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Martin Biel

Showing results (161-170 of 198) with videos related to

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JCI Insight|October 7, 2025
CRISPR/Cas-mediated activation of genes associated with inherited retinal dystrophies in human cells for diagnostic purposesValentin J Weber, Alice Reschigna, Maximilian J Gerhardt, et al.
Plos One|November 14, 2014
Identification of a common non-apoptotic cell death mechanism in hereditary retinal degenerationBlanca Arango-Gonzalez, Dragana Trifunović, Ayse Sahaboglu, et al.
The EMBO Journal|April 16, 2015
Expression of Ca²⁺-permeable two-pore channels rescues NAADP signalling in TPC-deficient cellsMargarida Ruas, Lianne C Davis, Cheng-Chang Chen, et al.
The EMBO Journal|January 7, 2003
Absence epilepsy and sinus dysrhythmia in mice lacking the pacemaker channel HCN2Andreas Ludwig, Thomas Budde, Juliane Stieber, 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.
Nature Communications|July 3, 2021
Redirected nuclear glutamate dehydrogenase supplies Tet3 with α-ketoglutarate in neuronsFranziska R Traube, Dilara Özdemir, Hanife Sahin, 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 Gene Therapy. Clinical Development|September 7, 2018
Development of Methodology and Study Protocol: Safety and Efficacy of a Single Subretinal Injection of rAAV.hCNGA3 in Patients with CNGA3-Linked Achromatopsia Investigated in an Exploratory Dose-Escalation TrialNadine A Kahle, Tobias Peters, Ditta Zobor, et al.
Human Molecular Genetics|April 10, 2015
Vitreal delivery of AAV vectored Cnga3 restores cone function in CNGA3-/-/Nrl-/- mice, an all-cone model of CNGA3 achromatopsiaWei Du, Ye Tao, Wen-Tao Deng, et al.
Pageof 20

Showing results (161-170 of 198) with videos related to

Sort By:
Pageof 20
JCI Insight|October 7, 2025
CRISPR/Cas-mediated activation of genes associated with inherited retinal dystrophies in human cells for diagnostic purposesValentin J Weber, Alice Reschigna, Maximilian J Gerhardt, et al.
Plos One|November 14, 2014
Identification of a common non-apoptotic cell death mechanism in hereditary retinal degenerationBlanca Arango-Gonzalez, Dragana Trifunović, Ayse Sahaboglu, et al.
The EMBO Journal|April 16, 2015
Expression of Ca²⁺-permeable two-pore channels rescues NAADP signalling in TPC-deficient cellsMargarida Ruas, Lianne C Davis, Cheng-Chang Chen, et al.
The EMBO Journal|January 7, 2003
Absence epilepsy and sinus dysrhythmia in mice lacking the pacemaker channel HCN2Andreas Ludwig, Thomas Budde, Juliane Stieber, 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.
Nature Communications|July 3, 2021
Redirected nuclear glutamate dehydrogenase supplies Tet3 with α-ketoglutarate in neuronsFranziska R Traube, Dilara Özdemir, Hanife Sahin, 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 Gene Therapy. Clinical Development|September 7, 2018
Development of Methodology and Study Protocol: Safety and Efficacy of a Single Subretinal Injection of rAAV.hCNGA3 in Patients with CNGA3-Linked Achromatopsia Investigated in an Exploratory Dose-Escalation TrialNadine A Kahle, Tobias Peters, Ditta Zobor, et al.
Human Molecular Genetics|April 10, 2015
Vitreal delivery of AAV vectored Cnga3 restores cone function in CNGA3-/-/Nrl-/- mice, an all-cone model of CNGA3 achromatopsiaWei Du, Ye Tao, Wen-Tao Deng, et al.
Pageof 20