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Journal Abstract Search

85 related items for PubMed ID: 3685870

  • 1. Normal activity of C27-steroid 26-hydroxylase in cultured sitosterolaemia fibroblasts.
    Boberg KM, Björkhem I, Skrede S.
    Scand J Clin Lab Invest; 1987 Nov; 47(7):701-4. PubMed ID: 3685870
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  • 5. Identification of new mutations in sterol 27-hydroxylase gene in Japanese patients with cerebrotendinous xanthomatosis (CTX).
    Kim KS, Kubota S, Kuriyama M, Fujiyama J, Björkhem I, Eggertsen G, Seyama Y.
    J Lipid Res; 1994 Jun; 35(6):1031-9. PubMed ID: 7915755
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  • 6. Cholic acid biosynthesis: the enzymatic defect in cerebrotendinous xanthomatosis.
    Salen G, Shefer S, Cheng FW, Dayal B, Batta AK, Tint GS.
    J Clin Invest; 1979 Jan; 63(1):38-44. PubMed ID: 762246
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  • 7. Increased (23R)-hydroxylase activity in patients suffering from cerebrotendinous xanthomatosis, resulting in (23R)-hydroxylation of bile acids.
    Koopman BJ, Wolthers BG, Van der Molen JC, Nagel GT, Rutgers H, Strijtveen B, Kaptein B.
    Biochim Biophys Acta; 1986 Oct 01; 883(3):585-92. PubMed ID: 3756224
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  • 9. Biosynthesis of bile acids in cerebrotendinous xanthomatosis. Relationship of bile acid pool sizes and synthesis rates to hydroxylations at C-12, C-25, and C-26.
    Salen G, Shefer S, Tint GS, Nicolau G, Dayal B, Batta AK.
    J Clin Invest; 1985 Aug 01; 76(2):744-51. PubMed ID: 4031069
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  • 10. Cerebrotendinous xanthomatosis: reduced serum 26-hydroxycholesterol.
    Javitt NB, Kok E, Cohen B, Burstein S.
    J Lipid Res; 1982 May 01; 23(4):627-30. PubMed ID: 7097127
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  • 11. Competitive inhibition of bile acid synthesis by endogenous cholestanol and sitosterol in sitosterolemia with xanthomatosis. Effect on cholesterol 7 alpha-hydroxylase.
    Shefer S, Salen G, Nguyen L, Batta AK, Packin V, Tint GS, Hauser S.
    J Clin Invest; 1988 Dec 01; 82(6):1833-9. PubMed ID: 3143743
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  • 12. Role of the 26-hydroxylase in the biosynthesis of bile acids in the normal state and in cerebrotendinous xanthomatosis. An in vivo study.
    Björkhem I, Fausa O, Hopen G, Oftebro H, Pedersen JI, Skrede S.
    J Clin Invest; 1983 Jan 01; 71(1):142-8. PubMed ID: 6848555
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  • 13. [A paradigm to elucidate a congenital disease, cerebrotendinous xanthomatosis].
    Okuda K, Setoguchi T.
    Tanpakushitsu Kakusan Koso; 1994 Sep 01; 39(12):2102-12. PubMed ID: 7938607
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  • 14. Quantitative analysis of the mitochondrial cytochrome P-450-linked monooxygenase system: NADPH-hepatoredoxin reductase, hepatoredoxin, and cytochrome P-450s27 in livers of patients with cerebrotendinous xanthomatosis.
    Miki H, Takeuchi H, Yamada A, Nishioka M, Matsuzawa Y, Hamamoto I, Hiwatashi A, Ichikawa Y.
    Clin Chim Acta; 1986 Nov 15; 160(3):255-63. PubMed ID: 3791635
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  • 18. Bile alcohol profiles in bile, urine, and feces of a patient with cerebrotendinous xanthomatosis.
    Shimazu K, Kuwabara M, Yoshii M, Kihira K, Takeuchi H, Nakano I, Ozawa S, Onuki M, Hatta Y, Hoshita T.
    J Biochem; 1986 Feb 15; 99(2):477-83. PubMed ID: 3700361
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  • 19. Genetic analysis of a Japanese cerebrotendinous xanthomatosis family: identification of a novel mutation in the adrenodoxin binding region of the CYP 27 gene.
    Chen W, Kubota S, Nishimura Y, Nozaki S, Yamashita S, Nakagawa T, Kameda-Takemura K, Menju M, Matsuzawa Y, Björkhem I, Eggertsen G, Seyama Y.
    Biochim Biophys Acta; 1996 Nov 15; 1317(2):119-26. PubMed ID: 8950197
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  • 20. [27-Hydroxylase deficiency (cerebrotendinous xanthomatosis)].
    Miyamoto K, Setoguchi T.
    Ryoikibetsu Shokogun Shirizu; 1998 Nov 15; (19 Pt 2):285-8. PubMed ID: 9645063
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