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Thibaut Eguether - Publications

Affiliations: 
Université Pierre et Marie Curie (Paris), Paris, Île-de-France, France 
Area:
Cilia and centrosome biology
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16 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Francis RJB, San Agustin JT, Szabo Rogers HL, Cui C, Jonassen JA, Eguether T, Follit JA, Lo CW, Pazour GJ. Autonomous and non-cell autonomous role of cilia in structural birth defects in mice. Plos Biology. 21: e3002425. PMID 38079449 DOI: 10.1371/journal.pbio.3002425  0.642
2023 Francis R, San Agustin JT, Szabo Rogers HL, Cui C, Jonassen JA, Eguether T, Follit JA, Lo CW, Pazour GJ. Autonomous and non-cell autonomous etiology of ciliopathy associated structural birth defects. Biorxiv : the Preprint Server For Biology. PMID 37333142 DOI: 10.1101/2023.06.07.544132  0.639
2023 Bakey Z, Cabrera OA, Hoefele J, Antony D, Wu K, Stuck MW, Micha D, Eguether T, Smith AO, van der Wel NN, Wagner M, Strittmatter L, Beales PL, Jonassen JA, Thiffault I, et al. IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans. Plos Genetics. 19: e1010796. PMID 37315079 DOI: 10.1371/journal.pgen.1010796  0.653
2023 Bakey Z, Cabrera OA, Hoefele J, Antony D, Wu K, Stuck MW, Micha D, Eguether T, Smith AO, van der Wel NN, Wagner M, Strittmatter L, Beales PL, Jonassen JA, Thiffault I, et al. variants cause skeletal ciliopathy and motile cilia defects in mice and humans. Medrxiv : the Preprint Server For Health Sciences. PMID 36865301 DOI: 10.1101/2023.02.23.23286106  0.613
2018 Eguether T, Hahne M. Mixed signals from the cell's antennae: primary cilia in cancer. Embo Reports. PMID 30348893 DOI: 10.15252/Embr.201846589  0.358
2018 Condemine W, Eguether T, Couroussé N, Etchebest C, Gardet A, Trugnan G, Chwetzoff S. The C-terminus of rotavirus VP4 protein contains an actin binding domain which requires co-operation with the coiled-coil domain for actin remodeling. Journal of Virology. PMID 30333172 DOI: 10.1128/Jvi.01598-18  0.343
2018 Eguether T, Cordelieres FP, Pazour GJ. Intraflagellar transport is deeply integrated in hedgehog signaling. Molecular Biology of the Cell. PMID 29540531 DOI: 10.1091/Mbc.E17-10-0600  0.637
2017 Yang N, Leung EL, Liu C, Li L, Eguether T, Jun Yao XJ, Jones EC, Norris DA, Liu A, Clark RA, Roop DR, Pazour GJ, Shroyer KR, Chen J. INTU is essential for oncogenic Hh signaling through regulating primary cilia formation in basal cell carcinoma. Oncogene. PMID 28459465 DOI: 10.1038/Onc.2017.117  0.468
2017 Bruel AL, Franco B, Duffourd Y, Thevenon J, Jego L, Lopez E, Deleuze JF, Doummar D, Giles RH, Johnson CA, Huynen MA, Chevrier V, Burglen L, Morleo M, Desguerres I, ... ... Eguether T, et al. Fifteen years of research on oral-facial-digital syndromes: from 1 to 16 causal genes. Journal of Medical Genetics. PMID 28289185 DOI: 10.1136/Jmedgenet-2016-104436  0.617
2016 Thevenon J, Duplomb L, Phadke S, Eguether T, Saunier A, Avila M, Carmignac V, Bruel AL, St-Onge J, Duffourd Y, Pazour GJ, Franco B, Attie-Bitach T, Masurel-Paulet A, Rivière JB, et al. Autosomal Recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangia. Clinical Genetics. PMID 27060890 DOI: 10.1111/Cge.12785  0.66
2015 Yang N, Li L, Eguether T, Sundberg JP, Pazour GJ, Chen J. Intraflagellar transport 27 is essential for hedgehog signaling but dispensable for ciliogenesis during hair follicle morphogenesis. Development (Cambridge, England). 142: 2860. PMID 26286943 DOI: 10.1242/dev.128751  0.577
2015 Yang N, Li L, Eguether T, Sundberg JP, Pazour GJ, Chen J. Intraflagellar transport 27 is essential for hedgehog signaling but dispensable for ciliogenesis during hair follicle morphogenesis. Development (Cambridge, England). 142: 2194-202. PMID 26023097 DOI: 10.1242/Dev.115261  0.681
2015 Damerla RR, Cui C, Gabriel GC, Liu X, Craige B, Gibbs BC, Francis R, Li Y, Chatterjee B, San Agustin JT, Eguether T, Subramanian R, Witman GB, Michaud JL, Pazour GJ, et al. Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies. Human Molecular Genetics. 24: 3994-4005. PMID 25877302 DOI: 10.1093/Hmg/Ddv137  0.681
2014 Eguether T, San Agustin JT, Keady BT, Jonassen JA, Liang Y, Francis R, Tobita K, Johnson CA, Abdelhamed ZA, Lo CW, Pazour GJ. IFT27 links the BBSome to IFT for maintenance of the ciliary signaling compartment. Developmental Cell. 31: 279-90. PMID 25446516 DOI: 10.1016/J.Devcel.2014.09.011  0.683
2014 Eguether T, Ermolaeva MA, Zhao Y, Bonnet MC, Jain A, Pasparakis M, Courtois G, Tassin AM. The deubiquitinating enzyme CYLD controls apical docking of basal bodies in ciliated epithelial cells. Nature Communications. 5: 4585. PMID 25134987 DOI: 10.1038/Ncomms5585  0.644
2012 Eguether T, Bonnet B, Ermolaeva E, Pasparakis P, Courtois C, Tassin T. CYLD tumour supressor regulates ciligenesis Cilia. 1: 66. DOI: 10.1186/2046-2530-1-S1-P66  0.493
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