-
1
-
-
0036189524
-
HDL and arteriosclerosis: Beyond reverse cholesterol transport
-
Nofer J.R., Kehrel B., Fobker M., Levkau B., Assmann G., von Eckardstein A. HDL and arteriosclerosis: beyond reverse cholesterol transport. Atherosclerosis. 161:2002;1-16.
-
(2002)
Atherosclerosis
, vol.161
, pp. 1-16
-
-
Nofer, J.R.1
Kehrel, B.2
Fobker, M.3
Levkau, B.4
Assmann, G.5
Von Eckardstein, A.6
-
2
-
-
0036276255
-
The cholesterol mobilizing transport ABCA1 as a new therapeutic target for cardiovascular disease
-
Oram J.F. The cholesterol mobilizing transport ABCA1 as a new therapeutic target for cardiovascular disease. Trends Cardiovasc. Med. 12:2002;170-175.
-
(2002)
Trends Cardiovasc. Med.
, vol.12
, pp. 170-175
-
-
Oram, J.F.1
-
3
-
-
0036186708
-
Altered distribution of platelet-activating factor-acetylhydrolase activity between LDL and HDL as a function of the severity of hypercholesterolemia
-
Tsimihodimos V., Karabina S.A., Tambaki A.P., Bairaktari E., Miltiadous G., Goudevenos J.A., Cariolou M.A., Chapman M.J., Tselepis A.D., Elisaf M. Altered distribution of platelet-activating factor-acetylhydrolase activity between LDL and HDL as a function of the severity of hypercholesterolemia. J. Lipid Res. 43:2002;256-263.
-
(2002)
J. Lipid Res.
, vol.43
, pp. 256-263
-
-
Tsimihodimos, V.1
Karabina, S.A.2
Tambaki, A.P.3
Bairaktari, E.4
Miltiadous, G.5
Goudevenos, J.A.6
Cariolou, M.A.7
Chapman, M.J.8
Tselepis, A.D.9
Elisaf, M.10
-
4
-
-
0027763632
-
Protection of low density lipoprotein against oxidative modification by high density lipoprotein associated with paraoxonase
-
Mackness M.I., Arrol S., Abbott C., Durrington P.N. Protection of low density lipoprotein against oxidative modification by high density lipoprotein associated with paraoxonase. Atherosclerosis. 104:1993;129-135.
-
(1993)
Atherosclerosis
, vol.104
, pp. 129-135
-
-
Mackness, M.I.1
Arrol, S.2
Abbott, C.3
Durrington, P.N.4
-
5
-
-
0032813808
-
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
-
Brook-Wilson A., Marcil M., Clee S.M., Zhang L.H., Roomp K., van Dam M., Yu K., Brewer C., Collins J.A., Molhuizen H.O., Loubster O., Ouelette B.F., Fichter K., Ashbourne-Excoffon K.J., Sensen C.W., Scherer S., Mott S., Denis M., Martindale D., Frohlich J., Morgan K., Koop B., Pimstone S., Kastelein J.J., Hayden M.R. Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. Nat. Genet. 22:1999;336-345.
-
(1999)
Nat. Genet.
, vol.22
, pp. 336-345
-
-
Brook-Wilson, A.1
Marcil, M.2
Clee, S.M.3
Zhang, L.H.4
Roomp, K.5
Van Dam, M.6
Yu, K.7
Brewer, C.8
Collins, J.A.9
Molhuizen, H.O.10
Loubster, O.11
Ouelette, B.F.12
Fichter, K.13
Ashbourne-Excoffon, K.J.14
Sensen, C.W.15
Scherer, S.16
Mott, S.17
Denis, M.18
Martindale, D.19
Frohlich, J.20
Morgan, K.21
Koop, B.22
Pimstone, S.23
Kastelein, J.J.24
Hayden, M.R.25
more..
-
6
-
-
0032813809
-
The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease
-
Bodzioch M., Orso E., Klucken J., Langmann T., Bottcher A., Diederich W., Drobnik W., Barlage S., Buchler C., Porsh-Ozcurumerz M., Kaminski W.E., Hahmann H.W., Oette K., Roche G., Aslannidis C., Lakner K.J., Schmitz G. The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease. Nat. Genet. 22:1999;347-351.
-
(1999)
Nat. Genet.
, vol.22
, pp. 347-351
-
-
Bodzioch, M.1
Orso, E.2
Klucken, J.3
Langmann, T.4
Bottcher, A.5
Diederich, W.6
Drobnik, W.7
Barlage, S.8
Buchler, C.9
Porsh-Ozcurumerz, M.10
Kaminski, W.E.11
Hahmann, H.W.12
Oette, K.13
Roche, G.14
Aslannidis, C.15
Lakner, K.J.16
Schmitz, G.17
-
7
-
-
0032813660
-
Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1
-
Rust S., Rosier M., Funke H., Real J., Amoura Z., Pietter J.C., Deleuze J.F., Brewer H.B., Duverger N., Denefle P., Assaman G. Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1. Nat. Genet. 22:1999;352-355.
-
(1999)
Nat. Genet.
, vol.22
, pp. 352-355
-
-
Rust, S.1
Rosier, M.2
Funke, H.3
Real, J.4
Amoura, Z.5
Pietter, J.C.6
Deleuze, J.F.7
Brewer, H.B.8
Duverger, N.9
Denefle, P.10
Assaman, G.11
-
8
-
-
0033576209
-
Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux
-
Marcil M., Brooks-Wilson A., Clee S., Roomp K., Zhang L.H., Yu L., Collins J.A., van Dam M., Molhuizen H.O., Loubster O., Ouellette B.F., Sensen C.W., Fichter K., Mott S., Denis M., Boucher B., Pimstone S., Genest J. Jr, Kastelein J.J., Hayden M.R. Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux. Lancet. 354:1999;1341-1346.
-
(1999)
Lancet
, vol.354
, pp. 1341-1346
-
-
Marcil, M.1
Brooks-Wilson, A.2
Clee, S.3
Roomp, K.4
Zhang, L.H.5
Yu, L.6
Collins, J.A.7
Van Dam, M.8
Molhuizen, H.O.9
Loubster, O.10
Ouellette, B.F.11
Sensen, C.W.12
Fichter, K.13
Mott, S.14
Denis, M.15
Boucher, B.16
Pimstone, S.17
Genest J., Jr.18
Kastelein, J.J.19
Hayden, M.R.20
more..
-
9
-
-
0015512255
-
Tangier disease. Report of a case and studies of lipid metabolism
-
Clifton-Bligh P., Nestel P.J., Whyte H.M. Tangier disease. Report of a case and studies of lipid metabolism. New Engl. J. Med. 286:1972;567-571.
-
(1972)
New Engl. J. Med.
, vol.286
, pp. 567-571
-
-
Clifton-Bligh, P.1
Nestel, P.J.2
Whyte, H.M.3
-
10
-
-
0343717914
-
High density lipoprotein deficiency and foam cell accumulation in mice with targeted disruption of ATP-binding cassette transporter-1
-
McNeish J., Aiello R.J., Guyot D., Turi T., Gabel C., Aldinger C., Hoppe K.L., Roach M.L., Royer L.J., de Wet J., Broccardo C., Chimini G., Francone O.L. High density lipoprotein deficiency and foam cell accumulation in mice with targeted disruption of ATP-binding cassette transporter-1. Proc. Natl. Acad. Sci. USA. 97:2000;4245-4250.
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 4245-4250
-
-
McNeish, J.1
Aiello, R.J.2
Guyot, D.3
Turi, T.4
Gabel, C.5
Aldinger, C.6
Hoppe, K.L.7
Roach, M.L.8
Royer, L.J.9
De Wet, J.10
Broccardo, C.11
Chimini, G.12
Francone, O.L.13
-
11
-
-
0033962086
-
Transport of lipids from golgi to plasma membrane is defective in Tangier disease patients and Abc1-deficient mice
-
Orso E., Broccardo C., Kaminski W.E., Bottcher A., Liebisch G., Drobnik W., Gotz A., Chambenoit O., Diederich W., Langmann T., Spruss T., Luciani M.F., Rothe G., Lackner K.J., Chimini G., Schmitz G. Transport of lipids from golgi to plasma membrane is defective in Tangier disease patients and Abc1-deficient mice. Nat. Genet. 24:2000;192-196.
-
(2000)
Nat. Genet.
, vol.24
, pp. 192-196
-
-
Orso, E.1
Broccardo, C.2
Kaminski, W.E.3
Bottcher, A.4
Liebisch, G.5
Drobnik, W.6
Gotz, A.7
Chambenoit, O.8
Diederich, W.9
Langmann, T.10
Spruss, T.11
Luciani, M.F.12
Rothe, G.13
Lackner, K.J.14
Chimini, G.15
Schmitz, G.16
-
12
-
-
0035947686
-
Regulation and activity of the human ABCA1 gene in transgenic mice
-
Cavelier L.B., Qiu Y., Bielicki J.K., Afzal V., Cheng J.F., Rubin E.M. Regulation and activity of the human ABCA1 gene in transgenic mice. J. Biol. Chem. 276:2001;18046-18051.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 18046-18051
-
-
Cavelier, L.B.1
Qiu, Y.2
Bielicki, J.K.3
Afzal, V.4
Cheng, J.F.5
Rubin, E.M.6
-
13
-
-
0034856194
-
High-density single-nucleotide polymorphism (SNP) map of the 150-kb region corresponding to the human ATP-binding cassette transporter A1 (ABCA1) gene
-
Iida A., Saito S., Sekine A., Kitamura Y., Kondo K., Mishima C., Osawa S., Harigae S., Nakamura Y. High-density single-nucleotide polymorphism (SNP) map of the 150-kb region corresponding to the human ATP-binding cassette transporter A1 (ABCA1) gene. J. Hum. Genet. 46:2001;522-528.
-
(2001)
J. Hum. Genet.
, vol.46
, pp. 522-528
-
-
Iida, A.1
Saito, S.2
Sekine, A.3
Kitamura, Y.4
Kondo, K.5
Mishima, C.6
Osawa, S.7
Harigae, S.8
Nakamura, Y.9
-
14
-
-
0035843968
-
Novel polymorphism in promoter region of ATP binding cassette transporter gene and plasma lipids, severity, progression, and regression of coronary atherosclerosis and response to therapy
-
Lutucuta S., Ballantyne C.M., Elghannam H., Gotto A.M. Jr, Marian A.J. Novel polymorphism in promoter region of ATP binding cassette transporter gene and plasma lipids, severity, progression, and regression of coronary atherosclerosis and response to therapy. Circ. Res. 88:2001;969-973.
-
(2001)
Circ. Res.
, vol.88
, pp. 969-973
-
-
Lutucuta, S.1
Ballantyne, C.M.2
Elghannam, H.3
Gotto A.M., Jr.4
Marian, A.J.5
-
15
-
-
0035864677
-
Common variants in the gene encoding ATP-binding cassette transporter 1 in men with low LDL cholesterol levels and coronary heart disease
-
Brousseau M.E., Bodzioch M., Schaefer E.J., Goldkamp A.L., Kielar D., Probst M., Ordovas J.M., Aslanidis C., Lackner K.J., Rubins H.B., Collins D., Robins S.J., Wilson P.W.F., Schitz G. Common variants in the gene encoding ATP-binding cassette transporter 1 in men with low LDL cholesterol levels and coronary heart disease. Atherosclerosis. 154:2001;607-611.
-
(2001)
Atherosclerosis
, vol.154
, pp. 607-611
-
-
Brousseau, M.E.1
Bodzioch, M.2
Schaefer, E.J.3
Goldkamp, A.L.4
Kielar, D.5
Probst, M.6
Ordovas, J.M.7
Aslanidis, C.8
Lackner, K.J.9
Rubins, H.B.10
Collins, D.11
Robins, S.J.12
Wilson, P.W.F.13
Schitz, G.14
-
16
-
-
0033903231
-
Common and rare ABCA1 variants affecting plasma HDL cholesterol
-
Wang J., Burnett J.R., Near S., Young K., Zinman B., Hanley A.J.G., Connelly P.W., Harris S.B., Hegele R.A. Common and rare ABCA1 variants affecting plasma HDL cholesterol. Arterioscler. Thromb. Vasc. Biol. 20:2000;1983-1989.
-
(2000)
Arterioscler. Thromb. Vasc. Biol.
, vol.20
, pp. 1983-1989
-
-
Wang, J.1
Burnett, J.R.2
Near, S.3
Young, K.4
Zinman, B.5
Hanley, A.J.G.6
Connelly, P.W.7
Harris, S.B.8
Hegele, R.A.9
-
17
-
-
0035814958
-
Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease
-
Clee S.M., Zwinderman A.H., Engert J.C., Zwarts K.Y., Molhuizen H.O.F., Roomp K., Jukema W., van Wijland M., van Dam M., Hudson T.J., Brooks-Wilson A., Genest J. Jr, Kastelein J.J.P., Hayden M.R. Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease. Circulation. 103:2001;1198-1205.
-
(2001)
Circulation
, vol.103
, pp. 1198-1205
-
-
Clee, S.M.1
Zwinderman, A.H.2
Engert, J.C.3
Zwarts, K.Y.4
Molhuizen, H.O.F.5
Roomp, K.6
Jukema, W.7
Van Wijland, M.8
Van Dam, M.9
Hudson, T.J.10
Brooks-Wilson, A.11
Genest J., Jr.12
Kastelein, J.J.P.13
Hayden, M.R.14
-
18
-
-
17444446649
-
Evidence for association between paraoxonase gene polymorphisms and atherosclerotic diseases
-
Imai Y., Morita H., Kurihara H., Sugiyama T., Kato N., Ebihara A., Hamada C., Kurihara Y., Shindo T., Oh-hashi Y., Yazaki Y. Evidence for association between paraoxonase gene polymorphisms and atherosclerotic diseases. Atherosclerosis. 49:2000;435-442.
-
(2000)
Atherosclerosis
, vol.49
, pp. 435-442
-
-
Imai, Y.1
Morita, H.2
Kurihara, H.3
Sugiyama, T.4
Kato, N.5
Ebihara, A.6
Hamada, C.7
Kurihara, Y.8
Shindo, T.9
Oh-hashi, Y.10
Yazaki, Y.11
-
19
-
-
0034805822
-
Human ABCA1 contains a large amino-terminal extracellular domain homologous to an epitope of Sjogren's syndrome
-
Tanaka A.R., Ikeda Y., Abe-Dohmae S., Arakawa R., Sadanami K., Kidera A., Nakagawa S., Nagase T., Aoki R., Kioka N., Amachi T., Yokoyama S., Ueda K. Human ABCA1 contains a large amino-terminal extracellular domain homologous to an epitope of Sjogren's syndrome. Biochem. Biophys. Res. Commun. 283:2001;1019-1025.
-
(2001)
Biochem. Biophys. Res. Commun.
, vol.283
, pp. 1019-1025
-
-
Tanaka, A.R.1
Ikeda, Y.2
Abe-Dohmae, S.3
Arakawa, R.4
Sadanami, K.5
Kidera, A.6
Nakagawa, S.7
Nagase, T.8
Aoki, R.9
Kioka, N.10
Amachi, T.11
Yokoyama, S.12
Ueda, K.13
-
20
-
-
0035958632
-
Novel mutations in ABCA1 gene in Japanese patients with Tangier disease and familial high density lipoprotein deficiency with coronary heart disease
-
Huang W., Moriyama K., Koga T., Hua H., Ageta M., Kawabata M., Teramoto T., Sasaki J. Novel mutations in ABCA1 gene in Japanese patients with Tangier disease and familial high density lipoprotein deficiency with coronary heart disease. Biochem. Biophys. Acta. 1537:2001;71-78.
-
(2001)
Biochem. Biophys. Acta
, vol.1537
, pp. 71-78
-
-
Huang, W.1
Moriyama, K.2
Koga, T.3
Hua, H.4
Ageta, M.5
Kawabata, M.6
Teramoto, T.7
Sasaki, J.8
-
21
-
-
18444396314
-
Expression and functional analyses of novel mutations of ATP-binding cassette transporter-1 in Japanese patients with high-density lipoprotein deficiency
-
Nishida Y., Hirano K., Tsukamoto K., Nagano M., Ikegami C., Roomp K., Ishihara M., Sakane N., Zhang Z., Tsujii Ki K., Matsuyama A., Ohama T., Matsuura F., Ishigami M., Sakai N., Hiraoka H., Hattori H., Wellington C., Yoshida Y., Misugi S., Hayden M.R., Egashira T., Yamashita S., Matsuzawa Y. Expression and functional analyses of novel mutations of ATP-binding cassette transporter-1 in Japanese patients with high-density lipoprotein deficiency. Biochem. Biophys. Res. Commun. 290:2002;713-721.
-
(2002)
Biochem. Biophys. Res. Commun.
, vol.290
, pp. 713-721
-
-
Nishida, Y.1
Hirano, K.2
Tsukamoto, K.3
Nagano, M.4
Ikegami, C.5
Roomp, K.6
Ishihara, M.7
Sakane, N.8
Zhang, Z.9
Tsujii Ki, K.10
Matsuyama, A.11
Ohama, T.12
Matsuura, F.13
Ishigami, M.14
Sakai, N.15
Hiraoka, H.16
Hattori, H.17
Wellington, C.18
Yoshida, Y.19
Misugi, S.20
Hayden, M.R.21
Egashira, T.22
Yamashita, S.23
Matsuzawa, Y.24
more..
-
22
-
-
0035125577
-
Lack of association between the platelet glycoprotein Ia C807T gene polymorphism and myocardial infarction in Japanese
-
Morita H., Kurihara H., Imai Y., Sugiyama T., Hamada C., Sakai E., Mori M., Nagai R. Lack of association between the platelet glycoprotein Ia C807T gene polymorphism and myocardial infarction in Japanese. Thromb. Haemost. 85:2001;226-230.
-
(2001)
Thromb. Haemost.
, vol.85
, pp. 226-230
-
-
Morita, H.1
Kurihara, H.2
Imai, Y.3
Sugiyama, T.4
Hamada, C.5
Sakai, E.6
Mori, M.7
Nagai, R.8
-
23
-
-
0029657765
-
Increased pre-β-HDL levels, cholesterol effulux, and LCAT mediated esterification in mice expressing the human chlesteryl ester transfer protein (CETP) and human apolipoprotein A-I (apo A-I) transgene
-
Francone O.L., Royer L., Haghpassand M. Increased pre-β-HDL levels, cholesterol effulux, and LCAT mediated esterification in mice expressing the human chlesteryl ester transfer protein (CETP) and human apolipoprotein A-I (apo A-I) transgene. J. Lipid Res. 37:1996;1268-1277.
-
(1996)
J. Lipid Res.
, vol.37
, pp. 1268-1277
-
-
Francone, O.L.1
Royer, L.2
Haghpassand, M.3
-
24
-
-
0029946953
-
Phospholipid transfer protein mediated conversion of high density lipoprotein (HDL) generates generation of pre-β1-HDL
-
von Eckardstein A., Jauhiainen M., Huang Y., Metso J., Langer C., Pussinen P., Wu S., Ehnholm C., Assmann G. Phospholipid transfer protein mediated conversion of high density lipoprotein (HDL) generates generation of pre-β1-HDL. Biochem. Biophys. Acta. 1301:1996;255-261.
-
(1996)
Biochem. Biophys. Acta
, vol.1301
, pp. 255-261
-
-
Von Eckardstein, A.1
Jauhiainen, M.2
Huang, Y.3
Metso, J.4
Langer, C.5
Pussinen, P.6
Wu, S.7
Ehnholm, C.8
Assmann, G.9
-
25
-
-
0028310839
-
Hepatic lipase induces the formation of pre-β-1-high density lipoprotein (HDL) from triacylglycerol-rich-HDL
-
Barrans A., Collet X., Barbaras R., Jaspard B., Manent J., Vieu C., Chap H., Perret B. Hepatic lipase induces the formation of pre-β-1-high density lipoprotein (HDL) from triacylglycerol-rich-HDL. J. Biol. Chem. 269:1994;11572-11577.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 11572-11577
-
-
Barrans, A.1
Collet, X.2
Barbaras, R.3
Jaspard, B.4
Manent, J.5
Vieu, C.6
Chap, H.7
Perret, B.8
-
26
-
-
0026486432
-
Regulation of the concentration of pre high density lipoprotein in normal plasma by cell membranes and lecitihin cholesterol acyltransferase
-
Miida T., Kawano M., Fielding C.J., Fielding P.E. Regulation of the concentration of pre high density lipoprotein in normal plasma by cell membranes and lecitihin cholesterol acyltransferase. Biochemistry. 31:1992;11112-11120.
-
(1992)
Biochemistry
, vol.31
, pp. 11112-11120
-
-
Miida, T.1
Kawano, M.2
Fielding, C.J.3
Fielding, P.E.4
-
27
-
-
0030046797
-
Identification of scavenger receptor receptor SR-BI as a high density lipoprotein receptor
-
Acton S., Rigotti A., Landchulz K.T., Xu S., Hobbs H.H., Krieger M. Identification of scavenger receptor receptor SR-BI as a high density lipoprotein receptor. Science. 271:1996;518-520.
-
(1996)
Science
, vol.271
, pp. 518-520
-
-
Acton, S.1
Rigotti, A.2
Landchulz, K.T.3
Xu, S.4
Hobbs, H.H.5
Krieger, M.6
-
28
-
-
0034007631
-
Endothelial lipase: A new member of the triglyceride lipase gene family
-
Rader D., Jaye M. Endothelial lipase: a new member of the triglyceride lipase gene family. Curr. Opin. Lipidol. 11:2000;141-148.
-
(2000)
Curr. Opin. Lipidol.
, vol.11
, pp. 141-148
-
-
Rader, D.1
Jaye, M.2
-
29
-
-
0034089291
-
Cubilin, a high density lipoprotein receptor
-
Moestrup S.K., Kozyraki R. Cubilin, a high density lipoprotein receptor. Curr. Opin. Lipidol. 11:2000;133-140.
-
(2000)
Curr. Opin. Lipidol.
, vol.11
, pp. 133-140
-
-
Moestrup, S.K.1
Kozyraki, R.2
-
30
-
-
0036335408
-
Relationship between ABCA1 genetic variation and HDL cholesterol level in subjects with ischemic heart disease in Japanese
-
Takagi S., Iwai N., miyazaki S., Nonogi H., Goto Y. Relationship between ABCA1 genetic variation and HDL cholesterol level in subjects with ischemic heart disease in Japanese. Thromb. Haemost. 88:2002;369-370.
-
(2002)
Thromb. Haemost.
, vol.88
, pp. 369-370
-
-
Takagi, S.1
Iwai, N.2
Miyazaki, S.3
Nonogi, H.4
Goto, Y.5
|