To investigate whether catalytic topoisomerase II activity by ICRF187, a compound that interferes with the catalytic cycle of topoisomerase II without causing DNA damage, could result in a modulation of X-ray-induced chromosomal damage in Werner's syndrome (WS) cell lines.4n
WRN is a RecQ helicase with an associated exonuclease activity important in DNA metabolism, includin...
Topoisomerase 2α (Topo2α) is an essential protein with DNA decatenating enzymatic properties, indisp...
Werner syndrome (WS) protein is involved in DNA repair and its truncation causes Werner syndrome, an...
To investigate whether catalytic topoisomerase II activity by ICRF187, a compound that interferes wi...
L'articolo è disponibile sul sito dell'editore: http://www.taylorandfrancisgroup.comPURPOSE: To inve...
Werner's syndrome (WS) is a recessive human genetic disorder associated with an elevated incidence o...
Werner's syndrome (WS) is a rare autosomal recessive human disorder and the patients exhibit many sy...
L'articolo é disponibile sul sito dell'editore: http://www.sciencedirect.comWerner's syndrome (WS) i...
L'articolo é disponibile sul sito dell'editore: http://www.sciencedirect.comWerner's syndrome (WS) i...
ICRF-187 (Cardioxane™, Chiron) is a catalytic inhibitor of DNA topoisomerase II (Topo II), proposed ...
Werner's syndrome (WS) is a rare autosomal recessive disorder that arises as a consequence of mutati...
Werner's syndrome (WS) is a rare autosomal recessive disorder that arises as a consequence of mutati...
WRN is a RecQ helicase with an associated exonuclease activity important in DNA metabolism, includin...
Topoisomerase 2α (Topo2α) is an essential protein with DNA decatenating enzymatic properties, indisp...
Werner syndrome (WS) protein is involved in DNA repair and its truncation causes Werner syndrome, an...
To investigate whether catalytic topoisomerase II activity by ICRF187, a compound that interferes wi...
L'articolo è disponibile sul sito dell'editore: http://www.taylorandfrancisgroup.comPURPOSE: To inve...
Werner's syndrome (WS) is a recessive human genetic disorder associated with an elevated incidence o...
Werner's syndrome (WS) is a rare autosomal recessive human disorder and the patients exhibit many sy...
L'articolo é disponibile sul sito dell'editore: http://www.sciencedirect.comWerner's syndrome (WS) i...
L'articolo é disponibile sul sito dell'editore: http://www.sciencedirect.comWerner's syndrome (WS) i...
ICRF-187 (Cardioxane™, Chiron) is a catalytic inhibitor of DNA topoisomerase II (Topo II), proposed ...
Werner's syndrome (WS) is a rare autosomal recessive disorder that arises as a consequence of mutati...
Werner's syndrome (WS) is a rare autosomal recessive disorder that arises as a consequence of mutati...
WRN is a RecQ helicase with an associated exonuclease activity important in DNA metabolism, includin...
Topoisomerase 2α (Topo2α) is an essential protein with DNA decatenating enzymatic properties, indisp...
Werner syndrome (WS) protein is involved in DNA repair and its truncation causes Werner syndrome, an...