-
1
-
-
0033560938
-
Triglyceride enrichment of HDL enhances in vivo metabolic clearance of HDL apo A-I in healthy men
-
Lamarche B., Uffelman K.D., Carpentier A., et al. Triglyceride enrichment of HDL enhances in vivo metabolic clearance of HDL apo A-I in healthy men. J Clin Invest 1999, 103:1191-1199.
-
(1999)
J Clin Invest
, vol.103
, pp. 1191-1199
-
-
Lamarche, B.1
Uffelman, K.D.2
Carpentier, A.3
-
2
-
-
0018126248
-
Cholesteryl ester exchange protein in human plasma isolation and characterization
-
Pattnaik N.M., Montes A., Hughes L.B., Zilversmit D.B. Cholesteryl ester exchange protein in human plasma isolation and characterization. Biochim Biophys Acta 1978, 530:428-438.
-
(1978)
Biochim Biophys Acta
, vol.530
, pp. 428-438
-
-
Pattnaik, N.M.1
Montes, A.2
Hughes, L.B.3
Zilversmit, D.B.4
-
3
-
-
33846989758
-
Crystal structure of cholesteryl ester transfer protein reveals a long tunnel and four bound lipid molecules
-
Qiu X., Mistry A., Ammirati M.J., et al. Crystal structure of cholesteryl ester transfer protein reveals a long tunnel and four bound lipid molecules. Nat Struct Mol Biol 2007, 14:106-113.
-
(2007)
Nat Struct Mol Biol
, vol.14
, pp. 106-113
-
-
Qiu, X.1
Mistry, A.2
Ammirati, M.J.3
-
4
-
-
0038241707
-
Genomic evidence for the absence of a functional cholesteryl ester transfer protein gene in mice and rats
-
Hogarth C.A., Roy A., Ebert D.L. Genomic evidence for the absence of a functional cholesteryl ester transfer protein gene in mice and rats. Physiology 2003, 135:71-81.
-
(2003)
Physiology
, vol.135
, pp. 71-81
-
-
Hogarth, C.A.1
Roy, A.2
Ebert, D.L.3
-
5
-
-
0020013576
-
Differences in plasma cholesteryl ester transfer activity in sixteen vertebrate species
-
Ha Y.C., Barter P.J. Differences in plasma cholesteryl ester transfer activity in sixteen vertebrate species. Comp Biochem Physiol B 1982, 71:265-269.
-
(1982)
Comp Biochem Physiol B
, vol.71
, pp. 265-269
-
-
Ha, Y.C.1
Barter, P.J.2
-
6
-
-
0022346576
-
Deficiency of serum cholesteryl-ester transfer activity in patients with familial hyperalphalipoproteinaemia
-
Koizumi J., Mabuchi H., Yoshimura A., et al. Deficiency of serum cholesteryl-ester transfer activity in patients with familial hyperalphalipoproteinaemia. Atherosclerosis 1985, 58:175-186.
-
(1985)
Atherosclerosis
, vol.58
, pp. 175-186
-
-
Koizumi, J.1
Mabuchi, H.2
Yoshimura, A.3
-
7
-
-
0025104275
-
Increased high-density lipoprotein levels caused by a common cholesteryl-ester transfer protein gene mutation
-
Inazu A., Brown M.L., Hesler C.B., et al. Increased high-density lipoprotein levels caused by a common cholesteryl-ester transfer protein gene mutation. N Engl J Med 1990, 323:1234-1238.
-
(1990)
N Engl J Med
, vol.323
, pp. 1234-1238
-
-
Inazu, A.1
Brown, M.L.2
Hesler, C.B.3
-
8
-
-
0027420629
-
A missense mutation in the cholesteryl ester transfer protein gene with possible dominant effects on plasma high density lipoproteins
-
Takahashi K., Jiang X.C., Sakai N., et al. A missense mutation in the cholesteryl ester transfer protein gene with possible dominant effects on plasma high density lipoproteins. J Clin Invest 1993, 92:2060-2064.
-
(1993)
J Clin Invest
, vol.92
, pp. 2060-2064
-
-
Takahashi, K.1
Jiang, X.C.2
Sakai, N.3
-
9
-
-
0028135441
-
Genetic cholesteryl ester transfer protein deficiency caused by two prevalent mutations as a major determinant of increased levels of high density lipoprotein cholesterol
-
Inazu A., Jiang X.C., Haraki T., et al. Genetic cholesteryl ester transfer protein deficiency caused by two prevalent mutations as a major determinant of increased levels of high density lipoprotein cholesterol. J Clin Invest 1994, 94:1872-1882.
-
(1994)
J Clin Invest
, vol.94
, pp. 1872-1882
-
-
Inazu, A.1
Jiang, X.C.2
Haraki, T.3
-
10
-
-
84856232921
-
Human cholesteryl ester transfer protein in human HDL metabolism
-
Springer, E.J. Schaefer (Ed.)
-
Mabuchi H., Inazu A. Human cholesteryl ester transfer protein in human HDL metabolism. High density lipoproteins, dyslipidemia, and coronary heart disease 2010, 95-101. Springer. E.J. Schaefer (Ed.).
-
(2010)
High density lipoproteins, dyslipidemia, and coronary heart disease
, pp. 95-101
-
-
Mabuchi, H.1
Inazu, A.2
-
11
-
-
84856208700
-
Plasma cholesteryl ester transfer protein (CETP) in relation to human pathophysiology
-
Biological functions and clinical implications, Elsevier B.V. T. Komoda (Ed.)
-
Inazu A. Plasma cholesteryl ester transfer protein (CETP) in relation to human pathophysiology. The HDL Handbook 2010, 35-60. Biological functions and clinical implications, Elsevier B.V. T. Komoda (Ed.).
-
(2010)
The HDL Handbook
, pp. 35-60
-
-
Inazu, A.1
-
12
-
-
0032559809
-
Enzyme immunoassay for cholesteryl ester transfer protein in human serum
-
Kiyohara T., Kiriyama R., Zamma S., et al. Enzyme immunoassay for cholesteryl ester transfer protein in human serum. Clin Chim Acta 1998, 271:109-118.
-
(1998)
Clin Chim Acta
, vol.271
, pp. 109-118
-
-
Kiyohara, T.1
Kiriyama, R.2
Zamma, S.3
-
13
-
-
34547591343
-
Primer3Plus, an enhanced web interface to Primer3
-
Web Server issue
-
Untergasser A., Nijveen H., Rao X., Bisseling T., Geurts R., Leunissen J.A.M. Primer3Plus, an enhanced web interface to Primer3. Nucleic Acids Res 2007, 35(Web Server issue):W71-W74.
-
(2007)
Nucleic Acids Res
, vol.35
-
-
Untergasser, A.1
Nijveen, H.2
Rao, X.3
Bisseling, T.4
Geurts, R.5
Leunissen, J.A.M.6
-
14
-
-
0025105228
-
Organization of the human cholesteryl ester transfer protein gene
-
Agellon L.B., Quinet E.M., Gillette T.G., Drayna D.T., Brown M.L., Tall A.R. Organization of the human cholesteryl ester transfer protein gene. Biochemistry 1990, 29:1372-1376.
-
(1990)
Biochemistry
, vol.29
, pp. 1372-1376
-
-
Agellon, L.B.1
Quinet, E.M.2
Gillette, T.G.3
Drayna, D.T.4
Brown, M.L.5
Tall, A.R.6
-
15
-
-
0027199766
-
Inhibition of the cellular secretion of cholesteryl ester transfer protein by a variant protein formed by alternative splicing of mRNA
-
Quinet E., Yang T.P., Marinos C., Tall A. Inhibition of the cellular secretion of cholesteryl ester transfer protein by a variant protein formed by alternative splicing of mRNA. J Biol Chem 1993, 268:16891-16894.
-
(1993)
J Biol Chem
, vol.268
, pp. 16891-16894
-
-
Quinet, E.1
Yang, T.P.2
Marinos, C.3
Tall, A.4
-
16
-
-
0026513630
-
Alternative splicing of the mRNA encoding the human cholesteryl ester transfer protein
-
Inazu A., Quinet E.M., Wang S., et al. Alternative splicing of the mRNA encoding the human cholesteryl ester transfer protein. Biochemistry 1992, 31:2352-2358.
-
(1992)
Biochemistry
, vol.31
, pp. 2352-2358
-
-
Inazu, A.1
Quinet, E.M.2
Wang, S.3
-
17
-
-
0029160083
-
A versatile vector for gene and oligonucleotide transfer into cells in culture and in vivo: polyethylenimine
-
Boussif O., Lezoualc'h F., Zanta M.A., et al. A versatile vector for gene and oligonucleotide transfer into cells in culture and in vivo: polyethylenimine. Proc Natl Acad Sci U S A 1995, 92:7297-7301.
-
(1995)
Proc Natl Acad Sci U S A
, vol.92
, pp. 7297-7301
-
-
Boussif, O.1
Lezoualc'h, F.2
Zanta, M.A.3
-
18
-
-
16944363594
-
Skipping of exon 14 and possible instability of both the mRNA and the resultant truncated protein underlie a common cholesteryl ester transfer protein deficiency in Japan
-
Gotoda T., Kinoshita M., Ishibashi S., et al. Skipping of exon 14 and possible instability of both the mRNA and the resultant truncated protein underlie a common cholesteryl ester transfer protein deficiency in Japan. Arterioscler Thromb Vasc Biol 1997, 17:1376-1381.
-
(1997)
Arterioscler Thromb Vasc Biol
, vol.17
, pp. 1376-1381
-
-
Gotoda, T.1
Kinoshita, M.2
Ishibashi, S.3
-
19
-
-
0032880399
-
Aberrant mRNAs with extended 3' UTRs are substrates for rapid degradation by mRNA surveillance
-
Muhlrad D., Parker R. Aberrant mRNAs with extended 3' UTRs are substrates for rapid degradation by mRNA surveillance. RNA 1999, 5:1299-1307.
-
(1999)
RNA
, vol.5
, pp. 1299-1307
-
-
Muhlrad, D.1
Parker, R.2
-
20
-
-
33947112390
-
Cholesteryl ester transfer protein and hyperalphalipoproteinemia in Caucasians
-
van der Steeg W.A., Hovingh G.K., Klerkx A.H.E.M., et al. Cholesteryl ester transfer protein and hyperalphalipoproteinemia in Caucasians. J Lipid Res 2007, 48:674-682.
-
(2007)
J Lipid Res
, vol.48
, pp. 674-682
-
-
van der Steeg, W.A.1
Hovingh, G.K.2
Klerkx, A.H.E.M.3
-
21
-
-
0142010558
-
Natural genetic variation as a tool in understanding the role of CETP in lipid levels and disease
-
Boekholdt S.M., Thompson J.F. Natural genetic variation as a tool in understanding the role of CETP in lipid levels and disease. J Lipid Res 2003, 44:1080-1093.
-
(2003)
J Lipid Res
, vol.44
, pp. 1080-1093
-
-
Boekholdt, S.M.1
Thompson, J.F.2
-
22
-
-
0035026352
-
Effects of hepatic lipase gene promoter nucleotide variations on serum HDL cholesterol concentration in the general Japanese population
-
Inazu A., Nishimura Y., Terada Y., Mabuchi H. Effects of hepatic lipase gene promoter nucleotide variations on serum HDL cholesterol concentration in the general Japanese population. J Hum Genet 2001, 46:172-177.
-
(2001)
J Hum Genet
, vol.46
, pp. 172-177
-
-
Inazu, A.1
Nishimura, Y.2
Terada, Y.3
Mabuchi, H.4
-
23
-
-
33644819092
-
Polymorphisms in four genes related to triglyceride and HDL-cholesterol levels in the general Japanese population in 2000 Serum Lipid Level Survey 2000 in Japan
-
Arai H., Yamamoto A., Matsuzawa Y., et al. Polymorphisms in four genes related to triglyceride and HDL-cholesterol levels in the general Japanese population in 2000 Serum Lipid Level Survey 2000 in Japan. J Atheroscler Thromb 2005, 12:240-250.
-
(2005)
J Atheroscler Thromb
, vol.12
, pp. 240-250
-
-
Arai, H.1
Yamamoto, A.2
Matsuzawa, Y.3
-
24
-
-
65249186429
-
Loss-of-function variants in endothelial lipase are a cause of elevated HDL cholesterol in humans
-
Edmondson A.C., Brown R.J., Kathiresan S., et al. Loss-of-function variants in endothelial lipase are a cause of elevated HDL cholesterol in humans. J Clin Invest 2009, 119:1042-1050.
-
(2009)
J Clin Invest
, vol.119
, pp. 1042-1050
-
-
Edmondson, A.C.1
Brown, R.J.2
Kathiresan, S.3
-
25
-
-
78651352098
-
Genetic variant of the scavenger receptor BI in humans
-
Vergeer M., Korporaal S.J.A., Franssen R., et al. Genetic variant of the scavenger receptor BI in humans. N Engl J Med 2011, 364:136-145.
-
(2011)
N Engl J Med
, vol.364
, pp. 136-145
-
-
Vergeer, M.1
Korporaal, S.J.A.2
Franssen, R.3
-
26
-
-
84856224632
-
Mutations in scavenger receptor-BI/II result in a novel dyslipidemia, with increased HDL and lipoprotein(a) (Abstract)
-
Yang X.P., Becker L.C., Becker D.M., et al. Mutations in scavenger receptor-BI/II result in a novel dyslipidemia, with increased HDL and lipoprotein(a) (Abstract). Circ Suppl 2008, 118:S-559.
-
(2008)
Circ Suppl
, vol.118
-
-
Yang, X.P.1
Becker, L.C.2
Becker, D.M.3
-
27
-
-
79957986626
-
CETP deficiency due to a novel mutation in the CETP gene promoter and its effect on cholesterol efflux and selective uptake into hepatocytes
-
Plengpanich W., Le Goff W., Poolsuk S., Julia Z., Guerin M., Khovidhunkit W. CETP deficiency due to a novel mutation in the CETP gene promoter and its effect on cholesterol efflux and selective uptake into hepatocytes. Atherosclerosis 2011, 216:370-373.
-
(2011)
Atherosclerosis
, vol.216
, pp. 370-373
-
-
Plengpanich, W.1
Le Goff, W.2
Poolsuk, S.3
Julia, Z.4
Guerin, M.5
Khovidhunkit, W.6
-
28
-
-
0035718873
-
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., et al. Point mutation (-69 G>A) in the promoter region of cholesteryl ester transfer protein gene in Japanese hyperalphalipoproteinemic subjects. Arterioscler Thromb Vasc Biol 2001, 21:985-990.
-
(2001)
Arterioscler Thromb Vasc Biol
, vol.21
, pp. 985-990
-
-
Nagano, M.1
Yamashita, S.2
Hirano, K.3
-
30
-
-
0036120909
-
A novel mutation in the intron 1 splice donor site of the cholesterol ester transfer protein (CETP) gene as a cause of hyperalphalipoproteinemia
-
Jap T.-S., Wu Y.-C., Tso Y.-C., Chiu C.-Y. A novel mutation in the intron 1 splice donor site of the cholesterol ester transfer protein (CETP) gene as a cause of hyperalphalipoproteinemia. Metabolism 2002, 51:394-397.
-
(2002)
Metabolism
, vol.51
, pp. 394-397
-
-
Jap, T.-S.1
Wu, Y.-C.2
Tso, Y.-C.3
Chiu, C.-Y.4
-
31
-
-
67650892211
-
A novel homozygous mutation in CETP gene as a cause of CETP deficiency in a Caucasian kindred
-
Calabresi L., Nilsson P., Pinotti E., et al. A novel homozygous mutation in CETP gene as a cause of CETP deficiency in a Caucasian kindred. Atherosclerosis 2009, 205:506-511.
-
(2009)
Atherosclerosis
, vol.205
, pp. 506-511
-
-
Calabresi, L.1
Nilsson, P.2
Pinotti, E.3
-
32
-
-
84856216186
-
Identification of mutations in the cholesterol ester transfer protein in Europeans with elevated high density lipoprotein cholesterol (Abstract)
-
Funke H., Wiebusch H., Fuer L., Muntoni S., Schulte H., Assmann G. Identification of mutations in the cholesterol ester transfer protein in Europeans with elevated high density lipoprotein cholesterol (Abstract). Circ Suppl 1994, 90:p23.
-
(1994)
Circ Suppl
, vol.90
-
-
Funke, H.1
Wiebusch, H.2
Fuer, L.3
Muntoni, S.4
Schulte, H.5
Assmann, G.6
-
33
-
-
0031457897
-
Deficiency of cholesteryl ester transfer protein. Description of the molecular defect and the dissociation of cholesteryl ester and triglyceride transport in plasma
-
Ritsch A., Drexel H., Amann F.W., Pfeifhofer C., Patsch J.R. Deficiency of cholesteryl ester transfer protein. Description of the molecular defect and the dissociation of cholesteryl ester and triglyceride transport in plasma. Arterioscler Thromb Vasc Biol 1997, 17:3433-3441.
-
(1997)
Arterioscler Thromb Vasc Biol
, vol.17
, pp. 3433-3441
-
-
Ritsch, A.1
Drexel, H.2
Amann, F.W.3
Pfeifhofer, C.4
Patsch, J.R.5
-
34
-
-
33746692493
-
The two novel CETP mutations Gln87X and Gln165X in a compound heterozygous state are associated with marked hyperalphalipoproteinemia and absence of significant coronary artery disease
-
Rhyne J., Ryan M.J., White C., Chimonas T., Miller M. The two novel CETP mutations Gln87X and Gln165X in a compound heterozygous state are associated with marked hyperalphalipoproteinemia and absence of significant coronary artery disease. J Mol Med 2006, 84:647-650.
-
(2006)
J Mol Med
, vol.84
, pp. 647-650
-
-
Rhyne, J.1
Ryan, M.J.2
White, C.3
Chimonas, T.4
Miller, M.5
-
35
-
-
0035987264
-
Two novel missense mutations in the CETP gene in Japanese hyperalphalipoproteinemic subjects: high-throughput assay by Invader assay
-
Nagano M., Yamashita S., Hirano K., et al. Two novel missense mutations in the CETP gene in Japanese hyperalphalipoproteinemic subjects: high-throughput assay by Invader assay. J Lipid Res 2006, 43:1011-1018.
-
(2006)
J Lipid Res
, vol.43
, pp. 1011-1018
-
-
Nagano, M.1
Yamashita, S.2
Hirano, K.3
-
36
-
-
10244232759
-
A novel nonsense mutation (G181X) in the human cholesteryl ester transfer protein gene in Japanese hyperalphalipoproteinemic subjects
-
Arai T., Yamashita S., Sakai N., et al. A novel nonsense mutation (G181X) in the human cholesteryl ester transfer protein gene in Japanese hyperalphalipoproteinemic subjects. J Lipid Res 1996, 37:2145-2154.
-
(1996)
J Lipid Res
, vol.37
, pp. 2145-2154
-
-
Arai, T.1
Yamashita, S.2
Sakai, N.3
-
37
-
-
84856219943
-
A novel nonsense mutation of cholesteryl ester transfer protein gene and the clinical characterization of Japanese primary hyperalphalipoproteinamias (Abstract)
-
Takata K., Mishima Y., Shirahata H., Umemoto S., Toyota Y., Hiraoka A. A novel nonsense mutation of cholesteryl ester transfer protein gene and the clinical characterization of Japanese primary hyperalphalipoproteinamias (Abstract). Atheroscler Suppl 2003, 4:301.
-
(2003)
Atheroscler Suppl
, vol.4
, pp. 301
-
-
Takata, K.1
Mishima, Y.2
Shirahata, H.3
Umemoto, S.4
Toyota, Y.5
Hiraoka, A.6
-
38
-
-
67749084417
-
Two novel mutations and functional analyses of the CETP and LIPC genes underlying severe hyperalphalipoproteinemia
-
Plengpanich W., Siriwong S., Khovidhunkit W. Two novel mutations and functional analyses of the CETP and LIPC genes underlying severe hyperalphalipoproteinemia. Metabolism 2009, 58:1178-1184.
-
(2009)
Metabolism
, vol.58
, pp. 1178-1184
-
-
Plengpanich, W.1
Siriwong, S.2
Khovidhunkit, W.3
-
39
-
-
0031910644
-
Human plasma CETP deficiency: identification of a novel mutation in exon 9 of the CETP gene in a Caucasian subject from North America
-
Teh E.M., Dolphin P.J., Breckenridge W.C., Tan M.H. Human plasma CETP deficiency: identification of a novel mutation in exon 9 of the CETP gene in a Caucasian subject from North America. J Lipid Res 1998, 39:442-456.
-
(1998)
J Lipid Res
, vol.39
, pp. 442-456
-
-
Teh, E.M.1
Dolphin, P.J.2
Breckenridge, W.C.3
Tan, M.H.4
-
40
-
-
0030984690
-
The cholesteryl ester transfer protein (CETP) locus as a candidate gene in abdominal aortic aneurysm
-
Ramsbottom D., O'Neill A., Sexton D.M., Gafoor R.A., Bouchier-Hayes D., Croke D.T. The cholesteryl ester transfer protein (CETP) locus as a candidate gene in abdominal aortic aneurysm. Clin Genet 1997, 51:241-245.
-
(1997)
Clin Genet
, vol.51
, pp. 241-245
-
-
Ramsbottom, D.1
O'Neill, A.2
Sexton, D.M.3
Gafoor, R.A.4
Bouchier-Hayes, D.5
Croke, D.T.6
-
41
-
-
1942503354
-
A novel missense mutation (L296Q) in cholesteryl ester transfer protein gene related to coronary heart disease
-
Zheng K.-Q., Zhang S.-Z., Zhang L., Huang D.-J., Liao L.-C., Hou Y.-P. A novel missense mutation (L296Q) in cholesteryl ester transfer protein gene related to coronary heart disease. Acta Biochim Biophys Sin 2004, 36:33-36.
-
(2004)
Acta Biochim Biophys Sin
, vol.36
, pp. 33-36
-
-
Zheng, K.-Q.1
Zhang, S.-Z.2
Zhang, L.3
Huang, D.-J.4
Liao, L.-C.5
Hou, Y.-P.6
-
42
-
-
57649184072
-
Frequency and function of CETP variants among individuals of Asian ancestry
-
Thompson J.F., Reynolds J.M., Williams S.P., Wood L.S., Paciga S.A., Lloyd D.B. Frequency and function of CETP variants among individuals of Asian ancestry. Atherosclerosis 2009, 202:241-247.
-
(2009)
Atherosclerosis
, vol.202
, pp. 241-247
-
-
Thompson, J.F.1
Reynolds, J.M.2
Williams, S.P.3
Wood, L.S.4
Paciga, S.A.5
Lloyd, D.B.6
-
43
-
-
0027227681
-
Cholesteryl ester transfer protein deficiency caused by a nonsense mutation detected in the patient's macrophage mRNA
-
Gotoda T., Kinoshita M., Shimano H., et al. Cholesteryl ester transfer protein deficiency caused by a nonsense mutation detected in the patient's macrophage mRNA. Biochem Biophys Res Commun 1993, 194:519-524.
-
(1993)
Biochem Biophys Res Commun
, vol.194
, pp. 519-524
-
-
Gotoda, T.1
Kinoshita, M.2
Shimano, H.3
-
44
-
-
0029859668
-
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 H.B. Exon 10 skipping caused by intron 10 splice donor site mutation in cholesteryl ester transfer protein gene results in abnormal downstream splice site selection. J Lipid Res 1996, 37:2065-2073.
-
(1996)
J Lipid Res
, vol.37
, pp. 2065-2073
-
-
Sakai, N.1
Santamarina-Fojo, S.2
Yamashita, S.3
Matsuzawa, Y.4
Brewer, H.B.5
-
45
-
-
0024415898
-
Molecular basis of lipid transfer protein deficiency in a family with increased high-density lipoproteins
-
Brown M.L., Inazu A., Hesler C.B., et al. Molecular basis of lipid transfer protein deficiency in a family with increased high-density lipoproteins. Nature 1989, 342:448-451.
-
(1989)
Nature
, vol.342
, pp. 448-451
-
-
Brown, M.L.1
Inazu, A.2
Hesler, C.B.3
-
46
-
-
67349108321
-
Novel mutations of CETP gene in Italian subjects with hyperalphalipoproteinemia
-
Cefalù A.B., Noto D., Magnolo L., et al. Novel mutations of CETP gene in Italian subjects with hyperalphalipoproteinemia. Atherosclerosis 2009, 204:202-207.
-
(2009)
Atherosclerosis
, vol.204
, pp. 202-207
-
-
Cefalù, A.B.1
Noto, D.2
Magnolo, L.3
|