Saito MK - Search Results

1

Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency.

Boisson B, Honda Y, Ajiro M, Bustamante J, Bendavid M, Gennery AR, Kawasaki Y, Ichishima J, Osawa M, Nihira H, Shiba T, Tanaka T, Chrabieh M, Bigio B, Hur H, Itan Y, Liang Y, Okada S, Izawa K, Nishikomori R, Ohara O, Heike T, Abel L, Puel A, Saito MK, Casanova JL, Hagiwara M, Yasumi T. Boisson B, et al. Among authors: saito mk. J Clin Invest. 2019 Feb 1;129(2):583-597. doi: 10.1172/JCI124011. Epub 2018 Dec 18. J Clin Invest. 2019. PMID: 30422821 Free PMC article.

2

Somatic mosaicism of CIAS1 in a patient with chronic infantile neurologic, cutaneous, articular syndrome.

Saito M, Fujisawa A, Nishikomori R, Kambe N, Nakata-Hizume M, Yoshimoto M, Ohmori K, Okafuji I, Yoshioka T, Kusunoki T, Miyachi Y, Heike T, Nakahata T. Saito M, et al. Arthritis Rheum. 2005 Nov;52(11):3579-85. doi: 10.1002/art.21404. Arthritis Rheum. 2005. PMID: 16255047 Free article.

3

Disease-associated mutations in CIAS1 induce cathepsin B-dependent rapid cell death of human THP-1 monocytic cells.

Fujisawa A, Kambe N, Saito M, Nishikomori R, Tanizaki H, Kanazawa N, Adachi S, Heike T, Sagara J, Suda T, Nakahata T, Miyachi Y. Fujisawa A, et al. Blood. 2007 Apr 1;109(7):2903-11. doi: 10.1182/blood-2006-07-033597. Blood. 2007. PMID: 17164343 Free article.

4

[Familial Mediterranean fever: MEFV gene mutations and treatment].

Saito M, Nishikomori R, Kambe N. Saito M, et al. Nihon Rinsho Meneki Gakkai Kaishi. 2007 Apr;30(2):78-85. doi: 10.2177/jsci.30.78. Nihon Rinsho Meneki Gakkai Kaishi. 2007. PMID: 17473509 Free article. Review. Japanese.

5

Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis.

Okafuji I, Nishikomori R, Kanazawa N, Kambe N, Fujisawa A, Yamazaki S, Saito M, Yoshioka T, Kawai T, Sakai H, Tanizaki H, Heike T, Miyachi Y, Nakahata T. Okafuji I, et al. Arthritis Rheum. 2009 Jan;60(1):242-50. doi: 10.1002/art.24134. Arthritis Rheum. 2009. PMID: 19116920 Free article.

6

Orderly hematopoietic development of induced pluripotent stem cells via Flk-1(+) hemoangiogenic progenitors.

Niwa A, Umeda K, Chang H, Saito M, Okita K, Takahashi K, Nakagawa M, Yamanaka S, Nakahata T, Heike T. Niwa A, et al. J Cell Physiol. 2009 Nov;221(2):367-77. doi: 10.1002/jcp.21864. J Cell Physiol. 2009. PMID: 19562687

7

A Japanese case of familial Mediterranean fever with a MEFV gene mutation.

Kawabata H, Murakami M, Nishikomori R, Saito M, Takaoka Y, Nanao K, Maezawa M. Kawabata H, et al. Hokkaido Igaku Zasshi. 2009 Nov;84(6):419-22. Hokkaido Igaku Zasshi. 2009. PMID: 19998717

8

The inflammasome, an innate immunity guardian, participates in skin urticarial reactions and contact hypersensitivity.

Kambe N, Nakamura Y, Saito M, Nishikomori R. Kambe N, et al. Allergol Int. 2010 Jun;59(2):105-13. doi: 10.2332/allergolint.09-RAI-0160. Epub 2010 Feb 25. Allergol Int. 2010. PMID: 20179416 Free article. Review.

9

Rapid diagnosis of FHL3 by flow cytometric detection of intraplatelet Munc13-4 protein.

Murata Y, Yasumi T, Shirakawa R, Izawa K, Sakai H, Abe J, Tanaka N, Kawai T, Oshima K, Saito M, Nishikomori R, Ohara O, Ishii E, Nakahata T, Horiuchi H, Heike T. Murata Y, et al. Blood. 2011 Aug 4;118(5):1225-30. doi: 10.1182/blood-2011-01-329540. Epub 2011 Jun 8. Blood. 2011. PMID: 21653941 Free article.

10

High incidence of NLRP3 somatic mosaicism in patients with chronic infantile neurologic, cutaneous, articular syndrome: results of an International Multicenter Collaborative Study.

Tanaka N, Izawa K, Saito MK, Sakuma M, Oshima K, Ohara O, Nishikomori R, Morimoto T, Kambe N, Goldbach-Mansky R, Aksentijevich I, de Saint Basile G, Neven B, van Gijn M, Frenkel J, Aróstegui JI, Yagüe J, Merino R, Ibañez M, Pontillo A, Takada H, Imagawa T, Kawai T, Yasumi T, Nakahata T, Heike T. Tanaka N, et al. Among authors: saito mk. Arthritis Rheum. 2011 Nov;63(11):3625-32. doi: 10.1002/art.30512. Arthritis Rheum. 2011. PMID: 21702021 Free PMC article.

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