The fidelity of double strand breaks processing is impaired in complementation groups B and D of Fanconi anemia, a genetic instability syndrome

scientific article published on 01 November 1997

The fidelity of double strand breaks processing is impaired in complementation groups B and D of Fanconi anemia, a genetic instability syndrome is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1007/BF02673750
P698PubMed publication ID9661703

P2093author name stringM Escarceller
S Rousset
E Moustacchi
D Papadopoulo
P433issue6
P407language of work or nameEnglishQ1860
P921main subjectFanconi anemiaQ845779
P304page(s)401-411
P577publication date1997-11-01
P1433published inSomatic Cell and Molecular GeneticsQ7559232
P1476titleThe fidelity of double strand breaks processing is impaired in complementation groups B and D of Fanconi anemia, a genetic instability syndrome
P478volume23

Reverse relations

cites work (P2860)
Q52830252A DNA double strand break repair defect in Fanconi anemia fibroblasts.
Q35131190A Rad50-dependent pathway of DNA repair is deficient in Fanconi anemia fibroblasts
Q28252640Cellular and molecular consequences of defective Fanconi anemia proteins in replication-coupled DNA repair: mechanistic insights
Q35105914DNA double strand breaks (DSB) and non-homologous end joining (NHEJ) pathways in human leukemia
Q31742444Deficient DNA end joining activity in extracts from fanconi anemia fibroblasts
Q54525290Deficient Regulation of DNA Double-strand Break Repair in Fanconi Anemia Fibroblasts
Q39065431Double-strand break repair based on short-homology regions is suppressed under terminal deoxynucleotidyltransferase expression, as revealed by a novel vector system for analysing DNA repair by nonhomologous end joining
Q40922341Drug sensitivity spectra in Fanconi anemia lymphoblastoid cell lines of defined complementation groups
Q24678530Fanconi anaemia
Q30307206Fanconi anemia proteins localize to chromatin and the nuclear matrix in a DNA damage- and cell cycle-regulated manner
Q40501792Homozygous deletions of CDKN2A caused by alternative mechanisms in various human cancer cell lines.
Q34966793Impact of DNA ligase IV on the fidelity of end joining in human cells
Q52121550Molecular pathogenesis of fanconi anemia.
Q34134667Radiation-induced chromatid breaks and deficient DNA repair in cancer predisposition
Q57961762Relationship between chromosome fragility, aneuploidy and severity of the haematological disease in Fanconi anaemia
Q40584861The DNA crosslink-induced S-phase checkpoint depends on ATR-CHK1 and ATR-NBS1-FANCD2 pathways
Q28201371The Fanconi anaemia/BRCA pathway
Q33601052The contribution of homologous recombination in preserving genome integrity in mammalian cells

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