Publishing research using ab58552? Please let us know so that we can cite the reference in this datasheet.

ab58552 has been referenced in 11 publications.

  • Hu LR  et al. Deregulated Ca(2+) cycling underlies the development of arrhythmia and heart disease due to mutant obscurin. Sci Adv 3:e1603081 (2017). WB, IF ; Mouse . PubMed: 28630914
  • Georgiou DK  et al. Ca2+ Binding/Permeation via Calcium Channel, CaV1.1, Regulates the Intracellular Distribution of the Fatty Acid Transport Protein, CD36, and Fatty Acid Metabolism. J Biol Chem 290:23751-65 (2015). PubMed: 26245899
  • Shelton GD  et al. X-linked myotubular myopathy in Rottweiler dogs is caused by a missense mutation in Exon 11 of the MTM1 gene. Skelet Muscle 5:1 (2015). PubMed: 25664165
  • Smith LL  et al. Bridging integrator 1 (Bin1) deficiency in zebrafish results in centronuclear myopathy. Hum Mol Genet N/A:N/A (2014). PubMed: 24549043
  • Besser J  et al. MiRNA-1/133a clusters regulate adrenergic control of cardiac repolarization. PLoS One 9:e113449 (2014). WB ; Mouse . PubMed: 25415383
  • Leiria LO  et al. Role of PKC and CaV1.2 in detrusor overactivity in a model of obesity associated with insulin resistance in mice. PLoS One 7:e48507 (2012). WB ; Mouse . PubMed: 23144896
  • Gezen-Ak D  et al. The Effects of Vitamin D Receptor Silencing on the Expression of LVSCC-A1C and LVSCC-A1D and the Release of NGF in Cortical Neurons. PLoS One 6:e17553 (2011). WB ; Rat . PubMed: 21408608
  • Dursun E  et al. A novel perspective for Alzheimer's disease: vitamin D receptor suppression by amyloid-ß and preventing the amyloid-ß induced alterations by vitamin D in cortical neurons. J Alzheimers Dis 23:207-19 (2011). WB ; Rat . PubMed: 20966550
  • Hu ST  et al. Protective effect of oxymatrine on chronic rat heart failure. J Physiol Sci 61:363-72 (2011). WB ; Rat . PubMed: 21691940
  • Beggs AH  et al. MTM1 mutation associated with X-linked myotubular myopathy in Labrador Retrievers. Proc Natl Acad Sci U S A 107:14697-14702 (2010). ICC/IF ; Dog . PubMed: 20682747
  • Durieux AC  et al. A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice. Hum Mol Genet 19:4820-36 (2010). PubMed: 20858595

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