The human XPC DNA repair gene: arrangement, splice site information content and influence of a single nucleotide polymorphism in a splice acceptor site on alternative splicing and function.
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Establishment of papillomavirus infection is enhanced by promyelocytic leukemia protein (PML) expressionGenetic variation in nucleotide excision repair pathway genes influence prostate and bladder cancer susceptibility in North Indian populationHost nucleotide polymorphism in hepatitis B virus-associated hepatocellular carcinomaChimeric negative regulation of p14ARF and TBX1 by a t(9;22) translocation associated with melanoma, deafness, and DNA repair deficiencyEthnicity and cutaneous melanoma in the city of Sao Paulo, Brazil: a case-control studyPolymorphisms in XPC, XPD, XRCC1, and XRCC3 DNA repair genes and lung cancer risk in a population of northern SpainRed meat and poultry intake, polymorphisms in the nucleotide excision repair and mismatch repair pathways and colorectal cancer risk.Matrix metalloproteinase-2 polymorphisms and clinical outcome of Chinese patients with nonsmall cell lung cancer treated with first-line, platinum-based chemotherapy.RICTOR polymorphisms affect efficiency of platinum-based chemotherapy in Chinese non-small-cell lung cancer patients.XPC branch-point sequence mutations disrupt U2 snRNP binding, resulting in abnormal pre-mRNA splicing in xeroderma pigmentosum patients.A functional analysis of G23A polymorphism and the alternative splicing in the expression of the XPA gene.The genotype of the transporter associated with antigen processing gene affects susceptibility to colorectal cancer in Japanese.Association between the BRCA2 rs144848 polymorphism and cancer susceptibility: a meta-analysis.Functional characterization of NIPBL physiological splice variants and eight splicing mutations in patients with Cornelia de Lange syndromeCyclosporin A inhibits nucleotide excision repair via downregulation of the xeroderma pigmentosum group A and G proteins, which is mediated by calcineurin inhibition.Deletion of XPC leads to lung tumors in mice and is associated with early events in human lung carcinogenesis.Overcoming transcription activator-like effector (TALE) DNA binding domain sensitivity to cytosine methylation.Computational comparative analyses of alternative splicing regulation using full-length cDNA of various eukaryotes.Xeroderma pigmentosum group C in an isolated region of Guatemala.DNA Repair Gene Polymorphisms in the Nucleotide Excision Repair Pathway and Lung Cancer Risk: A Meta-analysis.Association of XPC gene polymorphisms with susceptibility to prostate cancer: evidence from 3,936 subjects.Interpretation of mRNA splicing mutations in genetic disease: review of the literature and guidelines for information-theoretical analysis.XPC Lys939Gln polymorphism contributes to colorectal cancer susceptibility: evidence from a meta-analysis.A brief review of molecular information theory.Shining a light on xeroderma pigmentosum.Modulation of DNA damage/DNA repair capacity by XPC polymorphismsThe polyAT, intronic IVS11-6 and Lys939Gln XPC polymorphisms are not associated with transitional cell carcinoma of the bladderXeroderma pigmentosum complementation group C genotypes/diplotypes play no independent or interaction role with polycyclic aromatic hydrocarbons-DNA adducts for breast cancer risk.GTF2E2 Mutations Destabilize the General Transcription Factor Complex TFIIE in Individuals with DNA Repair-Proficient TrichothiodystrophyXeroderma pigmentosum-variant patients from America, Europe, and Asia.XPC Lys939Gln polymorphism, smoking and risk of sporadic colorectal cancer among MalaysiansAbnormal XPD-induced nuclear receptor transactivation in DNA repair disorders: trichothiodystrophy and xeroderma pigmentosum.Influence of DNA damage and repair upon the risk of treatment related leukemia.XPC initiation codon mutation in xeroderma pigmentosum patients with and without neurological symptomsPolymorphisms in the XPC gene and gastric cancer susceptibility in a Southern Chinese populationRepair of UV photolesions in xeroderma pigmentosum group C cells induced by translational readthrough of premature termination codons.IFIT1 polymorphisms predict interferon-α treatment efficiency for hepatitis B virus infection.Molecular regulation of UV-induced DNA repair.Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients.XPC intron11 C/A polymorphism as a risk factor for prostate cancer.
P2860
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P2860
The human XPC DNA repair gene: arrangement, splice site information content and influence of a single nucleotide polymorphism in a splice acceptor site on alternative splicing and function.
description
2002 nî lūn-bûn
@nan
2002 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
The human XPC DNA repair gene: ...... rnative splicing and function.
@ast
The human XPC DNA repair gene: ...... rnative splicing and function.
@en
The human XPC DNA repair gene: ...... rnative splicing and function.
@nl
type
label
The human XPC DNA repair gene: ...... rnative splicing and function.
@ast
The human XPC DNA repair gene: ...... rnative splicing and function.
@en
The human XPC DNA repair gene: ...... rnative splicing and function.
@nl
prefLabel
The human XPC DNA repair gene: ...... rnative splicing and function.
@ast
The human XPC DNA repair gene: ...... rnative splicing and function.
@en
The human XPC DNA repair gene: ...... rnative splicing and function.
@nl
P2093
P2860
P356
P1476
The human XPC DNA repair gene: ...... rnative splicing and function.
@en
P2093
Carl C Baker
Hiroki Inui
Kenneth H Kraemer
Sikandar G Khan
Steffen Emmert
Takahiro Ueda
Tala Shahlavi
Thomas D Schneider
Vanessa Muniz-Medina
P2860
P304
P356
10.1093/NAR/GKF469
P407
P577
2002-08-01T00:00:00Z