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The horse PYGM gene was broadly expressed in all tissues tested with the highest expression observed in skeletal muscle. It contains fewer mobile elements than its human ortholog, resulting in an increase in the structural stability of the gene sequence.
Data suggest that the irreversible inhibition of glycogen (zeige GYS1 Proteine) phosphorylase (GP) could represent one of the mechanisms that contribute to mercury-dependent muscle toxicity.
Data show that glycogen (zeige GYS1 Proteine) phosphorylase is irreversibly impaired by exposure to peroxynitrite, and suggest that the peroxynitrite-dependent inactivation of the enzyme could be due to the nitration of Tyr613 at the allosteric inhibitor site of the enzyme.
The formation of a complex between the denatured monomeric form of Phb (zeige PHB Proteine) and the dissociated forms of GroEL (zeige GroEL Proteine) is detected during heating at 46 degrees C.
alpha-crystallin interacts with the intermediates of unfolding of the Phb (zeige PHB Proteine) molecule
Because the NMD mechanism does not seem to operate in nonspecific cells, PBMCs were more suitable than muscle biopsies for detecting the pathogenicity of some PYGM mutations, notably the silent mutation whose effect in the splicing of intron 6 was unnoticed in previous muscle transcriptomic studies
Variations in AMPD1 (zeige AMPD1 Proteine), CPT2 (zeige CPT2 Proteine), and PGYM genes are not associated with the onset, susceptibility, or severity of chronic fatigue syndrome.
update of the reported mutations and polymorphisms in the PYGM gene [review]
study found that T lymphocytes expressed myophosphorylase in healthy donors, but expression was significantly lower in McArdle patients (p<0.001); PYGM mRNA levels were also lower in white blood cells from McArdle patients
biological significance of this PKCtheta (zeige PRKCQ Proteine);/alphaPIX (zeige ARHGEF6 Proteine)/Rac 1 GTPase (zeige RACGAP1 Proteine)/PYGM signaling pathway seems to be the control of different cellular responses such as migration and proliferation
5 different PYGM mutations were found in 8 Brazilian families: 4 previously described (p.R50X, p.T692kfs30, p.K609K, and p.G455R), and one, pI513V, a novel heterozygous mutation.
a novel mutation, in the PYGM gene c.632delG, in three unrelated families of Jewish descent originating from the Caucasus region
a new role for Rac1 in cell signaling, showing that this GTPase (zeige RACGAP1 Proteine) triggers T-cell proliferation upon IL-2 (zeige IL2 Proteine) stimulation by associating with PYGM and modulating its enzymatic activity.
No genotype-phenotype correlation is evident and that no gender effect is related to the phenotype of McArdle's disease (PYGM gene) in a cohort of 123 European McArdle's disease patients.
The current data add to the list of pathogenic mutations in the PYGM gene associated with McArdle disease
Data indicate that a G/T mutation in exon 8 in muscle glycogen phosphorylase (PYGM) was identified and association analysis with meat quality traits showed that it was significantly associated with lean meat percentage(p<0.05).
This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants.
, glycogen phosphorylase, muscle form
, phosphorylase, glycogen; muscle (McArdle syndrome, glycogen storage disease type V)
, phosphorylase, glycogen. muscle
, Phosphorylase glycogen
, Phosphorylase, glycogen; muscle (McArdle syndrome)
, muscle (McArdle syndrome)
, muscle glycogen phosphorylase
, glycogen myophosphorylase