Ariga T - Search Results

1

[Genetic analysis of two patients with adenosine deaminase (ADA)-deficiency: detection of three novel mutations and characterization of two paradoxical carriers].

Oda N, Ariga T, Ono S, Kobayashi I, Kawamura N, Okano M, Kobayashi Y, Taniuchi S, Terada K, Kataoka N, Sakiyama Y. Oda N, et al. Among authors: ariga t. Arerugi. 2000 Dec;49(12):1173-80. Arerugi. 2000. PMID: 11197883 Japanese.

2

Molecular basis for paradoxical carriers of adenosine deaminase (ADA) deficiency that show extremely low levels of ADA activity in peripheral blood cells without immunodeficiency.

Ariga T, Oda N, Sanstisteban I, Arredondo-Vega FX, Shioda M, Ueno H, Terada K, Kobayashi K, Hershfield MS, Sakiyama Y. Ariga T, et al. J Immunol. 2001 Feb 1;166(3):1698-702. doi: 10.4049/jimmunol.166.3.1698. J Immunol. 2001. PMID: 11160213

3

T-cell lines from 2 patients with adenosine deaminase (ADA) deficiency showed the restoration of ADA activity resulted from the reversion of an inherited mutation.

Ariga T, Oda N, Yamaguchi K, Kawamura N, Kikuta H, Taniuchi S, Kobayashi Y, Terada K, Ikeda H, Hershfield MS, Kobayashi K, Sakiyama Y. Ariga T, et al. Blood. 2001 May 1;97(9):2896-9. doi: 10.1182/blood.v97.9.2896. Blood. 2001. PMID: 11313286 Free article.

4

[Gene therapy for ADA deficiency].

Ariga T, Sakiyama Y. Ariga T, et al. Tanpakushitsu Kakusan Koso. 1995 Dec;40(17):2772-80. Tanpakushitsu Kakusan Koso. 1995. PMID: 8584735 Review. Japanese. No abstract available.

5

[The gene therapy for a patient with ADA deficiency; report of the first gene therapy trial in Japan].

Ariga T, Kawamura N, Sakiyama Y. Ariga T, et al. Nihon Rinsho. 1997 Jun;55(6):1572-9. Nihon Rinsho. 1997. PMID: 9200950 Review. Japanese.

6

Successful peripheral T-lymphocyte-directed gene transfer for a patient with severe combined immune deficiency caused by adenosine deaminase deficiency.

Onodera M, Ariga T, Kawamura N, Kobayashi I, Ohtsu M, Yamada M, Tame A, Furuta H, Okano M, Matsumoto S, Kotani H, McGarrity GJ, Blaese RM, Sakiyama Y. Onodera M, et al. Among authors: ariga t. Blood. 1998 Jan 1;91(1):30-6. Blood. 1998. PMID: 9414266 Free article. Clinical Trial.

7

[Study of T cell-directed gene transfer for a patient with ADA deficiency].

Sakiyama Y, Ariga T, Kawamura N. Sakiyama Y, et al. Among authors: ariga t. Nihon Rinsho. 1998 Mar;56(3):696-700. Nihon Rinsho. 1998. PMID: 9549359 Review. Japanese.

8

In vivo kinetics of transduced cells in peripheral T cell-directed gene therapy: role of CD8+ cells in improved immunological function in an adenosine deaminase (ADA)-SCID patient.

Kawamura N, Ariga T, Ohtsu M, Kobayashi I, Yamada M, Tame A, Furuta H, Okano M, Egashira M, Niikawa N, Kobayashi K, Sakiyama Y. Kawamura N, et al. Among authors: ariga t. J Immunol. 1999 Aug 15;163(4):2256-61. J Immunol. 1999. PMID: 10438969

9

Molecular genetic studies of two families with X-linked chronic granulomatous disease: mutation analysis and definitive determination of carrier status in patients' sisters.

Ariga T, Sakiyama Y, Furuta H, Matsumoto S. Ariga T, et al. Eur J Haematol. 1994 Feb;52(2):99-102. doi: 10.1111/j.1600-0609.1994.tb01293.x. Eur J Haematol. 1994. PMID: 7907031

10

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. Pediatr Res. 1997 Apr;41(4 Pt 1):535-40. doi: 10.1203/00006450-199704000-00013. Pediatr Res. 1997. PMID: 9098856

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