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Adaptor protein complex 4 deficiency: a paradigm of childhood-onset hereditary spastic paraplegia caused by defective protein trafficking.
Behne R, Teinert J, Wimmer M, D'Amore A, Davies AK, Scarrott JM, Eberhardt K, Brechmann B, Chen IP, Buttermore ED, Barrett L, Dwyer S, Chen T, Hirst J, Wiesener A, Segal D, Martinuzzi A, Duarte ST, Bennett JT, Bourinaris T, Houlden H, Roubertie A, Santorelli FM, Robinson M, Azzouz M, Lipton JO, Borner GHH, Sahin M, Ebrahimi-Fakhari D. Behne R, et al. Among authors: lipton jo. Hum Mol Genet. 2020 Jan 15;29(2):320-334. doi: 10.1093/hmg/ddz310. Hum Mol Genet. 2020. PMID: 31915823 Free PMC article.
The neurology of mTOR.
Lipton JO, Sahin M. Lipton JO, et al. Neuron. 2014 Oct 22;84(2):275-91. doi: 10.1016/j.neuron.2014.09.034. Epub 2014 Oct 22. Neuron. 2014. PMID: 25374355 Free PMC article. Review.
Impaired Mitochondrial Dynamics And Mitophagy In Neuronal Models Of Tuberous Sclerosis Complex.
Ebrahimi-Fakhari D, Saffari A, Wahlster L, DiNardo A, Turner D, Lewis TL Jr, Conrad C, Rothberg JM, Lipton JO, Kölker S, Hoffmann GF, Han MJ, Polleux F, Sahin M. Ebrahimi-Fakhari D, et al. Among authors: lipton jo. Cell Rep. 2016 Nov 15;17(8):2162. doi: 10.1016/j.celrep.2016.10.051. Cell Rep. 2016. PMID: 27851977 Free article. No abstract available.
mGluR5 Modulation of Behavioral and Epileptic Phenotypes in a Mouse Model of Tuberous Sclerosis Complex.
Kelly E, Schaeffer SM, Dhamne SC, Lipton JO, Lindemann L, Honer M, Jaeschke G, Super CE, Lammers SH, Modi ME, Silverman JL, Dreier JR, Kwiatkowski DJ, Rotenberg A, Sahin M. Kelly E, et al. Among authors: lipton jo. Neuropsychopharmacology. 2018 May;43(6):1457-1465. doi: 10.1038/npp.2017.295. Epub 2017 Dec 5. Neuropsychopharmacology. 2018. PMID: 29206810 Free PMC article.
Insomnia of childhood.
Lipton J, Becker RE, Kothare SV. Lipton J, et al. Curr Opin Pediatr. 2008 Dec;20(6):641-9. doi: 10.1097/MOP.0b013e32831897cb. Curr Opin Pediatr. 2008. PMID: 19005332 Review.
21 results