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Maheswaran Kesavan

Showing results (1-10 of 6) with videos related to

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International Journal of Molecular Sciences|November 13, 2021
Hsp90 Inhibition: A Promising Therapeutic Approach for ARSACSSuran Nethisinghe, Rosella Abeti, Maheswaran Kesavan, et al.
International Journal of Molecular Sciences|July 24, 2021
Interruptions of the <i>FXN</i> GAA Repeat Tract Delay the Age at Onset of Friedreich's Ataxia in a Location Dependent MannerSuran Nethisinghe, Maheswaran Kesavan, Heather Ging, et al.
Science (New York, N.Y.)|July 17, 2025
Polyglycine-mediated aggregation of FAM98B disrupts tRNA processing in GGC repeat disordersJason Yang, Yunhan Xu, David R Ziehr, et al.
Nature Genetics|May 26, 2025
Base editing of trinucleotide repeats that cause Huntington's disease and Friedreich's ataxia reduces somatic repeat expansions in patient cells and in miceZaneta Matuszek, Mandana Arbab, Maheswaran Kesavan, et al.
Nature Genetics|January 22, 2025
In vivo CRISPR-Cas9 genome editing in mice identifies genetic modifiers of somatic CAG repeat instability in Huntington's diseaseRicardo Mouro Pinto, Ryan Murtha, António Azevedo, et al.
Medrxiv : the Preprint Server for Health Sciences|February 12, 2026
Transcriptomic profiling uncovers mis-splicing and gene fusions in amyotrophic lateral sclerosisHuilin Xu, Tiziana Petrozziello, Adel Boudi, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
International Journal of Molecular Sciences|November 13, 2021
Hsp90 Inhibition: A Promising Therapeutic Approach for ARSACSSuran Nethisinghe, Rosella Abeti, Maheswaran Kesavan, et al.
International Journal of Molecular Sciences|July 24, 2021
Interruptions of the <i>FXN</i> GAA Repeat Tract Delay the Age at Onset of Friedreich's Ataxia in a Location Dependent MannerSuran Nethisinghe, Maheswaran Kesavan, Heather Ging, et al.
Science (New York, N.Y.)|July 17, 2025
Polyglycine-mediated aggregation of FAM98B disrupts tRNA processing in GGC repeat disordersJason Yang, Yunhan Xu, David R Ziehr, et al.
Nature Genetics|May 26, 2025
Base editing of trinucleotide repeats that cause Huntington's disease and Friedreich's ataxia reduces somatic repeat expansions in patient cells and in miceZaneta Matuszek, Mandana Arbab, Maheswaran Kesavan, et al.
Nature Genetics|January 22, 2025
In vivo CRISPR-Cas9 genome editing in mice identifies genetic modifiers of somatic CAG repeat instability in Huntington's diseaseRicardo Mouro Pinto, Ryan Murtha, António Azevedo, et al.
Medrxiv : the Preprint Server for Health Sciences|February 12, 2026
Transcriptomic profiling uncovers mis-splicing and gene fusions in amyotrophic lateral sclerosisHuilin Xu, Tiziana Petrozziello, Adel Boudi, et al.
Pageof 1