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

Prech Uapinyoying

Showing results (1-10 of 21) with videos related to

Pageof 3
Sort By:
Trends in Molecular Medicine|November 9, 2021
Pathogenic role and therapeutic potential of fibro-adipogenic progenitors in muscle diseaseMarshall W Hogarth, Prech Uapinyoying, Davi A G Mázala, et al.
Journal of Neuromuscular Diseases|February 20, 2025
Exploring the therapeutic potential of fibroadipogenic progenitors in muscle diseaseMarshall W Hogarth, Medha P Kurukunda, Karim Ismat, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 1, 2012
Toll/interleukin-1 receptor domain-containing adapter inducing interferon-β mediates microglial phagocytosis of degenerating axonsSuneil Hosmane, Million Adane Tegenge, Labchan Rajbhandari, et al.
Iscience|August 21, 2023
Single-cell transcriptomic analysis of the identity and function of fibro/adipogenic progenitors in healthy and dystrophic musclePrech Uapinyoying, Marshall Hogarth, Surajit Battacharya, et al.
Biorxiv : the Preprint Server for Biology|April 8, 2024
Allele-specific CRISPR/Cas9 editing inactivates a single nucleotide variant associated with collagen VI muscular dystrophyVéronique Bolduc, Katherine Sizov, Astrid Brull, et al.
Molecular Therapy. Nucleic Acids|August 22, 2024
Allele-specific CRISPR-Cas9 editing inactivates a single nucleotide variant associated with collagen VI muscular dystrophyVéronique Bolduc, Katherine Sizov, Astrid Brull, et al.
Genome Research|July 15, 2020
A long-read RNA-seq approach to identify novel transcripts of very large genesPrech Uapinyoying, Jeremy Goecks, Susan M Knoblach, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Differential inclusion of <i>NEB</i> exons 143 and 144 provides insight into <i>NEB</i>-related myopathy variant interpretation and disease manifestationSarah Silverstein, Rotem Orbach, Safoora Syeda, et al.
HGG Advances|September 25, 2024
Differential inclusion of NEB exons 143 and 144 provides insight into NEB-related myopathy variant interpretation and disease manifestationSarah Silverstein, Rotem Orbach, Safoora Syeda, et al.
Annals of Clinical and Translational Neurology|November 3, 2021
Transcriptome analysis of collagen VI-related muscular dystrophy muscle biopsiesEleonora Guadagnin, Payam Mohassel, Kory R Johnson, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Trends in Molecular Medicine|November 9, 2021
Pathogenic role and therapeutic potential of fibro-adipogenic progenitors in muscle diseaseMarshall W Hogarth, Prech Uapinyoying, Davi A G Mázala, et al.
Journal of Neuromuscular Diseases|February 20, 2025
Exploring the therapeutic potential of fibroadipogenic progenitors in muscle diseaseMarshall W Hogarth, Medha P Kurukunda, Karim Ismat, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 1, 2012
Toll/interleukin-1 receptor domain-containing adapter inducing interferon-β mediates microglial phagocytosis of degenerating axonsSuneil Hosmane, Million Adane Tegenge, Labchan Rajbhandari, et al.
Iscience|August 21, 2023
Single-cell transcriptomic analysis of the identity and function of fibro/adipogenic progenitors in healthy and dystrophic musclePrech Uapinyoying, Marshall Hogarth, Surajit Battacharya, et al.
Biorxiv : the Preprint Server for Biology|April 8, 2024
Allele-specific CRISPR/Cas9 editing inactivates a single nucleotide variant associated with collagen VI muscular dystrophyVéronique Bolduc, Katherine Sizov, Astrid Brull, et al.
Molecular Therapy. Nucleic Acids|August 22, 2024
Allele-specific CRISPR-Cas9 editing inactivates a single nucleotide variant associated with collagen VI muscular dystrophyVéronique Bolduc, Katherine Sizov, Astrid Brull, et al.
Genome Research|July 15, 2020
A long-read RNA-seq approach to identify novel transcripts of very large genesPrech Uapinyoying, Jeremy Goecks, Susan M Knoblach, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Differential inclusion of <i>NEB</i> exons 143 and 144 provides insight into <i>NEB</i>-related myopathy variant interpretation and disease manifestationSarah Silverstein, Rotem Orbach, Safoora Syeda, et al.
HGG Advances|September 25, 2024
Differential inclusion of NEB exons 143 and 144 provides insight into NEB-related myopathy variant interpretation and disease manifestationSarah Silverstein, Rotem Orbach, Safoora Syeda, et al.
Annals of Clinical and Translational Neurology|November 3, 2021
Transcriptome analysis of collagen VI-related muscular dystrophy muscle biopsiesEleonora Guadagnin, Payam Mohassel, Kory R Johnson, et al.
Pageof 3