Publishing research using ab2182? Please let us know so that we can cite the reference in this datasheet.

ab2182 has been referenced in 16 publications.

  • Samuel W  et al. Appropriately differentiated ARPE-19 cells regain phenotype and gene expression profiles similar to those of native RPE cells. Mol Vis 23:60-89 (2017). WB ; Human . PubMed: 28356702
  • Hazim RA  et al. Differentiation of RPE cells from integration-free iPS cells and their cell biological characterization. Stem Cell Res Ther 8:217 (2017). ICC ; Human . PubMed: 28969679
  • Carter DA  et al. Mislocalisation of BEST1 in iPSC-derived retinal pigment epithelial cells from a family with autosomal dominant vitreoretinochoroidopathy (ADVIRC). Sci Rep 6:33792 (2016). PubMed: 27653836
  • Blenkinsop TA  et al. Human Adult Retinal Pigment Epithelial Stem Cell-Derived RPE Monolayers Exhibit Key Physiological Characteristics of Native Tissue. Invest Ophthalmol Vis Sci 56:7085-99 (2015). PubMed: 26540654
  • Kuo YH  et al. Effects of alternative splicing on the function of bestrophin-1 calcium-activated chloride channels. Biochem J 458:575-83 (2014). PubMed: 24341532
  • Kanemura H  et al. Tumorigenicity studies of induced pluripotent stem cell (iPSC)-derived retinal pigment epithelium (RPE) for the treatment of age-related macular degeneration. PLoS One 9:e85336 (2014). ICC/IF ; Human . PubMed: 24454843
  • Brandl C  et al. In-depth characterisation of Retinal Pigment Epithelium (RPE) cells derived from human induced pluripotent stem cells (hiPSC). Neuromolecular Med 16:551-64 (2014). WB ; Human . PubMed: 24801942
  • Bowens NH  et al. DCPIB, the proposed selective blocker of volume-regulated anion channels, inhibits several glutamate transport pathways in glial cells. Mol Pharmacol 83:22-32 (2013). PubMed: 23012257
  • Guziewicz KE  et al. Molecular consequences of BEST1 gene mutations in canine multifocal retinopathy predict functional implications for human bestrophinopathies. Invest Ophthalmol Vis Sci 52:4497-505 (2011). PubMed: 21498618
  • Milenkovic VM  et al. Disease-associated missense mutations in bestrophin-1 affect cellular trafficking and anion conductance. J Cell Sci 124:2988-96 (2011). WB, ICC/IF ; Human . PubMed: 21878505
  • Neussert R  et al. The presence of bestrophin-1 modulates the Ca2+ recruitment from Ca2+ stores in the ER. Pflugers Arch 460:163-75 (2010). WB . PubMed: 20411394
  • Milenkovic VM  et al. Regulation of the renin expression in the retinal pigment epithelium by systemic stimuli. Am J Physiol Renal Physiol : (2010). ICC/IF ; Pig . PubMed: 20519377
  • Marmorstein LY  et al. Bestrophin interacts physically and functionally with protein phosphatase 2A. J Biol Chem 277:30591-7 (2002). PubMed: 12058047
  • Marmorstein AD  et al. Bestrophin, the product of the Best vitelliform macular dystrophy gene (VMD2), localizes to the basolateral plasma membrane of the retinal pigment epithelium. Proc Natl Acad Sci U S A 97:12758-63 (2000). PubMed: 11050159
  • Caldwell GM  et al. Bestrophin gene mutations in patients with Best vitelliform macular dystrophy. Genomics 58:98-101 (1999). PubMed: 10331951
  • Petrukhin K  et al. Identification of the gene responsible for Best macular dystrophy. Nat Genet 19:241-7 (1998). PubMed: 9662395


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