DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» Werner syndrome
Werner syndrome
Molecular Basis of Progeroid Syndromes–S–S– the Wwthe Erner Andanderner Hutchinson-Gilford Syndromes
Download PDF (1878K)
Werner and Hutchinson–Gilford Progeria Syndromes: Mechanistic Basis of Human Progeroid Diseases
Diabetes Mellitus Coexisted with Progeria: a Case Report of Atypical Werner Syndrome with Novel LMNA Mutations and Literature Review
Genes and Diseases
A Case of Werner's Syndrome L
Crystal Structure of the Werner's Syndrome Helicase
Roles of the Werner Syndrome Recq Helicase in DNA Replication
Boards Fodder Disorders of Dyschromia (Hypo- and Hyperpigmentation) by Parin Pearl Rimtepathip, MD, and Janna Mieko Vassantachart, MD
The Role of SMARCAD1 During Replication Stress Sarah Joseph
Werner Syndrome: Clinical Features, Pathogenesis and Potential Therapeutic Interventions
DNA Repair Disorders
Functional Analysis of POLD1 P.Ser605del Variant: the Aging Phenotype of MDPL Syndrome Is Associated with an Impaired DNA Repair Capacity
TEST CATALOGUE October 2020 ACHIEVING a POSITIVE CHANGE
Nijmegen Breakage Syndrome Disease Protein and MRE11 at PML Nuclear Bodies and Meiotic Telomeres1
Chromosome Instability Syndromes PRESENTER: Jude Abadie Slide 1
A Novel Splice-Site Mutation of WRN (C.IVS28+2T>C)
P53 Centrosomal Localization Diagnoses Ataxia-Telangiectasia
Top View
Epigenetic Signatures of Werner Syndrome Occur Early in Life and Are Distinct from Normal Epigenetic Aging Processes
Early Onset Werner Syndrome
Inherigen Plus Carrier Screen Disease List
Altered Nuclear Functions in Progeroid Syndromes: a Paradigm for Aging Research
Carrier Detection of Werner's Syndrome Using a Microsatellite That Exhibits Linkage Disequilibrium with the Werner's Syndrome Locus
Exome Sequencing Reveals a De Novo POLD1 Mutation Causing Phenotypic Variability in Mandibular Hypoplasia, Deafness, Progeroid F
Mismatch Repair in Extracts of Werner Syndrome Cell Lines
Hereditary Nonmelanoma Skin Cancer Vasiliki Nikolaou, MD,* Alexander J
The Werner Syndrome Protein Has Separable Recombination and Survival Functionsଝ
Mismatch Repair in Extracts of Werner Syndrome Cell Lines
WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects
Adermatoglyphia: Challenges and Prospects in Diagnosis
Review Werner's Syndrome: from Clinics to Genetics
Insights from Progeroid Syndromes Into Skin Cancer and Aging Brian C
Hallmarks of Progeroid Syndromes: Lessons from Mice and Reprogrammed Cells Dido Carrero, Clara Soria-Valles and Carlos López-Otıń*
WES Gene Package Multiple Congenital Anomalie
Bloom's Syndrome and the Ataxia-Telangiectasia- Mutated Protein, ATM
DNA Helicases and Human Disease