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Mathias W Seeliger

Showing results (111-120 of 128) with videos related to

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 25, 2011
PALS1 is essential for retinal pigment epithelium structure and neural retina stratificationBokyung Park, Celso Henrique Alves, Ditte M Lundvig, et al.
Advances in Experimental Medicine and Biology|December 21, 2011
Gene therapy restores missing cone-mediated vision in the CNGA3-/- mouse model of achromatopsiaStylianos Michalakis, Regine Mühlfriedel, Naoyuki Tanimoto, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 15, 2010
Restoration of cone vision in the CNGA3-/- mouse model of congenital complete lack of cone photoreceptor functionStylianos Michalakis, Regine Mühlfriedel, Naoyuki Tanimoto, et al.
Angewandte Chemie (International Ed. in English)|March 28, 2008
A portable albumin binder from a DNA-encoded chemical libraryChristoph E Dumelin, Sabrina Trüssel, Fabian Buller, et al.
Frontiers in Molecular Neuroscience|January 30, 2018
Disturbed Processing of Contextual Information in HCN3 Channel Deficient MiceMarc S Stieglitz, Stefanie Fenske, Verena Hammelmann, et al.
Human Molecular Genetics|July 19, 2015
Retinitis pigmentosa: impact of different Pde6a point mutations on the disease phenotypeVithiyanjali Sothilingam, Marina Garcia Garrido, Kangwei Jiao, et al.
Human Molecular Genetics|September 25, 2012
Loss of CRB2 in the mouse retina mimics human retinitis pigmentosa due to mutations in the CRB1 geneCelso Henrique Alves, Alicia Sanz Sanz, Bokyung Park, et al.
Vision Research|September 29, 2005
In vivo confocal imaging of the retina in animal models using scanning laser ophthalmoscopyMathias W Seeliger, Susanne C Beck, Naira Pereyra-Muñoz, et al.
Plos Genetics|December 17, 2013
Targeted ablation of CRB1 and CRB2 in retinal progenitor cells mimics Leber congenital amaurosisLucie P Pellissier, Celso Henrique Alves, Peter M Quinn, et al.
The Journal of Clinical Investigation|December 5, 2017
Patients and animal models of CNGβ1-deficient retinitis pigmentosa support gene augmentation approachSimon M Petersen-Jones, Laurence M Occelli, Paige A Winkler, et al.
Pageof 13

Showing results (111-120 of 128) with videos related to

Sort By:
Pageof 13
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 25, 2011
PALS1 is essential for retinal pigment epithelium structure and neural retina stratificationBokyung Park, Celso Henrique Alves, Ditte M Lundvig, et al.
Advances in Experimental Medicine and Biology|December 21, 2011
Gene therapy restores missing cone-mediated vision in the CNGA3-/- mouse model of achromatopsiaStylianos Michalakis, Regine Mühlfriedel, Naoyuki Tanimoto, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 15, 2010
Restoration of cone vision in the CNGA3-/- mouse model of congenital complete lack of cone photoreceptor functionStylianos Michalakis, Regine Mühlfriedel, Naoyuki Tanimoto, et al.
Angewandte Chemie (International Ed. in English)|March 28, 2008
A portable albumin binder from a DNA-encoded chemical libraryChristoph E Dumelin, Sabrina Trüssel, Fabian Buller, et al.
Frontiers in Molecular Neuroscience|January 30, 2018
Disturbed Processing of Contextual Information in HCN3 Channel Deficient MiceMarc S Stieglitz, Stefanie Fenske, Verena Hammelmann, et al.
Human Molecular Genetics|July 19, 2015
Retinitis pigmentosa: impact of different Pde6a point mutations on the disease phenotypeVithiyanjali Sothilingam, Marina Garcia Garrido, Kangwei Jiao, et al.
Human Molecular Genetics|September 25, 2012
Loss of CRB2 in the mouse retina mimics human retinitis pigmentosa due to mutations in the CRB1 geneCelso Henrique Alves, Alicia Sanz Sanz, Bokyung Park, et al.
Vision Research|September 29, 2005
In vivo confocal imaging of the retina in animal models using scanning laser ophthalmoscopyMathias W Seeliger, Susanne C Beck, Naira Pereyra-Muñoz, et al.
Plos Genetics|December 17, 2013
Targeted ablation of CRB1 and CRB2 in retinal progenitor cells mimics Leber congenital amaurosisLucie P Pellissier, Celso Henrique Alves, Peter M Quinn, et al.
The Journal of Clinical Investigation|December 5, 2017
Patients and animal models of CNGβ1-deficient retinitis pigmentosa support gene augmentation approachSimon M Petersen-Jones, Laurence M Occelli, Paige A Winkler, et al.
Pageof 13