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Items: 1 to 50 of 108

1.

Tissue-type plasminogen activator-primed human iPSC-derived neural progenitor cells promote motor recovery after severe spinal cord injury.

Shiga Y, Shiga A, Mesci P, Kwon H, Brifault C, Kim JH, Jeziorski JJ, Nasamran C, Ohtori S, Muotri AR, Gonias SL, Campana WM.

Sci Rep. 2019 Dec 17;9(1):19291. doi: 10.1038/s41598-019-55132-8.

2.

An extraskeletal osteosarcoma in the auricle of a Wistar Hannover rat.

Shiga A, Katoh Y, Ito T, Ohnuma-Koyama A, Takahashi N, Okazaki Y, Harada T.

J Toxicol Pathol. 2019 Jul;32(3):181-187. doi: 10.1293/tox.2018-0046. Epub 2019 Apr 15.

3.

Spontaneous malignant myoid thymoma in an aged female Fischer 344 rat.

Katoh Y, Ito T, Shimada Y, Ohnuma-Koyama A, Takahashi N, Okazaki Y, Shiga A, Kuwahara M, Yoshida T, Harada T.

J Toxicol Pathol. 2018 Apr;31(2):135-139. doi: 10.1293/tox.2017-0045. Epub 2017 Dec 23.

4.

Successful Post-Transplant Psychiatric Interventions During Long-Term Follow-Up of Patients Receiving Liver Transplants for Alcoholic Liver Disease.

Kimura H, Onishi Y, Kishi S, Kurata N, Ogiso S, Kamei H, Tsuboi C, Yamaguchi N, Shiga A, Kondo M, Yokoyama Y, Takasato F, Fujishiro H, Ishizuka K, Okada T, Ogura Y, Ozaki N.

Am J Case Rep. 2017 Nov 16;18:1215-1219.

5.

Prednisolone-responsive Postpartum IgG4-related Hypophysitis.

Koide H, Shiga A, Komai E, Yamato A, Fujimoto M, Tamura A, Kono T, Nakayama A, Takiguchi T, Higuchi S, Sakuma I, Nagano H, Hashimoto N, Suzuki S, Takeda Y, Shibuya M, Nishioka H, Yamada S, Inoshita N, Ishiwatari N, Horiguchi K, Yokote K, Tanaka T.

Intern Med. 2018 Feb 1;57(3):367-375. doi: 10.2169/internalmedicine.8446-16. Epub 2017 Nov 1.

6.

Multihormonal pituitary adenoma concomitant with Pit-1 and Tpit lineage cells causing acromegaly associated with subclinical Cushing's disease: a case report.

Takiguchi T, Koide H, Nagano H, Nakayama A, Fujimoto M, Tamura A, Komai E, Shiga A, Kono T, Higuchi S, Sakuma I, Hashimoto N, Suzuki S, Miyabayashi Y, Ishiwatari N, Horiguchi K, Nakatani Y, Yokote K, Tanaka T.

BMC Endocr Disord. 2017 Sep 2;17(1):54. doi: 10.1186/s12902-017-0203-5.

7.

SEVEN FAMILIAL DYSALBUMINEMIC HYPERTHYROXINEMIA CASES IN THREE UNRELATED JAPANESE FAMILIES AND HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY ANALYSIS OF THE THYROXINE BINDING PROFILE.

Nagano H, Nakagawa Y, Ishikawa N, Watanabe H, Miyabayashi Y, Nakayama A, Fujimoto M, Komai E, Shiga A, Tamura A, Kono T, Takiguchi T, Higuchi S, Sakuma I, Hashimoto N, Suzuki S, Koide H, Yokote K, Tanaka T.

Endocr Pract. 2017 Nov;23(11):1325-1332. doi: 10.4158/EP171964.OR. Epub 2017 Aug 17.

PMID:
28816534
8.

A spontaneous myoepithelial carcinoma in the mammary gland of an aged female ICR (CD-1) mouse.

Ito T, Yoshida T, Soma K, Katoh Y, Shimada Y, Ohnuma-Koyama A, Takahashi N, Okazaki Y, Shiga A, Kuwahara M, Harada T.

J Toxicol Pathol. 2017 Jul;30(3):245-250. doi: 10.1293/tox.2016-0080. Epub 2017 Apr 27.

9.

Determination of the positions of aluminum atoms introduced into SSZ-35 and the catalytic properties of the generated Brønsted acid sites.

Miyaji A, Kimura N, Shiga A, Hayashi Y, Nishitoba T, Motokura K, Baba T.

Phys Chem Chem Phys. 2017 Mar 1;19(9):6508-6518. doi: 10.1039/c6cp08143f.

PMID:
28197567
10.

Experimental and computational studies of the roles of MgO and Zn in talc for the selective formation of 1,3-butadiene in the conversion of ethanol.

Hayashi Y, Akiyama S, Miyaji A, Sekiguchi Y, Sakamoto Y, Shiga A, Koyama TR, Motokura K, Baba T.

Phys Chem Chem Phys. 2016 Sep 14;18(36):25191-25209.

PMID:
27711446
11.

Familial amyotrophic lateral sclerosis with an I104F mutation in the SOD1 gene: Multisystem degeneration with neurofilamentous aggregates and SOD1 inclusions.

Jiang H, Shimizu H, Shiga A, Tanaka M, Onodera O, Kakita A, Takahashi H.

Neuropathology. 2017 Feb;37(1):69-77. doi: 10.1111/neup.12324. Epub 2016 Jul 22.

PMID:
27444855
12.

Heterogeneity of cerebral TDP-43 pathology in sporadic amyotrophic lateral sclerosis: Evidence for clinico-pathologic subtypes.

Takeuchi R, Tada M, Shiga A, Toyoshima Y, Konno T, Sato T, Nozaki H, Kato T, Horie M, Shimizu H, Takebayashi H, Onodera O, Nishizawa M, Kakita A, Takahashi H.

Acta Neuropathol Commun. 2016 Jun 23;4(1):61. doi: 10.1186/s40478-016-0335-2.

13.

Increased cytoplasmic TARDBP mRNA in affected spinal motor neurons in ALS caused by abnormal autoregulation of TDP-43.

Koyama A, Sugai A, Kato T, Ishihara T, Shiga A, Toyoshima Y, Koyama M, Konno T, Hirokawa S, Yokoseki A, Nishizawa M, Kakita A, Takahashi H, Onodera O.

Nucleic Acids Res. 2016 Jul 8;44(12):5820-36. doi: 10.1093/nar/gkw499. Epub 2016 Jun 2.

14.

Distinct molecular mechanisms of HTRA1 mutants in manifesting heterozygotes with CARASIL.

Nozaki H, Kato T, Nihonmatsu M, Saito Y, Mizuta I, Noda T, Koike R, Miyazaki K, Kaito M, Ito S, Makino M, Koyama A, Shiga A, Uemura M, Sekine Y, Murakami A, Moritani S, Hara K, Yokoseki A, Kuwano R, Endo N, Momotsu T, Yoshida M, Nishizawa M, Mizuno T, Onodera O.

Neurology. 2016 May 24;86(21):1964-74. doi: 10.1212/WNL.0000000000002694. Epub 2016 Apr 27.

PMID:
27164673
15.

Cushing Syndrome Due to ACTH-Secreting Pheochromocytoma, Aggravated by Glucocorticoid-Driven Positive-Feedback Loop.

Sakuma I, Higuchi S, Fujimoto M, Takiguchi T, Nakayama A, Tamura A, Kohno T, Komai E, Shiga A, Nagano H, Hashimoto N, Suzuki S, Mayama T, Koide H, Ono K, Sasano H, Tatsuno I, Yokote K, Tanaka T.

J Clin Endocrinol Metab. 2016 Mar;101(3):841-6. doi: 10.1210/jc.2015-2855. Epub 2015 Dec 23.

16.

GERMLINE DELETION OF ARMC5 IN FAMILIAL PRIMARY MACRONODULAR ADRENAL HYPERPLASIA.

Suzuki S, Tatsuno I, Oohara E, Nakayama A, Komai E, Shiga A, Kono T, Takiguchi T, Higuchi S, Sakuma I, Nagano H, Hashimoto N, Mayama T, Koide H, Sasano H, Nakatani Y, Imamoto T, Ichikawa T, Yokote K, Tanaka T.

Endocr Pract. 2015 Oct;21(10):1152-60. doi: 10.4158/EP15756.OR. Epub 2015 Jul 27.

PMID:
26214113
17.

Comet assay evaluation of six chemicals of known genotoxic potential in rats.

Hobbs CA, Recio L, Streicker M, Boyle MH, Tanaka J, Shiga A, Witt KL.

Mutat Res Genet Toxicol Environ Mutagen. 2015 Jul;786-788:172-81. doi: 10.1016/j.mrgentox.2015.03.003. Epub 2015 Mar 7.

18.

Pathological and Clinical Spectrum of Progressive Supranuclear Palsy: With Special Reference to Astrocytic Tau Pathology.

Yokoyama Y, Toyoshima Y, Shiga A, Tada M, Kitamura H, Hasegawa K, Onodera O, Ikeuchi T, Someya T, Nishizawa M, Kakita A, Takahashi H.

Brain Pathol. 2016 Mar;26(2):155-66. doi: 10.1111/bpa.12265. Epub 2015 Jun 4.

PMID:
25974705
19.
20.

Globular Glial Mixed Four Repeat Tau and TDP-43 Proteinopathy with Motor Neuron Disease and Frontotemporal Dementia.

Takeuchi R, Toyoshima Y, Tada M, Tanaka H, Shimizu H, Shiga A, Miura T, Aoki K, Aikawa A, Ishizawa S, Ikeuchi T, Nishizawa M, Kakita A, Takahashi H.

Brain Pathol. 2016 Jan;26(1):82-94. doi: 10.1111/bpa.12262. Epub 2015 May 19.

PMID:
25787090
21.

Left jugular phlebectasia in an elderly patient.

Tanigawa T, Shibata R, Shiga A, Murohara T.

Circulation. 2014 Oct 14;130(16):1416-7. doi: 10.1161/CIRCULATIONAHA.114.012357. No abstract available.

PMID:
25311620
22.

C9ORF72 repeat-associated non-ATG-translated polypeptides are distributed independently of TDP-43 in a Japanese patient with c9ALS.

Konno T, Tada M, Shiga A, Tsujino A, Eguchi H, Masuda-Suzukake M, Hasegawa M, Nishizawa M, Onodera O, Kakita A, Takahashi H.

Neuropathol Appl Neurobiol. 2014 Oct;40(6):783-8. doi: 10.1111/nan.12157. No abstract available.

PMID:
24861677
23.

Minor splicing pathway is not minor any more: implications for the pathogenesis of motor neuron diseases.

Onodera O, Ishihara T, Shiga A, Ariizumi Y, Yokoseki A, Nishizawa M.

Neuropathology. 2014 Feb;34(1):99-107. doi: 10.1111/neup.12070. Epub 2013 Sep 22. Review.

PMID:
24112438
24.

Inhibition of SMG-8, a subunit of SMG-1 kinase, ameliorates nonsense-mediated mRNA decay-exacerbated mutant phenotypes without cytotoxicity.

Usuki F, Yamashita A, Shiraishi T, Shiga A, Onodera O, Higuchi I, Ohno S.

Proc Natl Acad Sci U S A. 2013 Sep 10;110(37):15037-42. doi: 10.1073/pnas.1300654110. Epub 2013 Aug 27.

25.

Sporadic ALS with compound heterozygous mutations in the SQSTM1 gene.

Shimizu H, Toyoshima Y, Shiga A, Yokoseki A, Arakawa K, Sekine Y, Shimohata T, Ikeuchi T, Nishizawa M, Kakita A, Onodera O, Takahashi H.

Acta Neuropathol. 2013 Sep;126(3):453-9. doi: 10.1007/s00401-013-1150-5. Epub 2013 Jun 28.

PMID:
23812289
26.

Decreased number of Gemini of coiled bodies and U12 snRNA level in amyotrophic lateral sclerosis.

Ishihara T, Ariizumi Y, Shiga A, Kato T, Tan CF, Sato T, Miki Y, Yokoo M, Fujino T, Koyama A, Yokoseki A, Nishizawa M, Kakita A, Takahashi H, Onodera O.

Hum Mol Genet. 2013 Oct 15;22(20):4136-47. doi: 10.1093/hmg/ddt262. Epub 2013 Jun 4.

PMID:
23740936
27.

Transportin 1 accumulates in FUS inclusions in adult-onset ALS without FUS mutation.

Takeuchi R, Toyoshima Y, Tada M, Shiga A, Tanaka H, Shimohata M, Kimura K, Morita T, Kakita A, Nishizawa M, Takahashi H.

Neuropathol Appl Neurobiol. 2013 Aug;39(5):580-4. doi: 10.1111/nan.12022. No abstract available.

PMID:
23362988
28.

Malignant peripheral nerve sheath tumor of the trigeminal nerve: clinicopathologic features in a young adult patient.

Nakayama Y, Watanabe M, Suzuki K, Usuda H, Emura I, Ogura R, Shiga A, Toyoshima Y, Takahashi H, Kawaguchi T, Kakita A.

Neuropathology. 2013 Oct;33(5):541-6. doi: 10.1111/neup.12004. Epub 2012 Dec 21.

PMID:
23279368
29.

Japanese amyotrophic lateral sclerosis patients with GGGGCC hexanucleotide repeat expansion in C9ORF72.

Konno T, Shiga A, Tsujino A, Sugai A, Kato T, Kanai K, Yokoseki A, Eguchi H, Kuwabara S, Nishizawa M, Takahashi H, Onodera O.

J Neurol Neurosurg Psychiatry. 2013 Apr;84(4):398-401. doi: 10.1136/jnnp-2012-302272. Epub 2012 Sep 25.

PMID:
23012445
30.

Cerebral astroblastoma in an adult: an immunohistochemical, ultrastructural and genetic study.

Fu YJ, Taniguchi Y, Takeuchi S, Shiga A, Okamoto K, Hirato J, Nobusawa S, Nakazato Y, Kakita A, Takahashi H.

Neuropathology. 2013 Jun;33(3):312-9. doi: 10.1111/j.1440-1789.2012.01351.x. Epub 2012 Sep 21.

PMID:
22994361
31.

Suppressed expression of autophagosomal protein LC3 in cortical tubers of tuberous sclerosis complex.

Miyahara H, Natsumeda M, Shiga A, Aoki H, Toyoshima Y, Zheng Y, Takeuchi R, Murakami H, Masuda H, Kameyama S, Izumi T, Fujii Y, Takahashi H, Kakita A.

Brain Pathol. 2013 May;23(3):254-62. doi: 10.1111/j.1750-3639.2012.00634.x. Epub 2012 Oct 23.

PMID:
22974335
32.

Alteration of POLDIP3 splicing associated with loss of function of TDP-43 in tissues affected with ALS.

Shiga A, Ishihara T, Miyashita A, Kuwabara M, Kato T, Watanabe N, Yamahira A, Kondo C, Yokoseki A, Takahashi M, Kuwano R, Kakita A, Nishizawa M, Takahashi H, Onodera O.

PLoS One. 2012;7(8):e43120. doi: 10.1371/journal.pone.0043120. Epub 2012 Aug 10.

33.

Coexistence of Huntington's disease and amyotrophic lateral sclerosis: a clinicopathologic study.

Tada M, Coon EA, Osmand AP, Kirby PA, Martin W, Wieler M, Shiga A, Shirasaki H, Tada M, Makifuchi T, Yamada M, Kakita A, Nishizawa M, Takahashi H, Paulson HL.

Acta Neuropathol. 2012 Nov;124(5):749-60. doi: 10.1007/s00401-012-1005-5. Epub 2012 Jun 27.

34.

Study on the pathogenesis of foreign body granulomatous inflammation in the livers of sprague-dawley rats.

Shiga A, Ota Y, Ueda Y, Hosoi M, Miyajima R, Hasegawa K, Mizuhashi F.

J Toxicol Pathol. 2010 Dec;23(4):253-60. doi: 10.1293/tox.23.253. Epub 2010 Dec 16.

35.

Primary lateral sclerosis: upper-motor-predominant amyotrophic lateral sclerosis with frontotemporal lobar degeneration--immunohistochemical and biochemical analyses of TDP-43.

Kosaka T, Fu YJ, Shiga A, Ishidaira H, Tan CF, Tani T, Koike R, Onodera O, Nishizawa M, Kakita A, Takahashi H.

Neuropathology. 2012 Aug;32(4):373-84. doi: 10.1111/j.1440-1789.2011.01271.x. Epub 2011 Nov 21.

PMID:
22098653
36.

[FTLD/ALS as TDP-43 proteinopathies].

Ishihara T, Ariizumi Y, Shiga A, Yokoseki A, Sato T, Toyoshima Y, Kakita A, Takahashi H, Nishizawa M, Onodera O.

Rinsho Shinkeigaku. 2010 Nov;50(11):1022-4. Review. Japanese.

PMID:
21921552
37.

Genotype-phenotype correlations in early onset ataxia with ocular motor apraxia and hypoalbuminaemia.

Yokoseki A, Ishihara T, Koyama A, Shiga A, Yamada M, Suzuki C, Sekijima Y, Maruta K, Tsuchiya M, Date H, Sato T, Tada M, Ikeuchi T, Tsuji S, Nishizawa M, Onodera O.

Brain. 2011 May;134(Pt 5):1387-99. doi: 10.1093/brain/awr069. Epub 2011 Apr 12.

PMID:
21486904
38.

A novel mutation in the HTRA1 gene causes CARASIL without alopecia.

Nishimoto Y, Shibata M, Nihonmatsu M, Nozaki H, Shiga A, Shirata A, Yamane K, Kosakai A, Takahashi K, Nishizawa M, Onodera O, Suzuki N.

Neurology. 2011 Apr 12;76(15):1353-5. doi: 10.1212/WNL.0b013e318215281d. No abstract available.

PMID:
21482952
39.

Visualization of endolymphatic hydrops after administration of a standard dose of an intravenous gadolinium-based contrast agent.

Tanigawa T, Tamaki T, Yamamuro O, Tanaka H, Nonoyama H, Shiga A, Sato T, Ueda H.

Acta Otolaryngol. 2011 Jun;131(6):596-601. doi: 10.3109/00016489.2010.548402. Epub 2011 Feb 25.

PMID:
21351819
40.

Cerebral small-vessel disease protein HTRA1 controls the amount of TGF-β1 via cleavage of proTGF-β1.

Shiga A, Nozaki H, Yokoseki A, Nihonmatsu M, Kawata H, Kato T, Koyama A, Arima K, Ikeda M, Katada S, Toyoshima Y, Takahashi H, Tanaka A, Nakano I, Ikeuchi T, Nishizawa M, Onodera O.

Hum Mol Genet. 2011 May 1;20(9):1800-10. doi: 10.1093/hmg/ddr063. Epub 2011 Feb 14.

PMID:
21320870
41.

Congenital cutaneous fibropapillomatosis with no evidence of papillomavirus infection in a piglet.

Nishiyama S, Akiba Y, Kobayashi Y, Shiga A, Kamiie J, Shirota K.

J Vet Med Sci. 2011 Feb;73(2):283-5. Epub 2010 Oct 12.

42.

[Molecular pathogenesis of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy].

Shiga A, Nozaki H, Nishizawa M, Onodera O.

Brain Nerve. 2010 Jun;62(6):595-9. Review. Japanese.

PMID:
20548119
43.

An epidemiological survey on pigs showing symptoms of infectious enteric diseases and dyspepsia in Japan.

Ushida K, Kishimoto A, Piao SJ, Itoh M, Shiga A, Nakanishi N, Tsukahara T.

Anim Sci J. 2009 Oct;80(5):556-61. doi: 10.1111/j.1740-0929.2009.00671.x.

PMID:
20163620
44.

Identification of independent APP locus duplication in Japanese patients with early-onset Alzheimer disease.

Kasuga K, Shimohata T, Nishimura A, Shiga A, Mizuguchi T, Tokunaga J, Ohno T, Miyashita A, Kuwano R, Matsumoto N, Onodera O, Nishizawa M, Ikeuchi T.

J Neurol Neurosurg Psychiatry. 2009 Sep;80(9):1050-2. doi: 10.1136/jnnp.2008.161703.

PMID:
19684239
45.

Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease.

Hara K, Shiga A, Fukutake T, Nozaki H, Miyashita A, Yokoseki A, Kawata H, Koyama A, Arima K, Takahashi T, Ikeda M, Shiota H, Tamura M, Shimoe Y, Hirayama M, Arisato T, Yanagawa S, Tanaka A, Nakano I, Ikeda S, Yoshida Y, Yamamoto T, Ikeuchi T, Kuwano R, Nishizawa M, Tsuji S, Onodera O.

N Engl J Med. 2009 Apr 23;360(17):1729-39. doi: 10.1056/NEJMoa0801560.

46.

Spontaneous ganglioneuroma possibly originating from the trigeminal ganglion in a B6C3F1 mouse.

Yasui Y, Ohta Y, Ueda Y, Hasegawa K, Kihara T, Hosoi M, Miyajima R, Shiga A, Imai K, Toyoda K.

Toxicol Pathol. 2009 Apr;37(3):343-7. doi: 10.1177/0192623309333786.

PMID:
19380843
47.

Prominent psychiatric symptoms and glucose hypometabolism in a family with a SNCA duplication.

Uchiyama T, Ikeuchi T, Ouchi Y, Sakamoto M, Kasuga K, Shiga A, Suzuki M, Ito M, Atsumi T, Shimizu T, Ohashi T.

Neurology. 2008 Oct 14;71(16):1289-91. doi: 10.1212/01.wnl.0000327607.28928.e6. No abstract available.

PMID:
18852445
48.

Total deletion and a missense mutation of ITPR1 in Japanese SCA15 families.

Hara K, Shiga A, Nozaki H, Mitsui J, Takahashi Y, Ishiguro H, Yomono H, Kurisaki H, Goto J, Ikeuchi T, Tsuji S, Nishizawa M, Onodera O.

Neurology. 2008 Aug 19;71(8):547-51. doi: 10.1212/01.wnl.0000311277.71046.a0. Epub 2008 Jun 25.

PMID:
18579805
49.

TDP-43 mutation in familial amyotrophic lateral sclerosis.

Yokoseki A, Shiga A, Tan CF, Tagawa A, Kaneko H, Koyama A, Eguchi H, Tsujino A, Ikeuchi T, Kakita A, Okamoto K, Nishizawa M, Takahashi H, Onodera O.

Ann Neurol. 2008 Apr;63(4):538-42. doi: 10.1002/ana.21392.

PMID:
18438952
50.

Patients homozygous and heterozygous for SNCA duplication in a family with parkinsonism and dementia.

Ikeuchi T, Kakita A, Shiga A, Kasuga K, Kaneko H, Tan CF, Idezuka J, Wakabayashi K, Onodera O, Iwatsubo T, Nishizawa M, Takahashi H, Ishikawa A.

Arch Neurol. 2008 Apr;65(4):514-9. doi: 10.1001/archneur.65.4.514.

PMID:
18413475

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