Tomoya Kubota - Publications

University of Chicago, Chicago, IL 

8/23 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
2020 Du X, Carvalho-de-Souza JL, Wei C, Carrasquel-Ursulaez W, Lorenzo Y, Gonzalez N, Kubota T, Staisch J, Hain T, Petrossian N, Xu M, Latorre R, Bezanilla F, Gomez CM. Loss-of-function BK channel mutation causes impaired mitochondria and progressive cerebellar ataxia. Proceedings of the National Academy of Sciences of the United States of America. PMID 32132200 DOI: 10.1073/pnas.1920008117  0.4
2017 Kubota T, Dang B, Carvalho-de-Souza JL, Correa AM, Bezanilla F. Nav channel binder containing a specific conjugation-site based on a low toxicity β-scorpion toxin. Scientific Reports. 7: 16329. PMID 29180755 DOI: 10.1038/s41598-017-16426-x  0.4
2017 Kubota T, Correa AM, Bezanilla F. Mechanism of functional interaction between potassium channel Kv1.3 and sodium channel NavBeta1 subunit. Scientific Reports. 7: 45310. PMID 28349975 DOI: 10.1038/srep45310  0.4
2017 Kubota T, Durek T, Dang B, Finol-Urdaneta RK, Craik DJ, Kent SB, French RJ, Bezanilla F, Correa AM. Mapping of voltage sensor positions in resting and inactivated mammalian sodium channels by LRET. Proceedings of the National Academy of Sciences of the United States of America. PMID 28202723 DOI: 10.1073/pnas.1700453114  0.4
2017 Dang B, Shen R, Kubota T, Mandal K, Bezanilla F, Roux B, Kent SB. Inversion of the Side-Chain Stereochemistry of Indvidual Thr or Ile Residues in a Protein Molecule: Impact on the Folding, Stability, and Structure of the ShK Toxin. Angewandte Chemie (International Ed. in English). PMID 28194851 DOI: 10.1002/anie.201612398  0.4
2016 Dang B, Kubota T, Mandal K, Correa AM, Bezanilla F, Kent SB. Elucidation of the Covalent and Tertiary Structures of Biologically Active Ts3 Toxin. Angewandte Chemie (International Ed. in English). PMID 27244051 DOI: 10.1002/anie.201603420  0.4
2014 Dang B, Kubota T, Correa AM, Bezanilla F, Kent SB. Total chemical synthesis of biologically active fluorescent dye-labeled Ts1 toxin. Angewandte Chemie (International Ed. in English). 53: 8970-4. PMID 24989851 DOI: 10.1002/anie.201404438  0.4
2013 Dang B, Kubota T, Mandal K, Bezanilla F, Kent SB. Native chemical ligation at Asx-Cys, Glx-Cys: chemical synthesis and high-resolution X-ray structure of ShK toxin by racemic protein crystallography. Journal of the American Chemical Society. 135: 11911-9. PMID 23919482 DOI: 10.1021/ja4046795  0.4
Low-probability matches
2016 Kato H, Kokunai Y, Dalle C, Kubota T, Madokoro Y, Yuasa H, Uchida Y, Ikeda T, Mochizuki H, Nicole S, Fontaine B, Takahashi MP, Mitake S. A case of non-dystrophic myotonia with concomitant mutations in the SCN4A and CLCN1 genes. Journal of the Neurological Sciences. 369: 254-8. PMID 27653901 DOI: 10.1016/j.jns.2016.08.030  0.28
2012 Kokunai Y, Goto K, Kubota T, Fukuoka T, Sakoda S, Ibi T, Doyu M, Mochizuki H, Sahashi K, Takahashi MP. A sodium channel myotonia due to a novel SCN4A mutation accompanied by acquired autoimmune myasthenia gravis. Neuroscience Letters. 519: 67-72. PMID 22617007 DOI: 10.1016/j.neulet.2012.05.023  0.28
2012 Yoshinaga H, Sakoda S, Good JM, Takahashi MP, Kubota T, Arikawa-Hirasawa E, Nakata T, Ohno K, Kitamura T, Kobayashi K, Ohtsuka Y. A novel mutation in SCN4A causes severe myotonia and school-age-onset paralytic episodes. Journal of the Neurological Sciences. 315: 15-9. PMID 22257501 DOI: 10.1016/j.jns.2011.12.015  0.28
2011 Matsumura T, Kimura T, Kokunai Y, Kubota T, Takahashi MP, Sakoda S. [A survey of cardiologists, diabetologists, gynecologists and ophthalmologists practicing in Osaka on the medical consultation behaviors of myotonic dystrophy patients]. Rinshō Shinkeigaku = Clinical Neurology. 51: 677-82. PMID 21946424 DOI: JST.JSTAGE/clinicalneurol/51.677  0.28
2011 Kubota T, Roca X, Kimura T, Kokunai Y, Nishino I, Sakoda S, Krainer AR, Takahashi MP. A mutation in a rare type of intron in a sodium-channel gene results in aberrant splicing and causes myotonia. Human Mutation. 32: 773-82. PMID 21412952 DOI: 10.1002/humu.21501  0.28
2009 Kubota T, Kinoshita M, Sasaki R, Aoike F, Takahashi MP, Sakoda S, Hirose K. New mutation of the Na channel in the severe form of potassium-aggravated myotonia. Muscle & Nerve. 39: 666-73. PMID 19347921 DOI: 10.1002/mus.21155  0.28
2020 Nakaza M, Kitamura Y, Furuta M, Kubota T, Sasaki R, Takahashi MP. Analysis of the genetic background associated with sporadic periodic paralysis in Japanese patients. Journal of the Neurological Sciences. 116795. PMID 32234253 DOI: 10.1016/j.jns.2020.116795  0.01
2020 Horie R, Kubota T, Koh J, Tanaka R, Nakamura Y, Sasaki R, Ito H, Takahashi MP. EF hand-like motif mutations of Nav1.4 C-terminus cause myotonic syndrome by impairing fast inactivation. Muscle & Nerve. PMID 32129495 DOI: 10.1002/mus.26849  0.01
2020 Kurokawa M, Torio M, Ohkubo K, Tocan V, Ohyama N, Toda N, Ishii K, Nishiyama K, Mushimoto Y, Sakamoto R, Nakaza M, Horie R, Kubota T, Takahashi MP, Sakai Y, et al. The expanding phenotype of hypokalemic periodic paralysis in a Japanese family with p.Val876Glu mutation in CACNA1S. Molecular Genetics & Genomic Medicine. e1175. PMID 32104981 DOI: 10.1002/mgg3.1175  0.01
2020 Takahashi MP, Yamamoto R, Kubota T, Matsuura T, Ishigaki K, Sunada Y, Komaki H, Takada H, Kuru S, Matsumura T. [Study of care practices for patients with myotonic dystrophy in Japan-Nationwide patient survey]. Rinsho Shinkeigaku = Clinical Neurology. PMID 31956156 DOI: 10.5692/  0.01
2019 Fukumura S, Yamauchi K, Kawanabe A, Yamamoto A, Nakaza M, Kubota T, Kato S, Sasaki R, Okamura Y, Takahashi MP. Functional analysis of a double-point mutation in the KCNJ2 gene identified in a family with Andersen-Tawil syndrome. Journal of the Neurological Sciences. 407: 116521. PMID 31669729 DOI: 10.1016/j.jns.2019.116521  0.01
2019 Kubota T, Lloyd K, Sakashita N, Minato S, Ishida K, Mitsui T. Clog and Release, and Reverse Motions of DNA in a Nanopore. Polymers. 11. PMID 30960068 DOI: 10.3390/polym11010084  0.01
2014 Kubota T, Lacroix JJ, Bezanilla F, Correa AM. Probing α-3(10) transitions in a voltage-sensing S4 helix. Biophysical Journal. 107: 1117-28. PMID 25185547 DOI: 10.1016/j.bpj.2014.07.042  0.4
2014 Kubota T, Nakamori M, Takahashi MP. [Myotonia and cardiac conduction defects in myotonic dystrophy and defect in ion channels]. Rinsho Byori. the Japanese Journal of Clinical Pathology. 62: 246-54. PMID 24800500  0.28
2014 Kokunai Y, Nakata T, Furuta M, Sakata S, Kimura H, Aiba T, Yoshinaga M, Osaki Y, Nakamori M, Itoh H, Sato T, Kubota T, Kadota K, Shindo K, Mochizuki H, et al. A Kir3.4 mutation causes Andersen-Tawil syndrome by an inhibitory effect on Kir2.1. Neurology. 82: 1058-64. PMID 24574546 DOI: 10.1212/WNL.0000000000000239  0.28
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