Literature DB >> 17721633

Congenital hypodysfibrinogenaemia (Fibrinogen Des Moines) due to a gamma320Asp deletion at the Ca2+ binding site.

Stephen O Brennan1, Ryan L Davis, Michael W Mosesson, Irene Hernandez, Robin Lowen, Saramma J Alexander.   

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Year:  2007        PMID: 17721633

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


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  5 in total

Review 1.  Fibrin Formation, Structure and Properties.

Authors:  John W Weisel; Rustem I Litvinov
Journal:  Subcell Biochem       Date:  2017

2.  Fibrin protofibril packing and clot stability are enhanced by extended knob-hole interactions and catch-slip bonds.

Authors:  Nathan L Asquith; Cédric Duval; Artem Zhmurov; Stephen R Baker; Helen R McPherson; Marco M Domingues; Simon D A Connell; Valeri Barsegov; Robert A S Ariëns
Journal:  Blood Adv       Date:  2022-07-12

3.  Congenital fibrinogen disorders with repeated thrombosis.

Authors:  Xiuli Zhang; Chuang Zhang; Baoheng Wang; Ningheng Chen; Gaihe Sun; Xueli Guo
Journal:  J Thromb Thrombolysis       Date:  2020-02       Impact factor: 2.300

4.  Congenital hypodysfibrinogenemia associated with a novel deletion of three residues (γAla289_Asp291del) in fibrinogen.

Authors:  Liqing Zhu; Misheng Zhao; Mingshan Wang; Zhefeng Lou; Xiaoli Chen; Liangliang Pan; Dandan Yu; Wenli Xia; Han Wang; Bin Zhou; Shenmeng Gao
Journal:  J Thromb Thrombolysis       Date:  2018-08       Impact factor: 2.300

5.  Recombinant γY278H Fibrinogen Showed Normal Secretion from CHO Cells, but a Corresponding Heterozygous Patient Showed Hypofibrinogenemia.

Authors:  Tomu Kamijo; Takahiro Kaido; Masahiro Yoda; Shinpei Arai; Kazuyoshi Yamauchi; Nobuo Okumura
Journal:  Int J Mol Sci       Date:  2021-05-14       Impact factor: 5.923

  5 in total

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