(Q41582295)

4 October 2017

Spectrum of spontaneous HPRT- mutations in TK6 human lymphoblasts (English)

1 reference

4 October 2017

Giver CR

1

1 reference

PubMed ID

8404873

4 October 2017

Nelson SL

series ordinal

2

1 reference

PubMed ID

8404873

4 October 2017

Grosovsky AJ

series ordinal

3

1 reference

4 October 2017

1 January 1993

1 reference

Environmental and Molecular Mutagenesis

4 October 2017

1 reference

4 October 2017

22

1 reference

4 October 2017

138-146

1 reference

4 October 2017

3

1 reference

Endogenous mutagens and the causes of aging and cancer

4 October 2017

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

Repair of intrinsic DNA lesions

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

Errors in DNA synthesis: a source of spontaneous mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

Endogenous genotoxic agents and processes as a basis of spontaneous carcinogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

Fine structure of the human hypoxanthine phosphoribosyltransferase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

Spontaneous mutagenesis: experimental, genetic and other factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

Frameshift mutations and the genetic code. This paper is dedicated to Professor Theodosius Dobzhansky on the occasion of his 66th birthday

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

The spectrum of cystic fibrosis mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

On the formation of spontaneous deletions: The importance of short sequence homologies in the generation of large deletions

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Too many rodent carcinogens: mitogenesis increases mutagenesis

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Molecular mechanisms of oxygen radical carcinogenesis and mutagenesis: the role of DNA base damage

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Human HPRT mutant database: software for data entry and retrieval

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Mutagenic deamination of cytosine residues in DNA

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

An immunoglobulin heavy chain variable region gene is generated from three segments of DNA: VH, D and JH.

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Automated DNA sequencing of the human HPRT locus

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Asymmetric cytosine deamination revealed by spontaneous mutational specificity in an Ung- strain of Escherichia coli.

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Large deletions are tolerated at the hprt locus of in vivo derived human T-lymphocytes

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Mapping large spontaneous deletion endpoints in the human HPRT gene

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Identification of mutations leading to the Lesch-Nyhan syndrome by automated direct DNA sequencing of in vitro amplified cDNA.

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Multiplex DNA deletion detection and exon sequencing of the hypoxanthine phosphoribosyltransferase gene in Lesch-Nyhan families

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Structural intermediates of deletion mutagenesis: a role for palindromic DNA

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

p53 mutations in human cancers

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Molecular spectrum of background mutation at the hprt locus in human T-lymphocytes

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Spectrum of spontaneous mutations in a cDNA of the human hprt gene integrated in chromosomal DNA

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Mutation assay at the thymidine kinase locus in diploid human lymphoblasts

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Kinds and locations of mutations arising spontaneously in the coding region of theHPRT gene of finite-life-span diploid human fibroblasts

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Nucleotide sequence analysis of human hypoxanthine phosphoribosyltransferase (HPRT) gene deletions

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

S-adenosylmethionine, an endogenous alkylating agent

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotype

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Longitudinal study of the in vivo hprt mutant frequency in human T-lymphocytes as determined by a cell cloning assay.

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

DNA sequence analysis of in vivo hprt mutation in human T lymphocytes

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Mutational specificity of animal cell DNA polymerases

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Mutations affecting RNA splicing in man are detected more frequently in somatic than in germ cells

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Mutations which alter splicing in the human hypoxanthine-guanine phosphoribosyltransferase gene

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Mutational spectrometry in animal toxicity testing

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Somatic generation of antibody diversity

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Enhanced hprt mutant frequency but no significant difference in mutation spectrum between a smoking and a non-smoking human population.

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Oncogenic point mutations in the human retinoblastoma gene: their application to genetic counseling

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Amplification and direct nucleotide sequencing of cDNA from the lysate of low numbers of diploid human cells

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Spectrum of spontaneously occurring mutations in the hprt gene of V79 Chinese hamster cells

1 reference

https://api.crossref.org/works/10.1002%2FEM.2850220305

7 January 2021

Identifiers

DOI

10.1002/EM.2850220305

1 reference

4 October 2017

1 reference

PubMed ID

8404873