 Connection
Emily Bates to Mutation
This is a "connection" page, showing publications Emily Bates has written about Mutation.
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Connection Strength |
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0.351 |
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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 03; 77(3-4):40-54.
Score: 0.081
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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 04 15; 28(8):1227-1243.
Score: 0.078
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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 12 01; 444 Suppl 1:S297-S307.
Score: 0.073
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Gartz Hanson M, Aiken J, Sietsema DV, Sept D, Bates EA, Niswander L, Moore JK. Novel a-tubulin mutation disrupts neural development and tubulin proteostasis. Dev Biol. 2016 Jan 15; 409(2):406-19.
Score: 0.062
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Brennan KC, Bates EA, Shapiro RE, Zyuzin J, Hallows WC, Huang Y, Lee HY, Jones CR, Fu YH, Charles AC, Pt?cek LJ. Casein kinase id mutations in familial migraine and advanced sleep phase. Sci Transl Med. 2013 May 01; 5(183):183ra56, 1-11.
Score: 0.052
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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.
Score: 0.005
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Connection Strength
The connection strength for concepts is the sum of the scores for each matching publication.
Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
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