Tctex1d2 associates with short-rib polydactyly syndrome proteins and is required for ciliogenesis

Short-rib polydactyly syndromes (SRPS) arise from mutations in genes involved in retrograde intraflagellar transport (IFT) and basal body homeostasis, which are critical for cilia assembly and function. Recently, mutations in WDR34 or WDR60 (candidate dynein intermediate chains) were identified in S...

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Publicat a:Cell Cycle
Autors principals: Gholkar, Ankur A., Senese, Silvia, Lo, Yu-Chen, Capri, Joseph, Deardorff, William J, Dharmarajan, Harish, Contreras, Ely, Hodara, Emmanuelle, Whitelegge, Julian P, Jackson, Peter K, Torres, Jorge Z
Format: Artigo
Idioma:Inglês
Publicat: Taylor & Francis 2015
Matèries:
Reports
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4614626/
https://ncbi.nlm.nih.gov/pubmed/25830415
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/15384101.2014.985066
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