BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

75 related articles for article (PubMed ID: 8695174)

  • 1. [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]  

  • 2. [Analysis of the allelic polymorphism of four short tandem repeats in a population from the northwestern region of Russia].
    Assev MV; Skakun VN; Baranov VS
    Genetika; 1995 Jun; 31(6):839-45. PubMed ID: 7635321
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Genetic polymorphism at D20S161 locus in Chinese populations].
    Li Y; Wu J; Jin Z; Hou Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Jun; 15(3):147-50. PubMed ID: 9621121
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Amplified fragment length polymorphism of the VNTR locus COL2A1 in Chinese population].
    Hou Y; Gou Q; Wu M
    Yi Chuan Xue Bao; 1995; 22(4):245-51. PubMed ID: 8703516
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The distribution of the vWF alleles and genotypes in the Palestinian population.
    Khatib H; Ezzughayyar M; Ayesh S
    J Forensic Sci; 1997 May; 42(3):504-5. PubMed ID: 9144940
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A common splice site mutation is shared by two families with different type 2N von Willebrand disease mutations.
    Nesbitt IM; Hampton KK; Preston FE; Peake IR; Goodeve AC
    Thromb Haemost; 1999 Sep; 82(3):1061-4. PubMed ID: 10494764
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Genetic polymorphism of 9 STR loci in Han nation population in Shandong Province].
    Zhu BF; Lü GP; Shen CM; Yao GF; Tian YF; Li T; Wang ZY
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2002 Dec; 24(6):620-5. PubMed ID: 12905692
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Amplified fragment length polymorphism analysis on D5S436 locus and its application to linkage analysis in gene diagnosis of asthma.
    Huang K; Weng X; Liu J; Zhu Z; Xiao B; Yan M; Zhang H; Wang C
    Chin Med J (Engl); 1999 Feb; 112(2):112-4. PubMed ID: 11593573
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Polymorphism of STR loci D12S391/D18S865 in Wenzhou Han population].
    Wu SZ; Zhang HQ; Bi YT
    Fa Yi Xue Za Zhi; 2004; 20(2):85-7. PubMed ID: 15311521
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Genetic linkage of polymorphisms of type I angiotensin II receptor gene to Chinese Han hypertension].
    Hu A; Zhou X; Ren X; Cui Z; Hui R; Liu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Apr; 16(2):81-4. PubMed ID: 10194251
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Prenatal determination of a variable number of tandem repeats in intron 40 of the von Willebrand factor gene from maternal peripheral blood using the polymerase chain reaction.
    Ni X; Guo J; Xia J; Li L
    Hum Hered; 2000; 50(3):201-4. PubMed ID: 10686501
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Microsatellite polymorphisms at the TNF locus in Hubei Han population].
    Fei B; Deng C; Xia B
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Dec; 18(6):467-71. PubMed ID: 11774218
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations in von Willebrand factor multimerization domains are not a common cause of classical type 1 von Willebrand disease.
    Keeney S; Cumming A; Hay C
    Thromb Haemost; 1999 Nov; 82(5):1446-50. PubMed ID: 10595636
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Practical application of three polymorphic microsatellites in intron 40 of the human von Willebrand factor gene.
    Casaña P; Martinez F; Aznar JA; Lorenzo JI; Jorquera JI
    Haemostasis; 1995; 25(6):264-71. PubMed ID: 8586316
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Mutation detection enhancement (MDE) gel electrophoresis method for analysis of the von Willebrand factor gene].
    Hagiwara T; Inaba H; Fukutake K
    Rinsho Byori; 1996 Jun; 44(6):574-8. PubMed ID: 8752737
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Von Willebrand factor short sequence repeat locus 2 (intron 40) consists of three polymorphic subloci.
    Othman M; Elbatarny HS; Byrne CD; O'Shaughnessy DF
    Acta Haematol; 2007; 117(3):177-80. PubMed ID: 17159339
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association between von Willebrand factor gene polymorphism and preeclampsia.
    Sun C; Chen Y; Zhang W; Yu S
    J Perinat Med; 2009; 37(1):36-42. PubMed ID: 19021456
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Genetic polymorphism of short tandem repeat loci D1S549, D3S1754 and D12S375 in Qingdao Han population].
    Qi QW; Zhang HY; Ma SZ; Xu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Apr; 21(2):184-6. PubMed ID: 15079809
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Application of HLA-DRB1 genotyping by oligonucleotide micro-array technology in forensic medicine.
    Jiang B; Li Y; Wu H; He X; Li C; Li L; Tang R; Xie Y; Mao Y
    Forensic Sci Int; 2006 Oct; 162(1-3):66-73. PubMed ID: 16884876
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.