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PUBMED FOR HANDHELDS

Journal Abstract Search


107 related items for PubMed ID: 5357026

  • 1. The stereochemistry of hydrogen elimination at C-7,C-22 and C-23 during the conversion of cholesterol (cholest-5-en-3 beta-ol) into cholesta-5,7,22-trien-3 beta-ol by Tetrahymena pyriformis.
    Bimpson T, Goad LJ, Goodwin TW.
    Biochem J; 1969 Dec; 115(4):857-8. PubMed ID: 5357026
    [No Abstract] [Full Text] [Related]

  • 2. The stereochemistry of hydrogen elimination during 7,8-double bond formation by Tetrahymena pyriformis.
    Wilton DC, Akhtar M.
    Biochem J; 1970 Feb; 116(3):337-9. PubMed ID: 5435681
    [Abstract] [Full Text] [Related]

  • 3. The conversion of cholesterol to delta-5,7,22-cholestatrien-3-beta-ol by Tetrahymena pyriformis.
    Conner RL, Mallory FB, Landrey JR, Iyengar CW.
    J Biol Chem; 1969 May 10; 244(9):2325-33. PubMed ID: 5783836
    [No Abstract] [Full Text] [Related]

  • 4. Sterol synthesis: studies of the metabolism of 14 alpha-methyl-5 alpha-cholest-7-en-3 beta-ol.
    Chan JT, Spike TE, Trowbridge ST, Schroepfer GJ.
    J Lipid Res; 1979 Nov 10; 20(8):1007-19. PubMed ID: 533823
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  • 5. The stereochemistry of hydrogen elimination in the biological conversion of 5 alpha-cholest-8-en-3 beta-ol to 5 alpha-cholest-7-en-3 beta-ol.
    Canonica L, Fiecchi A, Galli Kienle M, Scala A.
    Steroids; 1968 Jun 10; 11(6):749-53. PubMed ID: 5671483
    [No Abstract] [Full Text] [Related]

  • 6. 5 Alpha-cholest-8(14)-en-3 beta-ol, a possible intermediate in the biosynthesis of cholesterol. Enzymatic conversion to cholesterol and isolation from rat skin.
    Lee WH, Lutsky BN, chropfer GJ.
    J Biol Chem; 1969 Oct 25; 244(20):5440-8. PubMed ID: 5348596
    [No Abstract] [Full Text] [Related]

  • 7. Mode of formulation of cholesta-5,7-dien-3beta-ol from Cholest-5-en-3beta-ol by Larvae of Calliphora erythrocephala.
    Johnson P, Cook IF, Rees HH, Goodwin TW.
    Biochem J; 1975 Nov 25; 152(2):303-11. PubMed ID: 1220687
    [Abstract] [Full Text] [Related]

  • 8. 4,4-dimethyl-5-alpha-cholesta-8,14-dien-3-beta-ol. A new precursor of cholesterol in mammalian tissues.
    Fiecchi A, Canonica L, Scala A, Cattabeni F, Paoletti EG, Paoletti R.
    Life Sci; 1969 Jun 15; 8(12):629-34. PubMed ID: 5804656
    [No Abstract] [Full Text] [Related]

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  • 12. Studies on the mechanism of the enzymatic conversion of delta 8-cholesten-3 beta-ol to delta 7-cholesten-3 beta-ol.
    Lee WH, Kammereck R, Lutsky BN, McCloskey JA, Schroepfer GJ.
    J Biol Chem; 1969 Apr 25; 244(8):2033-40. PubMed ID: 5781997
    [No Abstract] [Full Text] [Related]

  • 13. The location of the 4-pro-R protons of mevalonic acid in cholesterol.
    Mulheirn LJ, Caspi E.
    J Biol Chem; 1971 Jun 25; 246(12):3948-52. PubMed ID: 5561468
    [No Abstract] [Full Text] [Related]

  • 14. A novel olefinic rearrangement. The enzymic conversion of cholesta-7,9-dien-3 -ol into cholesta-8,14-dien-3 -ol.
    Akhtar M, Freeman CW, Rahimtula AD, Wilton DC.
    Biochem J; 1972 Sep 25; 129(2):225-9. PubMed ID: 4404936
    [Abstract] [Full Text] [Related]

  • 15. Substrate activation in pyridine nucleotide-linked reactions: illustrations from the steroid field.
    Akhtar M, Wilton DC, Watkinson IA, Rahimtula AD.
    Proc R Soc Lond B Biol Sci; 1972 Feb 15; 180(1059):167-77. PubMed ID: 4401774
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  • 18. The role of a cholesta-8,14-dien-3-beta-ol system in cholesterol biosynthesis.
    Akhtar M, Watkinson IA, Rahimtula AD, Wilton DC, Munday KA.
    Biochem J; 1969 Mar 15; 111(5):757-61. PubMed ID: 5783476
    [Abstract] [Full Text] [Related]

  • 19. The stereospecificity of the cholesterol delta 22-dehydrogenase of Tetrahymena pyriformis and the origin of the C-22 protons of cholesterol.
    Zander JM, Caspi E.
    J Biol Chem; 1970 Apr 10; 245(7):1682-7. PubMed ID: 5438358
    [No Abstract] [Full Text] [Related]

  • 20. The formation of cholest-5-ene-3 ,26-diol as an intermediate in the conversion of cholesterol into bile acids by liver mitochondria.
    Mitropoulos KA, Avery MD, Myant NB, Gibbons GF.
    Biochem J; 1972 Nov 10; 130(2):363-71. PubMed ID: 4664570
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