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Journal Abstract Search

205 related items for PubMed ID: 6648427

  • 1. [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
    [Abstract] [Full Text] [Related]

  • 2. [Fibrinogen Bern III: a further case of hereditary fibrinogen variants with substitution A alpha 16 Arg----Cys].
    Furlan M, Leupin L, Biasiutti FD, Lämmle B.
    Schweiz Med Wochenschr; 1991 Jul 20; 121(29):1068-71. PubMed ID: 1891701
    [Abstract] [Full Text] [Related]

  • 3. 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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  • 5. 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 01; 2(4):501-6. PubMed ID: 1768762
    [Abstract] [Full Text] [Related]

  • 6. Fibrinogen Milano IV, another case of congenital dysfibrinogenemia with an abnormal fibrinopeptide A release (A alpha 16 Arg----His).
    Bögli C, Hofer A, Baudo F, Redaelli R, Furlan M.
    Haemostasis; 1992 Aug 01; 22(1):7-11. PubMed ID: 1521828
    [Abstract] [Full Text] [Related]

  • 7. 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 01; 10(2):93-9. PubMed ID: 10192658
    [Abstract] [Full Text] [Related]

  • 8. Fibrinogen Sapporo: dysfibrinogenemia characterized by the replacement of A alpha arginine-16 by histidine resulting in the delayed release of fibrinopeptide A by thrombin.
    Asakura S, Terukina S, Yamazumi K, Matsuda M, Murayama H, Higuchi A, Musashi M, Sakurada K, Miyazaki T.
    Nihon Ketsueki Gakkai Zasshi; 1989 Sep 01; 52(6):1094-104. PubMed ID: 2588959
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. Fibrinogen Manchester: identification of an abnormal fibrinopeptide A with a C-terminal arginine leads to histidine substitution.
    Southan C, Kehl M, Henschen A, Lane DA.
    Br J Haematol; 1983 May 30; 54(1):143-51. PubMed ID: 6849832
    [Abstract] [Full Text] [Related]

  • 11. [Fibrinogen Bern I and fibrinogen Bern II: 2 hereditary fibrinogen variants with diverse biochemical properties].
    Rupp C, Kuyas C, Haeberli A, Furlan M, von Fliedner V, Beck EA.
    Schweiz Med Wochenschr; 1981 Oct 10; 111(41):1543-5. PubMed ID: 7313627
    [Abstract] [Full Text] [Related]

  • 12. Fibrinogen Osaka IV: a congenital dysfibrinogenemia found in a patient originally reported in relation to surgery, now defined to have an A alpha arginine-16 to histidine substitution.
    Yamazumi K, Terukina S, Matsuda M, Kanbayashi J, Sakon M, Tsujinaka T.
    Surg Today; 1993 Oct 10; 23(1):45-50. PubMed ID: 8461606
    [Abstract] [Full Text] [Related]

  • 13. Fibrinogen Petoskey, a dysfibrinogenemia characterized by replacement of Arg-A alpha 16 by a histidyl residue. Evidence for thrombin-catalyzed hydrolysis at a histidyl residue.
    Higgins DL, Shafer JA.
    J Biol Chem; 1981 Dec 10; 256(23):12013-7. PubMed ID: 7298640
    [No Abstract] [Full Text] [Related]

  • 14. A kinetic method for characterization of heterogenous fibrinogen and its application to fibrinogen Grand Rapids, a congenital dysfibrinogenemia.
    Higgins DL, Lewis SD, Penner JA, Shafer JA.
    Thromb Haemost; 1982 Oct 29; 48(2):182-6. PubMed ID: 6217579
    [Abstract] [Full Text] [Related]

  • 15. Thrombin-induced fibrinopeptide release from a fibrinogen variant (fibrinogen Sydney I) with an Aalpha Arg-16----His substitution.
    Southan C, Lane DA, Bode W, Henschen A.
    Eur J Biochem; 1985 Mar 15; 147(3):593-600. PubMed ID: 3979390
    [Abstract] [Full Text] [Related]

  • 16. Fibrinogen Geneva, a new case of A alpha 16 Arg----Cys dysfibrinogenaemia.
    Furlan M, Bögli C, Hofer A, Bouvier CA, de Moerloose P.
    Blood Coagul Fibrinolysis; 1990 Jun 15; 1(2):139-43. PubMed ID: 2130925
    [Abstract] [Full Text] [Related]

  • 17. Fibrinogen Barcelona II: a new case of A alpha 16 Arg----His substitution.
    Borrell M, Vila L, Solá J, Coll I, Fontcuberta J.
    Haemostasis; 1990 Jun 15; 20(1):1-7. PubMed ID: 2323678
    [Abstract] [Full Text] [Related]

  • 18. [Inherited dysfibrinogenemia caused by Arg275His in the beta chain of fibrinogen].
    Fang Y, Wang X, Qi H, Wu W, Ding Q, Dai J, Zhou R, Wang W, Xie S, Wang H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr 15; 22(2):201-3. PubMed ID: 15793786
    [Abstract] [Full Text] [Related]

  • 19. Novel structure elucidation strategy for genetically abnormal fibrinogens with incomplete fibrinopeptide release as applied to fibrinogen Schwarzach.
    Henschen A, Kehl M, Deutsch E.
    Hoppe Seylers Z Physiol Chem; 1983 Dec 15; 364(12):1747-51. PubMed ID: 6667926
    [Abstract] [Full Text] [Related]

  • 20. 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 15; 53(4):587-97. PubMed ID: 6830702
    [Abstract] [Full Text] [Related]

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