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 *

60 related articles for article (PubMed ID: 2349107)

  • 1. Nucleotide and predicted protein sequence of rat retinal degeneration slow (rds).
    Begy C; Bridges CD
    Nucleic Acids Res; 1990 May; 18(10):3058. PubMed ID: 2349107
    [No Abstract]   [Full Text] [Related]  

  • 2. The human retinal degeneration slow (RDS) gene: chromosome assignment and structure of the mRNA.
    Travis GH; Christerson L; Danielson PE; Klisak I; Sparkes RS; Hahn LB; Dryja TP; Sutcliffe JG
    Genomics; 1991 Jul; 10(3):733-9. PubMed ID: 1679750
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The retinal degeneration slow (rds) gene product is a photoreceptor disc membrane-associated glycoprotein.
    Travis GH; Sutcliffe JG; Bok D
    Neuron; 1991 Jan; 6(1):61-70. PubMed ID: 1986774
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Retinal degeneration slow (rds) in mouse results from simple insertion of a t haplotype-specific element into protein-coding exon II.
    Ma J; Norton JC; Allen AC; Burns JB; Hasel KW; Burns JL; Sutcliffe JG; Travis GH
    Genomics; 1995 Jul; 28(2):212-9. PubMed ID: 8530028
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse.
    Connell G; Bascom R; Molday L; Reid D; McInnes RR; Molday RS
    Proc Natl Acad Sci U S A; 1991 Feb; 88(3):723-6. PubMed ID: 1992463
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea.
    Nichols BE; Drack AV; Vandenburgh K; Kimura AE; Sheffield VC; Stone EM
    Hum Mol Genet; 1993 May; 2(5):601-3. PubMed ID: 8251014
    [No Abstract]   [Full Text] [Related]  

  • 7. Cloning of the human and murine ROM1 genes: genomic organization and sequence conservation.
    Bascom RA; Schappert K; McInnes RR
    Hum Mol Genet; 1993 Apr; 2(4):385-91. PubMed ID: 8504299
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Preferential rod and cone photoreceptor abnormalities in heterozygotes with point mutations in the RDS gene.
    Jacobson SG; Cideciyan AV; Maguire AM; Bennett J; Sheffield VC; Stone EM
    Exp Eye Res; 1996 Nov; 63(5):603-8. PubMed ID: 8994365
    [No Abstract]   [Full Text] [Related]  

  • 9. Cellular mechanisms of retinal degenerations: RPE65, ABCA4, RDS, and bicarbonate transporter genes as examples.
    Bok D
    Retina; 2005 Dec; 25(8 Suppl):S18-S20. PubMed ID: 16374319
    [No Abstract]   [Full Text] [Related]  

  • 10. Polymorphic variation within "conserved" sequences at the 3' end of the human RDS gene which results in amino acid substitutions.
    Jordan SA; Farrar GJ; Kenna P; Humphries P
    Hum Mutat; 1992; 1(3):240-7. PubMed ID: 1301931
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A medley of retinal dystrophies.
    Travis GH; Hepler JE
    Nat Genet; 1993 Mar; 3(3):191-2. PubMed ID: 8485572
    [No Abstract]   [Full Text] [Related]  

  • 12. Complete rescue of photoreceptor dysplasia and degeneration in transgenic retinal degeneration slow (rds) mice.
    Travis GH; Groshan KR; Lloyd M; Bok D
    Neuron; 1992 Jul; 9(1):113-9. PubMed ID: 1385966
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Choroidal neovascularization in a patient with adult foveomacular dystrophy and a mutation in the retinal degeneration slow gene (Pro 210 Arg).
    Feist RM; White MF; Skalka H; Stone EM
    Am J Ophthalmol; 1994 Aug; 118(2):259-60. PubMed ID: 7519821
    [No Abstract]   [Full Text] [Related]  

  • 14. Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene.
    Nichols BE; Sheffield VC; Vandenburgh K; Drack AV; Kimura AE; Stone EM
    Nat Genet; 1993 Mar; 3(3):202-7. PubMed ID: 8485574
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Retinal pattern dystrophy associated with a 4 bp insertion at codon 140 in the RDS-peripherin gene.
    Keen TJ; Inglehearn CF; Kim R; Bird AC; Bhattacharya S
    Hum Mol Genet; 1994 Feb; 3(2):367-8. PubMed ID: 8004111
    [No Abstract]   [Full Text] [Related]  

  • 16. [Hereditary retinal dystrophies].
    Kellner U
    Ophthalmologe; 1997 Feb; 94(2):164-83. PubMed ID: 9156644
    [No Abstract]   [Full Text] [Related]  

  • 17. Upregulation of CD44 expression in the retina during the rds degeneration.
    Krishnamoorthy R; Agarwal N; Chaitin MH
    Brain Res Mol Brain Res; 2000 Apr; 77(1):125-30. PubMed ID: 10814838
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Tulp1 is involved in specific photoreceptor protein transport pathways.
    Hagstrom SA; Watson RF; Pauer GJ; Grossman GH
    Adv Exp Med Biol; 2012; 723():783-9. PubMed ID: 22183407
    [No Abstract]   [Full Text] [Related]  

  • 19. A sequence polymorphism in the human peripherin/RDS gene.
    Farrar GJ; Kenna P; Jordan SA; Kumar-Singh R; Humphries P
    Nucleic Acids Res; 1991 Dec; 19(24):6982. PubMed ID: 1762948
    [No Abstract]   [Full Text] [Related]  

  • 20. Identification of two rds/peripherin homologs in the chick retina.
    Weng J; Belecky-Adams T; Adler R; Travis GH
    Invest Ophthalmol Vis Sci; 1998 Feb; 39(2):440-3. PubMed ID: 9478005
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.