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Journal of Immunological Methods
|
July 16, 2008
A novel bioassay for B-cell activating factor (BAFF) based on expression of a BAFF-receptor ectodomain-tumour necrosis factor-related apoptosis-inducing ligand (TRAIL) receptor-2 endodomain fusion receptor in human rhabdomyosarcoma cells
Michelle McClements, Stella Williams, Christine Ball, et al.
Experimental Eye Research
|
December 27, 2011
Tetradecanoylphorbol-13-acetate (TPA) significantly increases AAV2/5 transduction of human neuronal cells in vitro
Qisheng You, Laurence A Brown, Michelle McClements, et al.
Investigative Ophthalmology & Visual Science
|
January 17, 2013
Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy
Michelle McClements, Wayne I L Davies, Michel Michaelides, et al.
Vision Research
|
January 23, 2013
X-linked cone dystrophy and colour vision deficiency arising from a missense mutation in a hybrid L/M cone opsin gene
Michelle McClements, Wayne I L Davies, Michel Michaelides, et al.
Investigative Ophthalmology & Visual Science
|
April 16, 2010
The PROM1 mutation p.R373C causes an autosomal dominant bull's eye maculopathy associated with rod, rod-cone, and macular dystrophy
Michel Michaelides, Marie-Claire Gaillard, Pascal Escher, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
Journal of Immunological Methods
|
July 16, 2008
A novel bioassay for B-cell activating factor (BAFF) based on expression of a BAFF-receptor ectodomain-tumour necrosis factor-related apoptosis-inducing ligand (TRAIL) receptor-2 endodomain fusion receptor in human rhabdomyosarcoma cells
Michelle McClements, Stella Williams, Christine Ball, et al.
Experimental Eye Research
|
December 27, 2011
Tetradecanoylphorbol-13-acetate (TPA) significantly increases AAV2/5 transduction of human neuronal cells in vitro
Qisheng You, Laurence A Brown, Michelle McClements, et al.
Investigative Ophthalmology & Visual Science
|
January 17, 2013
Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy
Michelle McClements, Wayne I L Davies, Michel Michaelides, et al.
Vision Research
|
January 23, 2013
X-linked cone dystrophy and colour vision deficiency arising from a missense mutation in a hybrid L/M cone opsin gene
Michelle McClements, Wayne I L Davies, Michel Michaelides, et al.
Investigative Ophthalmology & Visual Science
|
April 16, 2010
The PROM1 mutation p.R373C causes an autosomal dominant bull's eye maculopathy associated with rod, rod-cone, and macular dystrophy
Michel Michaelides, Marie-Claire Gaillard, Pascal Escher, et al.
Page
of 1