S.S. Sidney

Bile acids: regulation of apoptosis by ursodeoxycholic acid

From oxygen to erythropoietin: Relevance of hypoxia for retinal development, health and disease

Bile acid–microbiota crosstalk in gastrointestinal inflammation and carcinogenesis

Unfolding the therapeutic potential of chemical chaperones for age-related macular degeneration

Retinitis Pigmentosa: Genes and Disease Mechanisms

Improved Retinal Function in a Mouse Model of Dominant Retinitis Pigmentosa Following AAV-delivered Gene Therapy

Adeno-associated virus vector as a platform for gene therapy delivery

Retinal Ganglion Cells Survive and Maintain Normal Dendritic Morphology in a Mouse Model of Inherited Photoreceptor Degeneration

VEGF in Signaling and Disease: Beyond Discovery and Development

ER stress-induced cell death mechanisms

Autosomal-Recessive Early-Onset Retinitis Pigmentosa Caused by a Mutation in PDE6G, the Gene Encoding the Gamma Subunit of Rod cGMP Phosphodiesterase

Advances in Gene Therapy for Diseases of the Eye

Chiefs: Economic Development and Elite Control of Civil Society in Sierra Leone

Collective Action in Diverse Sierra Leone Communities

Reversible Photocontrol of Biological Systems by the Incorporation of Molecular Photoswitches

Piccolo and bassoon maintain synaptic vesicle clustering without directly participating in vesicle exocytosis

Early Synaptic Defects intulp1^−/−Mice

Genes and mutations causing retinitis pigmentosa

Two mouse retinal degenerations caused by missense mutations in the β-subunit of rod cGMP phosphodiesterase gene

Mitochondrial DNA genetic diversity among four ethnic groups in Sierra Leone

Tool from ancient pharmacopoeia prevents vision loss.

Tauroursodeoxycholic Acid Preservation of Photoreceptor Structure and Function in therd10Mouse through Postnatal Day 30