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Life Technologies Parkinson’s disease cell models—part 3

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31 Life Technologies ™ | lifetechnologies.com/parkinsons References 1. Olanow CW, Stern MB, Sethi K (2009) The scientific and clinical basis for the treatment of Parkinson disease. Neurology 72(21 Suppl 4):S1–S136. 2. Hockemeyer D, Wang H, Kiani S et al. (2011) Genetic engineering of human pluripotent cells using TALE nucleases. Nat Biotech 29(8):731–734. 3. Burn DJ, Jaros E (2001) Multiple system atrophy: cellular and molecular pathology. Mol Pathol 54(6):419–426. 4. Zhao J, Hermanson SB, Carlson CB et al. (2012) Pharmacological inhibition of LRRK2 cellular phosphorylation sites provides insight into LRRK2 biology. Biochem Soc Trans 40(5):1158–1162. 5. Murphy KE, Gysbers AM, Abbott SK et al. (2014) Reduced glucocerebrosidase is associated with increased α-synuclein in sporadic Parkinson's disease. Brain 137(Pt 3):834–848. 6. Thorvaldsdottir H, Robinson JT, Mesirov, JP (2012) Integrative Genomics Viewer (IGV): high- performance genomics data visualization and exploration. Brief Bioinform 14(2):178–192. 7. Ding Q, Regan SN, Xia Y et al. (2013) Enhanced efficiency of human pluripotent stem cell genome editing through replacing TALENs with CRISPRs. Cell Stem Cell 12(4):393–394.

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