ライフサイエンスコーパス: skinned

1 of rat hearts and were subsequently rapidly skinned.

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

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

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

5 most common type of malignant cancer in fair-skinned adults.

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

7 relaxation were examined in both chemically skinned and intact myocardial preparations from adult ra

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

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

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

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

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

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

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

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

16 Skinned cardiac fiber measurements showed a large leftwa

17 utants altered the contractile properties of skinned cardiac fibers.

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

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

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

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

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

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

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

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

26 tional consequences were analyzed in porcine skinned cardiac muscle.

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

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

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

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

31 Single skinned cardiac myocytes were attached between a force t

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

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

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

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

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

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

38 In skinned cardiac trabeculae reconstituted with a mono-cys

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

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

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

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

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

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

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

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

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

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

49 87.9% (95% CI: 76.8%, 99%) of fair- and dark-skinned children, respectively, achieved sufficient conc

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

70 3% decrease in maximum developed force), and skinned fibers (14% decrease in maximally activated forc

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

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

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

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

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

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

77 with nonischemic control hearts, bundles of skinned fibers from hearts subjected to ischemia alone d

78 Single, skinned fibers from rabbit psoas muscle were used to tes

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

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

81 exchanged for the endogenous RLC in single, skinned fibers from rabbit psoas muscle.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

97 In skinned fibers, I79N increased myofilamental calcium sen

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

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

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

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

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

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

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

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

106 Cardiac skinned fibres reconstituted with D145E are more sensiti

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

130 stating and stigmatising, especially in dark skinned individuals.

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

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

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

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

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

136 Mechanical experiments with skinned left ventricular myocardium revealed that PKCalp

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

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

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

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

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

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

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

144 f activation and relaxation were examined in skinned multicellular preparations using the caged Ca2+

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

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

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

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

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

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

151 ate (Pi) in actively contracting, chemically skinned muscle fibers has proved to be a useful probe of

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

153 ed shortening velocity was also increased in skinned muscle fibers, and at the whole organ level, bot

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

155 ochondrial respiration in situ using saponin skinned muscle fibers.

156 perturb the actomyosin interaction in active skinned muscle fibers.

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

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

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

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

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

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

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

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

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

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

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

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

169 In skinned myocardial strips, maximum isometric tension was

170 viscosity and oscillatory work production in skinned myocardial strips.

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

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

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

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

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

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

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

178 Skinned myocardium from thyroidectomized rats expressing

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

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

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

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

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

184 Skinned myocardium responded to stretch with an immediat

185 induced alteration of calcium sensitivity in skinned myocardium.

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

187 This study utilized a skinned myocyte preparation with low end compliance to e

188 a concentrations (pCa = -log[Ca2+]) past the skinned myocyte.

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

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

191 ve of the myosin head, was applied to single skinned myocytes to cooperatively promote strong binding

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

193 In single skinned myocytes, increased expression of beta-MHC did n

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

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

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

197 Skinned myofibre preparations from the TG hearts indicat

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

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

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

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

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

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

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

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

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

207 Skinned papillary muscle fibers from transgenic mice exp

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

226 In skinned psoas fibers reconstituted with sTnC labeled at

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

263 The skinned skeleton highly expressed GFP.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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.