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Genome-Edited Cell Lines for High-Throughput Screening.
Dranchak P, Moran JJ, MacArthur R, Lopez-Anido C, Inglese J, Svaren J. Dranchak P, et al. Among authors: svaren j. Methods Mol Biol. 2018;1755:1-17. doi: 10.1007/978-1-4939-7724-6_1. Methods Mol Biol. 2018. PMID: 29671259 Free PMC article.
Genome-Edited Coincidence and PMP22-HiBiT Fusion Reporter Cell Lines Enable an Artifact-Suppressive Quantitative High-Throughput Screening Strategy for PMP22 Gene-Dosage Disorder Drug Discovery.
Martinez NJ, Braisted JC, Dranchak PK, Moran JJ, Larson H, Queme B, Pak E, Dutra A, Rai G, Cheng KC, Svaren J, Inglese J. Martinez NJ, et al. Among authors: svaren j. ACS Pharmacol Transl Sci. 2021 Jun 10;4(4):1422-1436. doi: 10.1021/acsptsci.1c00110. eCollection 2021 Aug 13. ACS Pharmacol Transl Sci. 2021. PMID: 34423274 Free PMC article.
Neuregulin 1 type III improves peripheral nerve myelination in a mouse model of congenital hypomyelinating neuropathy.
Belin S, Ornaghi F, Shackleford G, Wang J, Scapin C, Lopez-Anido C, Silvestri N, Robertson N, Williamson C, Ishii A, Taveggia C, Svaren J, Bansal R, Schwab MH, Nave K, Fratta P, D'Antonio M, Poitelon Y, Feltri ML, Wrabetz L. Belin S, et al. Among authors: svaren j. Hum Mol Genet. 2019 Apr 15;28(8):1260-1273. doi: 10.1093/hmg/ddy420. Hum Mol Genet. 2019. PMID: 30535360 Free PMC article.
Variation in SIPA1L2 is correlated with phenotype modification in Charcot- Marie- Tooth disease type 1A.
Tao F, Beecham GW, Rebelo AP, Svaren J, Blanton SH, Moran JJ, Lopez-Anido C, Morrow JM, Abreu L, Rizzo D, Kirk CA, Wu X, Feely S, Verhamme C, Saporta MA, Herrmann DN, Day JW, Sumner CJ, Lloyd TE, Li J, Yum SW, Taroni F, Baas F, Choi BO, Pareyson D, Scherer SS, Reilly MM, Shy ME, Züchner S; Inherited Neuropathy Consortium. Tao F, et al. Among authors: svaren j. Ann Neurol. 2019 Mar;85(3):316-330. doi: 10.1002/ana.25426. Ann Neurol. 2019. PMID: 30706531 Free PMC article.
Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.
Tao F, Beecham GW, Rebelo AP, Blanton SH, Moran JJ, Lopez-Anido C, Svaren J, Abreu L, Rizzo D, Kirk CA, Wu X, Feely S, Verhamme C, Saporta MA, Herrmann DN, Day JW, Sumner CJ, Lloyd TE, Li J, Yum SW, Taroni F, Baas F, Choi BO, Pareyson D, Scherer SS, Reilly MM, Shy ME, Züchner S; Inherited Neuropathy Consortium. Tao F, et al. Among authors: svaren j. J Neuromuscul Dis. 2019;6(2):201-211. doi: 10.3233/JND-190377. J Neuromuscul Dis. 2019. PMID: 30958311 Free PMC article.
Regulation of the PMP22 gene through an intronic enhancer.
Jones EA, Lopez-Anido C, Srinivasan R, Krueger C, Chang LW, Nagarajan R, Svaren J. Jones EA, et al. Among authors: svaren j. J Neurosci. 2011 Mar 16;31(11):4242-50. doi: 10.1523/JNEUROSCI.5893-10.2011. J Neurosci. 2011. PMID: 21411665 Free PMC article.
131 results