Pages that link to "Q68501332"

The following pages link to Rodent and human acid -glucosidase. Purification, properties and inhibition by antibodies. Investigation in type II glycogenosis (Q68501332):

Displaying 37 items.

• Leaky splicing mutation in the acid maltase gene is associated with delayed onset of glycogenosis type II (Q24314311) (← links)
• Identification of the base-pair substitution responsible for a human acid alpha glucosidase allele with lower "affinity" for glycogen (GAA 2) and transient gene expression in deficient cells (Q24676487) (← links)
• Studies on the catabolism of the hydroxylysine-linked disaccharide units of basement membranes and collagens. Isolation and characterization of a rat kidney alpha-glucosidase of high specificity (Q34192478) (← links)
• Genetic heterogeneity in acid alpha-glucosidase deficiency. (Q35202542) (← links)
• Separation of acid and neutral α-glucosidase isoenzymes from fetal and adult tissues, cultivated fibroblasts and amniotic fluid cells by deae-cellulose and sephadex G-100 column chromatography (Q36468795) (← links)
• Uncommon case of type II glycogenosis (Q36486106) (← links)
• Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts (Q37034093) (← links)
• Partial purification and characterization of alpha-glucosidase from Pseudomonas fluorescens W. (Q38359732) (← links)
• Physico-chemical and immunological properties of acid α-glucosidase from various human tissues in relation to glycogenosis type II (pompe's disease) (Q39088633) (← links)
• Some properties of human liver acid α-glucosidase (Q39147527) (← links)
• The molecular heterogeneity of purified human liver lysosomal α-Glucosidase (acid α-Glucosidase) (Q39184333) (← links)
• Use of immobilized antibodies in investigating acid α-glucosidase in urine in relation to Pompe's disease (Q39251470) (← links)
• Acid maltase deficiency in non-identical adult twins. A morphological and biochemical study (Q39396054) (← links)
• The distribution of hydrolytic enzyme activities in human fibroblast cultures and their intercellular transfer (Q39622132) (← links)
• Glycogen storage diseases in animals and their potential value as models of human disease (Q40207697) (← links)
• Hydrolytic and transglucosylation activities of a purified calf spleen β-glucosidase (Q40324722) (← links)
• Acid ?-glucosidase: A new polymorphism in man demonstrable by ?affinity? electrophoresis (Q40350922) (← links)
• Biochemical, immunological, and cell genetic studies in glycogenosis type II (Q40896047) (← links)
• The apparent activity in vivo of the lysosomal pathway of glycogen catabolism in cultured human skin fibroblasts from patients with type III glycogen storage disease (Q40911219) (← links)
• Metabolism of hydrogenated palatinose, an equimolar mixture ofα-D-glucopyranosido-1,6-sorbitol andα-D-glucopyranosido-1,6-mannitol (Q40971979) (← links)
• Carbohydrate content of acid α-glucosidase (γ-amylase) from human liver (Q41047021) (← links)
• Adult-onset acid maltase deficiency: A postmortem study (Q41052901) (← links)
• Nosology of lysosomal glycogen storage diseases without in vitro acid maltase deficiency. Delineation of a neonatal form (Q41650566) (← links)
• Skeletal-muscle alpha-glucosidases in bovine generalized glycogenosis type II. (Q41790169) (← links)
• Soluble neutral and acid maltases in the suckling-rat intestine. The effect of cortisol and development (Q41809759) (← links)
• A serological investigation into the acidic alpha-D-mannosidase in normal Angus cattle and in a calf with mannosidosis (Q42046022) (← links)
• Immunological characterization of human liver alpha-D-mannosidase (Q42916225) (← links)
• Caveat to protein replacement therapy for genetic disease. Immunological implications of accurate molecular diagnosis (Q46341839) (← links)
• Morquio's disease type A: Absence of material cross reacting with antibodies against N-acetylgalactosamine-6-sulfate sulfatase (Q53967432) (← links)
• Subcellular distribution of acid alpha-glucosidase in fibroblasts and of antigenically cross-reactive material in Pompe's disease fibroblasts (Q68944096) (← links)
• The use of leucocytes as an aid in the diagnosis of glycogen storage disease type II (Pompe's disease) (Q69046547) (← links)
• Modulation of enzymatic activities during spontaneous and induced differentiation in a human pancreatic adenocarcinoma cell line CAPAN-1 (Q69350563) (← links)
• The glycogen storage diseases (Q69370671) (← links)
• Immunohistochemical demonstration of acid alpha-glucosidase in muscle in Pompe's disease (Q70269855) (← links)
• Demonstration of acid maltase protein in Pompe disease by use of immunohistochemical and enzyme immunoassay methods (Q70467679) (← links)
• Immunocytochemistry of lysosomal hydrolases and their precursor forms in normal and mutant human cells (Q70620382) (← links)
• Biosynthesis of acid alpha-glucosidase in late-onset forms of glycogenosis type II (Pompe's disease) (Q71476837) (← links)