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Proceedings of the National Academy of Sciences of the United States of America
|
October 1, 1985
Human apolipoprotein B cDNA clone isolation and demonstration that liver apolipoprotein B mRNA is 22 kilobases in length
L S Huang, S C Bock, S I Feinstein, et al.
Science (New York, N.Y.)
|
January 10, 1986
Modification of the active site of alkaline phosphatase by site-directed mutagenesis
S S Ghosh, S C Bock, S E Rokita, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 1, 1982
Hybridization-selected translation of Bombyx mori high-cysteine chorion proteins in Xenopus laevis oocytes
S C Bock, D C Tiemeier, K Mester, et al.
The Journal of Biological Chemistry
|
February 25, 1989
CpG mutations in the reactive site of human C1 inhibitor
K Skriver, E Radziejewska, J A Silbermann, et al.
Biochemistry
|
May 31, 2001
The antithrombin P1 residue is important for target proteinase specificity but not for heparin activation of the serpin. Characterization of P1 antithrombin variants with altered proteinase specificity but normal heparin activation
Y J Chuang, R Swanson, S M Raja, et al.
Analytical Biochemistry
|
October 15, 1979
Two-dimensional electrophoresis of small-molecular-weight proteins
M R Goldsmith, E C Rattner, M M Koehler, et al.
FEBS Letters
|
April 6, 1992
Antithrombin Budapest 3. An antithrombin variant with reduced heparin affinity resulting from the substitution L99F
R J Olds, D A Lane, M Boisclair, et al.
The Journal of Biological Chemistry
|
May 15, 1991
Substrate properties of C1 inhibitor Ma (alanine 434----glutamic acid). Genetic and structural evidence suggesting that the P12-region contains critical determinants of serine protease inhibitor/substrate status
K Skriver, W R Wikoff, P A Patston, et al.
American Journal of Human Genetics
|
January 1, 1985
Hereditary thrombosis in a Utah kindred is caused by a dysfunctional antithrombin III gene
S C Bock, J F Harris, C E Schwartz, et al.
The Biochemical Journal
|
August 15, 1995
Elimination of glycosylation heterogeneity affecting heparin affinity of recombinant human antithrombin III by expression of a beta-like variant in baculovirus-infected insect cells
E Ersdal-Badju, A Lu, X Peng, et al.
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of 4
Search research articles
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Showing results (21-30 of 33) with videos related to
Sort By:
Page
of 4
Proceedings of the National Academy of Sciences of the United States of America
|
October 1, 1985
Human apolipoprotein B cDNA clone isolation and demonstration that liver apolipoprotein B mRNA is 22 kilobases in length
L S Huang, S C Bock, S I Feinstein, et al.
Science (New York, N.Y.)
|
January 10, 1986
Modification of the active site of alkaline phosphatase by site-directed mutagenesis
S S Ghosh, S C Bock, S E Rokita, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 1, 1982
Hybridization-selected translation of Bombyx mori high-cysteine chorion proteins in Xenopus laevis oocytes
S C Bock, D C Tiemeier, K Mester, et al.
The Journal of Biological Chemistry
|
February 25, 1989
CpG mutations in the reactive site of human C1 inhibitor
K Skriver, E Radziejewska, J A Silbermann, et al.
Biochemistry
|
May 31, 2001
The antithrombin P1 residue is important for target proteinase specificity but not for heparin activation of the serpin. Characterization of P1 antithrombin variants with altered proteinase specificity but normal heparin activation
Y J Chuang, R Swanson, S M Raja, et al.
Analytical Biochemistry
|
October 15, 1979
Two-dimensional electrophoresis of small-molecular-weight proteins
M R Goldsmith, E C Rattner, M M Koehler, et al.
FEBS Letters
|
April 6, 1992
Antithrombin Budapest 3. An antithrombin variant with reduced heparin affinity resulting from the substitution L99F
R J Olds, D A Lane, M Boisclair, et al.
The Journal of Biological Chemistry
|
May 15, 1991
Substrate properties of C1 inhibitor Ma (alanine 434----glutamic acid). Genetic and structural evidence suggesting that the P12-region contains critical determinants of serine protease inhibitor/substrate status
K Skriver, W R Wikoff, P A Patston, et al.
American Journal of Human Genetics
|
January 1, 1985
Hereditary thrombosis in a Utah kindred is caused by a dysfunctional antithrombin III gene
S C Bock, J F Harris, C E Schwartz, et al.
The Biochemical Journal
|
August 15, 1995
Elimination of glycosylation heterogeneity affecting heparin affinity of recombinant human antithrombin III by expression of a beta-like variant in baculovirus-infected insect cells
E Ersdal-Badju, A Lu, X Peng, et al.
Page
of 4