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M Abrahamson

Showing results (81-90 of 118) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1993
Localization of the human cystatin D gene (CST5) to chromosome 20p11.21 by in situ hybridizationJ P Freije, A M Pendás, G Velasco, et al.
Immunology|September 1, 1991
Human monoclonal antibodies with different fine specificity for digoxin derivatives: cloning of heavy and light chain variable region sequencesL Danielsson, C Furebring, M Ohlin, et al.
Molecular Pathology : MP|July 8, 2000
Expression of an LDL receptor allele with two different mutations (E256K and I402T)U Ekström, M Abrahamson, T Sveger, et al.
The Journal of Biological Chemistry|June 26, 1999
Inhibition of mammalian legumain by some cystatins is due to a novel second reactive siteM Alvarez-Fernandez, A J Barrett, B Gerhartz, et al.
The Biochemical Journal|April 1, 1994
Differential changes in the association and dissociation rate constants for binding of cystatins to target proteinases occurring on N-terminal truncation of the inhibitors indicate that the interaction mechanism varies with different enzymesI Björk, E Pol, E Raub-Segall, et al.
Bone|April 25, 2000
A peptidyl derivative structurally based on the inhibitory center of cystatin C inhibits bone resorption in vitroL Johansson, A Grubb, M Abrahamson, et al.
Gene|July 15, 1989
High-level expression of active human cystatin C in Escherichia coliH Dalbøge, E B Jensen, H Tøttrup, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|June 10, 2000
Functional effects of the inhibition of the cysteine protease activity of the major house dust mite allergen Der p 1 by a novel peptide-based inhibitorR J John, C Rusznak, M Ramjee, et al.
Ophthalmic Genetics|November 12, 1998
A Swedish family with a mutation in the peripherin/RDS gene (Arg-172-Trp) associated with a progressive retinal degenerationU Ekström, S Andréasson, V Ponjavic, et al.
Ophthalmic Genetics|May 20, 1998
Phenotypic expression of autosomal dominant retinitis pigmentosa in a Swedish family expressing a Phe-211-Leu variant of peripherin/RDSU Ekström, V Ponjavic, M Abrahamson, et al.
Pageof 12

Showing results (81-90 of 118) with videos related to

Sort By:
Pageof 12
Cytogenetics and Cell Genetics|January 1, 1993
Localization of the human cystatin D gene (CST5) to chromosome 20p11.21 by in situ hybridizationJ P Freije, A M Pendás, G Velasco, et al.
Immunology|September 1, 1991
Human monoclonal antibodies with different fine specificity for digoxin derivatives: cloning of heavy and light chain variable region sequencesL Danielsson, C Furebring, M Ohlin, et al.
Molecular Pathology : MP|July 8, 2000
Expression of an LDL receptor allele with two different mutations (E256K and I402T)U Ekström, M Abrahamson, T Sveger, et al.
The Journal of Biological Chemistry|June 26, 1999
Inhibition of mammalian legumain by some cystatins is due to a novel second reactive siteM Alvarez-Fernandez, A J Barrett, B Gerhartz, et al.
The Biochemical Journal|April 1, 1994
Differential changes in the association and dissociation rate constants for binding of cystatins to target proteinases occurring on N-terminal truncation of the inhibitors indicate that the interaction mechanism varies with different enzymesI Björk, E Pol, E Raub-Segall, et al.
Bone|April 25, 2000
A peptidyl derivative structurally based on the inhibitory center of cystatin C inhibits bone resorption in vitroL Johansson, A Grubb, M Abrahamson, et al.
Gene|July 15, 1989
High-level expression of active human cystatin C in Escherichia coliH Dalbøge, E B Jensen, H Tøttrup, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|June 10, 2000
Functional effects of the inhibition of the cysteine protease activity of the major house dust mite allergen Der p 1 by a novel peptide-based inhibitorR J John, C Rusznak, M Ramjee, et al.
Ophthalmic Genetics|November 12, 1998
A Swedish family with a mutation in the peripherin/RDS gene (Arg-172-Trp) associated with a progressive retinal degenerationU Ekström, S Andréasson, V Ponjavic, et al.
Ophthalmic Genetics|May 20, 1998
Phenotypic expression of autosomal dominant retinitis pigmentosa in a Swedish family expressing a Phe-211-Leu variant of peripherin/RDSU Ekström, V Ponjavic, M Abrahamson, et al.
Pageof 12