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662 results

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Human and mouse single-nucleus transcriptomics reveal TREM2-dependent and TREM2-independent cellular responses in Alzheimer's disease.
Zhou Y, Song WM, Andhey PS, Swain A, Levy T, Miller KR, Poliani PL, Cominelli M, Grover S, Gilfillan S, Cella M, Ulland TK, Zaitsev K, Miyashita A, Ikeuchi T, Sainouchi M, Kakita A, Bennett DA, Schneider JA, Nichols MR, Beausoleil SA, Ulrich JD, Holtzman DM, Artyomov MN, Colonna M. Zhou Y, et al. Among authors: kakita a. Nat Med. 2020 Jan;26(1):131-142. doi: 10.1038/s41591-019-0695-9. Epub 2020 Jan 13. Nat Med. 2020. PMID: 31932797 Free PMC article.
Genetic association of CTNNA3 with late-onset Alzheimer's disease in females.
Miyashita A, Arai H, Asada T, Imagawa M, Matsubara E, Shoji M, Higuchi S, Urakami K, Kakita A, Takahashi H, Toyabe S, Akazawa K, Kanazawa I, Ihara Y, Kuwano R; Japanese Genetic Study Consortium for Alzeheimer's Disease. Miyashita A, et al. Among authors: kakita a. Hum Mol Genet. 2007 Dec 1;16(23):2854-69. doi: 10.1093/hmg/ddm244. Epub 2007 Aug 30. Hum Mol Genet. 2007. PMID: 17761686
Enhanced accumulation of phosphorylated alpha-synuclein and elevated beta-amyloid 42/40 ratio caused by expression of the presenilin-1 deltaT440 mutant associated with familial Lewy body disease and variant Alzheimer's disease.
Kaneko H, Kakita A, Kasuga K, Nozaki H, Ishikawa A, Miyashita A, Kuwano R, Ito G, Iwatsubo T, Takahashi H, Nishizawa M, Onodera O, Sisodia SS, Ikeuchi T. Kaneko H, et al. Among authors: kakita a. J Neurosci. 2007 Nov 28;27(48):13092-7. doi: 10.1523/JNEUROSCI.4244-07.2007. J Neurosci. 2007. PMID: 18045903 Free PMC article.
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. Yokoseki A, et al. Among authors: kakita a. Ann Neurol. 2008 Apr;63(4):538-42. doi: 10.1002/ana.21392. Ann Neurol. 2008. PMID: 18438952
Genetic association study on in and around the APOE in late-onset Alzheimer disease in Japanese.
Takei N, Miyashita A, Tsukie T, Arai H, Asada T, Imagawa M, Shoji M, Higuchi S, Urakami K, Kimura H, Kakita A, Takahashi H, Tsuji S, Kanazawa I, Ihara Y, Odani S, Kuwano R; Japanese Genetic Study Consortium for Alzheimer Disease. Takei N, et al. Among authors: kakita a. Genomics. 2009 May;93(5):441-8. doi: 10.1016/j.ygeno.2009.01.003. Epub 2009 Feb 3. Genomics. 2009. PMID: 19442637 Free article.
Sporadic four-repeat tauopathy with frontotemporal lobar degeneration, Parkinsonism, and motor neuron disease: a distinct clinicopathological and biochemical disease entity.
Fu YJ, Nishihira Y, Kuroda S, Toyoshima Y, Ishihara T, Shinozaki M, Miyashita A, Piao YS, Tan CF, Tani T, Koike R, Iwanaga K, Tsujihata M, Onodera O, Kuwano R, Nishizawa M, Kakita A, Ikeuchi T, Takahashi H. Fu YJ, et al. Among authors: kakita a. Acta Neuropathol. 2010 Jul;120(1):21-32. doi: 10.1007/s00401-010-0649-2. Epub 2010 Feb 7. Acta Neuropathol. 2010. PMID: 20140439
Increased levels of soluble LR11 in cerebrospinal fluid of patients with Alzheimer disease.
Ikeuchi T, Hirayama S, Miida T, Fukamachi I, Tokutake T, Ebinuma H, Takubo K, Kaneko H, Kasuga K, Kakita A, Takahashi H, Bujo H, Saito Y, Nishizawa M. Ikeuchi T, et al. Among authors: kakita a. Dement Geriatr Cogn Disord. 2010;30(1):28-32. doi: 10.1159/000315539. Epub 2010 Jul 30. Dement Geriatr Cogn Disord. 2010. PMID: 20689279
662 results