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Proceedings of the National Academy of Sciences of the United States of America
|
January 30, 2013
Retinal degeneration depends on Bmi1 function and reactivation of cell cycle proteins
Dusan Zencak, Karine Schouwey, Danian Chen, et al.
Plos One
|
September 9, 2011
Retinal degeneration progression changes lentiviral vector cell targeting in the retina
Maritza Calame, Maité Cachafeiro, Stéphanie Philippe, et al.
Plos One
|
February 10, 2017
Nephropathy in Pparg-null mice highlights PPARγ systemic activities in metabolism and in the immune system
Barbara Toffoli, Federica Gilardi, Carine Winkler, et al.
Advances in Experimental Medicine and Biology
|
January 15, 2008
Lentiviral gene transfer-mediated cone vision restoration in RPE65 knockout mice
Alexis-Pierre Bemelmans, Corinne Kostic, Maité Cachafeiro, et al.
Plos One
|
February 10, 2011
Gene therapy regenerates protein expression in cone photoreceptors in Rpe65(R91W/R91W) mice
Corinne Kostic, Sylvain Vincent Crippa, Vérène Pignat, et al.
Human Molecular Genetics
|
March 10, 2015
Interactome analysis reveals that FAM161A, deficient in recessive retinitis pigmentosa, is a component of the Golgi-centrosomal network
Silvio Alessandro Di Gioia, Pietro Farinelli, Stef J F Letteboer, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
February 2, 2017
Cone Genesis Tracing by the Chrnb4-EGFP Mouse Line: Evidences of Cellular Material Fusion after Cone Precursor Transplantation
Sarah Decembrini, Catherine Martin, Florian Sennlaub, et al.
Scientific Reports
|
December 23, 2016
Olaparib significantly delays photoreceptor loss in a model for hereditary retinal degeneration
Ayse Sahaboglu, Melanie Barth, Enver Secer, et al.
Investigative Ophthalmology & Visual Science
|
January 2, 2007
Retinal stem cells transplanted into models of late stages of retinitis pigmentosa preferentially adopt a glial or a retinal ganglion cell fate
Kriss Canola, Brigitte Angénieux, Meriem Tekaya, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 15, 2023
Gene augmentation therapy attenuates retinal degeneration in a knockout mouse model of Fam161a retinitis pigmentosa
Chen Matsevich, Prakadeeswari Gopalakrishnan, Ning Chang, et al.
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of 8
Search research articles
Search
Showing results (31-40 of 79) with videos related to
Sort By:
Page
of 8
Proceedings of the National Academy of Sciences of the United States of America
|
January 30, 2013
Retinal degeneration depends on Bmi1 function and reactivation of cell cycle proteins
Dusan Zencak, Karine Schouwey, Danian Chen, et al.
Plos One
|
September 9, 2011
Retinal degeneration progression changes lentiviral vector cell targeting in the retina
Maritza Calame, Maité Cachafeiro, Stéphanie Philippe, et al.
Plos One
|
February 10, 2017
Nephropathy in Pparg-null mice highlights PPARγ systemic activities in metabolism and in the immune system
Barbara Toffoli, Federica Gilardi, Carine Winkler, et al.
Advances in Experimental Medicine and Biology
|
January 15, 2008
Lentiviral gene transfer-mediated cone vision restoration in RPE65 knockout mice
Alexis-Pierre Bemelmans, Corinne Kostic, Maité Cachafeiro, et al.
Plos One
|
February 10, 2011
Gene therapy regenerates protein expression in cone photoreceptors in Rpe65(R91W/R91W) mice
Corinne Kostic, Sylvain Vincent Crippa, Vérène Pignat, et al.
Human Molecular Genetics
|
March 10, 2015
Interactome analysis reveals that FAM161A, deficient in recessive retinitis pigmentosa, is a component of the Golgi-centrosomal network
Silvio Alessandro Di Gioia, Pietro Farinelli, Stef J F Letteboer, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
February 2, 2017
Cone Genesis Tracing by the Chrnb4-EGFP Mouse Line: Evidences of Cellular Material Fusion after Cone Precursor Transplantation
Sarah Decembrini, Catherine Martin, Florian Sennlaub, et al.
Scientific Reports
|
December 23, 2016
Olaparib significantly delays photoreceptor loss in a model for hereditary retinal degeneration
Ayse Sahaboglu, Melanie Barth, Enver Secer, et al.
Investigative Ophthalmology & Visual Science
|
January 2, 2007
Retinal stem cells transplanted into models of late stages of retinitis pigmentosa preferentially adopt a glial or a retinal ganglion cell fate
Kriss Canola, Brigitte Angénieux, Meriem Tekaya, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 15, 2023
Gene augmentation therapy attenuates retinal degeneration in a knockout mouse model of Fam161a retinitis pigmentosa
Chen Matsevich, Prakadeeswari Gopalakrishnan, Ning Chang, et al.
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of 8