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de dchughes retina [7 articles]

Recent papers added to de dchughes library classified by the tag retina. You can also see everyone's retina.
  • Expression and functional analysis of Nr2e3, a photoreceptor-specific nuclear receptor, suggest common mechanisms in retinal development between avians and mammals
    Development Genes and Evolution, Vol. 218, No. 8. (2008), pp. 439-444.
    by Mime Kobayashi, Kenji Hara, Ruth Yu, Kunio Yasuda
    posted to nr2e3 retina by dchughes on 2008-08-05 14:07:07 as **
  • Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism
    Hum. Mol. Genet., Vol. 17, No. 15. (1 August 2008), pp. 2405-2415.
    by Samuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, Alexander Sumaroka, Alejandro J Roman, Leigh M Gardner, Haydn M Prosser, Monalisa Mishra, Torben N Bech-Hansen, Waldo Herrera, Sharon B Schwartz, Xue-Zhong Liu, William J Kimberling, Karen P Steel, David S Williams
    posted to myo7a retina retinal-dystrophy retinitis-pigmentosa usher-syndrome by dchughes on 2008-07-16 09:38:22 as **
  • Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7).
    Genomics, Vol. 81, No. 3. (March 2003), pp. 304-314.
    by S Johnson, S Halford, AG Morris, RJ Patel, SE Wilkie, AJ Hardcastle, AT Moore, K Zhang, DM Hunt
    posted to mir retina retinal-dystrophy rim1 by dchughes on 2008-07-10 13:01:15 as **
  • Regulation of rod phototransduction machinery by ciliary neurotrophic factor.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 26, No. 52. (27 December 2006), pp. 13523-13530.
    by R Wen, Y Song, S Kjellstrom, A Tanikawa, Y Liu, Y Li, L Zhao, RA Bush, AM Laties, PA Sieving
    posted to cntf mir retina rhodopsin by dchughes on 2008-07-07 16:22:35 as **
  • Genomic analysis of mouse retinal development.
    PLoS biology, Vol. 2, No. 9. (September 2004)
    by S Blackshaw, S Harpavat, J Trimarchi, L Cai, H Huang, WP Kuo, G Weber, K Lee, RE Fraioli, SH Cho, R Yung, E Asch, L Ohno-Machado, WH Wong, CL Cepko
    posted to retina by dchughes on 2008-07-01 11:16:31 as **
  • Mutations in the gene coding for guanylate cyclase-activating protein 2 (GUCA1B gene) in patients with autosomal dominant retinal dystrophies.
    Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie, Vol. 243, No. 3. (March 2005), pp. 235-242.
    by M Sato, M Nakazawa, T Usui, N Tanimoto, H Abe, H Ohguro
    posted to guca1b mir retina retinal-dystrophy by dchughes on 2008-06-26 14:24:59 as **
  • Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy.
    American journal of human genetics, Vol. 79, No. 5. (November 2006), pp. 973-977.
    by KA Wycisk, C Zeitz, S Feil, M Wittmer, U Forster, J Neidhardt, B Wissinger, E Zrenner, R Wilke, S Kohl, W Berger
    posted to cacna2d4 mir retina retinal-dystrophy by dchughes on 2008-06-26 14:15:07 as **
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