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Prech Uapinyoying

Showing results (11-20 of 21) with videos related to

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Glia|May 28, 2014
A selective thyroid hormone β receptor agonist enhances human and rodent oligodendrocyte differentiationEmily G Baxi, Jason T Schott, Amanda N Fairchild, et al.
Biorxiv : the Preprint Server for Biology|August 26, 2024
Failure to resolve inflammation contributes to juvenile onset cardiac damage in a mouse model of Duchenne Muscular DystrophyJames S Novak, Amy Lischin, Prech Uapinyoying, et al.
Research Square|February 6, 2026
Benchmarking RNA-seq Tools for Real-World Diagnostic ApplicationsSarah Silverstein, Kaushik Ganapathy, Sandra Donkervoort, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Benchmarking RNA-seq Tools for Real-World Diagnostic ApplicationsSarah Silverstein, Kaushik R Ganapathy, Sandra Donkervoort, et al.
Cell Death & Disease|July 9, 2025
Failure to resolve inflammation contributes to juvenile onset cardiac damage in a mouse model of Duchenne muscular dystrophyJames S Novak, Amy Lischin, Prech Uapinyoying, et al.
Scientific Reports|July 15, 2026
Use of organ transplant solution to preserve skeletal muscle for cellular and spatial transcriptomic analysesPrech Uapinyoying, Young Jae Moon, Aiping Zhang, et al.
Aging Cell|June 5, 2021
Human muscle stem cells are refractory to agingJames S Novak, Davi A G Mázala, Marie Nearing, et al.
Clinical Genetics|August 6, 2022
A recurrent homozygous missense DPM3 variant leads to muscle and brain diseaseSara Nagy, Tracy Lau, Shahryar Alavi, et al.
Journal of Neuromuscular Diseases|November 18, 2016
Targeted Re-Sequencing Emulsion PCR Panel for Myopathies: Results in 94 CasesJaya Punetha, Akanchha Kesari, Prech Uapinyoying, et al.
EMBO Molecular Medicine|November 15, 2021
BET1 variants establish impaired vesicular transport as a cause for muscular dystrophy with epilepsySandra Donkervoort, Niklas Krause, Mykola Dergai, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Glia|May 28, 2014
A selective thyroid hormone β receptor agonist enhances human and rodent oligodendrocyte differentiationEmily G Baxi, Jason T Schott, Amanda N Fairchild, et al.
Biorxiv : the Preprint Server for Biology|August 26, 2024
Failure to resolve inflammation contributes to juvenile onset cardiac damage in a mouse model of Duchenne Muscular DystrophyJames S Novak, Amy Lischin, Prech Uapinyoying, et al.
Research Square|February 6, 2026
Benchmarking RNA-seq Tools for Real-World Diagnostic ApplicationsSarah Silverstein, Kaushik Ganapathy, Sandra Donkervoort, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Benchmarking RNA-seq Tools for Real-World Diagnostic ApplicationsSarah Silverstein, Kaushik R Ganapathy, Sandra Donkervoort, et al.
Cell Death & Disease|July 9, 2025
Failure to resolve inflammation contributes to juvenile onset cardiac damage in a mouse model of Duchenne muscular dystrophyJames S Novak, Amy Lischin, Prech Uapinyoying, et al.
Scientific Reports|July 15, 2026
Use of organ transplant solution to preserve skeletal muscle for cellular and spatial transcriptomic analysesPrech Uapinyoying, Young Jae Moon, Aiping Zhang, et al.
Aging Cell|June 5, 2021
Human muscle stem cells are refractory to agingJames S Novak, Davi A G Mázala, Marie Nearing, et al.
Clinical Genetics|August 6, 2022
A recurrent homozygous missense DPM3 variant leads to muscle and brain diseaseSara Nagy, Tracy Lau, Shahryar Alavi, et al.
Journal of Neuromuscular Diseases|November 18, 2016
Targeted Re-Sequencing Emulsion PCR Panel for Myopathies: Results in 94 CasesJaya Punetha, Akanchha Kesari, Prech Uapinyoying, et al.
EMBO Molecular Medicine|November 15, 2021
BET1 variants establish impaired vesicular transport as a cause for muscular dystrophy with epilepsySandra Donkervoort, Niklas Krause, Mykola Dergai, et al.
Pageof 3