Disease: Xeroderma pigmentosum
- <sup>1</sup>H, <sup>15</sup>N, <sup>13</sup>C resonance assignments for proteasome shuttle factor hHR23a
- <sup>1</sup>H, <sup>15</sup>N, <sup>13</sup>C resonance assignments for proteasome shuttle factor hHR23a
- 1H, 15N, 13C resonance assignments for proteasome shuttle factor hHR23a
- A clickable melphalan for monitoring DNA interstrand crosslink accumulation and detecting ICL repair defects in Fanconi anemia patient cells
- A Significant Increasing Risk Association between Cigarette Smoking and <em>XPA</em> and <em>XPC</em> Genes Polymorphisms
- Acceptability and influence of a complex personalized intervention on changes in photoprotection behaviours among people with xeroderma pigmentosum
- Alkylation of nucleobases by 2-chloro-<em>N,N</em>-diethylethanamine hydrochloride (CDEAH) sensitizes <em>PARP1</em>-deficient tumors
- APE1-dependent base excision repair of DNA photodimers in human cells
- Bilateral limbal stem cell deficiency with xeroderma pigmentosum in a young Asian child
- Brazilian XP-E siblings carrying a novel DDB2 variant developed early-onset melanoma: a case report
- Can Cemiplimab Become a Life-Changer in Xeroderma Pigmentosum?
- 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
- Codelivery of ERCC2 small interfering RNA and cisplatin with macrophage-derived mimetic nanovesicles for enhanced bladder cancer treatment
- 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
- Conjunctival "Melanoma-In-Situ''-A Rare Neoplasia of Xeroderma Pigmentosum in Indian Scenario
- 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
- Deep intronic founder mutations identified in the <em>ERCC4</em>/<em>XPF</em> gene are potential therapeutic targets for a high-frequency form of xeroderma pigmentosum
- Deep intronic founder mutations identified in the ERCC4/XPF gene are potential therapeutic targets for a high-frequency form of xeroderma pigmentosum
- Dissection of DNA damage and repair pathways in live cells by femtosecond laser microirradiation and free-electron modeling
- 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-related heritable photosensitivity syndromes: Mutation landscape in a multiethnic cohort of 17 multigenerational families with high degree of consanguinity
- Early-onset gynecological tumors in DNA repair-deficient xeroderma pigmentosum group C patients: a case series
- Effects of unburned tobacco smoke on inflammatory and oxidative mediators in the rat prefrontal cortex
- 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
- 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
- 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 predisposition to ocular surface disorders and opportunities for gene-based therapies
- Genetic variability of oxidative stress and DNA repair genes associated with pre-treatment cancer-related fatigue in women with breast cancer
- 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>
- Genomic alterations related to HPV infection status in a cohort of Chinese prostate cancer patients
- Genomic analysis of a Palestinian family with inherited cancer syndrome: a next-generation sequencing study
- 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
- Impression cytology of ocular surface in xeroderma pigmentosum
- Interpretation on genetic tumour syndromes in the 5th WHO classification of paediatric tumours: part Ⅱ
- Investigation of XPD, miR-145 and miR-770 expression in patients with end-stage renal disease
- 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
- Mutational signatures and increased retrotransposon insertions in xeroderma pigmentosum variant skin tumors
- 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
- Polymerase iota plays a key role during translesion synthesis of UV-induced lesions in the absence of polymerase eta
- Prevalence and clinical implications of germline pathogenic variants in cancer predisposing genes in young patients across sarcoma subtypes
- Relation between interleukin-6 concentrations and oxidative status of HIV infected patients with /or at risk of Kaposi disease in Yaounde
- 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
- Sarcomatoid Carcinoma of Orbit in a Patient With Xeroderma Pigmentosum
- 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
- Successful treatment of non-melanoma skin cancer in three patients with Xeroderma Pigmentosum by modified ALA-PDT
- 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 Curcumin Analog PAC Is a Potential Solution for the Treatment of Triple-Negative Breast Cancer by Modulating the Gene Expression of DNA Repair Pathways
- The French Cohort of DNA Repair-Deficient Xeroderma Pigmentosum Patients: Risk of Hematological Malignancies
- The Multifold Etiologies of Limbal Stem Cell Deficiency: A Comprehensive Review on the Etiologies and Additional Treatment Options for Limbal Stem Cell Deficiency
- The Over-Irradiation Metabolite Derivative, 24-Hydroxylumister-ol<sub>3</sub>, Reduces UV-Induced Damage in Skin
- The Role of TFIIH Complex in Nucleotide Excision Repair
- The role of Transcription Factor IIH complex in nucleotide excision repair
- The therapeutic dental challenge of xeroderma pigmentosum patients: case report
- 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
- 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 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
- XPA tumor variants lead 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