal cords of totally gastrectomized rats. Ornithine decarboxylase induction, cobalamin status, and astroglial reaction.
BACKGROUND The totally gastrectomized (TGX) rat is a new experimental model with which to produce widespread spongy vacuolation… (More)
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