(Q33982784)

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The point mutation of hypoxanthine-guanine phosphoribosyltransferase (HPRTEdinburgh) and detection by allele-specific polymerase chain reaction

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scholarly article

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Europe PubMed Central

PubMed publication ID

30 July 2017

The point mutation of hypoxanthine-guanine phosphoribosyltransferase (HPRTEdinburgh) and detection by allele-specific polymerase chain reaction (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

author name string

Lightfoot T

1

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Joshi R

2

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Europe PubMed Central

PubMed publication ID

30 July 2017

Nuki G

3

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Europe PubMed Central

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30 July 2017

Snyder FF

4

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Europe PubMed Central

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30 July 2017

publication date

1 March 1992

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Europe PubMed Central

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30 July 2017

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Europe PubMed Central

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30 July 2017

88

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30 July 2017

6

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Europe PubMed Central

PubMed publication ID

30 July 2017

695-696

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Europe PubMed Central

PubMed publication ID

30 July 2017

Human hypoxanthine-guanine phosphoribosyltransferase

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Organization of the HPRT gene and related sequences in the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A specific enzyme defect in gout associated with overproduction of uric acid

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple and very efficient method for generating cDNA libraries

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and characterization of a full-length expressible cDNA for human hypoxanthine phosphoribosyl transferase

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A method for specific cloning and sequencing of human hprt cDNA for mutation analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA sequencing with chain-terminating inhibitors

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypoxanthine-guanine phosphoribosyltransferase deficiency in three brothers with gout: characterization of a variant, HPRTEdinburgh, having altered isoelectric point, increased thermal lability and normal levels of messenger RNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determination of the mutations responsible for the Lesch-Nyhan syndrome in 17 subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Empirical Predictions of Protein Conformation

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of 17 independent mutations responsible for human hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An integrated family of amino acid sequence analysis programs

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF02265300

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Dimensions Publication ID

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

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