Med Sci (Paris)
Volume 36, Number 11, Novembre 2020
|Page(s)||987 - 990|
|Published online||05 November 2020|
- Johnstone CN, Castellvi-Bel S, Chang LM, et al. ARHGAP8 is a novel member of the RHOGAP family related to ARHGAP1/CDC42GAP/p50RHOGAP: mutation and expression analyses in colorectal and breast cancers. Gene 2004 ; 336 : 59–71. [Google Scholar]
- Stengel K, Zheng Y. Cdc42 in oncogenic transformation, invasion, and tumorigenesis. Cell Signal 2011 ; 23 : 1415–1423. [CrossRef] [PubMed] [Google Scholar]
- Motokawa M, Watanabe S, Nakatomi A, et al. A hot-spot mutation in CDC42 (p.Tyr64Cys) and novel phenotypes in the third patient with Takenouchi-Kosaki syndrome. J Hum Genet 2018 ; 63 : 387–390. [CrossRef] [PubMed] [Google Scholar]
- Martinelli S, Krumbach OHF, Pantaleoni F, et al. Functional dysregulation of CDC42 causes diverse developmental phenotypes. Am J Hum Genet 2018 ; 102 : 309–320. [Google Scholar]
- Bekhouche B, Tourville A, Ravichandran Y, et al. A toxic palmitoylation of Cdc42 enhances NF-kB signaling and drives a severe autoinflammatory syndrome. J Allergy Clin Immunol 2020; S0091–6749(20)30426–7. [Google Scholar]
- Gernez Y, de Jesus AA, Alsaleem H, et al. Severe autoinflammation in four patients with C-terminal variants in cell division control protein 42 homolog (CDC42) successfully treated with IL-1b inhibition. J Allergy Clin Immunol 2019 ; 144 : 1122–5 e6. [Google Scholar]
- Lam MT, Coppola S, Krumbach OHF, et al. A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function. J Exp Med 2019 ; 216 : 2778–2799. [CrossRef] [PubMed] [Google Scholar]
- He T, Huang Y, Ling J, et al. A new patient with NOCARH syndrome due to CDC42 defect. J Clin Immunol 2020; 40 : 571–5. [CrossRef] [PubMed] [Google Scholar]
- Verboon JM, Mahmut D, Kim AR, et al. Infantile myelofibrosis and myeloproliferation with CDC42 dysfunction. J Clin Immunol 2020; 40 : 554–66. [CrossRef] [PubMed] [Google Scholar]
- Johnson JL, Erickson JW, Cerione RA. C-terminal di-arginine motif of Cdc42 protein is essential for binding to phosphatidylinositol 4,5-bisphosphate-containing membranes and inducing cellular transformation. J Biol Chem 2012 ; 287 : 5764–5774. [Google Scholar]
- Pfajfer L, Mair NK, Jiménez-Heredia R, et al. Mutations affecting the actin regulator WD repeat-containing protein 1 lead to aberrant lymphoid immunity. J Allergy Clin Immunol 2018; 142 : 1589–604. [CrossRef] [PubMed] [Google Scholar]
Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.
Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.
Initial download of the metrics may take a while.