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J Robins

Showing results (301-310 of 587) with videos related to

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Anti-Cancer Drug Design|July 20, 2000
Synthesis of new homochiral bispyrrolidines as potential DNA cross-linking antitumour agentsF M Anderson, C C O'Hare, J A Hartley, et al.
The American Journal of Physiology|December 1, 1989
Response of serum triglycerides of endogenous origin to the administration of triglyceride-rich lipid particlesS J Robins, J M Fasulo, V F Robins, et al.
The Journal of Organic Chemistry|October 9, 2007
Deoxygenative [1,2]-hydride shift rearrangements in nucleoside and sugar chemistry: analogy with the [1,2]-electron shift in the deoxygenation of ribonucleotides by ribonucleotide reductasesMorris J Robins, Ireneusz Nowak, Stanislaw F Wnuk, et al.
Journal of Lipid Research|June 1, 1991
Utilization of different fatty acids for hepatic and biliary phosphatidylcholine formation and the effect of changes in phosphatidylcholine molecular species on biliary lipid secretionS J Robins, J M Fasulo, V F Robins, et al.
Natural Product Reports|February 17, 2012
Biochemical and physiological determinants of intramolecular isotope patterns in sucrose from C₃, C₄ and CAM plants accessed by isotopic ¹³C NMR spectrometry: a viewpointAlexis Gilbert, Virginie Silvestre, Richard J Robins, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 1, 1972
Plasma amino acid abnormalities in chronic renal failureA J Robins, B K Milewczyk, E M Booth, et al.
Journal of Lipid Research|October 1, 1985
Cholesterol exchange and synthesis in the live ratS J Robins, J M Fasulo, M A Collins, et al.
Chemosphere|February 3, 2020
Intramolecular isotope effects during permanganate oxidation and acid hydrolysis of methyl tert-butyl etherMaxime Julien, Didier Gori, Patrick Höhener, et al.
Biochemistry|April 7, 1987
2'-Deoxy-2'-halonucleotides as alternate substrates and mechanism-based inactivators of Lactobacillus leichmannii ribonucleotide reductaseG Harris, G W Ashley, M J Robins, et al.
Biochemical and Biophysical Research Communications|May 29, 1987
The 2',3'-dideoxyriboside of 2,6-diaminopurine and its 2',3'-didehydro derivative inhibit the deamination of 2',3'-dideoxyadenosine, an inhibitor of human immunodeficiency virus (HIV) replicationJ Balzarini, M J Robins, R M Zou, et al.
Pageof 59

Showing results (301-310 of 587) with videos related to

Sort By:
Pageof 59
Anti-Cancer Drug Design|July 20, 2000
Synthesis of new homochiral bispyrrolidines as potential DNA cross-linking antitumour agentsF M Anderson, C C O'Hare, J A Hartley, et al.
The American Journal of Physiology|December 1, 1989
Response of serum triglycerides of endogenous origin to the administration of triglyceride-rich lipid particlesS J Robins, J M Fasulo, V F Robins, et al.
The Journal of Organic Chemistry|October 9, 2007
Deoxygenative [1,2]-hydride shift rearrangements in nucleoside and sugar chemistry: analogy with the [1,2]-electron shift in the deoxygenation of ribonucleotides by ribonucleotide reductasesMorris J Robins, Ireneusz Nowak, Stanislaw F Wnuk, et al.
Journal of Lipid Research|June 1, 1991
Utilization of different fatty acids for hepatic and biliary phosphatidylcholine formation and the effect of changes in phosphatidylcholine molecular species on biliary lipid secretionS J Robins, J M Fasulo, V F Robins, et al.
Natural Product Reports|February 17, 2012
Biochemical and physiological determinants of intramolecular isotope patterns in sucrose from C₃, C₄ and CAM plants accessed by isotopic ¹³C NMR spectrometry: a viewpointAlexis Gilbert, Virginie Silvestre, Richard J Robins, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 1, 1972
Plasma amino acid abnormalities in chronic renal failureA J Robins, B K Milewczyk, E M Booth, et al.
Journal of Lipid Research|October 1, 1985
Cholesterol exchange and synthesis in the live ratS J Robins, J M Fasulo, M A Collins, et al.
Chemosphere|February 3, 2020
Intramolecular isotope effects during permanganate oxidation and acid hydrolysis of methyl tert-butyl etherMaxime Julien, Didier Gori, Patrick Höhener, et al.
Biochemistry|April 7, 1987
2'-Deoxy-2'-halonucleotides as alternate substrates and mechanism-based inactivators of Lactobacillus leichmannii ribonucleotide reductaseG Harris, G W Ashley, M J Robins, et al.
Biochemical and Biophysical Research Communications|May 29, 1987
The 2',3'-dideoxyriboside of 2,6-diaminopurine and its 2',3'-didehydro derivative inhibit the deamination of 2',3'-dideoxyadenosine, an inhibitor of human immunodeficiency virus (HIV) replicationJ Balzarini, M J Robins, R M Zou, et al.
Pageof 59