(Q70413830)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5041886%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

title

Isoenzymes of hypoxanthine-guanine-phosphoribosyl transferase in a family with partial deficiency of the enzyme (English)

1 reference

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11 October 2019

0 references

B Bakay

1

1 reference

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11 October 2019

W L Nyhan

series ordinal

2

1 reference

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11 October 2019

N Fawcett

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5041886%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

M D Kogut

series ordinal

4

1 reference

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11 October 2019

publication date

1 August 1972

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11 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5041886%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

volume

7

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11 October 2019

issue

1

1 reference

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11 October 2019

page(s)

73-85

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00487011

11 October 2019

exact match

0 references

cites work

Genetic analysis of mutants producing defective β-galactosidase which can be activated by specific antibodies

1 reference

12 December 2020

Detection of radioactive components in polyacrylamide gel disc electropherograms by automated mechanical fractionation

1 reference

12 December 2020

Human hypoxanthine phosphoribosyltransferase. II. Kinetics and chemical modification.

1 reference

12 December 2020

Lesch-Nyhan syndrome: altered kinetic properties of mutant enzyme

1 reference

12 December 2020

Kinetic Studies of Hypoxanthine-Guanine Phosphoribosyltransferase

1 reference

12 December 2020

Inheritance of purine phosphoribosyltransferases in man

1 reference

12 December 2020

Electrophoretic properties of hypoxanthine-guanine phosphoribosyl transferase in erythrocytes of subjects with Lesch-Nyhan syndrome

1 reference

12 December 2020

Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells

1 reference

12 December 2020

X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: heterozygote has two clonal populations

1 reference

12 December 2020

A FAMILIAL DISORDER OF URIC ACID METABOLISM AND CENTRAL NERVOUS SYSTEM FUNCTION

1 reference

12 December 2020

Diagnostic test for congenital hyperuricemia with central nervous system dysfunction

1 reference

12 December 2020

Purine metabolism in heterozygous carriers of hypoxanthine-guanine phosphoribosyltransferase deficiency

1 reference

12 December 2020

Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency in Gout

1 reference

12 December 2020

Enzyme Defect Associated with a Sex-Linked Human Neurological Disorder and Excessive Purine Synthesis

1 reference

12 December 2020

Disorder of purine metabolism due to partial deficiency of hypoxanthine-guanine phosphoribosyltransferase

1 reference

12 December 2020

The separation of adenine and hypoxanthine-guanine phosphoribosyl transferases isoenzymes by disc gel electrophoresis

1 reference

12 December 2020

Hemizygous expression of glucose-6-phosphate dehydrogenase in erythrocytes of heterozygotes for the Lesch-Nyhan syndrome

1 reference

12 December 2020

Enhanced stability against heat denaturation of E. coli wild type and mutant beta-galactosidase in the presence of specific antibodies

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00487011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5041886%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

1 reference