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125 related items for PubMed ID: 8454281

  • 1. Rapid detection and prevalence of cholesteryl ester transfer protein deficiency caused by an intron 14 splicing defect in hyperalphalipoproteinemia.
    Inazu A, Koizumi J, Haraki T, Yagi K, Wakasugi T, Takegoshi T, Mabuchi H, Takeda R.
    Hum Genet; 1993 Mar; 91(1):13-6. PubMed ID: 8454281
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  • 2. Frequency of intron 14 splicing defect of cholesteryl ester transfer protein gene in the Japanese general population--relation between the mutation and hyperalphalipoproteinemia.
    Hirano K, Yamashita S, Funahashi T, Sakai N, Menju M, Ishigami M, Hiraoka H, Kameda-Takemura K, Tokunaga K, Hoshino T.
    Atherosclerosis; 1993 Apr; 100(1):85-90. PubMed ID: 8318066
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  • 3. Frequency of exon 15 missense mutation (442D:G) in cholesteryl ester transfer protein gene in hyperalphalipoproteinemic Japanese subjects.
    Sakai N, Yamashita S, Hirano K, Menju M, Arai T, Kobayashi K, Ishigami M, Yoshida Y, Hoshino T, Nakajima N.
    Atherosclerosis; 1995 Apr 24; 114(2):139-45. PubMed ID: 7605382
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  • 5. Exon 10 skipping caused by intron 10 splice donor site mutation in cholesteryl ester transfer protein gene results in abnormal downstream splice site selection.
    Sakai N, Santamarina-Fojo S, Yamashita S, Matsuzawa Y, Brewer HB.
    J Lipid Res; 1996 Oct 24; 37(10):2065-73. PubMed ID: 8906584
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  • 7. Cholesteryl ester transfer protein gene: two common mutations and their effect on plasma high-density lipoprotein cholesterol content.
    Akita H, Chiba H, Tsuchihashi K, Tsuji M, Kumagai M, Matsuno K, Kobayashi K.
    J Clin Endocrinol Metab; 1994 Dec 24; 79(6):1615-8. PubMed ID: 7989465
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  • 14. Point mutation (-69 G-->A) in the promoter region of cholesteryl ester transfer protein gene in Japanese hyperalphalipoproteinemic subjects.
    Nagano M, Yamashita S, Hirano K, Kujiraoka T, Ito M, Sagehashi Y, Hattori H, Nakajima N, Maruyama T, Sakai N, Egashira T, Matsuzawa Y.
    Arterioscler Thromb Vasc Biol; 2001 Jun 24; 21(6):985-90. PubMed ID: 11397708
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  • 16. Evaluation of G-to-A substitution in the apolipoprotein A-I gene promoter as a determinant of high-density lipoprotein cholesterol level in subjects with and without cholesteryl ester transfer protein deficiency.
    Akita H, Chiba H, Tsuji M, Hui SP, Takahashi Y, Matsuno K, Kobayashi K.
    Hum Genet; 1995 Nov 24; 96(5):521-6. PubMed ID: 8529997
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  • 18. A low prevalence of coronary heart disease among subjects with increased high-density lipoprotein cholesterol levels, including those with plasma cholesteryl ester transfer protein deficiency.
    Moriyama Y, Okamura T, Inazu A, Doi M, Iso H, Mouri Y, Ishikawa Y, Suzuki H, Iida M, Koizumi J, Mabuchi H, Komachi Y.
    Prev Med; 1998 Nov 24; 27(5 Pt 1):659-67. PubMed ID: 9808796
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  • 20. Human plasma CETP deficiency: identification of a novel mutation in exon 9 of the CETP gene in a Caucasian subject from North America.
    Teh EM, Dolphin PJ, Breckenridge WC, Tan MH.
    J Lipid Res; 1998 Feb 24; 39(2):442-56. PubMed ID: 9508004
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