Hunting for a cure: the therapeutic potential of gene therapy in Duchenne muscular dystrophy
Duchenne muscular dystrophy (DMD) is an incurable disease and the search for a cure is a challenging journey. However, with recent encouraging progress, we are seeing a light at the end of a long tunnel. This review focuses on several main strategies in gene therapy, including truncated dystrophin g...
| Main Authors: | Hashim, Hasnur Zaman, Che Abdullah, Shahrin Tarmizi, Wan Sulaiman, Wan Aliaa, Hoo, Fan Kee, Basri, Hamidon |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2014
|
| Online Access: | http://psasir.upm.edu.my/id/eprint/37897/ http://psasir.upm.edu.my/id/eprint/37897/1/Hunting%20for%20a%20cure%20the%20therapeutic%20potential%20of%20gene%20therapy%20in%20Duchenne%20muscular%20dystrophy.pdf |
Similar Items
Hunting for a cure: the therapeutic potential of gene therapy in Duchenne muscular dystrophy
by: Hashim, Hasnur Zaman, et al.
Published: (2014)
by: Hashim, Hasnur Zaman, et al.
Published: (2014)
Molecular analysis of Dystrophin gene in patients with Duchenne muscular
dystrophy
by: Salmi, Ab Aziz
Published: (2006)
by: Salmi, Ab Aziz
Published: (2006)
Effect of Sitting Posture on Development of Scoliosis in Duchenne Muscular Dystrophy Cases
by: Pokharel, R., et al.
Published: (2014)
by: Pokharel, R., et al.
Published: (2014)
Dystropathology increases energy expenditure and protein turnover in the mdx mouse model of Duchenne muscular dystrophy
by: Crabb, Hannah, et al.
Published: (2014)
by: Crabb, Hannah, et al.
Published: (2014)
A bioinformatic analysis of the Duchenne muscular dystrophy gene and associated gene variants across human cancers
by: Machado, Lee
Published: (2022)
by: Machado, Lee
Published: (2022)
Identification of muscle necrosis in the mdx mouse model of Duchenne muscular dystrophy using three - dimensional optical coherence tomography
by: Klyen, B., et al.
Published: (2011)
by: Klyen, B., et al.
Published: (2011)
Investigating the use of oligonucleotides for the treatment of muscular dystrophy
by: Moore, Rebecca L. L.
Published: (2016)
by: Moore, Rebecca L. L.
Published: (2016)
Assessment of dysphagia in people with Parkinson’s disease, multiple sclerosis and muscular dystrophy
by: Molokwu, Anuri Joy
Published: (2015)
by: Molokwu, Anuri Joy
Published: (2015)
Oxidative stress and pathology in muscular dystrophies: focus on protein thiol oxidation and dysferlinopathies
by: Terrill, J., et al.
Published: (2013)
by: Terrill, J., et al.
Published: (2013)
Managing post stroke hyperglycaemia: moderate glycaemic control is better? An update
by: Wan Sulaiman, Wan Aliaa, et al.
Published: (2014)
by: Wan Sulaiman, Wan Aliaa, et al.
Published: (2014)
Managing post stroke hyperglycaemia: moderate glycaemic control is better? An update
by: Wan Sulaiman, Wan Aliaa, et al.
Published: (2014)
by: Wan Sulaiman, Wan Aliaa, et al.
Published: (2014)
Development of assays for therapeutic screening in myotonic dystrophy
by: Udosen, Inyang Udofia
Published: (2012)
by: Udosen, Inyang Udofia
Published: (2012)
Understanding the pathogenesis and potential therapeutics of Myotonic dystrophy
by: Verma, Ayushri
Published: (2024)
by: Verma, Ayushri
Published: (2024)
Can human pluripotent stem cell-derived cardiomyocytes advance understanding of muscular dystrophies?
by: Kalra, Spandan, et al.
Published: (2016)
by: Kalra, Spandan, et al.
Published: (2016)
ChIP analysis of the histone modifications at the D4Z4 repeats in facioscapulohumeral muscular dystrophy (FSHD)
by: Vafadar-Isfahani, Natasha
Published: (2010)
by: Vafadar-Isfahani, Natasha
Published: (2010)
Mapping the Journey: Family Carers' Perceptions of Issues Related to End-Stage Care of Individuals with Muscular Dystrophy or Motor Neurone Disease
by: Dawson, Susan, et al.
Published: (2003)
by: Dawson, Susan, et al.
Published: (2003)
Investigating genome engineering of myotonic dystrophy cells and small molecules as potential therapeutic agents
by: López Morató, Marta
Published: (2018)
by: López Morató, Marta
Published: (2018)
Anti-Wolbachia therapy for onchocerciasis & lymphatic filariasis: current perspectives
by: Wan Sulaiman, Wan Aliaa, et al.
Published: (2019)
by: Wan Sulaiman, Wan Aliaa, et al.
Published: (2019)
Acute brachial plexopathy: an unusual complication from Bee Sting
by: Hoo, Fan Kee, et al.
Published: (2014)
by: Hoo, Fan Kee, et al.
Published: (2014)
The hunt for mutations
by: Chung, Clarissa
Published: (2021)
by: Chung, Clarissa
Published: (2021)
Posterior polymorphous dystrophy: an unusual presentation
by: Muhammad Syamil MS,, et al.
Published: (2019)
by: Muhammad Syamil MS,, et al.
Published: (2019)
Replay: for Matthew Hunt
by: Costantino, Thea
Published: (2011)
by: Costantino, Thea
Published: (2011)
The role of muscleblind-like proteins in myotonic dystrophy
by: Arya, Sukrat
Published: (2014)
by: Arya, Sukrat
Published: (2014)
Acute disseminated encephalomyelitis in dengue viral infection
by: Wan Sulaiman, Wan Aliaa, et al.
Published: (2017)
by: Wan Sulaiman, Wan Aliaa, et al.
Published: (2017)
Hunting the Mammoth, Pleistocene to Postmodern
by: Chrulew, Matthew
Published: (2011)
by: Chrulew, Matthew
Published: (2011)
Hunting down the agents of illness
by: New Sunday, Times
Published: (1998)
by: New Sunday, Times
Published: (1998)
No more the hunted in land of the hornbills
by: The Borneo, Post
Published: (2016)
by: The Borneo, Post
Published: (2016)
On A Hunt For More Men
by: The Star, Ng Wei Loon
Published: (2008)
by: The Star, Ng Wei Loon
Published: (2008)
Quantitative methods to monitor RNA biomarkers in myotonic dystrophy
by: Wojciechowska, Marzena, et al.
Published: (2018)
by: Wojciechowska, Marzena, et al.
Published: (2018)
Augmented reality treasure hunt game
by: Tan, Kean Hon
Published: (2024)
by: Tan, Kean Hon
Published: (2024)
Security monitoring tool system using threat intelligence vs threat hunting
by: Wan Ikbal Ismat Wan Kamal,
Published: (2021)
by: Wan Ikbal Ismat Wan Kamal,
Published: (2021)
A rare case of vein of galen thrombosis: exploring a potential role for novel oral anticoagulants (NOACs) in cerebral deep vein thrombosis
by: Inche Mat, Liyana Najwa, et al.
Published: (2017)
by: Inche Mat, Liyana Najwa, et al.
Published: (2017)
The future of osteoarthritis therapeutics: targeted
pharmacological therapy
by: Mobasheri, Ali
Published: (2013)
by: Mobasheri, Ali
Published: (2013)
Neuroaxonal dystrophy in a flock of pied imperial pigeons (Ducula bicolor)
by: Barrows, M., et al.
Published: (2017)
by: Barrows, M., et al.
Published: (2017)
Small molecules which improve pathogenesis of myotonic dystrophy type 1
by: López-Morató, Marta, et al.
Published: (2018)
by: López-Morató, Marta, et al.
Published: (2018)
The next step : Idris hunts for MAS talent
Published: (2008)
Published: (2008)
Mobile edutainment AR treasure hunt application
by: Chong, Jia Ni
Published: (2021)
by: Chong, Jia Ni
Published: (2021)
Treasure hunt mobile application with object recognition
by: Thew, Thung Liang
Published: (2018)
by: Thew, Thung Liang
Published: (2018)
Incomplete anterior choroidal artery syndrome in a pregnant female
by: Inche Mat, Liyana Najwa, et al.
Published: (2019)
by: Inche Mat, Liyana Najwa, et al.
Published: (2019)
A rare case of acute psychosis as an isolated manifestation of extrapontine myelinolysis
by: Wan Sulaiman, Wan Aliaa, et al.
Published: (2014)
by: Wan Sulaiman, Wan Aliaa, et al.
Published: (2014)
Similar Items
-
Hunting for a cure: the therapeutic potential of gene therapy in Duchenne muscular dystrophy
by: Hashim, Hasnur Zaman, et al.
Published: (2014) -
Molecular analysis of Dystrophin gene in patients with Duchenne muscular
dystrophy
by: Salmi, Ab Aziz
Published: (2006) -
Effect of Sitting Posture on Development of Scoliosis in Duchenne Muscular Dystrophy Cases
by: Pokharel, R., et al.
Published: (2014) -
Dystropathology increases energy expenditure and protein turnover in the mdx mouse model of Duchenne muscular dystrophy
by: Crabb, Hannah, et al.
Published: (2014) -
A bioinformatic analysis of the Duchenne muscular dystrophy gene and associated gene variants across human cancers
by: Machado, Lee
Published: (2022)