(Q41344681)

29 September 2017

title

Structure-function analysis of human glucose-6-phosphatase, the enzyme deficient in glycogen storage disease type 1a. (English)

1 reference

29 September 2017

main subject

glycogen storage disease

1 reference

Lei KJ

1

1 reference

29 September 2017

Pan CJ

2

1 reference

29 September 2017

Liu JL

3

1 reference

29 September 2017

Shelly LL

4

1 reference

29 September 2017

Chou JY

5

1 reference

29 September 2017

language of work or name

English

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publication date

1 May 1995

1 reference

Journal of Biological Chemistry

29 September 2017

published in

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29 September 2017

volume

270

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29 September 2017

issue

20

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29 September 2017

page(s)

11882-11886

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The salience of Garrod's 'molecular groupings' and 'Inborn Factors in Disease'.

29 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11882

Mutations in the glucose-6-phosphatase gene that cause glycogen storage disease type 1a

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11882

Identification of mutations in the gene for glucose-6-phosphatase, the enzyme deficient in glycogen storage disease type 1a

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11882

Mutations in the glucose-6-phosphatase gene are associated with glycogen storage disease types 1a and 1aSP but not 1b and 1c

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11882

Protein-bound phosphoryl histidine: a probable intermediate in the microsomal glucose-6-phosphatase-inorganic pyrophosphatase reaction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11882

Isolation of a cDNA for the catalytic subunit of rat liver glucose-6-phosphatase: regulation of gene expression in FAO hepatoma cells by insulin, dexamethasone and cAMP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11882

Cassette mutagenesis: an efficient method for generation of multiple mutations at defined sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11882

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11882

Molecular mechanism of uncompetitive inhibition of human placental and germ-cell alkaline phosphatase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11882

Reaction mechanism of alkaline phosphatase based on crystal structures. Two-metal ion catalysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11882

Evolution of a bifunctional enzyme: 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11882

Atomic environments of arginine side chains in proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11882

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11882

The detection and classification of membrane-spanning proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.20.11882

21 January 2018

Identifiers

DOI

10.1074/JBC.270.20.11882

1 reference

release_mkl6o5vkt5catgdmnkkesbqmxy

29 September 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/mkl6o5vkt5catgdmnkkesbqmxy

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference