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Charles Askew

Showing results (1-10 of 15) with videos related to

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Hearing Research|April 6, 2020
Adeno-associated virus gene replacement for recessive inner ear dysfunction: Progress and challengesCharles Askew, Wade W Chien
The American Journal of Pathology|April 28, 2005
Matrix metalloproteinase dysregulation in the stria vascularis of mice with Alport syndrome: implications for capillary basement membrane pathologyMichael Anne Gratton, Velidi H Rao, Daniel T Meehan, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 19, 2011
The postnatal accumulation of junctional E-cadherin is inversely correlated with the capacity for supporting cells to convert directly into sensory hair cells in mammalian balance organsMaria Sol Collado, Benjamin R Thiede, Wendy Baker, et al.
Plos One|November 23, 2020
Self-complementarity in adeno-associated virus enhances transduction and gene expression in mouse cochlear tissuesGraham Casey, Charles Askew, Mark A Brimble, et al.
Science Translational Medicine|July 10, 2015
Tmc gene therapy restores auditory function in deaf miceCharles Askew, Cylia Rochat, Bifeng Pan, et al.
Human Molecular Genetics|December 17, 2013
Deletion of PDZD7 disrupts the Usher syndrome type 2 protein complex in cochlear hair cells and causes hearing loss in miceJunhuang Zou, Tihua Zheng, Chongyu Ren, et al.
Hearing Research|June 23, 2009
Localization and expression of clarin-1, the Clrn1 gene product, in auditory hair cells and photoreceptorsMarisa Zallocchi, Daniel T Meehan, Duane Delimont, et al.
Biomaterials|January 8, 2022
Customized blood-brain barrier shuttle peptide to increase AAV9 vector crossing the BBB and augment transduction in the brainXintao Zhang, Zheng Chai, Amanda Lee Dobbins, et al.
Gene Therapy|October 2, 2019
Superior human hepatocyte transduction with adeno-associated virus vector serotype 7Wenwei Shao, Xiaolei Pei, Caibin Cui, et al.
Nature Biotechnology|February 7, 2017
A synthetic AAV vector enables safe and efficient gene transfer to the mammalian inner earLukas D Landegger, Bifeng Pan, Charles Askew, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Hearing Research|April 6, 2020
Adeno-associated virus gene replacement for recessive inner ear dysfunction: Progress and challengesCharles Askew, Wade W Chien
The American Journal of Pathology|April 28, 2005
Matrix metalloproteinase dysregulation in the stria vascularis of mice with Alport syndrome: implications for capillary basement membrane pathologyMichael Anne Gratton, Velidi H Rao, Daniel T Meehan, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 19, 2011
The postnatal accumulation of junctional E-cadherin is inversely correlated with the capacity for supporting cells to convert directly into sensory hair cells in mammalian balance organsMaria Sol Collado, Benjamin R Thiede, Wendy Baker, et al.
Plos One|November 23, 2020
Self-complementarity in adeno-associated virus enhances transduction and gene expression in mouse cochlear tissuesGraham Casey, Charles Askew, Mark A Brimble, et al.
Science Translational Medicine|July 10, 2015
Tmc gene therapy restores auditory function in deaf miceCharles Askew, Cylia Rochat, Bifeng Pan, et al.
Human Molecular Genetics|December 17, 2013
Deletion of PDZD7 disrupts the Usher syndrome type 2 protein complex in cochlear hair cells and causes hearing loss in miceJunhuang Zou, Tihua Zheng, Chongyu Ren, et al.
Hearing Research|June 23, 2009
Localization and expression of clarin-1, the Clrn1 gene product, in auditory hair cells and photoreceptorsMarisa Zallocchi, Daniel T Meehan, Duane Delimont, et al.
Biomaterials|January 8, 2022
Customized blood-brain barrier shuttle peptide to increase AAV9 vector crossing the BBB and augment transduction in the brainXintao Zhang, Zheng Chai, Amanda Lee Dobbins, et al.
Gene Therapy|October 2, 2019
Superior human hepatocyte transduction with adeno-associated virus vector serotype 7Wenwei Shao, Xiaolei Pei, Caibin Cui, et al.
Nature Biotechnology|February 7, 2017
A synthetic AAV vector enables safe and efficient gene transfer to the mammalian inner earLukas D Landegger, Bifeng Pan, Charles Askew, et al.
Pageof 2