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T Takafuta

Explore the profile of T Takafuta including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 20
Citations 115
Followers 0
Related Specialties
Hematology
Cardiology & Vascular Diseases
General Medicine
Top 10 Co-Authors
K Fujimura
A Kuramoto
T Shimomura
M Noda
T Fujimoto
H Kawano
S S Shapiro
S Katsutani
G F Murphy
T Fujii
Published In
Thromb Haemost
Nihon Rinsho
Int J Hematol
Blood
Rinsho Byori
Affiliations
Soon will be listed here.
Recent Articles
1.
Inhibitory effects of ticlopidine on platelet function as assessed by three different methods
Cuyun-Lira O, Kaneko M, Takafuta T, Satoh K, Ohnishi M, Yatomi Y, et al.
Eur J Pharm Sci . 2006 Oct; 30(1):21-5. PMID: 17070023
The inhibitory effects of ticlopidine on platelet function were evaluated in 18 healthy male volunteers using three different platelet function tests. Three methods include the recently developed small collagen-beads method,...
2.
Anti-endothelial cell antibodies in Behçet's disease
Dinc A, Takafuta T, Jiang D, Melikoglu M, Saruhan-Direskeneli G, Shapiro S
Clin Exp Rheumatol . 2004 Jan; 21(4 Suppl 30):S27-30. PMID: 14727455
Objective: Circulating antibodies that bind to human endothelial cells cultured in vitro have been detected in a variety of diseases, including Behçet's disease. In this disorder the reported prevalence of...
3.
T-cell receptor V beta gene usage of human cytotoxic T-cell clones obtained from gastric cancer patients
Miyahara E, Yamaguchi Y, Minami K, Hihara J, Noma K, Toge T, et al.
Anticancer Res . 1999 Sep; 19(3A):2057-66. PMID: 10470148
Nine T-cell clones have been established from tumor-infiltrating lymphocytes (TIL) isolated from ascitic fluid of a gastric cancer patient. Five of them retained cytotoxicity against autologous tumor cells (AuTu), and...
4.
Von Willebrand factor receptor GPIb alpha is expressed by human factor XIIIa-positive dermal dendrocytes and is upregulated by mast cell degranulation
Monteiro M, Shapiro S, Takafuta T, Menezes D, Murphy G
J Invest Dermatol . 1999 Sep; 113(2):272-6. PMID: 10469316
GPIb alpha, a glycoprotein component of the GPIb-IX-V complex, serves as a platelet membrane receptor that mediates adhesion to von Willebrand factor normally present in the vascular subendothelium. Recent data...
5.
Cloning and characterization of the gene encoding the murine glycoprotein V: the conserved thrombin-cleavable protein on platelet surface
Katsutani S, Fujimoto T, Noda M, Shimomura T, Takafuta T, Kimura A, et al.
Thromb Res . 1998 Oct; 92(1):43-51. PMID: 9783673
Glycoprotein V (GPV) is a platelet membrane protein present as a subunit of the GPIb/V/IX complex, a major receptor for von Willebrand factor, and is specifically cleaved by thrombin. In...
6.
Human beta-filamin is a new protein that interacts with the cytoplasmic tail of glycoprotein Ibalpha
Takafuta T, Wu G, Murphy G, Shapiro S
J Biol Chem . 1998 Jul; 273(28):17531-8. PMID: 9651345
We have cloned and sequenced a 9.4-kilobase cDNA specifying a new 280-kDa protein interacting with the cytoplasmic tail of glycoprotein (Gp) Ibalpha and showing considerable homology to actin-binding protein 280...
7.
Human endothelial cells in culture and in vivo express on their surface all four components of the glycoprotein Ib/IX/V complex
Wu G, Essex D, Meloni F, Takafuta T, Fujimura K, Konkle B, et al.
Blood . 1997 Nov; 90(7):2660-9. PMID: 9326233
The platelet glycoprotein Ib (GpIb) complex is composed of four polypeptides: the disulfide-linked GpIb alpha and GpIb beta and the noncovalently associated GpIX and GpV. GpIb alpha contains binding sites...
8.
Two distinct novel splice site mutations in a compound heterozygous patient with protein S deficiency
Yamazaki T, Katsumi A, Okamoto Y, Takafuta T, Tsuzuki S, Kagami K, et al.
Thromb Haemost . 1997 Jan; 77(1):14-20. PMID: 9031442
Genetic analysis revealed two distinct novel splice site mutations in a compound heterozygous patient with protein S deficiency. The paternal mutation was a G-to-T transition at position-1 of the acceptor...
9.
Oligoclonal accumulation of T cells in peripheral blood from patients with idiopathic thrombocytopenic purpura
Shimomura T, Fujimura K, Takafuta T, Fujii T, Katsutani S, Noda M, et al.
Br J Haematol . 1996 Dec; 95(4):732-7. PMID: 8982053
To determine whether clonal T cells accumulate in idiopathic thrombocytopenic purpura (ITP), we performed single-strand conformation polymorphism (SSCP) analysis to detect T-cell receptor (TCR) beta-chain usage of peripheral T cells....
10.
A point mutation in glycoprotein IX coding sequence (Cys73 (TGT) to Tyr(TAT)) causes impaired surface expression of GPIb/IX/V complex in two families with Bernard-Soulier syndrome
Noda M, Fujimura K, Takafuta T, Shimomura T, Fujii T, Katsutani S, et al.
Thromb Haemost . 1996 Dec; 76(6):874-8. PMID: 8972003
Bernard-Soulier syndrome (BSS) is a rare inherited bleeding disorder which is caused by abnormal expression or function of the glycoprotein (GP) Ib/IX/V complex, a platelet major receptor for von Willebrand...