Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Madhu, S.P."'
Autor:
Mahendra, M., Madhu, S.P., Doreswamy, B.H., Gopalakrishna, G.S., Sridhar, M.A., Prasad, J.Shashidhara, Ashamanjari, K.G.
Publikováno v:
In Materials Research Bulletin 2003 38(8):1309-1317
Autor:
Goplakrishna, G.S., Madhu, S.P., Mahendra, M., Doreswamy, B.H., Mahesh, M.J., Sridhar, M.A., Prasad, J. Shashidhara
Publikováno v:
In Materials Letters 2006 60(5):613-617
Autor:
Goplakrishna, G.S.1, Madhu, S.P.1, Mahendra, M.2, Doreswamy, B.H., Mahesh, M.J.1, Sridhar, M.A.2, Prasad, J. Shashidhara2 mas@physics.uni-mysore.ac.in
Publikováno v:
Materials Letters. Mar2006, Vol. 60 Issue 5, p613-617. 5p.
Autor:
Mahendra, M.1 mahendra@uomphysics.net, Madhu, S.P.2, Doreswamy, B.H.1, Gopalakrishna, G.S.2, Sridhar, M.A.1, Prasad, J. Shashidhara1, Ashamanjari, K.G.2
Publikováno v:
Materials Research Bulletin. Jul2003, Vol. 38 Issue 8, p1309. 9p.
Autor:
Knox Van Dyke, Madhu S.P. Manandhar
Publikováno v:
Analytical Biochemistry. 60:122-129
A novel method to purify and quantitate GTP is described. This method is simple to run and sensitive to detect GTP in picomole quantities. It is based on purfication and isolation of GTP on PEI-thin layer chromatograms and quantitation with the firef
Autor:
Madhu S.P. Manandhar, Knox Van Dyke
Publikováno v:
Microchemical Journal. 19:42-51
A discovery is reported of a new system that enables one to quantitate the amounts of separated nucleotide triphosphates in picomole quantities. This system of delayed luminescence analysis (DLA) is sensitive to both purine and pyrimidine ribose and
Autor:
Knox Van Dyke, Madhu S.P. Manandhar
Publikováno v:
Experimental parasitology. 37(2)
Purine utilization in the malarial parasite dependent on a “salvage” pathway was studied to determine the detailed mechanism of how purines were utilized and which precursor might be penetrating the membrane of the parasite. Erythrocyte-free mala
Autor:
Knox Van Dyke, Madhu S.P. Manandhar
Publikováno v:
Analytical biochemistry. 58(2)
The role and sources of adenosine tetraphosphate (AP 4 ) have not been extensively identified because its separation and quantitation necessitates analyses on a microscale. This article illustrates a method of separation and quantitation previously n
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