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Showing results (51-60 of 55) with videos related to

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Science Advances|October 2, 2024
Neuroinflammation as a cause of differential Müller cell regenerative responses to retinal injuryDiana García-García, Lorena Vidal-Gil, Karine Parain, et al.
Progress in Retinal and Eye Research|January 20, 2023
Shedding light on myopia by studying complete congenital stationary night blindnessChristina Zeitz, Jérome E Roger, Isabelle Audo, et al.
Immunity|August 20, 2020
The 10q26 Risk Haplotype of Age-Related Macular Degeneration Aggravates Subretinal Inflammation by Impairing Monocyte EliminationFanny Beguier, Michael Housset, Christophe Roubeix, et al.
Nature Communications|November 21, 2024
GPATCH11 variants cause mis-splicing and early-onset retinal dystrophy with neurological impairmentAndrea Zanetti, Gwendal Dujardin, Lucas Fares-Taie, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Biallelic germline variants in the hematologic malignancy predisposition gene <i>DDX41</i> cause retinal dystrophy through dysregulation of retinal homeostasisZoéline Mars, Andrea Zanetti, Karolina Kaminska, et al.
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Showing results (51-60 of 55) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 55 results.
Science Advances|October 2, 2024
Neuroinflammation as a cause of differential Müller cell regenerative responses to retinal injuryDiana García-García, Lorena Vidal-Gil, Karine Parain, et al.
Progress in Retinal and Eye Research|January 20, 2023
Shedding light on myopia by studying complete congenital stationary night blindnessChristina Zeitz, Jérome E Roger, Isabelle Audo, et al.
Immunity|August 20, 2020
The 10q26 Risk Haplotype of Age-Related Macular Degeneration Aggravates Subretinal Inflammation by Impairing Monocyte EliminationFanny Beguier, Michael Housset, Christophe Roubeix, et al.
Nature Communications|November 21, 2024
GPATCH11 variants cause mis-splicing and early-onset retinal dystrophy with neurological impairmentAndrea Zanetti, Gwendal Dujardin, Lucas Fares-Taie, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Biallelic germline variants in the hematologic malignancy predisposition gene <i>DDX41</i> cause retinal dystrophy through dysregulation of retinal homeostasisZoéline Mars, Andrea Zanetti, Karolina Kaminska, et al.
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