Page 1 | Search Results | Blood | American Society of Hematology

1-5 of 5

Sort by

Sort Order Select

Journal Articles

Screening Method for Hepatic Fibrinogen Storage Disease Associated with Congenital Hypofibrinogenemia

Shinpei Arai, MS, Saki Mukai, BA, Yuka Takezawa, PhD, Mitsutoshi Sugano, PhD, Takayuki Honda, MD PhD, Fumihiro Ishida, MD PhD, Nobuo Okumura, PhD

Blood (2015) 126 (23): 3504.

https://doi.org/10.1182/blood.V126.23.3504.3504

Published: 2015

Journal Articles

Analysis of fibrinogen variants at γ387Ile shows that the side chain of γ387 and the tertiary structure of the γC-terminal tail are important not only for assembly and secretion of fibrinogen but also for lateral aggregation of protofibrils and XIIIa-catalyzed γ-γ dimer formation

Satomi Kani, Fumiko Terasawa, Kazuyoshi Yamauchi, Minoru Tozuka, Nobuo Okumura

Blood (2006) 108 (6): 1887–1894.

https://doi.org/10.1182/blood-2006-04-016485

Published: 2006

Includes: Supplemental data

Journal Articles

Substitution of the γ-chain Asn308 disturbs the D:D interface affecting fibrin polymerization, fibrinopeptide B release, and FXIIIa-catalyzed cross-linking

Nobuo Okumura, Oleg V. Gorkun, Fumiko Terasawa, Susan T. Lord

Blood (2004) 103 (11): 4157–4163.

https://doi.org/10.1182/blood-2003-12-4296

Published: 2004

Journal Articles

Analysis of fibrinogen γ-chain truncations shows the C-terminus, particularly γIle387, is essential for assembly and secretion of this multichain protein

Nobuo Okumura, Fumiko Terasawa, Hitoshi Tanaka, Masako Hirota, Hiroyoshi Ota, Kiyoshi Kitano, Kendo Kiyosawa, Susan T. Lord

Blood (2002) 99 (10): 3654–3660.

https://doi.org/10.1182/blood.V99.10.3654

Published: 2002

Journal Articles

Hypofibrinogenemia Associated With a Heterozygous Missense Mutation γ153Cys to Arg (Matsumoto IV): In Vitro Expression Demonstrates Defective Secretion of the Variant Fibrinogen

Fumiko Terasawa, Nobuo Okumura, Kiyoshi Kitano, Nobuaki Hayashida, Makoto Shimosaka, Mitsuo Okazaki, Susan T. Lord

Blood (1999) 94 (12): 4122–4131.

https://doi.org/10.1182/blood.V94.12.4122

Published: 1999

NARROW

Screening Method for Hepatic Fibrinogen Storage Disease Associated with Congenital Hypofibrinogenemia

Analysis of fibrinogen variants at γ387Ile shows that the side chain of γ387 and the tertiary structure of the γC-terminal tail are important not only for assembly and secretion of fibrinogen but also for lateral aggregation of protofibrils and XIIIa-catalyzed γ-γ dimer formation

Substitution of the γ-chain Asn308 disturbs the D:D interface affecting fibrin polymerization, fibrinopeptide B release, and FXIIIa-catalyzed cross-linking

Analysis of fibrinogen γ-chain truncations shows the C-terminus, particularly γIle387, is essential for assembly and secretion of this multichain protein

Hypofibrinogenemia Associated With a Heterozygous Missense Mutation γ153Cys to Arg (Matsumoto IV): In Vitro Expression Demonstrates Defective Secretion of the Variant Fibrinogen

Email alerts

ASH Publications

American Society of Hematology

Screening Method for Hepatic Fibrinogen Storage Disease Associated with Congenital Hypofibrinogenemia

Analysis of fibrinogen variants at γ387Ile shows that the side chain of γ387 and the tertiary structure of the γC-terminal tail are important not only for assembly and secretion of fibrinogen but also for lateral aggregation of protofibrils and XIIIa-catalyzed γ-γ dimer formation

Substitution of the γ-chain Asn308 disturbs the D:D interface affecting fibrin polymerization, fibrinopeptide B release, and FXIIIa-catalyzed cross-linking

Analysis of fibrinogen γ-chain truncations shows the C-terminus, particularly γIle387, is essential for assembly and secretion of this multichain protein

Hypofibrinogenemia Associated With a Heterozygous Missense Mutation γ153Cys to Arg (Matsumoto IV): In Vitro Expression Demonstrates Defective Secretion of the Variant Fibrinogen

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only