These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

108 related articles for article (PubMed ID: 8547094)

  • 21. Factor VIII gene mutations found by a comparative study of SSCP, DGGE and CMC and their analysis on a molecular model of factor VIII protein.
    Schwaab R; Oldenburg J; Lalloz MR; Schwaab U; Pemberton S; Hanfland P; Brackmann HH; Tuddenham EG; Michaelides K
    Hum Genet; 1997 Dec; 101(3):323-32. PubMed ID: 9439662
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mutations in haemophilia A.
    Schwaab R; Oldenburg J; Tuddenham EG; Brackmann HH; Olek K
    Br J Haematol; 1993 Mar; 83(3):450-8. PubMed ID: 8485051
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Identification of 32 novel mutations in the factor VIII gene in Indian patients with hemophilia A.
    Ahmed RP; Ivaskevicius V; Kannan M; Seifried E; Oldenburg J; Saxena R
    Haematologica; 2005 Feb; 90(2):283-4. PubMed ID: 15710596
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A recurrent missense mutation (Arg----Gln) and a partial deletion in factor VIII gene causing severe haemophilia A.
    Bernardi F; Volinia S; Patracchini P; Gemmati D; Boninsegna S; Schwienbacher C; Marchetti G
    Br J Haematol; 1989 Feb; 71(2):271-6. PubMed ID: 2493803
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Screening for nonsense mutations in patients with severe hemophilia A can provide rapid, direct carrier detection.
    Reiner AP; Thompson AR
    Hum Genet; 1992 Apr; 89(1):88-94. PubMed ID: 1349567
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Three missense mutations in Arg codons of the factor VIII genes of mild to moderately severe hemophilia A patients.
    Reiner AP; Stray SM; Thompson AR
    Thromb Res; 1992 Apr; 66(1):93-9. PubMed ID: 1412186
    [No Abstract]   [Full Text] [Related]  

  • 28. Screening for mutations in haemophilia A patients by multiplex PCR-SSCP, Southern blotting and RNA analysis: the detection of a genetic abnormality in the factor VIII gene in 30 out of 35 patients.
    Pieneman WC; Deutz-Terlouw PP; Reitsma PH; Briët E
    Br J Haematol; 1995 Jun; 90(2):442-9. PubMed ID: 7794769
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Factor VIII Ise (R2159C) in a patient with mild hemophilia A, an abnormal factor VIII with retention of function but modification of C2 epitopes.
    Suzuki H; Shima M; Arai M; Kagawa K; Fukutake K; Kamisue S; Nakai H; Morichika S; Tanaka I; Inoue M; Gale K; Tuddenham EG; Yoshioka A
    Thromb Haemost; 1997 May; 77(5):862-7. PubMed ID: 9184393
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Analysis of factor VIII mRNA reveals defects in everyone of 28 haemophilia A patients.
    Naylor JA; Green PM; Rizza CR; Giannelli F
    Hum Mol Genet; 1993 Jan; 2(1):11-7. PubMed ID: 8490618
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Detection and sequence of mutations in the factor VIII gene of haemophiliacs.
    Gitschier J; Wood WI; Tuddenham EG; Shuman MA; Goralka TM; Chen EY; Lawn RM
    Nature; 1985 May 30-Jun 5; 315(6018):427-30. PubMed ID: 2987704
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Characterization of dysfunctional factor VIII molecules.
    Hoyer LW
    Methods Enzymol; 1993; 222():169-76. PubMed ID: 8412792
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mutations in a subgroup of patients with mild haemophilia A and a familial discrepancy between the one-stage and two-stage factor VIII:C methods.
    Rudzki Z; Duncan EM; Casey GJ; Neumann M; Favaloro EJ; Lloyd JV
    Br J Haematol; 1996 Aug; 94(2):400-6. PubMed ID: 8759905
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Identification of a missense mutation in the factor VIII gene of a mild hemophiliac.
    Gitschier J; Wood WI; Shuman MA; Lawn RM
    Science; 1986 Jun; 232(4756):1415-6. PubMed ID: 3012775
    [TBL] [Abstract][Full Text] [Related]  

  • 35. CRM+ haemophilia A due to a missense mutation (372----Cys) at the internal heavy chain thrombin cleavage site.
    Pattinson JK; McVey JH; Boon M; Ajani A; Tuddenham EG
    Br J Haematol; 1990 May; 75(1):73-7. PubMed ID: 1973901
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Characterization of genetic defects of hemophilia A in patients of Chinese origin.
    Lin SW; Lin SR; Shen MC
    Genomics; 1993 Dec; 18(3):496-504. PubMed ID: 8307558
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A domain mutations in 65 haemophilia A families and molecular modelling of dysfunctional factor VIII proteins.
    Liu M; Murphy ME; Thompson AR
    Br J Haematol; 1998 Dec; 103(4):1051-60. PubMed ID: 9886318
    [TBL] [Abstract][Full Text] [Related]  

  • 38. High throughput mutation screening of the factor VIII gene (F8C) in hemophilia A: 37 novel mutations and genotype-phenotype correlation.
    Citron M; Godmilow L; Ganguly T; Ganguly A
    Hum Mutat; 2002 Oct; 20(4):267-74. PubMed ID: 12325022
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Identification of mutations in two families with sporadic hemophilia A.
    Paynton C; Sarkar G; Sommer SS
    Hum Genet; 1991 Aug; 87(4):397-400. PubMed ID: 1908817
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Non-inversion factor VIII mutations in 80 hemophilia A families including 24 with alloimmune responses.
    Liu ML; Nakaya S; Thompson AR
    Thromb Haemost; 2002 Feb; 87(2):273-6. PubMed ID: 11858487
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.