Pages that link to "Q35849094"

The following pages link to Evidence for subcomplexes in the Fanconi anemia pathway (Q35849094):

Displaying 49 items.

• UBE2T, the Fanconi anemia core complex, and FANCD2 are recruited independently to chromatin: a basis for the regulation of FANCD2 monoubiquitination (Q24297826) (← links)
• FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway (Q24301340) (← links)
• FAAP20: a novel ubiquitin-binding FA nuclear core-complex protein required for functional integrity of the FA-BRCA DNA repair pathway (Q24305406) (← links)
• Defective mitochondrial peroxiredoxin-3 results in sensitivity to oxidative stress in Fanconi anemia (Q24308795) (← links)
• Mechanistic insight into site-restricted monoubiquitination of FANCD2 by Ube2t, FANCL, and FANCI (Q24311413) (← links)
• Fanconi anemia complementation group A (FANCA) protein has intrinsic affinity for nucleic acids with preference for single-stranded forms (Q24631719) (← links)
• How the fanconi anemia pathway guards the genome (Q24634556) (← links)
• The Fanconi anemia pathway and DNA interstrand cross-link repair (Q26851561) (← links)
• Insights into Fanconi Anaemia from the structure of human FANCE (Q27643858) (← links)
• Overexpression of Rad51C splice variants in colorectal tumors (Q28256773) (← links)
• The role of the Fanconi anemia network in the response to DNA replication stress (Q33347783) (← links)
• The genetic and biochemical basis of FANCD2 monoubiquitination (Q33735561) (← links)
• Small molecule amiloride modulates oncogenic RNA alternative splicing to devitalize human cancer cells (Q33939096) (← links)
• Coregulation of FANCA and BRCA1 in human cells (Q34084861) (← links)
• Cytoplasmic FANCA-FANCC complex interacts and stabilizes the cytoplasm-dislocalized leukemic nucleophosmin protein (NPMc) (Q34333634) (← links)
• A protein prioritization approach tailored for the FA/BRCA pathway (Q34689369) (← links)
• Damage-dependent regulation of MUS81-EME1 by Fanconi anemia complementation group A protein. (Q35028557) (← links)
• Defective FANCI binding by a fanconi anemia-related FANCD2 mutant (Q35502827) (← links)
• Human FAN1 promotes strand incision in 5'-flapped DNA complexed with RPA. (Q35617226) (← links)
• FANCI Regulates Recruitment of the FA Core Complex at Sites of DNA Damage Independently of FANCD2 (Q35796778) (← links)
• Diagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger Sequencing (Q36072260) (← links)
• FANCD2, FANCJ and BRCA2 cooperate to promote replication fork recovery independently of the Fanconi Anemia core complex (Q36187965) (← links)
• Fancb deficiency impairs hematopoietic stem cell function (Q36364040) (← links)
• Cell cycle-dependent chromatin loading of the Fanconi anemia core complex by FANCM/FAAP24. (Q36658074) (← links)
• Fanconi anemia proteins, DNA interstrand crosslink repair pathways, and cancer therapy (Q37069628) (← links)
• RAD51D- and FANCG-dependent base substitution mutagenesis at the ATP1A1 locus in mammalian cells (Q37218373) (← links)
• Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M. (Q37262472) (← links)
• Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group. (Q37384036) (← links)
• Elucidation of the Fanconi Anemia Protein Network in Meiosis and Its Function in the Regulation of Histone Modifications (Q37393820) (← links)
• Bloom syndrome complex promotes FANCM recruitment to stalled replication forks and facilitates both repair and traverse of DNA interstrand crosslinks (Q37516257) (← links)
• Maintenance of genome stability by Fanconi anemia proteins (Q37658498) (← links)
• Stress and DNA repair biology of the Fanconi anemia pathway (Q38252562) (← links)
• Biomarkers and mechanisms of FANCD2 function (Q38287129) (← links)
• What is the DNA repair defect underlying Fanconi anemia? (Q38619026) (← links)
• RNA interferences targeting the Fanconi anemia/BRCA pathway upstream genes reverse cisplatin resistance in drug-resistant lung cancer cells (Q38834205) (← links)
• Abundance of the Fanconi anaemia core complex is regulated by the RuvBL1 and RuvBL2 AAA+ ATPases (Q38937471) (← links)
• FANCD2 but not FANCA promotes cellular resistance to type II topoisomerase poisons (Q39574588) (← links)
• Regulated degradation of FANCM in the Fanconi anemia pathway during mitosis (Q39875666) (← links)
• Polymorphic variations in the FANCA gene in high-risk non-BRCA1/2 breast cancer individuals from the French Canadian population. (Q41133980) (← links)
• Modularized functions of the Fanconi anemia core complex (Q41915735) (← links)
• Towards a molecular understanding of the fanconi anemia core complex (Q42182034) (← links)
• FancJ regulates interstrand crosslinker induced centrosome amplification through the activation of polo-like kinase 1. (Q42681613) (← links)
• Several tetratricopeptide repeat (TPR) motifs of FANCG are required for assembly of the BRCA2/D1-D2-G-X3 complex, FANCD2 monoubiquitylation and phleomycin resistance (Q42733515) (← links)
• Cytokine overproduction and crosslinker hypersensitivity are unlinked in Fanconi anemia macrophages (Q46660348) (← links)
• Mutations in Fanconi anemia genes and the risk of esophageal cancer (Q47857337) (← links)
• Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M. (Q51629652) (← links)
• Fanconi anemia (Q83572053) (← links)
• Association of clinical severity with FANCB variant type in Fanconi anemia (Q89919498) (← links)
• The Fanconi Anemia Pathway in Cancer (Q92433763) (← links)