ab11425 を使用した論文を発表された方は、こちらまでお知らせください。データシートに掲載させていただきます。

ab11425 は 19 報の論文で使用されています。

  • Hakim CH  et al. A Five-Repeat Micro-Dystrophin Gene Ameliorated Dystrophic Phenotype in the Severe DBA/2J-mdx Model of Duchenne Muscular Dystrophy. Mol Ther Methods Clin Dev 6:216-230 (2017). PubMed: 28932757
  • Kountz TS  et al. Endogenous N-terminal Domain Cleavage Modulates a1D-Adrenergic Receptor Pharmacodynamics. J Biol Chem 291:18210-21 (2016). PubMed: 27382054
  • Barnabei MS  et al. Severe dystrophic cardiomyopathy caused by the enteroviral protease 2A-mediated C-terminal dystrophin cleavage fragment. Sci Transl Med 7:294ra106 (2015). PubMed: 26136477
  • Lundby A  et al. Annotation of loci from genome-wide association studies using tissue-specific quantitative interaction proteomics. Nat Methods 11:868-74 (2014). PubMed: 24952909
  • Tanabe Y  et al. Synaptic adhesion molecules in Cadm family at the neuromuscular junction. Cell Biol Int 37:731-6 (2013). Mouse . PubMed: 23505055
  • Shin JH  et al. Microdystrophin ameliorates muscular dystrophy in the canine model of duchenne muscular dystrophy. Mol Ther 21:750-7 (2013). PubMed: 23319056
  • D'Arcy CE  et al. Identification of FHL1 as a therapeutic target for Duchenne muscular dystrophy. Hum Mol Genet N/A:N/A (2013). PubMed: 24087791
  • Kraner SD  et al. Altered sodium channel-protein associations in critical illness myopathy. Skelet Muscle 2:17 (2012). WB . PubMed: 22935229
  • Johnson EK  et al. Proteomic analysis reveals new cardiac-specific dystrophin-associated proteins. PLoS One 7:e43515 (2012). PubMed: 22937058
  • Gentil C  et al. Variable phenotype of del45-55 Becker patients correlated with nNOSµ mislocalization and RYR1 hypernitrosylation. Hum Mol Genet 21:3449-60 (2012). Human . PubMed: 22589245
  • Smith BF  et al. An intronic LINE-1 element insertion in the dystrophin gene aborts dystrophin expression and results in Duchenne-like muscular dystrophy in the corgi breed. Lab Invest 91:216-31 (2011). IF, IHC ; Dog . PubMed: 20714321
  • Li D  et al. Sarcolemmal nNOS anchoring reveals a qualitative difference between dystrophin and utrophin. J Cell Sci 123:2008-13 (2010). WB ; Mouse . PubMed: 20483958
  • Li D  et al. Sub-physiological sarcoglycan expression contributes to compensatory muscle protection in mdx mice. Hum Mol Genet 18:1209-20 (2009). PubMed: 19131360
  • Sene A  et al. Functional implication of Dp71 in osmoregulation and vascular permeability of the retina. PLoS One 4:e7329 (2009). WB ; Mouse . PubMed: 19809515
  • Bostick B  et al. Prevention of dystrophin-deficient cardiomyopathy in twenty-one-month-old carrier mice by mosaic dystrophin expression or complementary dystrophin/utrophin expression. Circ Res 102:121-30 (2008). PubMed: 17967782
  • Li D  et al. Preservation of muscle force in Mdx3cv mice correlates with low-level expression of a near full-length dystrophin protein. Am J Pathol 172:1332-41 (2008). IHC-Fr ; Mouse . PubMed: 18385524
  • Yue Y  et al. C-terminal-truncated microdystrophin recruits dystrobrevin and syntrophin to the dystrophin-associated glycoprotein complex and reduces muscular dystrophy in symptomatic utrophin/dystrophin double-knockout mice. Mol Ther 14:79-87 (2006). PubMed: 16563874
  • Lai Y  et al. Efficient in vivo gene expression by trans-splicing adeno-associated viral vectors. Nat Biotechnol 23:1435-9 (2005). PubMed: 16244658
  • Camp ND  et al. Individual protomers of a G protein-coupled receptor dimer integrate distinct functional modules. Cell Discov 1:N/A (0). PubMed: 26617989