Congenital hypofibrinogenemia: Characterization of two missense mutations affecting fibrinogen assembly and secretion-Reference-Cited by-同舟云学术

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Congenital hypofibrinogenemia: Characterization of two missense mutations affecting fibrinogen assembly and secretion

Published:2008-11 Issue:3 Volume:41 Page:292-297
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Platè Manuela,Asselta Rosanna,Spena Silvia,Spreafico Marta,Fagoonee Sharmila,Peyvandi Flora,Tenchini Maria Luisa,Duga Stefano

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference25 articles.

1. Fibrinogen and fibrin;Doolittle;Annu. Rev. Biochem.,1984

2. Fibrinogen structure and fibrin clot assembly;Mosesson;Semin. Thromb. Haemost.,1998

3. The human genome browser at UCSC;Kent;Genome Res.,2002

4. Crystal structure of fragment D from human fibrinogen and its crosslinked counterpart from fibrin;Spraggon;Nature,1997

5. Fibrinogen biosynthesis. Assembly, intracellular degradation, and association with lipid synthesis and secretion;Redman;Ann. N.Y. Acad. Sci.,2001

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3. Recombinant γY278H Fibrinogen Showed Normal Secretion from CHO Cells, but a Corresponding Heterozygous Patient Showed Hypofibrinogenemia;International Journal of Molecular Sciences;2021-05-14

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5. Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders;International Journal of Molecular Sciences;2017-12-29

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