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Year | Number of Results |
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1981 | 1 |
1993 | 1 |
1996 | 1 |
2006 | 1 |
2008 | 1 |
2024 | 0 |
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Localization of a fibrin polymerization site.
J Biol Chem. 1981 Apr 10;256(7):3544-9.
J Biol Chem. 1981.
PMID: 6451630
Free article.
Paris I dysfibrinogenemia: a point mutation in intron 8 results in insertion of a 15 amino acid sequence in the fibrinogen gamma-chain.
Rosenberg JB, Newman PJ, Mosesson MW, Guillin MC, Amrani DL.
Rosenberg JB, et al.
Thromb Haemost. 1993 Mar 1;69(3):217-20.
Thromb Haemost. 1993.
PMID: 8470043
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The role of betagamma and alphagamma complexes in the assembly of human fibrinogen.
Huang S, Cao Z, Chung DW, Davie EW.
Huang S, et al.
J Biol Chem. 1996 Nov 1;271(44):27942-7. doi: 10.1074/jbc.271.44.27942.
J Biol Chem. 1996.
PMID: 8910396
Free article.
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The fibrinogen Aalpha R16C mutation results in fibrinolytic resistance.
Flood VH, Al-Mondhiry HA, Farrell DH.
Flood VH, et al.
Br J Haematol. 2006 Jul;134(2):220-6. doi: 10.1111/j.1365-2141.2006.06129.x.
Br J Haematol. 2006.
PMID: 16846481
Free article.
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Congenital hypofibrinogenemia: characterization of two missense mutations affecting fibrinogen assembly and secretion.
Platè M, Asselta R, Spena S, Spreafico M, Fagoonee S, Peyvandi F, Tenchini ML, Duga S.
Platè M, et al.
Blood Cells Mol Dis. 2008 Nov-Dec;41(3):292-7. doi: 10.1016/j.bcmd.2008.06.004. Epub 2008 Aug 3.
Blood Cells Mol Dis. 2008.
PMID: 18676163
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