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ERCC4
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Identification of Novel Pathogenic MSH2 Mutation and New DNA Repair Genes Variants: Investigation of a Tunisian Lynch Syndrome F
Fanconi Anemia, Bloom Syndrome and Breast Cancer
An ERCC4 Regulatory Variant Predicts Grade‐
Challenges in Reporting Pathogenic/Potentially
Gene Expression Responses to DNA Damage Are Altered in Human Aging and in Werner Syndrome
Predisposition to Hematologic Malignancies in Patients With
Patients Resistant Against PSMA-Targeting Α-Radiation Therapy Often Harbor Mutations in DNA Damage-Repair–Associated Genes
Bloom Syndrome Complex Promotes FANCM Recruitment to Stalled Replication Forks and Facilitates Both Repair and Traverse of DNA Interstrand Crosslinks
DNA Repair Pathway Profiling and Microsatellite Instability in Colorectal Cancer Jinshengyu,1, 6 Mary A
XPF Expression Correlates with Clinical Outcome in Squamous Cell Carcinoma of the Head and Neck
Functional Comparison of XPF Missense Mutations Associated to Multiple DNA Repair Disorders
And Other Nucleotide Excision Repair Polymorphisms in Individual Susceptibility to Well-Differentiated Thyroid Cancer
Nucleotide Excision Repair Is a Predictor of Early Relapse in Pediatric Acute Lymphoblastic Leukemia Omar M
Germline and Somatic DNA Damage Repair Gene Mutations and Overall Survival in Metastatic Pancreatic Adenocarcinoma Patients Trea
A Gene Expression Signature to Predict Nucleotide Excision Repair Defects and Novel Therapeutic Approaches
Cockayne Syndrome Group B (CSB): the Regulatory Framework Governing the Multifunctional Protein and Its Plausible Role in Cancer
Obesity and Genetic Polymorphism of ERCC2 and ERCC4 As Modifiers of Risk of Breast Cancer
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Role for Nucleotide-Excision Repair Gene Variants in Oxaliplatin-Induced Peripheral Neuropathy
Cancer Susceptibility Mutations in Patients with Urothelial Malignancies the Following Represents Disclosure Information Provided by Authors of This Manuscript
Genetic Variation in the Nucleotide Excision Repair Pathway and Bladder Cancer Risk
Genomic Instability — an Evolving Hallmark of Cancer
Multilocus Inherited Neoplasia Alleles Syndrome: a Case Series and Review
Interplay Between DNA Damage Repair and Apoptosis Shapes Cancer Evolution Through Aneuploidy and Microsatellite Instability ✉ ✉ Noam Auslander1 , Yuri I
Defining the Molecular Interface That Connects the Fanconi Anemia Protein FANCM to the Bloom Syndrome Dissolvasome
Formation of a Ternary Complex by Human XPA, ERCC1
Early Colorectal Cancers Provide New Evidence for a Lynch Syndrome-To-CMMRD Phenotypic Continuum
The Role of DNA Helicases and Their Interaction Partners in Genome Stability and Meiotic Recombination in Plants
Function and Interactions of ERCC1-XPF in DNA Damage Response
Hallmarks of Progeroid Syndromes: Lessons from Mice and Reprogrammed Cells Dido Carrero, Clara Soria-Valles and Carlos López-Otıń*
Genetics of Radiation-Related Cancer
Prevalence and Clinical Implications of Germline Predisposition Gene
Protective Mechanisms Against DNA Replication Stress in the Nervous System
Germline DNA Sequencing Reveals Novel Mutations Predictive of Overall Survival in a Cohort of Patients with Pancreatic Cancer Jennifer B
Investigation of DNA Repair Gene Expression and Protein Function in Human Oocytes and Preimplantation Embryos
Neurodegeneration As the Presenting Symptom in 2 Adults with Xeroderma Pigmentosum Complementation Group F
Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia
Gene ERCC4 (DNA Repi/Cl Ne UV41/Excdnuclease/Genefic Compemenaon/UV Rance) LARRY H
Structure Analysis of FAAP24 Reveals Single-Stranded DNA-Binding Activity and Domain Functions in DNA Damage Response
Retrovirus-Mediated Gene Transfer Corrects DNA Repair Defect of Xeroderma Pigmentosum Cells of Complementation Groups A, B and C
Patient-Level DNA Damage and Repair Pathway Profiles and Prognosis After Prostatectomy for High-Risk Prostate Cancer
Genomic Instability — an Evolving Hallmark of Cancer
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Comprehensive Profiling of DNA Repair Defects in Breast Cancer Identifies a Novel Class of Endocrine Therapy Resistance Drivers
Myotonic Dystrophy—A Progeroid Disease?
A Novel Function for FANCJ Helicase in Microsatellite Stabilization During Replication Stress
Genetic Variation in the Nucleotide Excision Repair Pathway and Bladder Cancer Risk
Malfunction of Nuclease ERCC1-XPF Results in Diverse Clinical Manifestations and Causes Cockayne Syndrome, Xeroderma Pigmentosum, and Fanconi Anemia
Associations of Individual and Joint Expressions of ERCC6 and ERCC8 with Clinicopathological Parameters and Prognosis of Gastric Cancer