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1 e biological responses via G protein-coupled serpentine receptors.
2 ost chemokine receptors and is rare in other serpentine receptors.
3 , and srd families of seven-transmembrane or serpentine receptors.
4 pression under free-running conditions; (iv) Serpentine receptor 10 (SR10) has a 24 h transcriptional
5  (ER) to prevent maturation of Frizzled (Fz) serpentine receptors and fibroblast growth factor recept
6 nary conservation of the switch mechanism of serpentine receptors and help to constrain models of how
7 rtussis toxin (PTX) is a potent inhibitor of serpentine receptor-associated inhibitory trimeric guani
8                                     Multiple Serpentine Receptor B (SRB) chemosensory receptors regul
9                 In contrast with other known serpentine receptors, CIRL has two subunits of the 120 a
10  but distinct from, the previously described serpentine receptor class a (sra) family and shows a dif
11  have identified a chemosensory gene family, serpentine receptor class ab (srab), which exists in bot
12 at disrupts the adjacent chemoreceptor genes serpentine receptor class g (srg)-36 and -37.
13 ent chemoattractant for cells expressing the serpentine receptor CMKLR1 (chemokine-like receptor 1),
14           The seven transmembrane helices of serpentine receptors comprise a conserved switch that re
15 ommunication that is mediated by a family of serpentine receptors containing seven transmembrane doma
16 riety of other chemoattractants that bind to serpentine receptors coupled to heterotrimeric G protein
17 , extracellular cAMP through activation of a serpentine receptor family.
18 rity in all three systems is mediated by the serpentine receptor Frizzled and a number of additional
19           In Drosophila, two closely related serpentine receptors, Frizzled (Fz) and D-Frizzled2 (Fz2
20                  The Frizzled (Fz) family of serpentine receptors function as Wnt receptors, but how
21 lassic components of this system include the serpentine receptors, heterotrimeric G-proteins, adenyly
22                    Caveolae harbor different serpentine receptors, intracellular components of signal
23 rimeric GTP-binding proteins (G-proteins) to serpentine receptors involves several independent contac
24 gnaling through the Frizzled (FZD) family of serpentine receptors is essential for embryogenesis and
25  We show that the mast cell-expressed orphan serpentine receptor mCCRL2 is not required for expressio
26                                     Frizzled serpentine receptors mediate distinct signaling pathways
27  interaction with receptors, and, in several serpentine receptors, regions similar to those in rhodop
28 ing seven-transmembrane G-protein-coupled or serpentine receptors related to the ODR-10 diacetyl chem
29  that inhibits Hh signaling by targeting the serpentine receptor Smoothened (SMO), has produced promi
30  key elements of a general mechanism for the serpentine receptor switch.
31                         C5L2 is an enigmatic serpentine receptor that is co-expressed with the C5a re
32 pressin, angiotensin II, and endothelin bind serpentine receptors that interact with G(q) and activat
33                   Frizzled (Fz) proteins are serpentine receptors that transduce critical cellular si
34 asmic ends of these two helices in two other serpentine receptors, the beta2-adrenoreceptor and the p
35 nding pockets within the seven-helix core of serpentine receptors, the topography of these binding po
36 eceptor that acts together with the Frizzled serpentine receptor to initiate Wnt signal transduction.
37        Hormones and sensory stimuli activate serpentine receptors, transmembrane switches that relay
38                                              Serpentine receptors usually signal to downstream effect
39 e findings show that acquired mutations in a serpentine receptor with features of a G protein-coupled