Related Experiment Video

Updated: Jul 7, 2026

Modeling Osteosarcoma Using Li-Fraumeni Syndrome Patient-derived Induced Pluripotent Stem Cells
08:52

Modeling Osteosarcoma Using Li-Fraumeni Syndrome Patient-derived Induced Pluripotent Stem Cells

Published on: June 13, 2018

9.2K

Comment on: "Myostatin inhibition in combination with antisense oligonucleotide therapy improves outcomes in spinal

Tai-Heng Chen1,2,3

  • 1Section of Neurobiology, Department of Biological Sciences, University of Southern California, Los Angeles, CA, USA.

Journal of Cachexia, Sarcopenia and Muscle
|July 28, 2020
PubMed
Abstract

No abstract available in PubMed .

More Related Videos

Skeletal Phenotype Analysis of a Conditional Stat3 Deletion Mouse Model
08:42

Skeletal Phenotype Analysis of a Conditional Stat3 Deletion Mouse Model

Published on: July 3, 2020

4.9K
Author Spotlight: Developing Gene Therapies for Muscular Dystrophies and Neuromuscular Disorders
05:03

Author Spotlight: Developing Gene Therapies for Muscular Dystrophies and Neuromuscular Disorders

Published on: August 23, 2024

2.2K

Related Experiment Videos

Last Updated: Jul 7, 2026

Modeling Osteosarcoma Using Li-Fraumeni Syndrome Patient-derived Induced Pluripotent Stem Cells
08:52

Modeling Osteosarcoma Using Li-Fraumeni Syndrome Patient-derived Induced Pluripotent Stem Cells

Published on: June 13, 2018

9.2K
Skeletal Phenotype Analysis of a Conditional Stat3 Deletion Mouse Model
08:42

Skeletal Phenotype Analysis of a Conditional Stat3 Deletion Mouse Model

Published on: July 3, 2020

4.9K
Author Spotlight: Developing Gene Therapies for Muscular Dystrophies and Neuromuscular Disorders
05:03

Author Spotlight: Developing Gene Therapies for Muscular Dystrophies and Neuromuscular Disorders

Published on: August 23, 2024

2.2K

Related Concept Videos

Formation of Muscle Fibers from Myoblasts01:13

Formation of Muscle Fibers from Myoblasts

De novo myogenesis, or the formation of muscle fibers, begins during the early embryonic stages. The skeletal muscle is formed from somites– blocks of embryonic cell layers. The somites are further divided into dermatomes, myotomes, sclerotomes, and syndetomes. Among these, the myotomes give rise to muscle fibers.
Muscle progenitor cells (MPCs) are formed from the myotomes. MPCs express genes that encode the transcription factors Pax3 and Pax7. Along with Pax 3/7, other transcription factors...
Satellite Stem Cells and Muscular Dystrophy01:21

Satellite Stem Cells and Muscular Dystrophy

Satellite stem cells or myosatellite cells are quiescent stem cells that Alexander Mauro first identified in 1961. These cells are located between the sarcolemma, the plasma membrane of muscle fibers, and the basal lamina, the connective tissue sheath covering it. These mononucleated cells are activated in response to muscle injury, can transform into myoblasts, and may form or repair muscle fibers. Myosatellite cells can provide additional myonuclei for muscle regeneration or return to a...

Articles linked to this work by shared authors, journal, and citation graph.

Circulating microRNAs as potential biomarkers and therapeutic targets in spinal muscular atrophy.

Therapeutic advances in neurological disorders·2021

Metabolic and Nutritional Issues Associated with Spinal Muscular Atrophy.

Nutrients·2020

Early-Onset Infantile Facioscapulohumeral Muscular Dystrophy: A Timely Review.

International journal of molecular sciences·2020

Respiratory management for patients with neuromuscular disorders during the COVID-19 pandemic.

Therapeutic advances in respiratory disease·2020

New and Developing Therapies in Spinal Muscular Atrophy: From Genotype to Phenotype to Treatment and Where Do We Stand?

International journal of molecular sciences·2020

Multifaceted roles of microRNAs: From motor neuron generation in embryos to degeneration in spinal muscular atrophy.

eLife·2019

Machine Learning Integrating Quantitative MRI and Clinical Features Predicts Loss of Ambulation in Duchenne Muscular Dystrophy.

Journal of cachexia, sarcopenia and muscle·2026

Circulating MicroRNAs Reflect Systemic Inflammation and Metabolic Dysfunction in Oesophageal Squamous Cell Carcinoma-Associated Cachexia.

Journal of cachexia, sarcopenia and muscle·2026

Underweight Versus Obesity and Gastrointestinal Cancer Mortality in Type 2 Diabetes: A Nationwide Cohort Study.

Journal of cachexia, sarcopenia and muscle·2026

Denosumab Versus Zoledronic Acid for Muscle Strength and Physical Performance in Postmenopausal Osteoporosis: A 3-Year Prospective Study.

Journal of cachexia, sarcopenia and muscle·2026

Plasma Lipidome Is Dysregulated in Amyotrophic Lateral Sclerosis and Associated With Life-Course Adiposity Polygenic Risk.

Journal of cachexia, sarcopenia and muscle·2026

Plasma Proteomic Signatures Predict Incident Amyotrophic Lateral Sclerosis: A Prospective Study Stratified by C9orf72 Expansion.

Journal of cachexia, sarcopenia and muscle·2026

Systemic and local delivery of siRNA to the CNS and periphery via anti-IGF1R antibody conjugation.

Molecular therapy. Nucleic acids·2026

Prevalence and impact of Thiopurine S-methyltransferase (TPMT) and Nudix hydrolase 15 (NUDT15) polymorphisms on the occurrence of myelosuppression in Thai patients with inflammatory bowel disease receiving thiopurine therapy.

Crohn's & colitis 360·2026

Sotagliflozin corrects myocardial phenotype, mitochondrial gene expression and oxidative stress in mice with hypertrophic cardiomyopathy.

Journal of molecular and cellular cardiology plus·2026

A biomimetic gas-protein co-delivery nanoplatform targets mitochondrial stress and GSDME activation for glioblastoma immunotherapy.

Materials today. Bio·2026

A Bispecific Biologic That Robustly Reverses HIV-1 and SIV Latency.

bioRxiv : the preprint server for biology·2026

A minimally modified AAV9 variant (AAV9fyhr) for enhanced CNS gene delivery by intra-CSF administration.

bioRxiv : the preprint server for biology·2026
See all related articles
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
Jove
Visualize
Contact Us