Futatani T - Search Results

1

Contiguous X-chromosome deletion syndrome encompassing the BTK, TIMM8A, TAF7L, and DRP2 genes.

Sedivá A, Smith CI, Asplund AC, Hadac J, Janda A, Zeman J, Hansíková H, Dvoráková L, Mrázová L, Velbri S, Koehler C, Roesch K, Sullivan KE, Futatani T, Ochs HD. Sedivá A, et al. Among authors: futatani t. J Clin Immunol. 2007 Nov;27(6):640-6. doi: 10.1007/s10875-007-9123-x. Epub 2007 Sep 12. J Clin Immunol. 2007. PMID: 17851739

2

Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes.

Arai T, Zhao M, Kanegane H, van Zelm MC, Futatani T, Yamada M, Ariga T, Ochs HD, Miyawaki T, Oh-ishi T. Arai T, et al. Among authors: futatani t. J Hum Genet. 2011 Aug;56(8):577-82. doi: 10.1038/jhg.2011.61. Epub 2011 Jul 14. J Hum Genet. 2011. PMID: 21753765

3

Survival of wild polio by a patient with XLA.

Sarpong S, Skolnick HS, Ochs HD, Futatani T, Winkelstein JA. Sarpong S, et al. Among authors: futatani t. Ann Allergy Asthma Immunol. 2002 Jan;88(1):59-60. doi: 10.1016/S1081-1206(10)63593-4. Ann Allergy Asthma Immunol. 2002. PMID: 11814279

4

Bruton's tyrosine kinase is present in normal platelets and its absence identifies patients with X-linked agammaglobulinaemia and carrier females.

Futatani T, Watanabe C, Baba Y, Tsukada S, Ochs HD. Futatani T, et al. Br J Haematol. 2001 Jul;114(1):141-9. doi: 10.1046/j.1365-2141.2001.02905.x. Br J Haematol. 2001. PMID: 11472359 Free article.

5

Absence of memory B cells in patients with common variable immunodeficiency.

Agematsu K, Futatani T, Hokibara S, Kobayashi N, Takamoto M, Tsukada S, Suzuki H, Koyasu S, Miyawaki T, Sugane K, Komiyama A, Ochs HD. Agematsu K, et al. Among authors: futatani t. Clin Immunol. 2002 Apr;103(1):34-42. doi: 10.1006/clim.2001.5197. Clin Immunol. 2002. PMID: 11987983

6

Severe neutropenia in Japanese patients with x-linked agammaglobulinemia.

Kanegane H, Taneichi H, Nomura K, Futatani T, Miyawaki T. Kanegane H, et al. Among authors: futatani t. J Clin Immunol. 2005 Sep;25(5):491-5. doi: 10.1007/s10875-005-5370-x. J Clin Immunol. 2005. PMID: 16160918

7

Developmental changes of FOXP3-expressing CD4+CD25+ regulatory T cells and their impairment in patients with FOXP3 gene mutations.

Fuchizawa T, Adachi Y, Ito Y, Higashiyama H, Kanegane H, Futatani T, Kobayashi I, Kamachi Y, Sakamoto T, Tsuge I, Tanaka H, Banham AH, Ochs HD, Miyawaki T. Fuchizawa T, et al. Among authors: futatani t. Clin Immunol. 2007 Dec;125(3):237-46. doi: 10.1016/j.clim.2007.08.004. Epub 2007 Oct 3. Clin Immunol. 2007. PMID: 17916446

8

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. Among authors: futatani t. J Allergy Clin Immunol. 2001 Dec;108(6):1012-20. doi: 10.1067/mai.2001.120133. J Allergy Clin Immunol. 2001. PMID: 11742281

9

Detection of Bruton's tyrosine kinase mutations in hypogammaglobulinaemic males registered as common variable immunodeficiency (CVID) in the Japanese Immunodeficiency Registry.

Kanegane H, Tsukada S, Iwata T, Futatani T, Nomura K, Yamamoto J, Yoshida T, Agematsu K, Komiyama A, Miyawaki T. Kanegane H, et al. Among authors: futatani t. Clin Exp Immunol. 2000 Jun;120(3):512-7. doi: 10.1046/j.1365-2249.2000.01244.x. Clin Exp Immunol. 2000. PMID: 10844531 Free PMC article.

10

[X-linked hyper-IGM syndrome associated to sclerosing cholangitis and gallbladder neoplasm: clinical case].

Rodríguez C, Carrión F, Marinovic MA, Chávez E, Preisler J, Pooley F, Futatani T, Ochs HD. Rodríguez C, et al. Among authors: futatani t. Rev Med Chil. 2003 Mar;131(3):303-8. Rev Med Chil. 2003. PMID: 12790080 Spanish.

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