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Tomoya Kubota - Publications

Affiliations: 
University of Chicago, Chicago, IL 
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39 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
2023 Kubota T, Takahashi S, Yamamoto R, Sato R, Miyanooto A, Yamamoto R, Yamauchi K, Homma K, Takahashi MP. Optical measurement of gating pore currents in hypokalemic periodic paralysis model cells. Disease Models & Mechanisms. PMID 37139703 DOI: 10.1242/dmm.049704  0.414
2023 Segawa K, Nishiyama M, Mori I, Kubota T, Takahashi MP. Hyperkalemic periodic paralysis associated with a novel missense variant located in the inner pore of Nav1.4. Brain & Development. PMID 36628799 DOI: 10.1016/j.braindev.2022.12.003  0.408
2022 Shibano M, Kubota T, Kokubun N, Miyaji Y, Kuriki H, Ito Y, Hamanoue H, Takahashi MP. Periodic paralysis due to cumulative effects of rare variants in SCN4A with small functional alterations. Muscle & Nerve. PMID 36116128 DOI: 10.1002/mus.27725  0.376
2020 Kubota T, Wu F, Vicart S, Nakaza M, Sternberg D, Watanabe D, Furuta M, Kokunai Y, Abe T, Kokubun N, Fontaine B, Cannon SC, Takahashi MP. Hypokalaemic periodic paralysis with a charge-retaining substitution in the voltage sensor. Brain Communications. 2: fcaa103. PMID 33005891 DOI: 10.1093/braincomms/fcaa103  0.38
2020 Sasaki R, Nakaza M, Furuta M, Fujino H, Kubota T, Takahashi MP. Mutation spectrum and health status in skeletal muscle channelopathies in Japan. Neuromuscular Disorders : Nmd. PMID 32660787 DOI: 10.1016/J.Nmd.2020.06.001  0.342
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  0.752
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  0.447
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  0.412
2020 Horie R, Kubota T, Koh J, Tanaka R, Nakamura Y, Ryogen S, Ito H, Takahashi MP. Myotonic Mutations of Nav1.4 Located At EF Hand-Like Motif in C-Terminus Impair Fast Inactivation Biophysical Journal. 118: 575a-576a. DOI: 10.1016/J.Bpj.2019.11.3127  0.314
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  0.405
2018 Nakaza M, Kubota T, Vicart S, Watanabe D, Kokubun N, Furuta M, Sternberg D, Kokunai Y, Abe T, Fontaine B, Takahashi MP. Hypokalemic Periodic Paralysis Cases with Substitutions from Arginine to Lysine in the Voltage Sensor Biophysical Journal. 114: 636a. DOI: 10.1016/J.Bpj.2017.11.3435  0.331
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  0.746
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  0.666
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  0.705
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  0.535
2017 Kubota T, Watanabe D, Kokubun N, Furuta M, Kokunai Y, Abe T, Takahashi M. Arginine-to-lysine mutations in the voltage sensor are associated with hypokalemic periodic paralysis Journal of the Neurological Sciences. 381: 660. DOI: 10.1016/J.Jns.2017.08.1857  0.37
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  0.428
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  0.588
2016 Kubota T, Durek T, Finol-Urdaneta RK, Craik DJ, French RJ, Bezanilla F, Correa AM. Probing Voltage-Dependent Structural Changes of the VSD in Mammalian Nav with LRET Biophysical Journal. 110: 113a. DOI: 10.1016/J.Bpj.2015.11.665  0.669
2016 Kubota T, Dang B, Carvalho-de-Souza JL, Kent SB, Correa AM, Bezanilla F. High Affinity Nav Channel Binder with Specific Conjugation Site Derived from Scorpion Toxin with Attenuated Toxicity Biophysical Journal. 110: 113a. DOI: 10.1016/J.Bpj.2015.11.664  0.758
2016 Carvalho-de-Souza JL, Kubota T, Du X, Latorre R, Gomez CM, Bezanilla F. A Missense Mutation in the Selectivity Filter of BK Affects the Channel's Potassium Conductance Biophysical Journal. 110: 449a. DOI: 10.1016/J.Bpj.2015.11.2412  0.764
2015 Kubota T, Correa AM, Bezanilla F. Exploring Molecular Mechanisms of the Functional Interaction between Kv1.3 and Nav Beta1 Biophysical Journal. 108: 279a. DOI: 10.1016/J.Bpj.2014.11.1527  0.668
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  0.555
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  0.671
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  0.316
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  0.474
2014 Kubota T, Brugarolas P, Dang B, Finol-Urdaneta RK, Frezza L, French RJ, Kent SB, Bezanilla F, Correa AM. Tracking Voltage-Dependent Conformational Changes of the VSD in Nav with LRET Biophysical Journal. 106: 133a. DOI: 10.1016/J.Bpj.2013.11.781  0.684
2014 Kubota T, Dang B, Finol-Urdaneta RK, Lacroix JJ, Frezza L, French RJ, Kent SB, Correa AM, Bezanilla F. Searching for the Interaction Sites of the Beta1 Subunit with the Voltage-Sensing Domains of Sodium Channels Using LRET Biophysical Journal. 106: 133a. DOI: 10.1016/J.Bpj.2013.11.780  0.578
2014 Treger JS, Priest MF, Kubota T, Frezza L, Bezanilla F. Single Molecule Fluorescence of an S4-Based Voltage Sensor Biophysical Journal. 106: 742a. DOI: 10.1016/J.Bpj.2013.11.4087  0.741
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  0.533
2013 Kokunai Y, Nakamori M, Kubota T, Mochizuki H, Takahashi MP, Nakata T, Ohno K, Sakata S, Okamura Y, Kimura H, Itoh H, Horie M, Osaki Y, Shindo K. P.12.10 Exome sequencing analysis reveals a mutation of Kir3.4 in a patient with Andersen–Tawil syndrome Neuromuscular Disorders. 23: 808. DOI: 10.1016/J.Nmd.2013.06.592  0.511
2013 Kubota T, Lacroix JJ, Bezanilla F, Correa AM. Probing S4 Re-Arrangement during Gating using Optical Tools Biophysical Journal. 104: 276a. DOI: 10.1016/J.Bpj.2012.11.1550  0.592
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  0.557
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  0.457
2012 Kubota T, Lacroix JJ, Bezanilla F, Correa AM. Probing S4 Length Changes during Gating with LRET Biophysical Journal. 102: 265a. DOI: 10.1016/J.Bpj.2011.11.1460  0.594
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  0.508
2010 Takahashi MP, Kubota T, Kokunai Y, Kimura T, Sakoda S. P2.34 A myotonia caused by aberrant splicing of voltage-gated sodium channel due to an intronic mutation of SCN4A Neuromuscular Disorders. 20: 628-629. DOI: 10.1016/J.Nmd.2010.07.106  0.531
2010 Kubota T, Takahashi MP, Kimura T, Sakoda S. An Intronic Mutation of SCN4A Associated with Myotonia Raises an Aberrantly Spliced Isoform with Disrupted Fast Inactivation Biophysical Journal. 98: 311a-312a. DOI: 10.1016/J.Bpj.2009.12.1692  0.524
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  0.522
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