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FANCM
Regulation of DNA Cross-Link Repair by the Fanconi Anemia/BRCA Pathway
An Overview of DNA Repair Mechanisms in Plants Compared to Mammals
Bloom Syndrome Complex Promotes FANCM Recruitment to Stalled Replication Forks and Facilitates Both Repair and Traverse of DNA Interstrand Crosslinks
A Structure-Specific Nucleic Acid-Binding Domain Conserved Among DNA Repair Proteins
The Fanconi Anemia DNA Damage Repair Pathway in the Spotlight for Germline Predisposition to Colorectal Cancer
Biochemical Activities and Genetic Functions of the Drosophila Melanogaster Fancm Helicase in Dna Repair
Homologous Recombination Nonhomologous End Joining Interstrand Cross-Link Repair Nucleotide Excision Repair Mismatch Repair
AAA-Atpase FIDGETIN-LIKE 1 and Helicase FANCM Antagonize
Functional Comparison of XPF Missense Mutations Associated to Multiple DNA Repair Disorders
A Homozygous FANCM Mutation Underlies a Familial Case of Non-Syndromic Primary Ovarian Insufficiency
The FANCM-BLM-TOP3A-RMI Complex Suppresses Alternative Lengthening of Telomeres (ALT)
Alternative Functions for Human FANCM at Telomeres
Methylation of Breast Cancer Predisposition Genes in Early-Onset Breast Cancer: Australian Breast Cancer Family Registry
Chapter 1: the Fanconi Anemia DNA Repair Pathway
The Concerted Roles of FANCM and Rad52 in the Protection of Common Fragile Sites
Protein Degradation Pathways Regulate the Functions of Helicases in the DNA Damage Response and Maintenance of Genomic Stability
Biallelic Truncating FANCM Mutations Cause Early-Onset Cancer but Not Fanconi Anemia
PFKFB3 Inhibition Sensitizes DNA Crosslinking Chemotherapies by Suppressing Fanconi Anemia Repair
Top View
Individuals with FANCM Biallelic Mutations Do Not Develop Fanconi Anemia, but Show Risk for Breast Cancer, Chemotherapy Toxicity and May Display Chromosome Fragility
WRN Helicase Defective in the Premature Aging Disorder Werner Syndrome Genetically Interacts with Topoisomerase 3 and Restores the Top3 Slow Growth Phenotype of Sgs1 Top3
FANCM Limits ALT Activity by Restricting Telomeric Replication Stress Induced by Deregulated BLM and R-Loops
FANCM As an Anti-Cancer Target in Alternative Lengthening of Telomeres
Canonical and Noncanonical Roles of Fanconi Anemia Proteins: Implications in Cancer Predisposition
The FANC/BRCA Pathway Releases Replication Blockades by Eliminating DNA Interstrand Cross-Links
FANCM, BRCA1, and BLM Cooperatively Resolve the Replication Stress at the ALT Telomeres
Cytokinesis Failure Occurs in Fanconi Anemia Pathway–Deficient Murine and Human Bone Marrow Hematopoietic Cells
The Regulation of Homologous Recombination by Helicases
FANCM Regulates Repair Pathway Choice at Stalled Replication Forks
Defining the Molecular Interface That Connects the Fanconi Anemia Protein FANCM to the Bloom Syndrome Dissolvasome
FANCM-Family Branchpoint Translocases Remove Co-Transcriptional R-Loops
Functions and Regulation of the Multitasking FANCM Family of DNA Motor Proteins
Regulation of DNA Pairing in Homologous Recombination
Fanconi Anemia FANCM/FNCM-1 and FANCD2/FCD-2 Are Required For
LOSS of BLOOM SYNDROME PROTEIN CAUSES DESTABILIZATION of GENOMIC ARCHITECTURE and IS COMPLEMENTED by ECTOPIC EXPRESSION of Escherichia Coli Recg in HUMAN CELLS
Fanconi Anemia FANCM/FNCM-1 and FANCD2/FCD-2 Are Required for Maintaining
Natural Variation Identifies SNI1, the SMC5/6 Component, As a Modifier of Meiotic Crossover in Arabidopsis
Structure Analysis of FAAP24 Reveals Single-Stranded DNA-Binding Activity and Domain Functions in DNA Damage Response
Dna Damage RESPONSE Complexes to Sites of ICL Formation to Prevent Sister Chromatid Exchange
Crosstalk Between BRCA-Fanconi Anemia and Mismatch Repair Pathways Prevents MSH2-Dependent Aberrant DNA Damage Responses
Report 46628
Advances in Understanding the Complex Mechanisms of DNA Interstrand Cross-Link Repair
MHF1 Plays Fanconi Anaemia Complementation Group M Protein (FANCM)Dependent and Fancmindependent Roles in DNA Repair and Homolog
Role of FANCM in Telomere Maintenance in Alternative Lengthening of Telomeres (ALT)
A Genome-Wide Association Study for Hypertensive Kidney Disease in Korean Men
FANCJ Localization by Mismatch Repair Is Vital to Maintain Genomic Integrity After UV Irradiation
A Novel Function for FANCJ Helicase in Microsatellite Stabilization During Replication Stress
Chapter 2: Diagnosis of Fanconi Anemia: Testing and Genetic Counseling