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FANCA
Structure and Function of the Human Recq DNA Helicases
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Fanconi Anemia, Bloom Syndrome and Breast Cancer
MECHANISMS in ENDOCRINOLOGY: Novel Genetic Causes of Short Stature
Epigenetic Regulation of DNA Repair Genes and Implications for Tumor Therapy ⁎ ⁎ Markus Christmann , Bernd Kaina
Posttranslational Regulation of the Fanconi Anemia Cancer Susceptibility Pathway
Deletion and Reduced Expression of the Fanconi Anemia FANCA Gene in Sporadic Acute Myeloid Leukemia
Evolutionary Genomics of Human Intellectual Disability Bernard Crespi,1 Kyle Summers2 and Steve Dorus3
Overexpression of the Fanconi Anemia a Gene in Hela and MCF10A Cells
Distinct Roles of BRCA2 in Replication Fork Protection in Response to Hydroxyurea and DNA Interstrand Cross-Links
Fanca Deficiency Reduces A/T Transitions in Somatic Hypermutation and Alters Class Switch Recombination Junctions in Mouse B Cells
Supplemental Table 1: Snps Genotyped for NCO, Listed Alphabetically by Gene Name
Spectrum of Mutations in the Fanconi Anaemia Group G Gene, FANCG/XRCC9
MSH2 Loss in Primary Prostate Cancer
The Fanconi Anemia DNA Damage Repair Pathway in the Spotlight for Germline Predisposition to Colorectal Cancer
Functional Comparison of XPF Missense Mutations Associated to Multiple DNA Repair Disorders
Pathogenic Mutations Identified by a Multimodality Approach in 117 Japanese Fanconi Anemia Patients
Chapter 1: Diagnosis and Evaluation
Top View
Cytogenetic and Molecular Diagnosis of Fanconi Anemia Revealed Two Hidden Phenotypes
Gene Therapy Clinical Trial for Fanconi Anemia Type a (FA-A) Additional Faqs for PATIENT DISCUSSIONS
HSP90 Inhibition Sensitizes Head and Neck Cancer to Platin-Based
1 Werner Syndrome Helicase Has a Critical Role in Dna
Characterization and Genotype-Phenotype Correlation of Patients with Fanconi Anemia in a Multi-Ethnic Population
FANCA Gene FA Complementation Group A
A Comprehensive Custom Panel Design for Routine Hereditary Cancer Testing
Canonical and Noncanonical Roles of Fanconi Anemia Proteins: Implications in Cancer Predisposition
History of DNA Helicases
Msh2 Depletion Mitigates Chromosomal Instability in Fancd2-Deficient Cells
Targeting Fanconi Anemia/BRCA2 Pathway Defects in Cancer: Thesignificanceofpreclinicalpharmacogenomicmodels Eike Gallmeier and Scott E
Investigation of FANCA Mutations in Greek Patients
Proteomic Analysis Reveals a FANCA-Modulated Neddylation Pathway Involved in CXCR5 Membrane Targeting and Cell Mobility
Fanconi Anemia Gene Sequencing Panel
Carboxy Terminal Region of the Fanconi Anemia Protein, FANCG/XRCC9, Is Required for Functional Activity
A Physical Complex of the Fanconi Anemia Proteins FANCG/XRCC9
Germline Mutations in DNA Repair Genes Predispose Asbestos-Exposed Patients to Malignant Pleural Mesothelioma
1 Germline Rare Deleterious Variant Load Alters Cancer Risk, Age of Onset
Defining the Molecular Interface That Connects the Fanconi Anemia Protein FANCM to the Bloom Syndrome Dissolvasome
Werner Syndrome Helicase Has a Critical Role in DNA Damage Responses in the Absence of a Functional Fanconi Anemia Pathway
Targeted Genes and Methodology Details for Hereditary Oncology Custom Gene Panel
Early Colorectal Cancers Provide New Evidence for a Lynch Syndrome-To-CMMRD Phenotypic Continuum
Exome Sequencing of Familial High-Grade Serous Ovarian Carcinoma Reveals Heterogeneity for Rare Candidate Susceptibility Genes
FANCA (H-300): Sc-28215
Genetics in Biomarkers for Prostate and Bladder Cancer
Gene Therapy for Fanconi Anemia: One Step Closer to the Clinic
Generating New FANCA-Deficient HNSCC Cell Lines by Genomic
Bloom's Syndrome and the Ataxia-Telangiectasia- Mutated Protein, ATM
Validation of Fanconi Anemia Complementation Group a Assignment Using Molecular Analysis Nabil N
Loss of the Homologous Recombination Gene Rad51 Leads To
Non-BRCA DNA Damage Repair Gene Alterations and Response To
Lasting DNA Damage and Aberrant DNA Repair Gene Expression Profile Are Associated with Post-Chronic Cadmium Exposure in Human Br
Fanconi Anemia: Guidelines for Diagnosis and Management, Fourth
MSH2 Loss in Primary Prostate Cancer Liana B
Crosstalk Between BRCA-Fanconi Anemia and Mismatch Repair Pathways Prevents MSH2-Dependent Aberrant DNA Damage Responses
FANCA Polymorphism Is Associated with the Rate of Proliferation in Uterine Leiomyoma in Korea
High Frequency of the V548A Fs X572 XPC Mutation in Tunisia: Implication for Molecular Diagnosis
Patient-Level DNA Damage and Repair Pathway Profiles and Prognosis After Prostatectomy for High-Risk Prostate Cancer
Differential Expression of DNA Repair Genes in Prognostically-Favorable
Rare Variants in FANCA Induce Premature Ovarian Insufficiency
Comprehensive Profiling of DNA Repair Defects in Breast Cancer Identifies a Novel Class of Endocrine Therapy Resistance Drivers
Modelling Fanconi Anemia Pathogenesis and Therapeutics Using Integration-Free Patient-Derived Ipscs
A Genetic Map of the Response to DNA Damage in Human Cells
A Novel Function for FANCJ Helicase in Microsatellite Stabilization During Replication Stress
Getting Ready for the Dance: FANCJ Irons out DNA Wrinkles
Fanca–/– Hematopoietic Stem Cells Demonstrate a Mobilization Defect Which Can Be Overcome by Administration of the Rac Inhibitor NSC23766
A Multiprotein Nuclear Complex Connects Fanconi Anemia and Bloom Syndrome Amom Ruhikanta Meetei,1 Salvatore Sechi,2† Michael Wallisch,3 Dafeng Yang,1 Mary K
Fanca Maintains Genomic Stability Through Regulating Bubr1