Tangier病家系に見られるLDL, HDLの異常
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| Published in | 動脈硬化 Vol. 11; no. 6; pp. 1223 - 1229 |
|---|---|
| Main Authors | , , , , , , , , |
| Format | Journal Article |
| Language | Japanese |
| Published |
一般社団法人 日本動脈硬化学会
01.02.1984
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| Online Access | Get full text |
| ISSN | 0386-2682 2185-8284 |
| DOI | 10.5551/jat1973.11.6_1223 |
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| Author | 木田, 信章 横山, 信治 田嶋, 正二 山本, 章 中村, 東樹 中川, 英彦 津田, 和矩 山村, 卓 大瀧, 幸哉 |
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| References | 12) 中村東樹, 津田和矩: 家族性HDL欠損症. 臨床医, 8: 1368-1372 (1983). 19) Yokoyama, S., Fukushima, D., Kupferberg, J. P., Kezdy, F. J., and Kaiser, E. T.: The mechanism of activation of lecithin-cholesterol acyltransferase by apolipoprotein A-I and amphiphilic peptide. J. Biol. Chem., 255: 7333-7339 (1980). 13) Folch, J., Lees, M. and Sloane-Stanley, G. H.: A simple method for the isolation and purification of a total lipides from animal tissues. J. Biol. Chem., 226: 497-509 (1957). 8) 中川英彦, 木田信章, 大滝幸哉, 中村東樹, 津田和矩: 家族性HDL欠損症 (Tangier病). 臨床病理, 30 (補冊): 254 (1982). 17) Utermann, G., Menzel, H. J. and Schoenborn, W.: Plasma lipoprotein abnormalities in a case of a primary high-density-lipoprotein (HDL) deficiency. Clin. Gen., 8: 258-268 (1975). 3) 大滝幸哉, 中川英彦, 木田信章, 鶴紀子, 池田暉親: 家族性HDL欠損症 (Tangier病). 医学のあゆみ, 119: 849-851 (1981). 10) Nagasaki, T. and Akanuma, Y.: A new colorimetric method for the determination of plasma lecithincholesterol acyltransferase activity. Clin. Chim. Acta, 75: 371-375 (1977). 15) Metcalfe, L. D., Schmitz, A. A. and Pelka, J. R.: Rapid preparation of fatty acid esters from lipids for gas chromatographic analysis. Anal. Chem., 38: 514 (1966). 16) Yao, J. K., Herbert, P. N., Fredrickson, D. S., Ellefson, R. D., Heinen, R. J., Forte, T. and Dyck, P. J.: Biochemical studies in a patient with a Tangier syndrome. J. Neuropathol. Exp. Neurol., 37: 138-154 (1978). 4) Schaefer, E. J., Heaton, W. H., Wetzel, M. G. and Brewer, Jr. H. B.: Plasma apolipoprotein A-I absence associated with a marked reduction of high density lipoprotein and premature coronary artery disease. Arteriosclerosis, 2: 16-26 (1982). 2) 大滝幸哉, 中川英彦: 家族性HDL欠損症 (Tangier病). 綜合臨床, 31: 2833-2842 (1982). 1) Fredrickson, D. S., Altrocchi, P. H., Avioli, L. V., Goodman, De W. S. and Goodman, H. C.: Tangier disease. Ann. Intern. Med., 55: 1016-1031 (1961). 5) Norum, R. A., Lakier, J. B., Goldstein, S., Angel, A., Goldberg, R. B., Block, W. D., Noffze, D. K., Dolphin, P. J., Edelglass, J., Bogorad, D. D. and Alaupovic, P.: Familial deficiency of apolipoproteins A-I and C-III and precocious coronary-artery disease. New Engl. J. Med., 306: 1513-1519 (1982). 7) Kay, L. L., Ronan, R., Schaefer, E. J. and Brewer Jr. H. B.: Tangier disease: A structural defect in apolipoprotein A-I (Apo A-I Tangier). Proc. Natl. Acad. Sci. USA, 79: 2485-2489 (1982). 20) Assman, G., Schmitz, G., Donath, N. and Lekim, D.: Phosphatidylcholine substrate specificity of lecithin: cholesterol acyltransferase. Scand. J. Clin. Lab. Invest., (Suppl. 150): 17-20 (1978). 14) Durrington, P. N., Bolton, C. H., Hartog, M., Angelinetta, R., Emmet, P. and Furniss, S.: The effect of a low-cholesterol, high-polysaturate diet on serum lipid levels, apolipoprotein B levels and triglyceride fatty acid composition. Atherosclerosis, 27: 465-475 (1977). 18) Albers, J. J.: Effect of human plasma apolipoproteins on the activity of purified lecithin-cholesterol acyltransferase. Scand. J. Clin. Lab. Invest., 38 (Suppl. 150): 48-52 (1978). 11) Glomset, J. A. and Wright, J. L.: Some properties of a cholesterol esterifying enzyme in plasma. Biochim. Biophys. Acta, 89: 266-276 (1964). 6) Zannis, V. I., Lees, A. M., Lees, R. S. and Breslow, J. L.: Abnormal apoprotein A-I isoprotein composition in patients with Tangier disease. J. Biol. Chem., 257: 4978-4986 (1982). 9) 中川英彦, 木田信章, 大滝幸哉, 中村東樹, 津田和矩, 横山信治, 山村卓, 田嶋正二, 山本章: 家族性HDL欠損症. 目本動脈硬化学会, 昭和57年度冬季大会 (1983). |
| References_xml | – reference: 12) 中村東樹, 津田和矩: 家族性HDL欠損症. 臨床医, 8: 1368-1372 (1983). – reference: 16) Yao, J. K., Herbert, P. N., Fredrickson, D. S., Ellefson, R. D., Heinen, R. J., Forte, T. and Dyck, P. J.: Biochemical studies in a patient with a Tangier syndrome. J. Neuropathol. Exp. Neurol., 37: 138-154 (1978). – reference: 13) Folch, J., Lees, M. and Sloane-Stanley, G. H.: A simple method for the isolation and purification of a total lipides from animal tissues. J. Biol. Chem., 226: 497-509 (1957). – reference: 19) Yokoyama, S., Fukushima, D., Kupferberg, J. P., Kezdy, F. J., and Kaiser, E. T.: The mechanism of activation of lecithin-cholesterol acyltransferase by apolipoprotein A-I and amphiphilic peptide. J. Biol. Chem., 255: 7333-7339 (1980). – reference: 1) Fredrickson, D. S., Altrocchi, P. H., Avioli, L. V., Goodman, De W. S. and Goodman, H. C.: Tangier disease. Ann. Intern. Med., 55: 1016-1031 (1961). – reference: 3) 大滝幸哉, 中川英彦, 木田信章, 鶴紀子, 池田暉親: 家族性HDL欠損症 (Tangier病). 医学のあゆみ, 119: 849-851 (1981). – reference: 4) Schaefer, E. J., Heaton, W. H., Wetzel, M. G. and Brewer, Jr. H. B.: Plasma apolipoprotein A-I absence associated with a marked reduction of high density lipoprotein and premature coronary artery disease. Arteriosclerosis, 2: 16-26 (1982). – reference: 5) Norum, R. A., Lakier, J. B., Goldstein, S., Angel, A., Goldberg, R. B., Block, W. D., Noffze, D. K., Dolphin, P. J., Edelglass, J., Bogorad, D. D. and Alaupovic, P.: Familial deficiency of apolipoproteins A-I and C-III and precocious coronary-artery disease. New Engl. J. Med., 306: 1513-1519 (1982). – reference: 15) Metcalfe, L. D., Schmitz, A. A. and Pelka, J. R.: Rapid preparation of fatty acid esters from lipids for gas chromatographic analysis. Anal. Chem., 38: 514 (1966). – reference: 20) Assman, G., Schmitz, G., Donath, N. and Lekim, D.: Phosphatidylcholine substrate specificity of lecithin: cholesterol acyltransferase. Scand. J. Clin. Lab. Invest., (Suppl. 150): 17-20 (1978). – reference: 11) Glomset, J. A. and Wright, J. L.: Some properties of a cholesterol esterifying enzyme in plasma. Biochim. Biophys. Acta, 89: 266-276 (1964). – reference: 8) 中川英彦, 木田信章, 大滝幸哉, 中村東樹, 津田和矩: 家族性HDL欠損症 (Tangier病). 臨床病理, 30 (補冊): 254 (1982). – reference: 2) 大滝幸哉, 中川英彦: 家族性HDL欠損症 (Tangier病). 綜合臨床, 31: 2833-2842 (1982). – reference: 14) Durrington, P. N., Bolton, C. H., Hartog, M., Angelinetta, R., Emmet, P. and Furniss, S.: The effect of a low-cholesterol, high-polysaturate diet on serum lipid levels, apolipoprotein B levels and triglyceride fatty acid composition. Atherosclerosis, 27: 465-475 (1977). – reference: 9) 中川英彦, 木田信章, 大滝幸哉, 中村東樹, 津田和矩, 横山信治, 山村卓, 田嶋正二, 山本章: 家族性HDL欠損症. 目本動脈硬化学会, 昭和57年度冬季大会 (1983). – reference: 17) Utermann, G., Menzel, H. J. and Schoenborn, W.: Plasma lipoprotein abnormalities in a case of a primary high-density-lipoprotein (HDL) deficiency. Clin. Gen., 8: 258-268 (1975). – reference: 10) Nagasaki, T. and Akanuma, Y.: A new colorimetric method for the determination of plasma lecithincholesterol acyltransferase activity. Clin. Chim. Acta, 75: 371-375 (1977). – reference: 18) Albers, J. J.: Effect of human plasma apolipoproteins on the activity of purified lecithin-cholesterol acyltransferase. Scand. J. Clin. Lab. Invest., 38 (Suppl. 150): 48-52 (1978). – reference: 6) Zannis, V. I., Lees, A. M., Lees, R. S. and Breslow, J. L.: Abnormal apoprotein A-I isoprotein composition in patients with Tangier disease. J. Biol. Chem., 257: 4978-4986 (1982). – reference: 7) Kay, L. L., Ronan, R., Schaefer, E. J. and Brewer Jr. H. B.: Tangier disease: A structural defect in apolipoprotein A-I (Apo A-I Tangier). Proc. Natl. Acad. Sci. USA, 79: 2485-2489 (1982). |
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| Title | Tangier病家系に見られるLDL, HDLの異常 |
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