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F E Hruska

Showing results (1-10 of 21) with videos related to

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Journal of the American Chemical Society|April 7, 1971
Molecular conformation of orotidine, a naturally occurring nucleoside, in the syn conformation in aqueous solutionF E Hruska
Biochimica Et Biophysica Acta|June 20, 1979
Proton magnetic resonance studies of 5,6-saturated thymidine derivatives produced by ionizing radiation. Conformational analysis of 6-hydroxylated diastereoisomersJ Cadet, R Ducolomb, F E Hruska
Biochimica Et Biophysica Acta|January 3, 1977
Effect of temperature and protonation upon the conformation of 2'-o-methyladenosine. Correlation of conformational parameters in purine nucleosidesF E Hruska, D J Wood, H Singh
Biopolymers|May 1, 1985
Crystal structure of the cis-syn photodimer of thymidylyl (3'-5') thymidine cyanoethyl esterJ Cadet, L Voituriez, F E Hruska, et al.
Journal of the American Chemical Society|August 25, 1971
A correlation of some structural parameters of pyrimidine nucleosides. A nuclear magnetic resonance studyF E Hruska, A A Smith, J G Dalton
Journal of the American Chemical Society|April 7, 1971
A model for the molecular conformation of alpha-pseudouridine from nuclear magnetic resonance dataA A Grey, I C Smith, F E Hruska
Journal of the American Chemical Society|January 14, 1970
Conformational analysis of a minor nucleoside from nuclear magnetic resonance data. PseudouridineF E Hruska, A A Grey, I C Smith
Biochemical and Biophysical Research Communications|October 1, 1971
Phase transitions in sphingomyelin thin filsm. A spin label studyR A Long, F E Hruska, H D Gesser
Journal of the American Chemical Society|July 1, 1970
A nuclear magnetic resonance study of the molecular conformation of beta-pseudouridine in aqueous solutionF E Hruska, A A Grey, I C Smith
FEBS Letters|October 15, 1973
1H, 1H-(31P), 31P, and 31P-(1H) fast Fourier transform NMR study of the solution conformation of the cofactors involved in glycogen synthesis: adenosinediphosphoglucose and uridinediphosphoglucoseR H Sarma, C H Lee, F E Hruska, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Journal of the American Chemical Society|April 7, 1971
Molecular conformation of orotidine, a naturally occurring nucleoside, in the syn conformation in aqueous solutionF E Hruska
Biochimica Et Biophysica Acta|June 20, 1979
Proton magnetic resonance studies of 5,6-saturated thymidine derivatives produced by ionizing radiation. Conformational analysis of 6-hydroxylated diastereoisomersJ Cadet, R Ducolomb, F E Hruska
Biochimica Et Biophysica Acta|January 3, 1977
Effect of temperature and protonation upon the conformation of 2'-o-methyladenosine. Correlation of conformational parameters in purine nucleosidesF E Hruska, D J Wood, H Singh
Biopolymers|May 1, 1985
Crystal structure of the cis-syn photodimer of thymidylyl (3'-5') thymidine cyanoethyl esterJ Cadet, L Voituriez, F E Hruska, et al.
Journal of the American Chemical Society|August 25, 1971
A correlation of some structural parameters of pyrimidine nucleosides. A nuclear magnetic resonance studyF E Hruska, A A Smith, J G Dalton
Journal of the American Chemical Society|April 7, 1971
A model for the molecular conformation of alpha-pseudouridine from nuclear magnetic resonance dataA A Grey, I C Smith, F E Hruska
Journal of the American Chemical Society|January 14, 1970
Conformational analysis of a minor nucleoside from nuclear magnetic resonance data. PseudouridineF E Hruska, A A Grey, I C Smith
Biochemical and Biophysical Research Communications|October 1, 1971
Phase transitions in sphingomyelin thin filsm. A spin label studyR A Long, F E Hruska, H D Gesser
Journal of the American Chemical Society|July 1, 1970
A nuclear magnetic resonance study of the molecular conformation of beta-pseudouridine in aqueous solutionF E Hruska, A A Grey, I C Smith
FEBS Letters|October 15, 1973
1H, 1H-(31P), 31P, and 31P-(1H) fast Fourier transform NMR study of the solution conformation of the cofactors involved in glycogen synthesis: adenosinediphosphoglucose and uridinediphosphoglucoseR H Sarma, C H Lee, F E Hruska, et al.
Pageof 3