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G L Long

Showing results (41-50 of 85) with videos related to

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The Journal of Biological Chemistry|June 13, 1998
Human protein S cleavage and inactivation by coagulation factor XaG L Long, D Lu, R L Xie, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1987
Cloning and characterization of human liver cDNA encoding a protein S precursorJ Hoskins, D K Norman, R J Beckmann, et al.
Somatic Cell and Molecular Genetics|January 1, 1988
Genes for human vitamin K-dependent plasma proteins C and S are located on chromosomes 2 and 3, respectivelyG L Long, A Marshall, J C Gardner, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1986
Evolution and organization of the human protein C geneJ Plutzky, J A Hoskins, G L Long, et al.
Thrombosis and Haemostasis|December 22, 1999
Hereditary thrombophilia as a model for multigenic diseaseE G Bovill, S J Hasstedt, M F Leppert, et al.
American Journal of Medical Genetics|October 1, 1986
Molecular detection of carriers of hereditary amyloidosis in a Swedish-American familyM R Wallace, P M Conneally, G L Long, et al.
Biochemistry|May 23, 2000
Self-association of human protein SJ E Pauls, M F Hockin, G L Long, et al.
The Journal of Biological Chemistry|November 5, 1991
beta-Hydroxyaspartic acid and beta-hydroxyasparagine residues in recombinant human protein S are not required for anticoagulant cofactor activity or for binding to C4b-binding proteinR M Nelson, W J VanDusen, P A Friedman, et al.
Journal of Deaf Studies and Deaf Education|September 30, 2004
Approaches to studying in deaf and hearing students in higher educationJ T Richardson, J MacLeod-Gallinger, B G McKee, et al.
American Journal of Human Genetics|July 31, 1998
An unknown genetic defect increases venous thrombosis risk, through interaction with protein C deficiencyS J Hasstedt, E G Bovill, P W Callas, et al.
Pageof 9

Showing results (41-50 of 85) with videos related to

Sort By:
Pageof 9
The Journal of Biological Chemistry|June 13, 1998
Human protein S cleavage and inactivation by coagulation factor XaG L Long, D Lu, R L Xie, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1987
Cloning and characterization of human liver cDNA encoding a protein S precursorJ Hoskins, D K Norman, R J Beckmann, et al.
Somatic Cell and Molecular Genetics|January 1, 1988
Genes for human vitamin K-dependent plasma proteins C and S are located on chromosomes 2 and 3, respectivelyG L Long, A Marshall, J C Gardner, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1986
Evolution and organization of the human protein C geneJ Plutzky, J A Hoskins, G L Long, et al.
Thrombosis and Haemostasis|December 22, 1999
Hereditary thrombophilia as a model for multigenic diseaseE G Bovill, S J Hasstedt, M F Leppert, et al.
American Journal of Medical Genetics|October 1, 1986
Molecular detection of carriers of hereditary amyloidosis in a Swedish-American familyM R Wallace, P M Conneally, G L Long, et al.
Biochemistry|May 23, 2000
Self-association of human protein SJ E Pauls, M F Hockin, G L Long, et al.
The Journal of Biological Chemistry|November 5, 1991
beta-Hydroxyaspartic acid and beta-hydroxyasparagine residues in recombinant human protein S are not required for anticoagulant cofactor activity or for binding to C4b-binding proteinR M Nelson, W J VanDusen, P A Friedman, et al.
Journal of Deaf Studies and Deaf Education|September 30, 2004
Approaches to studying in deaf and hearing students in higher educationJ T Richardson, J MacLeod-Gallinger, B G McKee, et al.
American Journal of Human Genetics|July 31, 1998
An unknown genetic defect increases venous thrombosis risk, through interaction with protein C deficiencyS J Hasstedt, E G Bovill, P W Callas, et al.
Pageof 9