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  • Search Condition : Filter (MeSH = Chemotaxis / physiology*)
Species Resource
Cellular slime molds S00143 , S00338 Differentiation-inducing factor-1 and -2 function also as modulators for Dictyostelium chemotaxis.
C.elegans tm501 The insulin/PI 3-kinase pathway regulates salt chemotaxis learning in Caenorhabditis elegans.
C.elegans tm445 , tm501 Caenorhabditis elegans integrates the signals of butanone and food to enhance chemotaxis to butanone.
C.elegans tm351 , tm903 , tm669 Gustatory plasticity in C. elegans involves integration of negative cues and NaCl taste mediated by serotonin, dopamine, and glutamate.
Cellular slime molds G90230 Ras-mediated activation of the TORC2-PKB pathway is critical for chemotaxis.
Cellular slime molds G01887 Myosin I links PIP3 signaling to remodeling of the actin cytoskeleton in chemotaxis.
C.intestinalis / (O.japonicus) Wild C. int Lipid rafts function in Ca2+ signaling responsible for activation of sperm motility and chemotaxis in the ascidian Ciona intestinalis.
Cellular slime molds G90237 , G90238 , G90239 , G90240 , G90241 , G90242 , G90243 , G90244 , G90245 , G90246 , ... Phosphoinositide-dependent protein kinase (PDK) activity regulates phosphatidylinositol 3,4,5-trisphosphate-dependent and -independent protein kinase B activation and chemotaxis.
Cellular slime molds S90421 , S90422 A developmentally regulated Na-H exchanger in Dictyostelium discoideum is necessary for cell polarity during chemotaxis.
Zebrafish Tg(isl1:GFP)/rw0 α2-Chimaerin regulates a key axon guidance transition during development of the oculomotor projection.
Silkworms Insect-controlled Robot: A Mobile Robot Platform to Evaluate the Odor-tracking Capability of an Insect.
C.elegans tm2816 O2-sensing neurons control CO2 response in C. elegans.
C.elegans tm1500 Roles for class IIA phosphatidylinositol transfer protein in neurotransmission and behavioral plasticity at the sensory neuron synapses of Caenorhabditis elegans.
C.elegans tm272 A sexually conditioned switch of chemosensory behavior in C. elegans.
Cellular slime molds S90686 , S90685 , S00342 , S00251 Heterotrimeric G-protein shuttling via Gip1 extends the dynamic range of eukaryotic chemotaxis.
C.elegans tm2816 , tm2669 , tm16530 , tm1449 , tm901 , tm4516 , tm2364 , tm4300 , tm2411 Receptor-type guanylate cyclase is required for carbon dioxide sensation by Caenorhabditis elegans.
Cellular slime molds G21638 , S00405 , S00406 , S90292 Chemotaxis in the absence of PIP3 gradients.
Cellular slime molds G90218 , G90219 , G90220 , G90221 , G90222 , G90223 , G90224 , G90225 , G90226 , G90227 , ... PIP3-independent activation of TorC2 and PKB at the cell's leading edge mediates chemotaxis.
Prokaryotes E. coli JW3441-KC(nikA) , JW3442-KC(nikB) , JW3443-KC(nikC) Repellent taxis in response to nickel ion requires neither Ni2+ transport nor the periplasmic NikA binding protein.
Cellular slime molds G02982 G03201 , S90289 Dynamics of the Dictyostelium Arp2/3 complex in endocytosis, cytokinesis, and chemotaxis.