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- 2010
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Mark
Phenotype associated with mutation in the recently identified autosomal dominant retinitis pigmentosa KLHL7 gene.
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- Contribution to journal › Article
- 2008
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Mark
rd1 Mouse retina shows an imbalance in the activity of cysteine protease cathepsins and their endogenous inhibitor cystatin C.
(
- Contribution to journal › Article
- 2006
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Mark
rd1 Mouse Retina Shows Imbalance in Cellular Distribution and Levels of TIMP-1/MMP-9, TIMP-2/MMP-2 and Sulfated Glycosaminoglycans.
(
- Contribution to journal › Article
- 2005
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Mark
Clinical phenotype in a Swedish family with a mutation in the IMPDH1 gene.
(
- Contribution to journal › Article
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Mark
Cystatin C uptake in the eye.
(
- Contribution to journal › Article
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Mark
Juvenile X-linked retinoschisis with normal scotopic b-wave in the electroretinogram at an early stage of the disease.
(
- Contribution to journal › Article
- 2004
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Mark
Glutathione S-transferase µ(GST) modifies activities of proteases and levels of cystatin C secreted by mouse retinal explants
(
- Contribution to journal › Published meeting abstract
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Mark
Cystatin C in the anterior segment of rat and mouse eyes.
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- Contribution to journal › Article
- 2003
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Mark
Cathepsin B in the rat eye.
(
- Contribution to journal › Article
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Mark
Macular appearance by means of OCT and electrophysiology in members of two families with different mutations in RDS (the peripherin/RDS gene).
(
- Contribution to journal › Article