-
1
-
-
0035960630
-
Global burden of cardiovascular diseases: Part I: General considerations, the epidemiologic transition, risk factors, and impact of urbanization
-
Yusuf S, Reddy S, Ounpuu S, Anand S. Global burden of cardiovascular diseases: part I: general considerations, the epidemiologic transition, risk factors, and impact of urbanization. Circulation. 2001;104:2746-2753.
-
(2001)
Circulation
, vol.104
, pp. 2746-2753
-
-
Yusuf, S.1
Reddy, S.2
Ounpuu, S.3
Anand, S.4
-
2
-
-
0031001720
-
Alternative projections of mortality and disability by cause 1990 to 2020: Global Burden of Disease Study
-
Murray CJL, Lopez AD. Alternative projections of mortality and disability by cause 1990 to 2020: Global Burden of Disease Study. Lancet. 1997;349:1498-1504.
-
(1997)
Lancet
, vol.349
, pp. 1498-1504
-
-
Murray, C.J.L.1
Lopez, A.D.2
-
3
-
-
0030996001
-
Global mortality, disability, and the contribution of risk factors: Global Burden of Disease Study
-
Murray CJL, Lopez AD. Global mortality, disability, and the contribution of risk factors: Global Burden of Disease Study. Lancet. 1997;349:1436-1442.
-
(1997)
Lancet
, vol.349
, pp. 1436-1442
-
-
Murray, C.J.L.1
Lopez, A.D.2
-
4
-
-
0027330899
-
Familial hypoalphalipoproteinemia in premature coronary artery disease
-
Genest J Jr, Bard J-M, Fruchart J-C, Ordovas JM, Schaefer EJ. Familial hypoalphalipoproteinemia in premature coronary artery disease. Arterioscler Thromb. 1993;13:1728-1737.
-
(1993)
Arterioscler Thromb
, vol.13
, pp. 1728-1737
-
-
Genest J., Jr.1
Bard, J.-M.2
Fruchart, J.-C.3
Ordovas, J.M.4
Schaefer, E.J.5
-
5
-
-
0026762806
-
Familial lipoprotein disorders in patients with premature coronary artery disease
-
Genest JJr., Martin-Munley SS, McNamara JR, Ordovas JM, Jenner J, Myers RH, Silberman SR, Wilson PWF, Salem DN, Schaefer EJ. Familial lipoprotein disorders in patients with premature coronary artery disease. Circulation. 1992;85:2025-2033.
-
(1992)
Circulation
, vol.85
, pp. 2025-2033
-
-
Genest J., Jr.1
Martin-Munley, S.S.2
McNamara, J.R.3
Ordovas, J.M.4
Jenner, J.5
Myers, R.H.6
Silberman, S.R.7
Wilson, P.W.F.8
Salem, D.N.9
Schaefer, E.J.10
-
6
-
-
0014264541
-
The plasma lecithin: Cholesterol acyltransferase reaction
-
Glomset JA. The plasma lecithin: cholesterol acyltransferase reaction. J Lipid Res. 1968;9:155-167.
-
(1968)
J Lipid Res
, vol.9
, pp. 155-167
-
-
Glomset, J.A.1
-
8
-
-
0019965825
-
Complete nucleotide sequence and identification of membrane components of the histidine transport operon of S. typhimurium
-
Higgins CF, Haag PD, Nikaido K, Ardeshir F, Garcia G, Ames GF. Complete nucleotide sequence and identification of membrane components of the histidine transport operon of S. typhimurium. Nature. 1982;298:723-727.
-
(1982)
Nature
, vol.298
, pp. 723-727
-
-
Higgins, C.F.1
Haag, P.D.2
Nikaido, K.3
Ardeshir, F.4
Garcia, G.5
Ames, G.F.6
-
9
-
-
0034917716
-
The human ATP-binding cassette (ABC) transporter superfamily
-
Dean M, Rzhetsky A, Allikmets R. The human ATP-binding cassette (ABC) transporter superfamily. Genome Res. 2001;11:1156-1166.
-
(2001)
Genome Res
, vol.11
, pp. 1156-1166
-
-
Dean, M.1
Rzhetsky, A.2
Allikmets, R.3
-
11
-
-
0032720231
-
Inventory and function of yeast ABC proteins: About sex, stress, pleiotropic drug and heavy metal resistance
-
Bauer BE, Wolfger H, Kuchler K. Inventory and function of yeast ABC proteins: about sex, stress, pleiotropic drug and heavy metal resistance. Biochim Biophys Acta. 1999;1461:217-236.
-
(1999)
Biochim Biophys Acta
, vol.1461
, pp. 217-236
-
-
Bauer, B.E.1
Wolfger, H.2
Kuchler, K.3
-
12
-
-
0031943304
-
The Escherichia coli ATP-binding cassette (ABC) proteins
-
Linton KJ, Higgins CF. The Escherichia coli ATP-binding cassette (ABC) proteins. Mol Microbiol. 1998;28:5-13.
-
(1998)
Mol Microbiol
, vol.28
, pp. 5-13
-
-
Linton, K.J.1
Higgins, C.F.2
-
13
-
-
0026621245
-
ABC transporters: From microorganisms to man
-
Higgins CF. ABC transporters: from microorganisms to man. Annu Rev Cell Biol. 1992;8:67-113.
-
(1992)
Annu Rev Cell Biol
, vol.8
, pp. 67-113
-
-
Higgins, C.F.1
-
14
-
-
0028249115
-
The MDR superfamily of genes and its biological implications
-
Childs S, Ling V. The MDR superfamily of genes and its biological implications. Important Adv Oncol 1994;1:21-36.
-
(1994)
Important Adv Oncol
, vol.1
, pp. 21-36
-
-
Childs, S.1
Ling, V.2
-
15
-
-
0029586715
-
Evolution of ATP-binding cassette transporter genes
-
Dean M, Allikmets R. Evolution of ATP-binding cassette transporter genes. Curr Opin Genet Dev. 1995;5:779-785
-
(1995)
Curr Opin Genet Dev
, vol.5
, pp. 779-785
-
-
Dean, M.1
Allikmets, R.2
-
16
-
-
0025374695
-
Structural model of ATP-binding proteins associated with cystic fibrosis, multidrug resistance and bacterial transport
-
Hyde SC, Emsley P, Hartshorn MJ, Mimmack MM, Gileadi U, Pearce SR, Gallagher MP, Gill DR, Hubbard RE, Higgins CF. Structural model of ATP-binding proteins associated with cystic fibrosis, multidrug resistance and bacterial transport. Nature. 1990;346:362-365.
-
(1990)
Nature
, vol.346
, pp. 362-365
-
-
Hyde, S.C.1
Emsley, P.2
Hartshorn, M.J.3
Mimmack, M.M.4
Gileadi, U.5
Pearce, S.R.6
Gallagher, M.P.7
Gill, D.R.8
Hubbard, R.E.9
Higgins, C.F.10
-
19
-
-
0034805822
-
Human ABCA1 contains a large amino-terminal extracellular domain homologous to an epitope of Sjogren's Syndrome
-
Tanaka AR, Ikeda Y, Abe-Dohmae S, Arakawa R, Sadanami K, Kidera A, Nakagawa S, Nagase T, Aoki R, Kioka N, Amach 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. 2001;283:1019-1025.
-
(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
Amach, T.11
Yokoyama, S.12
Ueda, K.13
-
20
-
-
0034953105
-
The human ATP-binding cassette (ABC) transporter superfamily
-
Dean M, Hamon Y, Chimini G. The human ATP-binding cassette (ABC) transporter superfamily. J Lipid Res. 2001;42:1007-1017.
-
(2001)
J Lipid Res
, vol.42
, pp. 1007-1017
-
-
Dean, M.1
Hamon, Y.2
Chimini, G.3
-
21
-
-
0032813808
-
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
-
Brooks-Wilson A, Marcil M, Clee SM, Zhang L, Roomp K, van Dam M, Yu L, Brewer C, Collins JA, Molhuizen HOF, Loubser O, Ouellette BFF, Fichte K, Ashbourne Excoffon KJD, Sensen CW, Scherer S, Mott S, Denis M, Martindale D, Frohlich J, Morgan K, Koop B, Pimstone SN, Kastelein JJP, Genest J Jr, Hayden MR. Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. Nat Genet. 1999;22:336-345.
-
(1999)
Nat Genet
, vol.22
, pp. 336-345
-
-
Brooks-Wilson, A.1
Marcil, M.2
Clee, S.M.3
Zhang, L.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
Ouellette, B.F.F.12
Fichte, 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.N.23
Kastelein, J.J.P.24
Genest J., Jr.25
Hayden, M.R.26
more..
-
22
-
-
0031037951
-
A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy
-
Allikmets R, Singh N, Sun H, Shroyer NF, Hutchinson A, Chidambaram A, Gerrard B, Baird L, Stauffer D, Peiffer A, Rattner A, Smallwood P, Li Y, Anderson KL, Lewis RA, Nathans J, Leppert M, Dean M, Lupski JR. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy. Nat Genet. 1997;15:236-245.
-
(1997)
Nat Genet
, vol.15
, pp. 236-245
-
-
Allikmets, R.1
Singh, N.2
Sun, H.3
Shroyer, N.F.4
Hutchinson, A.5
Chidambaram, A.6
Gerrard, B.7
Baird, L.8
Stauffer, D.9
Peiffer, A.10
Rattner, A.11
Smallwood, P.12
Li, Y.13
Anderson, K.L.14
Lewis, R.A.15
Nathans, J.16
Leppert, M.17
Dean, M.18
Lupski, J.R.19
-
23
-
-
0031568891
-
A new locus for autosomal recessive retinitis pigmentosa (RP19) maps to 1p13-1p21
-
Martinez-Mir A, Bayes M, Vilageliu L, Grinberg D, Ayuso C, del Rio T, Garcia-Sandoval B, Bussaglia E, Baiget M, Gonzalez-Duarte R, Balcells S. A new locus for autosomal recessive retinitis pigmentosa (RP19) maps to 1p13-1p21. Genomics. 1997;40:142-146.
-
(1997)
Genomics
, vol.40
, pp. 142-146
-
-
Martinez-Mir, A.1
Bayes, M.2
Vilageliu, L.3
Grinberg, D.4
Ayuso, C.5
Del Rio, T.6
Garcia-Sandoval, B.7
Bussaglia, E.8
Baiget, M.9
Gonzalez-Duarte, R.10
Balcells, S.11
-
24
-
-
17644443114
-
Heterozygous MDR3 missense mutation associated with intrahepatic cholestasis of pregnancy: Evidence for a defect in protein trafficking
-
Dixon PH, Weerasekera N, Linton KJ, Donaldson O, Chambers J, Egginton E, Weaver J, Nelson-Piercy C, de Swiet M, Warnes G, Elias E, Higgins CF, Johnston DG, McCarthy MI, Williamson C. Heterozygous MDR3 missense mutation associated with intrahepatic cholestasis of pregnancy: evidence for a defect in protein trafficking. Hum Mol Genet. 2000;9:1209-1217.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1209-1217
-
-
Dixon, P.H.1
Weerasekera, N.2
Linton, K.J.3
Donaldson, O.4
Chambers, J.5
Egginton, E.6
Weaver, J.7
Nelson-Piercy, C.8
De Swiet, M.9
Warnes, G.10
Elias, E.11
Higgins, C.F.12
Johnston, D.G.13
McCarthy, M.I.14
Williamson, C.15
-
25
-
-
0032920837
-
Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A)
-
Allikmets R, Raskind WH, Hutchinson A, Schueck ND, Dean M, Koeller DM. Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A). Hum Mol Genet. 1999;8:743-749.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 743-749
-
-
Allikmets, R.1
Raskind, W.H.2
Hutchinson, A.3
Schueck, N.D.4
Dean, M.5
Koeller, D.M.6
-
26
-
-
17344366172
-
A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis
-
Strautnieks SS, Bull LN, Knisely AS, Kocoshis SA, Dahl N, Arnell H, Sokal E, Dahan K, Childs S, Ling V, Tanner MS, Kagalwalla AF, Nemeth A, Pawlowska J, Baker A, Mieli-Vergani G, Freimer NB, Gardiner RM, Thompson RJ. A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis. Nat Genet. 1998;20:233-238.
-
(1998)
Nat Genet
, vol.20
, pp. 233-238
-
-
Strautnieks, S.S.1
Bull, L.N.2
Knisely, A.S.3
Kocoshis, S.A.4
Dahl, N.5
Arnell, H.6
Sokal, E.7
Dahan, K.8
Childs, S.9
Ling, V.10
Tanner, M.S.11
Kagalwalla, A.F.12
Nemeth, A.13
Pawlowska, J.14
Baker, A.15
Mieli-Vergani, G.16
Freimer, N.B.17
Gardiner, R.M.18
Thompson, R.J.19
-
27
-
-
0032711405
-
Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis
-
Jansen PL, Strautnieks SS, Jacquemin E, Hadchouel M, Sokal EM, Hooiveld GJ, Koning JH, Jager-Krikken A, Kuipers F, Stellaard F, Bijleveld CM, Gouw A, Van Goor H, Thompson RJ, Muller M. Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis. Gastroenterology. 1999;117:1370-1379.
-
(1999)
Gastroenterology
, vol.117
, pp. 1370-1379
-
-
Jansen, P.L.1
Strautnieks, S.S.2
Jacquemin, E.3
Hadchouel, M.4
Sokal, E.M.5
Hooiveld, G.J.6
Koning, J.H.7
Jager-Krikken, A.8
Kuipers, F.9
Stellaard, F.10
Bijleveld, C.M.11
Gouw, A.12
Van Goor, H.13
Thompson, R.J.14
Muller, M.15
-
28
-
-
0036790453
-
The role of bile salt export pump mutations in progressive familial intrahepatic cholestasis type II
-
Wang L, Soroka CJ, Boyer JL. The role of bile salt export pump mutations in progressive familial intrahepatic cholestasis type II. J Clin Invest. 2002;110:965-972.
-
(2002)
J Clin Invest
, vol.110
, pp. 965-972
-
-
Wang, L.1
Soroka, C.J.2
Boyer, J.L.3
-
29
-
-
0034123093
-
Mutations in ABCC6 cause pseudoxanthoma elasticum
-
Bergen AA, Plomp AS, Schuurman EJ, Terry S, Breuning M, Dauwerse H, Swart J, Kool M, van Soest S, Baas F, ten Brink JB, de Jong PT. Mutations in ABCC6 cause pseudoxanthoma elasticum. Nat Genet. 2000;25:228-231.
-
(2000)
Nat Genet
, vol.25
, pp. 228-231
-
-
Bergen, A.A.1
Plomp, A.S.2
Schuurman, E.J.3
Terry, S.4
Breuning, M.5
Dauwerse, H.6
Swart, J.7
Kool, M.8
Van Soest, S.9
Baas, F.10
Ten Brink, J.B.11
De Jong, P.T.12
-
30
-
-
0030016913
-
Adenosine diphosphate as an intracellular regulator of insulin secretion
-
Nichols CG, Shyng SL, Nestorowicz A, Glaser B, Clement JP, Gonzalez G, Aguilar-Bryan L, Permutt MA, Bryan J. Adenosine diphosphate as an intracellular regulator of insulin secretion. Science. 1996;272:1785-1787.
-
(1996)
Science
, vol.272
, pp. 1785-1787
-
-
Nichols, C.G.1
Shyng, S.L.2
Nestorowicz, A.3
Glaser, B.4
Clement, J.P.5
Gonzalez, G.6
Aguilar-Bryan, L.7
Permutt, M.A.8
Bryan, J.9
-
31
-
-
0032893407
-
X-linked adrenoleukodystrophy: Genes, mutations, and phenotypes
-
Smith KD, Kemp S, Braiterman LT, Lu JF, Wei HM, Geraghty M, Stetten G, Bergin JS, Pevsner J, Watkins PA. X-linked adrenoleukodystrophy: genes, mutations, and phenotypes. Neurochem Res. 1999;24:521-535.
-
(1999)
Neurochem Res
, vol.24
, pp. 521-535
-
-
Smith, K.D.1
Kemp, S.2
Braiterman, L.T.3
Lu, J.F.4
Wei, H.M.5
Geraghty, M.6
Stetten, G.7
Bergin, J.S.8
Pevsner, J.9
Watkins, P.A.10
-
32
-
-
0030994468
-
A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome
-
Paulusma CC, Kool M, Bosma PJ, Scheffer GL, ter Borg F, Scheper RJ, Tytgat GN, Borst P, Baas F, Oude Elferink RP. A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome. Hepatology. 1997;25:1539-1542.
-
(1997)
Hepatology
, vol.25
, pp. 1539-1542
-
-
Paulusma, C.C.1
Kool, M.2
Bosma, P.J.3
Scheffer, G.L.4
Ter Borg, F.5
Scheper, R.J.6
Tytgat, G.N.7
Borst, P.8
Baas, F.9
Oude Elferink, R.P.10
-
33
-
-
0024424270
-
Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA
-
Riordan JR, Rommens JM, Kerem B, Alon N, Rozmahel R, Grzelczak Z, Zielenski J, Lok S, Plavsic N, Chou JL, Drumm ML, Iannuzzi MC, Collins FC, Tsui LC. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science. 1989;245:1066-1073.
-
(1989)
Science
, vol.245
, pp. 1066-1073
-
-
Riordan, J.R.1
Rommens, J.M.2
Kerem, B.3
Alon, N.4
Rozmahel, R.5
Grzelczak, Z.6
Zielenski, J.7
Lok, S.8
Plavsic, N.9
Chou, J.L.10
Drumm, M.L.11
Iannuzzi, M.C.12
Collins, F.C.13
Tsui, L.C.14
-
34
-
-
0024423668
-
Identification of the cystic fibrosis gene: Genetic analysis
-
Kerem B, Rommens JM, Buchanan JA, Markiewicz D, Cox TK, Chakravarti A, Buchwald M, Tsui LC. Identification of the cystic fibrosis gene: genetic analysis. Science. 1989;245:1073-1080.
-
(1989)
Science
, vol.245
, pp. 1073-1080
-
-
Kerem, B.1
Rommens, J.M.2
Buchanan, J.A.3
Markiewicz, D.4
Cox, T.K.5
Chakravarti, A.6
Buchwald, M.7
Tsui, L.C.8
-
35
-
-
17744390348
-
Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters
-
Berge KE, Tian H, Graf GA, Yu L, Grishin NV, Schultz J, Kwiterovich P, Shan B, Barnes R, Hobbs HH. Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters. Science. 2000;290:1771-1775.
-
(2000)
Science
, vol.290
, pp. 1771-1775
-
-
Berge, K.E.1
Tian, H.2
Graf, G.A.3
Yu, L.4
Grishin, N.V.5
Schultz, J.6
Kwiterovich, P.7
Shan, B.8
Barnes, R.9
Hobbs, H.H.10
-
37
-
-
0037225279
-
Characterization of the ABCA transporter subfamily: Identification of prokaryotic and eukaryotic members, phylogeny and topology
-
Peelman F, Labeur C, Vanloo B, Roosbeek S, Devaud C, Duverger N, Denefle P, Rosier M, Vandekerckhove J, Rosseneu M. Characterization of the ABCA transporter subfamily: identification of prokaryotic and eukaryotic members, phylogeny and topology. J Mol Biol. 2003;325:259-274.
-
(2003)
J Mol Biol
, vol.325
, pp. 259-274
-
-
Peelman, F.1
Labeur, C.2
Vanloo, B.3
Roosbeek, S.4
Devaud, C.5
Duverger, N.6
Denefle, P.7
Rosier, M.8
Vandekerckhove, J.9
Rosseneu, M.10
-
38
-
-
0036827972
-
Lack of association between increased carotid intima-media thickening and decreased HDL-cholesterol in a family with a novel ABCA1 variant, G2265T
-
Hong SH, Riley W, Rhyne J, Friel G, Miller M. Lack of association between increased carotid intima-media thickening and decreased HDL-cholesterol in a family with a novel ABCA1 variant, G2265T. Clin Chem. 2002;48:2066-2070.
-
(2002)
Clin Chem
, vol.48
, pp. 2066-2070
-
-
Hong, S.H.1
Riley, W.2
Rhyne, J.3
Friel, G.4
Miller, M.5
-
39
-
-
0032813660
-
Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1
-
Rust S, Rosier M, Funke H, Amoura Z, Piette J-C, Deleuze J-F, Brewer HB Jr, Duverger N, Denèfle P, Assmann G. Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1. Nat Genet. 1999;22:352-355.
-
(1999)
Nat Genet
, vol.22
, pp. 352-355
-
-
Rust, S.1
Rosier, M.2
Funke, H.3
Amoura, Z.4
Piette, J.-C.5
Deleuze, J.-F.6
Brewer H.B., Jr.7
Duverger, N.8
Denèfle, P.9
Assmann, G.10
-
40
-
-
0032813809
-
The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease
-
Bodzioch M, Orsó E, Klucken J, Langmann T, Böttcher A, Diederich W, Drobnik W, Barlage S, Büchler C, Porsch-Özcürümez M, Kaminski WE, Hahmann HW, Oette K, Rothe G, Aslanidis C, Lackner KJ, Schmitz G. The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease. Nat Genet. 1999;22:347-351.
-
(1999)
Nat Genet
, vol.22
, pp. 347-351
-
-
Bodzioch, M.1
Orsó, E.2
Klucken, J.3
Langmann, T.4
Böttcher, A.5
Diederich, W.6
Drobnik, W.7
Barlage, S.8
Büchler, C.9
Porsch-Özcürümez, 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
-
41
-
-
0033903231
-
Common and rare ABCA1 variants affecting plasma HDL cholesterol
-
Wang J, Burnett JR, Near S, Young K, Zinman B, Hanley AJ, Connelly PW, Harris SB, Hegele RA. Common and rare ABCA1 variants affecting plasma HDL cholesterol. Arterioscler Thromb Vasc Biol. 2000;20:1983-1989.
-
(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.6
Connelly, P.W.7
Harris, S.B.8
Hegele, R.A.9
-
42
-
-
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 KK, Matsuyama A, Ohama T, Matsuura F, Ishigami M, Sakai N, Hiraoka H, Hattori H, Wellington C, Yoshida Y, Misugi S, Hayden MR, 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. 2002;290:713-721.
-
(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, K.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..
-
43
-
-
19244377100
-
Novel mutations in the gene encoding ATP-binding cassette 1 in four Tangier disease kindreds
-
Brousseau ME, Shaefer EJ, Dupuis J, Eustace B, Van Eerdewegh P, Goldkamp AL, Thurston LM, FitzGerald MG, Yasek-McKenna D, O'Neill G, Eberhart GP, Weiffenbach B, Ordovas JM, Freeman MW, Brown RH Jr, Gu JZ. Novel mutations in the gene encoding ATP-binding cassette 1 in four Tangier disease kindreds. J Lipid Res. 2000;41:433-441.
-
(2000)
J Lipid Res
, vol.41
, pp. 433-441
-
-
Brousseau, M.E.1
Shaefer, E.J.2
Dupuis, J.3
Eustace, B.4
Van Eerdewegh, P.5
Goldkamp, A.L.6
Thurston, L.M.7
FitzGerald, M.G.8
Yasek-McKenna, D.9
O'Neill, G.10
Eberhart, G.P.11
Weiffenbach, B.12
Ordovas, J.M.13
Freeman, M.W.14
Brown R.H., Jr.15
Gu, J.Z.16
-
44
-
-
0032725185
-
The Tangier disease gene product ABC1 controls the cellular apolipoprotein-mediated lipid removal pathway
-
Lawn RM, Wade DP, Garvin MR, Wang X, Schwartz K, Porter JG, Seilhamer JJ, Vaughan AM, Oram JF. The Tangier disease gene product ABC1 controls the cellular apolipoprotein-mediated lipid removal pathway. J Clin Invest. 1999;104:R25-R31.
-
(1999)
J Clin Invest
, vol.104
-
-
Lawn, R.M.1
Wade, D.P.2
Garvin, M.R.3
Wang, X.4
Schwartz, K.5
Porter, J.G.6
Seilhamer, J.J.7
Vaughan, A.M.8
Oram, J.F.9
-
45
-
-
0035958629
-
Homogeneous assay based on 52 primer sets to scan for mutations of the ABCA1 gene and its application in genetic analysis of a new patient with familial high-density lipoprotein deficiency syndrome
-
Lapicka-Bodzioch K, Bodzioch M, Krull M, Kielar D, Probst M, Kiec B, Andrikovics H, Bottcher A, Hubacek J, Aslanidis C, Suttorp N, Schmitz G. Homogeneous assay based on 52 primer sets to scan for mutations of the ABCA1 gene and its application in genetic analysis of a new patient with familial high-density lipoprotein deficiency syndrome. Biochim Biophys Acta. 2001;1537:42-48.
-
(2001)
Biochim Biophys Acta
, vol.1537
, pp. 42-48
-
-
Lapicka-Bodzioch, K.1
Bodzioch, M.2
Krull, M.3
Kielar, D.4
Probst, M.5
Kiec, B.6
Andrikovics, H.7
Bottcher, A.8
Hubacek, J.9
Aslanidis, C.10
Suttorp, N.11
Schmitz, G.12
-
46
-
-
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 S, Mawatari K, Imamura T, Eto T, Kawamura 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. Biochim Biophys Acta. 2001;1537:71-78.
-
(2001)
Biochim Biophys Acta
, vol.1537
, pp. 71-78
-
-
Huang, W.1
Moriyama, K.2
Koga, T.3
Hua, H.4
Ageta, M.5
Kawabata, S.6
Mawatari, K.7
Imamura, T.8
Eto, T.9
Kawamura, M.10
Teramoto, T.11
Sasaki, J.12
-
47
-
-
0036299871
-
Clinical variant of Tangier disease in Japan: Mutation of the ABCA1 gene in hypoalphalipoproteinemia with corneal lipidosis
-
Ishii J, Nagano M, Kujiraoka T, Ishihara M, Egashira T, Takada D, Tsuji M, Hattori H, Emi M. Clinical variant of Tangier disease in Japan: mutation of the ABCA1 gene in hypoalphalipoproteinemia with corneal lipidosis. J Hum Genet. 2002;47:366-369.
-
(2002)
J Hum Genet
, vol.47
, pp. 366-369
-
-
Ishii, J.1
Nagano, M.2
Kujiraoka, T.3
Ishihara, M.4
Egashira, T.5
Takada, D.6
Tsuji, M.7
Hattori, H.8
Emi, M.9
-
48
-
-
10744222201
-
Abnormal splicing of ABCA1 pre-mRNA in Tangier disease due to a IVS2 + 5G>C mutation in ABCA1 gene
-
Altilia S, Pisciotta L, Garuti R, Tarugi P, Cantafora A, Calabresi L, Tagliabue J, Maccari S, Bernini F, Zanotti I, Vergani C, Bertolini S, Calandra S. Abnormal splicing of ABCA1 pre-mRNA in Tangier disease due to a IVS2 + 5G>C mutation in ABCA1 gene. J Lipid Res. 2003;44:254-264.
-
(2003)
J Lipid Res
, vol.44
, pp. 254-264
-
-
Altilia, S.1
Pisciotta, L.2
Garuti, R.3
Tarugi, P.4
Cantafora, A.5
Calabresi, L.6
Tagliabue, J.7
Maccari, S.8
Bernini, F.9
Zanotti, I.10
Vergani, C.11
Bertolini, S.12
Calandra, S.13
-
49
-
-
0035987005
-
Double deletions and missense mutations in the first nucleotide-binding fold of the ATP-binding cassette transporter A1 (ABCA1) gene in Japanese patients with Tangier disease
-
Guo Z, Inazu A, Yu W, Suzumura T, Okamoto M, Nohara A, Higashikata T, Sano R, Wakasugi K, Hayakawa T, Yoshida K, Suehiro T, Schmitz G, Mabuchi H. Double deletions and missense mutations in the first nucleotide-binding fold of the ATP-binding cassette transporter A1 (ABCA1) gene in Japanese patients with Tangier disease. J Hum Genet. 2002;47:325-329.
-
(2002)
J Hum Genet
, vol.47
, pp. 325-329
-
-
Guo, Z.1
Inazu, A.2
Yu, W.3
Suzumura, T.4
Okamoto, M.5
Nohara, A.6
Higashikata, T.7
Sano, R.8
Wakasugi, K.9
Hayakawa, T.10
Yoshida, K.11
Suehiro, T.12
Schmitz, G.13
Mabuchi, H.14
-
50
-
-
0035864640
-
A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease
-
Bertolini S, Pisciotta L, Seri M, Cusano R, Cantafora A, Calabresi L, Franceschini G, Ravazzolo R, Calandra S. A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease. Atherosclerosis. 2001;154:599-605.
-
(2001)
Atherosclerosis
, vol.154
, pp. 599-605
-
-
Bertolini, S.1
Pisciotta, L.2
Seri, M.3
Cusano, R.4
Cantafora, A.5
Calabresi, L.6
Franceschini, G.7
Ravazzolo, R.8
Calandra, S.9
-
51
-
-
0037150282
-
Novel ABCA1 compound variant associated with HDL cholesterol deficiency
-
Hong SH, Rhyne J, Zeller K, Miller M. Novel ABCA1 compound variant associated with HDL cholesterol deficiency. Biochim Biophys Acta. 2002;1587:60-64.
-
(2002)
Biochim Biophys Acta
, vol.1587
, pp. 60-64
-
-
Hong, S.H.1
Rhyne, J.2
Zeller, K.3
Miller, M.4
-
52
-
-
0036801569
-
ABCA1(Alabama): A novel variant associated with HDL deficiency and premature coronary artery disease
-
Hong SH, Rhyne J, Zeller K, Miller M. ABCA1(Alabama): a novel variant associated with HDL deficiency and premature coronary artery disease. Atherosclerosis. 2002;164:245-250.
-
(2002)
Atherosclerosis
, vol.164
, pp. 245-250
-
-
Hong, S.H.1
Rhyne, J.2
Zeller, K.3
Miller, M.4
-
53
-
-
0342811295
-
Human ATP-binding cassette transporter 1 (ABC1): Genomic organization and identification of the genetic defect in the original Tangier disease kindred
-
Remaley AT, Rust S, Rosier M, Knapper C, Naudin L, Broccardo C, Peterson KM, Koch C, Arnould I, Prades C, Duverger N, Funke H, Assman G, Dinger M, Dean M, Chimini G, Santamarina-Fojo S, Fredrickson DS, Denefle P, Brewer HB Jr. Human ATP-binding cassette transporter 1 (ABC1): genomic organization and identification of the genetic defect in the original Tangier disease kindred. Proc Natl Acad Sci U S A. 1999;96:12685-12690.
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 12685-12690
-
-
Remaley, A.T.1
Rust, S.2
Rosier, M.3
Knapper, C.4
Naudin, L.5
Broccardo, C.6
Peterson, K.M.7
Koch, C.8
Arnould, I.9
Prades, C.10
Duverger, N.11
Funke, H.12
Assman, G.13
Dinger, M.14
Dean, M.15
Chimini, G.16
Santamarina-Fojo, S.17
Fredrickson, D.S.18
Denefle, P.19
Brewer H.B., Jr.20
more..
-
54
-
-
0035024968
-
Subpopulations of high density lipoproteins in homozygous and heterozygous Tangier disease
-
Asztalos BF, Brousseau ME, McNamara JR, Horvath KV, Roheim PS, Schaefer EJ. Subpopulations of high density lipoproteins in homozygous and heterozygous Tangier disease. Atherosclerosis. 2001;156:217-225.
-
(2001)
Atherosclerosis
, vol.156
, pp. 217-225
-
-
Asztalos, B.F.1
Brousseau, M.E.2
McNamara, J.R.3
Horvath, K.V.4
Roheim, P.S.5
Schaefer, E.J.6
-
55
-
-
0032509180
-
Caenorhabditis elegans is a nematode
-
Blaxter M. Caenorhabditis elegans is a nematode. Science. 1998;282:2041-2046.
-
(1998)
Science
, vol.282
, pp. 2041-2046
-
-
Blaxter, M.1
-
56
-
-
0030696044
-
Determining divergence times with a protein clock: Update and reevaluation
-
Feng DF, Cho G, Doolittle RF. Determining divergence times with a protein clock: update and reevaluation. Proc Natl Acad Sci U S A. 1997;94:13028-13033.
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 13028-13033
-
-
Feng, D.F.1
Cho, G.2
Doolittle, R.F.3
-
57
-
-
0035968213
-
Membrane topology of the ATP binding cassette transporter ABCR and its relationship to ABC1 and related ABCA transporters: Identification of N-linked glycosylation sites
-
Bungert S, Molday LL, Molday RS. Membrane topology of the ATP binding cassette transporter ABCR and its relationship to ABC1 and related ABCA transporters: identification of N-linked glycosylation sites. J Biol Chem. 2001;276:23539-23546.
-
(2001)
J Biol Chem
, vol.276
, pp. 23539-23546
-
-
Bungert, S.1
Molday, L.L.2
Molday, R.S.3
-
58
-
-
0037031835
-
Naturally occurring mutations in the largest extracellular loops of ABCA1 can disrupt its direct interaction with apolipoprotein A-1
-
Fitzgerald ML, Morris AL, Rhee JS, Andersson LP, Mendez AJ, Freeman MW. Naturally occurring mutations in the largest extracellular loops of ABCA1 can disrupt its direct interaction with apolipoprotein A-1. J Biol Chem. 2002;277:33178-33187.
-
(2002)
J Biol Chem
, vol.277
, pp. 33178-33187
-
-
Fitzgerald, M.L.1
Morris, A.L.2
Rhee, J.S.3
Andersson, L.P.4
Mendez, A.J.5
Freeman, M.W.6
-
59
-
-
0037424367
-
Effects of mutations of ABCA1 in the first extracellular domain on subcellular trafficking and ATP binding/ hydrolysis
-
Tanaka AR, Abe-Dohmae S, Ohnishi T, Aoki R, Morinaga G, Okuhira KI, Ikeda Y, Kano F, Matsuo M, Kioka N, Amachi T, Murata M, Yokoyama S, Ueda K. Effects of mutations of ABCA1 in the first extracellular domain on subcellular trafficking and ATP binding/ hydrolysis. J Biol Chem. 2002;278:8815-8819.
-
(2002)
J Biol Chem
, vol.278
, pp. 8815-8819
-
-
Tanaka, A.R.1
Abe-Dohmae, S.2
Ohnishi, T.3
Aoki, R.4
Morinaga, G.5
Okuhira, K.I.6
Ikeda, Y.7
Kano, F.8
Matsuo, M.9
Kioka, N.10
Amachi, T.11
Murata, M.12
Yokoyama, S.13
Ueda, K.14
-
60
-
-
0036906543
-
Distinct sites on ABCA1 control distinct steps required for cellular release of phospholipids
-
Rigot V, Hamon Y, Chambenoit O, Alibert M, Duverger N, Chimini G. Distinct sites on ABCA1 control distinct steps required for cellular release of phospholipids. J Lipid Res. 2002;43:2077-2086.
-
(2002)
J Lipid Res
, vol.43
, pp. 2077-2086
-
-
Rigot, V.1
Hamon, Y.2
Chambenoit, O.3
Alibert, M.4
Duverger, N.5
Chimini, G.6
-
61
-
-
0033775698
-
Biochemical defects in ABCR protein variants associated with human retinopathies
-
Sun, H Smallwood PM, Nathans J. Biochemical defects in ABCR protein variants associated with human retinopathies. Nat Genet. 2000;26:242-246.
-
(2000)
Nat Genet
, vol.26
, pp. 242-246
-
-
Sun, H.1
Smallwood, P.M.2
Nathans, J.3
-
62
-
-
0035902535
-
Nucleotide binding domain 1 of the human retinal ABC transporter functions as a general ribonucleotidase
-
Biswas EE. Nucleotide binding domain 1 of the human retinal ABC transporter functions as a general ribonucleotidase. Biochemistry. 2001;40:8181-8187.
-
(2001)
Biochemistry
, vol.40
, pp. 8181-8187
-
-
Biswas, E.E.1
-
63
-
-
0029113976
-
The first nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator can function as an active ATPase
-
Ko YH, Pedersen PL. The first nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator can function as an active ATPase. J Biol Chem. 1995;270:22093-22096.
-
(1995)
J Biol Chem
, vol.270
, pp. 22093-22096
-
-
Ko, Y.H.1
Pedersen, P.L.2
-
64
-
-
0030806301
-
A recombinant polypeptide model of the second nucleotide-binding fold of the cystic fibrosis transmembrane conductance regulator functions as an active ATPase, GTPase and adenylate kinase
-
Randak C, Neth P, Auerswald EA, Eckerskorn C, Assfalg-Machleidt I, Machleidt W. A recombinant polypeptide model of the second nucleotide-binding fold of the cystic fibrosis transmembrane conductance regulator functions as an active ATPase, GTPase and adenylate kinase. FEBS Lett. 1997;410:180-186.
-
(1997)
FEBS Lett
, vol.410
, pp. 180-186
-
-
Randak, C.1
Neth, P.2
Auerswald, E.A.3
Eckerskorn, C.4
Assfalg-Machleidt, I.5
Machleidt, W.6
-
65
-
-
0037423359
-
ATP binding, not hydrolysis, at the first nucleotide-binding domain of multidrug resistance-associated protein MRP1 enhances ADP: Vi trapping at the second domain
-
Hou YX, Riordan JR, Chang XB. ATP binding, not hydrolysis, at the first nucleotide-binding domain of multidrug resistance-associated protein MRP1 enhances ADP: Vi trapping at the second domain. J Biol Chem. 2003;278:3599-3605.
-
(2003)
J Biol Chem
, vol.278
, pp. 3599-3605
-
-
Hou, Y.X.1
Riordan, J.R.2
Chang, X.B.3
-
66
-
-
0037131297
-
PDZ domain interaction controls the endocytic recycling of the cystic fibrosis transmembrane conductance regulator
-
Swiatecka-Urban A, Duhaime M, Coutermarsh B, Karlson KH, Collawn J, Milewski M, Cutting GR, Guggino WB, Langford G, Stanton BA. PDZ domain interaction controls the endocytic recycling of the cystic fibrosis transmembrane conductance regulator. J Biol Chem. 2002;277:40099-40105.
-
(2002)
J Biol Chem
, vol.277
, pp. 40099-40105
-
-
Swiatecka-Urban, A.1
Duhaime, M.2
Coutermarsh, B.3
Karlson, K.H.4
Collawn, J.5
Milewski, M.6
Cutting, G.R.7
Guggino, W.B.8
Langford, G.9
Stanton, B.A.10
-
67
-
-
0032584744
-
An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton
-
Short, DB Trotter KW, Reczek D, Kreda SM, Bretscher A, Boucher RC, Stutts MJ, Milgram SL. An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton. J Biol Chem. 1998;273:19797-19801.
-
(1998)
J Biol Chem
, vol.273
, pp. 19797-19801
-
-
Short, D.B.1
Trotter, K.W.2
Reczek, D.3
Kreda, S.M.4
Bretscher, A.5
Boucher, R.C.6
Stutts, M.J.7
Milgram, S.L.8
-
68
-
-
0036297101
-
The carboxyterminus of the ATP-binding cassette transporter A1 interacts with a beta2-syntrophin/utrophin complex
-
Buechler C, Boettcher A, Bared SM, Probst MC, Schmitz G. The carboxyterminus of the ATP-binding cassette transporter A1 interacts with a beta2-syntrophin/utrophin complex. Biochem Biophys Res Commun. 2002;293:759-765.
-
(2002)
Biochem Biophys Res Commun
, vol.293
, pp. 759-765
-
-
Buechler, C.1
Boettcher, A.2
Bared, S.M.3
Probst, M.C.4
Schmitz, G.5
-
69
-
-
0036846003
-
Truncation mutations in ABCA1 suppress normal upregulation of full-length ABCA1 by 9-cis-retinoic acid and 22-R-hydroxycholesterol
-
Wellington CL, Yang YZ, Zhou S, Clee SM, Tan B, Hirano K, Zwarts K, Kwok A, Gelfer A, Marcil M, Newman S, Roomp K, Singaraja R, Collins J, Zhang LH, Groen AK, Hovingh K, Brownlie A, Tafuri S, Genest J Jr., Kastelein JJ, Hayden MR. Truncation mutations in ABCA1 suppress normal upregulation of full-length ABCA1 by 9-cis-retinoic acid and 22-R-hydroxycholesterol. J Lipid Res. 2002;43:1939-1949.
-
(2002)
J Lipid Res
, vol.43
, pp. 1939-1949
-
-
Wellington, C.L.1
Yang, Y.Z.2
Zhou, S.3
Clee, S.M.4
Tan, B.5
Hirano, K.6
Zwarts, K.7
Kwok, A.8
Gelfer, A.9
Marcil, M.10
Newman, S.11
Roomp, K.12
Singaraja, R.13
Collins, J.14
Zhang, L.H.15
Groen, A.K.16
Hovingh, K.17
Brownlie, A.18
Tafuri, S.19
Genest J., Jr.20
Kastelein, J.J.21
Hayden, M.R.22
more..
-
70
-
-
0033692757
-
Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 hererozygotes
-
Clee SM, Kastelein JJ, van Dam M, Marcil M, Roomp K, Zwarts KY, Collins JA, Roelants R, Tamasawa N, Stulc T, Suda T, Ceska R, Boucher B, Rondeau C, DeSouich C, Brooks-Wilson A, Molhuizen HO, Frohlich J, Genest J Jr, Hayden MR. Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 hererozygotes. J Clin Invest. 2000;106:1263-1270.
-
(2000)
J Clin Invest
, vol.106
, pp. 1263-1270
-
-
Clee, S.M.1
Kastelein, J.J.2
Van Dam, M.3
Marcil, M.4
Roomp, K.5
Zwarts, K.Y.6
Collins, J.A.7
Roelants, R.8
Tamasawa, N.9
Stulc, T.10
Suda, T.11
Ceska, R.12
Boucher, B.13
Rondeau, C.14
DeSouich, C.15
Brooks-Wilson, A.16
Molhuizen, H.O.17
Frohlich, J.18
Genest J., Jr.19
Hayden, M.R.20
more..
-
71
-
-
0017690994
-
Characterization of high density lipoproteins in patients heterozygous, for Tangier disease
-
Assmann G, Simantke O, Schaefer HE, Smootz E. Characterization of high density lipoproteins in patients heterozygous, for Tangier disease. J Clin Invest. 1977;60:1025-1035.
-
(1977)
J Clin Invest
, vol.60
, pp. 1025-1035
-
-
Assmann, G.1
Simantke, O.2
Schaefer, H.E.3
Smootz, E.4
-
72
-
-
0018953911
-
Coronary heart disease prevalence and other clinical features in familial high-density lipoprotein deficiency (Tangier disease)
-
Schaefer EJ, Zech LA, Schwartz DE, Brewer HB Jr. Coronary heart disease prevalence and other clinical features in familial high-density lipoprotein deficiency (Tangier disease). Ann Intern Med. 1980;93:261-266.
-
(1980)
Ann Intern Med
, vol.93
, pp. 261-266
-
-
Schaefer, E.J.1
Zech, L.A.2
Schwartz, D.E.3
Brewer H.B., Jr.4
-
73
-
-
0037022001
-
Association between in creased arterial-wall thickness and impairment in ABCA1-driven cholesterol efflux: An observational study
-
van Dam MJ, de Groot E, Clee SM, Hovingh GK, Roelants R, Brooks-Wilson A, Zwinderman AH, Smit AJ, Smelt AH, Groen AK, Hayden MR, Kastelein JJ. Association between in creased arterial-wall thickness and impairment in ABCA1-driven cholesterol efflux: an observational study. Lancet. 2002;359:37-42.
-
(2002)
Lancet
, vol.359
, pp. 37-42
-
-
Van Dam, M.J.1
De Groot, E.2
Clee, S.M.3
Hovingh, G.K.4
Roelants, R.5
Brooks-Wilson, A.6
Zwinderman, A.H.7
Smit, A.J.8
Smelt, A.H.9
Groen, A.K.10
Hayden, M.R.11
Kastelein, J.J.12
-
74
-
-
0042945903
-
Restoration of endothelial function by increasing high-density lipoprotein in subjects with isolated low high-density lipoprotein
-
Bisoendial RJ, Hovingh GK, Levels JHM, Lerch PG, Andresen I, Hayden MR, Kastelein JJP, Stroes ESG. Restoration of endothelial function by increasing high-density lipoprotein in subjects with isolated low high-density lipoprotein. Circulation. 2003;10:12944-2948.
-
(2003)
Circulation
, vol.10
, pp. 12944-12948
-
-
Bisoendial, R.J.1
Hovingh, G.K.2
Levels, J.H.M.3
Lerch, P.G.4
Andresen, I.5
Hayden, M.R.6
Kastelein, J.J.P.7
Stroes, E.S.G.8
-
75
-
-
0035814958
-
Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease
-
Clee SM, Zwinderman AH, Engert JC, Zwarts KY, Molhuizen HO, Roomp K, Jukema JW, van Wijland M, van Dam M, Hudson TJ, Brooks-Wilson A, Genest J Jr Kastelein JJ, Hayden MR. Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease. Circulation. 2001;103:1198-1205.
-
(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.5
Roomp, K.6
Jukema, J.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.13
Hayden, M.R.14
-
76
-
-
0035843968
-
Novel polymorphisms 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 CM, Elghannam H, Gotto AM Jr, Marian AJ. Novel polymorphisms 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. 2001;88:969-973.
-
(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
-
77
-
-
0035864677
-
Common variants in the gene encoding ATP-binding cassette transporter 1 in men with low HDL cholesterol levels and coronary heart disease
-
Brousseau ME, Bodzioch M, Schaefer EJ, Goldkamp AL, Kielar D, Probst M, Ordovas JM, Aslanidis C, Lackner KJ, Rubins HB, Collins D, Robins SJ, Wilson PWF, Schmitz G. Common variants in the gene encoding ATP-binding cassette transporter 1 in men with low HDL cholesterol levels and coronary heart disease. Atherosclerosis. 2001;154:607-611.
-
(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
Schmitz, G.14
-
78
-
-
0036488074
-
ABCA1 regulatory variants influence coronary artery disease independent of effects on plasma lipid levels
-
Zwarts KY, Clee SM, Zwinderman AH, Engert JC, Singaraja R, Loubser O, James E, Roomp K, Hudson TJ, Jukema JW, Kastelein JJ, Hayden MR. ABCA1 regulatory variants influence coronary artery disease independent of effects on plasma lipid levels. Clin Genet. 2002;61:115-125.
-
(2002)
Clin Genet
, vol.61
, pp. 115-125
-
-
Zwarts, K.Y.1
Clee, S.M.2
Zwinderman, A.H.3
Engert, J.C.4
Singaraja, R.5
Loubser, O.6
James, E.7
Roomp, K.8
Hudson, T.J.9
Jukema, J.W.10
Kastelein, J.J.11
Hayden, M.R.12
-
79
-
-
0036335408
-
Relationship between ABCA1 genetic variation and HDL cholesterol level in subjects with ischemic heart diseases 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 diseases in Japanese. Thromb Haemost. 2002;88:369-370.
-
(2002)
Thromb Haemost
, vol.88
, pp. 369-370
-
-
Takagi, S.1
Iwai, N.2
Miyazaki, S.3
Nonogi, H.4
Goto, Y.5
-
80
-
-
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. 2001;46:522-528.
-
(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
-
81
-
-
25744474712
-
A common promoter haplotype of ABCA1 gene reduces promoter activity, alters transcriptional factors binding and is associated with progression of coronary atherosclerosis
-
Abstract
-
Lutucuta S, Ballantyne CM, Gotto AM, Marian AJ. A common promoter haplotype of ABCA1 gene reduces promoter activity, alters transcriptional factors binding and is associated with progression of coronary atherosclerosis. Circulation. 2002;106:II-168-II-168. Abstract.
-
(2002)
Circulation
, vol.106
-
-
Lutucuta, S.1
Ballantyne, C.M.2
Gotto, A.M.3
Marian, A.J.4
-
82
-
-
0038583684
-
The association of the R219K polymorphism in the ATP-binding cassette transporter 1 (ABCA1) gene with coronary artery disease and hyperlipidemia
-
Evans D, Beil F-U. The association of the R219K polymorphism in the ATP-binding cassette transporter 1 (ABCA1) gene with coronary artery disease and hyperlipidemia. J Mol Med. 2003;81:264-270.
-
(2003)
J Mol Med
, vol.81
, pp. 264-270
-
-
Evans, D.1
Beil, F.-U.2
-
83
-
-
0037298521
-
ATP-binding cassette transporter A1 locus is not a major determinant of HDL-C levels in a population at high risk for coronary heart disease
-
Kakko S, Kelloniemi J, Kelloniemi J, von Rohr P, Hoeschele I, Tamminen M, Brousseau ME, Kesaniemi YA, Savolainen MJ, ATP-binding cassette transporter A1 locus is not a major determinant of HDL-C levels in a population at high risk for coronary heart disease. Atherosclerosis. 2003;166:285-290.
-
(2003)
Atherosclerosis
, vol.166
, pp. 285-290
-
-
Kakko, S.1
Kelloniemi, J.2
Kelloniemi, J.3
Von Rohr, P.4
Hoeschele, I.5
Tamminen, M.6
Brousseau, M.E.7
Kesaniemi, Y.A.8
Savolainen, M.J.9
-
84
-
-
0037337602
-
A common variant in the ABCA1 gene is associated with a lower risk for premature coronary heart disease in familial hypercholesterolaemia
-
Cenarro A, Artieda M, Castillo S, Mozas P, Reyes G, Tejedor D, Alonso R, Mata P, Pocovi M, Civeira F. A common variant in the ABCA1 gene is associated with a lower risk for premature coronary heart disease in familial hypercholesterolaemia. J Med Genet. 2003;40:163-168.
-
(2003)
J Med Genet
, vol.40
, pp. 163-168
-
-
Cenarro, A.1
Artieda, M.2
Castillo, S.3
Mozas, P.4
Reyes, G.5
Tejedor, D.6
Alonso, R.7
Mata, P.8
Pocovi, M.9
Civeira, F.10
-
85
-
-
0036120566
-
Increased atherosclerosis in hyperlipidemic mice with inactivation of ABCA1 in macrophages
-
Aiello RJ, Brees D, Bourassa PA, Royer L, Lindsey S, Coskran T, Haghpassand M, Francone OL. Increased atherosclerosis in hyperlipidemic mice with inactivation of ABCA1 in macrophages. Arterioscler Thromb Vasc Biol. 2002;22:630-637.
-
(2002)
Arterioscler Thromb Vasc Biol
, vol.22
, pp. 630-637
-
-
Aiello, R.J.1
Brees, D.2
Bourassa, P.A.3
Royer, L.4
Lindsey, S.5
Coskran, T.6
Haghpassand, M.7
Francone, O.L.8
-
86
-
-
0035191911
-
Monocyte/macrophage expression of ABCA1 has minimal contribution to plasma HDL levels
-
Haghpassand M, Bourassa PA, Francone OL, Aiello RJ. Monocyte/macrophage expression of ABCA1 has minimal contribution to plasma HDL levels. J Clin Invest. 2001;108:1315-1320.
-
(2001)
J Clin Invest
, vol.108
, pp. 1315-1320
-
-
Haghpassand, M.1
Bourassa, P.A.2
Francone, O.L.3
Aiello, R.J.4
-
87
-
-
0035823531
-
Human ABCA1 BAC transgenic mice show increased high density lipoprotein cholesterol and ApoA1-dependent efflux stimulated by an internal promoter containing liver X receptor response elements in intron 1
-
Singaraja RR, Bocher V, James ER, Clee SM, Zhang LH, Leavitt BR, Tan B, Brooks-Wilson A, Kwok A, Bissada N, Yang YZ, Liu G, Tafuri SR, Fievet C, Wellington CL, Staels B, Hayden MR. Human ABCA1 BAC transgenic mice show increased high density lipoprotein cholesterol and ApoA1-dependent efflux stimulated by an internal promoter containing liver X receptor response elements in intron 1. J Biol Chem. 2001;276:33969-33979.
-
(2001)
J Biol Chem
, vol.276
, pp. 33969-33979
-
-
Singaraja, R.R.1
Bocher, V.2
James, E.R.3
Clee, S.M.4
Zhang, L.H.5
Leavitt, B.R.6
Tan, B.7
Brooks-Wilson, A.8
Kwok, A.9
Bissada, N.10
Yang, Y.Z.11
Liu, G.12
Tafuri, S.R.13
Fievet, C.14
Wellington, C.L.15
Staels, B.16
Hayden, M.R.17
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