Rezultati pretrage autora

1

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

Izdano 2018

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2

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

Izdano 2017

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3

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

Izdano 2021

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4

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

Izdano 2022

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5

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

Izdano 2017

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6

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

Izdano 2015

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7

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

Izdano 2022

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8

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

Izdano 2014

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9

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... od Lee, Winston Y, Weinberg, Olga K, Evans, Andrew G, Pinkus, Geraldine S

Izdano 2018

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10

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

Izdano 2018

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11

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

Izdano 2018

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12

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

Izdano 2013

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13

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

Izdano 2016

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14

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

Izdano 2017

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15

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

Izdano 2020

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16

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

Izdano 2020

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17

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

Izdano 2022

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18

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

Izdano 2008

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19

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

Izdano 2009

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20

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

Izdano 2008

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Rezultati pretrage - LEE, WINSTON

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

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

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

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

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

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

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

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

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... od Lee, Winston Y, Weinberg, Olga K, Evans, Andrew G, Pinkus, Geraldine S

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

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

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

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

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

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

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

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

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

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

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

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