Multiple transport protein defects in a patient with glycogen storage disease type 1: GSD 1b/1c beta (Q70994522)

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15 October 2019

title

Multiple transport protein defects in a patient with glycogen storage disease type 1: GSD 1b/1c beta (English)

1 reference

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15 October 2019

main subject

glycogen storage disease

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glycogen metabolic process

inferred from title

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R A Hawkins

1

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15 October 2019

K R Kamath

series ordinal

2

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15 October 2019

H M Scott

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8598636%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

A Burchell

series ordinal

4

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15 October 2019

publication date

1 January 1995

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Journal of Inherited Metabolic Disease

15 October 2019

published in

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15 October 2019

volume

18

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15 October 2019

issue

5

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15 October 2019

page(s)

558-566

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Specific inactivation of the phosphohydrolase component of the hepatic microsomal glucose-6-phosphatase system by diethyl pyrocarbonate

15 October 2019

cites work

1 reference

12 December 2020

Evidence for the participation of independent translocation for phosphate and glucose 6-phosphate in the microsomal glucose-6-phosphatase system. Interactions of the system with orthophosphate, inorganic pyrophosphate, and carbamyl phosphate

1 reference

12 December 2020

Glycogen storage disease diagnosed in adults

1 reference

12 December 2020

Fatty acyl-CoA esters inhibit glucose-6-phosphatase in rat liver microsomes

1 reference

12 December 2020

A new microtechnique for the analysis of the human hepatic microsomal glucose-6-phosphatase system

1 reference

12 December 2020

Diagnosis of type 1B and 1C glycogen storage disease

1 reference

12 December 2020

Analysis of human hepatic microsomal glucose-6-phosphatase in clinical conditions where the T2 pyrophosphate/phosphate transport protein is absent

1 reference

12 December 2020

Microsomal membrane permeability and the hepatic glucose-6-phosphatase system. Interactions of the system with D-mannose 6-phosphate and D-mannose

1 reference

12 December 2020

Molecular pathology of glucose-6-phosphatase

1 reference

12 December 2020

Molecular pathologies of the hepatic endoplasmic reticulum

1 reference

12 December 2020

A simplification of the protein assay method of Lowry et al. which is more generally applicable

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12 December 2020

Diagnosis of a novel glycogen storage disease: type 1aSP

1 reference

12 December 2020

The hepatic glucose-6-phosphatase system in Ehrlich-ascites-tumour-bearing mice

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12 December 2020

LIVER MICROSOMAL GLUCOSE 6-PHOSPHATASE, INORGANIC PYROPHOSPHATASE, AND PYROPHOSPHATE-GLUCOSE PHOSPHOTRANSFERASE. II. KINETIC STUDIES

1 reference

12 December 2020

The mechanism of histone activation of the hepatic microsomal glucose-6-phosphatase system: a novel method to assay glucose-6-phosphatase activity.

1 reference

12 December 2020

A new variant of glycogen storage disease Type I probably due to a defect in the glucose-6-phosphate transport system

1 reference

12 December 2020

The molecular basis of the type 1 glycogen storage diseases

1 reference

12 December 2020

Protein measurement with the Folin phenol reagent

1 reference

12 December 2020

Glucose-6-phosphatase of the liver in glycogen storage disease

1 reference

12 December 2020

The importance of membrane integrity in kinetic characterizations of the microsomal glucose-6-phosphatase system

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02436000

1 reference

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15 October 2019

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