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Journal Abstract Search

124 related items for PubMed ID: 1421174

  • 21. Adjacent substitutions (γ352Gly→Cys and 353Thr→Pro) in fibrinogen Ilam cause diminished γ chain expression.
    Brennan SO, Oliver J, Davis RL.
    Thromb Haemost; 2011 Feb; 105(2):379-81. PubMed ID: 21057694
    [No 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 New Britain: characterization of an A alpha Arg 16-->His variant human fibrinogen.
    Webb CD, Hantgan RR, Byeff PD, Owen J.
    Blood Coagul Fibrinolysis; 1994 Apr 15; 5(2):233-8. PubMed ID: 8054455
    [Abstract] [Full Text] [Related]

  • 24. Fibrinogen Bern I: substitution gamma 337 Asn-->Lys is responsible for defective fibrin monomer polymerization.
    Steinmann C, Reber P, Jungo M, Lämmle B, Heinemann G, Wermuth B, Furlan M.
    Blood; 1993 Oct 01; 82(7):2104-8. PubMed ID: 8400260
    [Abstract] [Full Text] [Related]

  • 25. A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo.
    Margaglione M, Vecchione G, Santacroce R, D'Angelo F, Casetta B, Papa ML, Grandone E, Di Minno G.
    Thromb Haemost; 2001 Dec 01; 86(6):1483-8. PubMed ID: 11776317
    [Abstract] [Full Text] [Related]

  • 26. Abnormal polymerization and normal binding of plasminogen and t-PA in three new dysfibrinogenaemias: Barcelona III and IV (gamma Arg 275-->His) and Villajoyosa (gamma Arg 275-->Cys).
    Borrell M, Garí M, Coll I, Vallvé C, Tirado I, Soria JM, Sala N, Muñoz C, Oliver A, García A.
    Blood Coagul Fibrinolysis; 1995 May 01; 6(3):198-206. PubMed ID: 7654933
    [Abstract] [Full Text] [Related]

  • 27. Hypofibrinogenemia due to novel 316 Asp --> Tyr substitution in the fibrinogen Bbeta chain.
    Brennan SO, Wyatt JM, May S, De Caigney S, George PM.
    Thromb Haemost; 2001 Mar 01; 85(3):450-3. PubMed ID: 11307813
    [Abstract] [Full Text] [Related]

  • 28. [Functional analysis of heterozygous plasma dysfibrinogens derived from two families of gammaArg275Cys and three families of gammaArg275His, and haplotype analysis for these families].
    Kamijyo Y, Hirota-Kawadobora M, Fujihara N, Wakabayashi S, Matsuda K, Yamauchi K, Terasawa F, Okumura N, Honda T.
    Rinsho Byori; 2009 Jul 01; 57(7):651-8. PubMed ID: 19708534
    [Abstract] [Full Text] [Related]

  • 29. Fibrinogen Matsumoto II: gamma 308 Asn-->Lys (AAT-->AAG) mutation associated with bleeding tendency.
    Okumura N, Furihata K, Terasawa F, Ishikawa S, Ueno I, Katsuyama T.
    Br J Haematol; 1996 Sep 01; 94(3):526-8. PubMed ID: 8790154
    [Abstract] [Full Text] [Related]

  • 30. Fibrinogen Seoul (FGG Ala341Asp): a novel mutation associated with hypodysfibrinogenemia.
    Song KS, Park NJ, Choi JR, Doh HJ, Chung KH.
    Clin Appl Thromb Hemost; 2006 Jul 01; 12(3):338-43. PubMed ID: 16959688
    [Abstract] [Full Text] [Related]

  • 31. Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bbeta and gamma chain mutations.
    Castaman G, Giacomelli SH, Duga S, Rodeghiero F.
    Haemophilia; 2008 May 01; 14(3):630-3. PubMed ID: 18393984
    [No Abstract] [Full Text] [Related]

  • 32. 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 May 01; 121(1):75-84. PubMed ID: 17408725
    [Abstract] [Full Text] [Related]

  • 33. Fibrinogen Krakow: a novel hypo/dysfibrinogenemia mutation in fibrinogen gamma chain (Asn325Ile) affecting fibrin clot structure and function.
    Undas A, Zdziarska J, Iwaniec T, Stepien E, Skotnicki AB, de Moerloose P, Neerman-Arbez M.
    Thromb Haemost; 2009 May 01; 101(5):975-6. PubMed ID: 19404553
    [No Abstract] [Full Text] [Related]

  • 34. The amino acids that constitute sequence gamma 268-282 of fibrinogen are not involved in fibrin monomer polymerization.
    Janiak A, Plucinski T, Kupryszewski G, Cierniewski CS.
    Acta Biochim Pol; 1993 May 01; 40(4):515-20. PubMed ID: 8140826
    [Abstract] [Full Text] [Related]

  • 35. Fibrinogen Guarenas, an abnormal fibrinogen with an Aalpha-chain truncation due to a nonsense mutation at Aalpha 467 Glu (GAA)-->stop (TAA).
    Marchi R, Carvajal Z, Meyer M, Soria J, Ruiz-Saez A, Arocha-Piñango CL, Weisel JW.
    Thromb Res; 2006 May 01; 118(5):637-50. PubMed ID: 16406498
    [Abstract] [Full Text] [Related]

  • 36. Normal plasmic cleavage of the gamma-chain variant of "fibrinogen Saga" with an Arg-275 to His substitution.
    Yamazumi K, Terukina S, Onohara S, Matsuda M.
    Thromb Haemost; 1988 Dec 22; 60(3):476-80. PubMed ID: 2976995
    [Abstract] [Full Text] [Related]

  • 37. 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 22; 10(2):93-9. PubMed ID: 10192658
    [Abstract] [Full Text] [Related]

  • 38. A novel fibrinogen variant--Liberec: dysfibrinogenaemia associated with gamma Tyr262Cys substitution.
    Kotlín R, Sobotková A, Suttnar J, Salaj P, Walterová L, Riedel T, Reicheltová Z, Dyr JE.
    Eur J Haematol; 2008 Aug 22; 81(2):123-9. PubMed ID: 18485115
    [Abstract] [Full Text] [Related]

  • 39. Homophenotypic Aalpha R16H fibrinogen (Kingsport): uniquely altered polymerization associated with slower fibrinopeptide A than fibrinopeptide B release.
    Galanakis DK, Neerman-Arbez M, Scheiner T, Henschen A, Hubbs D, Nagaswami C, Weisel JW.
    Blood Coagul Fibrinolysis; 2007 Dec 22; 18(8):731-7. PubMed ID: 17982313
    [Abstract] [Full Text] [Related]

  • 40. Fibrinogen Saint-Germain II: hypofibrinogenemia due to heterozygous gamma N345S mutation.
    de Raucourt E, de Mazancourt P, Maghzal GJ, Brennan SO, Mosesson MW.
    Thromb Haemost; 2005 Nov 22; 94(5):965-8. PubMed ID: 16363237
    [Abstract] [Full Text] [Related]

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