|
JP2000166600A
|
|
Method for screening compound capable of inhibiting tumor growth
|
|
JP2000197483A
|
|
Method of inspecting disease due to mutation of recq dna helicase family gene
|
|
JPH11276173A
|
|
Gene encoding helicase, recq5
|
|
JPH10337183A
|
|
Human gene coding for helicase, cdc28-#46
|
|
JPH10327866A
|
|
Human gene, cdc28-#3 capable of coding helicase
|
|
JPH10260184A
|
|
Ligand detecting method for 7-time membrane penetration type orphan acceptor
|
|
JPH10248577A
|
|
Human-originated eternized b-lymphoblast-like cell line
|
|
JPH10201498A
|
|
Detection of mutation in pathogenic gene of human werner syndrome
|
|
JPH10146188A
|
|
Mouse gene corresponding to causative gene of human werner's syndrome and protein for which the gene codes
|
|
JPH1075789A
|
|
Killer protein
|
|
JPH09238683A
|
|
New ws-3 gene in region in which casual gene of werner's syndrome is present and protein for which the gene codes
|
|
JPH09206080A
|
|
New gene being in domain in which causative gene of werner syndrome exists, ws-2 and protein coded by the same gene
|
