101 – 110 of 188
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=""
width=""
height=""
allowtransparency="true"
frameborder="0">
</iframe>
- 1998
-
Mark
Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype
- Contribution to journal › Article
-
Mark
Two-step mechanism of inhibition of cathepsin B by cystatin C, due to the inhibitor displacing the occluding loop of the enzyme
- Contribution to journal › Article
-
Mark
A 50-year perspective of a family with chromosome 14-linked Alzheimer’s disease
- Contribution to journal › Article
-
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
-
Mark
Phenotype in a Swedish family with X-linked retinitis pigmentosa caused by a novel splice defect in the RPGR gene
- Contribution to journal › Article
-
Mark
Intracellular accumulation of the amyloidogenic L68Q variant of human cystatin C in NIH/3T3 cells
- Contribution to journal › Article
- 1997
-
Mark
Apolipoprotein E genotyping in Alzheimer’s disease and frontotemporal dementia
- Contribution to journal › Article
-
Mark
Affinity purification and elimination of methionine oxidation in recombinant human cystatin C
- Contribution to journal › Article
-
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
-
Mark
Cathepsin B and cysteine proteinase inhibitors in human lung cancer cell lines
- Contribution to journal › Article
