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fibrosis (5) 5
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duchenne muscular dystrophy (4) 4
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transforming growth factor beta1 - genetics (2) 2
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Cell and Tissue Research, ISSN 0302-766X, 2/2010, Volume 339, Issue 2, pp. 397 - 410
To probe pro-fibrotic mechanisms in dystrophic muscle, we isolated primary fibroblasts from Duchenne muscular dystrophy (DMD) and control muscle biopsies and... 
Human Genetics | Human | Biomedicine | Fibroblast cultures | Duchenne muscular dystrophy | Proteomics | Fibrosis | Extracellular matrix | Molecular Medicine | Myofibroblasts
Journal Article
Electrochemistry Communications, ISSN 1388-2481, 06/2019, Volume 103, pp. 31 - 36
Ethylene glycol-based solutions containing metal precursor chloride salts were investigated for the electrodeposition of cobalt thin films and nanowires. The... 
Organic solvent | Magnetization | Electroplating | Non-aqueous | Alumina template | ELECTROCHEMISTRY | CO NANOWIRES | BEHAVIOR | ARRAYS | SOLVENTS | COATINGS | FABRICATION | MAGNETIC-PROPERTIES | IONIC LIQUIDS | UREA | FE | Thin films | Ethylene glycol | Electrochemical reactions | Anisotropy | Animal behavior | Aluminum compounds | Dielectric films | Electric properties
Journal Article
Matrix Biology, ISSN 0945-053X, 12/2018, Volume 74, pp. 77 - 100
Exosomes, natural carriers of mRNAs, non-coding RNAs and proteins between donor and recipient cells, actively contribute to cell-cell communication. We... 
Fibroblasts | Myofibroblasts | miRNAs | Duchenne muscle dystrophy | Exosomes | Fibrosis | LUNG FIBROSIS | CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | MECHANISMS | MICRORNAS | CELL BIOLOGY | REGULATOR | INTERNALIZATION | EXTRACELLULAR-MATRIX | PROGRESSION | CAVEOLIN-1 | Fibronectins | MicroRNA | Actin | Collagen | Analysis | Muscles | Muscle proteins | Cells | Index Medicus
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 2017, Volume 27, Issue 5, pp. 481 - 486
Journal Article
Journal Article
Cell and Tissue Research, ISSN 0302-766X, 5/2014, Volume 356, Issue 2, pp. 427 - 443
The Sgcb-null mouse, with knocked-down β-sarcoglycan, develops severe muscular dystrophy as in type 2E human limb girdle muscular dystrophy. The mdx mouse,... 
Human Genetics | mdx | Decorin | Collagens | Macrophages | Muscle inflammation | Biomedicine | β-sarcoglycan | Proteomics | Muscle fibrosis | Extracellular matrix | TGF-β | Molecular Medicine | DYSTROPHIN-GLYCOPROTEIN COMPLEX | MESSENGER-RNA EXPRESSION | III COLLAGEN | GIRDLE MUSCULAR-DYSTROPHY | beta-sarcoglycan | CELL BIOLOGY | SKELETAL-MUSCLE | TGF-beta | GROWTH-FACTOR-BETA | GENE-EXPRESSION | MICE | Osteopontin - genetics | Diaphragm - pathology | Transforming Growth Factor beta1 - metabolism | Collagen Type III - metabolism | Collagen Type VI - metabolism | Muscular Dystrophy, Animal - pathology | Collagen Type VI - genetics | RNA, Messenger - biosynthesis | Collagen Type I - genetics | Muscular Dystrophies, Limb-Girdle - genetics | Mice, Inbred mdx | Diaphragm - metabolism | Quadriceps Muscle - pathology | Decorin - genetics | Extracellular Matrix Proteins - metabolism | Macrophages - immunology | Fibrosis - genetics | Collagen Type I - metabolism | Extracellular Matrix Proteins - genetics | Mice, Inbred C57BL | Inflammation - immunology | Transforming Growth Factor beta1 - genetics | Collagen Type III - genetics | Mice, Knockout | Animals | Sarcoglycans - genetics | Dystrophin - genetics | Inflammation - genetics | Mice | Quadriceps Muscle - metabolism | Extracellular Matrix - pathology | Decorin - metabolism | Usage | Collagen | Analysis | Fibrosis | Bone morphogenetic proteins | Inflammation | Transforming growth factors | Dystrophin | Muscular system | Gene expression | Rodents | Muscular dystrophy | Immune system
Journal Article
Toxicon, ISSN 0041-0101, 01/2015, Volume 93, p. S66
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 07/2015, Volume 1852, Issue 7, pp. 1451 - 1464
Excessive extracellular matrix deposition progressively replacing muscle fibres is the endpoint of most severe muscle diseases. Recent data indicate major... 
MiR-21 | mdx mouse | Duchenne muscular dystrophy | Fibrosis | Myoblast | MiR-29 | Fibroblast | Mdx mouse | COLLAGEN | BIOCHEMISTRY & MOLECULAR BIOLOGY | MUSCLE | PTEN | FIBROBLASTS | PATHOGENESIS | BIOPHYSICS | TRANSFORMING GROWTH-FACTOR-BETA-1 | THERAPEUTIC TARGET | EXTRACELLULAR-MATRIX | EXPRESSION | MICRORNA | Transforming growth factors | Collagen
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 05/2019, Volume 29, Issue 5, pp. 376 - 380
2 mutations cause the most frequent congenital muscular dystrophy subtype MDC1A and a variety of milder phenotypes, characterized by total or partial... 
LAMA2 | WES | Congenital muscular dystrophy type 1A | Laminin-α2 | POPULATION | NERVE | CONGENITAL MUSCULAR-DYSTROPHY | MEROSIN | NEUROSCIENCES | CLINICAL NEUROLOGY | Laminin-alpha 2 | NEUROPATHY | COHORT | SPECTRUM
Journal Article
Toxicology in Vitro, ISSN 0887-2333, 08/2018, Volume 50, p. 124
Botulin toxin (BTX) is widely used for treating skeletal muscle spasticity. Experimental reports on BTX treatment were mainly focused on the neuromuscular... 
Biotechnology | Transcription factors | Myotubes | Transcription | Genes | Muscles | Spasticity | Cultures | Muscular system | Gene expression | Botulinum toxin | Patients | Muscle contraction | Cells | Skeletal muscle | Myoblasts | Proteins | DNA microarrays | Biopsy | Botulinum Toxin Type A | Cell cycle | Fibroblasts | Extracellular matrix
Journal Article
Cell and Tissue Research, ISSN 0302-766X, 02/2010, Volume 339, Issue 2, p. 397
To probe pro-fibrotic mechanisms in dystrophic muscle, we isolated primary fibroblasts from Duchenne muscular dystrophy (DMD) and control muscle biopsies and... 
Enzymes | Collagen | Duchenne muscular dystrophy | Bone morphogenetic proteins | Transforming growth factors | Dystrophin | Enzyme-linked immunosorbent assay | Proteins | Muscular system | Cellular biology | Muscular dystrophy
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 03/2019, Volume 398, pp. 75 - 78
Variants in Filamin C (FLNC) gene may cause either cardiomyopathies or different myopathies. We describe a family affected by a distal myopathy with autosomal... 
Distal myopathy | Myofibrillar myopathy | NGS | FLNC | Filamin C | Hereditary myopathy | NEUROSCIENCES | CLINICAL NEUROLOGY | Neurosciences | Anopheles | Actin | Creatine kinase | Genetic aspects | Muscle proteins | Creatine | Protein binding
Journal Article
Journal Article
Toxicology in Vitro, ISSN 0887-2333, 08/2018, Volume 50, pp. 124 - 136
Botulin toxin (BTX) is widely used for treating skeletal muscle spasticity. Experimental reports on BTX treatment were mainly focused on the neuromuscular... 
Spasticity | Fibroblasts | Myotubes | Microarray | Botulinum toxin-A | Myoblasts | DNA-DAMAGE | DIFFERENTIALLY REGULATED GENES | NEUROTOXIN | CORD-INJURED SUBJECTS | LIMB SPASTICITY | SKELETAL-MUSCLE | IN-VITRO | EXTRACELLULAR-MATRIX | TOXICOLOGY | CEREBRAL-PALSY | Muscles | DNA microarrays | Botulinum toxin | Analysis | Cells
Journal Article