ライフサイエンスコーパス: mechanosensitive

1 ore domain K(+) (K2P) channel family and are mechanosensitive.

2 dynamic range neurons that were exclusively mechanosensitive.

3 ADAMTS13 cleaves VWF within the mechanosensitive A2 domain, which is believed to open un

4 cal theory behind how these proteins display mechanosensitive accumulation has allowed us to predict

5 cue myoII-null cytokinesis, and has impaired mechanosensitive accumulation.

6 y, this dermal cell aggregation triggers the mechanosensitive activation of beta-catenin in adjacent

7 fostered by adhesion-mediated signaling, and mechanosensitive activation of RhoA that promotes myosin

8 nvironment interaction models to reveal that mechanosensitive adhesions are necessary to reproduce th

9 r recordings, and the encoding properties of mechanosensitive afferents (serosal, mucosal, muscular,

10 These complexes are mechanosensitive and essential for the transmission of f

11 d to a negative residue, the channel is less mechanosensitive and has longer open dwell times.

12 sin II receptor type 1 (AT1 R) is inherently mechanosensitive and initiates this signalling pathway.

13 sitive, itch sensitive, type C low-threshold mechanosensitive and nociceptive neurons with markedly d

14 uires the obligatory combination of distinct mechanosensitive and thermosensitive pathways.

15 he articular cartilage is known to be highly mechanosensitive, and a number of mechanosensing mechani

16 Engineering mechanosensitive artificial cell through bottom-up in vi

17 droplets (aqueous/oil/aqueous) to prototype mechanosensitive artificial cells.

18 Targeting these mechanosensitive 'athero-miRs' may provide a new treatme

19 vestigated whether pannexins, which can form mechanosensitive ATP-permeable channels, are present in

20 Mechanosensitive biological nanomachines such as motor p

21 T cells are mechanosensitive but the effect of stiffness on their fu

22 re, we propose that a class of low-threshold mechanosensitive C fibers that innervate the hairy skin

23 er, Ca(2+) influx at the plasma membrane via mechanosensitive Ca(2+) permeable channels is only media

24 on and actomyosin contractility, but also by mechanosensitive Ca(2+) permeable channels on the plasma

25 evel, selective activation of TRPV4 restored mechanosensitive Ca(2+) signaling as well as the functio

26 functional status of TRPV4, which underlies mechanosensitive Ca(2+) signaling in CD cells, inversely

27 The activity of the mechanosensitive Ca(2+)-permeable TRPV4 channel underlie

28 channels function as a critical component of mechanosensitive, Ca(2+)-signaling machinery within the

29 Here, we have shown that the endothelial mechanosensitive cation channel PIEZO1 is required for f

30 s catastrophic Ca(2+) influx mediated by the mechanosensitive cation channel TRPC6, which activates h

31 d functional analyses localized the putative mechanosensitive cation channel TRPV4 to the plasma memb

32 assembly and dynamics of focal adhesions and mechanosensitive cell motility.

33 a new conceptual framework for understanding mechanosensitive cell scattering and EMT.

34 d cation channels that are expressed in many mechanosensitive cell types.

35 l cells that possess many of the features of mechanosensitive cells and mediate important defense and

36 ne receptors increases the activity of these mechanosensitive cells.

37 ractile force increase in different adherent mechanosensitive cells.

38 ognized that oligodendrocyte progenitors are mechanosensitive cells.

39 in alternating magnetic fields can activate mechanosensitive cellular functions or physically destru

40 mechanistic perspectives through which many mechanosensitive cellular processes could be quantitativ

41 ein beta-arrestin have been shown to mediate mechanosensitive cellular signaling, we tested the hypot

42 es of the urease operon, and mscL encoding a mechanosensitive chanel.

43 The large conductance mechanosensitive channel (MscL), acts as an osmoprotecti

44 provide a direct link between pathology and mechanosensitive channel dysfunction in nonsensory cells

45 discuss some future direction on repurposing mechanosensitive channel for mechanical actuation of spa

46 d comparison with MscL, a well-characterized mechanosensitive channel from bacteria that is driven by

47 re domain K(+) channel, was the first animal mechanosensitive channel identified at the molecular lev

48 eveloping a stable sensory chip containing a mechanosensitive channel in a Si/SiO(2) chip with a 3 mu

49 m, and has been shown to encode a functional mechanosensitive channel in all species where it has bee

50 the anthrax toxin pore and the 1.2-MDa mouse mechanosensitive channel MmPiezo1.

51 The bacterial mechanosensitive channel MscL gates in response to membr

52 screen to search for compounds targeting the mechanosensitive channel of large conductance (MscL) and

53 Using the mechanosensitive channel of large conductance (MscL) as

54 The bacterial mechanosensitive channel of large conductance (MscL) dir

55 We investigate the mechanosensitive channel of large conductance (MscL) fro

56 The mechanosensitive channel of large conductance (MscL) is

57 termined the conditions for releasing intact mechanosensitive channel of large conductance (MscL) pro

58 The bacterial mechanosensitive channel of large conductance (MscL) ser

59 ion of MPPNs for two unrelated proteins, the mechanosensitive channel of large conductance and the co

60 MscL, the highly conserved bacterial mechanosensitive channel of large conductance, is one of

61 The mechanosensitive channel of large conductance, MscL, is

62 The mechanosensitive channel of large conductance, which ser

63 Using the Escherichia coli mechanosensitive channel of small conductance (MscS) as

64 The mechanosensitive channel of small conductance (MscS) has

65 The mechanosensitive channel of small conductance (MscS) has

66 stid-localized mechanosensitive ion channels Mechanosensitive Channel of Small Conductance-Like2 (MSL

67 Here we examine whether the mechanosensitive channel PIEZO1 is activated by force-tr

68 This channel was identified to be the mechanosensitive channel Piezo1.

69 Mechanosensitive channel proteins are important safety v

70 R2456H and R2488Q mutations in PIEZO1 alter mechanosensitive channel regulation, leading to increase

71 The best understood mechanosensitive channel, MscL, opens a wide pore, which

72 y activating TRPV4, a Ca(2+)/Na(+)-permeable mechanosensitive channel.

73 ew insights into the quantitative biology of mechanosensitive channels and emphasizes the need for ca

74 It is one of the best studied mechanosensitive channels and serves as a paradigm of ho

75 Mechanosensitive channels are detected in all cells and

76 In prokaryotic cells, a direct gating of mechanosensitive channels by membrane tension was clearl

77 idence has been presented yet in the case of mechanosensitive channels from animal cells.

78 Furthermore, our findings suggest a role for mechanosensitive channels in bacterial calcium regulatio

79 in the mammalian auditory system depends on mechanosensitive channels in the hair bundles that proje

80 e Drosophila S2 cell line also gives rise to mechanosensitive channels in which ion selectivity can b

81 Understanding the gating mechanism of mechanosensitive channels is challenging because the sti

82 Our study also suggests that different mechanosensitive channels may be used to sense gentle to

83 lipid" principle established for prokaryotic mechanosensitive channels MscL and MscS to these eukaryo

84 of MJF465 Escherichia coli strain (devoid of mechanosensitive channels MscL, MscS, and MscK), or on p

85 The mechanosensitive channels of large conductance (MscL) ar

86 ts the possibility for specific targeting of mechanosensitive channels of pathogens by therapeutic dr

87 Mechanosensitive channels play important roles in the ph

88 Bacterial mechanosensitive channels protect cells from structural

89 mmation on the activity of the odontoblast's mechanosensitive channels remains unknown.

90 Bacterial mechanosensitive channels sense the changes in lateral t

91 iron oxide magnetite (Fe3O4) are coupled to mechanosensitive channels that elicit neuronal activity

92 s, TRPA1 and TRPV4 are emerging as candidate mechanosensitive channels that play a pivotal role in in

93 ecialized protein/lipid subdomains enclosing mechanosensitive channels to open with localized tension

94 essential elements such as water permeation, mechanosensitive channels, active ion pumps, and active

95 ductance, which serves as a model system for mechanosensitive channels, has previously been crystalli

96 robust expression of the recently identified mechanosensitive channels, PIEZO1 and PIEZO2.

97 ich sets the resting open probability of the mechanosensitive channels.

98 bda), are compared on two distinct bacterial mechanosensitive channels.

99 sing osmoprotective amino acids, in part via mechanosensitive channels.

100 assay for determining functional behavior in mechanosensitive channels.

101 hem of genes encoding putative homologues of mechanosensitive channels.

102 pomeroyi belongs to the family of MscS-type mechanosensitive channels.

103 in close analogy to the behavior of cellular mechanosensitive channels.

104 tly modulates responses and sensitization of mechanosensitive colorectal primary afferents.

105 Furthermore, we found that the neurite is a mechanosensitive compartment that becomes softer and ado

106 results indicate that the PECAM-1.Galphaq/11 mechanosensitive complex contains an endogenous heparan

107 shape results from force balance and FAs are mechanosensitive complexes transmitting tension from the

108 ire of behaviors, including light avoidance, mechanosensitive contraction, food selection, and even t

109 ess three potential activating mechanisms at mechanosensitive crosslinks as inputs to a mixture model

110 on by drugs or molecular knockdown decreases mechanosensitive currents, serotonin release and downstr

111 aterally with a dense plexus surrounding the mechanosensitive dendrites of the edge cells.

112 e this system by showing that it can support mechanosensitive differentiation of mesenchymal stem cel

113 Mechanosensitive differentiation was similarly evident i

114 -rich repeat domain (LRRD) and juxtamembrane mechanosensitive domain (MSD).

115 The identification of the mechanosensitive domain in GPIb-IX has significant impli

116 g under fluid shear induces unfolding of the mechanosensitive domain in GPIb-IX, which may possibly c

117 Recently, a relatively unstable and mechanosensitive domain in the GPIbalpha subunit of GPIb

118 nd enabled localization of this quasi-stable mechanosensitive domain of approximately 60 residues bet

119 that most large-diameter proprioceptive and mechanosensitive DRG neurons expressed maternal Ube3a an

120 chanism of signaling that may quickly couple mechanosensitive elements in crowded biological membrane

121 To find mechanosensitive elements in mammalian cells, we examine

122 cuit, whereas early-born ELs contribute to a mechanosensitive escape circuit.

123 known as P21-activated kinase (PAK), and the mechanosensitive factor, Yes-associated protein 1 (YAP-1

124 In the gut, high-threshold mechanosensitive fibres also express Nav1.1 and show enh

125 ograde flow and myosin II to the ECM through mechanosensitive focal adhesion proteins that are collec

126 y kinases to adhesion complexes and impaired mechanosensitive, force-induced Rho signaling, and rigid

127 MscL, opens a wide pore, which accounts for mechanosensitive gating due to in-plane area expansion.

128 gradation of that protein to achieve stable, mechanosensitive gene expression.

129 and shear-dependent miRNA that regulates key mechanosensitive gene in AV such as TGFbeta1.

130 hypermethylation within the promoters of 11 mechanosensitive genes and that 5Aza treatment restored

131 therosclerosis by altering the expression of mechanosensitive genes in the arterial endothelium.

132 Previously, we identified >580 mechanosensitive genes in the mouse arterial endothelium

133 s differentially express osteogenic factors, mechanosensitive genes, and signaling genes.

134 To investigate the role of metabo- and mechanosensitive group III/IV muscle afferents in limiti

135 The precise morphology of the mechanosensitive hair bundle requires seamless integrati

136 air cell is mediated by displacements of its mechanosensitive hair bundle which protrudes from the ap

137 ialized structure at the apical surface, the mechanosensitive hair bundle.

138 maintaining the structural integrity of the mechanosensitive hair bundles formed by the stereocilia.

139 ells exhibit functional properties of native mechanosensitive hair cells and form specialized synapse

140 So far, attempts to derive inner ear mechanosensitive hair cells and sensory neurons have res

141 Mechanosensitive hair cells and supporting cells compris

142 ere we investigate the potential to generate mechanosensitive hair cells from mouse embryonic stem ce

143 Inner ear sensory epithelia contain mechanosensitive hair cells that transmit information to

144 ying mechanism that regulates the opening of mechanosensitive hemichannels is largely unknown.

145 Mechanistically, CD2AP is required for mechanosensitive ICAM-1 downstream signaling toward acti

146 e (NOS) to alter its signaling, and augments mechanosensitive intracellular Ca(2+) influx.

147 ults have implications for ATP-dependent and mechanosensitive intracellular processes.

148 lular matrix and cell adhesion molecules, to mechanosensitive intracellular structures that regulate

149 Gliding motility induces mechanosensitive intraflagellar Ca(2+) elevations in tra

150 ssure-induced secretion was inhibited by the mechanosensitive ion channel antagonists gadolinium, rut

151 ng with the MEC-2 homolog podocin may form a mechanosensitive ion channel complex in podocytes.

152 families identified mutations in piezo-type mechanosensitive ion channel component 2 (PIEZO2) in eac

153 a synthetic small molecule that activates a mechanosensitive ion channel involved in a blood disorde

154 at is potentially sufficient to activate the mechanosensitive ion channel of the hair cell.

155 es the translation of mechanical energy into mechanosensitive ion channel opening, thereby generating

156 ction pharmacologically and knocked down the mechanosensitive ion channel piezo1.

157 study, we show, for the first time, that the mechanosensitive ion channel Piezo2 is specifically expr

158 esults of the present study suggest that the mechanosensitive ion channel Piezo2 is specifically expr

159 bowel GI epithelium selectively express the mechanosensitive ion channel Piezo2, and also that activ

160 PIEZO2 encodes a mechanosensitive ion channel that plays a major role in

161 Here we show that the mechanosensitive ion channel transient receptor potentia

162 nt receptor potential vanilloid 4 (TRPV4), a mechanosensitive ion channel, has been implicated in car

163 en traced to two individual mutations in the mechanosensitive ion channel, PIEZO1.

164 the present study we determine the role of a mechanosensitive ion channel, transient receptor potenti

165 an inactivating eukaryotic cation-selective mechanosensitive ion channel.

166 ypothesis, we expressed potassium and sodium mechanosensitive ion channels (channels of the two-pore-

167 depends on an influx of K(+) through apical mechanosensitive ion channels and its subsequent removal

168 Coupling between the gating of the mechanosensitive ion channels and this adaptation mechan

169 Mechanosensitive ion channels are force-transducing enzy

170 Mechanosensitive ion channels are sensors probing membra

171 Activation of mechanosensitive ion channels by physical force underlie

172 Mechanosensitive ion channels convert external mechanica

173 may mediate cellular discharge by activating mechanosensitive ion channels embedded within cellular m

174 h poration sites for fast ICWs or opening of mechanosensitive ion channels for slow ICWs, which then

175 Members of the MscS superfamily of mechanosensitive ion channels function as osmotic safety

176 ondrocyte mechanotransduction by identifying mechanosensitive ion channels functioning at injurious l

177 A variety of mechanosensitive ion channels have evolved to facilitate

178 e auditory and vestibular systems depends on mechanosensitive ion channels in the stereociliary bundl

179 Mechanosensitive ion channels initiate sensory signals b

180 al basis of force transduction in eukaryotic mechanosensitive ion channels is unknown.

181 emale gametes, and it has been proposed that mechanosensitive ion channels may sense the resulting me

182 nd illustrate the mechanisms that eukaryotic mechanosensitive ion channels may use to detect and fine

183 functional versions of the plastid-localized mechanosensitive ion channels Mechanosensitive Channel o

184 w that loss of MSL1, a member of a family of mechanosensitive ion channels related to the bacterial c

185 TMC1 and TMC2 proteins are components of the mechanosensitive ion channels that convert mechanical in

186 med tip links, which in turn convey force to mechanosensitive ion channels to open them.

187 Mechanosensitive ion channels underlie neuronal response

188 heart, gut) is mediated by biosensors (like mechanosensitive ion channels), which convert mechanical

189 n principle in the gating cycle of unrelated mechanosensitive ion channels, allowing the coupling of

190 vibrations of the hair-cell bundle activate mechanosensitive ion channels, giving birth to an electr

191 ing that local tissue stiffness, read out by mechanosensitive ion channels, is critically involved in

192 nsory hair cells in the cochlea, by means of mechanosensitive ion channels, the mechano-electrical tr

193 The key players involved in this process are mechanosensitive ion channels.

194 tanding of the evolution and significance of mechanosensitive ion channels.

195 repair of alkylated DNA and the synthesis of mechanosensitive ion channels.

196 r previous findings suggest that they form a mechanosensitive junctional complex that discriminates b

197 The mechanosensitive junctional protein alpha-catenin acts t

198 n recapitulated recently with two vertebrate mechanosensitive K(+) channels (TREK1 and TRAAK).

199 e channels MscL and MscS to these eukaryotic mechanosensitive K(+) channels.

200 brane interacting TM2-TM3 segment, unique to mechanosensitive K2Ps, against TM4 may further stabilize

201 Proteomics-detected targets of mechanosensitive lamin-A and retinoids underscore the co

202 , all parasites examined lack genes encoding mechanosensitive large-conductance (MscL), mini-conducta

203 hannel Piezo1 is an important determinant of mechanosensitive lineage choice in neural stem cells and

204 that these enzymes are induced in vivo in a mechanosensitive manner provides a clear and sensible un

205 by stimulating the cell wall machinery in a mechanosensitive manner.

206 lation status of these loci could serve as a mechanosensitive master switch in gene expression.

207 the same spindle pole, they activate another mechanosensitive mechanism to correct the monopolar atta

208 ogue MEC-2 have emerged as key components of mechanosensitive membrane protein signalling complexes.

209 for organ bud formation, demonstrating that mechanosensitive mesenchymal stem cells drive condensati

210 extracellular matrix (ECM) stiffening by the mechanosensitive microRNA-130/301 family, as activated b

211 Here, we hypothesized that dysregulation of mechanosensitive microRNAs (mechanomiRs) in dystrophic s

212 architecture of hair bundles, the arrays of mechanosensitive microvilli-like stereocilia crowning th

213 Here we identify miRNA-712 (miR-712) as a mechanosensitive miRNA upregulated by disturbed flow (d-

214 , correlate with applied force, supporting a mechanosensitive model for vinculin activation in which

215 correlated with applied force, supporting a mechanosensitive model in which forces stabilize vinculi

216 rved repeatedly in the beta-glomerulus only, mechanosensitive modulation of mitral cells and their po

217 main was proposed to constitute an intrinsic mechanosensitive module based on expression of a chimera

218 ha6-integrin is a matrix stiffness-regulated mechanosensitive molecule which confers an invasive fibr

219 longer lever arm (2xELC), producing a highly mechanosensitive motor, could also partially suppress th

220 The role of mechanosensitive (MS) Ca(2+)-permeable ion channels in p

221 tiscale continuum model is constructed for a mechanosensitive (MS) channel gated by tension in a lipi

222 e the role of these cytoskeletal proteins in mechanosensitive (MS) channel gating.

223 Mechanosensitive (MS) channels allow cells to sense and

224 ion in interciliary tip links, and anomalous mechanosensitive (MS) channels on the top surface of the

225 ential canonical 1 (TRPC1) subunits assemble mechanosensitive (MS) channels on Xenopus neuronal growt

226 id bilayer plays a crucial role in gating of mechanosensitive (MS) channels.

227 bust mechanosensors in the form of bacterial mechanosensitive (MS) channels.

228 which is compelling for the investigation of mechanosensitive (MS) ion channels, since they are highl

229 by continued regulation through the acutely mechanosensitive myocardin-related transcription factor-

230 This study unveils the self-organizing and mechanosensitive nature of human amniogenesis and establ

231 ry neurons, meaning that the distribution of mechanosensitive nerve endings can be inferred by visual

232 The mechanosensitive nociceptors in the fibromyalgia patient

233 -modulated upregulation of SIRPalpha and the mechanosensitive nuclear marker lamin-A.

234 unclear whether Merkel cells are inherently mechanosensitive or whether they can rapidly transmit su

235 e found that selective blockade of adherens, mechanosensitive, or gap junctions effectively inhibited

236 as the other ultrastructural elements in the mechanosensitive organelle were still present at 50% (or

237 Here, we demonstrate a major mechanosensitive pathway in which alpha-actinin triggers

238 The mechanosensitive pathway requires a conserved DEG/ENaC/A

239 Thus, we term this mechanosensitive pathway the "SMuSh" pathway, for Ste11

240 Such rheostasis involves a mechanosensitive pattern wherein ground states of cytosk

241 The mechanosensitive phenotypic switching in prostate cancer

242 a-rich structure-function study on mammalian mechanosensitive Piezo channels reveals a modular protei

243 gnals mediated in T cells by an activator of mechanosensitive Piezo1 channels.

244 s and highlight recent structural studies of mechanosensitive potassium channels.

245 Mechanosensitive PPAP2B plays a critical role in promoti

246 al spreading depression-evoked activation of mechanosensitive primary afferent meningeal nociceptors

247 ogenesis and increase in fat tissue mass are mechanosensitive processes and hence should be influence

248 an be used to control and understand diverse mechanosensitive processes in cell signaling.

249 Our understanding of the intrinsic mechanosensitive properties of human pluripotent stem ce

250 New work is shedding light on the mechanosensitive properties of SFs, including that these

251 ited functional TRPV4 with largely preserved mechanosensitive properties.

252 ught to be regulated/dysregulated by elusive mechanosensitive protein(s).

253 Mechanosensitive proteins are key players in cytoskeleta

254 Mechanosensitive proteins play a crucial role in this pr

255 force allosterically alters the functions of mechanosensitive proteins within adhesions to elicit bio

256 Finally, the mechanosensitive proteins YAP, Lamin A/C, Lamin B, MRTF-

257 ion channels has been identified as genuine mechanosensitive proteins.

258 e regulated by clustering of the endothelial mechanosensitive receptor intercellular adhesion molecul

259 patial and mechanical properties of targeted mechanosensitive receptors in live cells by adjusting th

260 cell through E-cadherin adhesions elicits a mechanosensitive response in neighbor cells that is nece

261 of the ion channel NompC, which mediates the mechanosensitive response.

262 les, together with a significant decrease in mechanosensitive responses, suggesting that a Pcdh15a-Tm

263 mechanisms for quantitatively recapitulating mechanosensitive rheostasis.

264 ogether, during bladder filling, the bladder mechanosensitive SAAs of Adelta-fibers were attenuated,

265 ere disruption of ordered lipids initiates a mechanosensitive signal for cell growth through mechanic

266 It operates a mechanosensitive signaling cascade known as the spindle

267 iated immunosuppressive pathways, as well as mechanosensitive signaling cascades that are activated b

268 These studies indicate that targeting mechanosensitive signaling in myofibroblasts to trigger

269 actile unit of striated muscle and also as a mechanosensitive signaling molecule during cell migratio

270 These forces elicit mechanosensitive signaling within the leading edge and a

271 Our study identifies an ECM-specific, mechanosensitive signalling pathway that regulates EC co

272 investigated the characteristics of bladder mechanosensitive single-unit afferent activities (SAAs)

273 Merkel cells are mechanosensitive skin cells whose production requires th

274 In this study, we tested how mechanosensitive small GTPases, RhoA and Rac1, coordinat

275 c protozoa have genes encoding homologues of mechanosensitive small-conductance (MscS) and K(+)-depen

276 quency than the vibrations measured near the mechanosensitive stereocilia.

277 tein complex at the ankle link region of the mechanosensitive stereociliary bundle in hair cells.

278 Integrin-dependent adhesions are mechanosensitive structures in which talin mediates a li

279 t is well established that stress fibers are mechanosensitive structures, physical mechanisms by whic

280 hese needs, we developed the first mammalian mechanosensitive synthetic gene network to monitor endot

281 rts that the insulin production of islets is mechanosensitive, these findings open up an exciting new

282 Cells are mechanosensitive to extracellular matrix (ECM) deformati

283 cell-derived cardiomyocytes also prove to be mechanosensitive to matrix and thus generalize the main

284 We illustrate that TRPM7 is mechanosensitive to shear force of 1.2 Pa, which is much

285 Down-regulation of the mechanosensitive transcription coactivators YAP and TAZ,

286 Although mechanosensitive transcription factor Kruppel-like facto

287 anslocation and downstream signalling of the mechanosensitive transcription factor megakaryoblastic l

288 The mechanosensitive transcription factor TWIST is expressed

289 /ROCK), actin cytoskeletal remodeling, and a mechanosensitive transcription factor, megakaryoblastic

290 YAP is a mechanosensitive transcriptional activator with a critic

291 Mechanosensitive transient receptor potential vanilloid

292 We found that Ca(2+) entry through mechanosensitive TRPV4 channels during bladder filling s

293 Polymodal thermo- and mechanosensitive two-pore domain potassium (K2P) channel

294 ABS2 is inhibited by the preceding mechanosensitive vinculin-binding R3 domain, and deletio

295 r of formerly 'silent' afferents that became mechanosensitive was increased five fold when the skin w

296 Because P2X4 channels are not intrinsically mechanosensitive, we investigated whether podocytes rele

297 Rodents use their mechanosensitive whiskers for a diverse range of tactile

298 We find that Jurkat T-cells are mechanosensitive, with cytoskeletal forces and signaling

299 This turnover is mechanosensitive, with the number of engaged units depen

300 e protein level and nuclear translocation of mechanosensitive Yes-associated protein 1 (YAP1), which