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Molecular Biology of the Cell|February 17, 2021
Roles for ELMOD2 and Rootletin in ciliogenesisRachel E Turn, Joshua Linnert, Eduardo D Gigante, et al.
Scientific Reports|January 22, 2021
A new mouse model for retinal degeneration due to Fam161a deficiencyAvigail Beryozkin, Chen Matsevich, Alexey Obolensky, et al.
Human Molecular Genetics|January 29, 2010
The retinitis pigmentosa protein RP2 links pericentriolar vesicle transport between the Golgi and the primary ciliumR Jane Evans, Nele Schwarz, Kerstin Nagel-Wolfrum, et al.
Neurobiology of Disease|May 20, 2015
A novel function of Huntingtin in the cilium and retinal ciliopathy in Huntington's disease miceAlice Karam, Lars Tebbe, Chantal Weber, et al.
Journal of Virology|October 5, 2018
The Abundant Tegument Protein pUL25 of Human Cytomegalovirus Prevents Proteasomal Degradation of pUL26 and Supports Its Suppression of ISGylationChristine Zimmermann, Nicole Büscher, Steffi Krauter, et al.
Development (Cambridge, England)|March 15, 2008
A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growthGaelle Lefèvre, Vincent Michel, Dominique Weil, et al.
Frontiers in Cell and Developmental Biology|February 27, 2023
The Usher syndrome 1C protein harmonin regulates canonical Wnt signalingJessica Schäfer, Nicole Wenck, Katharina Janik, et al.
Human Molecular Genetics|March 11, 2014
Phosphorylation of the Usher syndrome 1G protein SANS controls Magi2-mediated endocytosisKatharina Bauß, Barbara Knapp, Pia Jores, et al.
Plos Genetics|October 29, 2015
The GTP- and Phospholipid-Binding Protein TTD14 Regulates Trafficking of the TRPL Ion Channel in Drosophila Photoreceptor CellsAlexander C Cerny, André Altendorfer, Krystina Schopf, et al.
Frontiers in Cell and Developmental Biology|March 19, 2025
The BBS/CCT chaperonin complex ensures the localization of the adhesion G protein-coupled receptor ADGRV1 to the base of primary ciliaJoshua Linnert, Deva Krupakar Kusuluri, Baran E Güler, et al.
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