Matthew C. Judson, Ph.D. - Publications

Affiliations: 
2010 Vanderbilt University, Nashville, TN 
Area:
Neurobiology Biology, Human Development, Evolution and Development Biology

10 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, 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
2016 Judson MC, Wallace ML, Sidorov MS, Burette AC, Gu B, van Woerden GM, King IF, Han JE, Zylka MJ, Elgersma Y, Weinberg RJ, Philpot BD. GABAergic Neuron-Specific Loss of Ube3a Causes Angelman Syndrome-Like EEG Abnormalities and Enhances Seizure Susceptibility. Neuron. PMID 27021170 DOI: 10.1016/j.neuron.2016.02.040  0.68
2016 Berrios J, Stamatakis AM, Kantak PA, McElligott ZA, Judson MC, Aita M, Rougie M, Stuber GD, Philpot BD. Loss of UBE3A from TH-expressing neurons suppresses GABA co-release and enhances VTA-NAc optical self-stimulation. Nature Communications. 7: 10702. PMID 26869263 DOI: 10.1038/ncomms10702  0.68
2015 Bruinsma CF, Schonewille M, Gao Z, Aronica EM, Judson MC, Philpot BD, Hoebeek FE, van Woerden GM, De Zeeuw CI, Elgersma Y. Dissociation of locomotor and cerebellar deficits in a murine Angelman syndrome model. The Journal of Clinical Investigation. 125: 4305-15. PMID 26485287 DOI: 10.1172/JCI83541  0.68
2014 Judson MC, Sosa-Pagan JO, Del Cid WA, Han JE, Philpot BD. Allelic specificity of Ube3a expression in the mouse brain during postnatal development. The Journal of Comparative Neurology. 522: 1874-96. PMID 24254964 DOI: 10.1002/cne.23507  0.68
2011 Mabb AM, Judson MC, Zylka MJ, Philpot BD. Angelman syndrome: insights into genomic imprinting and neurodevelopmental phenotypes. Trends in Neurosciences. 34: 293-303. PMID 21592595 DOI: 10.1016/j.tins.2011.04.001  0.68
2011 Judson MC, Eagleson KL, Levitt P. A new synaptic player leading to autism risk: Met receptor tyrosine kinase. Journal of Neurodevelopmental Disorders. 3: 282-92. PMID 21509596 DOI: 10.1007/s11689-011-9081-8  0.96
2011 Judson MC, Amaral DG, Levitt P. Conserved subcortical and divergent cortical expression of proteins encoded by orthologs of the autism risk gene MET. Cerebral Cortex (New York, N.Y. : 1991). 21: 1613-26. PMID 21127014 DOI: 10.1093/cercor/bhq223  0.68
2011 Judson MC, Eagleson KL, Levitt P. A new synaptic player leading to autism risk: Met receptor tyrosine kinase Journal of Neurodevelopmental Disorders. 3: 282-292. DOI: 10.1007/s11689-011-9081-8  0.68
2010 Judson MC, Eagleson KL, Wang L, Levitt P. Evidence of cell-nonautonomous changes in dendrite and dendritic spine morphology in the met-signaling-deficient mouse forebrain. The Journal of Comparative Neurology. 518: 4463-78. PMID 20853516 DOI: 10.1002/cne.22467  0.68
2009 Judson MC, Bergman MY, Campbell DB, Eagleson KL, Levitt P. Dynamic gene and protein expression patterns of the autism-associated met receptor tyrosine kinase in the developing mouse forebrain. The Journal of Comparative Neurology. 513: 511-31. PMID 19226509 DOI: 10.1002/cne.21969  0.68
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