Kanazawa N - Search Results

1

The cytosolic pattern-recognition receptor Nod2 and inflammatory granulomatous disorders.

Kambe N, Nishikomori R, Kanazawa N. Kambe N, et al. Among authors: kanazawa n. J Dermatol Sci. 2005 Aug;39(2):71-80. doi: 10.1016/j.jdermsci.2005.04.001. J Dermatol Sci. 2005. PMID: 15927452 Review.

2

Presence of a sporadic case of systemic granulomatosis syndrome with a CARD15 mutation.

Kanazawa N, Matsushima S, Kambe N, Tachibana T, Nagai S, Miyachi Y. Kanazawa N, et al. J Invest Dermatol. 2004 Mar;122(3):851-2. doi: 10.1111/j.0022-202X.2004.22341.x. J Invest Dermatol. 2004. PMID: 15086578 Free article. No abstract available.

3

Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-kappaB activation: common genetic etiology with Blau syndrome.

Kanazawa N, Okafuji I, Kambe N, Nishikomori R, Nakata-Hizume M, Nagai S, Fuji A, Yuasa T, Manki A, Sakurai Y, Nakajima M, Kobayashi H, Fujiwara I, Tsutsumi H, Utani A, Nishigori C, Heike T, Nakahata T, Miyachi Y. Kanazawa N, et al. Blood. 2005 Feb 1;105(3):1195-7. doi: 10.1182/blood-2004-07-2972. Epub 2004 Sep 30. Blood. 2005. PMID: 15459013 Free article.

4

Dendritic cell immunoreceptors: C-type lectin receptors for pattern-recognition and signaling on antigen-presenting cells.

Kanazawa N. Kanazawa N. J Dermatol Sci. 2007 Feb;45(2):77-86. doi: 10.1016/j.jdermsci.2006.09.001. Epub 2006 Oct 13. J Dermatol Sci. 2007. PMID: 17046204 Review.

5

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. Among authors: kanazawa n. Blood. 2007 Apr 1;109(7):2903-11. doi: 10.1182/blood-2006-07-033597. Blood. 2007. PMID: 17164343 Free article.

6

[Clinical features of Blau syndrome and early-onset sarcoidosis and associating CARD15/NOD2 gene mutations].

Kanazawa N. Kanazawa N. Nihon Rinsho Meneki Gakkai Kaishi. 2007 Apr;30(2):123-32. doi: 10.2177/jsci.30.123. Nihon Rinsho Meneki Gakkai Kaishi. 2007. PMID: 17473515 Free article. Japanese.

7

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. Among authors: kanazawa n. Arthritis Rheum. 2009 Jan;60(1):242-50. doi: 10.1002/art.24134. Arthritis Rheum. 2009. PMID: 19116920 Free article.

8

Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair.

Yoshimasu T, Kanazawa N, Kambe N, Nakamura M, Furukawa F. Yoshimasu T, et al. Among authors: kanazawa n. J Dermatol. 2011 Sep;38(9):900-4. doi: 10.1111/j.1346-8138.2010.01101.x. Epub 2011 Feb 1. J Dermatol. 2011. PMID: 21352330

9

Autoimmunity versus autoinflammation from the 2nd JSID-Asia-Oceania-Forum, Wakayama, Japan, 5th December, 2010.

Furukawa F, Kanazawa N. Furukawa F, et al. Among authors: kanazawa n. J Dermatol Sci. 2011 Aug;63(2):132-7. doi: 10.1016/j.jdermsci.2011.05.001. Epub 2011 May 14. J Dermatol Sci. 2011. PMID: 21680156 No abstract available.

10

Rare hereditary autoinflammatory disorders: towards an understanding of critical in vivo inflammatory pathways.

Kanazawa N. Kanazawa N. J Dermatol Sci. 2012 Jun;66(3):183-9. doi: 10.1016/j.jdermsci.2012.01.004. Epub 2012 Jan 18. J Dermatol Sci. 2012. PMID: 22336993 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

379 results

Search Page

Filters