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 *

160 related articles for article (PubMed ID: 11377968)

  • 1. Molecular genetics and prospects for therapy of the inherited retinal dystrophies.
    Bessant DA; Ali RR; Bhattacharya SS
    Curr Opin Genet Dev; 2001 Jun; 11(3):307-16. PubMed ID: 11377968
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic testing for retinal dystrophies and dysfunctions: benefits, dilemmas and solutions.
    Koenekoop RK; Lopez I; den Hollander AI; Allikmets R; Cremers FP
    Clin Exp Ophthalmol; 2007 Jul; 35(5):473-85. PubMed ID: 17651254
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular genetics of Leber congenital amaurosis.
    Cremers FP; van den Hurk JA; den Hollander AI
    Hum Mol Genet; 2002 May; 11(10):1169-76. PubMed ID: 12015276
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Altered expression of the transcription factor Mef2c during retinal degeneration in Rpe65-/- mice.
    Escher P; Schorderet DF; Cottet S
    Invest Ophthalmol Vis Sci; 2011 Jul; 52(8):5933-40. PubMed ID: 21715356
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pathways to photoreceptor cell death in inherited retinal degenerations.
    Pierce EA
    Bioessays; 2001 Jul; 23(7):605-18. PubMed ID: 11462214
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Different effects of valproic acid on photoreceptor loss in Rd1 and Rd10 retinal degeneration mice.
    Mitton KP; Guzman AE; Deshpande M; Byrd D; DeLooff C; Mkoyan K; Zlojutro P; Wallace A; Metcalf B; Laux K; Sotzen J; Tran T
    Mol Vis; 2014; 20():1527-44. PubMed ID: 25489226
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Genetics of retinal dystrophies--an overview].
    Bolz H
    Ophthalmologe; 2005 Jul; 102(7):661-73. PubMed ID: 15782291
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular aspects of retinal degenerative diseases.
    Lev S
    Cell Mol Neurobiol; 2001 Dec; 21(6):575-89. PubMed ID: 12043834
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Vitamin A and Vision.
    Saari JC
    Subcell Biochem; 2016; 81():231-259. PubMed ID: 27830507
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Rapid restoration of visual pigment and function with oral retinoid in a mouse model of childhood blindness.
    Van Hooser JP; Aleman TS; He YG; Cideciyan AV; Kuksa V; Pittler SJ; Stone EM; Jacobson SG; Palczewski K
    Proc Natl Acad Sci U S A; 2000 Jul; 97(15):8623-8. PubMed ID: 10869443
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Signalling beyond photon absorption: extracellular retinoids and growth factors modulate rod photoreceptor sensitivity.
    McKeown AS; Pitale PM; Kraft TW
    J Physiol; 2016 Apr; 594(7):1841-54. PubMed ID: 26691896
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Differential dimerization of variants linked to enhanced S-cone sensitivity syndrome (ESCS) located in the NR2E3 ligand-binding domain.
    von Alpen D; Tran HV; Guex N; Venturini G; Munier FL; Schorderet DF; Haider NB; Escher P
    Hum Mutat; 2015 Jun; 36(6):599-610. PubMed ID: 25703721
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Biology and therapy of inherited retinal degenerative disease: insights from mouse models.
    Veleri S; Lazar CH; Chang B; Sieving PA; Banin E; Swaroop A
    Dis Model Mech; 2015 Feb; 8(2):109-29. PubMed ID: 25650393
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Emerging therapies for inherited retinal degeneration.
    Scholl HP; Strauss RW; Singh MS; Dalkara D; Roska B; Picaud S; Sahel JA
    Sci Transl Med; 2016 Dec; 8(368):368rv6. PubMed ID: 27928030
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Digoxin-induced retinal degeneration depends on rhodopsin.
    Landfried B; Samardzija M; Barben M; Schori C; Klee K; Storti F; Grimm C
    Cell Death Dis; 2017 Mar; 8(3):e2670. PubMed ID: 28300845
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Leber congenital amaurosis: genes, proteins and disease mechanisms.
    den Hollander AI; Roepman R; Koenekoop RK; Cremers FP
    Prog Retin Eye Res; 2008 Jul; 27(4):391-419. PubMed ID: 18632300
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Inherited retinal degeneration: exceptional genetic and clinical heterogeneity.
    Sullivan LS; Daiger SP
    Mol Med Today; 1996 Sep; 2(9):380-6. PubMed ID: 8885257
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Gene Therapy for Retinal Degeneration.
    Apte RS
    Cell; 2018 Mar; 173(1):5. PubMed ID: 29570997
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The Consequences of Hypomorphic RPE65 for Rod and Cone Photoreceptors.
    Samardzija M; Barben M; Geiger P; Grimm C
    Adv Exp Med Biol; 2016; 854():341-6. PubMed ID: 26427430
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Safety in nonhuman primates of ocular AAV2-RPE65, a candidate treatment for blindness in Leber congenital amaurosis.
    Jacobson SG; Boye SL; Aleman TS; Conlon TJ; Zeiss CJ; Roman AJ; Cideciyan AV; Schwartz SB; Komaromy AM; Doobrajh M; Cheung AY; Sumaroka A; Pearce-Kelling SE; Aguirre GD; Kaushal S; Maguire AM; Flotte TR; Hauswirth WW
    Hum Gene Ther; 2006 Aug; 17(8):845-58. PubMed ID: 16942444
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.