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Wooi Fang Lim

Showing results (1-10 of 7) with videos related to

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Journal of Neuromuscular Diseases|May 14, 2023
RNA Transcript Diversity in Neuromuscular ResearchWooi Fang Lim, Carlo Rinaldi
The American Journal of Pathology|March 5, 2023
Investigating Eukaryotic Elongation Factor 2 Kinase/Eukaryotic Translation Elongation Factor 2 Pathway Regulation and Its Role in Protein Synthesis Impairment during Disuse-Induced Skeletal Muscle AtrophyNatalia Vilchinskaya, Wooi Fang Lim, Svetlana Belova, et al.
EMBO Molecular Medicine|September 19, 2023
PRMT inhibitor promotes SMN2 exon 7 inclusion and synergizes with nusinersen to rescue SMA miceAnna J Kordala, Jessica Stoodley, Nina Ahlskog, et al.
Acta Neuropathologica|May 6, 2022
AR cooperates with SMAD4 to maintain skeletal muscle homeostasisMitra Forouhan, Wooi Fang Lim, Laura C Zanetti-Domingues, et al.
Nature Communications|February 6, 2023
LSD1/PRMT6-targeting gene therapy to attenuate androgen receptor toxic gain-of-function ameliorates spinobulbar muscular atrophy phenotypes in flies and miceRamachandran Prakasam, Angela Bonadiman, Roberta Andreotti, et al.
Life Science Alliance|August 14, 2021
Dystrophin involvement in peripheral circadian SRF signallingCorinne A Betts, Aarti Jagannath, Tirsa LE van Westering, et al.
Brain Communications|December 15, 2021
Variants in <i>ATP6V0A1</i> cause progressive myoclonus epilepsy and developmental and epileptic encephalopathyLaura C Bott, Mitra Forouhan, Maria Lieto, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Journal of Neuromuscular Diseases|May 14, 2023
RNA Transcript Diversity in Neuromuscular ResearchWooi Fang Lim, Carlo Rinaldi
The American Journal of Pathology|March 5, 2023
Investigating Eukaryotic Elongation Factor 2 Kinase/Eukaryotic Translation Elongation Factor 2 Pathway Regulation and Its Role in Protein Synthesis Impairment during Disuse-Induced Skeletal Muscle AtrophyNatalia Vilchinskaya, Wooi Fang Lim, Svetlana Belova, et al.
EMBO Molecular Medicine|September 19, 2023
PRMT inhibitor promotes SMN2 exon 7 inclusion and synergizes with nusinersen to rescue SMA miceAnna J Kordala, Jessica Stoodley, Nina Ahlskog, et al.
Acta Neuropathologica|May 6, 2022
AR cooperates with SMAD4 to maintain skeletal muscle homeostasisMitra Forouhan, Wooi Fang Lim, Laura C Zanetti-Domingues, et al.
Nature Communications|February 6, 2023
LSD1/PRMT6-targeting gene therapy to attenuate androgen receptor toxic gain-of-function ameliorates spinobulbar muscular atrophy phenotypes in flies and miceRamachandran Prakasam, Angela Bonadiman, Roberta Andreotti, et al.
Life Science Alliance|August 14, 2021
Dystrophin involvement in peripheral circadian SRF signallingCorinne A Betts, Aarti Jagannath, Tirsa LE van Westering, et al.
Brain Communications|December 15, 2021
Variants in <i>ATP6V0A1</i> cause progressive myoclonus epilepsy and developmental and epileptic encephalopathyLaura C Bott, Mitra Forouhan, Maria Lieto, et al.
Pageof 1