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Annual Review of Genomics and Human Genetics|June 2, 2022
The Joubert-Meckel-Nephronophthisis Spectrum of CiliopathiesJulie C Van De Weghe, Arianna Gomez, Dan DohertyTraffic (Copenhagen, Denmark)|March 2, 2017
Protein transport in growing and steady-state ciliaKarl F Lechtreck, Julie C Van De Weghe, James Aaron Harris, et al.Nature Cell Biology|August 29, 2017
Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert syndromeXiaoyu Shi, Galo Garcia, Julie C Van De Weghe, et al.Nature Cell Biology|November 1, 2017
Erratum: Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert syndromeXiaoyu Shi, Galo Garcia, Julie C Van De Weghe, et al.HGG Advances|April 1, 2021
TMEM218 dysfunction causes ciliopathies, including Joubert and Meckel syndromesJulie C Van De Weghe, Jessica L Giordano, Inge B Mathijssen, 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.Pageof 1