-
1
-
-
63749121093
-
Mutations and polymorphisms in the proprotein convertase subtilisin kexin 9 (PCSK9) gene in cholesterol metabolism and disease
-
Abifadel M., Rabès J.-P., Devillers M., et al. Mutations and polymorphisms in the proprotein convertase subtilisin kexin 9 (PCSK9) gene in cholesterol metabolism and disease. Hum Mutat 2009, 30:520-529.
-
(2009)
Hum Mutat
, vol.30
, pp. 520-529
-
-
Abifadel, M.1
Rabès, J.-P.2
Devillers, M.3
-
2
-
-
70449368195
-
The unique role of proprotein convertase subtilisin/kexin 9 in cholesterol homeostasis
-
Mousavi S.A., Berge K.E., Leren T.P. The unique role of proprotein convertase subtilisin/kexin 9 in cholesterol homeostasis. J Intern Med 2009, 266:507-519.
-
(2009)
J Intern Med
, vol.266
, pp. 507-519
-
-
Mousavi, S.A.1
Berge, K.E.2
Leren, T.P.3
-
3
-
-
66349126280
-
PCSK9: a convertase that coordinates LDL catabolism
-
Horton J.D., Cohen J.C., Hobbs H.H. PCSK9: a convertase that coordinates LDL catabolism. J Lipid Res 2009, 50:S172-S177.
-
(2009)
J Lipid Res
, vol.50
-
-
Horton, J.D.1
Cohen, J.C.2
Hobbs, H.H.3
-
4
-
-
70350746156
-
Dissection of the endogenous cellular pathways of PCSK9-induced low density lipoprotein receptor degradation. Evidence for an intracellular route
-
Poirier S., Mayer G., Poupon V., et al. Dissection of the endogenous cellular pathways of PCSK9-induced low density lipoprotein receptor degradation. Evidence for an intracellular route. J Biol Chem 2009, 384:28856-28864.
-
(2009)
J Biol Chem
, vol.384
, pp. 28856-28864
-
-
Poirier, S.1
Mayer, G.2
Poupon, V.3
-
5
-
-
67649652056
-
The molecular basis of familial hypercholesterolemia in Lebanon: spectrum of LDLR mutations and role of PCSK9 as a modifier gene
-
Abifadel M., Rabès J.-P., Jambart S., et al. The molecular basis of familial hypercholesterolemia in Lebanon: spectrum of LDLR mutations and role of PCSK9 as a modifier gene. Hum Mutat 2009, 30:E682-E691.
-
(2009)
Hum Mutat
, vol.30
-
-
Abifadel, M.1
Rabès, J.-P.2
Jambart, S.3
-
6
-
-
57349089246
-
A PCSK9 variant and familial combined hyperlipidaemia
-
Abifadel M., Bernier L., Dubuc G., et al. A PCSK9 variant and familial combined hyperlipidaemia. J Med Genet 2008, 45:780-786.
-
(2008)
J Med Genet
, vol.45
, pp. 780-786
-
-
Abifadel, M.1
Bernier, L.2
Dubuc, G.3
-
7
-
-
18944392912
-
A common PCSK9 haplotype, encompassing the E670G coding single nucleotide polymorphism, is a novel genetic marker for plasma low-density lipoprotein cholesterol levels and severity of coronary atherosclerosis
-
Chen S.N., Ballantyne C.M., Gotto A.M., Tan Y., Willerson J.T., Marian A.J. A common PCSK9 haplotype, encompassing the E670G coding single nucleotide polymorphism, is a novel genetic marker for plasma low-density lipoprotein cholesterol levels and severity of coronary atherosclerosis. J Am Coll Cardiol 2005, 45:1611-1619.
-
(2005)
J Am Coll Cardiol
, vol.45
, pp. 1611-1619
-
-
Chen, S.N.1
Ballantyne, C.M.2
Gotto, A.M.3
Tan, Y.4
Willerson, J.T.5
Marian, A.J.6
-
8
-
-
33646382116
-
The c.43_44insCTG variation in PCSK9 is associated with low plasma LDL-cholesterol in a Caucasian population
-
Yue P., Averna M., Lin X., Schonfeld G. The c.43_44insCTG variation in PCSK9 is associated with low plasma LDL-cholesterol in a Caucasian population. Hum Mutat 2006, 27:460-466.
-
(2006)
Hum Mutat
, vol.27
, pp. 460-466
-
-
Yue, P.1
Averna, M.2
Lin, X.3
Schonfeld, G.4
-
9
-
-
73149094934
-
A new method for measuring of total plasma PCSK9: clinical applications
-
Dubuc G., Tremblay M., Paré G., et al. A new method for measuring of total plasma PCSK9: clinical applications. J Lipid Res 2010, 51:140-149.
-
(2010)
J Lipid Res
, vol.51
, pp. 140-149
-
-
Dubuc, G.1
Tremblay, M.2
Paré, G.3
-
10
-
-
33646443979
-
Missense mutations in the PCSK9 gene are associated with hypocholesterolemia and possibly increased response to statin therapy
-
Berge K.E., Ose L., Leren T.P. Missense mutations in the PCSK9 gene are associated with hypocholesterolemia and possibly increased response to statin therapy. Arterioscler Thromb Vasc Biol 2006, 26:1094-1100.
-
(2006)
Arterioscler Thromb Vasc Biol
, vol.26
, pp. 1094-1100
-
-
Berge, K.E.1
Ose, L.2
Leren, T.P.3
-
11
-
-
2342592460
-
Genetic polymorphisms affecting the phenotypic expression in familial hypercholesterolemia
-
Bertolini S., Pisciotta L., Di Scala L., et al. Genetic polymorphisms affecting the phenotypic expression in familial hypercholesterolemia. Atherosclerosis 2004, 174:57-65.
-
(2004)
Atherosclerosis
, vol.174
, pp. 57-65
-
-
Bertolini, S.1
Pisciotta, L.2
Di Scala, L.3
-
12
-
-
0004136246
-
-
Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
-
Sambrook J., Fritsch E.F., Maniatis T. Molecular cloning: a laboratory manual 1989, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
-
(1989)
Molecular cloning: a laboratory manual
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
13
-
-
33646435074
-
Additive effect of mutations in LDLR and PCSK9 genes on the phenotype of familial hypercholesterolemia
-
Pisciotta L., Oliva C.P., Cefalu A.B., et al. Additive effect of mutations in LDLR and PCSK9 genes on the phenotype of familial hypercholesterolemia. Atherosclerosis 2006, 186:433-440.
-
(2006)
Atherosclerosis
, vol.186
, pp. 433-440
-
-
Pisciotta, L.1
Oliva, C.P.2
Cefalu, A.B.3
-
14
-
-
0025257612
-
Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with HhaI
-
Hixson J.E., Vernier D.T. Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with HhaI. J Lipid Res 1990, 31:545-548.
-
(1990)
J Lipid Res
, vol.31
, pp. 545-548
-
-
Hixson, J.E.1
Vernier, D.T.2
-
15
-
-
0034268668
-
Clinical expression of familial hypercholesterolemia in clusters of mutations of the LDL receptor gene that cause a receptor-defective or receptor-negative phenotype
-
Bertolini S., Cantafora A., Averna M., et al. Clinical expression of familial hypercholesterolemia in clusters of mutations of the LDL receptor gene that cause a receptor-defective or receptor-negative phenotype. Arterioscler Thromb Vasc Biol 2000, 20:e41-e52.
-
(2000)
Arterioscler Thromb Vasc Biol
, vol.20
-
-
Bertolini, S.1
Cantafora, A.2
Averna, M.3
-
16
-
-
72049130254
-
Meta-analysis of comparative efficacy of increasing dose of Atorvastatin versus Rosuvastatin versus simvastatin on lowering levels of atherogenic lipids (from VOYAGER)
-
Nicholls S.J., Brandrup-Wognsen G., Palmer M., Barter P.J. Meta-analysis of comparative efficacy of increasing dose of Atorvastatin versus Rosuvastatin versus simvastatin on lowering levels of atherogenic lipids (from VOYAGER). Am J Cardiol 2010, 105:69-76.
-
(2010)
Am J Cardiol
, vol.105
, pp. 69-76
-
-
Nicholls, S.J.1
Brandrup-Wognsen, G.2
Palmer, M.3
Barter, P.J.4
-
17
-
-
77749248851
-
A systematic review and meta-analysis on the therapeutic equivalence of statins
-
Weng T.-C., Kao Yang Y.-H., Lin S.-J., Tai S.-H. A systematic review and meta-analysis on the therapeutic equivalence of statins. J Clin Pharm Ther 2010, 35:139-151.
-
(2010)
J Clin Pharm Ther
, vol.35
, pp. 139-151
-
-
Weng, T.-C.1
Kao Yang, Y.-H.2
Lin, S.-J.3
Tai, S.-H.4
-
18
-
-
38049077373
-
Genetic variants in PCSK9 in the Japanese population: rare genetic variants in PCSK9 might collectively contribute to plasma LDL cholesterol levels in the general population
-
Miyake Y., Kimura R., Kokubo Y., et al. Genetic variants in PCSK9 in the Japanese population: rare genetic variants in PCSK9 might collectively contribute to plasma LDL cholesterol levels in the general population. Atherosclerosis 2008, 196:29-36.
-
(2008)
Atherosclerosis
, vol.196
, pp. 29-36
-
-
Miyake, Y.1
Kimura, R.2
Kokubo, Y.3
-
19
-
-
33847075832
-
A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol
-
Fasano T., Cefalù A.B., Di Leo E., et al. A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol. Arterioscler Thromb Vasc Biol 2007, 27:677-681.
-
(2007)
Arterioscler Thromb Vasc Biol
, vol.27
, pp. 677-681
-
-
Fasano, T.1
Cefalù, A.B.2
Di Leo, E.3
-
20
-
-
34547129121
-
Effects of pH and low density lipoprotein (LDL) on PCSK9-dependent LDL receptor regulation
-
Fisher T.S., Lo Surdo P., Pandit S., et al. Effects of pH and low density lipoprotein (LDL) on PCSK9-dependent LDL receptor regulation. J Biol Chem 2007, 282:20502-20512.
-
(2007)
J Biol Chem
, vol.282
, pp. 20502-20512
-
-
Fisher, T.S.1
Lo Surdo, P.2
Pandit, S.3
-
21
-
-
36849085368
-
The PCSK9 gene R46L variant is associated with lower plasma lipid levels and cardiovascular risk in healthy U.K. men
-
Scartezini M., Hubbart C., Whittall R.A., Cooper J.A., Neil A.H.W., Humphries S.E. The PCSK9 gene R46L variant is associated with lower plasma lipid levels and cardiovascular risk in healthy U.K. men. Clin Sci 2007, 113:435-441.
-
(2007)
Clin Sci
, vol.113
, pp. 435-441
-
-
Scartezini, M.1
Hubbart, C.2
Whittall, R.A.3
Cooper, J.A.4
Neil, A.H.W.5
Humphries, S.E.6
-
22
-
-
57649193160
-
Variation in PCSK9, low LDL cholesterol, and risk of peripheral arterial disease
-
Atherosclerosis Risk in Communities (ARIC) Study Investigators
-
Folsom A.R., Peacock J.M., Boerwinkle E., Atherosclerosis Risk in Communities (ARIC) Study Investigators Variation in PCSK9, low LDL cholesterol, and risk of peripheral arterial disease. Atherosclerosis 2009, 202:211-215.
-
(2009)
Atherosclerosis
, vol.202
, pp. 211-215
-
-
Folsom, A.R.1
Peacock, J.M.2
Boerwinkle, E.3
-
23
-
-
77953309816
-
PCSK9 R46L, low-density lipoprotein cholesterol levels, and risk of ischemic heart disease
-
Benn M., Nordestgaard B.G., Grande P., Schnohr P., Tybiærg-Hansen A. PCSK9 R46L, low-density lipoprotein cholesterol levels, and risk of ischemic heart disease. J Am Coll Cardiol 2010, 55:2833-2842.
-
(2010)
J Am Coll Cardiol
, vol.55
, pp. 2833-2842
-
-
Benn, M.1
Nordestgaard, B.G.2
Grande, P.3
Schnohr, P.4
Tybiærg-Hansen, A.5
-
24
-
-
72449203600
-
Loss-of-function mutation R46L in the PCSK9 gene has little impact on the levels of total serum cholesterol in familial hypercholesterolemia heterozygotes
-
Strøm T.B., Holla Ø. L., Cameron J., Berge K.E., Leren T.P. Loss-of-function mutation R46L in the PCSK9 gene has little impact on the levels of total serum cholesterol in familial hypercholesterolemia heterozygotes. Clin Chim Acta 2010, 411:229-233.
-
(2010)
Clin Chim Acta
, vol.411
, pp. 229-233
-
-
Strøm, T.B.1
Holla, Ø.L.2
Cameron, J.3
Berge, K.E.4
Leren, T.P.5
-
25
-
-
69849094785
-
Identification of genetic variants associated with response to statin therapy
-
Mega J.L., Morrow D.A., Brown A., Cannon C.P., Sabatine M.S. Identification of genetic variants associated with response to statin therapy. Arterioscler Thromb Vasc Biol 2009, 29:1310-1315.
-
(2009)
Arterioscler Thromb Vasc Biol
, vol.29
, pp. 1310-1315
-
-
Mega, J.L.1
Morrow, D.A.2
Brown, A.3
Cannon, C.P.4
Sabatine, M.S.5
-
26
-
-
71249136025
-
The role of HMGCR alternative splicing in statin efficacy
-
Medina M.W., Krauss R.M. The role of HMGCR alternative splicing in statin efficacy. Trends Cardiovasc Med 2009, 19:173-177.
-
(2009)
Trends Cardiovasc Med
, vol.19
, pp. 173-177
-
-
Medina, M.W.1
Krauss, R.M.2
-
27
-
-
3242736602
-
Interactions between common genetic polymorphisms in ABCG5/G8 and CYP7A1 on LDL cholesterol-lowering response to atorvastatin
-
Kajinami K., Brousseau M.E., Ordovas J.M., Schaefer E.J. Interactions between common genetic polymorphisms in ABCG5/G8 and CYP7A1 on LDL cholesterol-lowering response to atorvastatin. Atherosclerosis 2004, 175:287-293.
-
(2004)
Atherosclerosis
, vol.175
, pp. 287-293
-
-
Kajinami, K.1
Brousseau, M.E.2
Ordovas, J.M.3
Schaefer, E.J.4
-
28
-
-
75549088606
-
The influence of SLCO1B1 (OATP1B1) polymorphisms on response to statin therapy
-
Romaine S.P.R., Bailey K.M., Hall A.S., Balmforth A.J. The influence of SLCO1B1 (OATP1B1) polymorphisms on response to statin therapy. Pharmacogenomics J 2010, 10:1-11.
-
(2010)
Pharmacogenomics J
, vol.10
, pp. 1-11
-
-
Romaine, S.P.R.1
Bailey, K.M.2
Hall, A.S.3
Balmforth, A.J.4
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