A congenitally abnormal fibrinogen (Vlissingen) with a 6-base deletion in the gamma-chain gene, causing defective calcium binding and impaired fibrin polymerization-Reference-Cited by-同舟云学术

A congenitally abnormal fibrinogen (Vlissingen) with a 6-base deletion in the gamma-chain gene, causing defective calcium binding and impaired fibrin polymerization

Published:1991-07 Issue:20 Volume:266 Page:13456-13461
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Koopman J.,Haverkate F.,Briët E.,Lord S.T.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference54 articles.

1. Evidence for four different polymerization sites involved in human fibrin formation.

2. Localization of segments essential for polymerization and for calcium binding in the .gamma.-chain of human fibrinogen

3. A fibrinogen fragment D (D intermediate) with calcium binding but without anticlotting properties

4. Calcium binding to human fibrinogen — Localization of two calcium specific sites

5. Calcium-binding properties of human fibrin(ogen) and degradation products

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