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ZFIN ID:
ZDB-PERS-011004-1
Bahadori, Ronja
Email:
ronja.bahadori@imm.ox.ac.uk
URL:
Affiliation:
Patient Lab
Address:
MRC Molecular Haematology Unit Weatherall Institute of Molecular Medicine John Radcliffe Hospital Headington Oxford, OX3 9DS United Kingdom
Country:
United Kingdom
Phone:
41-1-635-3228
Fax:
41-1-635-3303
ORCID ID:
BIOGRAPHY AND RESEARCH INTERESTS
PUBLICATIONS
Schonthaler, H.B., Fleisch, V.C., Biehlmaier, O., Makhankov, Y., Rinner, O., Bahadori, R., Geisler, R., Schwarz, H., Neuhauss, S.C., and Dahm, R. (2008) The zebrafish mutant lbk/vam6 resembles human multi-systemic disorders caused by aberrant trafficking of endosomal vesicles. Development (Cambridge, England). 135(2):387-399
Bahadori, R., Rinner, O., Schonthaler, H.B., Biehlmaier, O., Makhankov, Y.V., Rao, P., Jagadeeswaran, P., and Neuhauss, S.C. (2006) The Zebrafish fade out Mutant: A Novel Genetic Model for Hermansky-Pudlak Syndrome. Investigative ophthalmology & visual science. 47(10):4523-4531
Bahadori, R., Biehlmaier, O., Zeitz, C., Labhart, T., Makhankov, Y.V., Forster, U., Gesemann, M., Berger, W., and Neuhauss, S.C. (2006) Nyctalopin is essential for synaptic transmission in the cone dominated zebrafish retina. The European journal of neuroscience. 24(6):1664-1674
Bahadori, R. (2005) Zebrafish as a genetic model system for human retinal disorders. Ph.D. Thesis. :116p
Bahadori, R., Huber, M., Rinner, O., Seeliger, M.W., Geiger-Rudolph, S., Geisler, R., and Neuhauss, S.C. (2003) Retinal function and morphology in two zebrafish models of oculo-renal syndromes. The European journal of neuroscience. 18(6):1377-1386
NON-ZEBRAFISH PUBLICATIONS
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