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GATM encodes a mitochondrial enzyme that belongs to the amidinotransferase family. Zusätzlich bieten wir Ihnen GATM Kits (22) und GATM Proteine (12) und viele weitere Produktgruppen zu diesem Protein an.
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Human Polyclonal GATM Primary Antibody für WB - ABIN1881365
Köttgen, Glazer, Dehghan, Hwang, Katz, Li, Yang, Gudnason, Launer, Harris, Smith, Arking, Astor, Boerwinkle, Ehret, Ruczinski: Multiple loci associated with indices of renal function and chronic kidney disease. in Nature genetics 2010
Show all 3 Pubmed References
Measurements of creatine and guanidinoacetate in plasma are recommended for the diagnosis of AGAT and GAMT (zeige GAMT Antikörper) deficiency.Definitive confirmation of the diagnosis requires DNA sequencing of the appropriate gene and (if molecular analysis is ambiguous) measurement of AGAT or GAMT (zeige GAMT Antikörper) enzyme activity or of CRTR (zeige SLC6A8 Antikörper)-mediated transport .
Results show the functional characterization of rare missense variants in GATM which cause GATM deficiency. Seven of them report 0% of wild-type GATM activity indicating a putative pathogenicity.
Data suggest that creatine is provided equally by diet and by endogenous synthesis from arginine and glycine with successive involvement of arginine glycine amidinotransferase [AGAT] and guanidinoacetate methyl transferase [GAMT (zeige GAMT Antikörper)]. [REVIEW]
AGAT deficiency is a treatable intellectual disability.
Meta-analysis yielded a marginal, but null, association of GATM rs9806699 with statin-induced myopathy.
Genome-wide association reveals that plasma homoarginine is strongly associated with single nucleotide polymorphisms in the AGAT gene.
promiscuous activity of AGAT, a key enzyme in creatine synthesis, plays a pivotal role in homoarginine synthesis
GATM sequencing revealed a homozygous single nucleotide insertion 1111_1112insA, producing a frame-shift at Met-371 and premature termination at codon 376.
AGAT mRNA expression was significantly elevated in all heart failure patients and returned to normal levels after recovery, suggesting a specific response to heart failure involving elevated local creatine synthesis.
For the GATM BseLI polymorphism, the Yorkshire and Duroc breeds have higher allele frequencies at the G allele, whereas the local pigs have higher allele frequencies at the A allele. (GATM; glycine amidinotransferase)
results show marked metabolic effects of creatine deficiency via the chronic activation of AMPK (zeige PRKAA1 Antikörper) in a first animal model of AGAT deficiency
The spatiotemporal expression pattern of gatm during zebrafish embryogenesis was revealed.
This gene encodes a mitochondrial enzyme that belongs to the amidinotransferase family. This enzyme is involved in creatine biosynthesis, whereby it catalyzes the transfer of a guanido group from L-arginine to glycine, resulting in guanidinoacetic acid, the immediate precursor of creatine. Mutations in this gene cause arginine:glycine amidinotransferase deficiency, an inborn error of creatine synthesis characterized by mental retardation, language impairment, and behavioral disorders.
, glycine amidinotransferase, mitochondrial
, arginine:glycine amidinotransferase
, L-arginine: glycine amidinotransferase
, l-arginine:glycine amidinotransferase