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Synthesis of a mouse model of the dysfibrinogen Vlissingen/Frankfurt IV.
Hogan, K A; Maeda, N; Kluckman, K D; Lord, S T.
Affiliation
  • Hogan KA; Department of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill, NC 27599-7525, USA.
Ann N Y Acad Sci ; 936: 117-21, 2001.
Article in En | MEDLINE | ID: mdl-11460467
ABSTRACT
The dysfibrinogen Vlissingen/Frankfurt IV is characterized as a deletion of Asn319 and Asp320 from the C-terminus of the gamma-chain of fibrinogen. This dysfibrinogen, which was identified in several family members that are all heterozygous for the in-frame 6-bp deletion, is associated with both venous and arterial thrombosis. Here, we describe the generation of a murine model of the V/F IV dysfibrinogen using gene targeting of mouse gamma-chain DNA. Preliminary analysis shows that the human and mouse variant fibrinogens are similar analogous to the human V/F IV protein, the D1 fragment of the variant mouse fibrinogen is partially protected from digestion in the presence of calcium or Gly-Pro-Arg-Pro. These heterozygous mice provide the first opportunity to examine the association of thrombophilia and dysfibrinogenemia in a controlled genetic background.
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Collection: 01-internacional Database: MEDLINE Main subject: Fibrinogens, Abnormal Limits: Animals / Female / Humans / Male Language: En Journal: Ann N Y Acad Sci Year: 2001 Document type: Article Affiliation country:
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Fibrinogens, Abnormal Limits: Animals / Female / Humans / Male Language: En Journal: Ann N Y Acad Sci Year: 2001 Document type: Article Affiliation country: