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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 hybridization
J 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 sequences
L 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 site
M 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 enzymes
I 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 vitro
L Johansson, A Grubb, M Abrahamson, et al.
Gene
|
July 15, 1989
High-level expression of active human cystatin C in Escherichia coli
H 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 inhibitor
R 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 degeneration
U 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/RDS
U Ekström, V Ponjavic, M Abrahamson, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 118) with videos related to
Sort By:
Page
of 12
Cytogenetics and Cell Genetics
|
January 1, 1993
Localization of the human cystatin D gene (CST5) to chromosome 20p11.21 by in situ hybridization
J 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 sequences
L 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 site
M 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 enzymes
I 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 vitro
L Johansson, A Grubb, M Abrahamson, et al.
Gene
|
July 15, 1989
High-level expression of active human cystatin C in Escherichia coli
H 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 inhibitor
R 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 degeneration
U 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/RDS
U Ekström, V Ponjavic, M Abrahamson, et al.
Page
of 12