Thibaut Eguether
Affiliations: | Université Pierre et Marie Curie (Paris), Paris, Île-de-France, France |
Area:
Cilia and centrosome biologyGoogle:
"Thibaut Eguether"Parents
Sign in to add mentor| Anne-Marie Tassin | grad student | CNRS | |
| Gregory Pazour | post-doc | UMASS Medical School |
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Publications
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| Francis RJB, San Agustin JT, Szabo Rogers HL, et al. (2023) Autonomous and non-cell autonomous role of cilia in structural birth defects in mice. Plos Biology. 21: e3002425 |
| Francis R, San Agustin JT, Szabo Rogers HL, et al. (2023) Autonomous and non-cell autonomous etiology of ciliopathy associated structural birth defects. Biorxiv : the Preprint Server For Biology |
| Bakey Z, Cabrera OA, Hoefele J, et al. (2023) IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans. Plos Genetics. 19: e1010796 |
| Bakey Z, Cabrera OA, Hoefele J, et al. (2023) variants cause skeletal ciliopathy and motile cilia defects in mice and humans. Medrxiv : the Preprint Server For Health Sciences |
| Eguether T, Hahne M. (2018) Mixed signals from the cell's antennae: primary cilia in cancer. Embo Reports |
| Condemine W, Eguether T, Couroussé N, et al. (2018) 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 |
| Eguether T, Cordelieres FP, Pazour GJ. (2018) Intraflagellar transport is deeply integrated in hedgehog signaling. Molecular Biology of the Cell |
| Yang N, Leung EL, Liu C, et al. (2017) INTU is essential for oncogenic Hh signaling through regulating primary cilia formation in basal cell carcinoma. Oncogene |
| Bruel AL, Franco B, Duffourd Y, et al. (2017) Fifteen years of research on oral-facial-digital syndromes: from 1 to 16 causal genes. Journal of Medical Genetics |
| Thevenon J, Duplomb L, Phadke S, et al. (2016) Autosomal Recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangia. Clinical Genetics |