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Derek J Blake

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

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Frontiers in Molecular Biosciences|January 1, 2024
Misfolding of fukutin-related protein (FKRP) variants in congenital and limb girdle muscular dystrophiesChristopher T Esapa, R A Jeffrey McIlhinney, Adrian J Waite, et al.
Stem Cells Translational Medicine|February 17, 2017
Potency of Human Cardiosphere-Derived Cells from Patients with Ischemic Heart Disease Is Associated with Robust Vascular Supportive AbilityEmma Harvey, Huajun Zhang, Pilar Sepúlveda, et al.
Annals of Neurology|April 1, 2003
Phenotypic spectrum associated with mutations in the fukutin-related protein geneEugenio Mercuri, Martin Brockington, Volker Straub, et al.
Annals of Neurology|June 6, 2015
C9orf72 ablation in mice does not cause motor neuron degeneration or motor deficitsMax Koppers, Anna M Blokhuis, Henk-Jan Westeneng, et al.
Investigative Ophthalmology & Visual Science|March 6, 2025
The TCF4 Gene Regulates Apoptosis of Corneal Endothelial Cells in Fuchs Endothelial Corneal DystrophyTatsuya Nakagawa, Tetsuro Honda, Taichi Yuasa, et al.
Investigative Ophthalmology & Visual Science|February 28, 2019
Effect of Trinucleotide Repeat Expansion on the Expression of TCF4 mRNA in Fuchs' Endothelial Corneal DystrophyNaoki Okumura, Ryosuke Hayashi, Masakazu Nakano, et al.
Nature Communications|January 15, 2022
Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variantsBret Sanders, Daniel D'Andrea, Mark O Collins, et al.
Nature Genetics|August 19, 2003
Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)Wei Li, Qing Zhang, Naoki Oiso, et al.
Journal of Neurology|September 12, 2014
SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotypeKathryn J Peall, Manju A Kurian, Mark Wardle, et al.
Brain : a Journal of Neurology|February 1, 2013
SGCE mutations cause psychiatric disorders: clinical and genetic characterizationKathryn J Peall, Daniel J Smith, Manju A Kurian, et al.
Pageof 6

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

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
Frontiers in Molecular Biosciences|January 1, 2024
Misfolding of fukutin-related protein (FKRP) variants in congenital and limb girdle muscular dystrophiesChristopher T Esapa, R A Jeffrey McIlhinney, Adrian J Waite, et al.
Stem Cells Translational Medicine|February 17, 2017
Potency of Human Cardiosphere-Derived Cells from Patients with Ischemic Heart Disease Is Associated with Robust Vascular Supportive AbilityEmma Harvey, Huajun Zhang, Pilar Sepúlveda, et al.
Annals of Neurology|April 1, 2003
Phenotypic spectrum associated with mutations in the fukutin-related protein geneEugenio Mercuri, Martin Brockington, Volker Straub, et al.
Annals of Neurology|June 6, 2015
C9orf72 ablation in mice does not cause motor neuron degeneration or motor deficitsMax Koppers, Anna M Blokhuis, Henk-Jan Westeneng, et al.
Investigative Ophthalmology & Visual Science|March 6, 2025
The TCF4 Gene Regulates Apoptosis of Corneal Endothelial Cells in Fuchs Endothelial Corneal DystrophyTatsuya Nakagawa, Tetsuro Honda, Taichi Yuasa, et al.
Investigative Ophthalmology & Visual Science|February 28, 2019
Effect of Trinucleotide Repeat Expansion on the Expression of TCF4 mRNA in Fuchs' Endothelial Corneal DystrophyNaoki Okumura, Ryosuke Hayashi, Masakazu Nakano, et al.
Nature Communications|January 15, 2022
Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variantsBret Sanders, Daniel D'Andrea, Mark O Collins, et al.
Nature Genetics|August 19, 2003
Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)Wei Li, Qing Zhang, Naoki Oiso, et al.
Journal of Neurology|September 12, 2014
SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotypeKathryn J Peall, Manju A Kurian, Mark Wardle, et al.
Brain : a Journal of Neurology|February 1, 2013
SGCE mutations cause psychiatric disorders: clinical and genetic characterizationKathryn J Peall, Daniel J Smith, Manju A Kurian, et al.
Pageof 6