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305 results

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Page 1
A de novo dominant-negative variant is associated with OTULIN-related autoinflammatory syndrome.
Takeda Y, Ueki M, Matsuhiro J, Walinda E, Tanaka T, Yamada M, Fujita H, Takezaki S, Kobayashi I, Tamaki S, Nagata S, Miyake N, Matsumoto N, Osawa M, Yasumi T, Heike T, Ohtake F, Saito MK, Toguchida J, Takita J, Ariga T, Iwai K. Takeda Y, et al. Among authors: takita j. J Exp Med. 2024 Jun 3;221(6):e20231941. doi: 10.1084/jem.20231941. Epub 2024 Apr 23. J Exp Med. 2024. PMID: 38652464 Free PMC article.
Functional evaluation of the pathological significance of MEFV variants using induced pluripotent stem cell-derived macrophages.
Shiba T, Tanaka T, Ida H, Watanabe M, Nakaseko H, Osawa M, Shibata H, Izawa K, Yasumi T, Kawasaki Y, Saito MK, Takita J, Heike T, Nishikomori R. Shiba T, et al. Among authors: takita j. J Allergy Clin Immunol. 2019 Nov;144(5):1438-1441.e12. doi: 10.1016/j.jaci.2019.07.039. Epub 2019 Sep 18. J Allergy Clin Immunol. 2019. PMID: 31542286 No abstract available.
Pluripotent stem cell model of Shwachman-Diamond syndrome reveals apoptotic predisposition of hemoangiogenic progenitors.
Hamabata T, Umeda K, Kouzuki K, Tanaka T, Daifu T, Nodomi S, Saida S, Kato I, Baba S, Hiramatsu H, Osawa M, Niwa A, Saito MK, Kamikubo Y, Adachi S, Hashii Y, Shimada A, Watanabe H, Osafune K, Okita K, Nakahata T, Watanabe K, Takita J, Heike T. Hamabata T, et al. Among authors: takita j. Sci Rep. 2020 Sep 9;10(1):14859. doi: 10.1038/s41598-020-71844-8. Sci Rep. 2020. PMID: 32908229 Free PMC article.
Author Correction: Pluripotent stem cell model of Shwachman-Diamond syndrome reveals apoptotic predisposition of hemoangiogenic progenitors.
Hamabata T, Umeda K, Kouzuki K, Tanaka T, Daifu T, Nodomi S, Saida S, Kato I, Baba S, Hiramatsu H, Osawa M, Niwa A, Saito MK, Kamikubo Y, Adachi S, Hashii Y, Shimada A, Watanabe H, Osafune K, Okita K, Nakahata T, Watanabe K, Takita J, Heike T. Hamabata T, et al. Among authors: takita j. Sci Rep. 2021 Jan 18;11(1):2107. doi: 10.1038/s41598-021-81066-1. Sci Rep. 2021. PMID: 33462257 Free PMC article. No abstract available.
Detailed analysis of Japanese patients with adenosine deaminase 2 deficiency reveals characteristic elevation of type II interferon signature and STAT1 hyperactivation.
Nihira H, Izawa K, Ito M, Umebayashi H, Okano T, Kajikawa S, Nanishi E, Keino D, Murakami K, Isa-Nishitani M, Shiba T, Honda Y, Hijikata A, Yasu T, Kubota T, Hasegawa Y, Kawashima Y, Nakano N, Takada H, Ohga S, Heike T, Takita J, Ohara O, Takei S, Takahashi M, Kanegane H, Morio T, Iwaki-Egawa S, Sasahara Y, Nishikomori R, Yasumi T. Nihira H, et al. Among authors: takita j. J Allergy Clin Immunol. 2021 Aug;148(2):550-562. doi: 10.1016/j.jaci.2021.01.018. Epub 2021 Jan 30. J Allergy Clin Immunol. 2021. PMID: 33529688 Clinical Trial.
Rapid Flow Cytometry-Based Assay for the Functional Classification of MEFV Variants.
Honda Y, Maeda Y, Izawa K, Shiba T, Tanaka T, Nakaseko H, Nishimura K, Mukoyama H, Isa-Nishitani M, Miyamoto T, Nihira H, Shibata H, Hiejima E, Ohara O, Takita J, Yasumi T, Nishikomori R. Honda Y, et al. Among authors: takita j. J Clin Immunol. 2021 Aug;41(6):1187-1197. doi: 10.1007/s10875-021-01021-7. Epub 2021 Mar 17. J Clin Immunol. 2021. PMID: 33733382
Augmentation of Stimulator of Interferon Genes-Induced Type I Interferon Production in COPA Syndrome.
Kato T, Yamamoto M, Honda Y, Orimo T, Sasaki I, Murakami K, Hemmi H, Fukuda-Ohta Y, Isono K, Takayama S, Nakamura H, Otsuki Y, Miyamoto T, Takita J, Yasumi T, Nishikomori R, Matsubayashi T, Izawa K, Kaisho T. Kato T, et al. Among authors: takita j. Arthritis Rheumatol. 2021 Nov;73(11):2105-2115. doi: 10.1002/art.41790. Arthritis Rheumatol. 2021. PMID: 33982886
Case Report: A Case of Epstein-Barr Virus-Associated Acute Liver Failure Requiring Hematopoietic Cell Transplantation After Emergent Liver Transplantation.
Nakajima K, Hiejima E, Nihira H, Kato K, Honda Y, Izawa K, Kawabata N, Kato I, Ogawa E, Sonoda M, Okamoto T, Okajima H, Yasumi T, Takita J. Nakajima K, et al. Among authors: takita j. Front Immunol. 2022 Jan 28;13:825806. doi: 10.3389/fimmu.2022.825806. eCollection 2022. Front Immunol. 2022. PMID: 35154146 Free PMC article.
An efficient diagnosis: A patient with X-linked inhibitor of apoptosis protein (XIAP) deficiency in the setting of infantile hemophagocytic lymphohistiocytosis was diagnosed using high serum interleukin-18 combined with common laboratory parameters.
Higuchi T, Izawa K, Miyamoto T, Honda Y, Nishiyama A, Shimizu M, Takita J, Yasumi T. Higuchi T, et al. Among authors: takita j. Pediatr Blood Cancer. 2022 Aug;69(8):e29606. doi: 10.1002/pbc.29606. Epub 2022 Feb 21. Pediatr Blood Cancer. 2022. PMID: 35187790 No abstract available.
305 results