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M Abrahamson

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Human Genetics|June 1, 1989
The human cystatin C gene (CST3), mutated in hereditary cystatin C amyloid angiopathy, is located on chromosome 20M Abrahamson, M Q Islam, J Szpirer, et al.
Protein Expression and Purification|November 5, 1997
Affinity purification and elimination of methionine oxidation in recombinant human cystatin CP J Berti, I Ekiel, P Lindahl, et al.
Ophthalmic Genetics|June 1, 1997
A mild phenotype of autosomal dominant retinitis pigmentosa is associated with the rhodopsin mutation Pro-267-LeuV Ponjavic, M Abrahamson, S Andréasson, et al.
Human Genetics|July 1, 1992
A novel mutation in the beta-protein coding region of the amyloid beta-protein precursor (APP) geneM Balbín, M Abrahamson, L Gustafson, et al.
Biochimica Et Biophysica Acta|May 25, 1994
Latency of cathepsin B secreted by human colon carcinoma cells is not linked to secretion of cystatin C and is relieved by neutrophil elastaseD Keppler, P Waridel, M Abrahamson, et al.
European Journal of Clinical Investigation|October 10, 1998
Mutations in the low-density lipoprotein receptor gene in Swedish familial hypercholesterolaemia patients: clinical expression and treatment responseU Ekström, M Abrahamson, A Wallmark, et al.
Biochemistry|April 12, 1994
Evidence for the interaction of valine-10 in cystatin C with the S2 subsite of cathepsin BP Lindahl, D Ripoll, M Abrahamson, et al.
Gene|January 23, 1995
Structural organization, expression and chromosomal mapping of the mouse cystatin-C-encoding gene (Cst3)C Huh, J W Nagle, C A Kozak, et al.
FEBS Letters|January 11, 2001
Cystatin inhibition of cathepsin B requires dislocation of the proteinase occluding loop. Demonstration By release of loop anchoring through mutation of his110A Pavlova, J C Krupa, J S Mort, et al.
Biochemistry|May 2, 1998
Structural basis for different inhibitory specificities of human cystatins C and DA Hall, I Ekiel, R W Mason, et al.
Pageof 12

Showing results (51-60 of 118) with videos related to

Sort By:
Pageof 12
Human Genetics|June 1, 1989
The human cystatin C gene (CST3), mutated in hereditary cystatin C amyloid angiopathy, is located on chromosome 20M Abrahamson, M Q Islam, J Szpirer, et al.
Protein Expression and Purification|November 5, 1997
Affinity purification and elimination of methionine oxidation in recombinant human cystatin CP J Berti, I Ekiel, P Lindahl, et al.
Ophthalmic Genetics|June 1, 1997
A mild phenotype of autosomal dominant retinitis pigmentosa is associated with the rhodopsin mutation Pro-267-LeuV Ponjavic, M Abrahamson, S Andréasson, et al.
Human Genetics|July 1, 1992
A novel mutation in the beta-protein coding region of the amyloid beta-protein precursor (APP) geneM Balbín, M Abrahamson, L Gustafson, et al.
Biochimica Et Biophysica Acta|May 25, 1994
Latency of cathepsin B secreted by human colon carcinoma cells is not linked to secretion of cystatin C and is relieved by neutrophil elastaseD Keppler, P Waridel, M Abrahamson, et al.
European Journal of Clinical Investigation|October 10, 1998
Mutations in the low-density lipoprotein receptor gene in Swedish familial hypercholesterolaemia patients: clinical expression and treatment responseU Ekström, M Abrahamson, A Wallmark, et al.
Biochemistry|April 12, 1994
Evidence for the interaction of valine-10 in cystatin C with the S2 subsite of cathepsin BP Lindahl, D Ripoll, M Abrahamson, et al.
Gene|January 23, 1995
Structural organization, expression and chromosomal mapping of the mouse cystatin-C-encoding gene (Cst3)C Huh, J W Nagle, C A Kozak, et al.
FEBS Letters|January 11, 2001
Cystatin inhibition of cathepsin B requires dislocation of the proteinase occluding loop. Demonstration By release of loop anchoring through mutation of his110A Pavlova, J C Krupa, J S Mort, et al.
Biochemistry|May 2, 1998
Structural basis for different inhibitory specificities of human cystatins C and DA Hall, I Ekiel, R W Mason, et al.
Pageof 12