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Biorxiv : the Preprint Server for Biology|September 2, 2025
AAV2-mediated intravitreal delivery of exon-specific U1 snRNA rescues optic neuropathy in a mouse model of familial dysautonomiaAnil Chekuri, Krishnakanth Kondabolu, Emily G Kirchner, et al.
Molecular Biology and Evolution|April 1, 2014
Evolutionary and molecular facts link the WWC protein family to Hippo signalingDirk Oliver Wennmann, Jürgen Schmitz, Michael C Wehr, et al.
Human Molecular Genetics|December 15, 2021
Selective retinal ganglion cell loss and optic neuropathy in a humanized mouse model of familial dysautonomiaAnil Chekuri, Emily M Logan, Aram J Krauson, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|December 13, 2021
Developmental regulation of neuronal gene expression by Elongator complex protein 1 dosageElisabetta Morini, Dadi Gao, Emily M Logan, et al.
Biorxiv : the Preprint Server for Biology|January 16, 2026
ELP1 Gene Augmentation Restores Visual Function in a Mouse Model of Familial DysautonomiaHui-Chen Cheng, Swanand Koli, Kate Lewis, et al.
Human Gene Therapy|December 1, 2018
Long-Term Effects of Gene Therapy in a Novel Mouse Model of Human MFRP-Associated RetinopathyAnil Chekuri, Bhubanananda Sahu, Venkata Ramana Murthy Chavali, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|April 26, 2026
ELP1 Gene Augmentation Restores Visual Function in a Mouse Model of Familial DysautonomiaHui-Chen Cheng, Swanand Koli, Kate Lewis, et al.
American Journal of Human Genetics|February 22, 2023
Development of an oral treatment that rescues gait ataxia and retinal degeneration in a phenotypic mouse model of familial dysautonomiaElisabetta Morini, Anil Chekuri, Emily M Logan, et al.
Nature Communications|June 8, 2021
A deep learning approach to identify gene targets of a therapeutic for human splicing disordersDadi Gao, Elisabetta Morini, Monica Salani, et al.
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