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T L Innerarity

Showing results (101-110 of 107) with videos related to

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The Journal of Biological Chemistry|March 15, 1988
Site-specific mutagenesis of human apolipoprotein E. Receptor binding activity of variants with single amino acid substitutionsA Lalazar, K H Weisgraber, S C Rall, et al.
Nature|October 23, 1986
Complete protein sequence and identification of structural domains of human apolipoprotein BT J Knott, R J Pease, L M Powell, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1988
Familial defective apolipoprotein B-100: enhanced binding of monoclonal antibody MB47 to abnormal low density lipoproteinsK H Weisgraber, T L Innerarity, Y M Newhouse, et al.
Science (New York, N.Y.)|October 4, 1985
Human apolipoprotein B: structure of carboxyl-terminal domains, sites of gene expression, and chromosomal localizationT J Knott, S C Rall, T L Innerarity, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1985
Human apolipoprotein E expression in Escherichia coli: structural and functional identity of the bacterially produced protein with plasma apolipoprotein ET Vogel, K H Weisgraber, M I Zeevi, et al.
Journal of Lipid Research|August 1, 1990
Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemiaT L Innerarity, R W Mahley, K H Weisgraber, et al.
The Journal of Clinical Investigation|October 1, 1981
Familial dysbetalipoproteinemia. Abnormal binding of mutant apoprotein E to low density lipoprotein receptors of human fibroblasts and membranes from liver and adrenal of rats, rabbits, and cowsW J Schneider, P T Kovanen, M S Brown, et al.
Pageof 11

Showing results (101-110 of 107) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 107 results.
The Journal of Biological Chemistry|March 15, 1988
Site-specific mutagenesis of human apolipoprotein E. Receptor binding activity of variants with single amino acid substitutionsA Lalazar, K H Weisgraber, S C Rall, et al.
Nature|October 23, 1986
Complete protein sequence and identification of structural domains of human apolipoprotein BT J Knott, R J Pease, L M Powell, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1988
Familial defective apolipoprotein B-100: enhanced binding of monoclonal antibody MB47 to abnormal low density lipoproteinsK H Weisgraber, T L Innerarity, Y M Newhouse, et al.
Science (New York, N.Y.)|October 4, 1985
Human apolipoprotein B: structure of carboxyl-terminal domains, sites of gene expression, and chromosomal localizationT J Knott, S C Rall, T L Innerarity, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1985
Human apolipoprotein E expression in Escherichia coli: structural and functional identity of the bacterially produced protein with plasma apolipoprotein ET Vogel, K H Weisgraber, M I Zeevi, et al.
Journal of Lipid Research|August 1, 1990
Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemiaT L Innerarity, R W Mahley, K H Weisgraber, et al.
The Journal of Clinical Investigation|October 1, 1981
Familial dysbetalipoproteinemia. Abnormal binding of mutant apoprotein E to low density lipoprotein receptors of human fibroblasts and membranes from liver and adrenal of rats, rabbits, and cowsW J Schneider, P T Kovanen, M S Brown, et al.
Pageof 11