Paper · 7004875

Dna repair: pathways and defects.

Bartram CR. Eur J Pediatr, 1980. Cited by 6 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

Cite this record

ConductScience Library. Dna repair: pathways and defects. Papers, record 7004875. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/7004875

On this page

Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title: Dna repair: pathways and defects.; PubMed
Journal: Eur J Pediatr; PubMed
Year: 1980; PubMed
Publication types: Journal Article, Review; PubMed
PubMed: https://pubmed.ncbi.nlm.nih.gov/7004875/; PubMed
DOI: https://doi.org/10.1007/bf00441631; PubMed
The journal: https://conductscience.org/library/journal-index/7603873; PubMed
Citations, by iCite: 6; iCite
Relative citation ratio, by iCite: 0.15; iCite
Revised in PubMed: 2026-10-10; PubMed

Authors1

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

Order	Author	Forename	Kind	ORCID iD
1	Bartram CR	C R

Source PubMed

Topics15

NLM's MeSH indexing of the paper, its major topics first.

MeSH term	Major
DNA Repair	Major topic
Ataxia Telangiectasia
Cell Transformation, Neoplastic
Cockayne Syndrome
DNA Replication
Deoxyribodipyrimidine Photo-Lyase
Fanconi Anemia
Growth Disorders
Humans
Light
Progeria
Risk
Syndrome
Werner Syndrome
Xeroderma Pigmentosum

Source PubMed

Grants0

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

None in this release.

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References91

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

Order	PMID	Title	Journal	Year	In Papers	Source
1	990,442	Somatic recombination as possible prelude to malignant transformation.	Birth Defects Orig Artic Ser	1976	https://conductscience.org/library/papers/990442	PubMed
2	6,024,234	Immunoglobulin deficiency in Bloom's syndrome.	Am J Dis Child	1967	https://conductscience.org/library/papers/6024234	PubMed
3	437,776	Frequency of sister chromatid exchanges in Bloom syndrome fibroblasts reduced by cocultivation with normal cells.	Hum Genet	1979	https://conductscience.org/library/papers/437776	PubMed
4	1,056,890	Human diseases with genetically altered DNA repair processes.	Genetics	1975	https://conductscience.org/library/papers/1056890	PubMed
5	4,140,506	A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes.	Proc Natl Acad Sci U S A	1974	https://conductscience.org/library/papers/4140506	PubMed
6	7,360,141	Increased sensitivity of cell strains from Cockayne's syndrome to sister-chromatid-exchange induction and cell killing by UV light.	Mutat Res	1980	https://conductscience.org/library/papers/7360141	PubMed
7	371,535	Human disorders showing increased sensitivity to the induction of genetic damage.	Annu Rev Genet	1978	https://conductscience.org/library/papers/371535	PubMed
8	14,997,609	Sister chromatid exchanges in ataxia telangiectasia.	Mutat Res	1976	https://conductscience.org/library/papers/14997609	PubMed
9	291,051	Postreplication repair: questions of its definition and possible alteration in xeroderma pigmentosum cell strains.	Proc Natl Acad Sci U S A	1979	https://conductscience.org/library/papers/291051	PubMed
10	990,439	Malignant disease in heterozygous carriers.	Birth Defects Orig Artic Ser	1976	https://conductscience.org/library/papers/990439	PubMed

1 to 10 of 91

See all 91 references

Cited by2

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 6 citations.

PMID	Title	Journal	Year	In Papers	Source
40,586,826	Association Between Seven Selected Genetic Polymorphisms in DNA Repair-Related Genes and Breast Cancer Risk: Evidence from a Comprehensive Meta-analysis Including 96 Studies.	Biochem Genet	2026	https://conductscience.org/library/papers/40586826	PubMed
3,098,567	Increased chromosomal breakage in epileptic children after long-term treatment.	Eur J Pediatr	1986	https://conductscience.org/library/papers/3098567	PubMed

Genes0

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

None in this release.

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed: 2026-11-06; PubMed
iCite: 2026-11-05; iCite
PMC's ID file: 2026-11-05; PMC's ID file
NIH RePORTER's grant and paper links: 2026-11-01; NIH RePORTER's grant and paper links
Trials: 2026-11-12
Gene search: 2026-11-11
Pipelines: 2026-09-18

Sources 11

ChEMBL, through Open TargetsCC BY-SA 3.0
ClinicalTrials.govNo license stated
HGNCCC0
iCiteCC BY 4.0
NCBI GenePublic domain (US government)
NIH RePORTER's grant and paper linksPublic domain
Open TargetsCC0 1.0
PMC's ID filePublic domain (US government)
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0

Each source's terms

ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
ClinicalTrials.govnone stated
HGNCCC0: https://www.genenames.org/about/license/
iCiteCC BY 4.0
NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this paper from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/papers/v1/7004875

GET https://conductscience.org/api/papers/v1/7004875/references?page=2

API reference For AI assistants