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Structure, expression, and mutation of the hypoxanthine phosphoribosyltransferase gene
scientific journal article
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
6326107
retrieved
24 January 2017
title
Structure, expression, and mutation of the hypoxanthine phosphoribosyltransferase gene
(English)
1 reference
stated in
PubMed
PubMed ID
6326107
retrieved
24 January 2017
main subject
Hypoxanthine guanine phosphoribosyl transferase
1 reference
stated in
GOA release 2020-03-11
author name string
D. W. Melton
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
6326107
retrieved
24 January 2017
D. S. Konecki
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
6326107
retrieved
24 January 2017
J. Brennand
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
6326107
retrieved
24 January 2017
C. T. Caskey
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
6326107
retrieved
24 January 2017
language of work or name
English
0 references
publication date
1 April 1984
1 reference
stated in
PubMed
PubMed ID
6326107
retrieved
24 January 2017
published in
Proceedings of the National Academy of Sciences of the United States of America
1 reference
stated in
PubMed
PubMed ID
6326107
retrieved
24 January 2017
volume
81
1 reference
stated in
PubMed
PubMed ID
6326107
retrieved
24 January 2017
page(s)
2147–2151
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stated in
PubMed
PubMed ID
6326107
retrieved
24 January 2017
issue
7
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stated in
PubMed
PubMed ID
6326107
retrieved
24 January 2017
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Isolation and characterization of a full-length expressible cDNA for human hypoxanthine phosphoribosyl transferase
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Cloned cDNA sequences of the hypoxanthine/guanine phosphoribosyltransferase gene from a mouse neuroblastoma cell line found to have amplified genomic sequences.
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In vitro translation of hypoxanthine/guanine phosphoribosyltransferase mRNA: characterization of a mouse neuroblastoma cell line that has elevated levels of hypoxanthine/guanine phosphoribosyltransferase protein.
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Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in a patient with the Lesch-Nyhan syndrome
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Human hypoxanthine (guanine) phosphoribosyltransferase: an amino acid substitution in a mutant form of the enzyme isolated from a patient with gout.
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Determination of RNA sequences by primer directed synthesis and sequencing of their cDNA transcripts
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https://pubmed.ncbi.nlm.nih.gov/6326107
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Promoter sequences of eukaryotic protein-coding genes
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PubMed
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https://pubmed.ncbi.nlm.nih.gov/6326107
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based on heuristic
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Reactivation of an inactive human X chromosome: evidence for X inactivation by DNA methylation
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6326107
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Human hypoxanthine-guanine phosphoribosyltransferase
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6326107
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Expression of human and Chinese hamster hypoxanthine-guanine phosphoribosyltransferase cDNA recombinants in cultured Lesch-Nyhan and Chinese hamster fibroblasts
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6326107
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1073/PNAS.81.7.2147
0 references
PMCID
345454
0 references
PubMed ID
6326107
1 reference
stated in
PubMed
PubMed ID
6326107
retrieved
24 January 2017
ResearchGate publication ID
16870395
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