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Nature Communications|March 12, 2022
Loss of the Bardet-Biedl protein Bbs1 alters photoreceptor outer segment protein and lipid compositionMarkus Masek, Christelle Etard, Claudia Hofmann, et al.
Open Biology|July 30, 2024
Glutamate transporters are involved in direct inhibitory synaptic transmission in the vertebrate retinaStephanie Niklaus, Stella M K Glasauer, Peter Kovermann, et al.
Elife|March 2, 2021
Endoglycan plays a role in axon guidance by modulating cell adhesionThomas Baeriswyl, Alexandre Dumoulin, Martina Schaettin, et al.
The European Journal of Neuroscience|September 18, 2007
Evidence for RPE65-independent vision in the cone-dominated zebrafish retinaHelia B Schonthaler, Johanna M Lampert, Andrea Isken, et al.
Biology Open|January 10, 2015
Proper migration and axon outgrowth of zebrafish cranial motoneuron subpopulations require the cell adhesion molecule MDGA2AEsther Ingold, Colette M Vom Berg-Maurer, Christoph J Burckhardt, et al.
Human Molecular Genetics|March 5, 2020
Biallelic variants in PSMB1 encoding the proteasome subunit β6 cause impairment of proteasome function, microcephaly, intellectual disability, developmental delay and short statureMuhammad Ansar, Frédéric Ebstein, Hayriye Özkoç, et al.
American Journal of Human Genetics|June 20, 2017
Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in ZebrafishJulie C Van De Weghe, Tamara D S Rusterholz, Brooke Latour, et al.
The Journal of Clinical Investigation|May 27, 2020
Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndromeBrooke L Latour, Julie C Van De Weghe, Tamara Ds Rusterholz, et al.
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