Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

C Frank Bennett

Showing results (31-40 of 169) with videos related to

Pageof 17
Sort By:
Genes & Development|January 14, 2015
Motor neuron cell-nonautonomous rescue of spinal muscular atrophy phenotypes in mild and severe transgenic mouse modelsYimin Hua, Ying Hsiu Liu, Kentaro Sahashi, et al.
Human Molecular Genetics|April 4, 2020
Systemic therapy in an RNA toxicity mouse model with an antisense oligonucleotide therapy targeting a non-CUG sequence within the DMPK 3'UTR RNARamesh S Yadava, Qing Yu, Mahua Mandal, et al.
Nature|October 8, 2011
Peripheral SMN restoration is essential for long-term rescue of a severe spinal muscular atrophy mouse modelYimin Hua, Kentaro Sahashi, Frank Rigo, et al.
Nature Chemical Biology|April 17, 2012
Synthetic oligonucleotides recruit ILF2/3 to RNA transcripts to modulate splicingFrank Rigo, Yimin Hua, Seung J Chun, et al.
Human Molecular Genetics|April 17, 2021
Modeling muscle regeneration in RNA toxicity miceRamesh S Yadava, Mahua Mandal, Jack M Giese, et al.
Methods in Molecular Biology (Clifton, N.J.)|June 2, 2018
Translating Antisense Technology into a Treatment for Huntington's DiseaseRoger M Lane, Anne Smith, Tiffany Baumann, et al.
Nature Medicine|March 12, 2021
Systematic screening identifies therapeutic antisense oligonucleotides for Hutchinson-Gilford progeria syndromeMadaiah Puttaraju, Michaela Jackson, Stephanie Klein, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 22, 2015
Synthetic CRISPR RNA-Cas9-guided genome editing in human cellsMeghdad Rahdar, Moira A McMahon, Thazha P Prakash, et al.
Brain Research|March 27, 2012
Misregulated RNA processing in amyotrophic lateral sclerosisMagdalini Polymenidou, Clotilde Lagier-Tourenne, Kasey R Hutt, et al.
Nature Medicine|June 2, 2021
Author Correction: Systematic screening identifies therapeutic antisense oligonucleotides for Hutchinson-Gilford progeria syndromeMadaiah Puttaraju, Michaela Jackson, Stephanie Klein, et al.
Pageof 17

Showing results (31-40 of 169) with videos related to

Sort By:
Pageof 17
Genes & Development|January 14, 2015
Motor neuron cell-nonautonomous rescue of spinal muscular atrophy phenotypes in mild and severe transgenic mouse modelsYimin Hua, Ying Hsiu Liu, Kentaro Sahashi, et al.
Human Molecular Genetics|April 4, 2020
Systemic therapy in an RNA toxicity mouse model with an antisense oligonucleotide therapy targeting a non-CUG sequence within the DMPK 3'UTR RNARamesh S Yadava, Qing Yu, Mahua Mandal, et al.
Nature|October 8, 2011
Peripheral SMN restoration is essential for long-term rescue of a severe spinal muscular atrophy mouse modelYimin Hua, Kentaro Sahashi, Frank Rigo, et al.
Nature Chemical Biology|April 17, 2012
Synthetic oligonucleotides recruit ILF2/3 to RNA transcripts to modulate splicingFrank Rigo, Yimin Hua, Seung J Chun, et al.
Human Molecular Genetics|April 17, 2021
Modeling muscle regeneration in RNA toxicity miceRamesh S Yadava, Mahua Mandal, Jack M Giese, et al.
Methods in Molecular Biology (Clifton, N.J.)|June 2, 2018
Translating Antisense Technology into a Treatment for Huntington's DiseaseRoger M Lane, Anne Smith, Tiffany Baumann, et al.
Nature Medicine|March 12, 2021
Systematic screening identifies therapeutic antisense oligonucleotides for Hutchinson-Gilford progeria syndromeMadaiah Puttaraju, Michaela Jackson, Stephanie Klein, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 22, 2015
Synthetic CRISPR RNA-Cas9-guided genome editing in human cellsMeghdad Rahdar, Moira A McMahon, Thazha P Prakash, et al.
Brain Research|March 27, 2012
Misregulated RNA processing in amyotrophic lateral sclerosisMagdalini Polymenidou, Clotilde Lagier-Tourenne, Kasey R Hutt, et al.
Nature Medicine|June 2, 2021
Author Correction: Systematic screening identifies therapeutic antisense oligonucleotides for Hutchinson-Gilford progeria syndromeMadaiah Puttaraju, Michaela Jackson, Stephanie Klein, et al.
Pageof 17