Neuromuscular

The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein

Membrane Proteins / Apoptosis / Gene expression / Cell line / Humans / Muscular Dystrophy / Cell Death / Rhabdomyosarcoma / Medical Physiology / Chromatin structure / Clinical Sciences / Nuclear envelope / Neuromuscular Disorders / Amino Acid Sequence / Neuromuscular / Neurosciences / Muscular Dystrophy / Cell Death / Rhabdomyosarcoma / Medical Physiology / Chromatin structure / Clinical Sciences / Nuclear envelope / Neuromuscular Disorders / Amino Acid Sequence / Neuromuscular / Neurosciences

Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?

Genetics / Cognitive Science / Neurology / Human Genetics / Complementary and Alternative Medicine / Skeletal muscle biology / Immunohistochemistry / Oxidative Stress / Stem Cell / Gene expression / Extracellular Matrix / Cell Culture / Biopsy / Western blotting / Cell line / Humans / Muscle / Mice / Muscular Dystrophy / Female / Muscular Dystrophies / Animals / Male / Muscles / Disease Control / Medical Physiology / Differentiation / Phenotype / Clinical Sciences / Middle Aged / Cell nucleus / Skeletal Muscle / Adult / Neuromuscular Disorders / HeLa cells / In Vitro Studies / Cell Cycle Arrest / Global Gene Expression / Expression analysis / Neuromuscular / Myofibrils / Neurosciences / Biochemistry and cell biology / Gene expression profiling / Extracellular Matrix Proteins / Case Control Studies / Myoblasts / Skeletal muscle biology / Immunohistochemistry / Oxidative Stress / Stem Cell / Gene expression / Extracellular Matrix / Cell Culture / Biopsy / Western blotting / Cell line / Humans / Muscle / Mice / Muscular Dystrophy / Female / Muscular Dystrophies / Animals / Male / Muscles / Disease Control / Medical Physiology / Differentiation / Phenotype / Clinical Sciences / Middle Aged / Cell nucleus / Skeletal Muscle / Adult / Neuromuscular Disorders / HeLa cells / In Vitro Studies / Cell Cycle Arrest / Global Gene Expression / Expression analysis / Neuromuscular / Myofibrils / Neurosciences / Biochemistry and cell biology / Gene expression profiling / Extracellular Matrix Proteins / Case Control Studies / Myoblasts

The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein

Membrane Proteins / Apoptosis / Gene expression / Cell line / Humans / Muscular Dystrophy / Cell Death / Rhabdomyosarcoma / Medical Physiology / Chromatin structure / Clinical Sciences / Nuclear envelope / Neuromuscular Disorders / Amino Acid Sequence / Neuromuscular / Neurosciences / Muscular Dystrophy / Cell Death / Rhabdomyosarcoma / Medical Physiology / Chromatin structure / Clinical Sciences / Nuclear envelope / Neuromuscular Disorders / Amino Acid Sequence / Neuromuscular / Neurosciences

Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?

Genetics / Cognitive Science / Neurology / Human Genetics / Complementary and Alternative Medicine / Skeletal muscle biology / Immunohistochemistry / Oxidative Stress / Stem Cell / Gene expression / Extracellular Matrix / Cell Culture / Biopsy / Western blotting / Cell line / Humans / Muscle / Mice / Muscular Dystrophy / Female / Muscular Dystrophies / Animals / Male / Muscles / Disease Control / Medical Physiology / Differentiation / Phenotype / Clinical Sciences / Middle Aged / Cell nucleus / Skeletal Muscle / Adult / Neuromuscular Disorders / HeLa cells / In Vitro Studies / Cell Cycle Arrest / Global Gene Expression / Expression analysis / Neuromuscular / Myofibrils / Neurosciences / Biochemistry and cell biology / Gene expression profiling / Extracellular Matrix Proteins / Case Control Studies / Myoblasts / Skeletal muscle biology / Immunohistochemistry / Oxidative Stress / Stem Cell / Gene expression / Extracellular Matrix / Cell Culture / Biopsy / Western blotting / Cell line / Humans / Muscle / Mice / Muscular Dystrophy / Female / Muscular Dystrophies / Animals / Male / Muscles / Disease Control / Medical Physiology / Differentiation / Phenotype / Clinical Sciences / Middle Aged / Cell nucleus / Skeletal Muscle / Adult / Neuromuscular Disorders / HeLa cells / In Vitro Studies / Cell Cycle Arrest / Global Gene Expression / Expression analysis / Neuromuscular / Myofibrils / Neurosciences / Biochemistry and cell biology / Gene expression profiling / Extracellular Matrix Proteins / Case Control Studies / Myoblasts

Telethonin-deficiency initially presenting as a congenital muscular dystrophy

Motor Development / Skeletal muscle biology / Magnetic Resonance Imaging / Limb Girdle Muscular Dystrophy / Sequence Analysis / Biopsy / Humans / Child / Muscular Dystrophy / Muscular Dystrophies / Male / Medical Physiology / Clinical Sciences / Neuromuscular Disorders / Neuromuscular / Neurosciences / Biopsy / Humans / Child / Muscular Dystrophy / Muscular Dystrophies / Male / Medical Physiology / Clinical Sciences / Neuromuscular Disorders / Neuromuscular / Neurosciences

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