The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases
about
Effects of DNA repair gene polymorphisms on DNA damage in human lymphocytes induced by a vinyl chloride metabolite in vitroA yeast four-hybrid system identifies Cdk-activating kinase as a regulator of the XPD helicase, a subunit of transcription factor IIHDNA nucleotide excision repair-dependent signaling to checkpoint activationHuman Nbp35 is essential for both cytosolic iron-sulfur protein assembly and iron homeostasisSingle-gene disorders: what role could moonlighting enzymes play?Trans-4-hydroxy-2-nonenal inhibits nucleotide excision repair in human cells: a possible mechanism for lipid peroxidation-induced carcinogenesisXPD helicase structures and activities: insights into the cancer and aging phenotypes from XPD mutationsThe BRCA1-associated protein BACH1 is a DNA helicase targeted by clinically relevant inactivating mutationsTrichothiodystrophy: a systematic review of 112 published cases characterises a wide spectrum of clinical manifestationsNucleotide Excision Repair, Genome Stability, and Human Disease: New Insight from Model SystemsFunctional characterization of polymorphisms in DNA repair genes using cytogenetic challenge assaysXRCC1 and XPD genetic polymorphisms, smoking and breast cancer risk in a Finnish case-control studyNucleotide Excision Repair and Vitamin D--Relevance for Skin Cancer TherapyAdaptive stress response in segmental progeria resembles long-lived dwarfism and calorie restriction in miceDrosophila Xpd regulates Cdk7 localization, mitotic kinase activity, spindle dynamics, and chromosome segregationStructure of the DNA Repair Helicase XPDCrystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPDTfb5 interacts with Tfb2 and facilitates nucleotide excision repair in yeastPlasmodium falciparum XPD translocates in 5' to 3' direction, is expressed throughout the blood stages, and interacts with p44A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group AComprehensive molecular characterization of urothelial bladder carcinomaPolymorphisms in XPD (Asp312Asn and Lys751Gln) genes, sunburn and arsenic-related skin lesionsReal-time quantification of Xeroderma pigmentosum mRNA from the mammalian cochlea.Collaborative dynamic DNA scanning by nucleotide excision repair proteins investigated by single- molecule imaging of quantum-dot-labeled proteins.Ordered conformational changes in damaged DNA induced by nucleotide excision repair factors.The DNA repair genes XPB and XPD defend cells from retroviral infectionPersistence of repair proteins at unrepaired DNA damage distinguishes diseases with ERCC2 (XPD) mutations: cancer-prone xeroderma pigmentosum vs. non-cancer-prone trichothiodystrophy.The 8,5'-cyclopurine-2'-deoxynucleosides: candidate neurodegenerative DNA lesions in xeroderma pigmentosum, and unique probes of transcription and nucleotide excision repair.Both XPD alleles contribute to the phenotype of compound heterozygote xeroderma pigmentosum patients.Phosphorylation of steroidogenic factor 1 is mediated by cyclin-dependent kinase 7Polymorphisms of DNA repair genes OGG1 and XPD and the risk of age-related cataract in Egyptians.Clinical utility gene card for: Xeroderma pigmentosum.Dysregulation of the peroxisome proliferator-activated receptor target genes by XPD mutationsTranscription inhibition by DRB potentiates recombinational repair of UV lesions in mammalian cells.Premature aging and cancer in nucleotide excision repair-disorders.Nucleotide excision repair in Trypanosoma brucei: specialization of transcription-coupled repair due to multigenic transcriptionThe evolution of controlled multitasked gene networks: the role of introns and other noncoding RNAs in the development of complex organisms.Potentially functional polymorphisms in the ERCC2 gene and risk of esophageal squamous cell carcinoma in Chinese populations.On the traces of XPD: cell cycle matters - untangling the genotype-phenotype relationship of XPD mutationsXPB and XPD helicases in TFIIH orchestrate DNA duplex opening and damage verification to coordinate repair with transcription and cell cycle via CAK kinase.
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P2860
The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases
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2001 nî lūn-bûn
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2001 թուականի Յունուարին հրատարակուած գիտական յօդուած
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2001 թվականի հունվարին հրատարակված գիտական հոդված
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2001年の論文
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2001年論文
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2001年論文
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2001年論文
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2001年論文
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2001年論文
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2001年论文
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The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases
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The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases
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The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases
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The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases
@ast
The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases
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The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases
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The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases
@ast
The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases
@en
The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases
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P3181
P356
P1433
P1476
The xeroderma pigmentosum group D (XPD) gene: one gene, two functions, three diseases
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P2093
A R Lehmann
P3181
P356
10.1101/GAD.859501
P407
P577
2001-01-01T00:00:00Z