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  • Search Condition : Filter (MeSH = Eye Abnormalities / genetics)
Species Resource Title
C.elegans An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes.
C.elegans tm1830 , tm324 , tm925 , tm2322 , tm3100 KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome.
Drosophila Members of the synaptobrevin/vesicle-associated membrane protein (VAMP) family in Drosophila are functionally interchangeable in vivo for neurotransmitter release and cell viability.
C.elegans tm925 , tm3083 TMEM107 recruits ciliopathy proteins to subdomains of the ciliary transition zone and causes Joubert syndrome.
Zebrafish Fucci Microcephaly models in the developing zebrafish retinal neuroepithelium point to an underlying defect in metaphase progression.
Rats KFRS4/Kyo(strainID=919) Deletion of a conserved regulatory element required for Hmx1 expression in craniofacial mesenchyme in the dumbo rat: a newly identified cause of congenital ear malformation.
Drosophila 6876R-1 , 6876R-4 The splicing factor Prp31 is essential for photoreceptor development in Drosophila.
Drosophila actin-GAL4 , GMR-GAL4 , ey-GAL4 , UAS-lacZ , UAS-GFP , 6390R-2 , 6390R-4 , 3002R-2 , 3002R-3 , 9388R-2 , ... AP-1 clathrin adaptor and CG8538/Aftiphilin are involved in Notch signaling during eye development in Drosophila melanogaster.
Drosophila Bax-like protein Drob-1 protects neurons from expanded polyglutamine-induced toxicity in Drosophila.