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European Journal of Biochemistry
|
May 13, 1998
The C-terminal helix of human apolipoprotein AII promotes the fusion of unilamellar liposomes and displaces apolipoprotein AI from high-density lipoproteins
G Lambert, A Decout, B Vanloo, et al.
The Journal of Biological Chemistry
|
February 5, 1993
Interaction of reconstituted high density lipoprotein discs containing human apolipoprotein A-I (ApoA-I) variants with murine adipocytes and macrophages. Evidence for reduced cholesterol efflux promotion by apoA-I(Pro165-->Arg)
A von Eckardstein, G Castro, I Wybranska, et al.
The Journal of Clinical Investigation
|
July 1, 1993
Fish eye syndrome: a molecular defect in the lecithin-cholesterol acyltransferase (LCAT) gene associated with normal alpha-LCAT-specific activity. Implications for classification and prognosis
H G Klein, S Santamarina-Fojo, N Duverger, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 14, 2000
High-level protein secretion into blood circulation after electric pulse-mediated gene transfer into skeletal muscle
M Bettan, F Emmanuel, R Darteil, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
February 17, 2000
Complete atherosclerosis regression after human ApoE gene transfer in ApoE-deficient/nude mice
C Desurmont, J M Caillaud, F Emmanuel, et al.
Human Molecular Genetics
|
June 22, 2000
Therapeutic liver repopulation in a mouse model of hypercholesterolemia
C Mitchell, A Mignon, J E Guidotti, et al.
European Journal of Biochemistry
|
June 1, 1995
Tissue-specific expression of the human gene for lecithin: cholesterol acyltransferase in transgenic mice alters blood lipids, lipoproteins and lipases towards a less atherogenic profile
A Mehlum, B Staels, N Duverger, et al.
Journal of Lipid Research
|
January 1, 1993
Two different allelic mutations in the lecithin:cholesterol acyltransferase (LCAT) gene resulting in classic LCAT deficiency: LCAT (tyr83-->stop) and LCAT (tyr156-->asn)
H G Klein, P Lohse, N Duverger, et al.
Circulation
|
January 13, 1999
Somatic gene transfer of human ApoA-I inhibits atherosclerosis progression in mouse models
P Benoit, F Emmanuel, J M Caillaud, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
November 14, 2000
Decreased susceptibility to diet-induced atherosclerosis in human apolipoprotein A-II transgenic mice
A Tailleux, M Bouly, G Luc, et al.
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of 6
Search research articles
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Showing results (21-30 of 59) with videos related to
Sort By:
Page
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European Journal of Biochemistry
|
May 13, 1998
The C-terminal helix of human apolipoprotein AII promotes the fusion of unilamellar liposomes and displaces apolipoprotein AI from high-density lipoproteins
G Lambert, A Decout, B Vanloo, et al.
The Journal of Biological Chemistry
|
February 5, 1993
Interaction of reconstituted high density lipoprotein discs containing human apolipoprotein A-I (ApoA-I) variants with murine adipocytes and macrophages. Evidence for reduced cholesterol efflux promotion by apoA-I(Pro165-->Arg)
A von Eckardstein, G Castro, I Wybranska, et al.
The Journal of Clinical Investigation
|
July 1, 1993
Fish eye syndrome: a molecular defect in the lecithin-cholesterol acyltransferase (LCAT) gene associated with normal alpha-LCAT-specific activity. Implications for classification and prognosis
H G Klein, S Santamarina-Fojo, N Duverger, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 14, 2000
High-level protein secretion into blood circulation after electric pulse-mediated gene transfer into skeletal muscle
M Bettan, F Emmanuel, R Darteil, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
February 17, 2000
Complete atherosclerosis regression after human ApoE gene transfer in ApoE-deficient/nude mice
C Desurmont, J M Caillaud, F Emmanuel, et al.
Human Molecular Genetics
|
June 22, 2000
Therapeutic liver repopulation in a mouse model of hypercholesterolemia
C Mitchell, A Mignon, J E Guidotti, et al.
European Journal of Biochemistry
|
June 1, 1995
Tissue-specific expression of the human gene for lecithin: cholesterol acyltransferase in transgenic mice alters blood lipids, lipoproteins and lipases towards a less atherogenic profile
A Mehlum, B Staels, N Duverger, et al.
Journal of Lipid Research
|
January 1, 1993
Two different allelic mutations in the lecithin:cholesterol acyltransferase (LCAT) gene resulting in classic LCAT deficiency: LCAT (tyr83-->stop) and LCAT (tyr156-->asn)
H G Klein, P Lohse, N Duverger, et al.
Circulation
|
January 13, 1999
Somatic gene transfer of human ApoA-I inhibits atherosclerosis progression in mouse models
P Benoit, F Emmanuel, J M Caillaud, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
November 14, 2000
Decreased susceptibility to diet-induced atherosclerosis in human apolipoprotein A-II transgenic mice
A Tailleux, M Bouly, G Luc, et al.
Page
of 6