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ab11576 has been referenced in 21 publications.

  • Aguilar CA  et al. Multiscale analysis of a regenerative therapy for treatment of volumetric muscle loss injury. Cell Death Discov 4:33 (2018). PubMed: 29531830
  • Mead AF  et al. Fundamental constraints in synchronous muscle limit superfast motor control in vertebrates. Elife 6:N/A (2017). PubMed: 29165242
  • Luo D  et al. Deltex2 represses MyoD expression and inhibits myogenic differentiation by acting as a negative regulator of Jmjd1c. Proc Natl Acad Sci U S A 114:E3071-E3080 (2017). PubMed: 28351977
  • Greising SM  et al. Unwavering Pathobiology of Volumetric Muscle Loss Injury. Sci Rep 7:13179 (2017). PubMed: 29030619
  • Nie Y  et al. Palmdelphin promotes myoblast differentiation and muscle regeneration. Sci Rep 7:41608 (2017). IF . PubMed: 28148961
  • Naito M  et al. Dnmt3a Regulates Proliferation of Muscle Satellite Cells via p57Kip2. PLoS Genet 12:e1006167 (2016). IHC-Fr . PubMed: 27415617
  • Meilleur KG  et al. Clinical, pathologic, and mutational spectrum of dystroglycanopathy caused by LARGE mutations. J Neuropathol Exp Neurol 73:425-41 (2014). PubMed: 24709677
  • Rodgers JT  et al. mTORC1 controls the adaptive transition of quiescent stem cells from G0 to G(Alert). Nature 509:393-6 (2014). Mouse . PubMed: 24870234
  • Park R  et al. Aß1-42 reduces P-glycoprotein in the blood-brain barrier through RAGE-NF-?B signaling. Cell Death Dis 5:e1299 (2014). PubMed: 24967961
  • Whitmore C  et al. The transgenic expression of LARGE exacerbates the muscle phenotype of dystroglycanopathy mice. Hum Mol Genet N/A:N/A (2013). Mouse . PubMed: 24234655
  • Aoki Y  et al. Highly efficient in vivo delivery of PMO into regenerating myotubes and rescue in laminin-a2 chain-null congenital muscular dystrophy mice. Hum Mol Genet 22:4914-28 (2013). PubMed: 23882132
  • Serra C  et al. Testosterone Improves the Regeneration of Old and Young Mouse Skeletal Muscle. J Gerontol A Biol Sci Med Sci : (2012). Mouse . PubMed: 22499765
  • Li Z  et al. An HMGA2-IGF2BP2 axis regulates myoblast proliferation and myogenesis. Dev Cell 23:1176-88 (2012). PubMed: 23177649
  • Cui CH  et al. Dystrophin conferral using human endothelium expressing HLA-E in the non-immunosuppressive murine model of Duchenne muscular dystrophy. Hum Mol Genet 20:235-44 (2011). IHC-P ; Human . PubMed: 20947660
  • Ackroyd MR  et al. Fukutin-related protein alters the deposition of laminin in the eye and brain. J Neurosci 31:12927-35 (2011). IHC-Fr . PubMed: 21900571
  • Weihl CC  et al. Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in mice. Hum Mol Genet 16:919-28 (2007). IHC-Fr ; Mouse . PubMed: 17329348
  • Guo LT  et al. Laminin alpha2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant mice. Neuromuscul Disord 13:207-15 (2003). IHC-Fr ; Mouse . PubMed: 12609502
  • Allamand V  et al. Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chain. Hum Mol Genet 6:747-52 (1997). PubMed: 9158149
  • Sewry CA  et al. Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsy. Lancet 347:582-4 (1996). PubMed: 8596321
  • Schuler F & Sorokin LM Expression of laminin isoforms in mouse myogenic cells in vitro and in vivo. J Cell Sci 108 ( Pt 12):3795-805 (1995). PubMed: 8719886
  • Burgeson RE  et al. A new nomenclature for the laminins. Matrix Biol 14:209-11 (1994). PubMed: 7921537


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