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Liver Glycogenosis, X-Linked, Type II

Known as: XLG2 
 

Topic mentions per year

Topic mentions per year

1996-2018
0119962018

Related topics

Related topics

2 relations

Broader (2)

Genetic Diseases, X-LinkedGlycogen Storage Disease

Related mentions per year

Related mentions per year

1944-2018
19401960198020002020
Liver Glycogenosis, X-Linked, Type II
Glycogen Storage Disease
Genetic Diseases, X-Linked

Papers overview

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2018
2018
The G protein β subunit, AGB1, interacts with FERONIA in RALF1-regulated stomatal movement.
Heterotrimeric guanine nucleotide-binding (G) proteins are composed of Gα, Gβ, and Gγ subunits, and function as molecular… (More)
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2016
2016
Arabidopsis heterotrimeric G proteins regulate immunity by directly coupling to the FLS2 receptor
The Arabidopsis immune receptor FLS2 perceives bacterial flagellin epitope flg22 to activate defenses through the central… (More)
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2015
2015
Membrane-localized extra-large G proteins and Gbg of the heterotrimeric G proteins form functional complexes engaged in plant immunity in Arabidopsis.
In animals, heterotrimeric G proteins, comprising Ga, Gb, and Gg subunits, are molecular switches whose function tightly depends… (More)
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2009
2009
Arabidopsis extra large G-protein 2 (XLG2) interacts with the Gbeta subunit of heterotrimeric G protein and functions in disease resistance.
Heterotrimeric GTP-binding proteins, which consist of Galpha, Gbeta, and Ggamma subunits, play important roles in transducing… (More)
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1998
1998
Variability of biochemical and clinical phenotype in X-linked liver glycogenosis with mutations in the phosphorylase kinase PHKA2 gene
X-linked liver glycogenosis (XLG) resulting from phosphorylase kinase (Phk) deficiency is one of the most common forms of… (More)
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1997
1997
Phosphorylase-kinase-deficient liver glycogenosis with an unusual biochemical phenotype in blood cells associated with a missense mutation in the β subunit gene (PHKB)
We have identified mutations in the phosphorylase kinase (Phk) β subunit gene in a male patient with liver glycogenosis caused by… (More)
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1996
1996
Mutation hotspots in the PHKA2 gene in X-linked liver glycogenosis due to phosphorylase kinase deficiency with atypical activity in blood cells (XLG2).
In five cases of X-linked liver glycogenosis subtype 2 (XLG2), we have identified mutations in the gene encoding the liver… (More)
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