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The American Journal of Pathology
|
June 17, 2015
IL-4 regulates specific Arg-1(+) macrophage sFlt-1-mediated inhibition of angiogenesis
Wei-Kang Wu, Anastasios Georgiadis, David A Copland, et al.
Investigative Ophthalmology & Visual Science
|
September 27, 2014
Nature of the visual loss in observers with Leber's congenital amaurosis caused by specific mutations in RPE65
Caterina Ripamonti, G Bruce Henning, Robin R Ali, et al.
Journal of Vision
|
November 26, 2015
Spectral sensitivity measurements reveal partial success in restoring missing rod function with gene therapy
Caterina Ripamonti, G Bruce Henning, Scott J Robbie, et al.
Human Molecular Genetics
|
August 23, 2014
The severity of retinal pathology in homozygous Crb1rd8/rd8 mice is dependent on additional genetic factors
Ulrich F O Luhmann, Livia S Carvalho, Sophia-Martha Kleine Holthaus, et al.
Human Molecular Genetics
|
December 23, 2020
RPGR isoform imbalance causes ciliary defects due to exon ORF15 mutations in X-linked retinitis pigmentosa (XLRP)
Laura Moreno-Leon, Emma L West, Michelle O'Hara-Wright, et al.
Angiogenesis
|
October 5, 2019
Stabilization of myeloid-derived HIFs promotes vascular regeneration in retinal ischemia
Pilar Villacampa, Sidath E Liyanage, Izabela P Klaska, et al.
Stem Cell Reports
|
May 6, 2022
Differentiation of brain and retinal organoids from confluent cultures of pluripotent stem cells connected by nerve-like axonal projections of optic origin
Milan Fernando, Scott Lee, Jesse R Wark, et al.
Plos One
|
May 1, 2012
Differential modulation of retinal degeneration by Ccl2 and Cx3cr1 chemokine signalling
Ulrich F O Luhmann, Clemens A Lange, Scott Robbie, et al.
Scientific Reports
|
February 21, 2019
Conditional Dicer1 depletion using Chrnb4-Cre leads to cone cell death and impaired photopic vision
Eduardo Zabala Aldunate, Valentina Di Foggia, Fabiana Di Marco, et al.
Human Molecular Genetics
|
December 7, 2019
Neonatal brain-directed gene therapy rescues a mouse model of neurodegenerative CLN6 Batten disease
Sophia-Martha Kleine Holthaus, Saul Herranz-Martin, Giulia Massaro, et al.
Page
of 18
Search research articles
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Showing results (131-140 of 175) with videos related to
Sort By:
Page
of 18
The American Journal of Pathology
|
June 17, 2015
IL-4 regulates specific Arg-1(+) macrophage sFlt-1-mediated inhibition of angiogenesis
Wei-Kang Wu, Anastasios Georgiadis, David A Copland, et al.
Investigative Ophthalmology & Visual Science
|
September 27, 2014
Nature of the visual loss in observers with Leber's congenital amaurosis caused by specific mutations in RPE65
Caterina Ripamonti, G Bruce Henning, Robin R Ali, et al.
Journal of Vision
|
November 26, 2015
Spectral sensitivity measurements reveal partial success in restoring missing rod function with gene therapy
Caterina Ripamonti, G Bruce Henning, Scott J Robbie, et al.
Human Molecular Genetics
|
August 23, 2014
The severity of retinal pathology in homozygous Crb1rd8/rd8 mice is dependent on additional genetic factors
Ulrich F O Luhmann, Livia S Carvalho, Sophia-Martha Kleine Holthaus, et al.
Human Molecular Genetics
|
December 23, 2020
RPGR isoform imbalance causes ciliary defects due to exon ORF15 mutations in X-linked retinitis pigmentosa (XLRP)
Laura Moreno-Leon, Emma L West, Michelle O'Hara-Wright, et al.
Angiogenesis
|
October 5, 2019
Stabilization of myeloid-derived HIFs promotes vascular regeneration in retinal ischemia
Pilar Villacampa, Sidath E Liyanage, Izabela P Klaska, et al.
Stem Cell Reports
|
May 6, 2022
Differentiation of brain and retinal organoids from confluent cultures of pluripotent stem cells connected by nerve-like axonal projections of optic origin
Milan Fernando, Scott Lee, Jesse R Wark, et al.
Plos One
|
May 1, 2012
Differential modulation of retinal degeneration by Ccl2 and Cx3cr1 chemokine signalling
Ulrich F O Luhmann, Clemens A Lange, Scott Robbie, et al.
Scientific Reports
|
February 21, 2019
Conditional Dicer1 depletion using Chrnb4-Cre leads to cone cell death and impaired photopic vision
Eduardo Zabala Aldunate, Valentina Di Foggia, Fabiana Di Marco, et al.
Human Molecular Genetics
|
December 7, 2019
Neonatal brain-directed gene therapy rescues a mouse model of neurodegenerative CLN6 Batten disease
Sophia-Martha Kleine Holthaus, Saul Herranz-Martin, Giulia Massaro, et al.
Page
of 18