About: Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage disease

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About: Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage disease Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	artículu científicu espublizáu en 1970 (ast) vědecký článek publikovaný v roce 1970 (cs) 1970 թուականի Մարտին հրատարակուած գիտական յօդուած (hyw) 1970 թվականի մարտին հրատարակված գիտական հոդված (hy) наукова стаття, опублікована в березні 1970 (uk) scientific journal article (en) im März 1970 veröffentlicher wissenschaftlicher Artikel (de) wetenschappelijk artikel (gepubliceerd op 1970/03/17) (nl) vedecký článok (publikovaný 1970/03/17) (sk) مقالة علمية (نشرت في 17-3-1970) (ar)
publication date	wds:Q28118525-1D52DC93-3B23-4EC7-B0C8-E2C33170FEC3
publication date	1970-03-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28118525-1C09A890-B0AD-4752-B8E4-0F2215F01605
language of work or name	English
author name string	wds:Q28118525-0BAA363E-B96E-4D27-8A57-5873DB5D5FD7 wds:Q28118525-512097B7-4640-41C5-880F-4054313CFB56 wds:Q28118525-DBAA0C22-7A10-441F-8FC7-E33F00D3FEF2
author name string	D H Brown P L Jeffrey B I Brown
rdfs:label	Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage disease (en) Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage disease (nl) Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage disease (ast)
skos:prefLabel	Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage disease (en) Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage disease (nl) Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage disease (ast)
name	Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage disease (en) Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage disease (nl) Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage disease (ast)
title	wds:Q28118525-01232224-820E-4E00-B61F-2B0BE19554C1
title	Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage disease (en)
page(s)	wds:Q28118525-685D6532-3F93-46F4-B566-815BE8FD2A20
page(s)	1423-1428
instance of	wds:Q28118525-12D6654B-C121-4FA3-BC48-E8AF931D5EBA
instance of	scholarly article
main subject	wds:Q28118525-BF1EF963-7173-4274-B39F-39E832AC7EC6
main subject	glycogen storage disease
PubMed ID	wds:Q28118525-71F5AAF9-98C0-4683-8C5F-1D152A768C18
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/5264799
PubMed ID	5264799
published in	wds:Q28118525-4EEFDF63-1BE2-417E-9359-EABA76CDE190
published in	Biochemistry
issue	wds:Q28118525-98D48F1B-01F8-4934-9DD0-650BB4A6BB25
volume	wds:Q28118525-B4AA49D0-071C-4753-AA74-BDDAAF057BE4
issue	6
volume	9
number of pages	wds:Q28118525-1B450A92-8872-45F0-A4FD-217A4F70E20F
number of pages	6 (xsd:decimal)
DOI	wds:Q28118525-BEED9B63-D5C6-441B-B2CC-70B5F319F6F6
DOI	http://dx.doi.org/10.1021/BI00808A017
DOI	10.1021/BI00808A017
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28118525
is cites work of	The Glycogenoses and Other Inherited Disorders of Carbohydrate Metabolism Autophagic degradation of glycogen in skeletal muscles of the newborn rat Leaky splicing mutation in the acid maltase gene is associated with delayed onset of glycogenosis type II Glycosylation-independent lysosomal targeting of acid α-glucosidase enhances muscle glycogen clearance in pompe mice Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts Use of immobilized antibodies in investigating acid α-glucosidase in urine in relation to Pompe's disease Alpha-glucosidase activity in human leucocytes: Choice of lymphocytes for the diagnosis of Pompe's disease and the carrier state Adult-onset acid maltase deficiency: A postmortem study Skeletal muscle glycogenosis type II: biochemical and electron microscopic investigations of one case. Maltase, isomaltase and glucoamylase activities of the acid α-d-glucoside glucohydrolase isolated from cattle liver Heat-stable protein that stimulates acid alpha-glucosidase Anaplerotic diet therapy in inherited metabolic disease: therapeutic potential Myopathies due to enzyme deficiencies Glycogen storage disease type II (GAA) Latency of some glycosidases of rat liver lysosomes Identification of a missense mutation in one allele of a patient with Pompe disease, and use of endonuclease digestion of PCR-amplified RNA to demonstrate lack of mRNA expression from the second allele Genetic heterogeneity in acid alpha-glucosidase deficiency. Type IV glycogen storage disease: branching enzyme deficiency in skin fibroblasts and possible heterozygote detection Defective GAA does not hydrolyze lysosomal glycogen Amniotic cell 4-methylumbelliferyl-alpha-glucosidase activity for prenatal diagnosis of Pompe's disease 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 Effect of acid maltase deficiency on the endosomal/lysosomal system and glucose transporter 4. Defective GAA does not hydrolyze alpha(1;4) linkages in lysosomal glycogen GAA hydrolyzes lysosomal glycogen An isozyme of acid alpha-glucosidase with reduced catalytic activity for glycogen Studies on type II glycogenosis. Effects of cortisone derivatives on acid -glucosidase Lysosomal glycogen catabolism GAA hydrolyzes alpha(1;4) linkages in lysosomal glycogen GAA hydrolyzes alpha(1;6) linkages in lysosomal glycogen Defective GAA does not hydrolyze alpha(1;6) linkages in lysosomal glycogen Type III glycogen storage disease: An adult case with mild disease but complete absence of debrancher protein The experimental production of glycogen storage in cultured human fibroblasts Glycogen metabolism A newly identified c.1824_1828dupATACG mutation in exon 13 of the GAA gene in infantile-onset glycogen storage disease type II (Pompe disease) Brain Glycogen Structure and Its Associated Proteins: Past, Present and Future
is cites work of	wds:Q38362656-822F80E1-E7A8-4B56-A1C7-A87A529AFA55 wds:Q42162821-BA0468DA-BC4E-46A4-9366-95ED70E1819F wds:Q36543643-B9F0A35C-29B6-4C89-AA55-C00EDFFC41B5 wds:Q39251470-A20077C8-DE6B-432B-9BF2-2DF7FE1B6CF9 wds:Q40911219-4831AD80-5D7C-4763-ACD6-29F9B73F5A05 wds:Q42186605-EEB47F32-2B89-42E5-AC7E-891E68BDAA87 wds:Q33586900-A8E51709-7D33-4761-9BDD-2C25ED79880C wds:Q45316420-74C013D8-986E-4011-9800-295ABA93C480 wds:Q50289086-538341B5-4D60-4D1E-AC51-D28271B74869 wds:Q36501326-BF9B4041-F388-4935-8DB7-4090B8C06759 wds:Q37074813-EB50ACF6-C2C7-4C6F-8253-B22416832967 wds:Q35202542-817E31DB-8C5E-4CA1-9C57-1F971036C830

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