Authors:
Tanaka, H
Terasawa, F
Ito, T
Tokunaga, S
Ishida, F
Kitano, K
Kiyosawa, K
Okumura, N
Citation: H. Tanaka et al., Fibrinogen Matsumoto V: a variant with a alpha 19 Arg -> Gly (AGG -> GGG) - Comparison between fibrin polymerization stimulated by thrombin or reptilase and fibrin monomer polymerization, THROMB HAEM, 85(1), 2001, pp. 108-113
Authors:
Hogan, KA
Lord, ST
Okumura, N
Terasawa, F
Galankis, DK
Scharrer, I
Gorkun, OV
Citation: Ka. Hogan et al., A functional assay suggests that heterodimers exist in two C-terminal gamma-chain dysfibrinogens: Matsumoto I and Vlissingen/Frankfurt IV, THROMB HAEM, 83(4), 2000, pp. 592-597
Authors:
Okumura, N
Terasawa, F
Fujita, K
Tozuka, M
Ota, H
Katsuyama, T
Citation: N. Okumura et al., Difference in electrophoretic mobility and plasmic digestion profile between four recombinant fibrinogens, gamma 308K, gamma 3081, gamma 308A, and wild type (gamma 308N), ELECTROPHOR, 21(12), 2000, pp. 2309-2315
Authors:
Terasawa, F
Fujita, K
Tozuka, M
Ota, H
Katsuyama, T
Okumura, N
Citation: F. Terasawa et al., Identification of a dysfibrinogen, the substitution of gamma 308Asn(AAT) to Lys(AAG), using coagulation tests, immunoblot analysis, and allele-specific polymerase chain reaction, CLIN CHIM A, 295(1-2), 2000, pp. 77-85
Authors:
Terasawa, F
Okumura, N
Higuchi, Y
Ishikawa, S
Tozuka, M
Ishida, F
Kitano, K
Katsuyama, T
Citation: F. Terasawa et al., Fibrinogen Matsumoto III: a variant with gamma 275 Arg -> Cys (CGC -> TGC)- Comparison of fibrin polymerization properties with those of Matsumoto I(gamma 364 Asp -> His) and Matsumoto II (gamma 308 Asn -> Lys), THROMB HAEM, 81(5), 1999, pp. 763-766
Authors:
Okumura, N
Terasawa, F
Ueno, I
Oki, K
Yamauchi, K
Hidaka, H
Tozuka, M
Okura, M
Katsuyama, T
Citation: N. Okumura et al., Genetic analyses in homozygous and heterozygous variants of lactate dehydrogenase-B (H) subunit - LD-B Matsumoto I and II (LD-B W323R), CLIN CHIM A, 287(1-2), 1999, pp. 163-171
Authors:
Terasawa, F
Okumura, N
Kitano, K
Hayashida, N
Shimosaka, M
Okazaki, M
Lord, ST
Citation: F. Terasawa et al., Hypofibrinogenemia associated with a heterozygous missense mutation gamma 153Cys to Arg (Matsumoto IV): In vitro expression demonstrates defective secretion of the variant fibrinogen, BLOOD, 94(12), 1999, pp. 4122-4131