Overactivation of Cdc42 GTPase Impairs the Cytotoxic Function of NK Cells From Old Individuals Towards Senescent Fibroblasts. [PDF]
Koroma AK +15 more
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Engineered interfaces in Rac1 and Cdc42 biosensors enhance sensitivity and reduce cell perturbation. [PDF]
Marston DJ +10 more
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Dual targeting of mitochondrial metabolism and Rho GTPase signaling to suppress cancer metastasis (Review). [PDF]
Daher A +4 more
europepmc +1 more source
Does Ras/Rho Have Skin in the Game: The Importance of the Isoprenoid Biosynthesis Pathway in Merkel Cell Carcinoma Cell Lines. [PDF]
Blaha LN +3 more
europepmc +1 more source
Membrane curvature initiates Cdc42-FBP17-N-WASP clustering and actin nucleation. [PDF]
Zhu K +6 more
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FABP7 controls radial glial scaffold stability during human cortical development. [PDF]
Wang Y +15 more
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Cholecystokinin A Receptor Knockdown Diminishes Colon Cancer Cell Invasive Potential via Modulation of Integrin/FAK, EMT, and uPA/uPAR/MMP2 Axis. [PDF]
Lin CS, Hsu TW, Lee HL, Kao SH.
europepmc +1 more source
Glabridin Inhibits Melanogenesis and Melanin Transfer via Wnt/β-Catenin Pathway and Rho Family GTPase-Mediated Dendritic Formation Suppression. [PDF]
Li L, Zhang X, Tang G, Wu J, Huang Q.
europepmc +1 more source
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Cdc42: Role in Cancer Management
Chemical Biology and Drug Design, 2015Contribution of Cdc42, a member of Rho family, has been characterized for the beginning of variety of cellular responses including cellular transformation, cell division, cell invasion, migration, invadopodia formation, enzyme activity, filopodia formation, and cell polarity in cells. Deregulation of Cdc42 can alter the normal functioning of the cells,
Muhammad Ali, Mi Qadir
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NMR assignment of Cdc42(T35A), an active Switch I mutant of Cdc42
Biomolecular NMR Assignments, 2007Cdc42(T35A) is an active construct of Cdc42, a Ras GTPase involved in signal transduction, containing a single-point mutation in an important effector-binding region. We determined the backbone and side chain resonance assignments of (13)C,(15)N-labelled Cdc42(T35A) from E. coli.
Adams, Paul D., Oswald, Robert E.
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