These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

75 related articles for article (PubMed ID: 9643300)

  • 1. Microsatellite markers for the cone-rod retinal dystrophy gene, CRX, on 19q13.3.
    Bellingham J; Gregory-Evans CY; Gregory-Evans K
    J Med Genet; 1998 Jun; 35(6):527. PubMed ID: 9643300
    [No Abstract]   [Full Text] [Related]  

  • 2. Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor.
    Freund CL; Gregory-Evans CY; Furukawa T; Papaioannou M; Looser J; Ploder L; Bellingham J; Ng D; Herbrick JA; Duncan A; Scherer SW; Tsui LC; Loutradis-Anagnostou A; Jacobson SG; Cepko CL; Bhattacharya SS; McInnes RR
    Cell; 1997 Nov; 91(4):543-53. PubMed ID: 9390563
    [TBL] [Abstract][Full Text] [Related]  

  • 3. From CRX to CRD.
    Abitbol M; DuFier JL
    Nat Med; 1998 Jan; 4(1):18-9. PubMed ID: 9427598
    [No Abstract]   [Full Text] [Related]  

  • 4. Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion.
    Evans K; Fryer A; Inglehearn C; Duvall-Young J; Whittaker JL; Gregory CY; Butler R; Ebenezer N; Hunt DM; Bhattacharya S
    Nat Genet; 1994 Feb; 6(2):210-3. PubMed ID: 8162077
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Meiotic drive at the myotonic dystrophy and the cone-rod dystrophy loci on chromosome 19q13.3.
    Inglehearn CF; Gregory CY
    Am J Hum Genet; 1997 Jun; 60(6):1562-3. PubMed ID: 9199584
    [No Abstract]   [Full Text] [Related]  

  • 6. Cloning and characterization of the canine photoreceptor specific cone-rod homeobox (CRX) gene and evaluation as a candidate for early onset photoreceptor diseases in the dog.
    Akhmedov NB; Baldwin VJ; Zangerl B; Kijas JW; Hunter L; Minoofar KD; Mellersh C; Ostrander EA; Acland GM; Farber DB; Aguirre GD
    Mol Vis; 2002 Mar; 8():79-84. PubMed ID: 11951083
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Refinement of the cone-rod retinal dystrophy locus on chromosome 19q.
    Gregory CY; Evans K; Whittaker JL; Fryer A; Weissenbach J; Bhattacharya SS
    Am J Hum Genet; 1994 Nov; 55(5):1061-3. PubMed ID: 7977344
    [No Abstract]   [Full Text] [Related]  

  • 8. Microsatellite (TTCC)n polymorphism in intron 6 of the canine rod photoreceptor cGMP-gated cation channel alpha-subunit gene.
    Veske A; Nilsson SE; Gal A
    Anim Genet; 1997 Oct; 28(5):374-5. PubMed ID: 9363608
    [No Abstract]   [Full Text] [Related]  

  • 9. Novel 615delC mutation in the CRX gene in a Japanese family with cone-rod dystrophy.
    Itabashi T; Wada Y; Sato H; Kawamura M; Shiono T; Tamai M
    Am J Ophthalmol; 2004 Nov; 138(5):876-7. PubMed ID: 15531334
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24.
    Khaliq S; Hameed A; Ismail M; Anwar K; Leroy BP; Mehdi SQ; Payne AM; Bhattacharya SS
    Invest Ophthalmol Vis Sci; 2000 Nov; 41(12):3709-12. PubMed ID: 11053266
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11.
    Wissinger B; Jägle H; Kohl S; Broghammer M; Baumann B; Hanna DB; Hedels C; Apfelstedt-Sylla E; Randazzo G; Jacobson SG; Zrenner E; Sharpe LT
    Genomics; 1998 Aug; 51(3):325-31. PubMed ID: 9721202
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Maternal uniparental isodisomy of chromosome 6 reveals a TULP1 mutation as a novel cause of cone dysfunction.
    Roosing S; van den Born LI; Hoyng CB; Thiadens AA; de Baere E; Collin RW; Koenekoop RK; Leroy BP; van Moll-Ramirez N; Venselaar H; Riemslag FC; Cremers FP; Klaver CC; den Hollander AI
    Ophthalmology; 2013 Jun; 120(6):1239-46. PubMed ID: 23499059
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) gene.
    Jacobson SG; Cideciyan AV; Huang Y; Hanna DB; Freund CL; Affatigato LM; Carr RE; Zack DJ; Stone EM; McInnes RR
    Invest Ophthalmol Vis Sci; 1998 Nov; 39(12):2417-26. PubMed ID: 9804150
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The photoreceptor-specific nuclear receptor Nr2e3 interacts with Crx and exerts opposing effects on the transcription of rod versus cone genes.
    Peng GH; Ahmad O; Ahmad F; Liu J; Chen S
    Hum Mol Genet; 2005 Mar; 14(6):747-64. PubMed ID: 15689355
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genotype-phenotype correlation in a German family with a novel complex CRX mutation extending the open reading frame.
    Paunescu K; Preising MN; Janke B; Wissinger B; Lorenz B
    Ophthalmology; 2007 Jul; 114(7):1348-1357.e1. PubMed ID: 17320181
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in man.
    Cideciyan AV; Hood DC; Huang Y; Banin E; Li ZY; Stone EM; Milam AH; Jacobson SG
    Proc Natl Acad Sci U S A; 1998 Jun; 95(12):7103-8. PubMed ID: 9618546
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A hybrid photoreceptor expressing both rod and cone genes in a mouse model of enhanced S-cone syndrome.
    Corbo JC; Cepko CL
    PLoS Genet; 2005 Aug; 1(2):e11. PubMed ID: 16110338
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new family of Greek origin maps to the CRD locus for autosomal dominant cone-rod dystrophy on 19q.
    Papaioannou M; Bessant D; Payne A; Bellingham J; Rougas C; Loutradis-Anagnostou A; Gregory-Evans C; Balassopoulou A; Bhattacharya S
    J Med Genet; 1998 May; 35(5):429-31. PubMed ID: 9610810
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Predominant rod photoreceptor degeneration in Leber congenital amaurosis.
    van der Spuy J; Munro PM; Luthert PJ; Preising MN; Bek T; Heegaard S; Cheetham ME
    Mol Vis; 2005 Jul; 11():542-53. PubMed ID: 16052170
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish families.
    Köhn L; Kadzhaev K; Burstedt MS; Haraldsson S; Sandgren O; Golovleva I
    Adv Exp Med Biol; 2008; 613():229-34. PubMed ID: 18188949
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.