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Ubiquitination of DNA Damage-Stalled RNAPII Promotes Transcription-Coupled Repair.
Nakazawa Y, Hara Y, Oka Y, Komine O, van den Heuvel D, Guo C, Daigaku Y, Isono M, He Y, Shimada M, Kato K, Jia N, Hashimoto S, Kotani Y, Miyoshi Y, Tanaka M, Sobue A, Mitsutake N, Suganami T, Masuda A, Ohno K, Nakada S, Mashimo T, Yamanaka K, Luijsterburg MS, Ogi T. Nakazawa Y, et al. Among authors: ogi t. Cell. 2020 Mar 19;180(6):1228-1244.e24. doi: 10.1016/j.cell.2020.02.010. Epub 2020 Mar 5. Cell. 2020. PMID: 32142649 Free article.
NUS1 mutation in a family with epilepsy, cerebellar ataxia, and tremor.
Araki K, Nakamura R, Ito D, Kato K, Iguchi Y, Sahashi K, Toyama M, Hamada K, Okamoto N, Wada Y, Nakamura T, Ogi T, Katsuno M. Araki K, et al. Among authors: ogi t. Epilepsy Res. 2020 Aug;164:106371. doi: 10.1016/j.eplepsyres.2020.106371. Epub 2020 May 22. Epilepsy Res. 2020. PMID: 32485575
Astrocytic phagocytosis is a compensatory mechanism for microglial dysfunction.
Konishi H, Okamoto T, Hara Y, Komine O, Tamada H, Maeda M, Osako F, Kobayashi M, Nishiyama A, Kataoka Y, Takai T, Udagawa N, Jung S, Ozato K, Tamura T, Tsuda M, Yamanaka K, Ogi T, Sato K, Kiyama H. Konishi H, et al. Among authors: ogi t. EMBO J. 2020 Nov 16;39(22):e104464. doi: 10.15252/embj.2020104464. Epub 2020 Sep 22. EMBO J. 2020. PMID: 32959911 Free PMC article.
The wide-ranging clinical and genetic features in Japanese families with valosin-containing protein proteinopathy.
Ando T, Nakamura R, Kuru S, Yokoi D, Atsuta N, Koike H, Suzuki M, Hara K, Iguchi Y, Harada Y, Yoshida Y, Hattori M, Murakami A, Noda S, Kimura S, Sone J, Nakamura T, Goto Y, Mano K, Okada H, Okuda S, Nishino I, Ogi T, Sobue G, Katsuno M. Ando T, et al. Among authors: ogi t. Neurobiol Aging. 2021 Apr;100:120.e1-120.e6. doi: 10.1016/j.neurobiolaging.2020.10.028. Epub 2020 Nov 14. Neurobiol Aging. 2021. PMID: 33339634
Metabolome and transcriptome analysis on muscle of sporadic inclusion body myositis.
Murakami A, Noda S, Kazuta T, Hirano S, Kimura S, Nakanishi H, Matsuo K, Tsujikawa K, Iida M, Koike H, Sakamoto K, Hara Y, Kuru S, Kadomatsu K, Shimamura T, Ogi T, Katsuno M. Murakami A, et al. Among authors: ogi t. Ann Clin Transl Neurol. 2022 Oct;9(10):1602-1615. doi: 10.1002/acn3.51657. Epub 2022 Sep 15. Ann Clin Transl Neurol. 2022. PMID: 36107781 Free PMC article.
A case of non-immune hydrops fetalis with maternal mirror syndrome diagnosed by trio-based exome sequencing: An autopsy case report and literature review.
Tano S, Kotani T, Yoshihara M, Nakamura N, Matsuo S, Ushida T, Imai K, Ito M, Oka Y, Sato E, Hayashi S, Ogi T, Kajiyama H. Tano S, et al. Among authors: ogi t. Mol Genet Metab Rep. 2022 Oct 14;33:100925. doi: 10.1016/j.ymgmr.2022.100925. eCollection 2022 Dec. Mol Genet Metab Rep. 2022. PMID: 36274670 Free PMC article.
Lysosomal cholesterol overload in macrophages promotes liver fibrosis in a mouse model of NASH.
Itoh M, Tamura A, Kanai S, Tanaka M, Kanamori Y, Shirakawa I, Ito A, Oka Y, Hidaka I, Takami T, Honda Y, Maeda M, Saito Y, Murata Y, Matozaki T, Nakajima A, Kataoka Y, Ogi T, Ogawa Y, Suganami T. Itoh M, et al. Among authors: ogi t. J Exp Med. 2023 Nov 6;220(11):e20220681. doi: 10.1084/jem.20220681. Epub 2023 Sep 19. J Exp Med. 2023. PMID: 37725372 Free PMC article.
237 results