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- 1998
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Mark
Two-step mechanism of inhibition of cathepsin B by cystatin C, due to the inhibitor displacing the occluding loop of the enzyme
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- Contribution to journal › Article
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Mark
A Swedish family with a mutation in the peripherin/RDS gene (Arg-172-Trp) associated with a progressive retinal degeneration
(
- Contribution to journal › Article
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Mark
Intracellular accumulation of the amyloidogenic L68Q variant of human cystatin C in NIH/3T3 cells
(
- Contribution to journal › Article
- 1997
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Mark
Apolipoprotein E genotyping in Alzheimer’s disease and frontotemporal dementia
(
- Contribution to journal › Article
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Mark
Cathepsin B and cysteine proteinase inhibitors in human lung cancer cell lines
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- Contribution to journal › Article
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Mark
Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: Paucity of mutations in the coding region, but splice defects in two families
(
- Contribution to journal › Article
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Mark
Cystatin E is a novel human cysteine proteinase inhibitor with structural resemblance to family 2 cystatins
(
- Contribution to journal › Article
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Mark
Affinity purification and elimination of methionine oxidation in recombinant human cystatin C
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- Contribution to journal › Article
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Mark
A mild phenotype of autosomal dominant retinitis pigmentosa is associated with the rhodopsin mutation Pro-267–Leu
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- Contribution to journal › Article
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Mark
Autosomal dominant retinitis pigmentosa with a rhodopsin mutation (Arg-135–Trp): Disease phenotype in a Swedish family
(
- Contribution to journal › Article