(Q33792430)

English

A comprehensive haplotype analysis of the XPC genomic sequence reveals a cluster of genetic variants associated with sensitivity to tobacco-smoke mutagens

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scholarly article

1 reference

Europe PubMed Central

29 July 2017

A comprehensive haplotype analysis of the XPC genomic sequence reveals a cluster of genetic variants associated with sensitivity to tobacco-smoke mutagens (English)

1 reference

Europe PubMed Central

29 July 2017

author name string

Catherine M Rondelli

1

1 reference

Europe PubMed Central

29 July 2017

Randa A El-Zein

2

1 reference

Europe PubMed Central

29 July 2017

Jeffrey K Wickliffe

3

1 reference

Europe PubMed Central

29 July 2017

Carol J Etzel

4

1 reference

Europe PubMed Central

29 July 2017

Sherif Z Abdel-Rahman

5

1 reference

Europe PubMed Central

29 July 2017

publication date

27 January 2010

1 reference

Europe PubMed Central

29 July 2017

Toxicological Sciences

1 reference

Europe PubMed Central

29 July 2017

115

1 reference

Europe PubMed Central

29 July 2017

1

1 reference

Europe PubMed Central

29 July 2017

41-50

1 reference

Europe PubMed Central

29 July 2017

Applications of computational algorithm tools to identify functional SNPs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

28 July 2018

Modulation of DNA damage/DNA repair capacity by XPC polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

28 July 2018

Nucleotide excision repair pathway genes and oral premalignant lesions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

28 July 2018

Disease-associated intronic variants in the ErbB4 gene are related to altered ErbB4 splice-variant expression in the brain in schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

28 July 2018

Biochemical and structural domain analysis of xeroderma pigmentosum complementation group C protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

28 July 2018

Nucleotide excision repair genotype and the incidence of endometrial cancer: effect of other risk factors on the association

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

28 July 2018

XRCC3 and XPD/ERCC2 single nucleotide polymorphisms and the risk of cancer: a HuGE review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

28 July 2018

The protein shuffle. Sequential interactions among components of the human nucleotide excision repair pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

28 July 2018

Molecular epidemiology of non-small cell lung cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

28 July 2018

Effect of VKORC1 haplotypes on transcriptional regulation and warfarin dose

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

28 July 2018

The structure of haplotype blocks in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

28 July 2018

How nucleotide excision repair protects against cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

28 July 2018

Centrosome protein centrin 2/caltractin 1 is part of the xeroderma pigmentosum group C complex that initiates global genome nucleotide excision repair

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

28 July 2018

Chromosomal aberrations in lymphocytes predict human cancer: a report from the European Study Group on Cytogenetic Biomarkers and Health (ESCH).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

28 July 2018

Cancer risk in humans predicted by increased levels of chromosomal aberrations in lymphocytes: Nordic study group on the health risk of chromosome damage

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

28 July 2018

Mutagen sensitivity as a biological marker of lung cancer risk in African Americans.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

28 July 2018

Mutagen sensitivity: a biological marker of cancer susceptibility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

28 July 2018

Human peripheral blood lymphocytes for the analysis of chromosome aberrations in mutagen tests

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

28 July 2018

On the use of phylogeny-based tests to detect association between quantitative traits and haplotypes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

30 October 2018

Single nucleotide polymorphisms 5' upstream the coding region of the NEIL2 gene influence gene transcription levels and alter levels of genetic damage

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

30 October 2018

Polymorphisms of the DNA repair gene xeroderma pigmentosum groups A and C and risk of esophageal squamous cell carcinoma in a population of high incidence region of North China

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

30 October 2018

XPA A23G, XPC Lys939Gln, XPD Lys751Gln and XPD Asp312Asn polymorphisms, interactions with smoking, alcohol and dietary factors, and risk of colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

30 October 2018

Comprehensive analysis of 22 XPC polymorphisms and bladder cancer risk.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

30 October 2018

Genotypes, haplotypes and diplotypes of XPC and risk of bladder cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

30 October 2018

Association of Vitamin K epoxide reductase complex 1 (VKORC1) variants with warfarin dose in a Hong Kong Chinese patient population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

30 October 2018

Use of biomarkers to characterize functions of polymorphic DNA repair genotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

30 October 2018

Effect of XPD/ERCC2 polymorphisms on chromosome aberration frequencies in smokers and on sensitivity to the mutagenic tobacco-specific nitrosamine NNK.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

30 October 2018

Smoking, DNA repair capacity and risk of nonsmall cell lung cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

30 October 2018

A simple correction for multiple comparisons in interval mapping genome scans.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

30 October 2018

Chromosomal aberrations in lymphocytes predict human cancer independently of exposure to carcinogens. European Study Group on Cytogenetic Biomarkers and Health.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

30 October 2018

Are chromosome aberrations in circulating lymphocytes predictive of future cancer onset in humans? Preliminary results of an Italian cohort study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855352

30 October 2018

The 399Gln polymorphism in the DNA repair gene XRCC1 modulates the genotoxic response induced in human lymphocytes by the tobacco-specific nitrosamine NNK

1 reference

https://pubmed.ncbi.nlm.nih.gov/20106949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotype tagging for the identification of common disease genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/20106949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An International System for Human Cytogenetic Nomenclature (1985) ISCN 1985. Report of the Standing Committee on Human Cytogenetic Nomenclature

1 reference

https://pubmed.ncbi.nlm.nih.gov/20106949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tobacco smoking

1 reference

https://pubmed.ncbi.nlm.nih.gov/20106949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reduced DNA repair capacity in head and neck cancer patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/20106949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms in the DNA nucleotide excision repair genes and lung cancer risk in Xuan Wei, China

1 reference

https://pubmed.ncbi.nlm.nih.gov/20106949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[The effect of gene polymorphism in promoter and intron 1 on human ApoA I expression]

1 reference

https://pubmed.ncbi.nlm.nih.gov/20106949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Potentially functional single nucleotide polymorphisms in the core nucleotide excision repair genes and risk of squamous cell carcinoma of the head and neck

1 reference

https://pubmed.ncbi.nlm.nih.gov/20106949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional significance of the TLR4/11367 polymorphism identified in Chinese Han population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20106949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of polymorphic CYP2E1 and CYP2D6 genes in NNK-induced chromosome aberrations in cultured human lymphocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/20106949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/TOXSCI/KFQ027

1 reference

Europe PubMed Central

29 July 2017

1 reference

Europe PubMed Central

29 July 2017

1 reference

Europe PubMed Central

29 July 2017

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