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Frontiers in Neuroscience
|
October 30, 2023
Reduction of <i>Kcnt1</i> is therapeutic in mouse models of <i>SCN1A</i> and <i>SCN8A</i> epilepsy
Sophie F Hill, Paymaan Jafar-Nejad, Frank Rigo, et al.
Molecular Therapy. Nucleic Acids
|
April 10, 2019
Delivery of GalNAc-Conjugated Splice-Switching ASOs to Non-hepatic Cells through Ectopic Expression of Asialoglycoprotein Receptor
Juergen Scharner, Sabrina Qi, Frank Rigo, et al.
Nucleic Acids Research
|
February 28, 2020
Comparison of the efficacy of MOE and PMO modifications of systemic antisense oligonucleotides in a severe SMA mouse model
Lei Sheng, Frank Rigo, C Frank Bennett, et al.
Nucleic Acids Research
|
March 5, 2014
Nonsense-mediated decay as a terminating mechanism for antisense oligonucleotides
Amanda J Ward, Michaela Norrbom, Seung Chun, et al.
Open Biology
|
November 17, 2012
Manipulation of PK-M mutually exclusive alternative splicing by antisense oligonucleotides
Zhenxun Wang, Hyun Yong Jeon, Frank Rigo, et al.
Experimental Cell Research
|
August 4, 2024
Targeting alternative splicing of fibronectin in human renal proximal tubule epithelial cells with antisense oligonucleotides to reduce EDA+ fibronectin production and block an autocrine loop that drives renal fibrosis
Mysore Keshavmurthy Phanish, Felicia Heidebrecht, Michaela Jackson, et al.
Epilepsia
|
July 27, 2022
Genetic interaction between Scn8a and potassium channel genes Kcna1 and Kcnq2
Sophie F Hill, Julie M Ziobro, Paymaan Jafar-Nejad, et al.
Cell Reports
|
December 15, 2021
Sarm1 haploinsufficiency or low expression levels after antisense oligonucleotides delay programmed axon degeneration
Stacey Anne Gould, Jonathan Gilley, Karen Ling, et al.
Nature
|
December 4, 2014
Towards a therapy for Angelman syndrome by targeting a long non-coding RNA
Linyan Meng, Amanda J Ward, Seung Chun, et al.
Molecular Therapy. Nucleic Acids
|
September 18, 2017
Antisense Oligonucleotide-Mediated Removal of the Polyglutamine Repeat in Spinocerebellar Ataxia Type 3 Mice
Lodewijk J A Toonen, Frank Rigo, Haico van Attikum, et al.
Page
of 17
Search research articles
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Showing results (11-20 of 163) with videos related to
Sort By:
Page
of 17
Frontiers in Neuroscience
|
October 30, 2023
Reduction of <i>Kcnt1</i> is therapeutic in mouse models of <i>SCN1A</i> and <i>SCN8A</i> epilepsy
Sophie F Hill, Paymaan Jafar-Nejad, Frank Rigo, et al.
Molecular Therapy. Nucleic Acids
|
April 10, 2019
Delivery of GalNAc-Conjugated Splice-Switching ASOs to Non-hepatic Cells through Ectopic Expression of Asialoglycoprotein Receptor
Juergen Scharner, Sabrina Qi, Frank Rigo, et al.
Nucleic Acids Research
|
February 28, 2020
Comparison of the efficacy of MOE and PMO modifications of systemic antisense oligonucleotides in a severe SMA mouse model
Lei Sheng, Frank Rigo, C Frank Bennett, et al.
Nucleic Acids Research
|
March 5, 2014
Nonsense-mediated decay as a terminating mechanism for antisense oligonucleotides
Amanda J Ward, Michaela Norrbom, Seung Chun, et al.
Open Biology
|
November 17, 2012
Manipulation of PK-M mutually exclusive alternative splicing by antisense oligonucleotides
Zhenxun Wang, Hyun Yong Jeon, Frank Rigo, et al.
Experimental Cell Research
|
August 4, 2024
Targeting alternative splicing of fibronectin in human renal proximal tubule epithelial cells with antisense oligonucleotides to reduce EDA+ fibronectin production and block an autocrine loop that drives renal fibrosis
Mysore Keshavmurthy Phanish, Felicia Heidebrecht, Michaela Jackson, et al.
Epilepsia
|
July 27, 2022
Genetic interaction between Scn8a and potassium channel genes Kcna1 and Kcnq2
Sophie F Hill, Julie M Ziobro, Paymaan Jafar-Nejad, et al.
Cell Reports
|
December 15, 2021
Sarm1 haploinsufficiency or low expression levels after antisense oligonucleotides delay programmed axon degeneration
Stacey Anne Gould, Jonathan Gilley, Karen Ling, et al.
Nature
|
December 4, 2014
Towards a therapy for Angelman syndrome by targeting a long non-coding RNA
Linyan Meng, Amanda J Ward, Seung Chun, et al.
Molecular Therapy. Nucleic Acids
|
September 18, 2017
Antisense Oligonucleotide-Mediated Removal of the Polyglutamine Repeat in Spinocerebellar Ataxia Type 3 Mice
Lodewijk J A Toonen, Frank Rigo, Haico van Attikum, et al.
Page
of 17