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Showing results (241-250 of 251) with videos related to

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Disease Models & Mechanisms|October 5, 2022
DUX4 expression activates JNK and p38 MAP kinases in myoblastsChristopher M Brennan, Abby S Hill, Michael St Andre, et al.
Human Molecular Genetics|July 17, 2012
Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesisTakako Iida Jones, Jennifer C J Chen, Fedik Rahimov, et al.
Annals of Neurology|May 15, 2023
Post-Translational Modifications of the DUX4 Protein Impact Toxic Function in FSHD Cell ModelsRenatta N Knox, Jocelyn O Eidahl, Lindsay M Wallace, et al.
Biorxiv : the Preprint Server for Biology|October 31, 2023
Addressing the dNTP bottleneck restricting prime editing activityKarthikeyan Ponnienselvan, Pengpeng Liu, Thomas Nyalile, et al.
Journal of Hazardous Materials|August 2, 2023
Accumulation mechanisms for contaminants on weak-base hybrid ion exchange resinsSarah A Saslow, Elsa A Cordova, Nancy M Escobedo, et al.
The CRISPR Journal|September 7, 2022
Efficient Homology-Directed Repair with Circular Single-Stranded DNA DonorsSukanya Iyer, Aamir Mir, Joel Vega-Badillo, et al.
Elife|January 25, 2022
iMyoblasts for ex vivo and in vivo investigations of human myogenesis and disease modelingDongsheng Guo, Katelyn Daman, Jennifer Jc Chen, et al.
Genome Biology|June 16, 2017
CRISPR/Cas9-mediated genome editing induces exon skipping by alternative splicing or exon deletionHaiwei Mou, Jordan L Smith, Lingtao Peng, et al.
Nature Communications|November 12, 2022
Impaired mitochondrial oxidative metabolism in skeletal progenitor cells leads to musculoskeletal disintegrationChujiao Lin, Qiyuan Yang, Dongsheng Guo, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 12, 2026
SORT LNPs encapsulating Cas9 mRNA achieve efficient editing in skeletal muscle in a dystrophic mouse modelSukanya Iyer, Katelyn Daman, Yehui Sun, et al.
Pageof 26

Showing results (241-250 of 251) with videos related to

Sort By:
Pageof 26
Disease Models & Mechanisms|October 5, 2022
DUX4 expression activates JNK and p38 MAP kinases in myoblastsChristopher M Brennan, Abby S Hill, Michael St Andre, et al.
Human Molecular Genetics|July 17, 2012
Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesisTakako Iida Jones, Jennifer C J Chen, Fedik Rahimov, et al.
Annals of Neurology|May 15, 2023
Post-Translational Modifications of the DUX4 Protein Impact Toxic Function in FSHD Cell ModelsRenatta N Knox, Jocelyn O Eidahl, Lindsay M Wallace, et al.
Biorxiv : the Preprint Server for Biology|October 31, 2023
Addressing the dNTP bottleneck restricting prime editing activityKarthikeyan Ponnienselvan, Pengpeng Liu, Thomas Nyalile, et al.
Journal of Hazardous Materials|August 2, 2023
Accumulation mechanisms for contaminants on weak-base hybrid ion exchange resinsSarah A Saslow, Elsa A Cordova, Nancy M Escobedo, et al.
The CRISPR Journal|September 7, 2022
Efficient Homology-Directed Repair with Circular Single-Stranded DNA DonorsSukanya Iyer, Aamir Mir, Joel Vega-Badillo, et al.
Elife|January 25, 2022
iMyoblasts for ex vivo and in vivo investigations of human myogenesis and disease modelingDongsheng Guo, Katelyn Daman, Jennifer Jc Chen, et al.
Genome Biology|June 16, 2017
CRISPR/Cas9-mediated genome editing induces exon skipping by alternative splicing or exon deletionHaiwei Mou, Jordan L Smith, Lingtao Peng, et al.
Nature Communications|November 12, 2022
Impaired mitochondrial oxidative metabolism in skeletal progenitor cells leads to musculoskeletal disintegrationChujiao Lin, Qiyuan Yang, Dongsheng Guo, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 12, 2026
SORT LNPs encapsulating Cas9 mRNA achieve efficient editing in skeletal muscle in a dystrophic mouse modelSukanya Iyer, Katelyn Daman, Yehui Sun, et al.
Pageof 26