John P. Svaren
Affiliations: | University of Wisconsin, Madison, Madison, WI |
Area:
Molecular Biology, Neuroscience BiologyGoogle:
"John Svaren"Mean distance: 17811
Children
Sign in to add traineeScott E. LeBlanc | grad student | 2007 | UW Madison |
Gennifer M. Mager | grad student | 2007 | UW Madison |
Sung-Wook Jang | grad student | 2008 | UW Madison |
Nolan G. Gokey | grad student | 2012 | UW Madison |
Holly A. Hung | grad student | 2014 | UW Madison |
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Publications
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Khullar S, Huang X, Ramesh R, et al. (2023) NetREm: Network Regression Embeddings reveal cell-type transcription factor coordination for gene regulation. Biorxiv : the Preprint Server For Biology |
Pipis M, Won S, Poh R, et al. (2023) Post-transcriptional microRNA repression of PMP22 dose in severe Charcot-Marie-Tooth disease type 1. Brain : a Journal of Neurology |
Duong P, Ramesh R, Schneider A, et al. (2023) Modulation of Schwann cell homeostasis by the BAP1 deubiquitinase. Glia |
Veneri FA, Prada V, Mastrangelo R, et al. (2022) A novel mouse model of CMT1B identifies hyperglycosylation as a new pathogenetic mechanism. Human Molecular Genetics |
Ramesh R, Manurung Y, Ma KH, et al. (2022) JUN Regulation of Injury-induced Enhancers in Schwann Cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience |
Park HJ, Tsai E, Huang D, et al. (2022) ACTL6a coordinates axonal caliber recognition and myelination in the peripheral nerve. Iscience. 25: 104132 |
Martinez NJ, Braisted JC, Dranchak PK, et al. (2021) Genome-Edited Coincidence and PMP22-HiBiT Fusion Reporter Cell Lines Enable an Artifact-Suppressive Quantitative High-Throughput Screening Strategy for Gene-Dosage Disorder Drug Discovery. Acs Pharmacology & Translational Science. 4: 1422-1436 |
Duong P, Ma KH, Ramesh R, et al. (2021) H3K27 demethylases are dispensable for activation of Polycomb-regulated injury response genes in peripheral nerve. The Journal of Biological Chemistry. 100852 |
Wagstaff LJ, Gomez-Sanchez JA, Fazal SV, et al. (2021) Failures of nerve regeneration caused by aging or chronic denervation are rescued by restoring Schwann cell c-Jun. Elife. 10 |
Lupo V, Won S, Frasquet M, et al. (2020) Bi-allelic mutations in EGR2 cause autosomal recessive demyelinating neuropathy by disrupting the EGR2-NAB complex. European Journal of Neurology |