• ¹H, ¹⁵N, ¹³C resonance assignments for proteasome shuttle factor hHR23a
• ¹H, ¹⁵N, ¹³C resonance assignments for proteasome shuttle factor hHR23a
• "Immunopeeling" Using Imiquimod for Xeroderma Pigmentosum
• 1H, 15N, 13C resonance assignments for proteasome shuttle factor hHR23a
• A case of xeroderma pigmentosum group C with rare compound heterozygous mutations
• A novel algorithm for the virtual screening of extensive small molecule libraries against ERCC1/XPF protein-protein interaction for the identification of resistance-bypassing potential anticancer molecules
• Adult-Onset Neuropsychiatric Symptoms as the Presenting Feature of Xeroderma Pigmentosum Group G: A Report of a Rare Case
• APE1-dependent base excision repair of DNA photodimers in human cells
• Case report: Xeroderma pigmentosum Group A with erythropoietic protoporphyria in a young Chinese patient
• Cell cycle arrest combined with CDK1 inhibition suppresses genome-wide mutations by activating alternative DNA repair genes during genome editing
• Characterisation of a novel missense mutation in the <em>ERCC5</em> gene leading to group G xeroderma pigmentosum/Cockayne syndrome overlap
• Characterisation of a novel missense mutation in the ERCC5 gene leading to group G xeroderma pigmentosum/Cockayne syndrome overlap
• Clinical prognostic significance of xeroderma pigmentosum group C and IFN-gamma in non-small cell lung cancer
• Cockayne Syndrome
• Community perspectives on the magnitude of Xeroderma pigmentosum and care-seeking practices in Micheweni district, Pemba: a mixed-methods cross-sectional study
• Complex Genomic Rearrangement Patterns in Malignant Pleural Mesothelioma due to Environmental Asbestos Exposure
• Cross-species investigation into the requirement of XPA for nucleotide excision repair
• Cutaneous angiosarcoma of the scalp in a pediatric patient with xeroderma pigmentosum
• De Sanctis-Cacchione Syndrome with Subdural Effusion: A Rare Case from India with Review of Literature
• Dermoscopy and In Vivo Confocal Microscopy Findings of Basal Cell Carcinomas in Xeroderma Pigmentosum Patients
• Development and evaluation of a personalised psychological intervention to improve adherence to photoprotection in adults with Xeroderma Pigmentosum (XP)
• Diffuse large B-cell lymphoma with cutaneous involvement in a patient with xeroderma pigmentosum type C
• Diseases with oral malignant potential: Need for change to inform research, policy, and practice
• DMC-siERCC2 hybrid nanoparticle enhances TRAIL sensitivity by inducing cell cycle arrest for glioblastoma treatment
• DNA repair ability in a patient with voriconazole-related squamous cell carcinoma that required differential diagnosis from xeroderma pigmentosum
• DNA Repair Genetics and the Risk of Radiation Pneumonitis in Patients With Lung Cancer: A Systematic Review and Meta-analysis
• DNA repair-related heritable photosensitivity syndromes: Mutation landscape in a multiethnic cohort of 17 multigenerational families with high degree of consanguinity
• Does the XPA-FEN1 Interaction Concern to Nucleotide Excision Repair or Beyond?
• Effects of unburned tobacco smoke on inflammatory and oxidative mediators in the rat prefrontal cortex
• ERCC2 mutations alter the genomic distribution pattern of somatic mutations and are independently prognostic in bladder cancer
• Evaluation of Meibomian gland dysfunction using meibography in patients with xeroderma pigmentosum
• Evaluation of the effectiveness and safety of combined oral and topical photoprotection with a standardized extract of Polypodium leucotomos (Fernblock) in a Moroccan population with xeroderma pigmentosum
• Evidence for persistent UV-induced DNA damage and altered DNA damage response in xeroderma pigmentosa patient corneas
• Evidence for the involvement of keratinocyte-derived microvesicle particles in the photosensitivity associated with xeroderma pigmentosum type A deficiency
• Expanding the phenotype of GTF2E2-associated trichothiodystrophy
• Familial Melanoma Phenotype With Xeroderma Pigmentosum Group C (XP-C) Genotype - The Putative Role of MC1R Polymorphism as Modifier
• Faulty Gap Filling in Nucleotide Excision Repair Leads to Double-Strand Break Formation in Senescent Cells
• Gemcitabine and cisplatin plus nivolumab as organ-sparing treatment for muscle-invasive bladder cancer: a phase 2 trial
• Generation of site-specifically labelled fluorescent human XPA to investigate DNA binding dynamics during nucleotide excision repair
• Genetic Polymorphisms of XPC, XPD, XPG Genes and their Association with Radiotherapy Induced Toxicity among Head and Neck Cancer Patients: A Hospital Based Study from Maharashtra
• Genetic Variants Associated With Response to Platinum-Based Chemotherapy in Non-Small Cell Lung Cancer Patients: A Field Synopsis and Meta-Analysis
• Genome-wide analysis of transcription-coupled repair reveals novel transcription events in <em>Caenorhabditis elegans</em>
• Genome-wide analysis of transcription-coupled repair reveals novel transcription events in Caenorhabditis elegans
• Genomic analysis of a Palestinian family with inherited cancer syndrome: a next-generation sequencing study
• Genomic patterns of somatic mutations provide new prognostic, therapeutic, and biological insights in cancer
• Genomic Tumor Correlates of Clinical Outcomes Following Organ-Sparing Chemoradiation Therapy for Bladder Cancer
• Germline mutational variants of Turkish ovarian cancer patients suspected of Hereditary Breast and Ovarian Cancer (HBOC) by next-generation sequencing
• High-Grade Sinonasal Small Cell Neuroendocrine Carcinoma in a Patient With Xeroderma Pigmentosum: A Case Report
• High-risk human papillomavirus-associated corneal/conjunctival intraepithelial neoplasia in a young patient
• Homozygous substitution of threonine 191 by proline in polymerase eta causes Xeroderma pigmentosum variant
• Homozygous substitution of threonine 191 by proline in polymerase η causes Xeroderma pigmentosum variant
• Impaired B-cell function in <em>ERCC2</em> deficiency
• Impression cytology of ocular surface in xeroderma pigmentosum
• Insights from multi-omic modeling of neurodegeneration in xeroderma pigmentosum using an induced pluripotent stem cell system
• Interpretation on genetic tumour syndromes in the 5th WHO classification of paediatric tumours: part Ⅱ
• Investigation of Polymorphisms in Global Genome Repair Genes in Patients With Ovarian Cancer in the Turkish Population
• Mechanisms of cancer cell death induction by triptolide: A comprehensive overview
• Molecular wrench activity of DNA helicases: Keys to modulation of rapid kinetics in DNA repair
• Multiple Facial Basal Cell Carcinoma With Xeroderma Pigmentosum
• Natural small-molecules reverse Xeroderma Pigmentosum Complementation Group C (XPC) deficient-mediated drug-resistance in renal cell carcinoma
• Neurological disease in xeroderma pigmentosum: prospective cohort study of its features and progression
• Noise Stress Abrogates Structure-Specific Endonucleases within the Mammalian Inner Ear
• Nucleotide excision repair deficiency is a targetable therapeutic vulnerability in clear cell renal cell carcinoma
• Oral mucosa involvement in pediatric patients with xeroderma pigmentosum: a comprehensive review
• p53 regulates diverse tissue-specific outcomes to endogenous DNA damage in mice
• PERIOCULAR HIGH RISK BCCS AFTER ADDITIONAL/PARALLEL INTAKE OF TORASEMIDE, MOXONIDINE AND MIRABEGRON: IMPORTANT LINKS TO SKIN CANCER RELATED (PHOTO-) NITROSOGENESIS IN THE CONTEXT OF PHARMACO-ONCOGENESIS
• Persistent TFIIH binding to non-excised DNA damage causes cell and developmental failure
• Photocarcinogenesis of Voriconazole Unraveled: A Likeness to Xeroderma Pigmentosum Is Key
• Photosensitivity
• Physical, oral, and swallowing functions of three patients with type a xeroderma pigmentosum: a report of three cases
• Pigmented skin lesions
• Polymerase iota plays a key role during translesion synthesis of UV-induced lesions in the absence of polymerase eta
• Protein-protein interactions in the core nucleotide excision repair pathway
• Proteome characterization of XPC-deficient melanocytes generated by CRISPR-Cas9 technology reveals alteration in the expression of several hundred proteins
• Relationship between <em>XPA</em>, <em>XPB/ERCC3</em>, <em>XPF/ERCC4</em>, and <em>XPG/ERCC5</em> Polymorphisms and the Susceptibility to Head and Neck Carcinoma: A Systematic Review, Meta-Analysis, and Tria
• Retrospective study of efficacy and adverse events of immune checkpoint inhibitors in 22 xeroderma pigmentosum patients with metastatic or unresectable cancers
• Revealing the UV response of melanocytes in xeroderma pigmentosum group A using patient-derived induced pluripotent stem cells
• Sequential post-translational modifications regulate damaged DNA-binding protein DDB2 function
• Skin cancer induction by the antimycotic drug voriconazole is caused by impaired DNA damage detection due to chromatin compaction
• Small Molecule Antagonists of the DNA Repair ERCC1/XPA Protein-Protein Interaction
• SNP Array Screening and Long Range PCR-Based Targeted Next Generation Sequencing for Autosomal Recessive Disease with Consanguinity: Insight from a Case of Xeroderma Pigmentosum Group C
• Subungual mass in a patient of xeroderma pigmentosum: Looking beyond malignant transformation
• TFIIH central activity in nucleotide excision repair to prevent disease
• The accurate bypass of pyrimidine dimers by DNA polymerase eta contributes to ultraviolet-induced mutagenesis
• The association between XPD rs13181 and rs1799793 polymorphism and oral cancer risk: evidence from a meta-analysis
• The Expression of PRAME as an Aid for Diagnosis and Evaluation of Histologic Margins of Intraepidermal Cutaneous Melanoma in Xeroderma Pigmentosum Patients
• The XRCC1 and TP53 gene polymorphisms are associated with advanced-stage disease and early distant metastasis at diagnosis in non-small cell lung cancer
• Translating patient needs into medical device development: co-design of a photoprotection visor for Xeroderma Pigmentosum using qualitative interviews
• Two siblings with Fanconi anemia (FANCQ, ERCC4/XPF) presenting with tumor-mimicking lesions in the brain and acute neurological deterioration
• Variability of DNA Repair and Oxidative Stress Genes Associated with Worst Pain in Breast Cancer Survivors on Aromatase Inhibitors
• Xeroderma Pigmentosum
• Xeroderma pigmentosum group G with pellagroid rash: A rare presentation
• Xeroderma Pigmentosum with a Rapidly Proliferating Squamous Cell Carcinoma in a 4-Year Old Kid: A Rare Entity in Indian Subcontinent
• Xeroderma Pigmentosum With Ocular Surface Squamous Neoplasia: A Case Report
• Xeroderma Pigmentosum: Novel Prophylactic and Therapeutic Approaches. Part III: Now More than Just a Therapeutic Challenge
• Xeroderma Pigmentosum: Novel Prophylactic and Therapeutic Approaches. Part One: Topical Zinc Sulfate 25% and Heat Dermabrasion plus Topical Trichloroacetic Acid
• Xeroderma Pigmentosum: Part Two: Treatment of Skin Tumors with Topical Podophyllin 25% in Benzoin
• XPA tumor variant leads to defects in NER that sensitize cells to cisplatin
• XPC Protects against Carcinogen-Induced Histologic Progression to Lung Squamous Cell Carcinoma by Reduced Basal Epithelial Cell Proliferation
• XRCC1 and XPD polymorphisms: clinical outcomes and risk of prostate cancer in Bangladeshi population