Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group G patients.
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Influence of XPB helicase on recruitment and redistribution of nucleotide excision repair proteins at sites of UV-induced DNA damageCell-autonomous progeroid changes in conditional mouse models for repair endonuclease XPG deficiencyA novel homozygous ERCC5 truncating mutation in a family with prenatal arthrogryposis--further evidence of genotype-phenotype correlationAssociation between the ERCC5 Asp1104His polymorphism and cancer risk: a meta-analysis.Chromosomal protein HMGN1 enhances the rate of DNA repair in chromatinThe cerebro-morphological fingerprint of a progeroid syndrome: white matter changes correlate with neurological symptoms in xeroderma pigmentosumCyclosporin A inhibits nucleotide excision repair via downregulation of the xeroderma pigmentosum group A and G proteins, which is mediated by calcineurin inhibition.Comparison of DNA damage responses following equimutagenic doses of UVA and UVB: a less effective cell cycle arrest with UVA may render UVA-induced pyrimidine dimers more mutagenic than UVB-induced ones.Deficiency in the nuclease activity of xeroderma pigmentosum G in mice leads to hypersensitivity to UV irradiation.Polymorphisms in the ERCC5 gene and risk of esophageal squamous cell carcinoma (ESCC) in Eastern Chinese populations.Epigenetic silencing of the human nucleotide excision repair gene, hHR23B, in interleukin-6-responsive multiple myeloma KAS-6/1 cells.UV-induced histone H2AX phosphorylation and DNA damage related proteins accumulate and persist in nucleotide excision repair-deficient XP-B cellsOxidative DNA damage and nucleotide excision repair.Non-catalytic Roles for XPG with BRCA1 and BRCA2 in Homologous Recombination and Genome StabilityThe Role of XPG in Processing (CAG)n/(CTG)n DNA HairpinsThe DNA repair endonuclease XPG interacts directly and functionally with the WRN helicase defective in Werner syndromeForty years of research on xeroderma pigmentosum at the US National Institutes of Health.Genotype-phenotype correlation of xeroderma pigmentosum in a Chinese Han population.Diagnosis of Xeroderma Pigmentosum and Related DNA Repair-Deficient Cutaneous DiseasesCancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repair.Polymorphisms of XPG/ERCC5 and risk of squamous cell carcinoma of the head and neck.Shining a light on xeroderma pigmentosum.Xeroderma pigmentosum complementation group G patient with a novel homozygous missense mutation and no neurological abnormalities.DNA repair capacity of zebrafish.Expansion of the genotypic and phenotypic spectrum of xeroderma pigmentosum in Chinese population.Expression of XPG protein in human normal and tumor tissues.Syndromes with genetic instability: model diseases for (skin) cancerogenesis.The involvement of DNA-damage and -repair defects in neurological dysfunctionLessons learned from DNA repair defective syndromes.Xeroderma pigmentosum-variant patients from America, Europe, and Asia.Strict sun protection results in minimal skin changes in a patient with xeroderma pigmentosum and a novel c.2009delG mutation in XPD (ERCC2).XPC initiation codon mutation in xeroderma pigmentosum patients with and without neurological symptomsXPG: its products and biological roles.Definition of a short region of XPG necessary for TFIIH interaction and stable recruitment to sites of UV damage.Xeroderma pigmentosum-Cockayne syndrome complex.Radiation therapy for high-risk squamous cell carcinomas in patients with xeroderma pigmentosum: report of two cases and review of the literature.Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients.XPG genetic polymorphisms and clinical outcome of patients with advanced non-small cell lung cancer under platinum-based treatment: a meta-analysis of 12 studies.Novel XPG (ERCC5) mutations affect DNA repair and cell survival after ultraviolet but not oxidative stress.Novel germline ERCC5 mutations identified in a xeroderma pigmentosum complementation group G pedigree.
P2860
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P2860
Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group G patients.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh
2002年學術文章
@zh-hant
name
Relationship of neurologic deg ...... pigmentosum group G patients.
@en
type
label
Relationship of neurologic deg ...... pigmentosum group G patients.
@en
prefLabel
Relationship of neurologic deg ...... pigmentosum group G patients.
@en
P2093
P1476
Relationship of neurologic deg ...... a pigmentosum group G patients
@en
P2093
Bari B Cunningham
Bassam Abu-Libdeh
David B Busch
Donna Coleman
Hanoch Slor
Hiroki Inui
James E Cleaver
Jill Crollick
John J DiGiovanna
Lawrence Grossman
P304
P356
10.1046/J.1523-1747.2002.01782.X
P407
P577
2002-06-01T00:00:00Z
P5875
P6179
1024053552