Canlyniadau Chwilio - LEE, WINSTON

Penetrance of the ABCA4 p.Asn1868Ile Allele in Stargardt Disease gan Allikmets, Rando, Zernant, Jana, Lee, Winston

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GATA1 Is a Sensitive and Specific Nuclear Marker for Erythroid and Megakaryocytic Lineages gan Lee, Winston Y., Weinberg, Olga K., Pinkus, Geraldine S.

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Reevaluating the Association of Sex With ABCA4 Alleles in Patients With Stargardt Disease gan Lee, Winston, Zernant, Jana, Nagasaki, Takayuki, Allikmets, Rando

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Identifying patients and assessing variant pathogenicity for an autosomal dominant disease-driving gene gan Lee, Winston, de Prisco, Nicola, Gennarino, Vincenzo A.

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Stem Cell Therapies in Retinal Disorders gan Garg, Aakriti, Yang, Jin, Lee, Winston, Tsang, Stephen H.

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Type 1 neovascularization may confer resistance to geographic atrophy amongst eyes treated for neovascular age-related macular degeneration gan Dhrami-Gavazi, Elona, Balaratnasingam, Chandrakumar, Lee, Winston, Freund, K. Bailey

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How to expand the method details in your Cell Press paper with step-by-step STAR Protocols gan Lee, Winston, de Prisco, Nicola, Gennarino, Vincenzo A., Buttery, Shawnna

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Structural and Genetic Assessment of the ABCA4-Associated Optical Gap Phenotype gan Nõupuu, Kalev, Lee, Winston, Zernant, Jana, Tsang, Stephen H., Allikmets, Rando

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Loss of Full-Length GATA1 Expression in Megakaryocytes Is a Sensitive and Specific Immunohistochemical Marker for the Diagnosis of Myeloid Proliferative Disorder Related to Down Sy... gan Lee, Winston Y, Weinberg, Olga K, Evans, Andrew G, Pinkus, Geraldine S

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Photoreceptor Cells as a Source of Fundus Autofluorescence in Recessive Stargardt Disease gan Paavo, Maarjaliis, Lee, Winston, Allikmets, Rando, Tsang, Stephen, Sparrow, Janet R.

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Deep Scleral Exposure: A Degenerative Outcome of End-Stage Stargardt Disease gan LEE, WINSTON, ZERNANT, JANA, NAGASAKI, TAKAYUKI, TSANG, STEPHEN H., ALLIKMETS, RANDO

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Disease Progression in Autosomal Dominant Cone-Rod Dystrophy Caused by a Novel Mutation (D100G) in the GUCA1A Gene gan Nong, Eva, Lee, Winston, Merriam, Joanna E., Allikmets, Rando, Tsang, Stephen H.

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Multimodal Imaging of Disease-Associated Pigmentary Changes in Retinitis Pigmentosa gan Schuerch, Kaspar, Marsiglia, Marcela, Lee, Winston, Tsang, Stephen H., Sparrow, Janet R.

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Peripapillary sparing in RDH12-associated Leber congenital amaurosis gan Garg, Aakriti, Lee, Winston, Sengillo, Jesse D., Allikmets, Rando, Tsang, Stephen H.

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Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations gan Cremers, Frans P.M., Lee, Winston, Collin, Rob W.J., Allikmets, Rando

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Pure erythroid leukemia gan Chen, Jason C., Lee, Winston Y., Schaefer, Jordan K., Bixby, Dale L.

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Protocol to assess the effect of disease-driving variants on mouse brain morphology and primary hippocampal neurons gan de Prisco, Nicola, Chemiakine, Alexei, Lee, Winston, Botta, Salvatore, Gennarino, Vincenzo A.

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Endothelial CD47 interaction with SIRPγ is required for human T-cell transendothelial migration under shear flow conditions in vitro gan Stefanidakis, Michael, Newton, Gail, Lee, Winston Y., Parkos, Charles A., Luscinskas, Francis W.

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Junctional Adhesion Molecule A Interacts with Afadin and PDZ-GEF2 to Activate Rap1A, Regulate β1 Integrin Levels, and Enhance Cell Migration gan Severson, Eric A., Lee, Winston Y., Capaldo, Christopher T., Nusrat, Asma, Parkos, Charles A.

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Neutrophil-mediated Activation of Epithelial Protease-Activated Receptors-1 and -2 Regulates Barrier Function and Transepithelial Migration gan Chin, Alex C., Lee, Winston Y., Nusrat, Asma, Vergnolle, Nathalie, Parkos, Charles A.

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