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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

385 related items for PubMed ID: 9501854

  • 1. Defective RNA splicing resulting from a mutation in the cyclic guanosine monophosphate-phosphodiesterase beta-subunit gene.
    Piriev NI, Shih JM, Farber DB.
    Invest Ophthalmol Vis Sci; 1998 Mar; 39(3):463-70. PubMed ID: 9501854
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Screening of the PDE6B gene in patients with autosomal dominant retinitis pigmentosa.
    Gao YQ, Danciger M, Zhao DY, Blaney J, Piriev NI, Shih J, Jacobson SG, Heckenlively JH, Farber DB.
    Exp Eye Res; 1996 Feb; 62(2):149-54. PubMed ID: 8698075
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. A substitution of G to C in the cone cGMP-phosphodiesterase gamma subunit gene found in a distinctive form of cone dystrophy.
    Piri N, Gao YQ, Danciger M, Mendoza E, Fishman GA, Farber DB.
    Ophthalmology; 2005 Jan; 112(1):159-66. PubMed ID: 15629837
    [Abstract] [Full Text] [Related]

  • 9. Identification of a novel R552O mutation in exon 13 of the beta-subunit of rod phosphodiesterase gene in a Spanish family with autosomal recessive retinitis pigmentosa.
    Valverde D, Baiget M, Seminago R, del Rio E, García-Sandoval B, del Rio T, Bayés M, Balcells S, Martínez A, Grinberg D, Ayuso C.
    Hum Mutat; 1996 Jan; 8(4):393-4. PubMed ID: 8956055
    [No Abstract] [Full Text] [Related]

  • 10. Evaluation of the gene encoding the gamma subunit of rod phosphodiesterase in retinitis pigmentosa.
    Hahn LB, Berson EL, Dryja TP.
    Invest Ophthalmol Vis Sci; 1994 Mar; 35(3):1077-82. PubMed ID: 8125719
    [Abstract] [Full Text] [Related]

  • 11. Molecular cloning and expression of human cGMP-binding cGMP-specific phosphodiesterase (PDE5).
    Stacey P, Rulten S, Dapling A, Phillips SC.
    Biochem Biophys Res Commun; 1998 Jun 18; 247(2):249-54. PubMed ID: 9642111
    [Abstract] [Full Text] [Related]

  • 12. [A study of PDE6B gene mutation and phenotype in Chinese cases with retinitis pigmentosa].
    Cui Y, Zhao KX, Wang L, Wang Q, Zhang W, Chen WY, Wang LM.
    Zhonghua Yan Ke Za Zhi; 2003 Jan 18; 39(1):28-32. PubMed ID: 12760810
    [Abstract] [Full Text] [Related]

  • 13. The human cGMP-PDE beta-subunit promoter region directs expression of the gene to mouse photoreceptors.
    Ogueta SB, Di Polo A, Flannery JG, Yamashita CK, Farber DB.
    Invest Ophthalmol Vis Sci; 2000 Dec 18; 41(13):4059-63. PubMed ID: 11095595
    [Abstract] [Full Text] [Related]

  • 14. Confirmation of tyrosine 698 in beta subunit of cGMP phosphodiesterase in patients with retinitis pigmentosa and population of the west of Mexico.
    Núñez-Gutiérrez IC, García-Cruz D, Fragoso-Herrera R, Medina-Lozano C.
    Rev Invest Clin; 2006 Dec 18; 58(4):359-61. PubMed ID: 17146947
    [No Abstract] [Full Text] [Related]

  • 15. Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesterase.
    Huang SH, Pittler SJ, Huang X, Oliveira L, Berson EL, Dryja TP.
    Nat Genet; 1995 Dec 18; 11(4):468-71. PubMed ID: 7493036
    [Abstract] [Full Text] [Related]

  • 16. cGMP phosphodiesterase-alpha mutation causes progressive retinal atrophy in the Cardigan Welsh corgi dog.
    Petersen-Jones SM, Entz DD, Sargan DR.
    Invest Ophthalmol Vis Sci; 1999 Jul 18; 40(8):1637-44. PubMed ID: 10393029
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Characterization of 3',5' cyclic nucleotide phosphodiesterase activity in Y79 retinoblastoma cells: absence of functional PDE6.
    White JB, Thompson WJ, Pittler SJ.
    Mol Vis; 2004 Oct 06; 10():738-49. PubMed ID: 15480303
    [Abstract] [Full Text] [Related]

  • 19. Mutations in the PDE6B gene in autosomal recessive retinitis pigmentosa.
    Danciger M, Blaney J, Gao YQ, Zhao DY, Heckenlively JR, Jacobson SG, Farber DB.
    Genomics; 1995 Nov 01; 30(1):1-7. PubMed ID: 8595886
    [Abstract] [Full Text] [Related]

  • 20. Ribozyme knockdown of the gamma-subunit of rod cGMP phosphodiesterase alters the ERG and retinal morphology in wild-type mice.
    Liu J, Timmers AM, Lewin AS, Hauswirth WW.
    Invest Ophthalmol Vis Sci; 2005 Oct 01; 46(10):3836-44. PubMed ID: 16186371
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 20.