124 related articles for article (PubMed ID: 15714754)
1. The dimeric Aalpha chain composition of dysfibrinogenemic molecules with mutations at Aalpha 16.
Meh DA; Siebenlist KR; Galanakis DK; Bergtrom G; Mosesson MW
Thromb Res; 1995 Jun; 78(6):531-9. PubMed ID: 15714754
[TBL] [Abstract][Full Text] [Related]
2. Confirmation of mendelian properties of heterodimeric fibrinogen molecules in a heterozygotic dysfibrinogenemia, "fibrinogen Amarillo," using gprphoresis to differentiate semifibrin molecules from fibrinogen and fibrin.
Shainoff JR; Ratnoff OD; Smejkal GB; DiBello PM; Welches WR; Lill H; Mitkevich OV; Periman P
Thromb Res; 2001 Jan; 101(2):91-9. PubMed ID: 11342210
[TBL] [Abstract][Full Text] [Related]
3. Fibrinogen Birmingham: a heterozygous dysfibrinogenemia (A alpha 16 Arg----His) containing heterodimeric molecules.
Siebenlist KR; Prchal JT; Mosesson MW
Blood; 1988 Mar; 71(3):613-8. PubMed ID: 3345340
[TBL] [Abstract][Full Text] [Related]
4. Sequence of release of fibrinopeptide A from fibrinogen molecules by thrombin or Atroxin.
Meh DA; Siebenlist KR; Bergtrom G; Mosesson MW
J Lab Clin Med; 1995 Mar; 125(3):384-91. PubMed ID: 7897305
[TBL] [Abstract][Full Text] [Related]
5. 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; 86(6):1483-8. PubMed ID: 11776317
[TBL] [Abstract][Full Text] [Related]
6. Fibrinogen Magdeburg I: a novel variant of human fibrinogen with an amino acid exchange in the fibrinopeptide A (Aalpha 9, Leu-->Pro).
Meyer M; Kutscher G; Stürzebecher J; Riesener G; Lutze G
Thromb Res; 2003 Jan; 109(2-3):145-51. PubMed ID: 12706644
[TBL] [Abstract][Full Text] [Related]
7. 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; 98(2):351-7. PubMed ID: 11435303
[TBL] [Abstract][Full Text] [Related]
8. Reactivity of fibrinogen and fibrinopeptide A containing fibrinogen fragments with antisera to fibrinopeptide A.
Canfield RE; Dean J; Nossel HL; Butler VP; Wilner GD
Biochemistry; 1976 Mar; 15(6):1203-9. PubMed ID: 943180
[TBL] [Abstract][Full Text] [Related]
9. Novel Aalpha chain truncation (fibrinogen Perth) resulting in low expression and impaired fibrinogen polymerization.
Homer VM; Mullin JL; Brennan SO; Barr A; George PM
J Thromb Haemost; 2003 Jun; 1(6):1245-50. PubMed ID: 12871326
[TBL] [Abstract][Full Text] [Related]
10. 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; 4(1):67-71. PubMed ID: 8457654
[TBL] [Abstract][Full Text] [Related]
11. Severe hypodysfibrinogenemia in compound heterozygotes of the fibrinogen AalphaIVS4 + 1G>T mutation and an AalphaGln328 truncation (fibrinogen Keokuk).
Lefebvre P; Velasco PT; Dear A; Lounes KC; Lord ST; Brennan SO; Green D; Lorand L
Blood; 2004 Apr; 103(7):2571-6. PubMed ID: 14615374
[TBL] [Abstract][Full Text] [Related]
12. A monoclonal antibody with ability to distinguish between NH2-terminal fragments derived from fibrinogen and fibrin.
Kudryk B; Rohoza A; Ahadi M; Chin J; Wiebe ME
Mol Immunol; 1983 Nov; 20(11):1191-200. PubMed ID: 6656769
[TBL] [Abstract][Full Text] [Related]
13. Evidence that heterodimers exist in the fibrinogen Matsumoto II (gamma308N-->K) proband and participate in fibrin fiber formation.
Okumura N; Terasawa F; Fujita K; Fujihara N; Tozuka M; Koh CS
Thromb Res; 2002 Aug; 107(3-4):157-62. PubMed ID: 12431483
[TBL] [Abstract][Full Text] [Related]
14. Habutobin recognizes Thr(7) in the sequence of fibrinopeptide A of rabbit fibrinogen.
Nejime T; Kinjoh K; Nakamura M; Hanashiro K; Sunagawa M; Eguchi Y; Kosugi T
Toxicon; 2000 Aug; 38(8):1029-41. PubMed ID: 10708795
[TBL] [Abstract][Full Text] [Related]
15. Aberrant hepatic processing causes removal of activation peptide and primary polymerisation site from fibrinogen Canterbury (A alpha 20 Val --> Asp).
Brennan SO; Hammonds B; George PM
J Clin Invest; 1995 Dec; 96(6):2854-8. PubMed ID: 8675656
[TBL] [Abstract][Full Text] [Related]
16. [Assembly and secretion of mutant fibrinogens with variant gamma-chain C terminal region (gamma313-gamma345)].
Terasawa F; Kamijyo Y; Fujihara N; Okumura N
Rinsho Byori; 2010 Aug; 58(8):772-8. PubMed ID: 20860169
[TBL] [Abstract][Full Text] [Related]
17. The cleavage sequence of fibrinopeptide A from fibrinogen fragment E by thrombin, atroxin or batroxobin.
Meh DA; Siebenlist KR; Bergtrom G; Mosesson MW
Blood Coagul Fibrinolysis; 1993 Feb; 4(1):107-12. PubMed ID: 8457636
[TBL] [Abstract][Full Text] [Related]
18. Fibrinogen αC-regions are not directly involved in fibrin polymerization as evidenced by a "Double-Detroit" recombinant fibrinogen mutant and knobs-mimic peptides.
Duval C; Profumo A; Aprile A; Salis A; Millo E; Damonte G; Gauer JS; Ariëns RAS; Rocco M
J Thromb Haemost; 2020 Apr; 18(4):802-814. PubMed ID: 31889430
[TBL] [Abstract][Full Text] [Related]
19. Hypofibrinogenemia in an individual with 2 coding (gamma82 A-->G and Bbeta235 P-->L) and 2 noncoding mutations.
Brennan SO; Fellowes AP; Faed JM; George PM
Blood; 2000 Mar; 95(5):1709-13. PubMed ID: 10688828
[TBL] [Abstract][Full Text] [Related]
20. Quantitative abnormality of an Aalpha chain molecular weight form in the fibrinogen of cirrhotic patients.
Weinstein MJ; Deykin D
Br J Haematol; 1978 Dec; 40(4):617-30. PubMed ID: 728374
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
