Related Experiment Video

Updated: May 9, 2026

Multi-exon Skipping Using Cocktail Antisense Oligonucleotides in the Canine X-linked Muscular Dystrophy
10:30

Multi-exon Skipping Using Cocktail Antisense Oligonucleotides in the Canine X-linked Muscular Dystrophy

Published on: May 24, 2016

Duchenne muscular dystrophy: Advances in molecular appraoch

Afaf Benitto1, Khalil Hamzi, Mohammed Itri

  • 1Department of Neuropediatrics, Ibn Rochd Hospital, Casablanca, Morocco.

Indian Journal of Human Genetics
|August 1, 2013
PubMed
Summary

No abstract available in PubMed .

More Related Videos

Characterizing Exon Skipping Efficiency in DMD Patient Samples in Clinical Trials of Antisense Oligonucleotides
05:16

Characterizing Exon Skipping Efficiency in DMD Patient Samples in Clinical Trials of Antisense Oligonucleotides

Published on: May 7, 2020

CRISPR/Cas9 Technology in Restoring Dystrophin Expression in iPSC-Derived Muscle Progenitors
07:44

CRISPR/Cas9 Technology in Restoring Dystrophin Expression in iPSC-Derived Muscle Progenitors

Published on: September 14, 2019

Related Experiment Videos

Last Updated: May 9, 2026

Multi-exon Skipping Using Cocktail Antisense Oligonucleotides in the Canine X-linked Muscular Dystrophy
10:30

Multi-exon Skipping Using Cocktail Antisense Oligonucleotides in the Canine X-linked Muscular Dystrophy

Published on: May 24, 2016

Characterizing Exon Skipping Efficiency in DMD Patient Samples in Clinical Trials of Antisense Oligonucleotides
05:16

Characterizing Exon Skipping Efficiency in DMD Patient Samples in Clinical Trials of Antisense Oligonucleotides

Published on: May 7, 2020

CRISPR/Cas9 Technology in Restoring Dystrophin Expression in iPSC-Derived Muscle Progenitors
07:44

CRISPR/Cas9 Technology in Restoring Dystrophin Expression in iPSC-Derived Muscle Progenitors

Published on: September 14, 2019

Related Concept Videos

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.

[Expression of NF-κB, EGFR, and HER3 in castration-resistant prostate adenocarcinoma: a clinical and molecular study of 88 Moroccan patients].

The Pan African medical journal·2026

Consensus Recommendations for the Diagnosis and Treatment of Neuromyelitis Optica Spectrum Disorders (NMOSD): The MENACTRIMS Guidelines.

CNS drugs·2026

Deep Brain Stimulation for Dystonia: Experience of a Moroccan University Hospital.

Pediatric neurology·2023

Lack of Association of C677T Methylenetetrahydrofolate Reductase Polymorphism with Breast Cancer Risk in Mali.

Genetics research·2023

Association of the Interleukin-10-592C/A Polymorphism and Cervical Cancer Risk: A Meta-Analysis.

Genetics research·2022

Influence of CYP2B6 and CYP3A4 polymorphisms on the virologic and immunologic responses of patients treated with efavirenz-containing regimen.

Pharmacogenetics and genomics·2022

Congenital anonychia and brachydactyly of the left foot - Cooks syndrome variant: Case report and review of literature.

Indian journal of human genetics·2014

Phenotypical characterization of 13q deletion syndrome: Report of two cases.

Indian journal of human genetics·2014

First report of c. 1499G>C mutation in a 6-month-child with cystic fibrosis.

Indian journal of human genetics·2014

Omphalocele, exstrophy of cloaca, imperforate anus and spinal defect (OEIS Complex) with overlapping features of body stalk anomaly (limb body wall complex).

Indian journal of human genetics·2014

Constitutional mismatch repair deficiency syndrome: Do we know it?

Indian journal of human genetics·2014

Wildervanck syndrome with hypoplastic frontal sinus: A rare case presentation.

Indian journal of human genetics·2014

Medical research and health care finance: Evidence from Academic Medical Centers.

Research policy·2026

Risk Factors for Peritonitis Associated With Endoscopic Ultrasound-guided Hepaticogastrostomy.

DEN open·2026

Demystifying Computational Biology: A Scalable Drug Discovery Framework for Medical Curricula.

Cureus·2026

Advances in antibiofilm strategies for medical implant-associated infections: emerging technologies and translational challenges.

Frontiers in microbiology·2026

Recent advances in ultrasound microbubble-mediated gold-based nanomaterials for cancer theranostics.

Frontiers in chemistry·2026

Reversing Antibiotic Resistance and Reprogramming Macrophage Polarization by Extracellular Vesicles from Fresh Schisandra chinensis: A Dual Pharmacological Strategy for Drug-Resistant Wound Infection and Sepsis.

Pharmacological research·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