|1.||Yowell, C A: 1 article (12/2001)|
|2.||Muller, R: 1 article (12/2001)|
|3.||Cawley, S E: 1 article (12/2001)|
|4.||Sturrock, K A: 1 article (12/2001)|
|5.||Mulder, N: 1 article (12/2001)|
|6.||Fluegge, M R: 1 article (12/2001)|
|7.||Galinski, M R: 1 article (12/2001)|
|8.||Carlton, J M: 1 article (12/2001)|
|9.||Dame, J B: 1 article (12/2001)|
|10.||Barnwell, J W: 1 article (12/2001)|
12/01/2001 - "A total of 5482 genome survey sequences (GSSs) and 5582 ESTs were generated from mung bean nuclease (MBN) and cDNA libraries, respectively, of the ANKA line of the rodent malaria parasite Plasmodium berghei, and 10,874 GSSs generated from MBN libraries of the Salvador I and Belem lines of Plasmodium vivax, the most geographically wide-spread human malaria pathogen. "
08/10/1984 - "Mung bean nuclease was found to cut the genomic DNA of the malaria parasite Plasmodium at positions before and after genes but not within gene-coding regions. "
06/01/1994 - "A clone expressing the 3' end of the RESA gene of the Palo Alto isolate of Plasmodium falciparum was isolated by screening a lambda expression library of Mung bean nuclease-digested genomic DNA fragments with antibodies from malaria patients. "
01/01/1993 - "Treatment with protease and nucleases revealed that each tubule consists of three layers: (i) an outer coat of protease-sensitive material; (ii) an intermediate layer that is digested by DNase and mung bean nuclease, and (iii) inner protease-resistant protein scrapie-associated fibril."
01/01/1991 - "Treatment by three proteolytic enzymes and subsequent treatment with DNase and mung bean nuclease of grids prepared from the infected animals confirmed previous observations that the tubulofilamentous particles observed in scrapie-effected brains are complex structures. "
09/01/1993 - "A broad DNA region directly 3' to the essential consensus is required and is easily unwound as indicated by: (i) hypersensitivity to nicking of an approximately 100-bp region by mung bean nuclease in a negatively supercoiled plasmid and (ii) helical instability determined by thermodynamic analysis of the nucleotide sequence. "
|1.||DNA (Deoxyribonucleic Acid)
|4.||Peptide Hydrolases (Proteases)