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Journal of Lipid Research
|
August 1, 1991
Characterization of the discoidal complexes formed between apoA-I-CNBr fragments and phosphatidylcholine
B Vanloo, J Morrison, N Fidge, et al.
The Biochemical Journal
|
February 26, 1999
Baculovirus expression and biochemical characterization of the human microsomal triglyceride transfer protein
P J Ritchie, A Decout, J Amey, et al.
Journal of Lipid Research
|
August 1, 1995
Association of synthetic peptide fragments of human apolipoprotein A-I with phospholipids
B Vanloo, L Demoor, C Boutillon, et al.
The Journal of Biological Chemistry
|
September 10, 1983
Interaction of the serum amyloid A proteins with phospholipid
L L Bausserman, P N Herbert, T Forte, et al.
Atherosclerosis
|
August 26, 1998
Displacement of apo A-I from HDL by apo A-II or its C-terminal helix promotes the formation of pre-beta1 migrating particles and decreases LCAT activation
C Labeur, G Lambert, T Van Cauteren, et al.
Biochimica Et Biophysica Acta
|
June 2, 1994
Structural domain of apolipoprotein A-I involved in its interaction with cells
J Luchoomun, N Theret, V Clavey, et al.
The Journal of Biological Chemistry
|
August 5, 1991
Catalytic triad residue mutation (Asp156----Gly) causing familial lipoprotein lipase deficiency. Co-inheritance with a nonsense mutation (Ser447----Ter) in a Turkish family
F Faustinella, A Chang, J P Van Biervliet, et al.
Clinical Chemistry
|
November 1, 1992
Plasma lipoprotein(a) values and severity of coronary artery disease in a large population of patients undergoing coronary angiography
C Labeur, D De Bacquer, G De Backer, et al.
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.
Journal of Lipid Research
|
April 29, 2000
Relationship between structure and biochemical phenotype of lecithin:cholesterol acyltransferase (LCAT) mutants causing fish-eye disease
B Vanloo, F Peelman, K Deschuymere, et al.
Page
of 19
Search research articles
Search
Showing results (161-170 of 189) with videos related to
Sort By:
Page
of 19
Journal of Lipid Research
|
August 1, 1991
Characterization of the discoidal complexes formed between apoA-I-CNBr fragments and phosphatidylcholine
B Vanloo, J Morrison, N Fidge, et al.
The Biochemical Journal
|
February 26, 1999
Baculovirus expression and biochemical characterization of the human microsomal triglyceride transfer protein
P J Ritchie, A Decout, J Amey, et al.
Journal of Lipid Research
|
August 1, 1995
Association of synthetic peptide fragments of human apolipoprotein A-I with phospholipids
B Vanloo, L Demoor, C Boutillon, et al.
The Journal of Biological Chemistry
|
September 10, 1983
Interaction of the serum amyloid A proteins with phospholipid
L L Bausserman, P N Herbert, T Forte, et al.
Atherosclerosis
|
August 26, 1998
Displacement of apo A-I from HDL by apo A-II or its C-terminal helix promotes the formation of pre-beta1 migrating particles and decreases LCAT activation
C Labeur, G Lambert, T Van Cauteren, et al.
Biochimica Et Biophysica Acta
|
June 2, 1994
Structural domain of apolipoprotein A-I involved in its interaction with cells
J Luchoomun, N Theret, V Clavey, et al.
The Journal of Biological Chemistry
|
August 5, 1991
Catalytic triad residue mutation (Asp156----Gly) causing familial lipoprotein lipase deficiency. Co-inheritance with a nonsense mutation (Ser447----Ter) in a Turkish family
F Faustinella, A Chang, J P Van Biervliet, et al.
Clinical Chemistry
|
November 1, 1992
Plasma lipoprotein(a) values and severity of coronary artery disease in a large population of patients undergoing coronary angiography
C Labeur, D De Bacquer, G De Backer, et al.
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.
Journal of Lipid Research
|
April 29, 2000
Relationship between structure and biochemical phenotype of lecithin:cholesterol acyltransferase (LCAT) mutants causing fish-eye disease
B Vanloo, F Peelman, K Deschuymere, et al.
Page
of 19