(Q77424682)

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Transition mutations at CpG dinucleotides are the most frequent in vivo spontaneous single-based substitution mutation in the human HPRT gene

scientific article published on 01 January 1998

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9776183%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

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Europe PubMed Central

Transition mutations at CpG dinucleotides are the most frequent in vivo spontaneous single-based substitution mutation in the human HPRT gene (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9776183%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

author name string

J P O'Neill

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9776183%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

B A Finette

2

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5 December 2019

publication date

1 January 1998

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9776183%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

Environmental and Molecular Mutagenesis

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9776183%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

32

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5 December 2019

2

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5 December 2019

188-191

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9776183%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

Lesch-Nyhan syndrome: carrier and prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2280%281998%2932%3A2%3C188%3A%3AAID-EM16%3E3.0.CO%3B2-Y

21 January 2018

The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2280%281998%2932%3A2%3C188%3A%3AAID-EM16%3E3.0.CO%3B2-Y

21 January 2018

Determination of hprt mutant frequencies in T-lymphocytes from a healthy pediatric population: statistical comparison between newborn, children and adult mutant frequencies, cloning efficiency and age.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2280%281998%2932%3A2%3C188%3A%3AAID-EM16%3E3.0.CO%3B2-Y

21 January 2018

Suggestions concerning the relationship between mutant frequency and mutation rate at the hprt locus in human peripheral T-lymphocytes.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2280%281998%2932%3A2%3C188%3A%3AAID-EM16%3E3.0.CO%3B2-Y

21 January 2018

Germinal HPRT splice donor site mutation results in multiple RNA splicing products in T-lymphocyte cultures

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2280%281998%2932%3A2%3C188%3A%3AAID-EM16%3E3.0.CO%3B2-Y

21 January 2018

Duplication-targeted DNA methylation and mutagenesis in the evolution of eukaryotic chromosomes

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2280%281998%2932%3A2%3C188%3A%3AAID-EM16%3E3.0.CO%3B2-Y

21 January 2018

5-Methylcytosine as an Endogenous Mutagen in the Human LDL Receptor and p53 Genes

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2280%281998%2932%3A2%3C188%3A%3AAID-EM16%3E3.0.CO%3B2-Y

21 January 2018

An analysis of in vivo hprt mutant frequency in circulating T-lymphocytes in the normal human population: a comparison of four datasets

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2280%281998%2932%3A2%3C188%3A%3AAID-EM16%3E3.0.CO%3B2-Y

21 January 2018

A review of the molecular basis of hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2280%281998%2932%3A2%3C188%3A%3AAID-EM16%3E3.0.CO%3B2-Y

21 January 2018

Characterization of mutations in phenotypic variants of hypoxanthine phosphoribosyltransferase deficiency

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2280%281998%2932%3A2%3C188%3A%3AAID-EM16%3E3.0.CO%3B2-Y

21 January 2018

Molecular analyses of a Lesch-Nyhan syndrome mutation (hprtMontreal) by use of T-lymphocyte cultures

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2280%281998%2932%3A2%3C188%3A%3AAID-EM16%3E3.0.CO%3B2-Y

21 January 2018

Identifiers

10.1002/(SICI)1098-2280(1998)32:2<188::AID-EM16>3.0.CO;2-Y

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9776183%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9776183%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

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