BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

74 related articles for article (PubMed ID: 9268643)

  • 1. Identification of a gene within the tandem array of red and green color pigment genes.
    Hanna MC; Platts JT; Kirkness EF
    Genomics; 1997 Aug; 43(3):384-6. PubMed ID: 9268643
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular cloning of tissue-specific transcripts of a transketolase-related gene: implications for the evolution of new vertebrate genes.
    Coy JF; Dübel S; Kioschis P; Thomas K; Micklem G; Delius H; Poustka A
    Genomics; 1996 Mar; 32(3):309-16. PubMed ID: 8838793
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Position of a 'green-red' hybrid gene in the visual pigment array determines colour-vision phenotype.
    Hayashi T; Motulsky AG; Deeb SS
    Nat Genet; 1999 May; 22(1):90-3. PubMed ID: 10319869
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The mouse lens fiber-cell intrinsic membrane protein MP19 gene (Lim2) and granule membrane protein GMP-17 gene (Nkg7): Isolation and sequence analysis of two neighboring genes.
    Zhou L; Li X; Church RL
    Mol Vis; 2001 Apr; 7():79-88. PubMed ID: 11290961
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
    Zhang DL; Ji L; Li YD
    Yi Chuan Xue Bao; 2004 May; 31(5):431-43. PubMed ID: 15478601
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp.
    Fisher SE; Ciccodicola A; Tanaka K; Curci A; Desicato S; D'urso M; Craig IW
    Genomics; 1997 Oct; 45(2):340-7. PubMed ID: 9344658
    [TBL] [Abstract][Full Text] [Related]  

  • 7. RINX(VSX1), a novel homeobox gene expressed in the inner nuclear layer of the adult retina.
    Hayashi T; Huang J; Deeb SS
    Genomics; 2000 Jul; 67(2):128-39. PubMed ID: 10903837
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. A novel gene for autosomal dominant Stargardt-like macular dystrophy with homology to the SUR4 protein family.
    Edwards AO; Donoso LA; Ritter R
    Invest Ophthalmol Vis Sci; 2001 Oct; 42(11):2652-63. PubMed ID: 11581213
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
    Pusch CM; Zeitz C; Brandau O; Pesch K; Achatz H; Feil S; Scharfe C; Maurer J; Jacobi FK; Pinckers A; Andreasson S; Hardcastle A; Wissinger B; Berger W; Meindl A
    Nat Genet; 2000 Nov; 26(3):324-7. PubMed ID: 11062472
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular cloning, expression and chromosomal localization of a novel human REG family gene, REG III.
    Nata K; Liu Y; Xu L; Ikeda T; Akiyama T; Noguchi N; Kawaguchi S; Yamauchi A; Takahashi I; Shervani NJ; Onogawa T; Takasawa S; Okamoto H
    Gene; 2004 Sep; 340(1):161-70. PubMed ID: 15556304
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of a conserved cluster of skin-specific genes encoding secreted proteins.
    Moffatt P; Salois P; St-Amant N; Gaumond MH; Lanctôt C
    Gene; 2004 Jun; 334():123-31. PubMed ID: 15256262
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Polymorphism in the number of genes encoding long-wavelength-sensitive cone pigments among males with normal color vision.
    Neitz M; Neitz J; Grishok A
    Vision Res; 1995 Sep; 35(17):2395-407. PubMed ID: 8594809
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The evolution of the novel Sdic gene cluster in Drosophila melanogaster.
    Ponce R; Hartl DL
    Gene; 2006 Jul; 376(2):174-83. PubMed ID: 16765537
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Adrenoleukodystrophy: overlapping deletions point to a gene location in Xq28.
    Sack GH; Morrell JC
    Biochem Biophys Res Commun; 1993 Mar; 191(3):955-60. PubMed ID: 8466536
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel form of a single X-linked visual pigment gene in a unique dichromatic color-vision defect.
    Hayashi T; Kubo A; Takeuchi T; Gekka T; Goto-Omoto S; Kitahara K
    Vis Neurosci; 2006; 23(3-4):411-7. PubMed ID: 16961974
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Characterization of novel promoter and enhancer elements of the mouse homologue of the Dent disease gene, CLCN5, implicated in X-linked hereditary nephrolithiasis.
    Tanaka K; Fisher SE; Craig IW
    Genomics; 1999 Jun; 58(3):281-92. PubMed ID: 10373326
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The molecular basis of variation in human color vision.
    Deeb SS
    Clin Genet; 2005 May; 67(5):369-77. PubMed ID: 15811001
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of fusion gene and encoded photopigment of colour-blind humans.
    Neitz J; Neitz M; Jacobs GH
    Nature; 1989 Dec; 342(6250):679-82. PubMed ID: 2574415
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular cloning and characterization of the human CLOCK gene: expression in the suprachiasmatic nuclei.
    Steeves TD; King DP; Zhao Y; Sangoram AM; Du F; Bowcock AM; Moore RY; Takahashi JS
    Genomics; 1999 Apr; 57(2):189-200. PubMed ID: 10198158
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.