BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

74 related articles for article (PubMed ID: 8432556)

  • 1. DNA polymorphisms in the 3' untranslated region of genes on human chromosome 21.
    Avramopoulos D; Chakravarti A; Antonarakis SE
    Genomics; 1993 Jan; 15(1):98-102. PubMed ID: 8432556
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Linkage mapping of the cystathionine beta-synthase (CBS) gene on human chromosome 21 using a DNA polymorphism in the 3' untranslated region.
    Avramopoulos D; Cox T; Kraus JP; Chakravarti A; Antonarakis SE
    Hum Genet; 1993 Jan; 90(5):566-8. PubMed ID: 8094069
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The cell adhesion regulator (CAR) gene, TaqI and insertion/deletion polymorphisms, and regional assignment to the peritelomeric region of 16q by linkage analysis.
    Koyama K; Emi M; Nakamura Y
    Genomics; 1993 Apr; 16(1):264-5. PubMed ID: 8098008
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41.
    Watanabe Y; Murray JC; Bjork BC; Bird CP; Chiang PW; Gregory SG; Kurnit DM; Schutte BC
    Hum Mutat; 2001 Nov; 18(5):422-34. PubMed ID: 11668635
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Linkage mapping of the human thromboxane A2 receptor (TBXA2R) to chromosome 19p13.3 using transcribed 3' untranslated DNA sequence polymorphisms.
    Schwengel DA; Nouri N; Meyers DA; Levitt RC
    Genomics; 1993 Nov; 18(2):212-5. PubMed ID: 8288221
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.
    Lee PL; Gelbart T; West C; Halloran C; Beutler E
    Blood Cells Mol Dis; 1998 Jun; 24(2):199-215. PubMed ID: 9642100
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A new betaA1-crystallin splice junction mutation in autosomal dominant cataract.
    Bateman JB; Geyer DD; Flodman P; Johannes M; Sikela J; Walter N; Moreira AT; Clancy K; Spence MA
    Invest Ophthalmol Vis Sci; 2000 Oct; 41(11):3278-85. PubMed ID: 11006214
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A new three allele polymorphism at distal 21q22.3, a region relatively devoid of polymorphic markers. Mutations in brief no. 212. Online.
    SertiƩ AL; Brahe C; Passos-Bueno MR
    Hum Mutat; 1999; 13(2):170. PubMed ID: 10094555
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Physical and linkage mapping of human chromosome 17 loci to dog chromosomes 9 and 5.
    Werner P; Raducha MG; Prociuk U; Henthorn PS; Patterson DF
    Genomics; 1997 May; 42(1):74-82. PubMed ID: 9177778
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genomic organization and sequence variation of the human integrin subunit alpha8 gene (ITGA8).
    Ekwa-Ekoka C; Diaz GA; Carlson C; Hasegawa T; Samudrala R; Lim KC; Yabu JM; Levy B; Schnapp LM
    Matrix Biol; 2004 Nov; 23(7):487-96. PubMed ID: 15579315
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of polymorphisms in the human Reprimo gene using public EST data.
    Ye Z; Parry JM
    Teratog Carcinog Mutagen; 2002; 22(6):485-93. PubMed ID: 12395409
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Complex high-resolution linkage disequilibrium and haplotype patterns of single-nucleotide polymorphisms in 2.5 Mb of sequence on human chromosome 21.
    Olivier M; Bustos VI; Levy MR; Smick GA; Moreno I; Bushard JM; Almendras AA; Sheppard K; Zierten DL; Aggarwal A; Carlson CS; Foster BD; Vo N; Kelly L; Liu X; Cox DR
    Genomics; 2001 Nov; 78(1-2):64-72. PubMed ID: 11707074
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Polymorphisms/mutations of TCR-zeta-chain promoter and 3' untranslated region and selective expression of TCR zeta-chain with an alternatively spliced 3' untranslated region in patients with systemic lupus erythematosus.
    Nambiar MP; Enyedy EJ; Warke VG; Krishnan S; Dennis G; Kammer GM; Tsokos GC
    J Autoimmun; 2001 Mar; 16(2):133-42. PubMed ID: 11247639
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Linkage localization of TGFB2 and the human homeobox gene HLX1 to chromosome 1q.
    Nishimura DY; Purchio AF; Murray JC
    Genomics; 1993 Feb; 15(2):357-64. PubMed ID: 8095486
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The HLA-DRw8 lineage was generated by a deletion in the DR B region followed by first domain diversification.
    Gorski J
    J Immunol; 1989 Jun; 142(11):4041-5. PubMed ID: 2785571
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Thirteen single-nucleotide polymorphisms (SNPs) in the alcohol dehydrogenase 4 (ADH4) gene locus.
    Iida A; Saito S; Sekine A; Kondo K; Mishima C; Kitamura Y; Harigae S; Osawa S; Nakamura Y
    J Hum Genet; 2002; 47(2):74-6. PubMed ID: 11916005
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of a new polymorphism in the 3'-untranslated region of the human serotonin receptor 2C (5-HT2C) gene.
    Song HR; Gu A; Schanen NC
    Mol Genet Metab; 1999 Mar; 66(3):224-7. PubMed ID: 10066392
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Polymorphism and genetic mapping of the human oxytocin receptor gene on chromosome 3.
    Michelini S; Urbanek M; Dean M; Goldman D
    Am J Med Genet; 1995 Jun; 60(3):183-7. PubMed ID: 7573168
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Frequency and polymorphism of simple sequence repeats in a contiguous 685-kb DNA sequence containing the human T-cell receptor beta-chain gene complex.
    Charmley P; Concannon P; Hood L; Rowen L
    Genomics; 1995 Oct; 29(3):760-5. PubMed ID: 8575771
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genomic structure and organization of the high grade Myopia-2 locus (MYP2) critical region: mutation screening of 9 positional candidate genes.
    Scavello GS; Paluru PC; Zhou J; White PS; Rappaport EF; Young TL
    Mol Vis; 2005 Feb; 11():97-110. PubMed ID: 15723005
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.