Muscle

Merosin-positive congenital muscular dystrophy with transient brain dysmyelination, pontocerebellar hypoplasia and mental retardation

Genetics / Pathology / Cognitive Science / Skeletal muscle biology / Magnetic Resonance Imaging / Epilepsy / Histology / Immunohistochemistry / Creatine / Magnetic Resonance Spectroscopy / Adolescent / Intellectual Disability / Brain development / Israel / Biopsy / Mental Retardation / London / Brain / Humans / Child / Cerebellum / Muscle / Cerebral Cortex / Haplotypes / Microcephaly / Female / Muscular Dystrophies / Male / Muscles / Infant / Developmental disabilities / Cataract / D-Aspartic Acid / Medical Physiology / Pedigree / Creatine Kinase / Genetic linkage analysis / Clinical Sciences / Spectrum / Fluorescent Antibody Technique / Family Health / Facies / Adult / Neuromuscular Disorders / Time Factors / Consanguinity / Nuclear Family / Neuronal Migration / Neuropediatrics / Dystrophin / X ray Computed Tomography / Choline / Nuclear Magnetic Resonance Imaging / Genetic Markers / Neurosciences / Linkage Analysis / Nino / Myelin Sheath / Magnetic resonance image / Laminin / Congenital muscular dystrophy / Child preschool / Epilepsy / Histology / Immunohistochemistry / Creatine / Magnetic Resonance Spectroscopy / Adolescent / Intellectual Disability / Brain development / Israel / Biopsy / Mental Retardation / London / Brain / Humans / Child / Cerebellum / Muscle / Cerebral Cortex / Haplotypes / Microcephaly / Female / Muscular Dystrophies / Male / Muscles / Infant / Developmental disabilities / Cataract / D-Aspartic Acid / Medical Physiology / Pedigree / Creatine Kinase / Genetic linkage analysis / Clinical Sciences / Spectrum / Fluorescent Antibody Technique / Family Health / Facies / Adult / Neuromuscular Disorders / Time Factors / Consanguinity / Nuclear Family / Neuronal Migration / Neuropediatrics / Dystrophin / X ray Computed Tomography / Choline / Nuclear Magnetic Resonance Imaging / Genetic Markers / Neurosciences / Linkage Analysis / Nino / Myelin Sheath / Magnetic resonance image / Laminin / Congenital muscular dystrophy / Child preschool

Long-lasting in vivo gene silencing by electrotransfer of shRNA expressing plasmid

Genetics / Skeletal muscle biology / Gene Silencing / Humans / Muscle / Mice / Electroporation / Female / Animals / shRNA / Gene / Plasmids / Green Fluorescent Protein / In Vivo / Gen / Transfection / Silencing / Plasmid / GFP / Mice / Electroporation / Female / Animals / shRNA / Gene / Plasmids / Green Fluorescent Protein / In Vivo / Gen / Transfection / Silencing / Plasmid / GFP

Trigemino-facial reflex inhibitory responses in some lower facial muscles

Humans / Muscle / Female / Male / Electromyography / Facial Nerve / Middle Aged / Adult / Reflex / Facial Movements / Trigeminal Nerve / Facial Nerve / Middle Aged / Adult / Reflex / Facial Movements / Trigeminal Nerve

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

Phospholipid Hydroperoxide Glutathione Peroxidase is a Seleno-Enzyme Distinct from the Classical Glutathione Peroxidase as Evident from Cdna and Amino Acid Sequencing

Kinetics / Aging / Phospholipids / Breeding / Fertility / Gene expression / Theriogenology / Free Radical / Italy / Biological Sciences / DNA / Antioxidants / Humans / Liver / Muscle / Selenium / Female / Animals / Male / Glutathione / Physical sciences / Heart / Glutathione Peroxidase / Blastocyst / Membrane Lipids / Vitamin E / Iron / Biochemical / tESTIS / Enzyme / Chromatin / CHEMICAL SCIENCES / Cattle / Hydrogen Peroxide / Cell nucleus / Active site / Rats / Myocardium / Specific Activity / Rat / Swine / Substrate Specificity / Wistar Rats / Biological markers / Molecular weight / Semen / Species Specificity / Amino Acid Sequence / Base Sequence / Spermatozoa / Sperm Motility / Detergents / Sperm Count / Subcellular Fractions / Protein Binding / Semen Quality / Polyethylene Glycols / Static Electricity / Biochemistry and cell biology / Gene expression / Theriogenology / Free Radical / Italy / Biological Sciences / DNA / Antioxidants / Humans / Liver / Muscle / Selenium / Female / Animals / Male / Glutathione / Physical sciences / Heart / Glutathione Peroxidase / Blastocyst / Membrane Lipids / Vitamin E / Iron / Biochemical / tESTIS / Enzyme / Chromatin / CHEMICAL SCIENCES / Cattle / Hydrogen Peroxide / Cell nucleus / Active site / Rats / Myocardium / Specific Activity / Rat / Swine / Substrate Specificity / Wistar Rats / Biological markers / Molecular weight / Semen / Species Specificity / Amino Acid Sequence / Base Sequence / Spermatozoa / Sperm Motility / Detergents / Sperm Count / Subcellular Fractions / Protein Binding / Semen Quality / Polyethylene Glycols / Static Electricity / Biochemistry and cell biology

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

Haootia quadriformis n. gen., n. sp., interpreted as a muscular cnidarian impression from the Late Ediacaran period (approx. 560 Ma)

Evolutionary Biology / Evolution / Palaeontology / Cnidaria / Newfoundland and Labrador / Biological Sciences / Phylogeny / Neoproterozoic / Ediacaran / Muscle / Fossils / Animals / Biological evolution / Species Specificity / Geologic Sediments / Biological Sciences / Phylogeny / Neoproterozoic / Ediacaran / Muscle / Fossils / Animals / Biological evolution / Species Specificity / Geologic Sediments

Merosin-positive congenital muscular dystrophy with transient brain dysmyelination, pontocerebellar hypoplasia and mental retardation

Pathology / Cognitive Science / Skeletal muscle biology / Magnetic Resonance Imaging / Epilepsy / Histology / Immunohistochemistry / Adolescent / Intellectual Disability / Brain development / Israel / Biopsy / Mental Retardation / London / Brain / Humans / Child / Cerebellum / Muscle / Cerebral Cortex / Haplotypes / Female / Muscular Dystrophies / Male / Muscles / Infant / Cataract / Central Nervous System / Medical Physiology / Pedigree / Creatine Kinase / Genetic linkage analysis / Clinical Sciences / Fluorescent Antibody Technique / Skeletal Muscle / Adult / Neuromuscular Disorders / Time Factors / Scoliosis / Consanguinity / Neuronal Migration / Neuropediatrics / Torticollis / Dystrophin / X ray Computed Tomography / Nuclear Magnetic Resonance Imaging / Mr Imaging / Genetic Markers / Neurosciences / Linkage Analysis / Occipital Lobe / Nino / Myelin Sheath / Histology / Immunohistochemistry / Adolescent / Intellectual Disability / Brain development / Israel / Biopsy / Mental Retardation / London / Brain / Humans / Child / Cerebellum / Muscle / Cerebral Cortex / Haplotypes / Female / Muscular Dystrophies / Male / Muscles / Infant / Cataract / Central Nervous System / Medical Physiology / Pedigree / Creatine Kinase / Genetic linkage analysis / Clinical Sciences / Fluorescent Antibody Technique / Skeletal Muscle / Adult / Neuromuscular Disorders / Time Factors / Scoliosis / Consanguinity / Neuronal Migration / Neuropediatrics / Torticollis / Dystrophin / X ray Computed Tomography / Nuclear Magnetic Resonance Imaging / Mr Imaging / Genetic Markers / Neurosciences / Linkage Analysis / Occipital Lobe / Nino / Myelin Sheath

Fatal familial infantile glycogen storage disease: Multisystem phosphofructokinase deficiency

Electron Microscopy / Israel / Biopsy / Humans / Muscle / Phosphofructokinase / Female / Male / Muscles / Infant / Ethnic Groups / Consanguinity / Glycogen / Phosphofructokinase / Female / Male / Muscles / Infant / Ethnic Groups / Consanguinity / Glycogen

Mitochondrial DNA mutation and muscle pathology in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

Mitochondrial DNA / Humans / Muscle / Mutation / Muscles / Base Sequence / Succinate Dehydrogenase / Cerebrovascular Disorders / Base Sequence / Succinate Dehydrogenase / Cerebrovascular Disorders

Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): Immunocytochemical and genetic analyses

Genetics / Face / Immunohistochemistry / Adolescent / Biopsy / DNA / Inflammatory Immune Response / Humans / Child / Muscle / Muscular Dystrophy / Female / Muscular Dystrophies / Male / Muscles / Middle Aged / Humerus / Adult / Myositis / Scapula / DNA / Inflammatory Immune Response / Humans / Child / Muscle / Muscular Dystrophy / Female / Muscular Dystrophies / Male / Muscles / Middle Aged / Humerus / Adult / Myositis / Scapula

A predictive robust cascade position-torque control strategy for Pneumatic Artificial Muscles

Robust control / Linear Matrix Inequalities / Muscle / Parallel Robot / Control Strategy / Nonlinear Model / Predictive Control / Torque Control / Nonlinear Model / Predictive Control / Torque Control
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