-
1
-
-
0017280786
-
Serum lipoproteins and coronary heart disease in a population study of Hawaii Japanese men
-
Rhoads, G. G., C. L. Gulbrandsen, and A. Kagan. 1976. Serum lipoproteins and coronary heart disease in a population study of Hawaii Japanese men. N. Engl. J. Med. 294: 293-298.
-
(1976)
N. Engl. J. Med.
, vol.294
, pp. 293-298
-
-
Rhoads, G.G.1
Gulbrandsen, C.L.2
Kagan, A.3
-
2
-
-
0018846624
-
High-density lipoproteins in human health and disease
-
Glomset, J. A. 1980. High-density lipoproteins in human health and disease. Adv. Intern. Med. 25: 91-116.
-
(1980)
Adv. Intern. Med.
, vol.25
, pp. 91-116
-
-
Glomset, J.A.1
-
3
-
-
0029082507
-
Defective removal of cellular cholesterol and phospholipids by apolipoprotein A-I in Tangier disease
-
Francis, G. A., R. H. Knopp, and J. F. Oram. 1995. Defective removal of cellular cholesterol and phospholipids by apolipoprotein A-I in Tangier disease. J. Clin. Invest. 96: 78-87.
-
(1995)
J. Clin. Invest.
, vol.96
, pp. 78-87
-
-
Francis, G.A.1
Knopp, R.H.2
Oram, J.F.3
-
4
-
-
0030852447
-
Decreased reverse cholesterol transport from Tangier disease fibroblasts. Acceptor specificity and effect of brefeldin on lipid efflux
-
Remaley, A. T., U. K. Schumacher, J. A. Stonik, B. D. Farsi, H. Nazih, and H. B. Brewer, Jr. 1997. Decreased reverse cholesterol transport from Tangier disease fibroblasts. Acceptor specificity and effect of brefeldin on lipid efflux. Arterioscler. Thromb. Vasc. Biol. 17: 1813-1821.
-
(1997)
Arterioscler. Thromb. Vasc. Biol.
, vol.17
, pp. 1813-1821
-
-
Remaley, A.T.1
Schumacher, U.K.2
Stonik, J.A.3
Farsi, B.D.4
Nazih, H.5
Brewer Jr., H.B.6
-
5
-
-
0032813660
-
Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1
-
Rust, S., M. Rosier, H. Funke, J. Real, Z. Amoura, J. C. Piette, J. F. Deleuze, H. B. Brewer, N. Duverger, P. Denefle, and G. Assmann. 1999. Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1. Nat. Genet. 22: 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
Piette, J.C.6
Deleuze, J.F.7
Brewer, H.B.8
Duverger, N.9
Denefle, P.10
Assmann, G.11
-
6
-
-
0032813809
-
The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease
-
Bodzioch, M., E. Orso, J. Klucken, T. Langmann, A. Bottcher, W. Diederich, W. Drobnik, S. Barlage, C. Buchler, M. Porsch-Ozcurumez, W. E. Kaminski, H. W. Hahmann, K. Oette, G. Rothe, C. Aslanidis, K. J. Lackner, and G. Schmitz. 1999. The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease. Nat. Genet. 22: 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
Porsch-Ozcurumez, M.10
Kaminski, W.E.11
Hahmann, H.W.12
Oette, K.13
Rothe, G.14
Aslanidis, C.15
Lackner, K.J.16
Schmitz, G.17
-
7
-
-
0032813808
-
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
-
Brooks-Wilson, A., M. Marcil, S. M. Clee, L-H. Zhang, K. Roomp, M. van Dam, L. Yu, C. Brewer, J. A. Collins, H. O. F. Molhuizen, O. Loubser, B. F. F. Ouelette, K. Fichter, K. J. D. Ashbourne-Excoffon, C. W. Sensen, S. Scherer, S. Mott, M. Denis, D. Martindale, J. Frohlich, K. Morgan, B. Koop, S. Pimstone, J. J. P. Kastelein, J. Genest Jr., and M. R. Hayden. 1999. Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. Nat. Genet. 22: 336-345.
-
(1999)
Nat. Genet.
, vol.22
, pp. 336-345
-
-
Brooks-Wilson, A.1
Marcil, M.2
Clee, S.M.3
Zhang, L.-H.4
Roomp, K.5
Van Dam, M.6
Yu, L.7
Brewer, C.8
Collins, J.A.9
Molhuizen, H.O.F.10
Loubser, O.11
Ouelette, B.F.F.12
Fichter, K.13
Ashbourne-Excoffon, K.J.D.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.P.24
Genest Jr., J.25
Hayden, M.R.26
more..
-
8
-
-
0034693064
-
Specific binding of apoA-I, enhanced cholesterol efflux, and altered plasma membrane morphology in cells expressing ABC1
-
Wang, N., D. L. Silver, P. Costet, and A. R. Tall. 2000. Specific binding of apoA-I, enhanced cholesterol efflux, and altered plasma membrane morphology in cells expressing ABC1. J. Biol. Chem. 275: 33053-33058.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 33053-33058
-
-
Wang, N.1
Silver, D.L.2
Costet, P.3
Tall, A.R.4
-
9
-
-
0037449210
-
Cloning of rat ABCA7 and its preferential expression in platelets
-
Sasaki, M., A. Shoji, Y. Kubo, S. Nada, and A. Yamaguchi. 2003. Cloning of rat ABCA7 and its preferential expression in platelets. Biochem. Biophys. Res. Commun. 304: 777-782.
-
(2003)
Biochem. Biophys. Res. Commun.
, vol.304
, pp. 777-782
-
-
Sasaki, M.1
Shoji, A.2
Kubo, Y.3
Nada, S.4
Yamaguchi, A.5
-
10
-
-
0033890964
-
Identification of a novel human sterol-sensitive ATP-binding cassette transporter (ABCA7)
-
Kaminski, W. E., E. Orso, W. Diederich, J. Klucken, W. Drobnik, and G. Schmitz. 2000. Identification of a novel human sterol-sensitive ATP-binding cassette transporter (ABCA7). Biochem. Biophys. Res. Commun. 273: 532-538.
-
(2000)
Biochem. Biophys. Res. Commun.
, vol.273
, pp. 532-538
-
-
Kaminski, W.E.1
Orso, E.2
Diederich, W.3
Klucken, J.4
Drobnik, W.5
Schmitz, G.6
-
11
-
-
0034937302
-
Comparative analysis of the promoter structure and genomic organization of the human and mouse ABCA7 gene encoding a novel ABCA transporter
-
Broccardo, C., J. Osorio, M. F. Luciani, L. M. Schriml, C. Prades, S. Shulenin, I. Arnould, L. Naudin, C. Lafargue, M. Rosier, B. Jordan, M. G. Mattei, M. Dean, P. Denefle, and G. Chimini. 2001. Comparative analysis of the promoter structure and genomic organization of the human and mouse ABCA7 gene encoding a novel ABCA transporter. Cytogenet. Cell Genet. 92: 264-270.
-
(2001)
Cytogenet. Cell Genet.
, vol.92
, pp. 264-270
-
-
Broccardo, C.1
Osorio, J.2
Luciani, M.F.3
Schriml, L.M.4
Prades, C.5
Shulenin, S.6
Arnould, I.7
Naudin, L.8
Lafargue, C.9
Rosier, M.10
Jordan, B.11
Mattei, M.G.12
Dean, M.13
Denefle, P.14
Chimini, G.15
-
12
-
-
0242353350
-
ATP-binding cassette transporter A7 (ABCA7) binds apolipoprotein A-I and mediates cellular phospholipid but not cholesterol efflux
-
Wang, N., D. Lan, M. Gerbod-Giannone, P. Linsel-Nitschke, A. W. Jehle, W. Chen, L. O. Martinez, and A. R. Tall. 2003. ATP-binding cassette transporter A7 (ABCA7) binds apolipoprotein A-I and mediates cellular phospholipid but not cholesterol efflux. J. Biol. Chem. 278: 42906-42912.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 42906-42912
-
-
Wang, N.1
Lan, D.2
Gerbod-Giannone, M.3
Linsel-Nitschke, P.4
Jehle, A.W.5
Chen, W.6
Martinez, L.O.7
Tall, A.R.8
-
13
-
-
0345791510
-
Human ABCA7 supports apolipoprotein-mediated release of cellular cholesterol and phospholipid to generate high density lipoprotein
-
Abe-Dohmae, S., Y. Ikeda, M. Matsuo, M. Hayashi, K. Okuhira, K. Ueda, and S. Yokoyama. 2004. Human ABCA7 supports apolipoprotein-mediated release of cellular cholesterol and phospholipid to generate high density lipoprotein. J. Biol. Chem. 279: 604-611.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 604-611
-
-
Abe-Dohmae, S.1
Ikeda, Y.2
Matsuo, M.3
Hayashi, M.4
Okuhira, K.5
Ueda, K.6
Yokoyama, S.7
-
14
-
-
3042798281
-
ATP-binding cassette transporters G1 and G4 mediate cellular cholesterol efflux to high-density lipoproteins
-
Wang, N., D. Lan, W. Chen, F. Matsuura, and A. R. Tall. 2004. ATP-binding cassette transporters G1 and G4 mediate cellular cholesterol efflux to high-density lipoproteins. Proc. Natl. Acad. Sci. USA. 101: 9774-9779.
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 9774-9779
-
-
Wang, N.1
Lan, D.2
Chen, W.3
Matsuura, F.4
Tall, A.R.5
-
15
-
-
0020511413
-
Tissue sites of degradation of apoprotein A-I in the rat
-
Glass, C. K., R. C. Pittman, G. A. Keller, and D. Steinberg. 1983. Tissue sites of degradation of apoprotein A-I in the rat. J. Biol. Chem. 258: 7161-7167.
-
(1983)
J. Biol. Chem.
, vol.258
, pp. 7161-7167
-
-
Glass, C.K.1
Pittman, R.C.2
Keller, G.A.3
Steinberg, D.4
-
16
-
-
0034490992
-
Functional loss of ABCA1 in mice causes severe placental malformation, aberrant lipid distribution, and kidney glomerulonephritis as well as high-density lipoprotein cholesterol deficiency
-
Christiansen-Weber, T. A., J. R. Voland, Y. Wu, K. Ngo, B. L. Roland, S. Nguyen, P. A. Peterson, and W. P. Fung-Leung. 2000. Functional loss of ABCA1 in mice causes severe placental malformation, aberrant lipid distribution, and kidney glomerulonephritis as well as high-density lipoprotein cholesterol deficiency. Am. J. Pathol. 157: 1017-1029.
-
(2000)
Am. J. Pathol.
, vol.157
, pp. 1017-1029
-
-
Christiansen-Weber, T.A.1
Voland, J.R.2
Wu, Y.3
Ngo, K.4
Roland, B.L.5
Nguyen, S.6
Peterson, P.A.7
Fung-Leung, W.P.8
-
17
-
-
12944286618
-
ABCG1 (ABC8), the human homolog of the Drosophila white gene, is a regulator of macrophage cholesterol and phospholipid transport
-
Klucken, J., C. Buchler, E. Orso, W. E. Kaminski, M. Porsch-Ozcurumez, G. Liebisch, M. Kapinsky, W. Diederich, W. Drobnik, M. Dean, R. Allikmets, and G. Schmitz. 2000. ABCG1 (ABC8), the human homolog of the Drosophila white gene, is a regulator of macrophage cholesterol and phospholipid transport. Proc. Natl. Acad. Sci. USA. 97: 817-822.
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 817-822
-
-
Klucken, J.1
Buchler, C.2
Orso, E.3
Kaminski, W.E.4
Porsch-Ozcurumez, M.5
Liebisch, G.6
Kapinsky, M.7
Diederich, W.8
Drobnik, W.9
Dean, M.10
Allikmets, R.11
Schmitz, G.12
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