BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

102 related articles for article (PubMed ID: 8105872)

  • 21. [An expert evaluation of molecular genetic individualizing systems based on the HUMvWFII and D6S366 tetranucleotide tandem repeats].
    Efremov IA; Zaiats MV; Ivanov PL
    Sud Med Ekspert; 1998; 41(2):33-6. PubMed ID: 9608260
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Structure of the gene for human von Willebrand factor.
    Mancuso DJ; Tuley EA; Westfield LA; Worrall NK; Shelton-Inloes BB; Sorace JM; Alevy YG; Sadler JE
    J Biol Chem; 1989 Nov; 264(33):19514-27. PubMed ID: 2584182
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A highly polymorphic (ACT)n VNTR (variable nucleotide of tandem repeats) locus inside intron 12 of COL1A2, one of the two genes involved in dominant osteogenesis imperfecta.
    Pepe G
    Hum Mutat; 1993; 2(4):300-5. PubMed ID: 8104634
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Allelic associations of two polymorphic microsatellites in intron 40 of the human von Willebrand factor gene.
    Pena SD; de Souza KT; de Andrade M; Chakraborty R
    Proc Natl Acad Sci U S A; 1994 Jan; 91(2):723-7. PubMed ID: 8290589
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Identification of newly polymorphic intron 40 markers of the von Willebrand factor gene in a Japanese population.
    Tamura A; Iwata M; Fukunishi S; Nishio H; Suzuki K
    Leg Med (Tokyo); 2009 May; 11(3):129-31. PubMed ID: 19144556
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The short tandem repeat locus VWF2 in Intron 40 of the von Willebrand factor gene consists of two polymorphic sub-loci.
    Haddad AP; Sparrow RL
    Forensic Sci Int; 2001 Jul; 119(3):299-304. PubMed ID: 11390143
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Characterisation of 98 alleles in 105 unrelated individuals in the F8VWF gene.
    Mercier B; Gaucher C; Mazurier C
    Nucleic Acids Res; 1991 Sep; 19(17):4800. PubMed ID: 1679932
    [No Abstract]   [Full Text] [Related]  

  • 28. Human von Willebrand factor gene and pseudogene: structural analysis and differentiation by polymerase chain reaction.
    Mancuso DJ; Tuley EA; Westfield LA; Lester-Mancuso TL; Le Beau MM; Sorace JM; Sadler JE
    Biochemistry; 1991 Jan; 30(1):253-69. PubMed ID: 1988024
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Intrinsic polymorphism of variable number tandem repeat loci in the human genome.
    Ali S; Wallace RB
    Nucleic Acids Res; 1988 Sep; 16(17):8487-96. PubMed ID: 2901724
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Investigation on VNTR in intron 40 of vWF gene in Chinese Han population].
    Ni X; Guo J; Xia J; Li L
    Yi Chuan Xue Bao; 1996; 23(1):1-10. PubMed ID: 8695174
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A further tetranucleotide repeat polymorphism in the vWF gene.
    Kimpton C; Walton A; Gill P
    Hum Mol Genet; 1992 Jul; 1(4):287. PubMed ID: 1303199
    [No Abstract]   [Full Text] [Related]  

  • 32. Novel mutation in the first intron of the spontaneously hypertensive rat renin gene upstream of the tandem repeat element.
    Di Nicolantonio R; Yu H; Wilks A; Lan L
    Clin Exp Pharmacol Physiol Suppl; 1995 Dec; 22(1):S10-11. PubMed ID: 9072312
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The application of restriction fragment length polymorphism to disputed paternity.
    Chow ST; Yap KH; Tai HE; Tan WF
    Ann Acad Med Singap; 1993 Jan; 22(1):23-7. PubMed ID: 8099262
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Allele frequencies of three STRs of the human von Willebrand factor gene (vWF) in a Brazilian population sample.
    Pagotto RC; Canas MC; Brito RO; Simões AL
    Int J Legal Med; 1999; 112(5):326-8. PubMed ID: 10460428
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A de novo mutation in exon 28 of the von Willebrand factor gene in a patient with type IIA von Willebrand's disease coincides with an MboI polymorphism in the von Willebrand factor pseudogene.
    Pérez-Casal M; Daly M; Peake I
    Hum Mol Genet; 1993 Dec; 2(12):2159-61. PubMed ID: 7906590
    [No Abstract]   [Full Text] [Related]  

  • 36. Characterization of polymorphic markers in the von Willebrand factor gene and pseudogene.
    Bernardi F; Marchetti G; Casonato A; Gemmati D; Patracchini P; Legnani C; DeRosa V; Girolami A; Conconi F
    Br J Haematol; 1990 Mar; 74(3):282-9. PubMed ID: 1970740
    [TBL] [Abstract][Full Text] [Related]  

  • 37. In-frame deletion of von Willebrand factor A domains in a dominant type of von Willebrand disease.
    Bernardi F; Patracchini P; Gemmati D; Pinotti M; Schwienbacher C; Ballerini G; Marchetti G
    Hum Mol Genet; 1993 May; 2(5):545-8. PubMed ID: 8518792
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Hemophilia A carrier detection by restriction fragment length polymorphism analysis and discriminant analysis based on ELISA of factor VIII and vWf.
    Poon MC; Hoar DI; Low S; Pon JK; Anand S; Sinclair GD
    J Lab Clin Med; 1992 Jun; 119(6):751-62. PubMed ID: 1350611
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Severe von Willebrand disease due to a defect at the level of von Willebrand factor mRNA expression: detection by exonic PCR-restriction fragment length polymorphism analysis.
    Nichols WC; Lyons SE; Harrison JS; Cody RL; Ginsburg D
    Proc Natl Acad Sci U S A; 1991 May; 88(9):3857-61. PubMed ID: 1673793
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Paternity testing with VNTR DNA systems. I. Matching criteria and population frequencies of the VNTR systems D2S44, D5S43, D7S21, D7S22, and D12S11 in Danes.
    Morling N; Hansen HE
    Int J Legal Med; 1993; 105(4):189-96. PubMed ID: 8094294
    [TBL] [Abstract][Full Text] [Related]  

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