ライフサイエンスコーパス: mechanosensitive

1 er mechanical stress (i.e. cbEGF domains are mechanosensitive).

2 lly, we find that Satb1-DNA interactions are mechanosensitive.

3 network, revealing that these junctions are mechanosensitive.

4 ckles, as defined by NEAT1 localization, are mechanosensitive.

5 steps in T cell receptor triggering are not mechanosensitive.

6 sion zones, both of which are, in principle, mechanosensitive.

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

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

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

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

11 The mechanosensitive adhesive blood protein, von Willebrand

12 sults, we propose that the kindlin2 dimer is mechanosensitive and can strengthen integrin-mediated fo

13 Filopodia can be mechanosensitive and function as cell-cell anchoring sit

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

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

16 es of LSECs and knockout mice, we identified mechanosensitive angiocrine signals released by LSECs wh

17 Engineering mechanosensitive artificial cell through bottom-up in vi

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

19 , and that cholangiocytes in the device were mechanosensitive (as demonstrated by changes in calcium

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

21 In the peripheral nerve, mechanosensitive axons are insulated by myelin, a multil

22 This demonstration of mechanosensitive beta-catenin/Wnt-dependent specificatio

23 Mechanosensitive biological nanomachines such as motor p

24 ging to evaluate the effect of osteocytes, a mechanosensitive bone cell, on the migratory behavior of

25 avior in response to transient activation of mechanosensitive bristle neurons and sweet-sensing chemo

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

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

28 potential vanilloid 4 (TRPV4) ion channel, a mechanosensitive Ca(2+)-permeable channel, may regulate

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

30 lfide bond mutations markedly disrupt normal mechanosensitive calcium binding dynamics.

31 IP(3) receptor, gap junction, and mechanosensitive calcium channel TRPC1 are involved in c

32 or asthma with SNP/protein expression of the mechanosensitive calcium channel, TRPV4.

33 O1 has recently been identified as a crucial mechanosensitive cation channel in multiple solid tumour

34 tial vanilloid 4 (TRPV4), a Ca(2+)-permeable mechanosensitive cation channel in the transient recepto

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

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

37 erstand the molecular mechanism by which the mechanosensitive cation channel, transient receptor pote

38 at allow Ca(2+) to enter RBCs through Piezo1 mechanosensitive cation-permeable channels.

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

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

41 Mammals detect sound through mechanosensitive cells of the cochlear organ of Corti th

42 ognized that oligodendrocyte progenitors are mechanosensitive cells.

43 ne receptors increases the activity of these mechanosensitive cells.

44 This mechanosensitive cellular behavior represents a conserve

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

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

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

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

49 structures of the E. coli small-conductance mechanosensitive channel (MscS) in nanodiscs (ND).

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

51 The bacterial mechanosensitive channel MscL gates in response to membr

52 entify nano-pockets on the large conductance mechanosensitive channel MscL, the high-pressure thresho

53 Subtle structural discrepancies on mechanosensitive channel nanopockets are known to affect

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

55 The mechanosensitive channel of large conductance (MscL) fro

56 The bacterial mechanosensitive channel of large conductance (MscL) nor

57 es previous reports of sequence coverage for mechanosensitive channel of large conductance (MscL).

58 model mechanosensitive channel protein, the mechanosensitive channel of large conductance, during ce

59 The mechanosensitive channel of large conductance, MscL, is

60 The mechanosensitive channel of small conductance (MscS) is

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

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

63 r interaction between phospholipase A2 and a mechanosensitive channel present in the internal membran

64 he folding and overall production of a model mechanosensitive channel protein, the mechanosensitive c

65 PIEZO1 is a mechanosensitive channel that converts applied force int

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

67 o unclear but recent work has implicated the mechanosensitive channel, PIEZO1.

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

69 Different mechanosensitive channels adapt distinctive structures a

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

71 Furthermore, we show that Piezo and TRP mechanosensitive channels are important factors modulati

72 g with surprising insights into well-studied mechanosensitive channels have driven further developmen

73 s provide a precedent for the involvement of mechanosensitive channels in axon regeneration and add a

74 nce suggests that insulin modulates putative mechanosensitive channels in the dorsal root ganglion (D

75 nce suggests that insulin modulates putative mechanosensitive channels in the dorsal root ganglion ne

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

77 The mechanosensitive channels of large conductance (MscL) ar

78 The mechanosensitive channels of small conductance (MscS) co

79 s, delineate a structural mechanism by which mechanosensitive channels open under increased membrane

80 Bacterial mechanosensitive channels protect cells from structural

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

82 Mechanosensitive channels sense tension through their in

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

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

85 How mechanosensitive channels work, especially in animals, h

86 Although MscL is one of the best studied mechanosensitive channels, no chemical that influenced b

87 ecrease the activating tension for bacterial mechanosensitive channels.

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

89 assay for determining functional behavior in mechanosensitive channels.

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

91 ns and adaptor proteins within NAs through a mechanosensitive coaggregation mechanism.

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

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

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

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

96 These two stimuli are detected by distinct mechanosensitive DEG/ENaC/ASIC channels, which trigger d

97 b)beta(3) to SLC44A2 on neutrophils leads to mechanosensitive-dependent production of highly prothrom

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

99 Mechanosensitive differentiation was similarly evident i

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

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

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

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

104 amics can be explained neither by the purely mechanosensitive dynamics (to breathing clean air) nor b

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

106 To find mechanosensitive elements in mammalian cells, we examine

107 Here, we identify a mechanosensitive EPHA2/LYN protein complex regulating EM

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

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

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

111 We have previously introduced a mechanosensitive flipper probe, which responds to the ch

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

113 Their frequent association with mechanosensitive functions suggests that processing of m

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

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

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

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

118 Genetic studies have identified mechanosensitive genes with causal roles in CVD.

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

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

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

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

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

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

125 capacity to activate YAP, an effector in the mechanosensitive Hippo pathway, correlates with regenera

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

127 her, TRPV4's modulation of the LPS signal is mechanosensitive in that both upstream activation of p38

128 that dental neurons are capable of providing mechanosensitive information to drive rapid behavioral r

129 tween matrix and cells induces expression of mechanosensitive integrins that drive fibroblast activat

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

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

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

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

134 These results demonstrate that Piezo1 is a mechanosensitive ion channel by which osteoblast lineage

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

136 w demonstrates a critical role of the Piezo1 mechanosensitive ion channel in guiding vascular tip cel

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

138 edlings and to test the contributions of the mechanosensitive ion channel MscS-like10 (MSL10).

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

140 ux and monocyte adhesion are mediated by the mechanosensitive ion channel Piezo-1.

141 Recently, gain-of-function mutations in the mechanosensitive ion channel PIEZO1 were shown to amelio

142 FRCs responded to conduit fluid flow via the mechanosensitive ion channel Piezo1.

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

144 Here we identify expression of the mechanosensitive ion channel PIEZO2 in lower urinary tra

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

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

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

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

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

150 gulation of soluble VEGF/VEGFR2 signaling by mechanosensitive ion channel TRPV4.

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

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

153 small interfering RNA (siRNA) knockdown of a mechanosensitive ion channel, transient receptor potenti

154 nt receptor potential vanilloid 4 (TRPV4), a mechanosensitive ion channel/receptor, is required for F

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

156 heterochromatin levels through activation of mechanosensitive ion channels (MSCs), without large-scal

157 e transfer across the skin and activation of mechanosensitive ion channels along the somatosensory ne

158 ing of the extracellular environment through mechanosensitive ion channels and consequent changes to

159 y of extracellular calcium due to opening of mechanosensitive ion channels and initiates a wave that

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

161 Mechanosensitive ion channels are crucial for normal cel

162 Mechanosensitive ion channels are force-transducing enzy

163 Mechanosensitive ion channels convert external mechanica

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

165 portance of cooperative interactions between mechanosensitive ion channels for hearing.

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

167 A variety of mechanosensitive ion channels have evolved to facilitate

168 ortance of this function, the involvement of mechanosensitive ion channels in human disease is poorly

169 suggest a previously unappreciated role for mechanosensitive ion channels in myelin development.

170 Mechanosensitive ion channels initiate sensory signals b

171 owth, it is important to investigate whether mechanosensitive ion channels may regulate axon regenera

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

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

174 Mechanosensitive ion channels rely on membrane compositi

175 PIEZO1 and PIEZO2 are newly identified mechanosensitive ion channels that exhibit a preference

176 Mechanosensitive ion channels transduce physical force i

177 Activation of mechanosensitive ion channels underlies a variety of fun

178 h-throughput suction-flow device for probing mechanosensitive ion channels(24) by back-calculating th

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

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

181 lular constituents, including gap junctions, mechanosensitive ion channels, energy-consuming ion pump

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

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

184 heterochromatin levels through activation of mechanosensitive ion channels, without large-scale cell

185 years, the identification of new families of mechanosensitive ion channels-such as PIEZO and OSCA/TME

186 brations, causing the opening and closing of mechanosensitive ion channels.

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

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

189 spond to cell swelling through the action of mechanosensitive ion channels.

190 that may have a role in recently discovered mechanosensitive ionic channels(23).

191 speculate on why nodes of Ranvier contain a mechanosensitive K(+) channel.

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

193 age TRPV4 in regulating innate immunity in a mechanosensitive manner through the modulation of dual-s

194 We also examined some well-characterized mechanosensitive markers, but found that lamin A express

195 These results point to a potential mechanosensitive mechanism for fibrillin-1 in regulating

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

197 These data also show that unidentified mechanosensitive mechanisms independent of known renal a

198 understanding of the molecular, cellular and mechanosensitive mechanisms of valve development, and hi

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

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

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

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

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

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

205 al species is reinterpreted, with a focus on mechanosensitive molecular motors.

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

207 hains, is used to activate covalent bonds in mechanosensitive molecules (mechanophores).

208 The reactivity of mechanophores (mechanosensitive molecules) can be controlled using vari

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

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

211 Prokaryotic mechanosensitive (MS) channels open by sensing the physi

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

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

214 Membrane tension perceived by mechanosensitive (MS) proteins mediates cellular respons

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

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

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

218 orted mode of platelet-neutrophil crosstalk, mechanosensitive NET production, and provide mechanistic

219 Chemical ablation of the mechanosensitive neuromast cells within the lateral line

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

221 of a tissue-stretching device, we uncover a mechanosensitive pathway that regulates tissue responses

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

223 Here, we assessed the mechanosensitive pathways involved during zebrafish outf

224 ar cells and immune cells, activated through mechanosensitive pathways or neurohumoral mediators may

225 tion of myocyte and non-myocyte responses to mechanosensitive pathways, which can alter gene expressi

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

227 The mechanosensitive phenotypic switching in prostate cancer

228 ulated by Notch and its interaction with the mechanosensitive piezo calcium channel.

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

230 evolutionarily and architecturally unrelated mechanosensitive Piezo channels.

231 Mechanosensitive Piezo1 and Piezo2 channels transduce va

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

233 This effect is observed at the level of mechanosensitive Piezo2 channels and can be replicated i

234 clearly indicated that Merkel cells and the mechanosensitive piezo2 ion channel play critical roles

235 Mechanosensitive PPAP2B plays a critical role in promoti

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

237 of substrate physical properties on distinct mechanosensitive processes and provide a premise to reco

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

239 ross-linkers such as alpha-actinin-4 exhibit mechanosensitive properties in their binding dynamics to

240 To understand the dynamics and mechanosensitive properties of NAs, a biophysical model

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

242 Previously, we identified a mechanosensitive protein, small proline-rich repeat 3 (S

243 Mechanosensitive proteins are key players in cytoskeleta

244 Mechanical signals regulate functions of mechanosensitive proteins by inducing structural changes

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

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

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

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

249 Increased mechanosensitive recruitment of vinculin to cell-cell ju

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

251 ge correlation spectroscopy, we measured the mechanosensitive response of integrin mobility at the wh

252 stimulation and data acquisition to capture mechanosensitive responses and suggest that mechanical c

253 mechanisms for quantitatively recapitulating mechanosensitive rheostasis.

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

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

256 It operates a mechanosensitive signaling cascade known as the spindle

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

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

259 A-sequencing of LSECs identified proteins in mechanosensitive signaling pathways that are altered in

260 ates actomyosin contractility and downstream mechanosensitive signaling to profoundly alter the tumor

261 tforms, for unbiased identification of novel mechanosensitive signalling pathways in arteries.

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

263 Merkel cells are mechanosensitive skin cells whose production requires th

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

265 Such mechanosensitive "smart" features may represent novel me

266 This reflects a mechanosensitive Src family kinase (SFK) signaling pathw

267 Cells typically use many mechanosensitive steps and different cell states to achi

268 dles possess tip links that interconnect the mechanosensitive stereocilia and convey force to the tra

269 quency than the vibrations measured near the mechanosensitive stereocilia.

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

271 d waves into electrical signals depends upon mechanosensitive stereociliary bundles that project from

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

273 for dynamic protein-protein interactions in mechanosensitive structures, such as focal adhesions, in

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

275 es use tyrosine kinase signalling to build a mechanosensitive, talin- and vinculin-mediated, focal ad

276 Taken together, the combination of mechanosensitive tension remodeling and junctional strai

277 ory and biophysical experiments to show that mechanosensitive tension remodeling of epithelial cell j

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

279 Trabecular meshwork (TM) is a highly mechanosensitive tissue in the eye that regulates intrao

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

281 Although mechanosensitive transcription factor Kruppel-like facto

282 The mechanosensitive transcription factor TWIST is expressed

283 thophysiology via differential regulation of mechanosensitive transcription factors (MSTFs) (KLF2, KL

284 The mechanosensitive transcription factors Yes-associated pr

285 wn of TRPV4 enhanced nuclear localization of mechanosensitive transcription factors, yes-associated p

286 YAP is a mechanosensitive transcriptional activator with a critic

287 Mechanosensitive transcriptional coactivators MRTF-A and

288 in alpha6beta4 regulates the activity of the mechanosensitive transcriptional regulator YAP through i

289 ce exclusion method, we demonstrate that the mechanosensitive transcriptional regulators YAP (Yes-ass

290 Mechanosensitive transient receptor potential vanilloid

291 cutely relieve nCa(V) inactivation, enabling mechanosensitive-triggered predatory attack.

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 at TREK-1 and TRAAK, the thermosensitive and mechanosensitive two-pore-domain potassium (K2P) channel

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

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

299 ithelial plasticity, fibrogenic activity and mechanosensitive Yap/Taz transcriptional activation.

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