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Simin K, Bates EA, Horner MA, Letsou A. Genetic analysis of punt, a type II Dpp receptor that functions throughout the Drosophila melanogaster life cycle. Genetics. 1998 Feb;148(2):801-13. doi: 10.1093/genetics/148.2.801. PubMed PMID: 9504926; PubMed Central PMCID: PMC1459835.

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Faber PW, Voisine C, King DC, Bates EA, Hart AC. Glutamine/proline-rich PQE-1 proteins protect Caenorhabditis elegans neurons from huntingtin polyglutamine neurotoxicity. Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):17131-6. doi: 10.1073/pnas.262544899. Epub 2002 Dec 16. PubMed PMID: 12486229; PubMed Central PMCID: PMC139281.

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Bates EA, Victor M, Jones AK, Shi Y, Hart AC. Differential contributions of Caenorhabditis elegans histone deacetylases to huntingtin polyglutamine toxicity. J Neurosci. 2006 Mar 8;26(10):2830-8. doi: 10.1523/JNEUROSCI.3344-05.2006. PubMed PMID: 16525063; PubMed Central PMCID: PMC6675170.

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Voisine C, Varma H, Walker N, Bates EA, Stockwell BR, Hart AC. Identification of potential therapeutic drugs for huntington's disease using Caenorhabditis elegans. PLoS One. 2007 Jun 6;2(6):e504. doi: 10.1371/journal.pone.0000504. PubMed PMID: 17551584; PubMed Central PMCID: PMC1876812.

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Bates EA, Nikai T, Brennan KC, Fu YH, Charles AC, Basbaum AI, Ptácek LJ, Ahn AH. Sumatriptan alleviates nitroglycerin-induced mechanical and thermal allodynia in mice. Cephalalgia. 2010 Feb;30(2):170-8. doi: 10.1111/j.1468-2982.2009.01864.x. PubMed PMID: 19489890; PubMed Central PMCID: PMC4854191.

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Dahal GR, Rawson J, Gassaway B, Kwok B, Tong Y, Ptácek LJ, Bates E. An inwardly rectifying K+ channel is required for patterning. Development. 2012 Oct;139(19):3653-64. doi: 10.1242/dev.078592. PubMed PMID: 22949619; PubMed Central PMCID: PMC3436115.

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Brennan KC, Bates EA, Shapiro RE, Zyuzin J, Hallows WC, Huang Y, Lee HY, Jones CR, Fu YH, Charles AC, Ptáček LJ. Casein kinase iδ mutations in familial migraine and advanced sleep phase. Sci Transl Med. 2013 May 1;5(183):183ra56, 1-11. doi: 10.1126/scitranslmed.3005784. PubMed PMID: 23636092; PubMed Central PMCID: PMC4220792.

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Bates EA. A potential molecular target for morphological defects of fetal alcohol syndrome: Kir2.1. Curr Opin Genet Dev. 2013 Jun;23(3):324-9. doi: 10.1016/j.gde.2013.05.001. Epub 2013 Jun 4. Review. PubMed PMID: 23756044.

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Bates E. Ion channels in development and cancer. Annu Rev Cell Dev Biol. 2015;31:231-47. doi: 10.1146/annurev-cellbio-100814-125338. Review. PubMed PMID: 26566112.

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Gartz Hanson M, Aiken J, Sietsema DV, Sept D, Bates EA, Niswander L, Moore JK. Novel α-tubulin mutation disrupts neural development and tubulin proteostasis. Dev Biol. 2016 Jan 15;409(2):406-19. doi: 10.1016/j.ydbio.2015.11.022. Epub 2015 Nov 30. PubMed PMID: 26658218; PubMed Central PMCID: PMC4724489.

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Kaufmann D, Bates EA, Yagen B, Bialer M, Saunders GH, Wilcox K, White HS, Brennan KC. sec-Butylpropylacetamide (SPD) has antimigraine properties. Cephalalgia. 2016 Sep;36(10):924-35. doi: 10.1177/0333102415612773. Epub 2015 Nov 13. PubMed PMID: 26568161; PubMed Central PMCID: PMC4887413.

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Dahal GR, Pradhan SJ, Bates EA. Inwardly rectifying potassium channels influence Drosophila wing morphogenesis by regulating Dpp release. Development. 2017 Aug 1;144(15):2771-2783. doi: 10.1242/dev.146647. Epub 2017 Jul 6. PubMed PMID: 28684627; PubMed Central PMCID: PMC5560040.

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Aiken J, Buscaglia G, Bates EA, Moore JK. The α-Tubulin gene TUBA1A in Brain Development: A Key Ingredient in the Neuronal Isotype Blend. J Dev Biol. 2017 Sep;5(3). doi: 10.3390/jdb5030008. Epub 2017 Sep 19. PubMed PMID: 29057214; PubMed Central PMCID: PMC5648057.

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Belus MT, Rogers MA, Elzubeir A, Josey M, Rose S, Andreeva V, Yelick PC, Bates EA. Kir2.1 is important for efficient BMP signaling in mammalian face development. Dev Biol. 2018 Dec 1;444 Suppl 1:S297-S307. doi: 10.1016/j.ydbio.2018.02.012. Epub 2018 Mar 20. PubMed PMID: 29571612; PubMed Central PMCID: PMC6148416.

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George LF, Pradhan SJ, Mitchell D, Josey M, Casey J, Belus MT, Fedder KN, Dahal GR, Bates EA. Ion Channel Contributions to Wing Development in Drosophila melanogaster. G3 (Bethesda). 2019 Apr 9;9(4):999-1008. doi: 10.1534/g3.119.400028. PubMed PMID: 30733380; PubMed Central PMCID: PMC6469425.

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Aiken J, Moore JK, Bates EA. TUBA1A mutations identified in lissencephaly patients dominantly disrupt neuronal migration and impair dynein activity. Hum Mol Genet. 2019 Apr 15;28(8):1227-1243. doi: 10.1093/hmg/ddy416. PubMed PMID: 30517687; PubMed Central PMCID: PMC6452179.

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George LF, Bates EA. Imaging Dpp Release from a Drosophila Wing Disc. J Vis Exp. 2019 Oct 30;(152). doi: 10.3791/60528. PubMed PMID: 31736481.

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Aiken J, Buscaglia G, Aiken AS, Moore JK, Bates EA. Tubulin mutations in brain development disorders: Why haploinsufficiency does not explain TUBA1A tubulinopathies. Cytoskeleton (Hoboken). 2020 Mar;77(3-4):40-54. doi: 10.1002/cm.21567. Epub 2019 Oct 31. PubMed PMID: 31574570.

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Buscaglia G, Northington KR, Moore JK, Bates EA. Reduced TUBA1A Tubulin Causes Defects in Trafficking and Impaired Adult Motor Behavior. eNeuro. 2020 Mar/Apr;7(2). doi: 10.1523/ENEURO.0045-20.2020. Print 2020 Mar/Apr. PubMed PMID: 32184299; PubMed Central PMCID: PMC7218002.

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Ozekin YH, Isner T, Bates EA. Ion Channel Contributions to Morphological Development: Insights From the Role of Kir2.1 in Bone Development. Front Mol Neurosci. 2020;13:99. doi: 10.3389/fnmol.2020.00099. eCollection 2020. Review. PubMed PMID: 32581710; PubMed Central PMCID: PMC7296152.

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