Tubulin transport by IFT is upregulated during ciliary growth by a cilium-autonomous mechanism JM Craft, JA Harris, S Hyman, P Kner, KF Lechtreck Journal of Cell Biology 208 (2), 223-237, 2015 | 230 | 2015 |
A differential cargo-loading model of ciliary length regulation by IFT KN Wren, JM Craft, D Tritschler, A Schauer, DK Patel, EF Smith, ME Porter, ... Current Biology 23 (24), 2463-2471, 2013 | 196 | 2013 |
Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert syndrome X Shi, G Garcia III, JC Van De Weghe, R McGorty, GJ Pazour, D Doherty, ... Nature cell biology 19 (10), 1178-1188, 2017 | 173 | 2017 |
Cycling of the signaling protein phospholipase D through cilia requires the BBSome only for the export phase KF Lechtreck, JM Brown, JL Sampaio, JM Craft, A Shevchenko, JE Evans, ... Journal of Cell Biology 201 (2), 249-261, 2013 | 156 | 2013 |
New, Combined, and Reduced Dosing Treatment Protocols Cure Trypanosoma cruzi Infection in Mice JM Bustamante, JM Craft, BD Crowe, SA Ketchie, RL Tarleton The Journal of infectious diseases 209 (1), 150-162, 2014 | 150 | 2014 |
Together, the IFT81 and IFT74 N-termini form the main module for intraflagellar transport of tubulin T Kubo, JM Brown, K Bellve, B Craige, JM Craft, K Fogarty, KF Lechtreck, ... Journal of cell science 129 (10), 2106-2119, 2016 | 116 | 2016 |
Mutations in ARMC9, which encodes a basal body protein, cause Joubert syndrome in humans and ciliopathy phenotypes in zebrafish JC Van De Weghe, TDS Rusterholz, B Latour, ME Grout, KA Aldinger, ... The American Journal of Human Genetics 101 (1), 23-36, 2017 | 102 | 2017 |
Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome BL Latour, JC Van De Weghe, TDS Rusterholz, SJF Letteboer, A Gomez, ... The Journal of clinical investigation 130 (8), 4423-4439, 2020 | 69 | 2020 |
Protein transport in growing and steady‐state cilia KF Lechtreck, JC Van De Weghe, JA Harris, P Liu Traffic 18 (5), 277-286, 2017 | 56 | 2017 |
Diffusion rather than intraflagellar transport likely provides most of the tubulin required for axonemal assembly in Chlamydomonas J Craft Van De Weghe, JA Harris, T Kubo, GB Witman, KF Lechtreck Journal of cell science 133 (17), jcs249805, 2020 | 46 | 2020 |
Oral Exposure to Trypanosoma cruzi Elicits a Systemic CD8+ T Cell Response and Protection against Heterotopic Challenge MH Collins, JM Craft, JM Bustamante, RL Tarleton Infection and immunity 79 (8), 3397-3406, 2011 | 44 | 2011 |
The Joubert–Meckel–nephronophthisis spectrum of ciliopathies JC Van De Weghe, A Gomez, D Doherty Annual Review of Genomics and Human Genetics 23 (1), 301-329, 2022 | 39 | 2022 |
TMEM218 dysfunction causes ciliopathies, including Joubert and Meckel syndromes JC Van De Weghe, JL Giordano, IB Mathijssen, M Mojarrad, ... Human Genetics and Genomics Advances 2 (1), 100016, 2020 | 14 | 2020 |
Diffusion rather than IFT provides most of the tubulin required for axonemal assembly JA Harris, JC Van De Weghe, T Kubo, GB Witman, KF Lechtreck BioRxiv, 268573, 2018 | 13 | 2018 |
Systematic analysis of cilia characteristics and Hedgehog signaling in five immortal cell lines AE Gómez, AK Christman, JC Van De Weghe, M Finn, D Doherty PLoS One 17 (12), e0266433, 2022 | 11 | 2022 |
ARMC9 and TOGARAM1 define a Joubert syndrome-associated protein module that regulates axonemal post-translational modifications and cilium stability BL Latour, JC Van De Weghe, TDS Rusterholz, SJF Letteboer, A Gomez, ... bioRxiv, 817213, 2019 | 7 | 2019 |
University of Washington Center for Mendelian Genomics Mutations in ARMC9, which encodes a basal body protein, cause Joubert syndrome in humans and ciliopathy phenotypes in … JC Van De Weghe, TDS Rusterholz, B Latour, ME Grout, KA Aldinger, ... Am. J. Hum. Genet 101, 23-36, 2017 | 5 | 2017 |
Erratum: Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert syndrome X Shi, G Garcia III, JC Van De Weghe, R McGorty, GJ Pazour, D Doherty, ... Nature Cell Biology 19 (11), 1379-1379, 2017 | 4 | 2017 |
eScholarship@ UMassChan J Craft Van De Weghe, JA Harris | | 2020 |
A novel ciliary Joubert Syndrome-associated protein module regulates axonemal post translational modifications and cilium stability B Latour, T Rusterholz, J Van de Weghe, M Gesemann, SCF Neuhauss, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1167-1168, 2019 | | 2019 |