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Werner syndrome helicase
Structure and Function of the Human Recq DNA Helicases
Curriculum Vitae
Neurodegeneration in Accelerated Aging
Werner Syndrome Protein Participates in a Complex with RAD51, RAD54
Human DNA Repair Genes Relatively Late-Diverging, Major Eukaryotic Taxa Whose Exact Order of Radiation Is Difficult to Deter- Richard D
University of Cincinnati
The Werner Syndrome Protein Is Distinguished from the Bloom Syndrome Protein by Its Capacity to Tightly Bind Diverse DNA Structures
Crystal Structure of the Werner's Syndrome Helicase
Roles of the Werner Syndrome Recq Helicase in DNA Replication
1 Research Article 29 July 2015 Werner Syndrome Helicase
WRN-Mutated Colorectal Cancer Is Characterized by a Distinct Genetic Phenotype
A Study of Genomic Instability in Chronic Lymphocytic Leukaemia
Phd Thesis, University of Helsinki, Finland, 2008
Atrx Deficiency Induces Telomere Dysfunction, Endocrine Defects, and Reduced Life Span
Werner Syndrome Helicase Is a Selective Vulnerability Of
P53 Modulates RPA-Dependent and RPA-Independent WRN Helicase Activity
History of DNA Helicases
Werner Helicase Is a Synthetic-Lethal Vulnerability in Mismatch Repair–Deficient Colorectal Cancer Refractory to Targeted Therapies, Chemotherapy and Immunotherapy
Top View
Genomic Instability — an Evolving Hallmark of Cancer
WRN Protein and Werner Syndrome
The Werner Syndrome Gene Reviews the Werner Syndrome Gene the Molecular Basis of Recq Helicase- Deficiency Diseases
The Regulation of Homologous Recombination by Helicases
Exploiting DNA Damage Repair in Precision Cancer Therapy: BRCA1 As a Prime Therapeutic Target
WRN Helicase Is a Synthetic Lethal Target in Microsatellite Unstable Cancers
Werner Syndrome Helicase Has a Critical Role in DNA Damage Responses in the Absence of a Functional Fanconi Anemia Pathway
SWITCH-LIKE PHOSPHORYLATION of WRN INTEGRATES END-RESECTION with REPAIR of Dsbs at REPLICATION FORKS
WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects
Werner Syndrome Helicase Is a Selective Vulnerability Of
WRN) Function in the Cellular Response to DNA Damage Or Replication Stress
Camptothecin Targets WRN Protein: Mechanism and Relevance in Clinical Breast Cancer
WRN Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian Family
DNA Helicases and Human Disease
G-Quadruplexes and Helicases Oscar Mendoza, Anne Bourdoncle, Jean-Baptiste Boulé, Robert Brosh, Jean-Louis Mergny
Supplementary Figures and Tables
Unwinding the Molecular Basis of the Werner Syndrome
WRN Gene Werner Syndrome Recq Like Helicase
Prioritizing Synthetic Lethal Targets with Functional Genomics
Biochemistry of Human Recq DNA Helicases and Their Role in DNA Repair
Genomic Instability — an Evolving Hallmark of Cancer
Recent Findings on Werner's and Hutchinson-Gilford Progeria
The Werner Syndrome Protein Is Required for Recruitment of Chromatin Assembly Factor 1 Following DNA Damage
Elevated Telomere–Telomere Recombination in WRN-Deficient, Telomere Dysfunctional Cells Promotes Escape from Senescence and Engagement of the ALT Pathway
Trf2 Interacting Proteins and Telomere Maintenance
Telomere Biology and Human Phenotype
Myotonic Dystrophy—A Progeroid Disease?
The Werner Syndrome Helicase/Exonuclease Processes Mobile D-Loops Through Branch Migration and Degradation