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1 nsor and has been proposed to act as a plant osmosensor.
2 ble channels, revealing that OSCA1 may be an osmosensor.
3 t role in ductal bile formation by acting as osmosensors.
4  we hypothesized that cilia also function as osmosensors.
5 HHP, rendering PLA2, next to being a primary osmosensor, a good candidate for a sensitive pressure se
6             The SLN1-YPD1-SSK1 two-component osmosensor activates the SSK2 and SSK22 MAPKKKs by direc
7 tic Lethal of N-end rule1 and SH3-containing Osmosensor and has been proposed to act as a plant osmos
8 tivation is independent of the two-component osmosensor and involves the SHO1 transmembrane protein a
9 um was recently shown to function as both an osmosensor and osmoregulator in proteoliposomes made fro
10  the ability of encoding afferent input from osmosensors and generating appropriate homeostatic respo
11 he Saccharomyces cerevisiae Sho1, acts as an osmosensor, and is required for plant penetration and me
12 2 MAPKKKs are activated by a 'two-component' osmosensor composed of SLN1, YPD1 and SSK1.
13 n this organism has revealed the presumptive osmosensors, downstream signaling components, and metabo
14                                          The osmosensor, EnvZ, has dual enzymatic functions with OmpR
15 urface and interacts with Cdc42 and with the osmosensor for the high osmolarity glycerol response (HO
16 ng in pollen and may serve as essential hypo-osmosensors for tracking rehydration in plants.
17          Here, we report that in yeast, Sln1 osmosensor histidine kinase monitors changes in turgor p
18 animals osmosensing Ca(2+) channels serve as osmosensors, hyperosmolality-induced [Ca(2+)]i increases
19  branch of the HOG pathway and that a second osmosensor in addition to Sho1p may activate Ste11p.
20 smembrane histidine kinase functioning as an osmosensor in Escherichia coli, consists of two distinct
21 Here we identify bona fide cell surface hypo-osmosensors in Arabidopsis and find that pollen Ca(2+) s
22 tential vanilloid isoform 4) channels as key osmosensors in nonpigmented epithelial (NPE) cells of th
23 s expressed on airway afferents and is a key osmosensor initiating reflex events in the lung.
24 east Sln1p sensor kinase is best known as an osmosensor involved in the regulation of the hyperosmola
25 osmotic stimulus and indicate that the Sln1p osmosensor is tied generally to osmotic balance, and may
26  Muller astroglia, but the identity of their osmosensor is unknown.
27      Very little is known about how cellular osmosensors monitor changes in osmolarity of the environ
28 sitivity of yeast (Saccharomyces cerevisiae) osmosensor mutants lacking Synthetic Lethal of N-end rul
29 asmic kinase domain of EnvZ, a transmembrane osmosensor of Escherichia coli can be further divided in
30 Sho1 osmosensing system, but not by the Sln1 osmosensor of the HOG pathway.
31                          Several presumptive osmosensors on the cell surface recruit and activate dow
32  cell-surface sensors/receptors, such as the osmosensor OSCA1.
33 of PBP 4 or by a transmembrane region of the osmosensor protein ProW, even though these hybrids were
34  suggest that AHK1 may not be the main plant osmosensor required for low psi(w) tolerance.
35  Our findings identify TRPM8 as a peripheral osmosensor responsible for the regulation of normal eye-
36 al analysis revealed that the membrane-bound osmosensor Sho1 is phosphorylated by Hog1 and that phosp
37 o function as a scaffold, since it binds the osmosensor Sho1, the upstream MAP kinase kinase kinase S
38                 This cross talk required the osmosensor Sho1p, as well as Ste20p, Ste50p, the pheromo
39                                     A second osmosensor, Sho1p, also activated Pbs2p and Hog1p, but d
40 kinase ATHK1 has been suggested to act as an osmosensor that detects water stress and initiates downs
41 nase, Sln1p, is a plasma membrane-associated osmosensor that regulates the activity of the osmotic st
42 trolled directly by water through these hypo-osmosensors-that is, Ca(2+) spiking is the second messen
43           The MAPKK Pbs2p bound to the Sho1p osmosensor, the MAPKKK Ste11p, and the MAPK Hog1p.
44      Because H-NS functions as a thermo- and osmosensor, these conformations may both be functionally
45  induces the Sln1p-Ypd1p-Ssk1p two-component osmosensor to activate a mitogen-activated protein (MAP)
46 s led us to propose the existence of another osmosensor upstream of Ste11.
47                          To identify such an osmosensor, we screened for mutants in which the residua