Levi P. Sowers, Ph.D. - Publications

Affiliations: 
2012 Molecular and Cell Biology University of Iowa, Iowa City, IA 
Area:
Neuroscience Biology, Molecular Biology

11 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Abbott PW, Hardie JB, Walsh KP, Nessler AJ, Farley SJ, Freeman JH, Wemmie JA, Wendt L, Kim YC, Sowers LP, Parker KL. Knockdown of the Non-canonical Wnt Gene Prickle2 Leads to Cerebellar Purkinje Cell Abnormalities While Cerebellar-Mediated Behaviors Remain Intact. Cerebellum (London, England). PMID 38165577 DOI: 10.1007/s12311-023-01648-9  0.337
2015 Taugher RJ, Ghobbeh A, Sowers LP, Fan R, Wemmie JA. ASIC1A in the bed nucleus of the stria terminalis mediates TMT-evoked freezing. Frontiers in Neuroscience. 9: 239. PMID 26257596 DOI: 10.3389/Fnins.2015.00239  0.316
2015 Paemka L, Mahajan VB, Ehaideb SN, Skeie JM, Tan MC, Wu S, Cox AJ, Sowers LP, Gecz J, Jolly L, Ferguson PJ, Darbro B, Schneider A, Scheffer IE, Carvill GL, et al. Seizures are regulated by ubiquitin-specific peptidase 9 X-linked (USP9X), a de-ubiquitinase. Plos Genetics. 11: e1005022. PMID 25763846 DOI: 10.1371/Journal.Pgen.1005022  0.558
2014 Massey CA, Sowers LP, Dlouhy BJ, Richerson GB. Mechanisms of sudden unexpected death in epilepsy: the pathway to prevention. Nature Reviews. Neurology. 10: 271-82. PMID 24752120 DOI: 10.1038/Nrneurol.2014.64  0.342
2014 Sowers LP, Yin T, Mahajan VB, Bassuk AG. Defective motile cilia in Prickle2-deficient mice. Journal of Neurogenetics. 28: 146-52. PMID 24708399 DOI: 10.3109/01677063.2014.885966  0.527
2013 Paemka L, Mahajan VB, Skeie JM, Sowers LP, Ehaideb SN, Gonzalez-Alegre P, Sasaoka T, Tao H, Miyagi A, Ueno N, Takao K, Miyakawa T, Wu S, Darbro BW, Ferguson PJ, et al. PRICKLE1 interaction with SYNAPSIN I reveals a role in autism spectrum disorders. Plos One. 8: e80737. PMID 24312498 DOI: 10.1371/Journal.Pone.0080737  0.589
2013 Sowers LP, Mouw TJ, Ferguson PJ, Wemmie JA, Mohapatra DP, Bassuk AG. The non-canonical Wnt ligand Wnt5a rescues morphological deficits in Prickle2-deficient hippocampal neurons Molecular Psychiatry. 18: 1049. PMID 24056908 DOI: 10.1038/Mp.2013.119  0.477
2013 Sowers LP, Loo L, Wu Y, Campbell E, Ulrich JD, Wu S, Paemka L, Wassink T, Meyer K, Bing X, El-Shanti H, Usachev YM, Ueno N, Manak JR, Manak RJ, et al. Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction. Molecular Psychiatry. 18: 1077-89. PMID 23711981 DOI: 10.1038/Mp.2013.71  0.598
2013 Sowers LP, Massey CA, Gehlbach BK, Granner MA, Richerson GB. Sudden unexpected death in epilepsy: fatal post-ictal respiratory and arousal mechanisms. Respiratory Physiology & Neurobiology. 189: 315-23. PMID 23707877 DOI: 10.1016/J.Resp.2013.05.010  0.343
2013 Sowers LP, Loo L, Wu Y, Campbell E, Ulrich JD, Wu S, Paemka L, Wassink T, Meyer K, Bing X, El-Shanti H, Usachev YM, Ueno N, Manak RJ, Shepherd AJ, et al. Erratum: Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction Molecular Psychiatry. 19: 742-742. DOI: 10.1038/Mp.2013.143  0.556
2011 Tao H, Manak JR, Sowers L, Mei X, Kiyonari H, Abe T, Dahdaleh NS, Yang T, Wu S, Chen S, Fox MH, Gurnett C, Montine T, Bird T, Shaffer LG, et al. Mutations in prickle orthologs cause seizures in flies, mice, and humans. American Journal of Human Genetics. 88: 138-49. PMID 21276947 DOI: 10.1016/J.Ajhg.2010.12.012  0.575
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