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Noonan Syndrome-Associated SHP2 Dephosphorylates GluN2B to Regulate NMDA Receptor Function.
Cell Rep. 2018 Aug 7;24(6):1523-1535. doi: 10.1016/j.celrep.2018.07.006.
Cell Rep. 2018.
PMID: 30089263
Free PMC article.
Trio Haploinsufficiency Causes Neurodevelopmental Disease-Associated Deficits.
Katrancha SM, Shaw JE, Zhao AY, Myers SA, Cocco AR, Jeng AT, Zhu M, Pittenger C, Greer CA, Carr SA, Xiao X, Koleske AJ.
Katrancha SM, et al.
Cell Rep. 2019 Mar 5;26(10):2805-2817.e9. doi: 10.1016/j.celrep.2019.02.022.
Cell Rep. 2019.
PMID: 30840899
Free PMC article.
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SNARE Complex Dysfunction: A Unifying Hypothesis for Schizophrenia.
Katrancha SM, Koleske AJ.
Katrancha SM, et al.
Biol Psychiatry. 2015 Sep 15;78(6):356-8. doi: 10.1016/j.biopsych.2015.07.013.
Biol Psychiatry. 2015.
PMID: 26296424
Free PMC article.
No abstract available.
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Neurodevelopmental disease-associated de novo mutations and rare sequence variants affect TRIO GDP/GTP exchange factor activity.
Katrancha SM, Wu Y, Zhu M, Eipper BA, Koleske AJ, Mains RE.
Katrancha SM, et al.
Hum Mol Genet. 2017 Dec 1;26(23):4728-4740. doi: 10.1093/hmg/ddx355.
Hum Mol Genet. 2017.
PMID: 28973398
Free PMC article.
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