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Identifying hub genes and dysregulated pathways in Duchenne muscular dystrophy

Identifying hub genes and dysregulated pathways in Duchenne muscular dystrophy
This research explores differentially expressed genes (DEGs) and hub genes in Duchenne muscular dystrophy, analyzing their role in disease progression and treatment targets.
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Moving towards successful exon-skipping therapy for Duchenne muscular dystrophy

Moving towards successful exon-skipping therapy for Duchenne muscular dystrophy
This review explores exon skipping therapy for Duchenne muscular dystrophy, discussing preclinical and clinical trials, therapeutic challenges, and future developments.
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The Dysferlinopathies Conundrum: Clinical Spectra, Disease Mechanism and Genetic Approaches for Treatments

The Dysferlinopathies Conundrum: Clinical Spectra, Disease Mechanism and Genetic Approaches for Treatments
This review examines dysferlinopathies, highlighting clinical features, molecular mechanisms, genetic therapies, and the latest research in treatment development.
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Duchenne muscular dystrophy: promising early-stage clinical trials to watch

Duchenne muscular dystrophy: promising early-stage clinical trials to watch
This review highlights early-stage clinical trials for Duchenne muscular dystrophy, covering exon-skipping therapies, gene therapy, and novel treatment strategies.
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Wnt7a is Required for Regeneration of Dystrophic Skeletal Muscle

Wnt7a is Required for Regeneration of Dystrophic Skeletal Muscle
This study examines the role of Wnt7a in muscle regeneration, highlighting its necessity for muscle repair and its potential as a therapy for Duchenne muscular dystrophy.
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Isolation of small extracellular vesicles from regenerating muscle tissue using Tangential Flow Filt

Isolation of small extracellular vesicles from regenerating muscle tissue using Tangential Flow Filt
This study presents an optimized protocol for isolating extracellular vesicles (EVs) from regenerating muscle tissue using TFF and SEC, ensuring purity and efficiency.
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Satellite Cell Heterogeneity in Skeletal Muscle Homeostasis

Satellite Cell Heterogeneity in Skeletal Muscle Homeostasis
This article explores the role of satellite cell heterogeneity in skeletal muscle homeostasis, highlighting its impact on muscle repair, self-renewal, and differentiation.
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Vamorolone improves Becker muscular dystrophy and increases dystrophin protein in bmx model mice

Vamorolone improves Becker muscular dystrophy and increases dystrophin protein in bmx model mice
This study highlights vamorolone’s ability to improve Becker muscular dystrophy by reducing inflammation and increasing dystrophin levels in BMX model mice.
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The X-linked Becker muscular dystrophy (bmx) mouse models Becker muscular dystrophy via deletion of

The X-linked Becker muscular dystrophy (bmx) mouse models Becker muscular dystrophy via deletion of
This study introduces the BMX mouse model for Becker muscular dystrophy, providing a new tool for studying disease mechanisms and testing potential therapies.
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Interrogation of Dystrophin and Dystroglycan Complex Protein Turnover After Exon Skipping Therapy

Interrogation of Dystrophin and Dystroglycan Complex Protein Turnover After Exon Skipping Therapy
This study examines dystrophin and dystroglycan protein turnover after exon skipping therapy in DMD, highlighting protein stability changes and implications for gene correction strategies.
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Membrane Stabilization by Modified Steroid Offers a Potential Therapy for Muscular Dystrophy Due to

Membrane Stabilization by Modified Steroid Offers a Potential Therapy for Muscular Dystrophy Due to
This study explores the potential of membrane stabilization therapy for LGMD2B using vamorolone, showing it outperforms prednisolone in muscle repair and strength restoration.
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