S. Azarian

发表

DEPHOSPHORYLATION ON RHODOPSIN CHARACTERISTICS AND ITS EFFECT Calpain: MOLECULAR Selective Proteolysis of Arrestin by Enzymology:

A. King, S. Azarian, 2014 .

Characterization of calpain II in the retina and photoreceptor outer segments.

D. S. Williams, C. L. Schlamp, S. Azarian, 1993, Journal of cell science.

Three homologs of rds/peripherin in Xenopus laevis photoreceptors that exhibit covalent and non-covalent interactions.

D. Bok, G. Travis, W. Moghrabi, 1996, Journal of cell science.

Calpain activity in the retinas of normal and RCS rats.

D. S. Williams, S. Azarian, 1995, Current eye research.

Selective Proteolysis of Arrestin by Calpain

A. King, M. Hallett, S. Azarian, 1995, The Journal of Biological Chemistry.

Mechanistic studies of the immunochemical termination of self-tolerance with unnatural amino acids

G. S. Hunt, R. Lerner, P. Schultz, 2009, Proceedings of the National Academy of Sciences.

Insights into the Function of Rim Protein in Photoreceptors and Etiology of Stargardt's Disease from the Phenotype in abcr Knockout Mice

D. Birch, G. Travis, N. Mata, 1999, Cell.

Role of myosin VIIa and Rab27a in the motility and localization of RPE melanosomes

K. Steel, C. Lillo, David S. Williams, 2004, Journal of Cell Science.

The human photoreceptor rim protein gene (ABCR): genomic structure and primer set information for mutation analysis

G. Travis, J. Weng, C. F. Megarity, 1998, Human Genetics.

The photoreceptor rim protein is an ABC transporter encoded by the gene for recessive Stargardt's disease (ABCR)

G. Travis, S. Azarian, 1997, FEBS letters.

Time-resolved fluorescence resonance energy transfer and surface plasmon resonance-based assays for retinoid and transthyretin binding to retinol-binding protein 4.

Paul W Anderson, Richard E Trager, J. Caldwell, 2009, Analytical biochemistry.

Lack of Involvement of CEP Adducts in TLR Activation and in Angiogenesis

B. Jaffee, R. Cepeda, Yubin Qiu, 2014, PLoS ONE.

Proteomic analysis of mature melanosomes from the retinal pigmented epithelium.

J. Yates, C. Lillo, David S. Williams, 2006, Journal of proteome research.

Lentiviral gene replacement therapy of retinas in a mouse model for Usher syndrome type 1B

D. S. Williams, C. Lillo, D. Gibbs, 2007, Gene Therapy.

Screen for usher syndrome 1B mutations in the ovine myosin VIIa gene.

Tania L. Slatter, David S. Williams, S. Tebbutt, 2003, Advances in experimental medicine and biology.