Sakiyama Y - Search Results

1

Confirming or excluding the diagnosis of Wiskott-Aldrich syndrome in children with thrombocytopenia of an unknown etiology.

Ariga T, Nakajima M, Yoshida J, Yamato K, Nagatoshi Y, Yanai F, Caviles AP, Nelson DL, Sakiyama Y. Ariga T, et al. Among authors: sakiyama y. J Pediatr Hematol Oncol. 2004 Jul;26(7):435-40. doi: 10.1097/00043426-200407000-00007. J Pediatr Hematol Oncol. 2004. PMID: 15218418

2

Mixed chimera status of 12 patients with Wiskott-Aldrich syndrome (WAS) after hematopoietic stem cell transplantation: evaluation by flow cytometric analysis of intracellular WAS protein expression.

Yamaguchi K, Ariga T, Yamada M, Nelson DL, Kobayashi R, Kobayashi C, Noguchi Y, Ito Y, Katamura K, Nagatoshi Y, Kondo S, Katoh H, Sakiyama Y. Yamaguchi K, et al. Among authors: sakiyama y. Blood. 2002 Aug 15;100(4):1208-14. doi: 10.1182/blood-2002-01-0211. Blood. 2002. PMID: 12149199 Free article.

3

Detection of lymphocytes and granulocytes expressing the mutant WASP message in carriers of Wiskott-Aldrich syndrome.

Ariga T, Yamada M, Wada T, Saitoh S, Sakiyama Y. Ariga T, et al. Among authors: sakiyama y. Br J Haematol. 1999 Mar;104(4):893-900. doi: 10.1046/j.1365-2141.1999.01248.x. Br J Haematol. 1999. PMID: 10192456 Free article.

4

Determination of carrier status for the Wiskott-Aldrich syndrome by flow cytometric analysis of Wiskott-Aldrich syndrome protein expression in peripheral blood mononuclear cells.

Yamada M, Ariga T, Kawamura N, Yamaguchi K, Ohtsu M, Nelson DL, Kondoh T, Kobayashi I, Okano M, Kobayashi K, Sakiyama Y. Yamada M, et al. Among authors: sakiyama y. J Immunol. 2000 Jul 15;165(2):1119-22. doi: 10.4049/jimmunol.165.2.1119. J Immunol. 2000. PMID: 10878391

5

Spontaneous in vivo reversion of an inherited mutation in the Wiskott-Aldrich syndrome.

Ariga T, Kondoh T, Yamaguchi K, Yamada M, Sasaki S, Nelson DL, Ikeda H, Kobayashi K, Moriuchi H, Sakiyama Y. Ariga T, et al. Among authors: sakiyama y. J Immunol. 2001 Apr 15;166(8):5245-9. doi: 10.4049/jimmunol.166.8.5245. J Immunol. 2001. PMID: 11290809

6

Detection of a novel splice-site mutation that results in skipping exon 3 of the WASP gene in a patient with Wiskott-Aldrich syndrome.

Ariga T, Yamada M, Pudua FR, Sakiyama Y. Ariga T, et al. Among authors: sakiyama y. Biochim Biophys Acta. 1996 Dec 16;1317(3):158-60. doi: 10.1016/s0925-4439(96)00058-0. Biochim Biophys Acta. 1996. PMID: 8988230 Free article.

7

Mutation analysis of five Japanese families with Wiskott-Aldrich syndrome and determination of the family members' carrier status using three different methods.

Ariga T, Yamada M, Sakiyama Y. Ariga T, et al. Among authors: sakiyama y. Pediatr Res. 1997 Apr;41(4 Pt 1):535-40. doi: 10.1203/00006450-199704000-00013. Pediatr Res. 1997. PMID: 9098856

8

The role of common gamma chain in human monocytes in vivo; evaluation from the studies of X-linked severe combined immunodeficiency (X-SCID) carriers and X-SCID patients who underwent cord blood stem cell transplantation.

Ariga T, Yamaguchi K, Yoshida J, Miyanoshita A, Watanabe T, Date T, Miura J, Kumaki S, Ishii N, Sakiyama Y. Ariga T, et al. Among authors: sakiyama y. Br J Haematol. 2002 Sep;118(3):858-63. doi: 10.1046/j.1365-2141.2002.03679.x. Br J Haematol. 2002. PMID: 12181059 Free article.

9

Possible application of flow cytometry for evaluation of the structure and functional status of WASP in peripheral blood mononuclear cells.

Nakajima M, Yamada M, Yamaguchi K, Sakiyama Y, Oda A, Nelson DL, Yawaka Y, Ariga T. Nakajima M, et al. Among authors: sakiyama y. Eur J Haematol. 2009 Mar;82(3):223-30. doi: 10.1111/j.1600-0609.2008.01180.x. Epub 2008 Nov 5. Eur J Haematol. 2009. PMID: 19018864

10

Characterization of a deletion mutation involving exons 3-7 of the WASP gene detected in a patient with Wiskott-Aldrich syndrome.

Ariga T, Yamada M, Ito S, Iwamura M, Iseki M, Sakiyama Y. Ariga T, et al. Among authors: sakiyama y. Hum Mutat. 1997;10(4):310-6. doi: 10.1002/(SICI)1098-1004(1997)10:4<310::AID-HUMU7>3.0.CO;2-K. Hum Mutat. 1997. PMID: 9338585

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