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Discovery of XL01126: A Potent, Fast, Cooperative, Selective, Orally Bioavailable, and Blood-Brain Barrier Penetrant PROTAC Degrader of Leucine-Rich Repeat Kinase 2.
J Am Chem Soc. 2022 Sep 21;144(37):16930-16952. doi: 10.1021/jacs.2c05499. Epub 2022 Aug 25.
J Am Chem Soc. 2022.
PMID: 36007011
Free PMC article.
Impact of 100 LRRK2 variants linked to Parkinson's disease on kinase activity and microtubule binding.
Kalogeropulou AF, Purlyte E, Tonelli F, Lange SM, Wightman M, Prescott AR, Padmanabhan S, Sammler E, Alessi DR.
Kalogeropulou AF, et al.
Biochem J. 2022 Sep 16;479(17):1759-1783. doi: 10.1042/BCJ20220161.
Biochem J. 2022.
PMID: 35950872
Free PMC article.
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Endogenous Rab29 does not impact basal or stimulated LRRK2 pathway activity.
Kalogeropulou AF, Freemantle JB, Lis P, Vides EG, Polinski NK, Alessi DR.
Kalogeropulou AF, et al.
Biochem J. 2020 Nov 27;477(22):4397-4423. doi: 10.1042/BCJ20200458.
Biochem J. 2020.
PMID: 33135724
Free PMC article.
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P62/SQSTM1 is a novel leucine-rich repeat kinase 2 (LRRK2) substrate that enhances neuronal toxicity.
Kalogeropulou AF, Zhao J, Bolliger MF, Memou A, Narasimha S, Molitor TP, Wilson WH, Rideout HJ, Nichols RJ.
Kalogeropulou AF, et al.
Biochem J. 2018 Apr 9;475(7):1271-1293. doi: 10.1042/BCJ20170699.
Biochem J. 2018.
PMID: 29519959
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