Molecular analysis of Dystrophin gene in patients with Duchenne muscular dystrophy
Duchenne muscular dystrophy (DMD) is an inherited disorder characterized by rapidly progressive muscle weakness, which start in the legs and pelvis and later affects the whole body. The responsible gene for DMD has been mapped on the Xp21, namely dystrophin gene. This gene is the largest gene in...
| Main Author: | Salmi, Ab Aziz |
|---|---|
| Format: | Monograph |
| Language: | English |
| Published: |
Universiti Sains Malaysia
2006
|
| Subjects: | |
| Online Access: | http://eprints.usm.my/48621/ http://eprints.usm.my/48621/1/Salimi%20Binti%20AB%20Aziz%20-%2024%20pages.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)
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)
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)
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)
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)
Biochemical characterisation of dystrophin in sensory dendrite and epithelial cells of drosophila melanogaster
by: Wei, Tee Chee
Published: (2020)
by: Wei, Tee Chee
Published: (2020)
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)
Characterization of the dystrophin gene in Macrobrachium rosenbergii / Noor Anees Fathima
by: Noor Anees , Fathima
Published: (2016)
by: Noor Anees , Fathima
Published: (2016)
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)
Molecular Analysis Of Cyp21 Gene In Patients Presenting With Ambiguous Genitalia.
by: Fuziah, M Z, et al.
Published: (2002)
by: Fuziah, M Z, et al.
Published: (2002)
Effects of combined aerobic dance exercise and honey
supplementation on bone metabolism and muscular strength in
women
by: Rahim, Marhasiyah
Published: (2011)
by: Rahim, Marhasiyah
Published: (2011)
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)
Comparison of bone health status, muscular performance and anaerobic capacity between physically active hikers and sedentary individuals
by: Zarian, Nur Syara Afiqa
Published: (2021)
by: Zarian, Nur Syara Afiqa
Published: (2021)
Development of dystrophin-based biomarker for penaeid shrimps / Raji Fatimah Omotayo
by: Raji Fatimah , Omotayo
Published: (2019)
by: Raji Fatimah , Omotayo
Published: (2019)
Effects of combined channa striatus supplementation with countermovement jumping exercise on bone parameters, muscular performance and antioxidant status in young physically inactive males
by: Abd. Hadi, Nurul Hidayah
Published: (2022)
by: Abd. Hadi, Nurul Hidayah
Published: (2022)
Development Of EZ DNA Diagnostic Kit For The Detection Of Homozygous Deletion Of SMN1 Gene In Spinal Muscular Atrophy (SMA) Patients
by: Marzuki, Marini
Published: (2012)
by: Marzuki, Marini
Published: (2012)
Ace and Actn3 Polymorphisms,
Aerobic and Anaerobic Capacities, Bone
and Muscular Performance
in Malay Athletes and Non-athletes
by: Xiao, Li
Published: (2016)
by: Xiao, Li
Published: (2016)
Association of MMP-9 gene polymorphisms with nephrolithiasis patients
by: Mehde, Atheer Awad, et al.
Published: (2017)
by: Mehde, Atheer Awad, et al.
Published: (2017)
Combined effect of plant-based protein supplementation with resistance training on muscular strength, protein catabolism, immune functions and bone metabolism markers in adult males
by: Ahmad, Azaizirawati
Published: (2018)
by: Ahmad, Azaizirawati
Published: (2018)
Analysis of p27 and cyclin 01 genes in
gliomas and meningiomas using
molecular genetic,
immunohistochemical and immunogold
electron microscopic techniques
by: Farizan, Ahmad
Published: (2008)
by: Farizan, Ahmad
Published: (2008)
Determination of alpha-2-MRAP gene polymorphisms innephrolithiasis patients
by: Mehde, Atheer Awad, et al.
Published: (2017)
by: Mehde, Atheer Awad, et al.
Published: (2017)
Data of Effects of Combined L-Carnitine Supplementation and Moderateintensity Exercise on Body Composition, Metabolic and Oxidative Stress Markers, Bone Parameters and Muscular Performance in Overweight and Obese Individuals
by: Ahmad, Nur Syamsina
Published: (2022)
by: Ahmad, Nur Syamsina
Published: (2022)
Aerobic and anaerobic capacities, flexibility and
muscular performance of young female
sedentary individuals, silat and taekwondo
practitioners
by: Anowar, Muhamad Nazri Mohd
Published: (2017)
by: Anowar, Muhamad Nazri Mohd
Published: (2017)
Detection of pia2 gene polymorphism in
glycoprotein III in patients with :migraine
by: Bhaskar, Shalini, et al.
Published: (2006)
by: Bhaskar, Shalini, et al.
Published: (2006)
Correlation of clinical and molecular features in myotonic dystrophy type 1 (DM1)
by: Sedehizadeh, Saam
Published: (2019)
by: Sedehizadeh, Saam
Published: (2019)
Assessment of factor VIII gene
in haemophilia a patients in east coast Malaysia
by: Mustaffa, Rapiaah, et al.
Published: (2004)
by: Mustaffa, Rapiaah, et al.
Published: (2004)
Patient-doctor relationships and its associated factors perceived by patients at non govermental hemodialysis clinics in Malaysia
by: Aziz, Ab Farid Fajilah Ab
Published: (2025)
by: Aziz, Ab Farid Fajilah Ab
Published: (2025)
Molecular characterisation of the plasmodium falciparum pfcrt gene involved in chloroquine resistance
by: Lau, Hui Chong
Published: (2008)
by: Lau, Hui Chong
Published: (2008)
Exon skipping and gene transfer restore dystrophin expression in human induced pluripotent stem cells-cardiomyocytes harboring DMD mutations
by: Dick, Emily, et al.
Published: (2013)
by: Dick, Emily, et al.
Published: (2013)
Study of DNA for molecular analysis and biochemical markers from non-invasive samples in beta-thalassaemia major patients / Mohd Rashdan Abd Rahim
by: Mohd Rashdan, Abd Rahim
Published: (2015)
by: Mohd Rashdan, Abd Rahim
Published: (2015)
The effects of angiotensin-converting enzyme gene polymorphism on the progression of immunoglobulin A nephropathy in Malaysian patients
by: Draman, Che Rosle, et al.
Published: (2008)
by: Draman, Che Rosle, et al.
Published: (2008)
Posterior polymorphous dystrophy: an unusual presentation
by: Muhammad Syamil MS,, et al.
Published: (2019)
by: Muhammad Syamil MS,, et al.
Published: (2019)
Identification of MSXl gene mutation in Kelantanese patients with various
types of non-syndromic cleft lip and palate
by: Nurhanini, Abd Rahman
by: Nurhanini, Abd Rahman
Characterisation of the human thyroid peroxidase gene mutations (S) in patients with congenital dyshormonogenetic hypothyroidism / Lee Ching Chin
by: Lee, Ching Chin
Published: (2013)
by: Lee, Ching Chin
Published: (2013)
Demographic and molecular genetic studies of neural tube defects in a cohort of Malaysian patients / Adibah Sahmat
by: Adibah, Sahmat
Published: (2018)
by: Adibah, Sahmat
Published: (2018)
Molecular genetic study of selected ribosomal protein genes in nasopharyngeal carcinoma cases.
by: Ma, Xiang Ru
Published: (2015)
by: Ma, Xiang Ru
Published: (2015)
Similar Items
-
Hunting for a cure: the therapeutic potential of gene therapy in Duchenne muscular dystrophy
by: Hashim, Hasnur Zaman, et al.
Published: (2014) -
Hunting for a cure: the therapeutic potential of gene therapy in Duchenne muscular dystrophy
by: Hashim, Hasnur Zaman, 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) -
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)