Institut de Recherche en Ophtalmologie

IRO

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Publications 2006

  • Pubmed

    Sub-foveal choroidal blood flow by LDF: measurement and application to the physiology and pathology of the choroidal circulation.
    Riva CE.
    Bull Soc Belge Ophtalmol. 2006;(302):185-94.

  • PDFPubmed

    Microarray analysis reveals retinal stem cell characteristics of the adult human eye. For contributed volumes.
    Angenieux B, Michaut L, Schorderet DE, Munier FL, Gehring W, Arsenijevic Y.
    Adv Exp Med Biol. 2006;572:377-80.

  • PDFPubmed

    Lentiviral vectors containing a retinal pigment epithelium specific promoter for leber congenital amaurosis gene therapy. Lentiviral gene therapy for LCA.
    Bemelmans AP, Kostic C, Hornfeld D, Jaquet M, Crippa SV, Hauswirth WW, Lem J, Wang Z, Schorderet DE, Munier FL, Wenzel A, Arsenijevic Y.
    Adv Exp Med Biol. 2006;572:247-53

  • PDFPubmed

    BMI1 loss delays photoreceptor degeneration in Rd1 mice. Bmi1 loss and neuroprotection in Rd1 mice.
    Zencak D, Crippa SV, Tekaya M, Tanger E, Schorderet DE, Munier FL, van Lohuizen M, Arsenijevic Y.
    Adv Exp Med Biol. 2006;572:209-15.

  • PDFPubmed

    Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
    Vieira V, David G, Roche O, de la Houssaye G, Boutboul S, Arbogast L, Kobetz A, Orssaud C, Camand O, Schorderet DF, Munier F, Rossi A, Delezoide AL, Marsac C, Ricquier D, Dufier JL, Menasche M, Abitbol M.
    Mol Vis. 2006 Dec 1;12:1448-60.

  • PDFPubmed

    Homogeneous and nonradioactive high-throughput screening platform for the characterization of kinase inhibitors in cell lysates.
    Guenat S, Rouleau N, Bielmann C, Bedard J, Maurer F, Allaman-Pillet N, Nicod P, Bielefeld-Sevigny M, Beckmann JS, Bonny C, Bosse R, Roduit R.
    J Biomol Screen. 2006 Dec;11(8):1015-26.

  • PDFPubmed

    Biological characterization of gene response in Rpe65-/- mouse model of Leber's congenital amaurosis during progression of the disease.
    Cottet S, Michaut L, Boisset G, Schlecht U, Gehring W, Schorderet DF.
    FASEB J. 2006 Oct;20(12):2036-49.

  • PDFPubmed

    Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness.
    Zeitz C, Kloeckener-Gruissem B, Forster U, Kohl S, Magyar I, Wissinger B, Matyas G, Borruat FX, Schorderet DF, Zrenner E, Munier FL, Berger W.
    Am J Hum Genet. 2006 Oct;79(4):657-67.

  • PDFPubmed

    Systemic investigation of keratoepithelin deposits in TGFBI/BIGH3-related corneal dystrophy.
    El Kochairi I, Letovanec I, Uffer S, Munier FL, Chaubert P, Schorderet DF.
    Mol Vis. 2006 May 10;12:461-6.

  • PDFPubmed

    Keratoepithelin suppresses the progression of experimental human neuroblastomas.
    Becker J, Erdlenbruch B, Noskova I, Schramm A, Aumailley M, Schorderet DF, Schweigerer L.
    Cancer Res. 2006 May 15;66(10):5314-21.

  • PDFPubmed

    Evanescent white linear flecks and posterior microphthalmos: new features of a recently established disease.
    Tran HV, Borruat FX, Reymond-Gruber S, Schorderet D, Munier F.
    Klin Monatsbl Augenheilkd. 2006 May;223(5):397-9.

  • PDFPubmed

    A subset of patients with epithelial basement membrane corneal dystrophy have mutations in TGFBI/BIGH3.
    Boutboul S, Black GC, Moore JE, Sinton J, Menasche M, Munier FL, Laroche L, Abitbol M, Schorderet DF.
    Hum Mutat. 2006 Jun;27(6):553-7.

  • PDFPubmed

    Eight previously unidentified mutations found in the OA1 ocular albinism gene.
    Mayeur H, Roche O, Vetu C, Jaliffa C, Marchant D, Dollfus H, Bonneau D, Munier FL, Schorderet DF, Levin AV, Heon E, Sutherland J, Lacombe D, Said E, Mezer E, Kaplan J, Dufier JL, Marsac C, Menasche M, Abitbol M.Mayeur H, Roche O, Vetu C, Jaliffa C, Marcha
    BMC Med Genet. 2006 Apr 28;7:41

  • PDFPubmed

    Regulation of subfoveal choroidal blood flow in age-related macular degeneration.
    Pournaras CJ, Logean E, Riva CE, Petrig BL, Chamot SR, Coscas G, Soubrane G.
    Graefes Arch Clin Exp Ophthalmol. 2006 Jun;244(6):725-31

  • PDFPubmed

    Phenotype of three consanguineous Tunisian families with early-onset retinal degeneration caused by an R91W homozygous mutation in the RPE65 gene.
    El Matri L, Ambresin A, Schorderet DF, Kawasaki A, Seeliger MW, Wenzel A, Arsenijevic Y, Borruat FX, Munier FL.
    Graefes Arch Clin Exp Ophthalmol. 2006 Sep;244(9):1104-12.

  • PDFPubmed

    Keratoepithelin in secondary corneal amyloidosis.
    Suesskind D, Auw-Haedrich C, Schorderet DF, Munier FL, Loeffler KU.
    Graefes Arch Clin Exp Ophthalmol. 2006 Jun;244(6):725-31

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