BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

138 related articles for article (PubMed ID: 8236150)

  • 1. A deletion located in the 3' non translated part of the factor IX gene responsible for mild haemophilia B.
    de la Salle C; Charmantier JL; Baas MJ; Schwartz A; Wiesel ML; Grunebaum L; Cazenave JP
    Thromb Haemost; 1993 Aug; 70(2):370-1. PubMed ID: 8236150
    [No Abstract]   [Full Text] [Related]  

  • 2. Severe haemophilia B due to a 6 kb factor IX gene deletion including exon 4: non-homologous recombination associated with a shortened transcript from whole blood.
    Hsu TC; Nakaya SM; Thompson AR
    Thromb Haemost; 2007 Feb; 97(2):176-80. PubMed ID: 17264943
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Partial deletion by illegitimate recombination of the factor IX gene in a haemophilia B family with two inhibitor patients.
    Green PM; Bentley DR; Mibashan RS; Giannelli F
    Mol Biol Med; 1988 Apr; 5(2):95-106. PubMed ID: 3398774
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Deletions with inversions: report of a mutation and review of the literature.
    Ketterling RP; Ricke DO; Wurster MW; Sommer SS
    Hum Mutat; 1993; 2(1):53-7. PubMed ID: 8477264
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular characterization of hemophilia B in North Indian families: identification of novel and recurrent molecular events in the factor IX gene.
    Mahajan A; Chavali S; Kabra M; Chowdhury MR; Bharadwaj D
    Haematologica; 2004 Dec; 89(12):1498-503. PubMed ID: 15590401
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Twenty-five novel mutations of the factor IX gene in haemophilia B.
    Wulff K; Schröder W; Wehnert M; Herrmann FH
    Hum Mutat; 1995; 6(4):346-8. PubMed ID: 8680410
    [No Abstract]   [Full Text] [Related]  

  • 7. A single base pair deletion in the promoter region of the factor IX gene is associated with haemophilia B.
    Hall AJ; Chuansumrit A; Peake IR; Winship PR
    Thromb Haemost; 1994 Dec; 72(6):799-803. PubMed ID: 7740444
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel mutation (Val-373 to Glu) in the catalytic domain of factor IX, resulting in moderately/severe hemophilia B in a southern French patient.
    Aguilar-Martinez P; Romey MC; Gris JC; Schved JF; Demaille J; Claustres M
    Hum Mutat; 1994; 3(2):156-8. PubMed ID: 8199596
    [No Abstract]   [Full Text] [Related]  

  • 9. Novel human pathological mutations. Gene symbol: F9. Disease: Haemophilia B.
    Niazi G; Shaukat Z; Masood K; Hussain R
    Hum Genet; 2009 Aug; 126(2):332. PubMed ID: 19693996
    [No Abstract]   [Full Text] [Related]  

  • 10. Haemophilia B caused by a missense mutation in the prepeptide sequence of factor IX.
    Green PM; Mitchell VE; McGraw A; Goldman E; Giannelli F
    Hum Mutat; 1993; 2(2):103-7. PubMed ID: 8318985
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular pathology of haemophilia B: identification of five novel mutations including a LINE 1 insertion in Indian patients.
    Mukherjee S; Mukhopadhyay A; Banerjee D; Chandak GR; Ray K
    Haemophilia; 2004 May; 10(3):259-63. PubMed ID: 15086324
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of factor IX mutations in Iranian haemophilia B patients by SSCP and sequencing.
    Karimipoor M; Zeinali S; Nafissi N; Tuddenham EG; Lak M; Safaee R
    Thromb Res; 2007; 120(1):135-9. PubMed ID: 17014892
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular genotyping of the Italian cohort of patients with hemophilia B.
    Belvini D; Salviato R; Radossi P; Pierobon F; Mori P; Castaldo G; Tagariello G;
    Haematologica; 2005 May; 90(5):635-42. PubMed ID: 15921378
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Complete deletion of factor IX gene and inhibition of factor IX activity in a labrador retriever with hemophilia B.
    Brooks MB; Gu W; Ray K
    J Am Vet Med Assoc; 1997 Dec; 211(11):1418-21. PubMed ID: 9394892
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Spectrum of factor IX gene mutations causing haemophilia B from India.
    Ghosh K; Quadros L; Shetty S
    Blood Coagul Fibrinolysis; 2009 Jul; 20(5):333-6. PubMed ID: 19357501
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Regulatory mechanism of the factor IX gene.
    Kurachi K; Kurachi S
    Thromb Haemost; 1995 Mar; 73(3):333-9. PubMed ID: 7667813
    [No Abstract]   [Full Text] [Related]  

  • 17. Two distinct mutations cause severe hemophilia B in two unrelated canine pedigrees.
    Gu W; Brooks M; Catalfamo J; Ray J; Ray K
    Thromb Haemost; 1999 Oct; 82(4):1270-5. PubMed ID: 10544912
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Factor IX gene analysis in 70 unrelated patients with haemophilia B: description of 13 new mutations.
    Attali O; Vinciguerra C; Trzeciak MC; Durin A; Pernod G; Gay V; Ménart C; Sobas F; Dechavanne M; Négrier C
    Thromb Haemost; 1999 Nov; 82(5):1437-42. PubMed ID: 10595634
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Marker and real-time quantitative analyses to confirm hemophilia B carrier diagnosis of a complete deletion of the F9 gene.
    Venceslá A; Barceló MJ; Baena M; Quintana M; Baiget M; Tizzano EF
    Haematologica; 2007 Nov; 92(11):1583-4. PubMed ID: 18024414
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular characterization of factor IX gene mutations in 53 patients with haemophilia B in India.
    Jayandharan GR; Shaji RV; Baidya S; Nair SC; Chandy M; Srivastava A
    Thromb Haemost; 2005 Oct; 94(4):883-6. PubMed ID: 16270648
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.