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M R Murthy

Showing results (71-80 of 82) with videos related to

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FEBS Letters|November 24, 1999
Thermodynamics of target peptide recognition by calmodulin and a calmodulin analogue: implications for the role of the central linkerA K Moorthy, B Gopal, P R Satish, et al.
Structure (London, England : 1993)|June 15, 1997
Triosephosphate isomerase from Plasmodium falciparum: the crystal structure provides insights into antimalarial drug designS S Velanker, S S Ray, R S Gokhale, et al.
Journal of Psychiatric Research|January 1, 1984
Biological markers in major psychosis and alcoholism: phenotypic and genotypic markersS Radouco-Thomas, F Garcin, M R Murthy, et al.
FEBS Letters|January 7, 1999
Induction of a spectroscopically defined transition by guanidinium hydrochloride on a recombinant calcium binding protein from Entamoeba histolyticaB Gopal, J V Krishna Rao, C J Thomas, et al.
The Journal of Biological Chemistry|January 5, 1986
The structure of rabbit muscle phosphoglucomutase at intermediate resolutionZ Lin, M Konno, C Abad-Zapatero, et al.
Journal of Molecular Biology|June 17, 1999
Three-dimensional structure of physalis mottle virus: implications for the viral assemblyS S Krishna, C N Hiremath, S K Munshi, et al.
Human Mutation|February 6, 1998
Dyslipidemias associated with heterozygous lipoprotein lipase mutations in the French-Canadian populationP Julien, C Gagné, M R Murthy, et al.
Protein Science : a Publication of the Protein Society|April 22, 1999
Disulfide engineering at the dimer interface of Lactobacillus casei thymidylate synthase: crystal structure of the T155C/E188C/C244T mutantS S Velanker, R S Gokhale, S S Ray, et al.
Human Biology|February 1, 1993
Genealogy and regional distribution of lipoprotein lipase deficiency in French-Canadians of QuebecC Dionne, C Gagné, P Julien, et al.
The Journal of Clinical Investigation|September 1, 1990
A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestriesM V Monsalve, H Henderson, G Roederer, et al.
Pageof 9

Showing results (71-80 of 82) with videos related to

Sort By:
Pageof 9
FEBS Letters|November 24, 1999
Thermodynamics of target peptide recognition by calmodulin and a calmodulin analogue: implications for the role of the central linkerA K Moorthy, B Gopal, P R Satish, et al.
Structure (London, England : 1993)|June 15, 1997
Triosephosphate isomerase from Plasmodium falciparum: the crystal structure provides insights into antimalarial drug designS S Velanker, S S Ray, R S Gokhale, et al.
Journal of Psychiatric Research|January 1, 1984
Biological markers in major psychosis and alcoholism: phenotypic and genotypic markersS Radouco-Thomas, F Garcin, M R Murthy, et al.
FEBS Letters|January 7, 1999
Induction of a spectroscopically defined transition by guanidinium hydrochloride on a recombinant calcium binding protein from Entamoeba histolyticaB Gopal, J V Krishna Rao, C J Thomas, et al.
The Journal of Biological Chemistry|January 5, 1986
The structure of rabbit muscle phosphoglucomutase at intermediate resolutionZ Lin, M Konno, C Abad-Zapatero, et al.
Journal of Molecular Biology|June 17, 1999
Three-dimensional structure of physalis mottle virus: implications for the viral assemblyS S Krishna, C N Hiremath, S K Munshi, et al.
Human Mutation|February 6, 1998
Dyslipidemias associated with heterozygous lipoprotein lipase mutations in the French-Canadian populationP Julien, C Gagné, M R Murthy, et al.
Protein Science : a Publication of the Protein Society|April 22, 1999
Disulfide engineering at the dimer interface of Lactobacillus casei thymidylate synthase: crystal structure of the T155C/E188C/C244T mutantS S Velanker, R S Gokhale, S S Ray, et al.
Human Biology|February 1, 1993
Genealogy and regional distribution of lipoprotein lipase deficiency in French-Canadians of QuebecC Dionne, C Gagné, P Julien, et al.
The Journal of Clinical Investigation|September 1, 1990
A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestriesM V Monsalve, H Henderson, G Roederer, et al.
Pageof 9