154 related articles for article (PubMed ID: 33322044)
1. A Novel Amino Acid Substitution, Fibrinogen Bβp.Pro234Leu, Associated with Hypofibrinogenemia Causing Impairment of Fibrinogen Assembly and Secretion.
Kaido T; Yoda M; Kamijo T; Arai S; Taira C; Higuchi Y; Okumura N
Int J Mol Sci; 2020 Dec; 21(24):. PubMed ID: 33322044
[TBL] [Abstract][Full Text] [Related]
2. Congenital fibrinogen disorder with a compound heterozygote possessing two novel FGB mutations, one qualitative and the other quantitative.
Yoda M; Kaido T; Taira C; Higuchi Y; Arai S; Okumura N
Thromb Res; 2020 Dec; 196():152-158. PubMed ID: 32871307
[TBL] [Abstract][Full Text] [Related]
3. Comparison of molecular structure and fibrin polymerization between two Bβ-chain N-terminal region fibrinogen variants, Bβp.G45C and Bβp.R74C.
Kaido T; Yoda M; Kamijo T; Taira C; Higuchi Y; Okumura N
Int J Hematol; 2020 Sep; 112(3):331-340. PubMed ID: 32562089
[TBL] [Abstract][Full Text] [Related]
4. Novel variant fibrinogen γp.C352R produced hypodysfibrinogenemia leading to a bleeding episode and failure of infertility treatment.
Yoda M; Kaido T; Kamijo T; Taira C; Higuchi Y; Arai S; Okumura N
Int J Hematol; 2021 Sep; 114(3):325-333. PubMed ID: 34117991
[TBL] [Abstract][Full Text] [Related]
5. [Role of fibrinogen Bbeta-chain D-region 454-458 residues for assembly and secretion of intact fibrinogen].
Terasawa F; Takezawa Y; Hirota-Kawadobora M; Okumura N
Rinsho Byori; 2011 Aug; 59(8):741-8. PubMed ID: 21942083
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 31957968
[TBL] [Abstract][Full Text] [Related]
7. 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; 18(11):. PubMed ID: 29156616
[TBL] [Abstract][Full Text] [Related]
8. Recombinant γY278H Fibrinogen Showed Normal Secretion from CHO Cells, but a Corresponding Heterozygous Patient Showed Hypofibrinogenemia.
Kamijo T; Kaido T; Yoda M; Arai S; Yamauchi K; Okumura N
Int J Mol Sci; 2021 May; 22(10):. PubMed ID: 34069309
[TBL] [Abstract][Full Text] [Related]
9. 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. PubMed ID: 26573395
[TBL] [Abstract][Full Text] [Related]
10. Hypofibrinogenemia associated with a heterozygous missense mutation gamma153Cys to arg (Matsumoto IV): in vitro expression demonstrates defective secretion of the variant fibrinogen.
Terasawa F; Okumura N; Kitano K; Hayashida N; Shimosaka M; Okazaki M; Lord ST
Blood; 1999 Dec; 94(12):4122-31. PubMed ID: 10590057
[TBL] [Abstract][Full Text] [Related]
11. Residue gamma153Cys is essential for the formation of the complexes Aalphagamma and Bbetagamma, assembly intermediates for the AalphaBbetagamma complex and intact fibrinogen.
Terasawa F; Fujita K; Okumura N
Clin Chim Acta; 2005 Mar; 353(1-2):157-64. PubMed ID: 15698603
[TBL] [Abstract][Full Text] [Related]
12. A C-terminal amino acid substitution in the gamma-chain caused by a novel heterozygous frameshift mutation (Fibrinogen Matsumoto VII) results in hypofibrinogenaemia.
Fujihara N; Haneishi A; Yamauchi K; Terasawa F; Ito T; Ishida F; Okumura N
Thromb Haemost; 2010 Aug; 104(2):213-23. PubMed ID: 20589319
[TBL] [Abstract][Full Text] [Related]
13. 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. PubMed ID: 27837696
[TBL] [Abstract][Full Text] [Related]
14. A novel missense mutation (FGG c.1168G > T) in the gamma chain of fibrinogen causing congenital hypodysfibrinogenemia with bleeding phenotype.
Xu N; Zheng L; Dai Z; Zhu J; Xie P; Yang S; Chen F
Hereditas; 2024 Jan; 161(1):4. PubMed ID: 38233949
[TBL] [Abstract][Full Text] [Related]
15. Recombinant variant fibrinogens substituted at residues gamma326Cys and gamma339Cys demonstrated markedly impaired secretion of assembled fibrinogen.
Haneishi A; Terasawa F; Fujihara N; Yamauchi K; Okumura N; Katsuyama T
Thromb Res; 2009 Jul; 124(3):368-72. PubMed ID: 19419756
[TBL] [Abstract][Full Text] [Related]
16. 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
Thromb Res; 2014 Jan; 133(1):101-7. PubMed ID: 24210681
[TBL] [Abstract][Full Text] [Related]
17. [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
Rinsho Byori; 2012 Sep; 60(9):831-8. PubMed ID: 23157111
[TBL] [Abstract][Full Text] [Related]
18. 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
Blood Coagul Fibrinolysis; 2012 Jan; 23(1):87-90. PubMed ID: 22001526
[TBL] [Abstract][Full Text] [Related]
19. A novel mutation in the FGB: c.1105C>T turns the codon for amino acid Bβ Q339 into a stop codon causing hypofibrinogenemia.
Marchi R; Brennan S; Meyer M; Rojas H; Kanzler D; De Agrela M; Ruiz-Saez A
Blood Cells Mol Dis; 2013 Mar; 50(3):177-81. PubMed ID: 23266225
[TBL] [Abstract][Full Text] [Related]
20. Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders.
Simurda T; Zolkova J; Snahnicanova Z; Loderer D; Skornova I; Sokol J; Hudecek J; Stasko J; Lasabova Z; Kubisz P
Int J Mol Sci; 2017 Dec; 19(1):. PubMed ID: 29286337
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
