ライフサイエンスコーパス: skinned

1 temperatures (5-30 degrees C) in chemically skinned (0.5 % Brij) rabbit psoas muscle fibres.

2 ximately 0.3 ms) were examined in chemically skinned (0.5 % Brij), maximally Ca(2+)-activated rabbit

3 rees N, respectively) in both fair- and dark-skinned 5- to 7-y-old children.

4 inase with emerging myocardial functions; in skinned adult rat ventricular myocytes (ARVMs), recombin

5 The 10 varieties, representing five red-skinned and five white-skinned berries, were all cultiva

6 athy (FHC) phenotype were generated, and the skinned and intact papillary muscle fibers from the Tg-D

7 solated by mechanical homogenization, Triton-skinned, and attached to micropipettes that projected fr

8 d-skinned apple cv. Red Delicious and yellow-skinned apple cv. Golden Delicious.

9 titative RT-PCR (qRT-PCR) using fruit of red-skinned apple cv. Red Delicious and yellow-skinned apple

10 mulates pathways otherwise inactive in white-skinned berries, leading to a greater accumulation of co

11 characterized by a restricted flux in white-skinned berries, was a common outcome of noble rot and r

12 representing five red-skinned and five white-skinned berries, were all cultivated in the same experim

13 s, was a common outcome of noble rot and red-skinned berry ripening.

14 Skinned cardiac fiber measurements showed a large leftwa

15 utants altered the contractile properties of skinned cardiac fibers.

16 etric force and ATPase activity in detergent-skinned cardiac fibre bundles from three transgenic (TG)

17 Using skinned cardiac muscle fibers, we determined that in com

18 pendent conformational behavior of N-cTnC in skinned cardiac muscle fibers.

19 Detergent-skinned cardiac muscle fibre bundles were used to study

20 efore, we incorporated the mutant CTnCs into skinned cardiac muscle in order to determine if their ef

21 hese TnT FHC mutants were reconstituted into skinned cardiac muscle preparations and characterized fo

22 nsitivity and cooperativity of activation of skinned cardiac muscle were unchanged.

23 s modulated by changes in lattice spacing in skinned cardiac muscle.

24 tional consequences were analyzed in porcine skinned cardiac muscle.

25 mere length (SL) dependence of activation in skinned cardiac muscles with different titin-based passi

26 +) for 50% activation (Ca(50)) in intact and skinned cardiac muscles.

27 Skinned cardiac myocytes from wild-type (WT) and MyBP-C

28 es of force development were examined in rat skinned cardiac myocytes that contained either alpha-myo

29 Single skinned cardiac myocytes were attached between a force t

30 of intact cardiac myocytes and incubation of skinned cardiac myocytes with PKA.

31 ases the power output-generating capacity of skinned cardiac myocytes, in part, by speeding the step(

32 g the McTnT deletion proteins into detergent-skinned cardiac papillary fibres harvested from non-tran

33 n proteins were reconstituted into detergent-skinned cardiac papillary fibres harvested from transgen

34 y ratio (I(1,1)/I(1,0)) were made in relaxed skinned cardiac trabeculae from rats.

35 by X-ray diffraction as a function of SL in skinned cardiac trabeculae in the passive state from bot

36 In skinned cardiac trabeculae reconstituted with a mono-cys

37 93) or human cTnI-(1-192) was exchanged into skinned cardiac trabeculae; Western blot analysis confir

38 fluence the level and rate of demembranated (skinned) cardiac muscle force development by exchanging

39 omere shortening-Ca2+ relationship in Triton-skinned cardiomyocytes revealed a significant reduction

40 s 110-121 that inhibited force production in skinned carotid artery.

41 alysis, 90.2% (95% CI: 81.1%, 99.3%) of fair-skinned children randomly assigned to supplementation of

42 skin type (greater concentrations in lighter-skinned children than in darker-skinned children), and,

43 skin type (greater concentrations in lighter-skinned children than in darker-skinned children), formu

44 rations, whereas 25 mug/d was needed in dark-skinned children to reach sufficiency in 95.1% (95% CI:

45 s in lighter-skinned children than in darker-skinned children), and, inversely, serum calcium and pho

46 s in lighter-skinned children than in darker-skinned children), formula use (higher intakes), season

47 87.9% (95% CI: 76.8%, 99%) of fair- and dark-skinned children, respectively, achieved sufficient conc

48 takes of 6 and 20 mug/d are required in fair-skinned children, whereas 14 and 28 mug/d are required i

49 re distinctive to the normal ripening of red-skinned cultivars.

50 the uplifting of deep crustal rocks ('thick-skinned' deformation) far from plate boundaries, and for

51 We found that the in vitro power produced by skinned Drosophila asynchronous flight muscle fibers inc

52 arying phosphate and MgATP concentrations in skinned Drosophila IFM fibers.

53 When skinned embryos are embedded in Matrigel, basal and supe

54 Dark-skinned ethnic subgroups had much higher (3- to 71-fold)

55 ump (T-jump) experiments and from intact and skinned fast mammalian muscle fibres.

56 ium-induced force development was studied in skinned fast skeletal muscle fibers from wildtype (WT) a

57 Skinned fast type IIa and slow type I fibres were prepar

58 depression in tension and ATPase activity in skinned fiber bundles from a TG model in which cTnI is r

59 of tension and ATPase activity of detergent-skinned fiber bundles from left ventricular papillary mu

60 Exchange of cTnI in skinned fiber bundles with cTnI(146G) induced enhanced C

61 ated hearts, isolated papillary muscles, and skinned fiber preparations), biochemical and molecular b

62 lopment of cardiac disease include increased skinned fiber sensitivity to calcium and, at the whole o

63 ), were expressed, purified, and utilized in skinned fiber studies and in reconstituted actomyosin AT

64 ions in cTnI, actomyosin ATPase activity and skinned fiber studies were carried out.

65 In skinned fiber studies, TnT1-wild-type (WT)-treated fiber

66 both the Ca(2+) binding measurements and the skinned fiber tension measurements, the presence of cTnI

67 Exposure of skinned fiber to caspase-3 decreased maximal Ca(2+)-acti

68 tension development in detergent-extracted (skinned) fiber bundles isolated from mouse left ventricu

69 3% decrease in maximum developed force), and skinned fibers (14% decrease in maximally activated forc

70 mbinant HCTnTs was incorporated into porcine skinned fibers along with human cardiac troponin I (HCTn

71 related with increased Ca(2+) sensitivity in skinned fibers and vice versa.

72 and structural role of the RLC in chemically skinned fibers at various thick and thin filament lattic

73 cross-bridge cycling kinetics as measured in skinned fibers derived from the diseased muscle.

74 Porcine papillary skinned fibers displaced with HSSTnT1, -2, or -3 and rec

75 with severe mitochondrial damage, and their skinned fibers failed to activate with calcium.

76 ric tension over a wide range of [Ca(2+)] in skinned fibers from rabbit psoas muscle.

77 C-5'ATR), in sTnC-5'ATR reconstituted single skinned fibers from rabbit psoas muscle.

78 influence in intact hearts, trabeculae, and skinned fibers from wild-type (+/+) and homozygous trunc

79 Ca(2+) sensitivity of contraction in skinned fibers increased with mutant gene dose: KI-TnC-A

80 ction in elastic modulus in Dmlc2(Delta2-46) skinned fibers is consistent with the N-terminal extensi

81 Surprisingly when the kinetics of skinned fibers isolated from the ELC1vDelta5-14 or ELC1a

82 Investigation of cardiac skinned fibers isolated from WT and heterozygous mice re

83 oncentration (Vmax) have been assessed using skinned fibers prepared from two oxidative muscles (vent

84 roteins reconstituted into porcine papillary skinned fibers showed decreased Ca(2+) sensitivity of fo

85 e/decrease the Ca(2+) sensitivity of cardiac skinned fibers to create the characteristic effects of D

86 spacing of dissected, osmotically compressed skinned fibers to native muscle fibers in living flies.

87 ociated with increased Ca(2+) sensitivity in skinned fibers was identified; and 3) the F27W reporter

88 The maximal force in reconstituted skinned fibers was significantly greater for the cTnT1 (

89 Skinned fibers were maximally Ca(2+)-activated at 20 deg

90 TnC-extracted cardiac skinned fibers were reconstituted with the cTnC-A31S mut

91 Small step-stretches of single skinned fibers were used to study the effect of phosphor

92 In troponin-exchanged skinned fibers, each mutant caused a significant increas

93 In skinned fibers, I79N increased myofilamental calcium sen

94 In maximally activated skinned fibers, the rate of tension redevelopment (ktr)

95 red abilities to inhibit ATPase and to relax skinned fibers.

96 eration and rate of tension redevelopment in skinned fibers.

97 ot other contractile proteins in "chemically skinned" fibers, we substantially reduced the contractil

98 scle (IFM) and assessed myofibril structure, skinned fibre mechanical properties, and flight ability.

99 pCa(2+)-tension relationships in skinned fibre preparations indicate decreased calcium se

100 egulates the unloaded shortening velocity in skinned fibres by reducing the number of crossbridges ab

101 ilisation during active shortening of single skinned fibres from rabbit psoas muscle at 10 degrees C

102 esence of Ca(2+) was characterized in single skinned fibres from rabbit psoas muscle.

103 iculum (SR) was investigated in mechanically skinned fibres from the rat extensor digitorum longus (E

104 Cardiac skinned fibres reconstituted with D145E are more sensiti

105 Treatment of skinned fibres with 5 microM NEM-S1 eliminated the low-v

106 usly proposed from studies on Ca2+-activated skinned fibres, that the elementary force generation ste

107 lower contents of hexanol and heptanol than skinned fish; moreover, the samples with the skin had a

108 Recently, double-skinned flat sheet cellulose acetate (CA) membranes cons

109 The double-skinned FO membrane comprises a fully porous sublayer sa

110 Therefore, a novel double-skinned FO membrane with a high water flux has been aime

111 rom small bundles of one to three chemically skinned frog sartorius muscle fibres (time resolution 25

112 calcium along the length of A and I bands in skinned frog semitendinosus muscles using electron probe

113 and dynamic contractile indices in detergent-skinned guinea pig (Cavia porcellus) cardiac muscle fibe

114 f 20,000 s(-1)) and initiated contraction of skinned guinea pig cardiac muscle.

115 of Ca(2+)-induced contractions of chemically skinned guinea pig trabeculae was studied using laser ph

116 ssively exchanged for the endogenous form in skinned guinea pig trabeculae.

117 Slack-test recordings of single, skinned human masseter fibers at 15 degrees C revealed m

118 ndogenous troponin was exchanged in isolated skinned human myocardium for recombinant troponin contai

119 rivative viscoelasticity, we used chemically skinned human skeletal muscle as a one-dimensional model

120 Here we found that melanocytes from light-skinned humans and albino mice secrete high levels of fi

121 sensitivity (CHS) responses in healthy white-skinned humans in vivo (n = 93).

122 ere obtained from rabbit psoas muscle fibers skinned in oil and transferred to physiological salt sol

123 or epidemiological differences between light-skinned individuals of mixed European descent and Africa

124 nfantile hemangioma are more common in light-skinned individuals of mixed European descent than in Af

125 Previous studies have suggested that darker-skinned individuals tend to have more inner ear melanin,

126 understudied population groups such as dark-skinned individuals, infants, adolescents, reproductive-

127 inoma (BCC), the most common cancer in light-skinned individuals.

128 stating and stigmatising, especially in dark skinned individuals.

129 duced tanning is defective in numerous 'fair-skinned' individuals, many of whom contain functional di

130 cing to changes in muscle length in relaxed, skinned isolated muscle preparations.

131 Mechanical studies on skinned left ventricle myocardium measured total and tit

132 analysis to compare crossbridge function in skinned left ventricular (LV) epicardial muscle strips f

133 dependence of force development between rat skinned left ventricular cardiac myocytes and fast-twitc

134 Mechanical experiments with skinned left ventricular myocardium revealed that PKCalp

135 ysis to examine the mechanical properties of skinned left ventricular papillary muscle strips from mo

136 R luminal Ca(2+) was studied in mechanically skinned malignant hyperthermia susceptible (MHS) and non

137 The resultant double-skinned membrane exhibits a high water flux of 17.2 LMH

138 The double-skinned membrane outperforms the single-skinned membrane

139 uble-skinned membrane outperforms the single-skinned membrane with much lower fouling propensity for

140 P and fouling propensity over typical single-skinned membranes.

141 We used detergent-skinned mouse cardiac fiber bundles to measure changes i

142 le contractile performance was determined in skinned muscle activated with exogenous Ca(2+), as well

143 Ca(2+)-activated stress in skinned muscle and stress produced by intact nebulin-fre

144 plays a role in muscle contraction by using skinned muscle fiber bundles from a nebulin knock-out (N

145 Importantly, in skinned muscle fiber preparations, we found markedly imp

146 oduction by measuring the force generated by skinned muscle fibers as the strength of the actomyosin

147 in maximal force and ATPase were observed in skinned muscle fibers from Tg-D166V mice compared with c

148 (T13C/N51C)AEDANS-DDPM was incorporated into skinned muscle fibers to monitor N-cTnC opening.

149 can reduce thick-to-thin filament spacing in skinned muscle fibers, thereby increasing force producti

150 for dantrolene to inhibit Ca(2+) release in skinned muscle fibers.

151 ochondrial respiration in situ using saponin skinned muscle fibers.

152 perturb the actomyosin interaction in active skinned muscle fibers.

153 was selectively removed from bovine cardiac skinned muscle fibres by gelsolin, and the actin filamen

154 regulation were investigated in mechanically skinned muscle fibres from rat extensor digitorum longus

155 tration (MC) decreased in both type 1 and 2A skinned muscle fibres.

156 Extraction of myosin binding protein-C from skinned muscle normalized myofilament Ca(2+) sensitivity

157 by synchrotron X-ray diffraction in relaxed, skinned muscle preparations.

158 ncreased unloaded shortening velocity in t/t skinned muscle strips, and dramatically reduced myofilam

159 For skinned muscle, an increase in MgADP or inorganic phosph

160 The demembranated (skinned) muscle fiber preparation is widely used to inve

161 zo-2 to rapidly decrease the [Ca(2+)] within skinned muscles from the mouse ventricles.

162 amic XB behavior were measured in chemically skinned myocardial preparations isolated from human dono

163 equatorial intensity ratio, I(11)/I(10), in skinned myocardial preparations isolated from wild-type

164 ses of the myofilament lattice in chemically skinned myocardial strips of the following mouse models:

165 In skinned myocardial strips, maximum isometric tension was

166 viscosity and oscillatory work production in skinned myocardial strips.

167 pha revealed that titin is phosphorylated in skinned myocardial tissues; this effect is exacerbated b

168 cMyBPC content in cMyBPC(-/-) skinned myocardium after in vivo cMyBPC gene transfer or

169 pendence that is similar to that measured in skinned myocardium after PKCalpha phosphorylation.

170 echanical experiments were also performed on skinned myocardium before and after phosphorylation.

171 Sudden stretch of skinned myocardium during maximal or submaximal Ca2+ act

172 o assess the inter-thick filament spacing in skinned myocardium following treatment with either MLCK

173 myosin subfragment-1 (NEM-S1) in chemically skinned myocardium from adult rats.

174 Skinned myocardium from thyroidectomized rats expressing

175 Skinned myocardium isolated from cMyBPC(+/-) hearts disp

176 and mechanical experiments were conducted on skinned myocardium isolated from cMyBPC(-/-) hearts 21 d

177 Cross-bridge kinetics in skinned myocardium isolated from cMyBPC(-/-) hearts afte

178 Skinned myocardium isolated from cMyBPC(-/-) hearts disp

179 f the rate of force redevelopment (k(tr)) in skinned myocardium isolated from wild-type (WT) and cMyB

180 Skinned myocardium responded to stretch with an immediat

181 induced alteration of calcium sensitivity in skinned myocardium.

182 cture during Ca2+-activation of force in rat skinned myocardium.

183 BP-C on LDA in the heart, we examined LDA in skinned myocytes from a non-transgenic (NTG) and a trans

184 hin filament.Confocal images of Triton X-100-skinned myocytes incubated with a fluorescent conjugate

185 Functional assessment of skinned myocytes, however, revealed that myofilament Ca(

186 + sensitivity of tension, measured in single skinned myocytes, was reduced in cMyBP-C(-/-) but not cM

187 es and 0.35 +/- 0.05 muscle lengths/s in pig skinned myocytes.

188 Complementary experiments in "skinned" myocytes confirmed reduced myofilament Ca(2+) s

189 Skinned myofibre preparations from the TG hearts indicat

190 on tissue explants, isolated cardiomyocytes, skinned myofibrils, and purified actin/myosin preparatio

191 ophis couchii) and sympatric prey, the rough-skinned newt (Taricha granulosa), Sierra newt (Ta. sierr

192 precedence and storage patterns in the rough-skinned newt (Taricha granulosa).

193 An earlier study in rough-skinned newts (Taricha granulosa) indicated that the neu

194 Rough-skinned newts (Taricha granulosa) use tetrodotoxin (TTX)

195 creased cross-bridge kinetics as observed in skinned papillary bundles from young transgenic mice pri

196 measurements of ATPase activity and force in skinned papillary fibers from hcTnI R145G transgenic mic

197 measurements of ATPase activity and force in skinned papillary fibers from hcTnI R145W transgenic mic

198 Studies of the pCa-force relations in skinned papillary fibers regulated by these forms of cTn

199 were decreased approximately 20% in Tg-E22K skinned papillary muscle fibers and intracellular [Ca2+]

200 ements of the ATPase and force in transgenic skinned papillary muscle fibers from mutated versus cont

201 Detergent-skinned papillary muscle fibers from non-TG (NTG) and TG

202 Skinned papillary muscle fibers from transgenic mice exp

203 ation rates (g(app)) was observed in freshly skinned papillary muscle fibers.

204 esults suggesting 3 factors in fair and dark skinned patients ("Psychological effects on daily life",

205 s suggesting three factors in fair- and dark-skinned patients ("Psychological effects on daily life,"

206 Light-skinned patients had an increased risk of BCC (P = .01).

207 Skin cancer incidence is highest in white-skinned people.

208 rse data on key vulnerable populations (dark-skinned persons, reproducing women, infants, children, a

209 ocyanin biosynthesis, is associated with red-skinned phenotype.

210 anoma incidence has been increasing in light-skinned populations worldwide, but the reasons for the i

211 SCC), are the most common cancers among fair-skinned populations worldwide.

212 SCC), are the most common cancers among fair-skinned populations worldwide.

213 de on mean concentrations of 25(OH)D in dark-skinned populations.

214 (NMSCs) are the most common cancers in fair-skinned populations.

215 are the second most frequent cancers in fair-skinned populations; yet, because of their genetic heter

216 For all astronauts, single chemically skinned post-flight fibres expressing only type I myosin

217 namic mechanical properties of multicellular skinned preparations isolated from the sub-endocardial a

218 steady-state activations in both intact and skinned preparations, propofol and isoflurane depressed

219 e responsible for unmasking Ca(2+) sparks in skinned preparations.

220 ancer burden were Australian born, were fair skinned (prevalence ratio = 1.61, 95% confidence interva

221 reased the Ca2+ sensitivity of force in both skinned psoas fibers and trabeculae.

222 In skinned psoas fibers reconstituted with sTnC labeled at

223 However, in skinned psoas fibers, neither SL changes or force inhibi

224 ced by flash photolysis of diazo-2 in rabbit skinned psoas fibres was investigated at 15 degrees C.

225 Exchange of G34DTnC(F29W) into skinned psoas muscle fibers decreased fiber calcium sens

226 atterns on passive fiber bundles from rabbit skinned psoas muscle.

227 approximately 95% of the myosin heads in the skinned rabbit psoas muscle contain the hydrolysis produ

228 -ray diffraction patterns were recorded from skinned rabbit psoas muscle fiber bundles stretched to n

229 The mechanical behavior of skinned rabbit psoas muscle fiber contractions and in vi

230 Contractility of skinned rabbit psoas muscle fibers was inhibited by trea

231 x-ray diffraction patterns from the relaxed skinned rabbit psoas muscle fibers where ATP hydrolysis

232 The endogenous RLC was removed from skinned rabbit psoas muscle fibers, and replaced with ei

233 The unloaded shortening velocity of skinned rabbit psoas muscle fibres is sensitive to [Ca2+

234 a2+ on loaded shortening and power output in skinned rat cardiac myocyte preparations, and fast- and

235 ded shortening velocity, and power output in skinned rat cardiac myocytes before and after treatment

236 otron x-ray diffraction as function of SL in skinned rat cardiac trabeculae bathed in 0% to 6% dextra

237 combinant cardiac TnT/TnC and exchanged into skinned rat cardiac trabeculae.

238 comere lengths (SL) of 2.0 and 2.3 microm in skinned rat cardiac trabeculae.

239 relaxation rate were investigated in Triton-skinned rat caudal arterial smooth muscle strips.

240 the rate of force redevelopment measured in skinned rat myocardial preparations.

241 ed in the tubular (t) system of mechanically skinned rat skeletal muscle fibres to measure SOCE durin

242 In single skinned rat soleus fibers, 30 mM caffeine produced a lef

243 ady-state force-pCa and ATPase-pCa data from skinned rat soleus fibers.

244 on chemo-mechanical transduction in isolated skinned rat trabeculae.

245 force-[Ca(2+)] relationships were studied in skinned rat trabeculae.

246 and ATPase rate in whole troponin-exchanged skinned rat trabeculae.

247 Piperine increased ATPase activity of skinned relaxed fibers by 66 +/- 15%.

248 single glycerinated rabbit psoas fibers and skinned right ventricular trabeculae from rats.

249 re juxtaposed between the Sephadex beads and skinned semitendinosus muscle fibers under oil.

250 Contractile forces generated by chemically skinned single fiber preparations from Mtm1delta4 muscle

251 Mechanical properties of skinned single fibres from rabbit psoas muscle have been

252 ng various length-change protocols to active skinned single fibres from rabbit psoas muscle, and obse

253 ched to the myosin regulatory light chain in skinned skeletal fibers, allowing us to perform a high-t

254 Activation in skinned skeletal muscle fibers was enhanced with all TnI

255 lated force and relaxation were performed in skinned skeletal muscle fibers whose endogenous TnI (alo

256 unds also decrease RyR1 Ca(2+) leak in human skinned skeletal muscle fibers.

257 Ca2+ regulation was studied in mechanically skinned skeletal muscle fibres from rat extensor digitor

258 levels of activation, unloaded shortening of skinned skeletal muscle fibres takes place in two phases

259 sitivity of tension to [Ca2+] that occurs in skinned skeletal muscle fibres upon stretch also occurs

260 The skinned skeleton highly expressed GFP.

261 ither a rat cardiac myocyte preparation or a skinned slow-twitch skeletal muscle fibre.

262 e relationship of relaxation to 8-Br-cGMP in skinned smooth muscle and the relative expression of LZ+

263 ion constant of approximately 110 microM for skinned smooth muscle fibers and approximately 730 micro

264 oximately 730 microM for thiophosphorylated, skinned smooth muscle fibers.

265 state of the light chain domain of myosin in skinned smooth muscle.

266 Skinned SOL muscles and ventricular PMs of R58Q animals

267 red sarcomere length-dependent properties in skinned soleus (SSM), psoas (FSM) and ventricular trabec

268 ss-bridge cycling and MgADP release rates in skinned soleus fibers using stochastic length-perturbati

269 in solution and after substitution into rat skinned soleus fibers.

270 ents and performed additional experiments on skinned strips osmotically compressed to the intact latt

271 ceptibility to cutaneous melanoma, with fair skinned subjects at highest risk of developing this neop

272 The study population consisted of eight fair-skinned sun-sensitive healthy young adults.

273 P20110-121 abolished Ca2+-activated force in skinned swine carotid artery.

274 ereas ultraviolet B-induced tanning of light-skinned swine was inhibited using these agents.

275 insufficiency is strongest, but rather fair-skinned teenagers and young adults, who are at highest r

276 ions of extracellular Ca and then chemically skinned to clamp the contractile system.

277 force-calcium relationships were measured in skinned trabeculae and/or myocytes.

278 nd that moderate compression (1% dextran) of skinned trabeculae at SL=2.02 microm reduced LS (LS=42.2

279 rease, respectively, in [Ca2+] within Triton-skinned trabeculae from rat and guinea pig hearts (22 de

280 equatorial intensity ratio, I(11)/I(10), in skinned trabeculae isolated from wild-type and cMyBP-C n

281 + sensitivity of both force and dichroism in skinned trabeculae.

282 sin ATPase activity, and force generation in skinned trabeculae.

283 rn of UVB radiation and a predominantly dark-skinned urban population who suffer high HIV-1 prevalenc

284 rot-infected berries of cv Semillon, a white-skinned variety, were collected over 3 years from a comm

285 PKA treatment of wild-type and cTnI(ala2) skinned ventricular myocardium accelerated stretch activ

286 pment and the stretch activation response in skinned ventricular myocardium from both wild-type (WT)

287 of tension development was studied in a rat skinned ventricular myocyte preparation.

288 ities of 1.1 +/- 0.8 muscle lengths/s in rat skinned ventricular myocytes and 0.35 +/- 0.05 muscle le

289 rminal peptide fragments to human and rodent skinned ventricular myocytes.

290 Single-nucleotide turnover in skinned ventricular preparations demonstrated that phosp

291 yBP-C on the stretch activation responses of skinned ventricular preparations from wild-type (WT) and

292 t myocardium on the mechanical properties of skinned ventricular preparations.

293 ce showed no discernable mutant phenotype in skinned ventricular strips.

294 lysed for the force vs. Ca2+ relationship in skinned ventricular trabeculae of transgenic mice in com

295 Herein, we used skinned, ventricular papillary muscle strips from rats t

296 Healthy white-skinned volunteers were used (n=119).

297 sured using a coupled assay system on fibres skinned with saponin.

298 Dark-skinned Yucatan swine treated with these agents showed v

299 ct and results in depigmentation of the dark skinned Yucatan swine, suggesting a new class of depigme

300 dependent skin lightening effect in the dark-skinned Yucatan swine.