Lack of an alpha-1,4-glucan: alpha-1,4-glucan 6-glycosyl transferase in a case of type IV glycogenosis

scientific article

Lack of an alpha-1,4-glucan: alpha-1,4-glucan 6-glycosyl transferase in a case of type IV glycogenosis is …
instance of (P31):
scholarly articleQ13442814

External links are
P819ADS bibcode1966PNAS...56..725B
P356DOI10.1073/PNAS.56.2.725
P953full work available at URLhttps://europepmc.org/articles/pmc224432?pdf=render
https://europepmc.org/articles/PMC224432
https://europepmc.org/articles/PMC224432?pdf=render
https://pnas.org/doi/pdf/10.1073/pnas.56.2.725
P932PMC publication ID224432
P698PubMed publication ID5229990
P5875ResearchGate publication ID253256870

P2093author name stringD. H. Brown
B. I. Brown
P2860cites workFamilial cirrhosis of the liver with storage of abnormal glycogenQ28212138
The de novo synthesis of polysaccharide by phosphorylaseQ36407141
THE MECHANISM OF THE DE NOVO SYNTHESIS OF POLYSACCHARIDE BY PHOSPHORYLASE.Q36407185
A study of the reaction catalysed by the liver branching enzymeQ42119328
Type IV glycogenosisQ70879897
Structure of glycogens and amylopectins. III. Normal and abnormal human glycogenQ73065832
The action of branching enzymes on outer chains of glycogenQ73182327
a-1,4-glucan: a-1,4-glucan 6-glycosyltransferase from liverQ76490029
AMYLO-1,6-GLUCOSIDASE ACTIVITY IN NORMAL LEUCOCYTES AND IN LEUCOCYTES OF PATIENTS WITH GLYCOGEN-STORAGE DISEASEQ76829032
TRANSFER OF GLUCOSYL UNITS TO OLIGOSACCHARIDES AND POLYSACCHARIDES BY THE ACTION OF URIDINE DIPHOSPHOGLUCOSE-ALPHA-GLUCAN TRANSGLUCOSYLASEQ78430626
Type IV glycogenosis. Report of a case proven by characterization of glycogen and studied at necropsyQ79667644
P433issue2
P407language of work or nameEnglishQ1860
P921main subjectglucosyltransferasesQ5572361
P1104number of pages5
P304page(s)725-729
P577publication date1966-08-01
P1433published inProceedings of the National Academy of Sciences of the United States of AmericaQ1146531
P1476titleLack of an alpha-1,4-glucan: alpha-1,4-glucan 6-glycosyl transferase in a case of type IV glycogenosis
P478volume56

Reverse relations

cites work (P2860)
Q381625861 Clinical Enzymology
Q57820545A Case of Glycogen Storage Disease IV with Rare Homozygous Mutations in the Glycogen Branching Enzyme Gene
Q37415869A Modified Enzymatic Method for Measurement of Glycogen Content in Glycogen Storage Disease Type IV.
Q34606916A complex rearrangement in GBE1 causes both perinatal hypoglycemic collapse and late-juvenile-onset neuromuscular degeneration in glycogen storage disease type IV of Norwegian forest cats
Q59182919A juvenile variant of glycogenosis IV (Andersen disease)
Q48589781A mild juvenile variant of type IV glycogenosis
Q40788188A new variant of type IV glycogenosis: deficiency of branching enzyme activity without apparent progressive liver disease
Q44555356A simple, rapid test for the differential diagnosis of glycogen storage disease type 3.
Q42518307Abnormal glycogen in astrocytes is sufficient to cause adult polyglucosan body disease
Q58743384Analysis of mutations via protein expression studies in glycogen storage disease type IV: A report on a non-progressive form with a literature review
Q67906323Apparent absence of glycogen branching enzyme activity in phosphofructokinase deficiency
Q77923035Branching action of amylo-1,6-glucosidase/oligo-1,4-->1,4-glucantransferase
Q35247186Branching enzyme activity of cultured amniocytes and chorionic villi: prenatal testing for type IV glycogen storage disease
Q70063744Branching enzyme in erythrocytes. Detection of type IV glycogenosis homozygotes and heterozygotes
Q36061863Branching enzyme-deficiency glycogenosis: studies in therapy
Q36296501Cardiac Involvement in Glycogen Storage Disease Type IV: Two Cases and the Two Ends of a Spectrum
Q34241674Cell migration and chimerism after whole-organ transplantation: the basis of graft acceptance
Q33229028Characterization of the role of gamma2 R531G mutation in AMP-activated protein kinase in cardiac hypertrophy and Wolff-Parkinson-White syndrome
Q28378665Chimerism after liver transplantation for type IV glycogen storage disease and type 1 Gaucher's disease
Q77343248Corpora-amylacea and the family of polyglucosan diseases
Q27661326Crystal Structure of Full-length Mycobacterium tuberculosis H37Rv Glycogen Branching Enzyme
Q35120208Dysfunctional muscle and liver glycogen metabolism in mdx dystrophic mice
Q70612108Enzyme studies on white blood cells and their significance for genetics
Q24531487Enzymic explorations of the structures of starch and glycogen
Q39975282Genetic Heterogeneity
Q45058157Glycogen branching enzyme (GBE1) mutation causing equine glycogen storage disease IV.
Q41825382Glycogen storage disease type IV, amylopectinosis
Q43540623Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder
Q93726856Glycogen storage diseases
Q34098766Glycogen storage diseases: new perspectives
Q33598826Glycogenosis type IV (Andersen disease). Clinical data, pathology, and genetics in a fatal perinatal case
Q24336056Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene
Q48632175Hereditary branching enzyme dysfunction in adult polyglucosan body disease: A possible metabolic cause in two patients
Q68518755Hypoglycemia in type IV glycogenosis: hepatic improvement in two patients with nutritional management
Q36127081Increased laforin and laforin binding to glycogen underlie Lafora body formation in malin-deficient Lafora disease.
Q72078323Juvenile hereditary polyglucosan body disease with complete branching enzyme deficiency (type IV glycogenosis)
Q71072947Light and electron microscopy of skeletal muscle in type IV glycogenosis
Q34280991Liver transplantation for type I and type IV glycogen storage disease
Q34965080Liver transplantation for type IV glycogen storage disease
Q40605304Living Donor Liver Transplantation in a Korean Child with Glycogen Storage Disease Type IV and a GBE1 Mutation.
Q49321379Molecular basis of hereditary disease
Q47571287Multisystem involvement in a patient due to accumulation of amylopectin-like material with diminished branching enzyme activity.
Q39477219Myopathies due to enzyme deficiencies
Q48212544Neonatal hypotonia and cardiomyopathy secondary to type IV glycogenosis
Q48027504Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of glycogen storage disease type IV associated with a new mutation in GBE1 gene.
Q28829068Nrf2-Mediated Regulation of Skeletal Muscle Glycogen Metabolism
Q44454793Overexpression of glycogen synthase in mouse muscle results in less branched glycogen
Q40245324Prenatal diagnosis of inherited metabolic diseases; principles, pitfalls, and prospects.
Q68147087Progressive cardiac failure following orthotopic liver transplantation for type IV glycogenosis
Q68765046Severe cardiopathy in branching enzyme deficiency
Q45237555Severe neonatal onset of glycogenosis type IV: clinical and laboratory findings leading to diagnosis in two siblings.
Q64078021Skeletal Muscle Glycogen Chain Length Correlates with Insolubility in Mouse Models of Polyglucosan-Associated Neurodegenerative Diseases
Q61861032Soluble starch synthases and starch branching enzymes from cotyledons of smooth- and wrinkled-seeded lines of Pisum sativum L
Q37074813The Glycogenoses and Other Inherited Disorders of Carbohydrate Metabolism
Q39973110The Role of Glycogen in Blood Cells
Q39867513The histochemical evaluation of the glycogen storage diseases. A review of techniques and their limitations
Q69006676Type 3 glycogenosis: atypical enzyme activities in blood cells in two siblings
Q71047723Type IV glycogen storage disease: branching enzyme deficiency in skin fibroblasts and possible heterozygote detection
Q49578189Variable clinical presentation of glycogen storage disease type IV: from severe hepatosplenomegaly to cardiac insufficiency. Some discrepancies in genetic and biochemical abnormalities

Search more.