BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

113 related articles for article (PubMed ID: 2137199)

  • 1. Molecular genetics. Insight into blindness.
    Applebury ML
    Nature; 1990 Jan; 343(6256):316-7. PubMed ID: 2137199
    [No Abstract]   [Full Text] [Related]  

  • 2. A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.
    Dryja TP; McGee TL; Reichel E; Hahn LB; Cowley GS; Yandell DW; Sandberg MA; Berson EL
    Nature; 1990 Jan; 343(6256):364-6. PubMed ID: 2137202
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Unexpected findings partly explain the causes of retinitis pigmentosa].
    Ehinger B
    Lakartidningen; 1990 Apr; 87(17):1458. PubMed ID: 2338852
    [No Abstract]   [Full Text] [Related]  

  • 4. Rhodopsin transgenic pigs as a model for human retinitis pigmentosa.
    Li ZY; Wong F; Chang JH; Possin DE; Hao Y; Petters RM; Milam AH
    Invest Ophthalmol Vis Sci; 1998 Apr; 39(5):808-19. PubMed ID: 9538889
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa.
    Dryja TP; Hahn LB; Cowley GS; McGee TL; Berson EL
    Proc Natl Acad Sci U S A; 1991 Oct; 88(20):9370-4. PubMed ID: 1833777
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rod and cone opsin mislocalization in an autopsy eye from a carrier of X-linked retinitis pigmentosa with a Gly436Asp mutation in the RPGR gene.
    Adamian M; Pawlyk BS; Hong DH; Berson EL
    Am J Ophthalmol; 2006 Sep; 142(3):515-8. PubMed ID: 16935610
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Pathology of opsins and vision disorders].
    Abitbol M; Eppelbaum M; Dolfuss H; Dufier JL
    Rev Prat; 1994 May; 44(9):1173-6. PubMed ID: 7939339
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Loss of cone molecular markers in rhodopsin-mutant human retinas with retinitis pigmentosa.
    John SK; Smith JE; Aguirre GD; Milam AH
    Mol Vis; 2000 Nov; 6():204-15. PubMed ID: 11063754
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pigment gene scrutinized.
    Lewin R
    Science; 1984 Oct; 226(4670):35. PubMed ID: 6236555
    [No Abstract]   [Full Text] [Related]  

  • 10. Molecular genetics of human visual pigments.
    Nathans J; Merbs SL; Sung CH; Weitz CJ; Wang Y
    Annu Rev Genet; 1992; 26():403-24. PubMed ID: 1482119
    [No Abstract]   [Full Text] [Related]  

  • 11. Amino acid residues responsible for the meta-III decay rates in rod and cone visual pigments.
    Kuwayama S; Imai H; Morizumi T; Shichida Y
    Biochemistry; 2005 Feb; 44(6):2208-15. PubMed ID: 15697246
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa.
    McLaughlin ME; Sandberg MA; Berson EL; Dryja TP
    Nat Genet; 1993 Jun; 4(2):130-4. PubMed ID: 8394174
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Acuity recovery and cone pigment regeneration after a bleach in patients with retinitis pigmentosa and rhodopsin mutations.
    Sandberg MA; Pawlyk BS; Berson EL
    Invest Ophthalmol Vis Sci; 1999 Sep; 40(10):2457-61. PubMed ID: 10476820
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ectopic expression of a minor Drosophila opsin in the major photoreceptor cell class: distinguishing the role of primary receptor and cellular context.
    Zuker CS; Mismer D; Hardy R; Rubin GM
    Cell; 1988 May; 53(3):475-82. PubMed ID: 2966681
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapy.
    Mendes HF; van der Spuy J; Chapple JP; Cheetham ME
    Trends Mol Med; 2005 Apr; 11(4):177-85. PubMed ID: 15823756
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Autosomal dominant retinitis pigmentosa caused by the threonine-17-methionine rhodopsin mutation: retinal histopathology and immunocytochemistry.
    Li ZY; Jacobson SG; Milam AH
    Exp Eye Res; 1994 Apr; 58(4):397-408. PubMed ID: 7925677
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Retinitis pigmentosa: pathogenic progress and therapeutic hopes].
    Sahel JA
    Rev Prat; 2002 Oct; 52(16):1745-7. PubMed ID: 12564163
    [No Abstract]   [Full Text] [Related]  

  • 18. Retinopathy mutations in the bZIP protein NRL alter phosphorylation and transcriptional activity.
    Kanda A; Friedman JS; Nishiguchi KM; Swaroop A
    Hum Mutat; 2007 Jun; 28(6):589-98. PubMed ID: 17335001
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A mutation in NRL is associated with autosomal dominant retinitis pigmentosa.
    Bessant DA; Payne AM; Mitton KP; Wang QL; Swain PK; Plant C; Bird AC; Zack DJ; Swaroop A; Bhattacharya SS
    Nat Genet; 1999 Apr; 21(4):355-6. PubMed ID: 10192380
    [No Abstract]   [Full Text] [Related]  

  • 20. Regeneration of rhodopsin and isorhodopsin in rod outer segment preparations: absence of effect of solvent parameters.
    Lacy ME; Veronee CD; Crouch RK
    Physiol Chem Phys Med NMR; 1984; 16(4):275-81. PubMed ID: 6240663
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.