Kanegane H - Search Results

1

Protein-tyrosine phosphatase, nonreceptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndrome.

Yoshida R, Hasegawa T, Hasegawa Y, Nagai T, Kinoshita E, Tanaka Y, Kanegane H, Ohyama K, Onishi T, Hanew K, Okuyama T, Horikawa R, Tanaka T, Ogata T. Yoshida R, et al. Among authors: kanegane h. J Clin Endocrinol Metab. 2004 Jul;89(7):3359-64. doi: 10.1210/jc.2003-032091. J Clin Endocrinol Metab. 2004. PMID: 15240615

2

Bruton tyrosine kinase gene mutations in Turkish patients with presumed X-linked agammaglobulinemia.

Wang Y, Kanegane H, Sanal O, Ersoy F, Tezcan I, Futatani T, Tsukada S, Miyawaki T. Wang Y, et al. Among authors: kanegane h. Hum Mutat. 2001 Oct;18(4):356. doi: 10.1002/humu.1200. Hum Mutat. 2001. PMID: 11668622

3

Identification of FOXP3-negative regulatory T-like (CD4(+)CD25(+)CD127(low)) cells in patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.

Otsubo K, Kanegane H, Kamachi Y, Kobayashi I, Tsuge I, Imaizumi M, Sasahara Y, Hayakawa A, Nozu K, Iijima K, Ito S, Horikawa R, Nagai Y, Takatsu K, Mori H, Ochs HD, Miyawaki T. Otsubo K, et al. Among authors: kanegane h. Clin Immunol. 2011 Oct;141(1):111-20. doi: 10.1016/j.clim.2011.06.006. Epub 2011 Jul 12. Clin Immunol. 2011. PMID: 21802372

4

Cartilage-hair hypoplasia with T-cell dysfunction.

Tomomasa D, Sato T, Hasegawa T, Morio T, Kanegane H. Tomomasa D, et al. Among authors: kanegane h. Pediatr Int. 2022 Jan;64(1):e15080. doi: 10.1111/ped.15080. Pediatr Int. 2022. PMID: 35278261 No abstract available.

5

Point mutation in intron 11 of Bruton's tyrosine kinase in atypical X-linked agammaglobulinemia.

Shinomiya N, Kanegane H, Watanabe A, Yamaguchi Y, Futatani T, Miyawaki T. Shinomiya N, et al. Among authors: kanegane h. Pediatr Int. 2000 Dec;42(6):689-92. doi: 10.1046/j.1442-200x.2000.01293.x. Pediatr Int. 2000. PMID: 11192530 No abstract available.

6

Maternal germinal mosaicism of X-linked agammaglobulinemia.

Sakamoto M, Kanegane H, Fujii H, Tsukada S, Miyawaki T, Shinomiya N. Sakamoto M, et al. Among authors: kanegane h. Am J Med Genet. 2001 Mar 15;99(3):234-7. doi: 10.1002/1096-8628(2001)9999:9999<::aid-ajmg1159>3.0.co;2-m. Am J Med Genet. 2001. PMID: 11241495

7

Clinical and mutational characteristics of X-linked agammaglobulinemia and its carrier identified by flow cytometric assessment combined with genetic analysis.

Kanegane H, Futatani T, Wang Y, Nomura K, Shinozaki K, Matsukura H, Kubota T, Tsukada S, Miyawaki T. Kanegane H, et al. J Allergy Clin Immunol. 2001 Dec;108(6):1012-20. doi: 10.1067/mai.2001.120133. J Allergy Clin Immunol. 2001. PMID: 11742281

8

Identification of mutations of Bruton's tyrosine kinase gene (BTK) in Brazilian patients with X-linked agammaglobulinemia.

Tani SM, Wang Y, Kanegane H, Futatani T, Pinto J, Vilela MM, Miyawaki T. Tani SM, et al. Among authors: kanegane h. Hum Mutat. 2002 Sep;20(3):235-6. doi: 10.1002/humu.9060. Hum Mutat. 2002. PMID: 12204007

9

Activation-dependent T cell expression of the X-linked lymphoproliferative disease gene product SLAM-associated protein and its assessment for patient detection.

Shinozaki K, Kanegane H, Matsukura H, Sumazaki R, Tsuchida M, Makita M, Kimoto Y, Kanai R, Tsumura K, Kondoh T, Moriuchi H, Miyawaki T. Shinozaki K, et al. Among authors: kanegane h. Int Immunol. 2002 Oct;14(10):1215-23. doi: 10.1093/intimm/dxf084. Int Immunol. 2002. PMID: 12356686

10

Membranoproliferative glomerulonephritis in a patient with X-linked agammaglobulinemia.

Yoshino A, Honda M, Kanegane H, Obata K, Matsukura H, Sakazume S, Katada Y, Miyawaki T, Ueda Y, Nagai T. Yoshino A, et al. Among authors: kanegane h. Pediatr Nephrol. 2006 Jan;21(1):36-8. doi: 10.1007/s00467-005-2029-z. Epub 2005 Nov 11. Pediatr Nephrol. 2006. PMID: 16550363

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