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Journal Abstract Search

210 related items for PubMed ID: 4082078

  • 1. Fibrinogen Bergamo I (A alpha 16Arg----Cys): susceptibility towards thrombin following aminoethylation, methylation or carboxamidomethylation of cysteine residues.
    Reber P, Furlan M, Beck EA, Finazzi G, Buelli M, Barbui T.
    Thromb Haemost; 1985 Aug 30; 54(2):390-3. PubMed ID: 4082078
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  • 4. Fibrinogen Kiel: a congenital dysfibrinogenaemia with (A alpha-16 Arg----His) substitution characterized by HPLC without prior isolation of fibrinogen.
    Seydewitz HH, Gram J, Bruhn HD, Witt I.
    Blood Coagul Fibrinolysis; 1991 Aug 30; 2(4):501-6. PubMed ID: 1768762
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  • 7. [Fibrinogen Bern II: hereditary fibrinogen variant with amino acid substitution of arginine replaced by histidine in position 16 of the A alpha chain].
    Rupp C, Sievi R, Furlan M, Beck EA.
    Schweiz Med Wochenschr; 1983 Oct 08; 113(40):1460-2. PubMed ID: 6648427
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  • 10. Fibrinogen Seattle releases half the normal amount of fibrinopeptide B.
    Branson HE, Schmer G, Theodor I, Pirkle H.
    Acta Haematol; 1983 Oct 08; 70(4):257-63. PubMed ID: 6414212
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  • 11. Delayed release of an abnormal fibrinopeptide A from fibrinogen Manchester: effect of the A alpha 16 Arg leads to His substitution upon fibrin monomer polymerization and the immunological crossreactivity of the peptide.
    Lane DA, Southan C, Ireland H, Thompson E, Kehl M, Henschen A.
    Br J Haematol; 1983 Apr 08; 53(4):587-97. PubMed ID: 6830702
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  • 13. Unusual A alpha 16Arg-->Cys dysfibrinogenaemic family: absence of normal A alpha-chains in fibrinogen from two of four heterozygous siblings.
    Galanakis D, Spitzer S, Scharrer I.
    Blood Coagul Fibrinolysis; 1993 Feb 08; 4(1):67-71. PubMed ID: 8457654
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  • 14. Substitution of tyrosine for phenylalanine in fibrinopeptide A results in preferential thrombin cleavage of fibrinopeptide B from fibrinogen.
    Rooney MM, Mullin JL, Lord ST.
    Biochemistry; 1998 Sep 29; 37(39):13704-9. PubMed ID: 9753458
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  • 15. Fibrinogens Bern IV, Bern V and Milano XI: three dysfunctional variants with amino acid substitutions in the thrombin cleavage site of the Aalpha-chain.
    Stucki B, Zenhäusern R, Biedermann B, Baudo F, Redaelli R, Lämmle B, Furlan M.
    Blood Coagul Fibrinolysis; 1999 Mar 29; 10(2):93-9. PubMed ID: 10192658
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  • 16. Fibrinogen Kanazawa: a congenital dysfibrinogenaemia with delayed polymerization having a replacement of proline-18 by leucine in the A alpha-chain.
    Uotani C, Miyata T, Kumabashiri I, Asakura H, Saito M, Matsuda T, Kajiyama S, Iwanaga S.
    Blood Coagul Fibrinolysis; 1991 Jun 29; 2(3):413-7. PubMed ID: 1932527
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  • 17. Fibrinogen kaiserslautern III: a new case of congenital dysfibrinogenemia with aalpha 16 arg-->cys substitution.
    Loreth RM, Meyer M, Albert FW.
    Haemostasis; 2001 Jun 29; 31(1):12-7. PubMed ID: 11408744
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  • 18. Fibrinogen Milano. VI: A heterozygous dysfibrinogenemia (A alpha 16 Arg----His) with bleeding tendency.
    Bögli C, Cofrancesco E, Cortellaro M, Della Volpe A, Hofer A, Furlan M, Zanussi C.
    Eur J Haematol; 1990 Jul 29; 45(1):26-30. PubMed ID: 2379562
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  • 19. Fibrinogen Seattle II: congenital dysfibrinogenemia with an Arg (A alpha 16)----his substitution.
    Ebert RF, Schreiler WE, Bell WR.
    Thromb Res; 1986 Jul 01; 43(1):7-13. PubMed ID: 3726812
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