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Items: 1 to 20 of 74

1.

Heterozygous variant fibrinogen γA289V (Kanazawa III) was confirmed as hypodysfibrinogenemia by plasma and recombinant fibrinogens.

Kaido T, Yoda M, Kamijo T, Taira C, Higuchi Y, Okumura N.

Int J Lab Hematol. 2020 Apr;42(2):190-197. doi: 10.1111/ijlh.13152. Epub 2020 Jan 20.

PMID:
31957968
2.

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.

Thromb Res. 2019 Oct;182:150-158. doi: 10.1016/j.thromres.2019.08.017. Epub 2019 Aug 20.

PMID:
31484085
3.

Fibrin monomers derived from thrombogenic dysfibrinogenemia, Naples-type variant (BβAla68Thr), showed almost entirely normal polymerization.

Kamijo T, Nagata K, Taira C, Higuchi Y, Arai S, Okumura N.

Thromb Res. 2018 Dec;172:1-3. doi: 10.1016/j.thromres.2018.10.004. Epub 2018 Oct 4. No abstract available.

PMID:
30321757
4.

Hereditary Fibrinogen Aα-Chain Amyloidosis in Asia: Clinical and Molecular Characteristics.

Yazaki M, Yoshinaga T, Sekijima Y, Kametani F, Okumura N.

Int J Mol Sci. 2018 Jan 22;19(1). pii: E320. doi: 10.3390/ijms19010320. Review.

5.

A Novel Mutation in the Fibrinogen Bβ Chain (c.490G>A; End of Exon 3) Causes a Splicing Abnormality and Ultimately Leads to Congenital Hypofibrinogenemia.

Taira C, Matsuda K, Arai S, Sugano M, Uehara T, Okumura N.

Int J Mol Sci. 2017 Nov 20;18(11). pii: E2470. doi: 10.3390/ijms18112470.

6.

A novel frameshift mutation in the fibrinogen γC terminal region, FGG c.1169_1170 del AT, leading to hypofibrinogenemia.

Nagata K, Arai S, Taira C, Sugano M, Honda T, Okumura N.

Thromb Res. 2017 Nov;159:82-85. doi: 10.1016/j.thromres.2017.10.002. Epub 2017 Oct 2. No abstract available.

PMID:
28992465
7.

Congenital dysfibrinogenemia in a Japanese family with fibrinogen Naples (BβAla68Thr) manifesting as superior sagittal sinus thrombosis.

Yoshida S, Kibe T, Matsubara R, Koizumi SI, Nara K, Amano K, Okumura N.

Blood Coagul Fibrinolysis. 2017 Oct;28(7):580-584. doi: 10.1097/MBC.0000000000000641.

PMID:
28537987
8.

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.

Cardiology. 2017;137(3):167-172. doi: 10.1159/000457899. Epub 2017 Apr 19.

PMID:
28419986
9.

Causal mechanisms of seismo-EM phenomena during the 1965-1967 Matsushiro earthquake swarm.

Enomoto Y, Yamabe T, Okumura N.

Sci Rep. 2017 Mar 21;7:44774. doi: 10.1038/srep44774.

10.

Rapid ABO genotyping by high-speed droplet allele-specific PCR using crude samples.

Taira C, Matsuda K, Takeichi N, Furukawa S, Sugano M, Uehara T, Okumura N, Honda T.

J Clin Lab Anal. 2018 Jan;32(1). doi: 10.1002/jcla.22196. Epub 2017 Mar 13.

11.

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.

Int J Hematol. 2017 Jun;105(6):758-768. doi: 10.1007/s12185-017-2185-5. Epub 2017 Feb 4.

PMID:
28161763
12.

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.

Thromb Res. 2016 Dec;148:111-117. doi: 10.1016/j.thromres.2016.11.002. Epub 2016 Nov 5.

PMID:
27837696
13.

Familial discrepancy of clinical outcomes associated with fibrinogen Dorfen: A case of huge genital hematoma after episiotomy.

Kagami K, Yamazaki R, Minami T, Okumura N, Morishita E, Fujiwara H.

J Obstet Gynaecol Res. 2016 Jun;42(6):722-725. doi: 10.1111/jog.12972. Epub 2016 Mar 23.

PMID:
27005882
14.

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.

Thromb Res. 2015 Dec;136(6):1318-24. doi: 10.1016/j.thromres.2015.11.011. Epub 2015 Nov 10.

PMID:
26573395
15.

[A Case of Secondary Cryofibrinogenemia with Cholangiocarcinoma and Deep Venous Thrombosis].

Arai S, Sugano M, Honda T, Kameko F, Terasawa F, Okumura N.

Rinsho Byori. 2015 Apr;63(4):421-6. Japanese.

PMID:
26536774
16.
17.

Rapid single nucleotide polymorphism based method for hematopoietic chimerism analysis and monitoring using high-speed droplet allele-specific PCR and allele-specific quantitative PCR.

Taira C, Matsuda K, Yamaguchi A, Uehara M, Sugano M, Okumura N, Honda T.

Clin Chim Acta. 2015 May 20;445:101-6. doi: 10.1016/j.cca.2015.03.018. Epub 2015 Mar 20.

PMID:
25797898
18.

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.

Thromb Res. 2015 Apr;135(4):710-7. doi: 10.1016/j.thromres.2015.01.013. Epub 2015 Jan 15.

PMID:
25613923
19.

[College education for medical technologists of the next generation].

Okumura N.

Rinsho Byori. 2014 May;62(5):487-92. Review. Japanese.

PMID:
25051665
20.

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.

Thromb Res. 2014 Aug;134(2):518-25. doi: 10.1016/j.thromres.2014.06.002. Epub 2014 Jun 11.

PMID:
24968960

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