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Items: 1 to 50 of 396

1.

Correction to: In Vitro Seeding Activity of Glycoform-Deficient Prions from Variably Protease-Sensitive Prionopathy and Familial CJD Associated with PrPV180I Mutation.

Wang Z, Yuan J, Shen P, Abskharon R, Lang Y, Dang J, Adornato A, Xu L, Chen J, Feng J, Moudjou M, Kitamoto T, Langeveld J, Appleby B, Ma J, Kong Q, Petersen RB, Zou WQ, Cui L.

Mol Neurobiol. 2019 Feb 1. doi: 10.1007/s12035-019-1508-3. [Epub ahead of print]

PMID:
30707392
2.

Sensitive quantification of BB-22 and its metabolite BB-22 3-carboxyindole, and characterization of new metabolites in authentic urine and/or serum specimens obtained from three individuals by LC-QTRAP-MS/MS and high-resolution LC-Orbitrap-MS/MS.

Minakata K, Hasegawa K, Nozawa H, Yamagishi I, Saitoh T, Yoshino A, Suzuki M, Kitamoto T, Suzuki O, Watanabe K.

Forensic Toxicol. 2019;37(1):164-173. doi: 10.1007/s11419-018-0448-3. Epub 2018 Oct 16.

3.

In Vitro Seeding Activity of Glycoform-Deficient Prions from Variably Protease-Sensitive Prionopathy and Familial CJD Associated with PrPV180I Mutation.

Wang Z, Yuan J, Shen P, Abskharon R, Lang Y, Dang J, Adornato A, Xu L, Chen J, Feng J, Moudjou M, Kitamoto T, Langeveld J, Appleby B, Ma J, Kong Q, Petersen RB, Zou WQ, Cui L.

Mol Neurobiol. 2019 Jan 5. doi: 10.1007/s12035-018-1459-0. [Epub ahead of print] Erratum in: Mol Neurobiol. 2019 Feb 1;:.

PMID:
30612334
4.

Ganglioside Synthase Knockout Reduces Prion Disease Incubation Time in Mouse Models.

Kobayashi A, Qi Z, Shimazaki T, Munesue Y, Miyamoto T, Isoda N, Sawa H, Aoshima K, Kimura T, Mohri S, Kitamoto T, Yamashita T, Miyoshi I.

Am J Pathol. 2018 Dec 13. pii: S0002-9440(18)30757-0. doi: 10.1016/j.ajpath.2018.11.009. [Epub ahead of print]

PMID:
30553837
5.

Intermolecular crosslinking of abnormal prion protein is efficiently induced by a primuline-sensitized photoreaction.

Teruya K, Nishizawa K, Oguma A, Sakasegawa Y, Kitamoto T, Doh-Ura K.

Biochim Biophys Acta Gen Subj. 2019 Feb;1863(2):384-394. doi: 10.1016/j.bbagen.2018.11.008. Epub 2018 Nov 14.

PMID:
30447252
6.

An autopsied case of MM1-type sporadic Creutzfeldt-Jakob disease with pathology of Wernicke encephalopathy.

Iwasaki Y, Hashimoto R, Saito Y, Aiba I, Inukai A, Akagi A, Mimuro M, Miyahara H, Kitamoto T, Yoshida M.

Prion. 2019 Jan;13(1):13-20. doi: 10.1080/19336896.2018.1545525. Epub 2018 Nov 14.

PMID:
30409087
7.

Specific amyloid-β42 deposition in the brain of a Gerstmann-Sträussler-Scheinker disease patient with a P105L mutation on the prion protein gene.

Furukawa F, Sanjo N, Kobayashi A, Hamaguchi T, Yamada M, Kitamoto T, Mizusawa H, Yokota T.

Prion. 2018;12(5-6):315-319. doi: 10.1080/19336896.2018.1541689. Epub 2018 Nov 13.

PMID:
30394185
8.

[Genetic Creutzfeldt-Jakob disease with a glutamate-to-lysine substitution at codon 219 (E219K) in the presence of the E200K mutation presenting with rapid progressive dementia following slowly progressive clinical course].

Takayanagi M, Suzuki K, Nakamura T, Hirata K, Satoh K, Kitamoto T.

Rinsho Shinkeigaku. 2018 Nov 28;58(11):682-687. doi: 10.5692/clinicalneurol.cn-001206. Epub 2018 Oct 27. Japanese.

PMID:
30369528
9.

Tumor Cell Subtypes Based on the Intracellular Hormonal Activity in KCNJ5-Mutated Aldosterone-Producing Adenoma.

Yamazaki Y, Omata K, Tezuka Y, Ono Y, Morimoto R, Adachi Y, Ise K, Nakamura Y, Gomez-Sanchez CE, Shibahara Y, Kitamoto T, Nishikawa T, Ito S, Satoh F, Sasano H.

Hypertension. 2018 Sep;72(3):632-640. doi: 10.1161/HYPERTENSIONAHA.118.10907.

PMID:
30354756
10.

A case of intoxication with a mixture of synthetic cannabinoids EAM-2201, AB-PINACA and AB-FUBINACA, and a synthetic cathinone α-PVP.

Yamagishi I, Minakata K, Nozawa H, Hasegawa K, Suzuki M, Kitamoto T, Suzuki O, Watanabe K.

Leg Med (Tokyo). 2018 Nov;35:44-49. doi: 10.1016/j.legalmed.2018.08.004. Epub 2018 Aug 6.

PMID:
30268690
11.

An autopsy report of three kindred in a Gerstmann-Sträussler-Scheinker disease P105L family with a special reference to prion protein, tau, and beta-amyloid.

Ishizawa K, Mitsufuji T, Shioda K, Kobayashi A, Komori T, Nakazato Y, Kitamoto T, Araki N, Yamamoto T, Sasaki A.

Brain Behav. 2018 Oct;8(10):e01117. doi: 10.1002/brb3.1117. Epub 2018 Sep 21.

12.

Autopsy case of V180I genetic Creutzfeldt-Jakob disease presenting with early disease pathology.

Iwasaki Y, Kato H, Ando T, Akagi A, Mimuro M, Miyahara H, Kitamoto T, Yoshida M.

Neuropathology. 2018 Dec;38(6):638-645. doi: 10.1111/neup.12516. Epub 2018 Sep 14.

PMID:
30216556
13.

Identification of differentially methylated region (DMR) networks associated with progression of nonalcoholic fatty liver disease.

Hotta K, Kitamoto A, Kitamoto T, Ogawa Y, Honda Y, Kessoku T, Yoneda M, Imajo K, Tomeno W, Saito S, Nakajima A.

Sci Rep. 2018 Sep 11;8(1):13567. doi: 10.1038/s41598-018-31886-5.

14.

PrPres deposition in the retina is a common finding of sporadic, familial and iatrogenic Creutzfeldt-Jakob diseases (CJD).

Takao M, Kimura H, Kitamoto T, Mihara B.

Acta Neuropathol Commun. 2018 Aug 10;6(1):78. doi: 10.1186/s40478-018-0582-5. No abstract available.

15.

Autopsied case of non-plaque-type dura mater graft-associated Creutzfeldt-Jakob disease presenting with extensive amyloid-β deposition.

Iwasaki Y, Imamura K, Iwai K, Kobayashi Y, Akagi A, Mimuro M, Miyahara H, Kitamoto T, Yoshida M.

Neuropathology. 2018 Oct;38(5):549-556. doi: 10.1111/neup.12503. Epub 2018 Aug 6.

PMID:
30084170
16.

A domain responsible for spontaneous conversion of bank vole prion protein.

Kobayashi A, Matsuura Y, Takeuchi A, Yamada M, Miyoshi I, Mohri S, Kitamoto T.

Brain Pathol. 2018 Jul 27. doi: 10.1111/bpa.12638. [Epub ahead of print]

PMID:
30051525
17.

Aldosterone Suppression by Dexamethasone in Patients With KCNJ5-Mutated Aldosterone-Producing Adenoma.

Inoue K, Yamazaki Y, Kitamoto T, Hirose R, Saito J, Omura M, Sasano H, Nishikawa T.

J Clin Endocrinol Metab. 2018 Sep 1;103(9):3477-3485. doi: 10.1210/jc.2018-00738.

PMID:
30020487
18.

Neuroimaging-pathological correlations of [18F]THK5351 PET in progressive supranuclear palsy.

Ishiki A, Harada R, Kai H, Sato N, Totsune T, Tomita N, Watanuki S, Hiraoka K, Ishikawa Y, Funaki Y, Iwata R, Furumoto S, Tashiro M, Sasano H, Kitamoto T, Kudo Y, Yanai K, Furukawa K, Okamura N, Arai H.

Acta Neuropathol Commun. 2018 Jun 29;6(1):53. doi: 10.1186/s40478-018-0556-7.

19.

Immune-mediated acquired lecithin-cholesterol acyltransferase deficiency: A case report and literature review.

Ishibashi R, Takemoto M, Tsurutani Y, Kuroda M, Ogawa M, Wakabayashi H, Uesugi N, Nagata M, Imai N, Hattori A, Sakamoto K, Kitamoto T, Maezawa Y, Narita I, Hiroi S, Furuta A, Miida T, Yokote K.

J Clin Lipidol. 2018 Jul - Aug;12(4):888-897.e2. doi: 10.1016/j.jacl.2018.05.002. Epub 2018 May 15.

PMID:
29937398
20.

Iatrogenic Creutzfeldt-Jakob disease.

Kobayashi A, Kitamoto T, Mizusawa H.

Handb Clin Neurol. 2018;153:207-218. doi: 10.1016/B978-0-444-63945-5.00012-X.

PMID:
29887137
21.

Creutzfeldt-Jakob disease with Alzheimer pathology, presenting with status epilepticus following repeated partial seizures: a case report and literature review.

Miyake K, Hara T, Oshima E, Kawada K, Ishizu H, Yamauchi Y, Satoh K, Kitamoto T, Takenoshita S, Terada S, Yamada N.

BMC Neurol. 2018 Apr 25;18(1):54. doi: 10.1186/s12883-018-1055-y. Review.

22.

Biochemical features of genetic Creutzfeldt-Jakob disease with valine-to-isoleucine substitution at codon 180 on the prion protein gene.

Ito Y, Sanjo N, Hizume M, Kobayashi A, Ohgami T, Satoh K, Hamaguchi T, Yamada M, Kitamoto T, Mizusawa H, Yokota T.

Biochem Biophys Res Commun. 2018 Feb 19;496(4):1055-1061. doi: 10.1016/j.bbrc.2018.01.119. Epub 2018 Jan 31.

PMID:
29382530
23.

Development of a quick bioassay for the evaluation of transmission properties of acquired prion diseases.

Munesue Y, Shimazaki T, Qi Z, Isoda N, Sawa H, Aoshima K, Kimura T, Mohri S, Kitamoto T, Kobayashi A.

Neurosci Lett. 2018 Mar 6;668:43-47. doi: 10.1016/j.neulet.2018.01.014. Epub 2018 Jan 9.

PMID:
29329906
24.

Distinct roles of systemic and local actions of insulin on pancreatic β-cells.

Kitamoto T, Sakurai K, Lee EY, Yokote K, Accili D, Miki T.

Metabolism. 2018 May;82:100-110. doi: 10.1016/j.metabol.2017.12.017. Epub 2018 Jan 7.

PMID:
29320716
25.

Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study.

Cali I, Cohen ML, Haik S, Parchi P, Giaccone G, Collins SJ, Kofskey D, Wang H, McLean CA, Brandel JP, Privat N, Sazdovitch V, Duyckaerts C, Kitamoto T, Belay ED, Maddox RA, Tagliavini F, Pocchiari M, Leschek E, Appleby BS, Safar JG, Schonberger LB, Gambetti P.

Acta Neuropathol Commun. 2018 Jan 8;6(1):5. doi: 10.1186/s40478-017-0503-z.

26.

Pathological progression of genetic Creutzfeldt-Jakob disease with a PrP V180I mutation.

Akagi A, Iwasaki Y, Mimuro M, Kitamoto T, Yamada M, Yoshida M.

Prion. 2018 Jan 2;12(1):54-62. doi: 10.1080/19336896.2017.1414130. Epub 2018 Jan 31.

27.

Area-Specific Regulation of Quiescent Neural Stem Cells by Notch3 in the Adult Mouse Subependymal Zone.

Kawai H, Kawaguchi D, Kuebrich BD, Kitamoto T, Yamaguchi M, Gotoh Y, Furutachi S.

J Neurosci. 2017 Dec 6;37(49):11867-11880. doi: 10.1523/JNEUROSCI.0001-17.2017. Epub 2017 Nov 3.

28.

Evolutionarily Conserved Roles for Blood-Brain Barrier Xenobiotic Transporters in Endogenous Steroid Partitioning and Behavior.

Hindle SJ, Munji RN, Dolghih E, Gaskins G, Orng S, Ishimoto H, Soung A, DeSalvo M, Kitamoto T, Keiser MJ, Jacobson MP, Daneman R, Bainton RJ.

Cell Rep. 2017 Oct 31;21(5):1304-1316. doi: 10.1016/j.celrep.2017.10.026.

29.

Identification of the genomic region under epigenetic regulation during non-alcoholic fatty liver disease progression.

Hotta K, Kitamoto T, Kitamoto A, Ogawa Y, Honda Y, Kessoku T, Yoneda M, Imajo K, Tomeno W, Saito S, Nakajima A.

Hepatol Res. 2018 Feb;48(3):E320-E334. doi: 10.1111/hepr.12992. Epub 2017 Nov 17.

PMID:
29059699
30.

KCNJ5 mutation as a predictor for resolution of hypertension after surgical treatment of aldosterone-producing adenoma.

Kitamoto T, Omura M, Suematsu S, Saito J, Nishikawa T.

J Hypertens. 2018 Mar;36(3):619-627. doi: 10.1097/HJH.0000000000001578.

PMID:
29016532
31.

Clinical findings of a probable case of MM2-cortical-type sporadic Creutzfeldt-Jakob disease with antibodies to anti-N-terminus of α-enolase.

Hayashi Y, Yamada M, Kimura A, Asano T, Satoh K, Kitamoto T, Yoneda M, Inuzuka T.

Prion. 2017 Nov 2;11(6):454-464. doi: 10.1080/19336896.2017.1377876. Epub 2017 Oct 30.

32.

Correlations of 18F-THK5351 PET with Postmortem Burden of Tau and Astrogliosis in Alzheimer Disease.

Harada R, Ishiki A, Kai H, Sato N, Furukawa K, Furumoto S, Tago T, Tomita N, Watanuki S, Hiraoka K, Ishikawa Y, Funaki Y, Nakamura T, Yoshikawa T, Iwata R, Tashiro M, Sasano H, Kitamoto T, Yanai K, Arai H, Kudo Y, Okamura N.

J Nucl Med. 2018 Apr;59(4):671-674. doi: 10.2967/jnumed.117.197426. Epub 2017 Sep 1.

PMID:
28864633
33.

Protective Effect of Val129-PrP against Bovine Spongiform Encephalopathy but not Variant Creutzfeldt-Jakob Disease.

Fernández-Borges N, Espinosa JC, Marín-Moreno A, Aguilar-Calvo P, Asante EA, Kitamoto T, Mohri S, Andréoletti O, Torres JM.

Emerg Infect Dis. 2017 Sep;23(9):1522-1530. doi: 10.3201/eid2309.161948.

34.

An autopsy-verified case of steroid-responsive encephalopathy with convulsion and a false-positive result from the real-time quaking-induced conversion assay.

Hayashi Y, Iwasaki Y, Yoshikura N, Asano T, Mimuro M, Kimura A, Satoh K, Kitamoto T, Yoshida M, Inuzuka T.

Prion. 2017 Jul 4;11(4):284-292. doi: 10.1080/19336896.2017.1345416. Epub 2017 Jul 27.

35.

An autopsy case of Creutzfeldt-Jakob disease with a prion protein gene codon 180 mutation presenting with pathological laughing and an exaggerated startle reaction.

Iwasaki Y, Mori K, Ito M, Akagi A, Mimuro M, Kitamoto T, Yoshida M.

Neuropathology. 2017 Dec;37(6):575-581. doi: 10.1111/neup.12399. Epub 2017 Jul 13.

PMID:
28703419
36.

Viral Population Changes during Murine Norovirus Propagation in RAW 264.7 Cells.

Kitamoto T, Takai-Todaka R, Kato A, Kanamori K, Takagi H, Yoshida K, Katayama K, Nakanishi A.

Front Microbiol. 2017 Jun 15;8:1091. doi: 10.3389/fmicb.2017.01091. eCollection 2017.

37.

Laparoscopic Sleeve Gastrectomy Resolves Low GHRP-2-Stimulated Growth Hormone Levels in Obese Patients.

Ohara E, Tokuyama H, Kitamoto T, Kitahara A, Hayashi A, Hayashi H, Takemoto M, Yokote K.

Obes Surg. 2017 Aug;27(8):2214-2217. doi: 10.1007/s11695-017-2769-4.

PMID:
28623445
38.

An autopsied case of MV2K + C-type sporadic Creutzfeldt-Jakob disease presenting with widespread cerebral cortical involvement and Kuru plaques.

Iwasaki Y, Saito Y, Aiba I, Kobayashi A, Mimuro M, Kitamoto T, Yoshida M.

Neuropathology. 2017 Jun;37(3):241-248. doi: 10.1111/neup.12350. Epub 2016 Nov 7.

PMID:
28568896
39.

Modulation of neuronal activity in the Drosophila mushroom body by DopEcR, a unique dual receptor for ecdysone and dopamine.

Lark A, Kitamoto T, Martin JR.

Biochim Biophys Acta Mol Cell Res. 2017 Oct;1864(10):1578-1588. doi: 10.1016/j.bbamcr.2017.05.015. Epub 2017 May 26. Review.

40.

MM1-type sporadic Creutzfeldt-Jakob disease with 1-month total disease duration and early pathologic indicators.

Iwasaki Y, Kato H, Ando T, Mimuro M, Kitamoto T, Yoshida M.

Neuropathology. 2017 Oct;37(5):420-425. doi: 10.1111/neup.12379. Epub 2017 Apr 12.

PMID:
28402042
41.

Recent Trends in WRN Gene Mutation Patterns in Individuals with Werner Syndrome.

Yamaga M, Takemoto M, Takada-Watanabe A, Koizumi N, Kitamoto T, Sakamoto K, Ishikawa T, Koshizaka M, Maezawa Y, Yokote K.

J Am Geriatr Soc. 2017 Aug;65(8):1853-1856. doi: 10.1111/jgs.14906. Epub 2017 Apr 10.

PMID:
28394436
42.

Outcomes of laparoscopic sleeve gastrectomy in elderly obese Japanese patients.

Hayashi A, Maeda Y, Takemoto M, Tokuyama H, Koide H, Kitahara A, Hayashi H, Kitamoto T, Yamaga M, Kobayashi K, Yokote K.

Geriatr Gerontol Int. 2017 Nov;17(11):2068-2073. doi: 10.1111/ggi.13022. Epub 2017 Mar 30.

PMID:
28371292
43.

Identification of core gene networks and hub genes associated with progression of non-alcoholic fatty liver disease by RNA sequencing.

Hotta K, Kikuchi M, Kitamoto T, Kitamoto A, Ogawa Y, Honda Y, Kessoku T, Kobayashi K, Yoneda M, Imajo K, Tomeno W, Nakaya A, Suzuki Y, Saito S, Nakajima A.

Hepatol Res. 2017 Dec;47(13):1445-1458. doi: 10.1111/hepr.12877. Epub 2017 Mar 29.

PMID:
28219123
44.

Risk factors for the delayed onset of neuropsychologic sequelae following carbon monoxide poisoning.

Kitamoto T, Tsuda M, Kato M, Saito F, Kamijo Y, Kinoshita T.

Acute Med Surg. 2016 Oct;3(4):315-319. doi: 10.1002/ams2.197. Epub 2016 Apr 26.

45.

An autopsy-verified case of FTLD-TDP type A with upper motor neuron-predominant motor neuron disease mimicking MM2-thalamic-type sporadic Creutzfeldt-Jakob disease.

Hayashi Y, Iwasaki Y, Takekoshi A, Yoshikura N, Asano T, Mimuro M, Kimura A, Satoh K, Kitamoto T, Yoshida M, Inuzuka T.

Prion. 2016 Nov;10(6):492-501.

46.

Acute onset of a tonic seizure in a phenytoin-overdosed patient who had taken phenytoin and levetiracetam daily.

Kitamoto T, Nakamori Y, Hayakawa K, Saito F, Kinoshita T.

Chudoku Kenkyu. 2016 Dec;29(4):360-362. English, Japanese.

PMID:
30461233
47.
48.

Lithium-Responsive Seizure-Like Hyperexcitability Is Caused by a Mutation in the Drosophila Voltage-Gated Sodium Channel Gene paralytic.

Kaas GA, Kasuya J, Lansdon P, Ueda A, Iyengar A, Wu CF, Kitamoto T.

eNeuro. 2016 Nov 10;3(5). pii: ENEURO.0221-16.2016. eCollection 2016 Sep-Oct.

49.

Preserved regional cerebral blood flow in the occipital cortices, brainstem, and cerebellum of patients with V180I-129M genetic Creutzfeldt-Jakob disease in serial SPECT studies.

Hayashi Y, Yoshikura N, Takekoshi A, Yamada M, Asano T, Kimura A, Satoh K, Kitamoto T, Inuzuka T.

J Neurol Sci. 2016 Nov 15;370:145-151. doi: 10.1016/j.jns.2016.09.043. Epub 2016 Sep 22.

PMID:
27772745
50.

Mutation of orthologous prickle genes causes a similar epilepsy syndrome in flies and humans.

Ehaideb SN, Wignall EA, Kasuya J, Evans WH, Iyengar A, Koerselman HL, Lilienthal AJ, Bassuk AG, Kitamoto T, Manak JR.

Ann Clin Transl Neurol. 2016 Aug 3;3(9):695-707. doi: 10.1002/acn3.334. eCollection 2016 Sep.

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