F1.652

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$40.00
SKU: F1.652
View product citations for antibody F1.652 on CiteAb

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DSHB Data Sheet

Catalog Fields

Antigen: myosin (embryonic)
Hybridoma Cells Available: Yes
Antigen Species: Human
Depositor: Blau, H.M.
Isotype: MIgG1
Antigen Sequence:
Host Species: mouse
Depositors Institution: Baxter Lab for Stem Cell Biology, Stanford University
Positive Tested Species Reactivity: Guinea Pig, Human, Mouse, Rat, Rodent
Depositors Notes:
Antigen Molecular Weight: Predicted 224kDa; Apparent: 200, 222 or 250kDa
Human Protein Atlas:
Predicted Species Reactivity:  
Gene: MYH3
Immunogen: partially purified (pyrophosphate extracted) fetal human myosin (15 weeks gestation)
Alternate Gene Names: HEMHC; SMHCE; MYHSE1; MYHC-EMB
Alternate Antibody Name:
Clonality: Monoclonal
Alternate Antigen Name:
Epitope Mapped:
Myeloma Strain: SP2/2
Epitope Location or Sequence:
Uniprot ID: P11055 
Immunogen Sequence: Total protein
Entrez Gene ID: 4621 
Additional Characterization:
Antibody Registry ID: AB_528358 
Additional Information: Embryonic myosin is a marker of newly forming fibers. F1.652 is useful to assess muscle regeneration/remodeling.
Recommended Applications: FFPE, Immunofluorescence, Immunohistochemistry, Western Blot
These hybridomas were created by your colleagues. Please acknowledge the hybridoma contributor and the Developmental Studies Hybridoma Bank (DSHB) in the Materials and Methods of your publications. Please email the citation to us.
For your Materials & Methods section:
F1.652 was deposited to the DSHB by Blau, H.M. (DSHB Hybridoma Product F1.652)
Storage and Handling Recommendations
Although many cell products are maintained at 4°C for years without loss of activity, shelf-life at 4°C is highly variable. To ensure retention of antibody activity, we recommend aliquotting the product into two parts: 1) a volume of antibody stored at 4°C to be used within two weeks. 2) the remaining product diluted with an equal volume of molecular grade glycerol and stored at -20°C.
Usage Recommendations
While optimal Ig concentration for an application will vary, a good starting concentration for immunohistochemistry (IHC), immunofluorescence(IF) and staining is 2-5 µg/ml. For Western blots, the concentration is decreased by one order of magnitude (that is, 0.2-0.5 µg/ml).
All cell products contain the antimicrobial ProClin. Click here for additional information.

57 References

  • Initial Publication
  • IF References
  • WB References
  • IHC References
  • ELISA References
  • FFPE References
  • Epitope Map References
  • All References
  • Initial Publication
    IF References

    In vitro Differentiation of Functional Human Skeletal Myotubes in a Defined System.
    Hickman J
    Biomaterials science 2.1 (2014 Jan 1): 131-138.

    Laminin α2 Chain-Deficiency is Associated with microRNA Deregulation in Skeletal Muscle and Plasma.
    Durbeej M
    Frontiers in aging neuroscience 6. (2014): 155.

    Whey protein supplementation accelerates satellite cell proliferation during recovery from eccentric exercise.
    Vissing K
    Amino acids 46.11 (2014 Nov): 2503-16.

    Influence of exercise contraction mode and protein supplementation on human skeletal muscle satellite cell content and muscle fiber growth.
    Vissing K
    Journal of applied physiology (Bethesda, Md. : 1985) 117.8 (2014 Oct 15): 898-909.

    Cyclosporin A Promotes in vivo Myogenic Response in Collagen VI-Deficient Myopathic Mice.
    Bonaldo P
    Frontiers in aging neuroscience 6. (2014): 244.

    Coffee treatment prevents the progression of sarcopenia in aged mice in vivo and in vitro.
    Nagatomi R
    Experimental gerontology 50. (2014 Feb): 1-8.

    Generation of muscular dystrophy model rats with a CRISPR/Cas system.
    Nishihara M
    Scientific reports 4. (2014 Jul 9): 5635.

    Metformin protects skeletal muscle from cardiotoxin induced degeneration.
    Cesareni G
    PloS one 9.12 (2014): e114018.

    Loss of dystrophin and β-sarcoglycan significantly exacerbates the phenotype of laminin α2 chain-deficient animals.
    Durbeej M
    The American journal of pathology 184.3 (2014 Mar): 740-52.

    Oxytocin is an age-specific circulating hormone that is necessary for muscle maintenance and regeneration.
    Conboy IM
    Nature communications 5. (2014 Jun 10): 4082.

    Resveratrol induces expression of the slow, oxidative phenotype in mdx mouse muscle together with enhanced activity of the SIRT1-PGC-1α axis.
    Jasmin BJ
    American journal of physiology. Cell physiology 307.1 (2014 Jul 1): C66-82.

    Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy.
    Blau HM
    Cell 52.4 (1988 Feb 26): 503-13.

    Protein turnover and cellular stress in mildly and severely affected muscles from patients with limb girdle muscular dystrophy type 2I.
    Krag TO
    PloS one 8.6 (2013): e66929.

    Development transitions of thin filament proteins in rat extraocular muscles.
    Andrade FH
    Experimental cell research 319.3 (2013 Feb 1): 23-31.

    CuZnSOD gene deletion targeted to skeletal muscle leads to loss of contractile force but does not cause muscle atrophy in adult mice.
    Van Remmen H
    FASEB journal : official publication of the Federation of American Societies for Experimental Biology 27.9 (2013 Sep): 3536-48.

    Royal jelly prevents the progression of sarcopenia in aged mice in vivo and in vitro.
    Nagatomi R
    The journals of gerontology. Series A, Biological sciences and medical sciences 68.12 (2013 Dec): 1482-92.

    Normal muscle regeneration requires tight control of muscle cell fusion by tetraspanins CD9 and CD81.
    Rubinstein E
    Nature communications 4. (2013): 1674.

    c-MET regulates myoblast motility and myocyte fusion during adult skeletal muscle regeneration.
    Fan CM
    PloS one 8.11 (2013): e81757.

    Increased sarcolipin expression and decreased sarco(endo)plasmic reticulum Ca2+ uptake in skeletal muscles of mouse models of Duchenne muscular dystrophy.
    Babu GJ
    Journal of muscle research and cell motility 34.5-6 (2013 Dec): 349-56.

    Increased sphingosine-1-phosphate improves muscle regeneration in acutely injured mdx mice.
    Reyes M
    Skeletal muscle 3.1 (2013 Aug 1): 20.

    The localization of VAMP5 in skeletal and cardiac muscle.
    Yorifuji H
    Histochemistry and cell biology 139.4 (2013 Apr): 573-82.

    PKCθ signaling is required for myoblast fusion by regulating the expression of caveolin-3 and β1D integrin upstream focal adhesion kinase.
    Bouché M
    Molecular biology of the cell 22.8 (2011 Apr 15): 1409-19.

    Regulation of differentiation potential of human mesenchymal stem cells by intracytoplasmic delivery of coactivator-associated arginine methyltransferase 1 protein using cell-penetrating peptide.
    Lee DR
    Stem cells (Dayton, Ohio) 30.8 (2012 Aug): 1703-13.

    Sarcospan-dependent Akt activation is required for utrophin expression and muscle regeneration.
    Crosbie-Watson RH
    The Journal of cell biology 197.7 (2012 Jun 25): 1009-27.

    Dystrophin and utrophin expression require sarcospan: loss of α7 integrin exacerbates a newly discovered muscle phenotype in sarcospan-null mice.
    Crosbie-Watson RH
    Human molecular genetics 21.20 (2012 Oct 15): 4378-93.

    Acetylation is important for MyoD function in adult mice.
    Harel-Bellan A
    EMBO reports 7.11 (2006 Nov): 1140-6.

    Clathrin isoform CHC22, a component of neuromuscular and myotendinous junctions, binds sorting nexin 5 and has increased expression during myogenesis and muscle regeneration.
    Brodsky FM
    Molecular biology of the cell 15.7 (2004 Jul): 3181-95.

    The ER-bound RING finger protein 5 (RNF5/RMA1) causes degenerative myopathy in transgenic mice and is deregulated in inclusion body myositis.
    Ronai Z
    PloS one 3.2 (2008 Feb 13): e1609.

    Evidence for myoblast-extrinsic regulation of slow myosin heavy chain expression during muscle fiber formation in embryonic development.
    Blau HM
    The Journal of cell biology 121.4 (1993 May): 795-810.

    Regulation of myosin heavy chain expression during rat skeletal muscle development in vitro.
    Daniels MP
    Molecular biology of the cell 12.5 (2001 May): 1499-508.

    Exercise-induced activation of NMDA receptor promotes motor unit development and survival in a type 2 spinal muscular atrophy model mouse.
    Charbonnier F
    The Journal of neuroscience : the official journal of the Society for Neuroscience 28.4 (2008 Jan 23): 953-62.

    Autophagy regulates satellite cell ability to regenerate normal and dystrophic muscles.
    Latella L
    Cell death and differentiation 23.11 (2016 Nov 1): 1839-1849.

    BAMBI shuttling between cytosol and membrane is required for skeletal muscle development and regeneration.
    Xie L
    Biochemical and biophysical research communications 509.1 (2019 Jan 29): 125-132.

    Isometric resistance training increases strength and alters histopathology of dystrophin-deficient mouse skeletal muscle.
    Lowe DA
    Journal of applied physiology (Bethesda, Md. : 1985) 126.2 (2019 Feb 1): 363-375.

    Fate decision of satellite cell differentiation and self-renewal by miR-31-IL34 axis.
    Meng Q
    Cell death and differentiation . (2019 Jul 22): .

    miR-146a deficiency does not aggravate muscular dystrophy in mdx mice.
    Dulak J
    Skeletal muscle 9.1 (2019 Aug 14): 22.

    WB References

    Absence of developmental and unconventional myosin heavy chain in human suprahyoid muscles.
    Sokoloff AJ
    Muscle and nerve 49.4 (2014 Apr): 534-44.

    Calpain-6 deficiency promotes skeletal muscle development and regeneration.
    Sorimachi H
    PLoS genetics 9.8 (2013): e1003668.

    Murine muscle engineered from dermal precursors: an in vitro model for skeletal muscle generation, degeneration, and fatty infiltration.
    López de Munain A
    Tissue engineering. Part C, Methods 20.1 (2014 Jan): 28-41.

    Disruption of basal lamina components in neuromotor synapses of children with spastic quadriplegic cerebral palsy.
    Akins RE
    PloS one 8.8 (2013): e70288.

    PKCθ signaling is required for myoblast fusion by regulating the expression of caveolin-3 and β1D integrin upstream focal adhesion kinase.
    Bouché M
    Molecular biology of the cell 22.8 (2011 Apr 15): 1409-19.

    Ndrg2 is a PGC-1α/ERRα target gene that controls protein synthesis and expression of contractile-type genes in C2C12 myotubes.
    Russell AP
    Biochimica et biophysica acta 1833.12 (2013 Dec): 3112-3123.

    Insulin-like growth factor-I downregulates embryonic myosin heavy chain (eMyHC) in myoblast nuclei.
    Rodgers BD
    Growth hormone and IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society 15.6 (2005 Dec): 377-83.

    Decreased levels of myotonic dystrophy protein kinase (DMPK) and delayed differentiation in human myotonic dystrophy myoblasts.
    Puymirat J
    Neuromuscular disorders : NMD 11.8 (2001 Nov): 728-35.

    Acetylation is important for MyoD function in adult mice.
    Harel-Bellan A
    EMBO reports 7.11 (2006 Nov): 1140-6.

    IL-1beta impairs insulin-like growth factor i-induced differentiation and downstream activation signals of the insulin-like growth factor i receptor in myoblasts.
    Kelley KW
    Journal of immunology (Baltimore, Md. : 1950) 172.12 (2004 Jun 15): 7713-20.

    Myogenic stage, sarcomere length, and protease activity modulate localization of muscle-specific calpain.
    Sorimachi H
    The Journal of biological chemistry 282.19 (2007 May 11): 14493-504.

    C-jun N-terminal kinase mediates tumor necrosis factor-alpha suppression of differentiation in myoblasts.
    Kelley KW
    Endocrinology 147.9 (2006 Sep): 4363-73.

    Evidence for myoblast-extrinsic regulation of slow myosin heavy chain expression during muscle fiber formation in embryonic development.
    Blau HM
    The Journal of cell biology 121.4 (1993 May): 795-810.

    Tumor necrosis factor-alpha gene transfer induces cachexia and inhibits muscle regeneration.
    Sassoon D
    Genesis (New York, N.Y. : 2000) 43.3 (2005 Nov): 120-8.

    Hypertrophy and transcriptional regulation induced in myogenic cell line L6-C5 by an increase of extracellular calcium.
    Naro F
    Journal of cellular physiology 202.3 (2005 Mar): 787-95.

    Fate decision of satellite cell differentiation and self-renewal by miR-31-IL34 axis.
    Meng Q
    Cell death and differentiation . (2019 Jul 22): .

    Fast myosin heavy chains expressed in secondary mammalian muscle fibers at the time of their inception.
    Blau HM
    Journal of cell science 107 ( Pt 9). (1994 Sep): 2361-71.

    IHC References

    Absence of developmental and unconventional myosin heavy chain in human suprahyoid muscles.
    Sokoloff AJ
    Muscle and nerve 49.4 (2014 Apr): 534-44.

    Geriatric muscle stem cells switch reversible quiescence into senescence.
    Muñoz-Cánoves P
    Nature 506.7488 (2014 Feb 20): 316-21.

    Src mediates the mechanical activation of myogenesis by activating TNFα-converting enzyme.
    Li YP
    Journal of cell science 126.Pt 19 (2013 Oct 1): 4349-57.

    Increased sphingosine-1-phosphate improves muscle regeneration in acutely injured mdx mice.
    Reyes M
    Skeletal muscle 3.1 (2013 Aug 1): 20.

    Conditional over-expression of PITX1 causes skeletal muscle dystrophy in mice.
    Chen YW
    Biology open 1.7 (2012 Jul): 629-639.

    p38/MKP-1-regulated AKT coordinates macrophage transitions and resolution of inflammation during tissue repair.
    Muñoz-Cánoves P
    The Journal of cell biology 195.2 (2011 Oct 17): 307-22.

    Abnormal palatopharyngeal muscle morphology in sleep-disordered breathing.
    Stål PS
    Journal of the neurological sciences 195.1 (2002 Mar 15): 11-23.

    Neutrophils contribute to muscle injury and impair its resolution after lengthening contractions in mice.
    Koh TJ
    The Journal of physiology 562.Pt 3 (2005 Feb 1): 899-913.

    Molecular indicators of denervation in aging human skeletal muscle.
    Mackey AL
    Muscle and nerve 60.4 (2019 Oct): 453-463.

    miR-146a deficiency does not aggravate muscular dystrophy in mdx mice.
    Dulak J
    Skeletal muscle 9.1 (2019 Aug 14): 22.

    Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy.
    Blau HM
    Cell 52.4 (1988 Feb 26): 503-13.

    Fast myosin heavy chains expressed in secondary mammalian muscle fibers at the time of their inception.
    Blau HM
    Journal of cell science 107 ( Pt 9). (1994 Sep): 2361-71.

    ELISA References
    FFPE References
    Epitope Map References
    All References

    Absence of developmental and unconventional myosin heavy chain in human suprahyoid muscles.
    Sokoloff AJ
    Muscle and nerve 49.4 (2014 Apr): 534-44.

    Geriatric muscle stem cells switch reversible quiescence into senescence.
    Muñoz-Cánoves P
    Nature 506.7488 (2014 Feb 20): 316-21.

    Src mediates the mechanical activation of myogenesis by activating TNFα-converting enzyme.
    Li YP
    Journal of cell science 126.Pt 19 (2013 Oct 1): 4349-57.

    Increased sphingosine-1-phosphate improves muscle regeneration in acutely injured mdx mice.
    Reyes M
    Skeletal muscle 3.1 (2013 Aug 1): 20.

    Conditional over-expression of PITX1 causes skeletal muscle dystrophy in mice.
    Chen YW
    Biology open 1.7 (2012 Jul): 629-639.

    p38/MKP-1-regulated AKT coordinates macrophage transitions and resolution of inflammation during tissue repair.
    Muñoz-Cánoves P
    The Journal of cell biology 195.2 (2011 Oct 17): 307-22.

    Abnormal palatopharyngeal muscle morphology in sleep-disordered breathing.
    Stål PS
    Journal of the neurological sciences 195.1 (2002 Mar 15): 11-23.

    Neutrophils contribute to muscle injury and impair its resolution after lengthening contractions in mice.
    Koh TJ
    The Journal of physiology 562.Pt 3 (2005 Feb 1): 899-913.

    Molecular indicators of denervation in aging human skeletal muscle.
    Mackey AL
    Muscle and nerve 60.4 (2019 Oct): 453-463.

    miR-146a deficiency does not aggravate muscular dystrophy in mdx mice.
    Dulak J
    Skeletal muscle 9.1 (2019 Aug 14): 22.

    Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy.
    Blau HM
    Cell 52.4 (1988 Feb 26): 503-13.

    Fast myosin heavy chains expressed in secondary mammalian muscle fibers at the time of their inception.
    Blau HM
    Journal of cell science 107 ( Pt 9). (1994 Sep): 2361-71.

    In vitro Differentiation of Functional Human Skeletal Myotubes in a Defined System.
    Hickman J
    Biomaterials science 2.1 (2014 Jan 1): 131-138.

    Laminin α2 Chain-Deficiency is Associated with microRNA Deregulation in Skeletal Muscle and Plasma.
    Durbeej M
    Frontiers in aging neuroscience 6. (2014): 155.

    Whey protein supplementation accelerates satellite cell proliferation during recovery from eccentric exercise.
    Vissing K
    Amino acids 46.11 (2014 Nov): 2503-16.

    Influence of exercise contraction mode and protein supplementation on human skeletal muscle satellite cell content and muscle fiber growth.
    Vissing K
    Journal of applied physiology (Bethesda, Md. : 1985) 117.8 (2014 Oct 15): 898-909.

    Cyclosporin A Promotes in vivo Myogenic Response in Collagen VI-Deficient Myopathic Mice.
    Bonaldo P
    Frontiers in aging neuroscience 6. (2014): 244.

    Coffee treatment prevents the progression of sarcopenia in aged mice in vivo and in vitro.
    Nagatomi R
    Experimental gerontology 50. (2014 Feb): 1-8.

    Generation of muscular dystrophy model rats with a CRISPR/Cas system.
    Nishihara M
    Scientific reports 4. (2014 Jul 9): 5635.

    Metformin protects skeletal muscle from cardiotoxin induced degeneration.
    Cesareni G
    PloS one 9.12 (2014): e114018.

    Loss of dystrophin and β-sarcoglycan significantly exacerbates the phenotype of laminin α2 chain-deficient animals.
    Durbeej M
    The American journal of pathology 184.3 (2014 Mar): 740-52.

    Oxytocin is an age-specific circulating hormone that is necessary for muscle maintenance and regeneration.
    Conboy IM
    Nature communications 5. (2014 Jun 10): 4082.

    Resveratrol induces expression of the slow, oxidative phenotype in mdx mouse muscle together with enhanced activity of the SIRT1-PGC-1α axis.
    Jasmin BJ
    American journal of physiology. Cell physiology 307.1 (2014 Jul 1): C66-82.

    Protein turnover and cellular stress in mildly and severely affected muscles from patients with limb girdle muscular dystrophy type 2I.
    Krag TO
    PloS one 8.6 (2013): e66929.

    Development transitions of thin filament proteins in rat extraocular muscles.
    Andrade FH
    Experimental cell research 319.3 (2013 Feb 1): 23-31.

    CuZnSOD gene deletion targeted to skeletal muscle leads to loss of contractile force but does not cause muscle atrophy in adult mice.
    Van Remmen H
    FASEB journal : official publication of the Federation of American Societies for Experimental Biology 27.9 (2013 Sep): 3536-48.

    Royal jelly prevents the progression of sarcopenia in aged mice in vivo and in vitro.
    Nagatomi R
    The journals of gerontology. Series A, Biological sciences and medical sciences 68.12 (2013 Dec): 1482-92.

    Normal muscle regeneration requires tight control of muscle cell fusion by tetraspanins CD9 and CD81.
    Rubinstein E
    Nature communications 4. (2013): 1674.

    c-MET regulates myoblast motility and myocyte fusion during adult skeletal muscle regeneration.
    Fan CM
    PloS one 8.11 (2013): e81757.

    Increased sarcolipin expression and decreased sarco(endo)plasmic reticulum Ca2+ uptake in skeletal muscles of mouse models of Duchenne muscular dystrophy.
    Babu GJ
    Journal of muscle research and cell motility 34.5-6 (2013 Dec): 349-56.

    The localization of VAMP5 in skeletal and cardiac muscle.
    Yorifuji H
    Histochemistry and cell biology 139.4 (2013 Apr): 573-82.

    PKCθ signaling is required for myoblast fusion by regulating the expression of caveolin-3 and β1D integrin upstream focal adhesion kinase.
    Bouché M
    Molecular biology of the cell 22.8 (2011 Apr 15): 1409-19.

    Regulation of differentiation potential of human mesenchymal stem cells by intracytoplasmic delivery of coactivator-associated arginine methyltransferase 1 protein using cell-penetrating peptide.
    Lee DR
    Stem cells (Dayton, Ohio) 30.8 (2012 Aug): 1703-13.

    Sarcospan-dependent Akt activation is required for utrophin expression and muscle regeneration.
    Crosbie-Watson RH
    The Journal of cell biology 197.7 (2012 Jun 25): 1009-27.

    Dystrophin and utrophin expression require sarcospan: loss of α7 integrin exacerbates a newly discovered muscle phenotype in sarcospan-null mice.
    Crosbie-Watson RH
    Human molecular genetics 21.20 (2012 Oct 15): 4378-93.

    Acetylation is important for MyoD function in adult mice.
    Harel-Bellan A
    EMBO reports 7.11 (2006 Nov): 1140-6.

    Clathrin isoform CHC22, a component of neuromuscular and myotendinous junctions, binds sorting nexin 5 and has increased expression during myogenesis and muscle regeneration.
    Brodsky FM
    Molecular biology of the cell 15.7 (2004 Jul): 3181-95.

    The ER-bound RING finger protein 5 (RNF5/RMA1) causes degenerative myopathy in transgenic mice and is deregulated in inclusion body myositis.
    Ronai Z
    PloS one 3.2 (2008 Feb 13): e1609.

    Evidence for myoblast-extrinsic regulation of slow myosin heavy chain expression during muscle fiber formation in embryonic development.
    Blau HM
    The Journal of cell biology 121.4 (1993 May): 795-810.

    Regulation of myosin heavy chain expression during rat skeletal muscle development in vitro.
    Daniels MP
    Molecular biology of the cell 12.5 (2001 May): 1499-508.

    Exercise-induced activation of NMDA receptor promotes motor unit development and survival in a type 2 spinal muscular atrophy model mouse.
    Charbonnier F
    The Journal of neuroscience : the official journal of the Society for Neuroscience 28.4 (2008 Jan 23): 953-62.

    Autophagy regulates satellite cell ability to regenerate normal and dystrophic muscles.
    Latella L
    Cell death and differentiation 23.11 (2016 Nov 1): 1839-1849.

    BAMBI shuttling between cytosol and membrane is required for skeletal muscle development and regeneration.
    Xie L
    Biochemical and biophysical research communications 509.1 (2019 Jan 29): 125-132.

    Isometric resistance training increases strength and alters histopathology of dystrophin-deficient mouse skeletal muscle.
    Lowe DA
    Journal of applied physiology (Bethesda, Md. : 1985) 126.2 (2019 Feb 1): 363-375.

    Fate decision of satellite cell differentiation and self-renewal by miR-31-IL34 axis.
    Meng Q
    Cell death and differentiation . (2019 Jul 22): .

    Calpain-6 deficiency promotes skeletal muscle development and regeneration.
    Sorimachi H
    PLoS genetics 9.8 (2013): e1003668.

    Murine muscle engineered from dermal precursors: an in vitro model for skeletal muscle generation, degeneration, and fatty infiltration.
    López de Munain A
    Tissue engineering. Part C, Methods 20.1 (2014 Jan): 28-41.

    Disruption of basal lamina components in neuromotor synapses of children with spastic quadriplegic cerebral palsy.
    Akins RE
    PloS one 8.8 (2013): e70288.

    Ndrg2 is a PGC-1α/ERRα target gene that controls protein synthesis and expression of contractile-type genes in C2C12 myotubes.
    Russell AP
    Biochimica et biophysica acta 1833.12 (2013 Dec): 3112-3123.

    Insulin-like growth factor-I downregulates embryonic myosin heavy chain (eMyHC) in myoblast nuclei.
    Rodgers BD
    Growth hormone and IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society 15.6 (2005 Dec): 377-83.

    Decreased levels of myotonic dystrophy protein kinase (DMPK) and delayed differentiation in human myotonic dystrophy myoblasts.
    Puymirat J
    Neuromuscular disorders : NMD 11.8 (2001 Nov): 728-35.

    IL-1beta impairs insulin-like growth factor i-induced differentiation and downstream activation signals of the insulin-like growth factor i receptor in myoblasts.
    Kelley KW
    Journal of immunology (Baltimore, Md. : 1950) 172.12 (2004 Jun 15): 7713-20.

    Myogenic stage, sarcomere length, and protease activity modulate localization of muscle-specific calpain.
    Sorimachi H
    The Journal of biological chemistry 282.19 (2007 May 11): 14493-504.

    C-jun N-terminal kinase mediates tumor necrosis factor-alpha suppression of differentiation in myoblasts.
    Kelley KW
    Endocrinology 147.9 (2006 Sep): 4363-73.

    Tumor necrosis factor-alpha gene transfer induces cachexia and inhibits muscle regeneration.
    Sassoon D
    Genesis (New York, N.Y. : 2000) 43.3 (2005 Nov): 120-8.

    Hypertrophy and transcriptional regulation induced in myogenic cell line L6-C5 by an increase of extracellular calcium.
    Naro F
    Journal of cellular physiology 202.3 (2005 Mar): 787-95.

    Developmental progression of myosin gene expression in cultured muscle cells.
    Blau HM
    Cell 46.7 (1986 Sep 26): 1075-81.

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