BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

409 related articles for article (PubMed ID: 19357501)

  • 21. Factor IX mutations in haemophilia B patients in Malaysia: a preliminary study.
    Balraj P; Ahmad M; Khoo AS; Ayob Y
    Malays J Pathol; 2012 Jun; 34(1):67-9. PubMed ID: 22870602
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Factor IX gene haplotypes and its relevance for the indirect genetic analysis of haemophilia B in its Indian perspective.
    Singh M; Singh P
    Blood Coagul Fibrinolysis; 2008 Jul; 19(5):429-32. PubMed ID: 18600094
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Gene diagnosis of 3 haemophilia B families].
    Zhang Y; Yang LH; Lu YL; Ding QL; Wang XF; Liu XE; Zhang L
    Zhonghua Xue Ye Xue Za Zhi; 2008 Mar; 29(3):179-82. PubMed ID: 18788618
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Identification of twenty-one new mutations in the factor IX gene by SSCP analysis.
    Montejo JM; Magallón M; Tizzano E; Solera J
    Hum Mutat; 1999; 13(2):160-5. PubMed ID: 10094553
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Methylation of the factor IX gene--a basic reason for the mutation causing hemophilia B].
    Mazin AL
    Mol Biol (Mosk); 1995; 29(1):71-90. PubMed ID: 7723765
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Allelic heterogeneity of molecular events in human coagulation factor IX in Asian Indians. Mutation in brief #965. Online.
    Mahajan A; Chavali S; Ghosh S; Kabra M; Chowdhury MR; ; Bharadwaj D
    Hum Mutat; 2007 May; 28(5):526. PubMed ID: 17397055
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Insight into molecular changes of the FIX protein in a series of Italian patients with haemophilia B.
    Bicocchi MP; Pasino M; Rosano C; Molinari AC; Della Valle E; Lanza T; Bottini F; Acquila M
    Haemophilia; 2006 May; 12(3):263-70. PubMed ID: 16643212
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. G244E in the canine factor IX gene leads to severe haemophilia B in Rhodesian Ridgebacks.
    Mischke R; Kühnlein P; Kehl A; Langbein-Detsch I; Steudle F; Schmid A; Dandekar T; Czwalinna A; Müller E
    Vet J; 2011 Jan; 187(1):113-8. PubMed ID: 20303304
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Heteroduplex analysis in hemophilia B: detection of two novel factor IX gene mutations.
    Driscoll MC; Chu A; Hilgartner MW
    Am J Hematol; 1996 Apr; 51(4):324-7. PubMed ID: 8602635
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mutation analysis of Swedish haemophilia B families - high frequency of unique mutations.
    Mårtensson A; Letelier A; Halldén C; Ljung R
    Haemophilia; 2016 May; 22(3):440-5. PubMed ID: 26612714
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Molecular diagnosis of inherited coagulation disorders--sequence analysis of hemophilia B patients with anti-factor IX antibodies].
    Tanimoto M; Matsushita T; Takamatsu J; Saito H
    Rinsho Byori; 1990 Sep; 38(9):1041-6. PubMed ID: 2232265
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Establishment of a new mismatch PCR-RFLP technique for detection of G10430A common mutation present in moderate to mild haemophilia B patients belonging to Gujarati community from the western part of India.
    Quadros L; Ghosh K; Shetty S
    Haemophilia; 2008 May; 14(3):628-9. PubMed ID: 18393981
    [No Abstract]   [Full Text] [Related]  

  • 35. Two mutations of the factor IX gene including a donor splice consensus deletion and a point mutation in a Dutch patient with severe hemophilia B.
    Poort SR; Briët E; Bertina RM; Reitsma PH
    Thromb Haemost; 1990 Nov; 64(3):379-84. PubMed ID: 2096489
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Heterogeneity of the factor IX locus in nine hemophilia B inhibitor patients.
    Matthews RJ; Anson DS; Peake IR; Bloom AL
    J Clin Invest; 1987 Mar; 79(3):746-53. PubMed ID: 3029178
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Identification of factor VIII gene mutations in 101 patients with haemophilia A: mutation analysis by inversion screening and multiplex PCR and CSGE and molecular modelling of 10 novel missense substitutions.
    Jayandharan G; Shaji RV; Baidya S; Nair SC; Chandy M; Srivastava A
    Haemophilia; 2005 Sep; 11(5):481-91. PubMed ID: 16128892
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Structural analysis of factor IX protein variants to predict functional aberration causing haemophilia B.
    Mukherjee S; Saha A; Biswas P; Mandal C; Ray K
    Haemophilia; 2008 Sep; 14(5):1076-81. PubMed ID: 18540896
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Fast and efficient mutation detection method using multiplex PCR and cycle sequencing--application to haemophilia B.
    Costa JM; Ernault P; Vidaud D; Vidaud M; Meyer D; Lavergne JM
    Thromb Haemost; 2000 Feb; 83(2):244-7. PubMed ID: 10739381
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 21.