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

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