Fetal myosin immunoreactivity in human dystrophic muscle

No abstract is available for this paper.

• Publication year

  1986

• Venue

  Muscle and Nerve

• Publication date

  1986-01-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1002/mus.880090108PMID 3513005
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Regenerated muscle fibers in Duchenne muscular dystrophy

  1984cited by this paper
• Hypothesis: Duchenne dystrophy viewed as a disturbance of nerve‐muscle interactions

  1983cited by this paper
• Defective myoblasts identified in Duchenne muscular dystrophy.

  1983cited by this paper
• Maturational defect of regenerating muscle fibers in cases with duchenne and congenital muscular dystrophies

  1983cited by this paper
• Human fetal muscle and cultured myotubes derived from it contain a fetal-specific myosin light chain.

  1983cited by this paper
• Fetal myosin heavy chains in regenerating muscle

  1982cited by this paper
• The significance of type 2C muscle fibers in duchenne muscular dystrophy

  1981cited by this paper
• Embryonic and foetal myosins in human skeletal muscle. The presence of foetal myosins in duchenne muscular dystrophy and infantile spinal muscular atrophy.

  1981cited by this paper
• Three myosin heavy-chain isozymes appear sequentially in rat muscle development

  1981cited by this paper
• "Fast" isomyosins and fiber types in mammalian skeletal muscle.

  1981cited by this paper
• "Slow" myosins in vertebrate skeletal muscle. An immunofluorescence study

  1980cited by this paper
• Rabbit skeletal myosin isoenzymes from fetal, fast-twitch and slow-twitch muscles

  1979cited by this paper
• Contractile protein isozymes in muscle development: identification of an embryonic form of myosin heavy chain.

  1979cited by this paper
• Identification of a novel form of myosin light chain present in embryonic muscle tissue and cultured muscle cells.

  1978cited by this paper
• Collateral Innervation of Muscle Fibres by Motor Axons of Dystrophic Motor Units

  1973cited by this paper
• Regeneration of human muscle. A morphologic and histochemical study of normal and dystrophic muscle after injury.

  1972cited by this paper
• The behavior of four fiber types in developing and reinnervated muscle.

  1971cited by this paper

• The Controlled Release of Platelet-Rich Plasma–Loaded Alginate Repairs Muscle Damage With Less Fibrosis

  2025cites this paper
• Mitochondrial Dynamics Drive Muscle Stem Cell Progression from Quiescence to Myogenic Differentiation

  2024cites this paper
• Functional specialisation and coordination of myonuclei

  2024cites this paper
• Platelet-derived chemokines promote skeletal muscle regeneration by guiding neutrophil recruitment to injured muscles

  2023cites this paper
• Histological Methods to Assess Skeletal Muscle Degeneration and Regeneration in Duchenne Muscular Dystrophy

  2022cites this paper
• Inhibiting the inflammasome with MCC950 counteracts muscle pyroptosis and improves Duchenne muscular dystrophy

  2022cites this paper
• The Emergence of Embryonic Myosin Heavy Chain during Branchiomeric Muscle Development

  2022cites this paper
• Molecular and cellular basis of genetically inherited skeletal muscle disorders

  2021cites this paper
• Identification of candidate miRNA biomarkers for facioscapulohumeral muscular dystrophy using DUX4-based mouse models

  2021cites this paper
• Immunohistochemical analysis of laryngeal muscle of horses clinically affected with recurrent laryngeal neuropathy.

  2020cites this paper
• A high–throughput digital script for multiplexed immunofluorescent analysis and quantification of sarcolemmal and sarcomeric proteins in muscular dystrophies

  2020cites this paper
• Skeletal muscle regeneration in facioscapulohumeral muscular dystrophy is correlated with pathological severity

  2020cites this paper
• Clinically Differentiated Abnormalities of the Architecture and Expression of Myosin Isoforms of the Human Cremaster Muscle in Cryptorchidism and Retractile Testis

  2020cites this paper
• Myosin heavy chain-embryonic regulates skeletal muscle differentiation during mammalian development

  2020influential citation
• Aging: Influence on Duchenne Muscular Dystrophy (DMD) and Becker Muscular Dystrophy (BMD)

  2019cites this paper
• Regenerative biomarkers for Duchenne muscular dystrophy

  2019cites this paper
• Embryonic myosin is a regeneration marker to monitor utrophin-based therapies for DMD

  2018influential citation
• Myosin Heavy Chain-embryonic is a crucial regulator of skeletal muscle development and differentiation

  2018cites this paper
• Muscle fiber type diversity revealed by anti‐myosin heavy chain antibodies

  2018cites this paper
• Nfix Regulates Temporal Progression of Muscle Regeneration through Modulation of Myostatin Expression

  2016cites this paper
• Chapter 30 – Dystrophinopathies

  2015cites this paper
• Developmental myosins: expression patterns and functional significance

  2015cites this paper
• Fibre typing of intrafusal fibres

  2015cites this paper
• Comparative myogenesis in teleosts and mammals

  2014cites this paper
• Muscle regeneration and inflammation in patients with facioscapulohumeral muscular dystrophy

  2013cites this paper
• Re-Evaluation of Sarcolemma Injury and Muscle Swelling in Human Skeletal Muscles after Eccentric Exercise

  2013cites this paper
• Fiber types in mammalian skeletal muscles.

  2011cites this paper
• IIb or not IIb? Regulation of myosin heavy chain gene expression in mice and men

  2011cites this paper
• Cyclosporine A in Ullrich Congenital Muscular Dystrophy: Long-Term Results

  2011cites this paper
• Level of muscle regeneration in limb-girdle muscular dystrophy type 2I relates to genotype and clinical severity

  2011cites this paper
• Regeneration of mammalian skeletal muscle. Basic mechanisms and clinical implications.

  2010cites this paper
• Myofiber stress-response in myositis: parallel investigations on patients and experimental animal models of muscle regeneration and systemic inflammation

  2010cites this paper
• A hypoplastic model of skeletal muscle development displaying reduced foetal myoblast cell numbers, increased oxidative myofibres and improved specific tension capacity.

  2010cites this paper
• Evidence for low muscle capillary supply as a pathogenic factor in chronic compartment syndrome

  2010cites this paper
• Capillary Supply of the Soft Palate Muscles Is Reduced in Long-Term Habitual Snorers

  2009cites this paper
• Childhood spinal muscular atrophy induces alterations in contractile and regulatory protein isoform expressions

  2008cites this paper
• Multipotential mesoangioblast stem cell therapy in the mdx/utrn-/- mouse model for Duchenne muscular dystrophy.

  2007cites this paper
• Expression of late myogenic differentiation markers in sarcoplasmic masses of patients with myotonic dystrophy

  2005cites this paper
• Myosin isoform expression in rat rhabdomyosarcoma induced by Moloney murine sarcoma virus

  2004cites this paper
• Immunohistochemical demonstration of embryonic myosin heavy chains in adult mammalian intrafusal fibers

  2004cites this paper
• Functional properties of skinned rabbit skeletal and cardiac muscle preparations containing α-cardiac myosin heavy chain

  2004cites this paper
• Distribution of sarcoplasmic reticulum Ca-ATPase and of calsequestrin at the polar regions of rat, rabbit and cat intrafusal fibers

  2004cites this paper
• Human muscle spindles : complex morphology and structural organisation

  2004cites this paper
• Abnormal palatopharyngeal muscle morphology in sleep-disordered breathing.

  2002cites this paper
• Familial cardioneuromyopathy with hyaline masses and nemaline rods: A novel phenotype

  2002cites this paper
• Human skeletal muscle fibres: molecular and functional diversity.

  2000cites this paper
• Muscle fiber types of human extraocular muscles: a histochemical and immunohistochemical study.

  2000cites this paper
• Regeneration in sarcoglycanopathies: expression studies of sarcoglycans and other muscle proteins.

  1999cites this paper
• Transient expression of myosin heavy chain MHCIα in rabbit muscle during fast-to-slow transition

  1999cites this paper
• Distribution of ten laminin chains in dystrophic and regenerating muscles.

  1999cites this paper
• Acute quadriplegic myopathy: Analysis of myosin isoforms and evidence for calpain‐mediated proteolysis

  1997cites this paper
• Mammalian skeletal muscle fiber type transitions.

  1997cites this paper
• Expression of an α-cardiac like myosin heavy chain in diaphragm, chronically stimulated, and denervated fast-twitch muscles of rabbit

  1997cites this paper
• Human skeletal muscle fiber types: delineation, development, and distribution.

  1997cites this paper
• "Goldin" : a triton-insoluble protein specifically upregulated in MDX skeletal muscle

  1996cites this paper
• Broad A band disease: A new, benign congenital myopathy

  1996cites this paper
• Myofibrillar Myopathy with Abnormal Foci of Desmin Positivity. II. Immunocytochemical Analysis Reveals Accumulation of Multiple Other Proteins

  1996cites this paper
• Ubiquitin expression in acute steroid myopathy with loss of myosin thick filaments

  1996cites this paper
• Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathy

  1996cites this paper
• Absence of dystrophin and spectrin in regenerating muscle fibers from Becker dystrophy patients.

  1994cites this paper
• Immunohistochemical characterization of human masseter muscle spindles

  1994cites this paper
• Chronic exertional compartment syndrome of the lower leg.

  1994cites this paper
• The pituitary-muscle axis in mdx dystrophic mice.

  1994cites this paper
• Differences in myosin composition between human oro-facial, masticatory and limb muscles: enzyme-, immunohisto-and biochemical studies

  1994cites this paper
• Experimental regeneration in canine muscular dystrophy--2. Expression of myosin heavy chain isoforms.

  1994cites this paper
• Fibres of intermediate type 1C and 2C are found continuously in mdx soleus muscle up to 52 weeks

  1993cites this paper
• Age-related failure of muscle regeneration in the dystrophic DY2J/DY2J mouse

  1993cites this paper
• Ridotta capacità rigenerativa del muscolo distrofico di topo DY2J/DY2J in rapporto all’età

  1993cites this paper
• Corticosteroid therapy in Duchenne muscular dystrophy.

  1993cites this paper
• Myosin isoforms in hindlimb muscles of normal and dystrophic (ReJ129 dy/sol;dy) mice

  1992cites this paper
• Immunocytochemical localization of proteins in striated muscle.

  1992cites this paper
• Acute quadriplegic myopathy

  1992cites this paper
• Expression of myosin heavy chain isoforms in Duchenne muscular dystrophy patients and carriers.

  1991cites this paper
• Myotube phospholipid synthesis and sarcolemmal ATPase activity in dystrophic (mdx) mouse muscle.

  1991cites this paper
• Progressive depletion of fast alpha‐actinin‐positive muscle fibers in Duchenne muscular dystrophy

  1991cites this paper
• Myosin expression in hypertrophied fast twitch and slow tonic muscles of normal and dystrophic chickens

  1991cites this paper
• Transition of myosin isozymes during development of human masseter muscle. Persistence of developmental isoforms during postnatal stage.

  1990cites this paper
• Werdnig-Hoffmann disease: myosin isoform expression not arrested at prenatal stage of development.

  1990cites this paper
• Cellular and molecular diversities of mammalian skeletal muscle fibers.

  1990cites this paper
• Ultrastructural and metabolic characteristics of single muscle fibres belonging to the same type in various muscles in rats

  1990cites this paper
• Identification of three developmentally controlled isoforms of human myosin heavy chains.

  1990cites this paper
• Identification of a novel type 2 fiber population in mammalian skeletal muscle by combined use of histochemical myosin ATPase and anti-myosin monoclonal antibodies.

  1990cites this paper
• Myosin heavy chain composition of muscle fibers in spinal muscular atrophy

  1989cites this paper
• Coexpression of myosin isoforms in muscle of patients with neurogenic disease

  1989cites this paper
• Myosin heavy chain expression in human muscle cocultured with mouse spinal cord.

  1989cites this paper
• Atypical persisting fibres in explants of human muscle cocultured with embryonic nerve cells.

  1988cites this paper
• Neonatal myosin heavy chains are not expressed in Ni-induced rat rhabdomyosarcoma.

  1988cites this paper
• Nodal Myosin Distribution in the Bovine Heart During Prenatal Development: An Immunohistochemical Study

  1988cites this paper
• Comparison of force and stiffness in normal and dystrophic mouse muscles

  1988cites this paper
• Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy.

  1988influential citation
• Binding of Ricinus communis I lectin to developing dystrophic muscle in human fetus.

  1988cites this paper
• Postnatal development of Ca2+-sequestration by the sarcoplasmic reticulum of fast and slow muscles in normal and dystrophic mice.

  1988cites this paper
• Differential effects of calcium on the metabolism of Duchenne muscular dystrophy fibroblasts in vitro

  1987cites this paper
• Expression of myosin light chains during fetal development of human skeletal muscle.

  1987cites this paper
• Primary, secondary and tertiary myotubes in developing skeletal muscle: a new approach to the analysis of human myogenesis.

  1987cites this paper
• Immunocytochemical analysis of myosin heavy chains in human fetal skeletal muscles.

  1986cites this paper