Takezawa Y - Search Results

1

Real-time nanodiamond thermometry probing in vivo thermogenic responses.

Fujiwara M, Sun S, Dohms A, Nishimura Y, Suto K, Takezawa Y, Oshimi K, Zhao L, Sadzak N, Umehara Y, Teki Y, Komatsu N, Benson O, Shikano Y, Kage-Nakadai E. Fujiwara M, et al. Among authors: takezawa y. Sci Adv. 2020 Sep 11;6(37):eaba9636. doi: 10.1126/sciadv.aba9636. Print 2020 Sep. Sci Adv. 2020. PMID: 32917703 Free PMC article.

2

Glass-patternable notch-shaped microwave architecture for on-chip spin detection in biological samples.

Oshimi K, Nishimura Y, Matsubara T, Tanaka M, Shikoh E, Zhao L, Zou Y, Komatsu N, Ikado Y, Takezawa Y, Kage-Nakadai E, Izutsu Y, Yoshizato K, Morita S, Tokunaga M, Yukawa H, Baba Y, Teki Y, Fujiwara M. Oshimi K, et al. Among authors: takezawa y. Lab Chip. 2022 Jun 28;22(13):2519-2530. doi: 10.1039/d2lc00112h. Lab Chip. 2022. PMID: 35510631 Free article.

3

siRNA down-regulation of FGA mRNA in HepG2 cells demonstrated that heterozygous abnormality of the Aα-chain gene does not affect the plasma fibrinogen level.

Takezawa Y, Matsuda K, Terasawa F, Sugano M, Honda T, Okumura N. Takezawa Y, et al. Thromb Res. 2013 Apr;131(4):342-8. doi: 10.1016/j.thromres.2013.01.010. Epub 2013 Feb 13. Thromb Res. 2013. PMID: 23414568

4

Nonsense-mediated mRNA decay was demonstrated in two hypofibrinogenemias caused by heterozygous nonsense mutations of FGG, Shizuoka III and Kanazawa II.

Soya K, Takezawa Y, Okumura N, Terasawa F. Soya K, et al. Among authors: takezawa y. Thromb Res. 2013 Oct;132(4):465-70. doi: 10.1016/j.thromres.2013.08.010. Epub 2013 Aug 17. Thromb Res. 2013. PMID: 24011387

5

Heterozygous Bβ-chain C-terminal 12 amino acid elongation variant, BβX462W (Kyoto VI), showed dysfibrinogenemia.

Okumura N, Terasawa F, Takezawa Y, Hirota-Kawadobora M, Inaba T, Fujita N, Saito M, Sugano M, Honda T. Okumura N, et al. Among authors: takezawa y. Blood Coagul Fibrinolysis. 2012 Jan;23(1):87-90. doi: 10.1097/MBC.0b013e32834cb243. Blood Coagul Fibrinolysis. 2012. PMID: 22001526

6

Molecular analysis of afibrinogenemic mutations caused by a homozygous FGA1238 bp deletion, and a compound heterozygous FGA1238 bp deletion and novel FGA c.54+3A>C substitution.

Takezawa Y, Terasawa F, Matsuda K, Sugano M, Tanaka A, Fujiwara M, Kainuma K, Okumura N. Takezawa Y, et al. Int J Hematol. 2012 Jul;96(1):39-46. doi: 10.1007/s12185-012-1100-3. Epub 2012 May 26. Int J Hematol. 2012. PMID: 22639050 Free article.

7

[Comparison of fibrinogen synthesis and secretion between novel variant fibrinogen, nagakute (gamma305Thr --> Ala), and other variants located in gamma305-308 residues].

Kobayashi T, Takezawa Y, Terasawa F, Okumura N. Kobayashi T, et al. Among authors: takezawa y. Rinsho Byori. 2012 Sep;60(9):831-8. Rinsho Byori. 2012. PMID: 23157111 Japanese.

8

γ375W fibrinogen-synthesizing CHO cells indicate the accumulation of variant fibrinogen within endoplasmic reticulum.

Kobayashi T, Arai S, Ogiwara N, Takezawa Y, Nanya M, Terasawa F, Okumura N. Kobayashi T, et al. Among authors: takezawa y. Thromb Res. 2014 Jan;133(1):101-7. doi: 10.1016/j.thromres.2013.10.033. Epub 2013 Oct 28. Thromb Res. 2014. PMID: 24210681

9

Recombinant γT305A fibrinogen indicates severely impaired fibrin polymerization due to the aberrant function of hole 'A' and calcium binding sites.

Ikeda M, Kobayashi T, Arai S, Mukai S, Takezawa Y, Terasawa F, Okumura N. Ikeda M, et al. Among authors: takezawa y. Thromb Res. 2014 Aug;134(2):518-25. doi: 10.1016/j.thromres.2014.06.002. Epub 2014 Jun 11. Thromb Res. 2014. PMID: 24968960

10

Novel heterozygous dysfibrinogenemia, Sumida (AαC472S), showed markedly impaired lateral aggregation of protofibrils and mildly lower functional fibrinogen levels.

Ikeda M, Arai S, Mukai S, Takezawa Y, Terasawa F, Okumura N. Ikeda M, et al. Among authors: takezawa y. Thromb Res. 2015 Apr;135(4):710-7. doi: 10.1016/j.thromres.2015.01.013. Epub 2015 Jan 15. Thromb Res. 2015. PMID: 25613923

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