(Q41330895)

29 September 2017

title

Spontaneous and ionizing radiation induced mutations involve large events when selecting for loss of an autosomal locus (English)

1 reference

chromosomal deletion syndrome

29 September 2017

main subject

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7603506

8 June 2024

2

K. A. Walker

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7603506

8 June 2024

author name string

M. Turker

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7603506

8 June 2024

C. D. Jennings

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7603506

8 June 2024

I. Mellon

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7603506

8 June 2024

A. Yusufji

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7603506

8 June 2024

M. Urano

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7603506

8 June 2024

language of work or name

English

0 references

publication date

1 July 1995

1 reference

full work available at URL

29 September 2017

https://api.elsevier.com/content/article/PII:002751079500046L?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/0027-5107(95)00046-L

https://api.elsevier.com/content/article/PII:002751079500046L?httpAccept=text/plain

8 June 2024

1 reference

https://api.crossref.org/works/10.1016/0027-5107(95)00046-L

8 June 2024

1 reference

29 September 2017

volume

329

1 reference

29 September 2017

issue

2

1 reference

29 September 2017

page(s)

97-105

1 reference

Rapid screening for deletion mutations in the hprt gene using the polymerase chain reaction: X-ray and alpha-particle mutant spectra

29 September 2017

cites work

1

1 reference

https://api.crossref.org/works/10.1016/0027-5107(95)00046-L

A comparison of induced mutation at homologous alleles of the tk locus in human cells

8 June 2024

2

1 reference

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Molecular dissection of mutations at the heterozygous thymidine kinase locus in mouse lymphoma cells

8 June 2024

3

1 reference

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Molecular analysis of hypoxanthine phosphoribosyltransferase gene deletions induced by alpha- and X-radiation in human lymphoblastoid cells

8 June 2024

4

1 reference

https://api.crossref.org/works/10.1016/0027-5107(95)00046-L

X rays induce interallelic homologous recombination at the human thymidine kinase gene

8 June 2024

5

1 reference

https://api.crossref.org/works/10.1016/0027-5107(95)00046-L

The aprt heterozygote/hemizygote system for screening mutagenic agents allows detection of large deletions

8 June 2024

6

1 reference

https://api.crossref.org/works/10.1016/0027-5107(95)00046-L

Molecular analysis of APRT deficiency in mouse P19 teratocarcinoma stem cell line

8 June 2024

7

1 reference

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At least two distinct epigenetic mechanisms are correlated with high-frequency "switching" for APRT phenotypic expression in mouse embryonal carcinoma stem cells

8 June 2024

8

1 reference

https://api.crossref.org/works/10.1016/0027-5107(95)00046-L

The nature of ultraviolet light-induced mutations at the heterozygous aprt locus in Chinese hamster ovary cells

8 June 2024

9

1 reference

https://api.crossref.org/works/10.1016/0027-5107(95)00046-L

The specificity of UV-induced mutations at an endogenous locus in mammalian cells

8 June 2024

10

1 reference

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Nucleotide sequence and organization of the mouse adenine phosphoribosyltransferase gene: presence of a coding region common to animal and bacterial phosphoribosyltransferases that has a variable intron/exon arrangement

8 June 2024

11

1 reference

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Allelic losses in mutations at the aprt locus of human lymphoblastoid cells

8 June 2024

12

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Molecular and biochemical elucidation of a cellular phenotype characterized by adenine analogue resistance in the presence of high levels of adenine phosphoribosyltransferase activity

8 June 2024

14

1 reference

https://api.crossref.org/works/10.1016/0027-5107(95)00046-L

Reduction to homozygosity is the predominant spontaneous mutational event in cultured human lymphoblastoid cells

8 June 2024

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Mutation and cancer: statistical study of retinoblastoma

8 June 2024

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Loss of constitutional heterozygosity in human cancer.

8 June 2024

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Molecular mechanisms of spontaneous and induced loss of heterozygosity in human cells in vitro

8 June 2024

18

1 reference

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Wilms' tumor-specific methylation pattern in 11p13 detected by PFGE

8 June 2024

20

1 reference

https://api.crossref.org/works/10.1016/0027-5107(95)00046-L

Allele-specific hypermethylation of the retinoblastoma tumor-suppressor gene

8 June 2024

21

1 reference

https://api.crossref.org/works/10.1016/0027-5107(95)00046-L

Ionizing radiation, genetic risk estimation and molecular biology: impact and inferences

8 June 2024

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The biology of alkylating-agent cellular injury.

8 June 2024

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Investigation of the mutagenic specificity of X-rays using a retroviral shuttle vector in CHO cells

8 June 2024

24

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Genetic instability on chromosome 16 in a human B lymphoblastoid cell line

8 June 2024

25

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Effect of gamma rays at the dihydrofolate reductase locus: deletions and inversions.

8 June 2024

26

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Loss of heterozygosity in mammalian cell mutagenesis: molecular analysis of spontaneous mutations at the aprt locus in CHO cells

8 June 2024

27

1 reference

https://api.crossref.org/works/10.1016/0027-5107(95)00046-L

Somatic mutations at a heterozygous autosomal locus in human cells occur more frequently by allele loss than by intragenic structural alterations

8 June 2024

28

1 reference

https://api.crossref.org/works/10.1016/0027-5107(95)00046-L

Loss of heterozygosity: the most frequent cause of recessive phenotype expression at the heterozygous human adenine phosphoribosyltransferase locus

8 June 2024

29

1 reference

https://api.crossref.org/works/10.1016/0027-5107(95)00046-L

8 June 2024

Identifiers

1 reference

29 September 2017

1 reference