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Journal Abstract Search

255 related items for PubMed ID: 7841300

  • 21. 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.
    Thromb Haemost; 1993 Mar 01; 69(3):217-20. PubMed ID: 8470043
    [Abstract] [Full Text] [Related]

  • 22. Three abnormal fibrinogen variants with the same amino acid substitution (gamma 275 Arg----His): fibrinogens Bergamo II, Essen and Perugia.
    Reber P, Furlan M, Henschen A, Kaudewitz H, Barbui T, Hilgard P, Nenci GG, Berrettini M, Beck EA.
    Thromb Haemost; 1986 Dec 15; 56(3):401-6. PubMed ID: 3563970
    [Abstract] [Full Text] [Related]

  • 23. Fibrinogen Nový Jicín and Praha II: cases of hereditary Aalpha 16 Arg-->Cys and Aalpha 16 Arg-->His dysfibrinogenemia.
    Kotlín R, Chytilová M, Suttnar J, Riedel T, Salaj P, Blatný J, Santrůcek J, Klener P, Dyr JE.
    Thromb Res; 2007 Dec 15; 121(1):75-84. PubMed ID: 17408725
    [Abstract] [Full Text] [Related]

  • 24. Fibrinogen Oviedo I. A new Spanish dysfibrinogenaemia.
    Fernández FJ, Rodríguez Pinto C, Páramo J, Cuesta B, Collado M, Rocha E.
    Blood Coagul Fibrinolysis; 1990 Oct 15; 1(4-5):571-5. PubMed ID: 2133236
    [Abstract] [Full Text] [Related]

  • 25. Fibrinogen Longmont. A heterozygous abnormal fibrinogen with B beta Arg-166 to Cys substitution associated with defective fibrin polymerization.
    Lounes KC, Lefkowitz JB, Coates AI, Hantgan RR, Henschen-Edman A, Lord ST.
    Ann N Y Acad Sci; 2001 Oct 15; 936():129-32. PubMed ID: 11460470
    [Abstract] [Full Text] [Related]

  • 26. Fibrinogen Matsumoto III: a variant with gamma275 Arg-->Cys (CGC-->TGC)--comparison of fibrin polymerization properties with those of Matsumoto I (gamma364 Asp-->His) and Matsumoto II (gamma308 Asn-->Lys).
    Terasawa F, Okumura N, Higuchi Y, Ishikawa S, Tozuka M, Ishida F, Kitano K, Katsuyama T.
    Thromb Haemost; 1999 May 15; 81(5):763-6. PubMed ID: 10365751
    [Abstract] [Full Text] [Related]

  • 27. A case of congenital afibrinogenemia: fibrinogen Hakata, a novel nonsense mutation of the fibrinogen gamma-chain gene.
    Iida H, Ishii E, Nakahara M, Urata M, Wakiyama M, Kurihara M, Watanabe K, Kai T, Ihara K, Kinoshita S, Hamasaki N.
    Thromb Haemost; 2000 Jul 15; 84(1):49-53. PubMed ID: 10928469
    [Abstract] [Full Text] [Related]

  • 28. A frameshift mutation in Exon V of the A alpha-chain gene leading to truncated A alpha-chains in the homozygous dysfibrinogen Milano III.
    Furlan M, Steinmann C, Jungo M, Bögli C, Baudo F, Redaelli R, Fedeli F, Lämmle B.
    J Biol Chem; 1994 Dec 30; 269(52):33129-34. PubMed ID: 7806542
    [Abstract] [Full Text] [Related]

  • 29. Fibrinogen Milano XII: a dysfunctional variant containing 2 amino acid substitutions, Aalpha R16C and gamma G165R.
    Bolliger-Stucki B, Lord ST, Furlan M.
    Blood; 2001 Jul 15; 98(2):351-7. PubMed ID: 11435303
    [Abstract] [Full Text] [Related]

  • 30. 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 15; 2(4):501-6. PubMed ID: 1768762
    [Abstract] [Full Text] [Related]

  • 31. Novel fibrinogen mutation (gamma 313 Ser-->Asn) associated with hypofibrinogenemia in two unrelated families.
    Meyer M, Bergmann F, Brennan SO.
    Blood Coagul Fibrinolysis; 2006 Jan 15; 17(1):63-7. PubMed ID: 16607083
    [Abstract] [Full Text] [Related]

  • 32. Abnormal fibrinogens IJmuiden (B beta Arg14----Cys) and Nijmegen (B beta Arg44----Cys) form disulfide-linked fibrinogen-albumin complexes.
    Koopman J, Haverkate F, Grimbergen J, Engesser L, Nováková I, Kerst AF, Lord ST.
    Proc Natl Acad Sci U S A; 1992 Apr 15; 89(8):3478-82. PubMed ID: 1565641
    [Abstract] [Full Text] [Related]

  • 33. The mutation in fibrinogen Bicêtre II (gamma Asn308-->Lys) does not affect the binding of t-PA and plasminogen to fibrin.
    Grailhe P, Boyer-Neumann C, Haverkate F, Grimbergen J, Larrieu MJ, Anglés-Cano E.
    Blood Coagul Fibrinolysis; 1993 Oct 15; 4(5):679-87. PubMed ID: 8292717
    [Abstract] [Full Text] [Related]

  • 34. Fibrinogen Alès: a homozygous case of dysfibrinogenemia (gamma-Asp(330)-->Val) characterized by a defective fibrin polymerization site "a".
    Lounes KC, Soria C, Mirshahi SS, Desvignes P, Mirshahi M, Bertrand O, Bonnet P, Koopman J, Soria J.
    Blood; 2000 Nov 15; 96(10):3473-9. PubMed ID: 11071644
    [Abstract] [Full Text] [Related]

  • 35. Fibrinogen Caracas V, an abnormal fibrinogen with an Aalpha 532 Ser-->Cys substitution associated with thrombosis.
    Marchi R, Lundberg U, Grimbergen J, Koopman J, Torres A, de Bosch NB, Haverkate F, Arocha Piñango CL.
    Thromb Haemost; 2000 Aug 15; 84(2):263-70. PubMed ID: 10959699
    [Abstract] [Full Text] [Related]

  • 36. A congenitally abnormal fibrinogen (Vlissingen) with a 6-base deletion in the gamma-chain gene, causing defective calcium binding and impaired fibrin polymerization.
    Koopman J, Haverkate F, Briët E, Lord ST.
    J Biol Chem; 1991 Jul 15; 266(20):13456-61. PubMed ID: 2071611
    [Abstract] [Full Text] [Related]

  • 37. 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 15; 2(3):413-7. PubMed ID: 1932527
    [Abstract] [Full Text] [Related]

  • 38. Dysfibrinogen Kagoshima with the amino acid substitution gammaThr-314 to Ile: analyses of molecular abnormalities and thrombophilic nature of this abnormal molecule.
    Niwa K, Mimuro J, Miyata M, Sugo T, Ohmori T, Madoiwa S, Tei C, Sakata Y.
    Thromb Res; 2008 Jun 15; 121(6):773-80. PubMed ID: 17854865
    [Abstract] [Full Text] [Related]

  • 39. A C-terminal amino acid substitution in the gamma-chain caused by a novel heterozygous frameshift mutation (Fibrinogen Matsumoto VII) results in hypofibrinogenaemia.
    Fujihara N, Haneishi A, Yamauchi K, Terasawa F, Ito T, Ishida F, Okumura N.
    Thromb Haemost; 2010 Aug 15; 104(2):213-23. PubMed ID: 20589319
    [Abstract] [Full Text] [Related]

  • 40. Fibrinogen Lima. A new dysfibrinogenaemia with a high-molecular-weight alpha-chain and effective polymerization.
    Arocha-Piñango CL, Rodriguez S, Nagy H, Perez Requejo JL.
    Blood Coagul Fibrinolysis; 1990 Oct 15; 1(4-5):561-5. PubMed ID: 2133234
    [Abstract] [Full Text] [Related]

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