Showing 1 - 13 results of 13 for search 'G.J Schroepfer, Jr', query time: 0.04s Refine Results
  1. 1
    Inhibitors of sterol synthesis. Reverse phase high performance liquid chromatography for the separation of cholesterol, 5 alpha-cholest-8(14)-en-3 beta-ol-15-one, and their fatty acid esters.

    Inhibitors of sterol synthesis. Reverse phase high performance liquid chromatography for the separation of cholesterol, 5 alpha-cholest-8(14)-en-3 beta-ol-15-one, and their fatty a... by A Chu, G J Schroepfer, Jr

    Published 1988-02-01
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  2. 2
    Inhibitors of sterol synthesis. Synthesis and spectral characterization of fatty acids esters of 5 alpha-cholest-8(14)-en-3 beta-ol-15-one

    Inhibitors of sterol synthesis. Synthesis and spectral characterization of fatty acids esters of 5 alpha-cholest-8(14)-en-3 beta-ol-15-one by J St Pyrek, G J Schroepfer, Jr

    Published 1987-11-01
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  3. 3
    Sterol synthesis. A simplified method for the synthesis of 32-oxygenated derivatives of 24,25-dihydrolanosterol.

    Sterol synthesis. A simplified method for the synthesis of 32-oxygenated derivatives of 24,25-dihydrolanosterol. by E J Parish, G J Schroepfer, Jr

    Published 1981-07-01
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  4. 4
    Sterol synthesis. Chemical synthesis of 5 alpha-cholest-7-en-3 beta, 14 alpha-diol.

    Sterol synthesis. Chemical synthesis of 5 alpha-cholest-7-en-3 beta, 14 alpha-diol. by R A Pascal, Jr, G J Schroepfer, Jr

    Published 1980-01-01
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  5. 5
    Improved separation of sterols by column chromatography

    Improved separation of sterols by column chromatography by Auste M. Paliokas, Wen-Hui Lee, G.J. Schroepfer, Jr.

    Published 1968-01-01
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  6. 6
    Inhibitors of sterol synthesis. Tritium-labeled 26-hydroxycholesterol of high specific activity from a byproduct of the Clemmensen reduction of diosgenin.

    Inhibitors of sterol synthesis. Tritium-labeled 26-hydroxycholesterol of high specific activity from a byproduct of the Clemmensen reduction of diosgenin. by Y Ni, A Kisic, W K Wilson, G J Schroepfer, Jr

    Published 1994-03-01
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  7. 7
    Sterol synthesis. A timely look at the capabilities of conventional and silver ion high performance liquid chromatography for the separation of C27 sterols related to cholesterol biosynthesis

    Sterol synthesis. A timely look at the capabilities of conventional and silver ion high performance liquid chromatography for the separation of C27 sterols related to cholesterol b... by B Ruan, N Gerst, G T Emmons, J Shey, G J Schroepfer, Jr

    Published 1997-12-01
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  8. 8
    An updated look at the analysis of unsaturated C27 sterols by gas chromatography and mass spectrometry

    An updated look at the analysis of unsaturated C27 sterols by gas chromatography and mass spectrometry by N Gerst, B Ruan, J Pang, W K Wilson, G J Schroepfer, Jr

    Published 1997-08-01
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  9. 9
    Inhibitors of sterol synthesis. Chemical synthesis of 5 beta-cholest-8-ene-3 beta,15 alpha-diol and its effects on 3-hydroxy-3-methylglutaryl coenzyme A reductase activity in CHO-K1 cells.

    Inhibitors of sterol synthesis. Chemical synthesis of 5 beta-cholest-8-ene-3 beta,15 alpha-diol and its effects on 3-hydroxy-3-methylglutaryl coenzyme A reductase activity in CHO-K... by W K Wilson, F D Pinkerton, N D Kirkpatrick, G J Schroepfer, Jr

    Published 1989-06-01
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  10. 10
    Sphingolipid bases. A revisitation of the O-methyl derivatives of sphingosine. Isolation and characterization of diacetate derivatives, with revised 13C nuclear magnetic resonance assignments for D-erythro-sphingosine.

    Sphingolipid bases. A revisitation of the O-methyl derivatives of sphingosine. Isolation and characterization of diacetate derivatives, with revised 13C nuclear magnetic resonance... by A Kisic, M Tsuda, R J Kulmacz, W K Wilson, G J Schroepfer, Jr

    Published 1995-04-01
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  11. 11
    Analysis of unsaturated C27 sterols by nuclear magnetic resonance spectroscopy.

    Analysis of unsaturated C27 sterols by nuclear magnetic resonance spectroscopy. by W K Wilson, R M Sumpter, J J Warren, P S Rogers, B Ruan, G J Schroepfer, Jr

    Published 1996-01-01
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  12. 12
    Inhibitors of sterol synthesis. Submicromolar 14 alpha-ethyl-5 alpha-cholest-7-ene-3 beta, 15 alpha-diol causes a major modification of the sterol composition of CHO-K1 cells and a marked change in cell morphology.

    Inhibitors of sterol synthesis. Submicromolar 14 alpha-ethyl-5 alpha-cholest-7-ene-3 beta, 15 alpha-diol causes a major modification of the sterol composition of CHO-K1 cells and a... by A Izumi, F.D Pinkerton, S.O Nelson, J.S Pyrek, P.J Neill, J H Smith, G.J Schroepfer, Jr

    Published 1994-07-01
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  13. 13
    Inhibitors of sterol synthesis. Chemical synthesis, structure, and biological activities of (25R)-3 beta,26-dihydroxy-5 alpha-cholest-8(14)-en-15-one, a metabolite of 3 beta-hydroxy-5 alpha-cholest-8(14)-en-15-one.

    Inhibitors of sterol synthesis. Chemical synthesis, structure, and biological activities of (25R)-3 beta,26-dihydroxy-5 alpha-cholest-8(14)-en-15-one, a metabolite of 3 beta-hydrox... by H S Kim, W K Wilson, D H Needleman, F D Pinkerton, D K Wilson, F A Quiocho, G J Schroepfer, Jr

    Published 1989-02-01
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