Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

3,847 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
[Girl with IPEX syndrome with low expression of Foxp3].
Horiuchi S, Ishiguro A, Nakagawa T, Shoji K, Nagai A, Arai K, Horikawa R, Kawai T, Watanabe N, Onodera M. Horiuchi S, et al. Among authors: kawai t. Nihon Rinsho Meneki Gakkai Kaishi. 2012;35(6):526-32. doi: 10.2177/jsci.35.526. Nihon Rinsho Meneki Gakkai Kaishi. 2012. PMID: 23291488 Free article. Japanese.
Two novel gain-of-function mutations of STAT1 responsible for chronic mucocutaneous candidiasis disease: impaired production of IL-17A and IL-22, and the presence of anti-IL-17F autoantibody.
Yamazaki Y, Yamada M, Kawai T, Morio T, Onodera M, Ueki M, Watanabe N, Takada H, Takezaki S, Chida N, Kobayashi I, Ariga T. Yamazaki Y, et al. Among authors: kawai t. J Immunol. 2014 Nov 15;193(10):4880-7. doi: 10.4049/jimmunol.1401467. Epub 2014 Oct 6. J Immunol. 2014. PMID: 25288569
Thymitis in chronic granulomatous disease.
Kanamori K, Tamura E, Onodera M, Ishiguro A, Kawai T. Kanamori K, et al. Among authors: kawai t. Pediatr Int. 2019 Apr;61(4):429-431. doi: 10.1111/ped.13810. Epub 2019 Apr 14. Pediatr Int. 2019. PMID: 30983070 No abstract available.
Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet's disease.
Tsuchida N, Kirino Y, Soejima Y, Onodera M, Arai K, Tamura E, Ishikawa T, Kawai T, Uchiyama T, Nomura S, Kobayashi D, Taguri M, Mitsuhashi S, Mizuguchi T, Takata A, Miyake N, Nakajima H, Miyatake S, Matsumoto N. Tsuchida N, et al. Among authors: kawai t. Arthritis Res Ther. 2019 Jun 4;21(1):137. doi: 10.1186/s13075-019-1928-5. Arthritis Res Ther. 2019. PMID: 31164164 Free PMC article.
3,847 results