ライフサイエンスコーパス: SM

1 SM and kidney mass decreased in both groups.

2 SM antagonize inhibitor of apoptosis (IAP) proteins and

3 SM is the ability of stimuli in the surround of a neuron

4 SM production is energy-consuming and thus tightly regul

5 SM undergoes cholesterol-dependent proteasomal degradati

6 SM was subsequently diagnosed in five of these, whereas

7 SM-OCT accomplishes this by creating and averaging an un

8 total of 59.9% of institutions performed 10 SM procedures or fewer, whereas 66.9% of institutions pe

9 tures of SIV infection in SMs, we treated 12 SMs with a potent antiretroviral therapy (ART) regimen f

10 (reviewed in [2]), including the SNAREs [3], SM proteins [4, 5], ion channels [6, 7], and receptors (

11 Of the 48 SM patients, 90% tested D816V-positive.

12 neurocognitive deficits in SM including 551 SM children, 71 uncomplicated malaria (UM) and 172 healt

13 ulation, we hypothesized that genes within a SM pathway would form tight associations (modules) with

14 phobic loop-that are essential for accessing SM in bile salt micelles.

15 tions in vascular smooth muscle alpha-actin (SM alpha-actin), encoded by ACTA2, are the most common c

16 A total of 14 adult SM patients (10 ISM, 2 BMM, 1 SSM, and 1 ASM-AHN) receiv

17 ay serve as a therapeutic target in advanced SM remains to be determined in forthcoming studies.

18 levels were higher in patients with advanced SM and were found to correlate with poor survival.

19 t of this hypothesis revealed that affecting SM homeostasis converted flat cisternae into highly curl

20 tions (3.3%, 3.8%, and 1.7%; P < .001) after SM was lower in higher-volume centers when stratified by

21 th new mechanisms of action directed against SM and homologous essential proteins in other herpesviru

22 ns have long indicated that immunity against SM is acquired relatively rapidly, but prospective studi

23 e development of vaccines to protect against SM.

24 NM myosin II plays a critical role in airway SM contraction that is independent and distinct from the

25 ted during contractile stimulation of airway SM tissues by RhoA-mediated NM myosin RLC phosphorylatio

26 In our patient cohort, we evaluated all SM patients treated with omalizumab.

27 the mechanistic in vivo relationships among SM high-energy phosphate concentrations, mitochondrial f

28 the Qc SNARE, and a fourth HOPS subunit, an SM protein, has conserved grooves that bind R- and Qa-SN

29 ched/paired synchronous metastases (SM#1 and SM#2) prospectively enrolled in the MOSCATO-01 clinical

30 tin suppressed adhesome complex assembly and SM contraction without inhibiting NM myosin Ser1943 phos

31 ACh-induced NM myosin filament assembly and SM contraction, and also inhibits the assembly of membra

32 required for NM myosin filament assembly and SM contraction.

33 lds such as electrochemistry, catalysis, and SM electronics, which all benefit from the vibrational c

34 uman dermal fibroblasts were established and SM alpha-actin expression induced with adenovirus encodi

35 NAREs of the R, Qa, Qb, and Qc families, and SM SNARE-binding proteins catalyze intracellular membran

36 PC species (observed at odd m/z values) and SM species (observed at even m/z values).

37 C, von Lindern I, von Braun M, Lind D, Anka SM, Abdullahi A.

38 Appendicular SM was regained during the second year whereas trunk SM

39 1.4 +/- 0.2 kg; P < 0.001) with appendicular SM regained during year 2.

40 si R, Shin HM, Vieira VM, Savitz DA, Bartell SM.

41 Laurent O, Hu J, Li L, Kleeman MJ, Bartell SM, Cockburn M, Escobedo L, Wu J.

42 ver, the precise mode of interaction between SM proteins and SNAREs is debated, as contrasting bindin

43 , based on the key residues in Deg1, blunted SM cholesterol-mediated turnover.

44 that p38 inhibitors increased TNF induced by SM.

45 Decreased overall survival was predicted by SM depletion before RT (hazard ratio [HR], 1.92; 95% CI,

46 ding is important for sterol/SM and ceramide/SM interactions, as well as for the lateral segregation

47 hed case-control study of well-characterized SM clinical phenotypes nested within a longitudinal birt

48 NPP7 is the only paralog that can cleave SM, and its activity requires the presence of bile salts

49 logical finding and its relation to clinical SM is not fully understood.

50 ls in all subjects, consistent with a common SM energetic limit.

51 Given that genes comprising SM pathways exhibit environmentally dependent coregulati

52 branes composed of lipid mixtures containing SM and Chol.

53 ion and to identify how degradation controls SM export at the catchment scale.

54 ns under grazing were AGB, height, coverage, SM, NH4(+)-N and NO3(-)N.

55 Consistent with these data, SM-ARKO VSMCs showed a reduction in Osterix mRNA express

56 This group was denoted SM.

57 The first 100 amino acids of SM (designated SM N100) are necessary for this degradative process and

58 , and enantiomers were combined to determine SM degradation at plot and catchment scales.

59 a marked reduction in the odds of developing SM (OR = 0.07; 95% CI = 0.006 to 0.82;P= 0.03).

60 evaluate the prospective odds of developing SM in the first 2 years of life.

61 nine patients did not fulfill any diagnostic SM criteria (excluding tryptase criterion).

62 Diminished SM mass assessed by CT imaging or BMI can predict oncolo

63 Mutlu E, Warren SH, Ebersviller SM, Kooter IM, Schmid JE, Dye JA, Linak WP, Gilmour MI,

64 we searched for drugs active against the EBV SM protein, which is essential for infectious virus prod

65 To enhance SM efficacy, we screened kinase inhibitors for their abi

66 Enantioselective degradation enriched SM in the R-enantiomer over longer periods and may be as

67 I (Eqt), into a nontoxic reporter termed Eqt-SM and used it to monitor intracellular trafficking of S

68 Here, we examined SM variation in 66 cosmopolitan strains of a single spec

69 species shown here are sufficient to explain SM cluster macroevolutionary patterns.

70 Flushing SM with sodium caprate prior to transplantation resulted

71 g the World Health Organization criteria for SM, our findings allowed us to establish the systemic na

72 The greatest TAA was measured for SM followed by SUM, RM, WM and WUM.

73 Understanding the circuit and mechanisms for SM can reveal fundamental principles of computations in

74 d the plasmonic nanostructures necessary for SM detection, the past and current methodologies for ver

75 est power conversion efficiency reported for SM-OPVs to date and the first time to combine high Jsc o

76 egion (residues Gln-62-Leu-73), required for SM cholesterol-mediated turnover.

77 PI group and decreased from 5.7 to 3.7 in FP/SM-pMDI group.

78 chnique (32 of BUD/FM-DPI group and 30 of FP/SM-pMDI group) were included into this study.

79 M-DPI group and in 86.6% (26/30 cases) of FP/SM-pMDI group.

80 ripheral blood mononuclear cells (PBMC) from SM or vervet AGM.

81 the function of representative A. fumigatus SM gene clusters, such as those involved in the producti

82 s nidulans for negative regulators of fungal SM gene clusters and we have used this screen to isolate

83 edforward or intracortical circuits generate SM, and whether this results from increased inhibition o

84 at most predicted plant BGCs are not genuine SM pathways and argue that BGCs are not a hallmark of pl

85 y pattern was associated with high BMD, high SM, low BR, and low risk of fractures [HR (95% CI) for o

86 rn was associated with high bone width, high SM, high BR, and high risk of fractures [HR (95% CI) for

87 ession of EBV viral capsid antigen is highly SM dependent, and spironolactone inhibits viral capsid a

88 of essential benefit when targeting the HSA-SM adduct for verification analysis.

89 Stability of the HSA-SM adduct in dried and liquid plasma is shown under cond

90 oethyl-CysPro (HETE-CP) derived from the HSA-SM adduct that was detected by microbore liquid chromato

91 haracterize this mutation in expressed human SM alpha-actin.

92 esult in a screening blood sample identifies SM among patients with hymenoptera venom-induced anaphyl

93 If SM could be verified histologically or MP radiologically

94 vascular cell migration and angiogenesis in SM.

95 ules triggering fibrosis and angiogenesis in SM.

96 st early, rapid exercise-induced declines in SM high-energy phosphates and reduced oxidative capacity

97 s associated with neurocognitive deficits in SM including 551 SM children, 71 uncomplicated malaria (

98 GABA puffs diluted in SM/CSF solution or SM/CSF solution alone showed no signi

99 co-workers identify an N-terminal domain in SM that interconverts in a cholesterol-sensitive manner

100 tic genes, and module genes were enriched in SM functions.

101 ate linear analysis revealed that entropy in SM#1 is significantly associated with (i) primary tumor

102 with (i) primary tumor type; (ii) entropy in SM#2 (same malignant process); (iii) ROI area size; (iv)

103 other MC-driven diseases, but experiences in SM are limited.

104 arrow microenvironment are commonly found in SM.

105 ort a model whereby the amphipathic helix in SM N100 attaches reversibly to the ER membrane depending

106 le tissues, however the role of NM myosin in SM contraction is unknown.

107 ess the efficacy and safety of omalizumab in SM.

108 ppears to be a promising treatment option in SM, effectively preventing anaphylaxis and improving chr

109 diesterase (SMase) enzymes may play roles in SM differences across the three cell lines.

110 -phosphorylatable mutant NM myosin S1943A in SM tissues inhibited ACh-induced endogenous NM myosin Se

111 table NM myosin mutant, NM myosin S1943A, in SM tissues inhibits ACh-induced NM myosin filament assem

112 issolved or particulate phases or as TPs (in SM mass equivalent).

113 ion revealed 5 general types of variation in SM gene clusters: nonfunctional gene polymorphisms; gene

114 ved in the benign course of SIV infection in SMs are the absence of chronic immune activation and low

115 mining the main features of SIV infection in SMs, we treated 12 SMs with a potent antiretroviral ther

116 ecific immunological changes in SIV-infected SMs, thus suggesting that virus replication affects immu

117 and contraction, although it did not inhibit SM RLC phosphorylation.

118 tagonist approved for clinical use, inhibits SM function and infectious EBV production.

119 ble trans-complex, catalyzed by HOPS and its SM subunit Vps33, is followed by subsequent zippering tr

120 Aaron CP, Chervona Y, Kawut SM, Diez Roux AV, Shen M, Bluemke DA, Van Hee VC, Kaufma

121 52.6% of modules contained two or more known SM biosynthetic genes, and module genes were enriched in

122 Severe malaria (SM) is a life-threatening complication of infection with

123 can green monkeys (AGM) and sooty mangabeys (SM) are well-studied natural hosts of simian immunodefic

124 ciency virus (SIV)-infected sooty mangabeys (SMs) do not develop AIDS despite high levels of viremia.

125 ncer (LAHNC) with negative surgical margins (SM negative) and no extracapsular extension (ECE).

126 on 325 patients to form the Spetzler-Martin (SM) grade, the supplemented SM (sSM) grade, the ICH scor

127 is a rare variant of systemic mastocytosis (SM) characterized by bone marrow (BM) infiltration by ma

128 Systemic mastocytosis (SM) is characterized by abnormal accumulation of neoplas

129 Patients with systemic mastocytosis (SM) may suffer from mast cell (MC) mediator-related symp

130 tigation in suspected systemic mastocytosis (SM).

131 Moreover, the superior mechanosensitivity, SM 3.4 VPa(-1) of the FTNG enables the design of a wea

132 hen cells are transplanted into scala media (SM) of the cochlea, they promptly die due to the high po

133 Sclerosing mesenteritis (SM) is sometimes used as an umbrella-term for idiopathic

134 Fungal secondary metabolites (SMs) are extremely important in medicine and agriculture

135 ce a diverse array of secondary metabolites (SMs) critical for defense, virulence, and communication.

136 nts produce diverse specialized metabolites (SMs), but the genes responsible for their production and

137 with matched/paired synchronous metastases (SM#1 and SM#2) prospectively enrolled in the MOSCATO-01

138 ation of the chiral herbicide S-metolachlor (SM) in soil in relation to its transport in runoff.

139 (WM) and partially skimmed pasteurised milk (SM).

140 w the gel to Lalpha phase transition of milk-SM (Tm approximately 34 degrees C).

141 quid condensed (LC) phase transition of milk-SM monolayers was observed at surface pressures of 10-15

142 effect of different physical states of milk-SM on its interactions with cholesterol was determined b

143 A phase diagram pressure - milk-SM/cholesterol composition was established.

144 The miscibility of milk sphingomyelin (milk-SM) and cholesterol was investigated in this study.

145 re affected the miscibility between the milk-SM and cholesterol.

146 For T=43 degrees C>Tm, the milk-SM molecules were in a LE phase regardless of the surfac

147 ntified for 30mol% cholesterol when the milk-SM was in the LE phase state.

148 Salvia miltiorrhiza (SM) is widely used to treat microcirculatory disturbance

149 ponent of the YQHX was Salviae miltiorrhiza (SM).

150 Smac mimetics (SMs), a class of drugs that can promote tumor cell death

151 logous information is obtained from modified SM lipid anions via amide bond cleavage.

152 Surround modulation (SM) is a fundamental property of sensory neurons in many

153 BMD, bone width, section modulus (SM; reflecting bending strength) and cortical buckling r

154 ely correlated with rainfall, soil moisture (SM), the carbon to nitrogen ratio (C/N ratio), soil avai

155 Single-molecule (SM) surface-enhanced Raman spectroscopy (SERS) and tip-e

156 Squalene monooxygenase (SM) is the second rate-limiting enzyme in cholesterol bi

157 Squalene monooxygenase (SM), which synthesizes a cholesterol precursor, is degra

158 fujikuroi revealed the presence of far more SM-encoding genes than known products.

159 s were used in this experiment: straw mulch (SM), plastic film mulch (PM) and conventional covering w

160 signal averaging (SA), single multiplexing (SM), and double multiplexing (DM) IMS modes to optimize

161 TX11) and its binding partner, the Sec/Munc (SM) protein Munc18-2, facilitate cytolytic granule relea

162 e fusion requires tethering and Sec1-Munc18 (SM) function to catalyze R-, Qa-, Qb-, and Qc-SNARE comp

163 orchestrated by the binding of Sec1/Munc18 (SM) proteins to specific syntaxin SNARE proteins.

164 e (HF), the extent to which skeletal muscle (SM) energy metabolic abnormalities occur and contribute

165 weight-loss intervention on skeletal muscle (SM) mass and selected organs over 2 y using MRI in overw

166 s available for analysis of skeletal muscle (SM).

167 issense mutations in vascular smooth muscle (SM) alpha-actin encoded by ACTA2 We focus here on ACTA2-

168 Y POINTS: Non-muscle (NM) and smooth muscle (SM) myosin II are both expressed in smooth muscle tissue

169 (NM) isoforms of myosin II in smooth muscle (SM) tissues and their possible role in contraction are l

170 duce transition of PAECs to a smooth muscle (SM)-like mesenchymal phenotype (endothelial-to-mesenchym

171 ere performed on bronchi from smooth muscle (SM)-specific Rac1 knockout mice and human individuals.

172 f the chemical warfare agent sulfur mustard (SM) produces a covalent adduct with human serum albumin

173 irmed induction of both wild-type and mutant SM alpha-actin in heterozygous ACTA2-R258C cells.

174 Expression of mutant SM alpha-actin in heterozygous ACTA2-R258C fibroblasts a

175 Mutating SM residues Phe-35/Ser-37/Leu-65/Ile-69 into alanine, ba

176 responses were similar in trachea from MYPT1(SM+/+) , MYPT1(SM-/-) and the knock-in mutant mice conta

177 similar in trachea from MYPT1(SM+/+) , MYPT1(SM-/-) and the knock-in mutant mice containing nonphosph

178 ur results demonstrate the sorting of native SM at the TGN and its transport to the plasma membrane b

179 the plasma membrane, we engineered a natural SM-binding pore-forming toxin, equinatoxin II (Eqt), int

180 ry light chain (RLC) phosphorylation but not SM myosin RLC phosphorylation is regulated by RhoA GTPas

181 these tissues accumulated ceramides but not SMs.

182 Here we show speckle-modulating OCT (SM-OCT), a method based purely on light manipulation tha

183 At the catchment outlet, 11% of SM applied was exported in dissolved or particulate phas

184 leaching (8%) and runoff (3%), while 13% of SM persisted in topsoil.

185 ent 1 week after application exported 96% of SM, which underlined the potential importance of severe

186 tate effects by inducing the accumulation of SM precursors and impairing insulin signaling and mitoch

187 The first 100 amino acids of SM (designated SM N100) are necessary for this degradati

188 The addition of SM synergistically modified the effects of FP modestly-o

189 l line exhibited 30-65-fold lower amounts of SM principally in the amount of 16:0.

190 Analyses of SM, transformation products (TPs, i.e., MESA and MOXA),

191 ts play a crucial role in the computation of SM.

192 he genetic basis and evolutionary drivers of SM gene cluster divergence.

193 oblasts abrogated the significant effects of SM alpha-actin induction on formation of stress fibers a

194 ndependent and distinct from the function of SM myosin.

195 Summarily, tanshinones in micronized GP of SM had higher oral bioavailability and lower individual

196 GP of SM resulted in a significant increase in mean maximum pl

197 An oral dose of TD or GP of SM was administrated to subjects and blood samples were

198 e whether micronized granular powder (GP) of SM could improve the bioavailability of tanshinones comp

199 here, is a roadmap for the implementation of SM-SERS as a routine tool for quantification at ultralow

200 hat CCR5 is dispensable for SIV infection of SM in vivo and that blocking of CCR5 does not prevent ex

201 e YQHX and that SAB, the major ingredient of SM, alleviates experimental pulmonary fibrosis both in v

202 anolic acid B (SAB), the major ingredient of SM, had strong anti-inflammatory and anti-fibrotic effec

203 ng cells with a pharmacological inhibitor of SM synthase or using CRISPR to knock out the Sms2 gene r

204 (LDAS) and without (CNTL) initialization of SM/ST dataset.

205 vitro callus cultures of stems and leaves of SM.

206 s tightly regulated, leaving the majority of SM gene clusters silent under laboratory conditions.

207 MRI-derived measurements of SM, heart, liver, kidney, spleen, and pancreas were acqu

208 found that the main dissipation pathways of SM at the plot scale were degradation (71%), volatilizat

209 their ability to increase TNF production of SM-treated cells.

210 gether with our previously presented role of SM in controlling the location of proteins involved in g

211 rmation, our data reveal the significance of SM metabolism in the structural organization and functio

212 To address the specificity of SM transport to the plasma membrane, we engineered a nat

213 The lowest tertile of SM volume among hospitals was an independent predictor o

214 d it to monitor intracellular trafficking of SM.

215 Decreased levels of SMs and increased levels of LysoPCs may be important mar

216 ditions, palmitate failed to alter levels of SMs, which are the most abundant sphingolipids, suggesti

217 r 17 mA cm(-2) and high FF over 77% into one SM-OPV.

218 GABA puffs diluted in SM/CSF solution or SM/CSF solution alone showed no significant differences

219 spironolactone inhibits expression of other SM-dependent genes necessary for infectious virion forma

220 rol association with fluid dihydro-palmitoyl SM bilayers was stronger than seen with palmitoyl SM und

221 layers was stronger than seen with palmitoyl SM under similar conditions.

222 small-molecule-based organic photovoltaics (SM-OPVs) using two electron donors (p-DTS(FBTTh2 )2 and

223 Mervish NA, Pajak A, Teitelbaum SL, Pinney SM, Windham GC, Kushi LH, Biro FM, Valentin-Blasini L, B

224 ht loss after RT initiation does not predict SM loss or survival.

225 A high resolution (3 km foot print) SM/ST dataset prepared from a land data assimilation sys

226 The metabolic pathways that produce SMs are found in contiguous gene clusters in fungal geno

227 One of the four putative SM gene clusters, named STC5, was analysed in more detai

228 e, we show that the majority of the putative SM gene clusters in F. fujikuroi are located within facu

229 nd analytical approaches enabled to quantify SM degradation and to identify how degradation controls

230 METHODS AND Resting SM high-energy phosphate concentrations and ATP flux rat

231 physical studies on model membranes revealed SM and Chol driven micrometer-sized liquid-ordered domai

232 with fluticasone propionate (FP)/salmeterol (SM) (50/500, 4 wk).

233 uticasone propionate (FP) and of salmeterol (SM), on the response of well-differentiated cultured bro

234 Furthermore, with saturated SM in the presence of 15 mol % cholesterol, cholesterol

235 os AJ, Lee SY, Thevenet-Morrison K, Schwartz SM, Verner MA, Palkovicova Murinova L, Drobna B, Kocan A

236 al importance of severe rainfall on seasonal SM export.

237 aracteristic radiologic changes and secondly SM with atypical radiology and a more aggressive clinica

238 Fatigue occurred at similar SM energetic levels in all subjects, consistent with a c

239 olecule surface-enhanced Raman spectroscopy (SM-SERS) has the potential to revolutionize quantitative

240 regression model combining the sphingolipid SM C22:3 and the glycerophospholipid lysoPCaC24:0 was di

241 Sphingomyelin (SM) species exhibited neither an increased nor decreased

242 phosphatidylcholine (PC), and sphingomyelin (SM) cations with dicarboxylate anions are shown to charg

243 Absorption of dietary sphingomyelin (SM) requires its initial degradation into ceramide, a pr

244 amide (Cer) and a decrease in sphingomyelin (SM) and dihydrosphingomyelin (dhSM) levels, and a decrea

245 l lines with lower amounts of sphingomyelin (SM) in SP2/0 compared to CHO and HEK, which was subseque

246 ) induced the accumulation of sphingomyelin (SM) precursors such as sphinganine, dihydroceramide, and

247 ipal site of the synthesis of sphingomyelin (SM), an abundant sphingolipid that is transported.

248 hology led us to propose that sphingomyelin (SM) metabolism at the trans-Golgi membranes in mammalian

249 iology and biophysics whether sphingomyelin (SM)- and cholesterol (Chol)- driven nanodomains exist in

250 n di- and triacylglycerides, sphingomyelins (SMs), lysophosphatidylcholines (LysoPCs), and esterified

251 hat hydrogen bonding is important for sterol/SM and ceramide/SM interactions, as well as for the late

252 e for hydrogen bonding in stabilizing sterol/SM interactions.

253 Deletion of mcrA stimulates SM production even in strains carrying a deletion of the

254 s (Swiss Multicentre Bypass Or Sleeve Study; SM-BOSS).

255 Spetzler-Martin (SM) grade, the supplemented SM (sSM) grade, the ICH score and the AVICH score.

256 nts with clear signs of, or highly suspected SM, regardless of the KIT mutation status.

257 sample" used to guide BM biopsy in suspected SM to the outcome of the subsequent BM investigation.

258 Fifty-eight adult patients with suspected SM were included.

259 ions such as soil moisture/soil temperature (SM/ST) can significantly improve the modeling of mesosca

260 ains reveal that mcrA regulates at least ten SM gene clusters.

261 We propose that the term SM should be reserved for this latter condition.

262 d Q-SNAREs were incubated with the tethering/SM protein complex HOPS and the two other soluble SNAREs

263 genotype was more frequent in CC (4.1%) than SM (0.6%, P = 0.002).

264 ese results further support the concept that SM proteins in general are part of the core fusion machi

265 theoretical and experimental evidence, that SM results from feedforward, horizontal, and feedback in

266 ese data lend support to our hypothesis that SM metabolism controls the structural organization of a

267 f filamentous fungal species have shown that SM gene clusters are often either highly divergent or un

268 Taken together, our results suggest that SM is the key anti-fibrotic component of the YQHX and th

269 ow-fatigability HF patients, suggesting that SM metabolism is a potentially important target for futu

270 nd causes NM myosin filament assembly at the SM cell cortex.

271 ical parameters in sera collected before the SM event in cases and their individually matched control

272 usly described a method for conditioning the SM to make it more hospitable to implanted cells and sho

273 AVM size, all single parameters forming the SM, sSM, ICH and AVICH score and the scores itself were

274 ducing the concentration of potassium in the SM facilitate survival of hESCs for at least one week.

275 S is absent, suggesting that ejection of the SM is a rate-limiting step.

276 have been found for different members of the SM protein family, including the three vertebrate Munc18

277 n even in strains carrying a deletion of the SM regulator laeA, and deletion of mcrA homologs in Aspe

278 In 43 of these, SM was subsequently diagnosed in the BM investigation.

279 Thirteen SM patients presented with Hymenoptera venom-induced ana

280 ased on precursor labeling, the flux through SM synthase also increases, which is exacerbated in HepG

281 isrupts cytoskeletal functions attributed to SM alpha-actin in fibroblasts and are consistent with de

282 hibition of growth suppression attributed to SM alpha-actin.

283 een previously hypothesized to contribute to SM gene cluster diversity across entire fungal classes a

284 MPR2 signaling can transition endothelium to SM-like cells associated with PAH.

285 Total SM decreased in both groups during year 1 (-1.4 +/- 0.2

286 g contractile stimulation of canine tracheal SM tissues.

287 NM myosin heavy chain on Ser1943 in tracheal SM tissues, which can regulate NM myosin IIA filament as

288 egained during the second year whereas trunk SM was not.

289 the quantification is to realize that, under SM-SERS conditions, the Raman intensity generated by a m

290 Using SM-OCT, we reveal small structures in the tissues of liv

291 ntification at ultralow concentrations using SM-SERS is proposed.

292 ules recovered many experimentally validated SM pathways, including all six known to form biosyntheti

293 thetic marker) expression were reduced while SM-MHC (SMC contractile marker) levels were increased.

294 (heart, liver, kidney, spleen) compared with SM was found.

295 ant CRT in patients with resected LAHNC with SM negative and no ECE is common.

296 ults Among patients with resected LAHNC with SM negative and no ECE, 47% received adjuvant CRT.

297 d CCL2 serum concentrations in patients with SM and found that CCL2 levels were significantly increas

298 We identified a subset of patients with SM negative and no ECE (n = 10,870).

299 Recent biochemical results with SM alpha-actin-R258C predicted that this variant will co

300 and exhibits 42% amino acid similarity with SM N100.

301 critical concentration for assembly than WT SM alpha-actin, driven by a high disassembly rate.