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Journal Abstract Search

65 related items for PubMed ID: 5121749

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  • 2. 6-amino derivatives of stigmastanol and cholestanol.
    Pinhas H, Loiseau A, Krikorian-Manoukian A, Courmarcel D, Buu-Hoi NP, Jacquignon P.
    J Med Chem; 1971 Nov; 14(11):1048-9. PubMed ID: 5115200
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  • 8. In vivo demonstration of the cholesterol feedback system by means of a desmosterol suppression technique.
    Bricker LA, Weis HJ, Siperstein MD.
    J Clin Invest; 1972 Feb; 51(2):197-205. PubMed ID: 5009109
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  • 9. [Biological properties of oxide with Rf 0.53--the product of 7-dehydrocholesterol oxidation].
    Morozova RP.
    Ukr Biokhim Zh; 1969 Feb; 41(5):480-4. PubMed ID: 5368734
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  • 10. 22-trans-cholesta-5,22,24-trien-3-beta-OL -- an intermediate in the conversion of stigmasterol to cholesterol in the tobacco hornworm, Manduca sexta (Johannson).
    Svoboda JA, Hutchins RF, Thompson MJ, Robbins WE.
    Steroids; 1969 Nov; 14(5):469-76. PubMed ID: 5356908
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  • 11. Synthesis of stereoisomeric 4-hydroxymethyl-4-methyl-3beta-hydroxy-cholestanes, -androstanes, and -10-methyl-trans-decalins.
    Czarny MR, Maheshwari KK, Nelson JA, Spencer TA.
    J Org Chem; 1975 Jul 11; 40(14):2079-85. PubMed ID: 1142043
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  • 14. Cerebrotendinous xanthomatosis: in vivo labeling of cerebral sterols and sterol esters.
    Gardner-Medwin D, Kishimoto Y, Derby BM, Moser HW.
    Trans Am Neurol Assoc; 1971 Jul 11; 96():241-4. PubMed ID: 5159092
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  • 17. Synthesis of polyhydroxysterols (III): synthesis and structural elucidation of 24-methylenecholest-4-en-3beta,6 alpha-diol.
    Cui JG, Lin CW, Zeng LM, Su JY.
    Steroids; 2002 Dec 11; 67(13-14):1015-9. PubMed ID: 12441186
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  • 18. The enzymatic aromatization of the B ring of delta5,7-sterols.
    Korn ED, Ulsamer AG, Weihing RR, Wetzel MG, Wright PL.
    Biochim Biophys Acta; 1969 Dec 17; 187(4):555-63. PubMed ID: 5362515
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  • 19. The synthesis of 25-hydroxycholecalciferol. A biologically active metabolite of vitamin D3.
    Blunt JW, DeLuca HF.
    Biochemistry; 1969 Feb 17; 8(2):671-5. PubMed ID: 4307413
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  • 20. Two isomeric epoxysitosterols from Rhododendron formosanum: 1H and 13C NMR chemical shift assignments.
    Krishna V, Chang CI, Chou CH.
    Magn Reson Chem; 2006 Aug 17; 44(8):817-9. PubMed ID: 16724364
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