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Expression and DNA sequence analysis of a human embryonic skeletal muscle mvosin heavy chain gene
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Developmental appearance of myosin heavy and light chain isoforms in vivo and in vitro in chicken skeletal muscle
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Substructure of the myosin molecule
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Recombinant DNA approach for defining the primary structure of monoclonal antibody epitopes
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Complete nucleotide and encoded amino acid sequence of a mammalian myosin heavy chain gene
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Embryonic and foetal myosins in human skeletal muscle
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Developmental progression of myosin gene expression in cultured muscle cells
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Developmental pattern of mouse skeletal myosin heavy chain gene transcripts in vivo and in vitro
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Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy
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Characterization of cDNA and genomic sequences corresponding to an embryonic myosin heavy chain.
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The sequence of an embryonic myosin heavy chain gene and isolation of its corresponding cDNA.
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Detection of specific sequences among DNA fragments separated by gel electrophoresis
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Ribonucleic acid isolated by cesium chloride centrifugation
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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
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Three myosin heavy-chain isozymes appear sequentially in rat muscle development
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Molecular characterization of two myosin heavy chain genes expressed in the adult heart
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Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.
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Molecular evidence for genetic exchanges among ribosomal genes on nonhomologous chromosomes in man and apes.
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Isolation and characterization of human myosin heavy chain genes.
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Cardiac alpha- and beta-myosin heavy chain genes are organized in tandem.
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Characterization of a mammalian smooth muscle myosin heavy chain cDNA clone and its expression in various smooth muscle types.
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Co-expression of multiple myosin heavy chain genes, in addition to a tissue-specific one, in extraocular musculature.
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Contractile activity is required for the expression of neonatal myosin heavy chain in embryonic chick pectoral muscle cultures.
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Distribution of fast myosin heavy chain isoforms in thick filaments of developing chicken pectoral muscle.
inferredcites →https://doi.org/10.1083/jcb.108.5.1791openalex-snapshot
Molecular genetic characterization of a developmentally regulated human perinatal myosin heavy chain.
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Characterization of diverse forms of myosin heavy chain expressed in adult human skeletal muscle
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Human cardiac myosin heavy chain genes and their linkage in the genome
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Identification and Characterization of mRnas Regulated by Nerve Growth Factor in PC12 Cells
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MOLECULAR GENETICS OF MYOSIN
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Myosin Structure and Function in Cell Motility
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Short-Term Effects of Nose-Only Cigarette Smoke Exposure on Glutathione Redox Homeostasis, Cytochrome P450 1A1/2 and Respiratory Enzyme Activities in Mice Tissues
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Developmental and hormonal regulation of sarcomeric myosin heavy chain gene family.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Tumor necrosis factor-α gene transfer induces cachexia and inhibits muscle regeneration
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Stromal derived factor‐1 and granulocyte‐colony stimulating factor treatment improves regeneration of Pax7−/− mice skeletal muscles
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Myogenesis modelled by human pluripotent stem cells: a multi‐omic study of Duchenne myopathy early onset
inferred← citeshttps://doi.org/10.1006/jmbi.1996.0790openalex-snapshot
A 29 residue region of the sarcomeric myosin rod is necessary for filament formation 1 1Edited by J. Karn
inferred← citeshttps://doi.org/10.1006/jmbi.1999.2865openalex-snapshot
Comparative sequence analysis of the complete human sarcomeric myosin heavy chain family: implications for functional diversity 1 1Edited by J. Karn
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Expression of human β-myosin heavy chain fragments inEscherichia coli; localization of actin interfaces on cardiac myosin
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Myosinopathies: pathology and mechanisms
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Remarkable heterogeneity in myosin heavy-chain composition of the human young masseter compared with young biceps brachii
inferred← citeshttps://doi.org/10.1016/0378-1119(90)90020-ropenalex-snapshot
Generation of a full-length human perinatal myosin heavy-chain-encoding cDNA
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Ndrg2 is a PGC-1α/ERRα target gene that controls protein synthesis and expression of contractile-type genes in C2C12 myotubes
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Implication of anti-inflammatory macrophages in regenerative moto-neuritogenesis: Promotion of myoblast migration and neural chemorepellent semaphorin 3A expression in injured muscle
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Prolonged myosin binding increases muscle stiffness in Drosophila models of Freeman-Sheldon syndrome
inferred← citeshttps://doi.org/10.1016/j.cellsig.2014.07.006openalex-snapshot
Ret finger protein mediates Pax7-induced ubiquitination of MyoD in skeletal muscle atrophy
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The expression of multiple myosin heavy chain genes during skeletal muscle development of torafugu Takifugu rubripes embryos and larvae
inferred← citeshttps://doi.org/10.1016/j.ghir.2005.08.001openalex-snapshot
Insulin-like growth factor-I downregulates embryonic myosin heavy chain (eMyHC) in myoblast nuclei
inferred← citeshttps://doi.org/10.1016/j.nmd.2007.02.008openalex-snapshot
Hereditary myosin myopathies
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A MYH3 mutation identified for the first time in a Chinese family with Sheldon-Hall syndrome (DA2B)
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Slow myosin heavy chain 1 is required for slow myofibril and muscle fibre growth but not for myofibril initiation
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Engineered clustered myoblast cell injection augments angiogenesis and muscle regeneration in peripheral artery disease
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Muscle adaptation during distraction osteogenesis in skeletally immature and mature rabbits
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Dynamic nature of fibre-type specific expression of myosin heavy chain transcripts in 14 different human skeletal muscles
inferred← citeshttps://doi.org/10.1038/cdd.2011.72openalex-snapshot
Ret finger protein inhibits muscle differentiation by modulating serum response factor and enhancer of polycomb1
inferred← citeshttps://doi.org/10.1038/ejhg.2013.250openalex-snapshot
Recessive myosin myopathy with external ophthalmoplegia associated with MYH2 mutations
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Comparative transcriptome analysis of muscular dystrophy models Largemyd, Dmdmdx/Largemyd and Dmdmdx: what makes them different?
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Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathy
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Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome
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Gene expression dynamics of human and mouse craniofacial development at the single-cell level
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Critical Limb Ischemia Induces Remodeling of Skeletal Muscle Motor Unit, Myonuclear-, and Mitochondrial-Domains
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Early and non-destructive prediction of the differentiation efficiency of human induced pluripotent stem cells using imaging and machine learning
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Organization of the human skeletal myosin heavy chain gene cluster.
inferred← citeshttps://doi.org/10.1080/10495398.2022.2149549openalex-snapshot
Effect of bovine myosin heavy chain 3 on proliferation and differentiation of myoblast
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Evidence for myoblast-extrinsic regulation of slow myosin heavy chain expression during muscle fiber formation in embryonic development.
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Clathrin Isoform CHC22, a Component of Neuromuscular and Myotendinous Junctions, Binds Sorting Nexin 5 and Has Increased Expression during Myogenesis and Muscle Regeneration
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New nucleotide sequence data on the EMBL File Server
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Evaluation of Embryonic and Perinatal Myosin Gene Mutations and the Etiology of Congenital Idiopathic Clubfoot
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Gene expression patterns of the developing human face at single cell resolution reveal cell type contributions to normal facial variation and disease risk
inferred← citeshttps://doi.org/10.1152/ajpcell.1994.267.6.c1723openalex-snapshot
Type IIx myosin heavy chain transcripts are expressed in type IIb fibers of human skeletal muscle
inferred← citeshttps://doi.org/10.1177/1179069519842157openalex-snapshot
Myo-granules Connect Physiology and Pathophysiology
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Myosin individualized: single nucleotide polymorphisms in energy transduction
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Expression profiles of muscle disease-associated genes and their isoforms during differentiation of cultured human skeletal muscle cells
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Transcription and proteome changes involved in re-innervation muscle following nerve crush in rats
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Novel potential causative genes in carotid paragangliomas
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Reconstructing the ancestral gene pool to uncover the origins and genetic links of Hmong–Mien speakers
inferred← citeshttps://doi.org/10.1186/s13395-020-00241-6openalex-snapshot
Drosophila myosin mutants model the disparate severity of type 1 and type 2B distal arthrogryposis and indicate an enhanced actin affinity mechanism
inferred← citeshttps://doi.org/10.1242/dmm.047886openalex-snapshot
Impaired muscle morphology in a Drosophila model of myosin storage myopathy was suppressed by overexpression of an E3 ubiquitin ligase
inferred← citeshttps://doi.org/10.1242/jcs.107.9.2361openalex-snapshot
Fast myosin heavy chains expressed in secondary mammalian muscle fibers at the time of their inception
inferred← citeshttps://doi.org/10.1242/jeb.01263openalex-snapshot
Temperature and the expression of myogenic regulatory factors (MRFs) and myosin heavy chain isoforms during embryogenesis in the common carpCyprinus carpioL.
inferred← citeshttps://doi.org/10.1242/jeb.202.9.1081openalex-snapshot
Identification and expression analysis of two developmentally regulated myosin heavy chain gene transcripts in carp (Cyprinus carpio)
inferred← citeshttps://doi.org/10.1371/journal.pone.0003750openalex-snapshot
Gene Expression Profiling in Limb-Girdle Muscular Dystrophy 2A
inferred← citeshttps://doi.org/10.1371/journal.pone.0009866openalex-snapshot
Ozz-E3 Ubiquitin Ligase Targets Sarcomeric Embryonic Myosin Heavy Chain during Muscle Development
inferred← citeshttps://doi.org/10.1371/journal.pone.0070288openalex-snapshot
Disruption of Basal Lamina Components in Neuromotor Synapses of Children with Spastic Quadriplegic Cerebral Palsy
inferred← citeshttps://doi.org/10.1371/journal.pone.0142094openalex-snapshot
Developmental MYH3 Myopathy Associated with Expression of Mutant Protein and Reduced Expression Levels of Embryonic MyHC
inferred← citeshttps://doi.org/10.2217/17460751.3.3.287openalex-snapshot
The ACTCellerate Initiative: Large-Scale Combinatorial Cloning of Novel Human Embryonic Stem Cell Derivatives
inferred← citeshttps://doi.org/10.3390/genes15010125openalex-snapshot
A Study of Polish Family with Scoliosis and Limb Contractures Expands the MYH3 Disease Spectrum
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Additional file 1 of Reconstructing the ancestral gene pool to uncover the origins and genetic links of Hmong–Mien speakers
inferred← citeshttps://doi.org/10.6084/m9.figshare.26692621openalex-snapshot
Additional file 2 of Reconstructing the ancestral gene pool to uncover the origins and genetic links of Hmong–Mien speakers
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