Mukai S - Search Results

1

γD318Y fibrinogen shows no fibrin polymerization due to defective "A-a" and "B-b" interactions, whereas that of γK321E fibrinogen is nearly normal.

Kamijo T, Mukai S, Taira C, Higuchi Y, Okumura N. Kamijo T, et al. Among authors: mukai s. Thromb Res. 2019 Oct;182:150-158. doi: 10.1016/j.thromres.2019.08.017. Epub 2019 Aug 20. Thromb Res. 2019. PMID: 31484085

2

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: mukai s. 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

3

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: mukai s. 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

4

Differences in the function and secretion of congenital aberrant fibrinogenemia between heterozygous γD320G (Okayama II) and γΔN319-ΔD320 (Otsu I).

Mukai S, Ikeda M, Takezawa Y, Sugano M, Honda T, Okumura N. Mukai S, et al. Thromb Res. 2015 Dec;136(6):1318-24. doi: 10.1016/j.thromres.2015.11.011. Epub 2015 Nov 10. Thromb Res. 2015. PMID: 26573395

5

Genetic analyses of novel compound heterozygous hypodysfibrinogenemia, Tsukuba I: FGG c.1129+62_65 del AATA and FGG c.1299+4 del A.

Mukai S, Nagata K, Ikeda M, Arai S, Sugano M, Honda T, Okumura N. Mukai S, et al. Thromb Res. 2016 Dec;148:111-117. doi: 10.1016/j.thromres.2016.11.002. Epub 2016 Nov 5. Thromb Res. 2016. PMID: 27837696

6

The fibrous form of intracellular inclusion bodies in recombinant variant fibrinogen-producing cells is specific to the hepatic fibrinogen storage disease-inducible variant fibrinogen.

Arai S, Ogiwara N, Mukai S, Takezawa Y, Sugano M, Honda T, Okumura N. Arai S, et al. Among authors: mukai s. Int J Hematol. 2017 Jun;105(6):758-768. doi: 10.1007/s12185-017-2185-5. Epub 2017 Feb 4. Int J Hematol. 2017. PMID: 28161763

7

Hypodysfibrinogenemia with a Heterozygous Mutation of γCys326Ser by the Novel Transversion of TGT to TCT in a Patient with Pulmonary Thromboembolism and Right Ventricular Thrombus.

Ushijima A, Komai T, Masukawa A, Oikawa K, Morita N, Asai S, Mukai S, Okumura N, Kobayashi Y, Miyachi H. Ushijima A, et al. Among authors: mukai s. Cardiology. 2017;137(3):167-172. doi: 10.1159/000457899. Epub 2017 Apr 19. Cardiology. 2017. PMID: 28419986

8

Complete measurable residual disease response after combination chemotherapy with AML-type and ALL-type regimens in pediatric B/myeloid acute bilineal leukemia.

Saito S, Taira C, Matsuda K, Yanagisawa R, Morita D, Shigemura T, Yoshikawa K, Tanaka M, Sakashita K, Mukai S, Shimodaira S, Koike K, Nakazawa Y. Saito S, et al. Among authors: mukai s. Leuk Lymphoma. 2020 Apr;61(4):967-970. doi: 10.1080/10428194.2019.1697813. Epub 2019 Dec 6. Leuk Lymphoma. 2020. PMID: 31809628 No abstract available.

9

Factor H gene variants in Japanese: its relation to atypical hemolytic uremic syndrome.

Mukai S, Hidaka Y, Hirota-Kawadobora M, Matsuda K, Fujihara N, Takezawa Y, Kubota S, Koike K, Honda T, Yamauchi K. Mukai S, et al. Mol Immunol. 2011 Oct;49(1-2):48-55. doi: 10.1016/j.molimm.2011.07.017. Epub 2011 Aug 24. Mol Immunol. 2011. PMID: 21868097 Free article.

10

Clinical utility of urinary mulberry bodies/cells testing in the diagnosis of Fabry disease.

Nakamura K, Mukai S, Takezawa Y, Natori Y, Miyazaki A, Ide Y, Takebuchi M, Nanato K, Katoh M, Suzuki H, Sakyu A, Kojima T, Kise E, Hanafusa H, Kosho T, Kuwahara K, Sekijima Y. Nakamura K, et al. Among authors: mukai s. Mol Genet Metab Rep. 2023 Jun 7;36:100983. doi: 10.1016/j.ymgmr.2023.100983. eCollection 2023 Sep. Mol Genet Metab Rep. 2023. PMID: 37323223 Free PMC article.

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