Research ExplorerJournalsMOL VIS

MOL VIS - MOLECULAR VISION

Bibliographical data

ISSNs1090-0535

Publications

Horizontal gaze palsy with progressive scoliosis: three novel ROBO3 mutations and descriptions of the phenotypes of four patients.
Volk, A. E., Carter, O., Fricke, J., Herkenrath, P., Poggenborg, J., Borck, G., Demant, A. W., Ivo, R., Eysel, P., Kubisch, C. & Neugebauer, A., 2011, In: MOL VIS. 17, p. 1978-1986

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

Identification of a novel LCA5 mutation in a Pakistani family with Leber congenital amaurosis and cataracts.
Ahmad, A., Daud, S., Kakar, N., Nürnberg, G., Nürnberg, P., Babar, M. E., Thoenes, M., Kubisch, C., Ahmad, J. & Bolz, H. J., 2011, In: MOL VIS. 17, p. 1940-1945

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

SU5416 induces premature senescence in endothelial progenitor cells from patients with age-related macular degeneration.
Berna-Thill, M., Berna, M., Kunst, F., Wege, H., Strunnikova, N. V., Gordiyenko, N., Grierson, R., Richard, G. & Csaky, K. G., 2011, In: MOL VIS. 17, p. 85-98

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

Regeneration of corneal endothelium following complete endothelial cell loss in rat keratoplasty.
Schwartzkopff, J., Bredow, L., Mahlenbrey, S., Boehringer, D. & Reinhard, T., 2010, In: MOL VIS. 16, p. 2368-2375

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa.
Azam, M., Khan, M. I., Gal, A., Hussain, A., Shah, S. T. A., Khan, M. S., Sadeque, A., Bokhari, H., Collin, R. W. J., Orth, U., Genderen, V., Maria, M., den Hollander, A. I., Cremers, F. P. M. & Qamar, R., 2009, In: MOL VIS. 15, p. 2526-2534

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

Ultra high throughput sequencing excludes MDH1 as candidate gene for RP28-linked retinitis pigmentosa.
Frio, T. R., Panek, S., Iseli, C., Gioia, D., Alessandro, S., Gal, A., Gal, A. & Rivolta, C., 2009, In: MOL VIS. 15, p. 2627-2633

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

Identification of novel mutations in X-linked retinitis pigmentosa families and implications for diagnostic testing.
Neidhardt, J., Glaus, E., Lorenz, B., Netzer, C., Li, Y., Schambeck, M., Wittmer, M., Feil, S., Kirschner-Schwabe, R., Rosenberg, T., Cremers, F. P. M., Bergen, A. A. B., Barthelmes, D., Baraki, H., Schmid, F., Tanner, G., Fleischhauer, J., Orth, U., Becker, C., Wegscheider, E., Nürnberg, G., Nürnberg, P., Bolz, H. J., Gal, A. & Berger, W., 2008, In: MOL VIS. 14, p. 1081-1093

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

Voltage-dependent Ca2+ channels, not ryanodine receptors, activate Ca2+-dependent BK potassium channels in human retinal pigment epithelial cells.
Wimmers, S., Halsband, C., Seyler, S., Milenkovic, V. & Strauss, O., 2008, In: MOL VIS. 14, p. 2340-2348

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

Ca2+ channels in retinal pigment epithelial cells regulate vascular endothelial growth factor secretion rates in health and disease.
Rosenthal, R., Heimann, H., Agostini, H., Martin, G., Hansen, L. L. & Strauss, O., 2007, In: MOL VIS. 13, p. 443-456

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

HCCS loss-of-function missense mutation in a female with bilateral microphthalmia and sclerocornea: a novel gene for severe ocular malformations?
Rau, I., Shaw, G. M. & Kutsche, K., 2007, In: MOL VIS. 13, p. 1475-1482

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

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