GAA 抗体
(Glucosidase, Alpha, Acid (GAA))
This gene encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008].
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Latest Publications for our GAA 抗体
: "Discovery of a novel noniminosugar acid ? glucosidase chaperone series." in: Journal of medicinal chemistry, Vol. 55, Issue 17, pp. 7546-59, (2012) (PubMed).: "Glycosylation-related gene expression is linked to differentiation status in glioblastomas undifferentiated cells." in: Cancer letters, Vol. 312, Issue 1, pp. 24-32, (2011) (PubMed).
Aliases for GAA 抗体
glucosidase alpha, acid (GAA) 抗体glucosidase, alpha, acid (Gaa) 抗体
transmembrane and coiled-coil domain family 1 (TMCC1) 抗体
glucosidase, alpha; acid (Pompe disease, glycogen storage disease type II) (gaa) 抗体
glucosidase alpha, acid (Gaa) 抗体
E430018M07Rik 抗体
LYAG 抗体
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