BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

68 related articles for article (PubMed ID: 11161804)

  • 1. The Werner syndrome gene and global sequence variation.
    Passarino G; Shen P; Van Kirk JB; Lin AA; De Benedictis G; Cavalli Sforza LL; Oefner PJ; Underhill PA
    Genomics; 2001 Jan; 71(1):118-22. PubMed ID: 11161804
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic association between chromosome 8 microsatellite (MS8-134) and Werner syndrome (WRN): chromosome microdissection and homozygosity mapping.
    Ye L; Nakura J; Mitsuda N; Fujioka Y; Kamino K; Ohta T; Jinno Y; Niikawa N; Miki T; Ogihara T
    Genomics; 1995 Aug; 28(3):566-9. PubMed ID: 7490095
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Polymorphisms at the Werner locus: I. Newly identified polymorphisms, ethnic variability of 1367Cys/Arg, and its stability in a population of Finnish centenarians.
    Castro E; Ogburn CE; Hunt KE; Tilvis R; Louhija J; Penttinen R; Erkkola R; Panduro A; Riestra R; Piussan C; Deeb SS; Wang L; Edland SD; Martin GM; Oshima J
    Am J Med Genet; 1999 Feb; 82(5):399-403. PubMed ID: 10069711
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Variation in the type I interferon gene cluster on 9p21 influences susceptibility to asthma and atopy.
    Chan A; Newman DL; Shon AM; Schneider DH; Kuldanek S; Ober C
    Genes Immun; 2006 Mar; 7(2):169-78. PubMed ID: 16437122
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 6. High-density single-nucleotide polymorphism (SNP) map in the 96-kb region containing the entire human DiGeorge syndrome critical region 2 (DGCR2) gene at 22q11.2.
    Iida A; Ohnishi Y; Ozaki K; Ariji Y; Nakamura Y; Tanaka T
    J Hum Genet; 2001; 46(10):604-8. PubMed ID: 11589220
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Comparison of methods for identifying transcription units and transcription map of the Werner syndrome gene region.
    Hisama FM; Oshima J; Yu CE; Fu YH; Mulligan J; Weissman SM; Schellenberg GD
    Genomics; 1998 Sep; 52(3):352-7. PubMed ID: 9790753
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Catalog of 46 single-nucleotide polymorphisms (SNPs) in the microsomal glutathione S-transferase 1 (MGST1) gene.
    Iida A; Saito S; Sekine A; Harigae S; Osawa S; Mishima C; Kondo K; Kitamura Y; Nakamura Y
    J Hum Genet; 2001; 46(10):590-4. PubMed ID: 11587073
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Polymorphisms at the Werner locus: II. 1074Leu/Phe, 1367Cys/Arg, longevity, and atherosclerosis.
    Castro E; Edland SD; Lee L; Ogburn CE; Deeb SS; Brown G; Panduro A; Riestra R; Tilvis R; Louhija J; Penttinen R; Erkkola R; Wang L; Martin GM; Oshima J
    Am J Med Genet; 2000 Dec; 95(4):374-80. PubMed ID: 11186893
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Detection of alpha-galactosidase a mutations causing Fabry disease by denaturing high performance liquid chromatography.
    Shabbeer J; Robinson M; Desnick RJ
    Hum Mutat; 2005 Mar; 25(3):299-305. PubMed ID: 15712228
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Functional analysis of human promoter polymorphisms.
    Hoogendoorn B; Coleman SL; Guy CA; Smith K; Bowen T; Buckland PR; O'Donovan MC
    Hum Mol Genet; 2003 Sep; 12(18):2249-54. PubMed ID: 12915441
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Functional analysis of yeast homologue gene associated with human DNA helicase causative syndromes].
    Miyajima A
    Kokuritsu Iyakuhin Shokuhin Eisei Kenkyusho Hokoku; 2002; (120):53-74. PubMed ID: 12638184
    [TBL] [Abstract][Full Text] [Related]  

  • 15. DNA sequence analysis of monoamine oxidase B gene coding and promoter regions in Parkinson's disease cases and unrelated controls.
    Costa-Mallen P; Afsharinejad Z; Kelada SN; Costa LG; Franklin GM; Swanson PD; Longstreth WT; Viernes HM; Farin FM; Smith-Weller T; Checkoway H
    Mov Disord; 2004 Jan; 19(1):76-83. PubMed ID: 14743364
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutational analysis of the NF2 gene in sporadic meningiomas by denaturing high-performance liquid chromatography.
    Kim JH; Kim IS; Kwon SY; Jang BC; Suh SI; Shin DH; Jeon CH; Son EI; Kim SP
    Int J Mol Med; 2006 Jul; 18(1):27-32. PubMed ID: 16786152
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Evaluation of Lipin 2 as a candidate gene for autosomal dominant 1 high-grade myopia.
    Zhou J; Young TL
    Gene; 2005 Jun; 352():10-9. PubMed ID: 15862761
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Global survey of haplotype frequencies and linkage disequilibrium at the RET locus.
    Chattopadhyay P; Pakstis AJ; Mukherjee N; Iyengar S; Odunsi A; Okonofua F; Bonne-Tamir B; Speed W; Kidd JR; Kidd KK
    Eur J Hum Genet; 2003 Oct; 11(10):760-9. PubMed ID: 14512966
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Excess of rare cancers in Werner syndrome (adult progeria).
    Goto M; Miller RW; Ishikawa Y; Sugano H
    Cancer Epidemiol Biomarkers Prev; 1996 Apr; 5(4):239-46. PubMed ID: 8722214
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A high-throughput denaturing high-performance liquid chromatography method for the identification of variant alleles associated with dihydropyrimidine dehydrogenase deficiency.
    Ezzeldin H; Okamoto Y; Johnson MR; Diasio RB
    Anal Biochem; 2002 Jul; 306(1):63-73. PubMed ID: 12069415
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.