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Items: 1 to 50 of 653

1.

The association between microRNA-21 and hypertension-induced cardiac remodeling.

Watanabe K, Narumi T, Watanabe T, Otaki Y, Takahashi T, Aono T, Goto J, Toshima T, Sugai T, Wanezaki M, Kutsuzawa D, Kato S, Tamura H, Nishiyama S, Takahashi H, Arimoto T, Shishido T, Watanabe M.

PLoS One. 2020 Feb 10;15(2):e0226053. doi: 10.1371/journal.pone.0226053. eCollection 2020.

2.

Neonatal hydrocephalus leads to white matter neuroinflammation and injury in the corpus callosum of Ccdc39 hydrocephalic mice.

Goulding DS, Vogel RC, Pandya CD, Shula C, Gensel JC, Mangano FT, Goto J, Miller BA.

J Neurosurg Pediatr. 2020 Feb 7:1-8. doi: 10.3171/2019.12.PEDS19625. [Epub ahead of print]

PMID:
32032950
3.

On the Differential Roles of Mg2+, Zn2+, and Cu2+ in the Equilibrium of β-N-Methyl-Amino-L-Alanine (BMAA) and its Carbamates.

Diaz-Parga P, Goto JJ, Krishnan VV.

Neurotox Res. 2020 Jan 18. doi: 10.1007/s12640-019-00157-0. [Epub ahead of print]

PMID:
31955368
4.

Depotentiation depends on IP3 receptor activation sustained by synaptic inputs after LTP induction.

Fujii S, Yamazaki Y, Goto JI, Fujiwara H, Mikoshiba K.

Learn Mem. 2020 Jan 16;27(2):52-66. doi: 10.1101/lm.050344.119. Print 2020 Feb.

PMID:
31949037
5.

Factors regulating the differential uptake of persistent organic pollutants in cucurbits and non-cucurbits.

Iwabuchi A, Katte N, Suwa M, Goto J, Inui H.

J Plant Physiol. 2020 Feb;245:153094. doi: 10.1016/j.jplph.2019.153094. Epub 2019 Dec 11.

PMID:
31862647
6.

Impaired neural differentiation and glymphatic CSF flow in the Ccdc39 rat model of neonatal hydrocephalus: genetic interaction with L1cam.

Emmert AS, Iwasawa E, Shula C, Schultz P, Lindquist D, Dunn RS, Fugate EM, Hu YC, Mangano FT, Goto J.

Dis Model Mech. 2019 Nov 21;12(11). pii: dmm040972. doi: 10.1242/dmm.040972.

7.

Sex Mysteries of the Fly Courtship Master Regulator Fruitless.

Sato K, Goto J, Yamamoto D.

Front Behav Neurosci. 2019 Oct 18;13:245. doi: 10.3389/fnbeh.2019.00245. eCollection 2019. Review.

8.

Novel SLC20A2 variant in a Japanese patient with idiopathic basal ganglia calcification-1 (IBGC1) associated with dopa-responsive parkinsonism.

Ichikawa Y, Tanaka M, Kurita E, Nakajima M, Tanaka M, Oishi C, Goto J, Tsuji S, Chiba A.

Hum Genome Var. 2019 Sep 4;6:44. doi: 10.1038/s41439-019-0073-7. eCollection 2019.

9.

Evaluation of health and quality of life in apheresis patients - data from the WAA register.

Goto J, Newman E, Witt V, Deeren D, Blaha M, Lanska M, Gasova Z, Bhuiyan-Ludvikova Z, Hrdlickova R, Ramlow W, Prophet H, Liumbruno G, Griskevicius A, Audzijoniene J, Vrielink H, Aandahl A, Sanchez SO, Strineholm V, Berlin G, Mörtzell-Henriksson M, Stegmayr BG, Eich T, Ilhan O.

Transfus Apher Sci. 2019 Oct;58(5):641-644. doi: 10.1016/j.transci.2019.08.024. Epub 2019 Sep 5.

PMID:
31519525
10.

Therapeutic inhibition of microRNA-34a ameliorates aortic valve calcification via modulation of Notch1-Runx2 signalling.

Toshima T, Watanabe T, Narumi T, Otaki Y, Shishido T, Aono T, Goto J, Watanabe K, Sugai T, Takahashi T, Yokoyama M, Kinoshita D, Tamura H, Kato S, Nishiyama S, Arimoto T, Takahashi H, Miyamoto T, Sadahiro M, Watanabe M.

Cardiovasc Res. 2020 Apr 1;116(5):983-994. doi: 10.1093/cvr/cvz210.

PMID:
31393559
11.

Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease.

Ishiura H, Shibata S, Yoshimura J, Suzuki Y, Qu W, Doi K, Almansour MA, Kikuchi JK, Taira M, Mitsui J, Takahashi Y, Ichikawa Y, Mano T, Iwata A, Harigaya Y, Matsukawa MK, Matsukawa T, Tanaka M, Shirota Y, Ohtomo R, Kowa H, Date H, Mitsue A, Hatsuta H, Morimoto S, Murayama S, Shiio Y, Saito Y, Mitsutake A, Kawai M, Sasaki T, Sugiyama Y, Hamada M, Ohtomo G, Terao Y, Nakazato Y, Takeda A, Sakiyama Y, Umeda-Kameyama Y, Shinmi J, Ogata K, Kohno Y, Lim SY, Tan AH, Shimizu J, Goto J, Nishino I, Toda T, Morishita S, Tsuji S.

Nat Genet. 2019 Aug;51(8):1222-1232. doi: 10.1038/s41588-019-0458-z. Epub 2019 Jul 22.

PMID:
31332380
12.

Prominent Spasticity and Hyperreflexia of the Legs in a Nepalese Patient with Friedreich Ataxia.

Naruse H, Takahashi Y, Ishiura H, Matsukawa T, Mitsui J, Ichikawa Y, Hamada M, Shimizu J, Goto J, Toda T, Tsuji S.

Intern Med. 2019 Oct 1;58(19):2865-2869. doi: 10.2169/internalmedicine.2953-19. Epub 2019 Jun 7.

13.

Association of ATXN2 intermediate-length CAG repeats with amyotrophic lateral sclerosis correlates with the distributions of normal CAG repeat alleles among individual ethnic populations.

Naruse H, Matsukawa T, Ishiura H, Mitsui J, Takahashi Y, Takano H, Goto J, Toda T, Tsuji S.

Neurogenetics. 2019 May;20(2):65-71. doi: 10.1007/s10048-019-00570-9. Epub 2019 Mar 7.

PMID:
30847648
14.

Establishing extracorporeal membrane oxygenation team increased number of patients and improved data recording.

Komindr A, Abe R, Tateishi Y, Takahashi Y, Goto J, Wada K, Furukawa Y, Sugiura A, Imaeda T, Suga N, Hattori N, Oda S.

J Intensive Care. 2019 Feb 7;7:11. doi: 10.1186/s40560-019-0366-4. eCollection 2019.

15.

Characterization of a novel rat model of X-linked hydrocephalus by CRISPR-mediated mutation in L1cam.

Emmert AS, Vuong SM, Shula C, Lindquist D, Yuan W, Hu YC, Mangano FT, Goto J.

J Neurosurg. 2019 Feb 8:1-14. doi: 10.3171/2018.10.JNS181015. [Epub ahead of print]

PMID:
30738385
16.

Associations among behavioral and psychological symptoms of dementia, care burden, and family-to-work conflict of employed family caregivers.

Sakka M, Goto J, Kita S, Sato I, Soejima T, Kamibeppu K.

Geriatr Gerontol Int. 2019 Jan;19(1):51-55. doi: 10.1111/ggi.13556. Epub 2018 Dec 16.

PMID:
30556370
17.

Neuroimaging, genetic, and enzymatic study in a Japanese family with a GBA gross deletion.

Ichinose Y, Ishiura H, Tanaka M, Yoshimura J, Doi K, Umeda T, Yamauchi H, Tsuchiya M, Koh K, Yamashiro N, Mitsui J, Goto J, Onishi H, Ohtsuka T, Shindo K, Morishita S, Tsuji S, Takiyama Y.

Parkinsonism Relat Disord. 2019 Apr;61:57-63. doi: 10.1016/j.parkreldis.2018.11.028. Epub 2018 Dec 2.

PMID:
30528172
18.

Burden of rare variants in causative genes for amyotrophic lateral sclerosis (ALS) accelerates age at onset of ALS.

Naruse H, Ishiura H, Mitsui J, Takahashi Y, Matsukawa T, Tanaka M, Doi K, Yoshimura J, Morishita S, Goto J, Toda T, Tsuji S.

J Neurol Neurosurg Psychiatry. 2019 May;90(5):537-542. doi: 10.1136/jnnp-2018-318568. Epub 2018 Oct 24.

PMID:
30355605
19.

Decreased Psoas Muscle Computed Tomography Value Predicts Poor Outcome in Peripheral Artery Disease.

Sugai T, Watanabe T, Otaki Y, Goto J, Watanabe K, Toshima T, Takahashi T, Yokoyama M, Tamura H, Nishiyama S, Arimoto T, Takahashi H, Shishido T, Watanabe M.

Circ J. 2018 Nov 24;82(12):3069-3075. doi: 10.1253/circj.CJ-18-0726. Epub 2018 Sep 29.

20.

Plasma Exchange Downregulates Activated Monocytes and Restores Regulatory T Cells in Kawasaki Disease.

Koizumi K, Hoshiai M, Moriguchi T, Katsumata N, Toda T, Kise H, Hasebe Y, Kono Y, Sunaga Y, Yoshizawa M, Watanabe A, Harii N, Goto J, Kagami K, Abe M, Matsuda K, Sugita K.

Ther Apher Dial. 2019 Feb;23(1):92-98. doi: 10.1111/1744-9987.12754. Epub 2018 Sep 21.

PMID:
30239141
21.
22.

Correction to: Outcomes of plasma exchange for severe dilated cardiomyopathy in children.

Koizumi K, Hoshiai M, Moriguchi T, Toda T, Katsumata N, Kise H, Hasebe Y, Kouno Y, Goto J, Harii N, Matsuda K, Kaga S, Suzuki S, Sugita K.

Heart Vessels. 2018 Dec;33(12):1584-1585. doi: 10.1007/s00380-018-1163-z.

PMID:
29671045
23.

Super-long single-molecule tracking reveals dynamic-anchorage-induced integrin function.

Tsunoyama TA, Watanabe Y, Goto J, Naito K, Kasai RS, Suzuki KGN, Fujiwara TK, Kusumi A.

Nat Chem Biol. 2018 May;14(5):497-506. doi: 10.1038/s41589-018-0032-5. Epub 2018 Apr 2.

PMID:
29610485
24.

Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy.

Ishiura H, Doi K, Mitsui J, Yoshimura J, Matsukawa MK, Fujiyama A, Toyoshima Y, Kakita A, Takahashi H, Suzuki Y, Sugano S, Qu W, Ichikawa K, Yurino H, Higasa K, Shibata S, Mitsue A, Tanaka M, Ichikawa Y, Takahashi Y, Date H, Matsukawa T, Kanda J, Nakamoto FK, Higashihara M, Abe K, Koike R, Sasagawa M, Kuroha Y, Hasegawa N, Kanesawa N, Kondo T, Hitomi T, Tada M, Takano H, Saito Y, Sanpei K, Onodera O, Nishizawa M, Nakamura M, Yasuda T, Sakiyama Y, Otsuka M, Ueki A, Kaida KI, Shimizu J, Hanajima R, Hayashi T, Terao Y, Inomata-Terada S, Hamada M, Shirota Y, Kubota A, Ugawa Y, Koh K, Takiyama Y, Ohsawa-Yoshida N, Ishiura S, Yamasaki R, Tamaoka A, Akiyama H, Otsuki T, Sano A, Ikeda A, Goto J, Morishita S, Tsuji S.

Nat Genet. 2018 Apr;50(4):581-590. doi: 10.1038/s41588-018-0067-2. Epub 2018 Mar 5.

PMID:
29507423
25.

Frequency and characteristics of the TBK1 gene variants in Japanese patients with sporadic amyotrophic lateral sclerosis.

Tohnai G, Nakamura R, Sone J, Nakatochi M, Yokoi D, Katsuno M, Watanabe H, Watanabe H, Ito M, Li Y, Izumi Y, Morita M, Taniguchi A, Kano O, Oda M, Kuwabara S, Abe K, Aiba I, Okamoto K, Mizoguchi K, Hasegawa K, Aoki M, Hattori N, Onodera O, Naruse H, Mitsui J, Takahashi Y, Goto J, Ishiura H, Morishita S, Yoshimura J, Doi K, Tsuji S, Nakashima K, Kaji R, Atsuta N, Sobue G; Japanese Consortium for Amyotrophic Lateral Sclerosis Research (JaCALS).

Neurobiol Aging. 2018 Apr;64:158.e15-158.e19. doi: 10.1016/j.neurobiolaging.2017.12.005. Epub 2017 Dec 11.

PMID:
29398122
26.

[A case of duodenal neuroendocrine carcinoma composed of small- and large-cell types].

Muto M, Ichiki K, Muto M, Ishikawa C, Inoue M, Goto J, Inaba S, Aoki T, Sato K.

Nihon Shokakibyo Gakkai Zasshi. 2018;115(1):79-86. doi: 10.11405/nisshoshi.115.79. Japanese.

PMID:
29353854
27.

A mutation in Ccdc39 causes neonatal hydrocephalus with abnormal motile cilia development in mice.

Abdelhamed Z, Vuong SM, Hill L, Shula C, Timms A, Beier D, Campbell K, Mangano FT, Stottmann RW, Goto J.

Development. 2018 Jan 9;145(1). pii: dev154500. doi: 10.1242/dev.154500.

28.

Molecular epidemiological study of familial amyotrophic lateral sclerosis in Japanese population by whole-exome sequencing and identification of novel HNRNPA1 mutation.

Naruse H, Ishiura H, Mitsui J, Date H, Takahashi Y, Matsukawa T, Tanaka M, Ishii A, Tamaoka A, Hokkoku K, Sonoo M, Segawa M, Ugawa Y, Doi K, Yoshimura J, Morishita S, Goto J, Tsuji S.

Neurobiol Aging. 2018 Jan;61:255.e9-255.e16. doi: 10.1016/j.neurobiolaging.2017.08.030. Epub 2017 Sep 6.

PMID:
29033165
29.

Scalaradial Is a Potent Inhibitor of Transient Receptor Potential Melastatin 2 (TRPM2) Ion Channels.

Starkus JG, Poerzgen P, Layugan K, Kawabata KG, Goto JI, Suzuki S, Myers G, Kelly M, Penner R, Fleig A, Horgen FD.

J Nat Prod. 2017 Oct 27;80(10):2741-2750. doi: 10.1021/acs.jnatprod.7b00515. Epub 2017 Oct 11.

30.

A case of synchronous quintuple gastric cancer with large-cell endocrine carcinoma.

Muto M, Muto M, Ichiki K, Ishikawa C, Hosoki T, Inoue M, Goto J, Inaba S.

Nihon Shokakibyo Gakkai Zasshi. 2017;114(10):1845-1852. doi: 10.11405/nisshoshi.114.1845. Review. Japanese.

PMID:
28978884
31.

Chemistry and Chemical Equilibrium Dynamics of BMAA and Its Carbamate Adducts.

Diaz-Parga P, Goto JJ, Krishnan VV.

Neurotox Res. 2018 Jan;33(1):76-86. doi: 10.1007/s12640-017-9801-2. Epub 2017 Sep 18.

32.

Clinicopathologic features of myositis patients with CD8-MHC-1 complex pathology.

Ikenaga C, Kubota A, Kadoya M, Taira K, Uchio N, Hida A, Maeda MH, Nagashima Y, Ishiura H, Kaida K, Goto J, Tsuji S, Shimizu J.

Neurology. 2017 Sep 5;89(10):1060-1068. doi: 10.1212/WNL.0000000000004333. Epub 2017 Aug 9.

PMID:
28794251
33.

Partial duplication of DHH causes minifascicular neuropathy: A novel mutation detection of DHH.

Sato NS, Maekawa R, Ishiura H, Mitsui J, Naruse H, Tokushige SI, Sugie K, Tate G, Shimizu J, Goto J, Tsuji S, Shiio Y.

Ann Clin Transl Neurol. 2017 May 22;4(6):415-421. doi: 10.1002/acn3.417. eCollection 2017 Jun.

34.

Plasma exchange for the patients with dilated cardiomyopathy in children is safe and effective in improving both cardiac function and daily activities.

Moriguchi T, Koizumi K, Matsuda K, Harii N, Goto J, Harada D, Sugawara H, Hoshiai M, Kise H, Baba A.

J Artif Organs. 2017 Sep;20(3):236-243. doi: 10.1007/s10047-017-0956-7. Epub 2017 Apr 5.

PMID:
28382424
35.

[An Autopsied Case of Familial Spinocerebellar Degeneration Presenting with Late-Onset Autonomic Dysfunction].

Yamazaki M, Fukuda T, Ishikawa K, Goto J.

Brain Nerve. 2017 Mar;69(3):277-286. doi: 10.11477/mf.1416200739. Japanese. No abstract available.

PMID:
28270637
36.

Three-Year Follow-Up of High-Dose Ubiquinol Supplementation in a Case of Familial Multiple System Atrophy with Compound Heterozygous COQ2 Mutations.

Mitsui J, Koguchi K, Momose T, Takahashi M, Matsukawa T, Yasuda T, Tokushige SI, Ishiura H, Goto J, Nakazaki S, Kondo T, Ito H, Yamamoto Y, Tsuji S.

Cerebellum. 2017 Jun;16(3):664-672. doi: 10.1007/s12311-017-0846-9.

37.

Preference of Conjugated Bile Acids over Unconjugated Bile Acids as Substrates for OATP1B1 and OATP1B3.

Suga T, Yamaguchi H, Sato T, Maekawa M, Goto J, Mano N.

PLoS One. 2017 Jan 6;12(1):e0169719. doi: 10.1371/journal.pone.0169719. eCollection 2017.

38.

Slowly progressive d-bifunctional protein deficiency with survival to adulthood diagnosed by whole-exome sequencing.

Matsukawa T, Koshi KM, Mitsui J, Bannai T, Kawabe M, Ishiura H, Terao Y, Shimizu J, Murayama K, Yoshimura J, Doi K, Morishita S, Tsuji S, Goto J.

J Neurol Sci. 2017 Jan 15;372:6-10. doi: 10.1016/j.jns.2016.11.009. Epub 2016 Nov 9.

PMID:
28017249
39.

Cellular Prion Protein Combined with Galectin-3 and -6 Affects the Infectivity Titer of an Endogenous Retrovirus Assayed in Hippocampal Neuronal Cells.

Kim BH, Shin HY, Goto JJ, Carp RI, Choi EK, Kim YS.

PLoS One. 2016 Dec 9;11(12):e0167293. doi: 10.1371/journal.pone.0167293. eCollection 2016.

40.

A case of mixed adenoneuroendocrine carcinoma of the stomach.

Muto M, Muto M, Ichiki K, Ishikawa C, Inoue M, Ishii D, Goto J, Inaba S, Aoki T, Kondo N.

Nihon Shokakibyo Gakkai Zasshi. 2016;113(10):1769-1776. Review. Japanese.

PMID:
27725466
41.

Equilibrium Dynamics of β-N-Methylamino-L-Alanine (BMAA) and Its Carbamate Adducts at Physiological Conditions.

Zimmerman D, Goto JJ, Krishnan VV.

PLoS One. 2016 Aug 11;11(8):e0160491. doi: 10.1371/journal.pone.0160491. eCollection 2016.

42.

Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses.

Ishiura H, Takahashi Y, Hayashi T, Saito K, Furuya H, Watanabe M, Murata M, Suzuki M, Sugiura A, Sawai S, Shibuya K, Ueda N, Ichikawa Y, Kanazawa I, Goto J, Tsuji S.

J Hum Genet. 2016 Apr;61(4):363-4. doi: 10.1038/jhg.2015.159. No abstract available.

PMID:
27108959
43.

Prior activation of inositol 1,4,5-trisphosphate receptors suppresses the subsequent induction of long-term potentiation in hippocampal CA1 neurons.

Fujii S, Yamazaki Y, Goto J, Fujiwara H, Mikoshiba K.

Learn Mem. 2016 Apr 15;23(5):208-20. doi: 10.1101/lm.041053.115. Print 2016 May.

44.

CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.

Williams KL, Topp S, Yang S, Smith B, Fifita JA, Warraich ST, Zhang KY, Farrawell N, Vance C, Hu X, Chesi A, Leblond CS, Lee A, Rayner SL, Sundaramoorthy V, Dobson-Stone C, Molloy MP, van Blitterswijk M, Dickson DW, Petersen RC, Graff-Radford NR, Boeve BF, Murray ME, Pottier C, Don E, Winnick C, McCann EP, Hogan A, Daoud H, Levert A, Dion PA, Mitsui J, Ishiura H, Takahashi Y, Goto J, Kost J, Gellera C, Gkazi AS, Miller J, Stockton J, Brooks WS, Boundy K, Polak M, Muñoz-Blanco JL, Esteban-Pérez J, Rábano A, Hardiman O, Morrison KE, Ticozzi N, Silani V, de Belleroche J, Glass JD, Kwok JB, Guillemin GJ, Chung RS, Tsuji S, Brown RH Jr, García-Redondo A, Rademakers R, Landers JE, Gitler AD, Rouleau GA, Cole NJ, Yerbury JJ, Atkin JD, Shaw CE, Nicholson GA, Blair IP.

Nat Commun. 2016 Apr 15;7:11253. doi: 10.1038/ncomms11253.

45.

Atypical parkinsonism caused by Pro105Leu mutation of prion protein: A broad clinical spectrum.

Mano KK, Matsukawa T, Mitsui J, Ishiura H, Tokushige S, Takahashi Y, Sato NS, Nakamoto FK, Ichikawa Y, Nagashima Y, Terao Y, Shimizu J, Hamada M, Uesaka Y, Oyama G, Ogawa G, Yoshimura J, Doi K, Morishita S, Tsuji S, Goto J.

Neurol Genet. 2016 Jan 7;2(1):e48. doi: 10.1212/NXG.0000000000000048. eCollection 2016 Feb.

46.

Role of postsynaptic inositol 1, 4, 5-trisphosphate receptors in depotentiation in guinea pig hippocampal CA1 neurons.

Sugita M, Yamazaki Y, Goto JI, Fujiwara H, Aihara T, Mikoshiba K, Fujii S.

Brain Res. 2016 Jul 1;1642:154-162. doi: 10.1016/j.brainres.2016.03.033. Epub 2016 Mar 25.

PMID:
27018292
47.

Activation of inositol 1,4,5-trisphosphate receptors during preconditioning low-frequency stimulation suppresses subsequent induction of long-term potentiation in hippocampal CA1 neurons.

Yamazaki Y, Fujii S, Goto JI, Fujiwara H, Mikoshiba K.

Neuroscience. 2015 Dec 17;311:195-206. doi: 10.1016/j.neuroscience.2015.10.030. Epub 2015 Oct 20.

PMID:
26500182
48.

Synthesis and Properties of Ethene-Bridged Terthiophenes.

Mitsudo K, Sato H, Yamasaki A, Kamimoto N, Goto J, Mandai H, Suga S.

Org Lett. 2015 Oct 2;17(19):4858-61. doi: 10.1021/acs.orglett.5b02417.

PMID:
26381709
49.

Directed evolution of the Escherichia coli cAMP receptor protein at the cAMP pocket.

Gunasekara SM, Hicks MN, Park J, Brooks CL, Serate J, Saunders CV, Grover SK, Goto JJ, Lee JW, Youn H.

J Biol Chem. 2015 Oct 30;290(44):26587-96. doi: 10.1074/jbc.M115.678474. Epub 2015 Sep 16.

50.

A systematic immunoprecipitation approach reinforces the concept of common conformational alterations in amyotrophic lateral sclerosis-linked SOD1 mutants.

Fujisawa T, Yamaguchi N, Kadowaki H, Tsukamoto Y, Tsuburaya N, Tsubota A, Takahashi H, Naguro I, Takahashi Y, Goto J, Tsuji S, Nishitoh H, Homma K, Ichijo H.

Neurobiol Dis. 2015 Oct;82:478-486. doi: 10.1016/j.nbd.2015.08.010. Epub 2015 Aug 18.

PMID:
26297318

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