ライフサイエンスコーパス: neonatal rat

1 ng organotypic hippocampal slice cultures of neonatal rat.

2 nsights into the E. coli K1 infection of the neonatal rat.

3 Escherichia coli K1 can be replicated in the neonatal rat.

4 in ventricular cardiomyocytes isolated from neonatal rats.

5 udens protein 1 was also better preserved in neonatal rats.

6 was reported to disrupt myelin formation in neonatal rats.

7 pulation in the dorsal root ganglia (DRG) of neonatal rats.

8 ortex and ventral midline thalamic nuclei of neonatal rats.

9 spontaneous activity in the visual system of neonatal rats.

10 fused than in glucose-perfused intestines of neonatal rats.

11 fields (RFs) in decerebrate spinal adult and neonatal rats.

12 ce and abrogated bacteremia and mortality in neonatal rats.

13 the ventilatory response to hyperthermia in neonatal rats.

14 role of cytokine regulation following TBI in neonatal rats.

15 Neonatal rat 6-hydroxydopamine lesion-induced hyperactiv

16 cholamine secretion and [Ca2+]i responses in neonatal rat adrenal chromaffin cells and involves react

17 ective cyclooxygenase-2 inhibition protected neonatal rats against death, progression of brain injury

18 rowth hormone release in male Sprague-Dawley neonatal rats, although to a lesser degree than GHRP-6.

19 e demonstrated that hypoxia induced GRP78 in neonatal rat and isolated adult mouse ventricular myocyt

20 phological reconstruction of interneurons in neonatal rat and mouse slices in vitro.

21 passage cultures of primary astrocytes from neonatal rats and cultures of the C6 rat glioma cells we

22 l types in brain slices from male and female neonatal rats and mice, including raphe neurons, cortica

23 Osteoclasts were isolated from long bones of neonatal rats and rabbits.

24 ort that, in intact hippocampi prepared from neonatal rats and transgenic mice expressing Clomeleon,

25 e induction of a high level of bacteremia in neonatal rats, and RDI 4 mutants exhibited a moderate de

26 r was injected subretinally into the eyes of neonatal rats, and this was followed by electroporation.

27 The results of these experiments with neonatal rats are inconsistent with the hypothesis that

28 and apoptosis were assessed in (i) cultured neonatal rat astrocytes treated with astrogliosis-induci

29 Neonatal rat atrial cardiomyocyte cultures and intact at

30 METHODS AND Neonatal rat atrial cardiomyocyte monolayers expressing

31 Additionally, in brain slices from P7 neonatal rats, BAPTA induced significant loss of calcium

32 the whisker-to-barrel cortex pathway of the neonatal rat barrel cortex in vivo.

33 ia with iN-IGF-1 significantly protected the neonatal rat brain from HI injury.

34 looked for HI neuroprotection from FBP in a neonatal rat brain slice model, using 14.1 T (1)H/(31)P/

35 Exposing the neonatal rat brain to propofol induces acute neurotrophi

36 When grafted into neonatal rat brain, they show potential for integration

37 ion, and leads to white matter injury in the neonatal rat brain.

38 In neonatal rat brains in vitro, the rostral ventral respir

39 tiated-human neuronal progenitors and in the neonatal rat brains.

40 identification of hypoxic-ischemic injury in neonatal rat brains.

41 cordings from hypoglossal motoneurons in the neonatal rat brainstem slice preparation.

42 Inhibition of endogenous ROCK activity in neonatal rat brainstem slices failed to modulate intrins

43 Neonatal rats, C57BL/6J, C3HeB/FeJ (TLR4 wild type), and

44 s in their conductance and driving forces in neonatal rat CA3 pyramidal cells during GDPs.

45 Neonatal rat cardiac fibroblasts, myocytes, and adult fi

46 tion increased promoter activity in cultured neonatal rat cardiac myocytes and human HEK fibroblasts

47 rized mitochondria and rescues cell death in neonatal rat cardiac myocytes subjected to hypoxia/reoxy

48 into SW13 and human smooth muscle cells and neonatal rat cardiac myocytes, and the effects on cytosk

49 TRAF2 localizes to the mitochondria in neonatal rat cardiac myocytes, and TNF treatment transcr

50 ation of depolarized mitochondria in resting neonatal rat cardiac myocytes, as well as in those treat

51 ast and independent nuclear Ca(2+) signal in neonatal rat cardiac myocytes, human embryonic cardiac m

52 ant in heart tissue and isolated ventricular neonatal rat cardiac myocytes.

53 agy effector, on depolarized mitochondria in neonatal rat cardiac myocytes.

54 We also used a neonatal rat cardiomyocyte culture system to elucidate t

55 We report that in neonatal rat cardiomyocyte culture, subtle out-of-plane

56 Adult hMSCs affect arrhythmicity of neonatal rat cardiomyocyte cultures by heterocellular co

57 Similarly, Pim-1 overexpression in neonatal rat cardiomyocyte cultures inhibits hypertrophy

58 MSC-derived exosomes did not increase APD in neonatal rat cardiomyocyte cultures.

59 cathepsin G (Cat.G) has been shown to induce neonatal rat cardiomyocyte detachment and apoptosis by a

60 cocultures, hMSCs dose-dependently decreased neonatal rat cardiomyocyte excitability, slowed conducti

61 ew preribosomal RNA synthesis occurs in both neonatal rat cardiomyocytes (NRCM) and cardiac progenito

62 ith these findings, adenoviral-induced Pim-1 neonatal rat cardiomyocytes (NRCMs) retain a reticular m

63 Neonatal rat cardiomyocytes (NRCMs) transduced with GFP

64 Knockdown of alpha-catenins in neonatal rat cardiomyocytes also resulted in increased p

65 Cocultures of 4x10(5) neonatal rat cardiomyocytes and 7% or 28% adult human MS

66 DNA breaks associated with DOXO exposure in neonatal rat cardiomyocytes and human cardiomyocytes der

67 nuated cardiomyocyte hypertrophy in cultured neonatal rat cardiomyocytes and in the intact adult hear

68 Cellular sorting experiments in neonatal rat cardiomyocytes are consistent with the view

69 TA4 in both co-transfected HEK293T cells and neonatal rat cardiomyocytes by co-immunoprecipitation.

70 Reoxygenation increased cell death in neonatal rat cardiomyocytes compared with hypoxia alone,

71 s attenuated in PPT.CG.H1.beta(2)-transduced neonatal rat cardiomyocytes compared with nonsilencing c

72 Immunohistochemical staining in neonatal rat cardiomyocytes demonstrates that ZASP1-D117

73 SiRNA knockdown of MURF2 in neonatal rat cardiomyocytes disrupts posttranslational m

74 mical analysis of the patient myocardium and neonatal rat cardiomyocytes expressing mutant MYPN.

75 tissue-derived stem cells (hASCs) fused with neonatal rat cardiomyocytes in vitro.

76 In neonatal rat cardiomyocytes induced to hypertrophy with

77 scent probe Vybrant DiO were cocultured with neonatal rat cardiomyocytes labeled with the red fluores

78 Neonatal rat cardiomyocytes plated on PPy-chitosan showe

79 Furthermore, ABCB10 knockdown in neonatal rat cardiomyocytes resulted in a significant de

80 g and overexpression experiments in isolated neonatal rat cardiomyocytes showed that Hsp22 activates

81 Inhibition of OGT or OGA activity within neonatal rat cardiomyocytes significantly affects energy

82 CryAB overexpression in cultured neonatal rat cardiomyocytes significantly attenuated adr

83 Overexpression of miR-539 in neonatal rat cardiomyocytes significantly suppressed OGA

84 ully associate with TM5 when introduced into neonatal rat cardiomyocytes was also associated with an

85 AB(R120G) protein misfolding and aggregates, neonatal rat cardiomyocytes were infected with adenoviru

86 Neonatal rat cardiomyocytes were treated with DEHP at a

87 Treatment of neonatal rat cardiomyocytes with 0.5 mm 2-DG dramaticall

88 Using cultured neonatal rat cardiomyocytes with adenoviral gene deliver

89 We treated neonatal rat cardiomyocytes with an inhibitory erbB2 ant

90 Mice and cultured neonatal rat cardiomyocytes with transgenic (TG) express

91 In cultured neonatal rat cardiomyocytes, AMPK activates FoxOs, and A

92 evels were detected in Rnd3-null embryos, in neonatal rat cardiomyocytes, and noncardiac cell lines w

93 In neonatal rat cardiomyocytes, L-type calcium channel acce

94 In neonatal rat cardiomyocytes, NN and NRG induced similar

95 In neonatal rat cardiomyocytes, TrpC4alpha, but not TrpC4be

96 ntihypertrophic (class II) HDACs in cultured neonatal rat cardiomyocytes.

97 R and the endogenously expressed receptor in neonatal rat cardiomyocytes.

98 re demonstrated both in vitro and in primary neonatal rat cardiomyocytes.

99 died in human embryonic kidney-293 cells and neonatal rat cardiomyocytes.

100 man embryonic kidney-293 cells and by 32% in neonatal rat cardiomyocytes.

101 scription of hypertrophy-associated genes in neonatal rat cardiomyocytes.

102 asome surrogate substrate (GFPu) in cultured neonatal rat cardiomyocytes.

103 protection against DOX toxicity in cultured neonatal rat cardiomyocytes.

104 glucose-induced mitochondrial dysfunction in neonatal rat cardiomyocytes.

105 T) RII and performed adenoviral infection of neonatal rat cardiomyocytes.

106 Similar results were obtained with primary neonatal rat cardiomyocytes.

107 ation calorimetry and sorting experiments in neonatal rat cardiomyocytes.

108 Here, we conducted two experiments using neonatal rat cells and an incomplete cervical injury mod

109 which contribute to Bax-related apoptosis in neonatal rat cerebellum at ages of peak ethanol sensitiv

110 in cocultures of A. culbertsoni and primary neonatal rat cerebral cortex microglia, induced apoptosi

111 s inhibitory effect in the nasal passages of neonatal rats, colonization experiments were performed w

112 s with naturally occurring cell death in the neonatal rat cortex and hippocampus.

113 In CA3 pyramidal neurons from neonatal rats, dendritic BDNF release causes long-term p

114 eta is in newly generated cells in adult and neonatal rat dentate gyrus.

115 Consistent with observations in neonatal rats, depletion of microglia before tMCAO in P9

116 CTGF expression was lower in neonatal rat discs than in skeletally mature rat discs.

117 Such gating is observed in neonatal rats during wake-related movements.

118 lung ECFCs exposed to hyperoxia in vitro and neonatal rat ECFCs isolated from hyperoxic alveolar grow

119 In both adults and neonatal rats, ERbeta immunoreactivity was found in a su

120 ration in striatal medium spiny neurons from neonatal rats exposed to antiepileptic drugs with proapo

121 DSLNnT and DS'LNT were shown to protect neonatal rats from necrotizing enterocolitis (NEC) and a

122 uroprotection of axotomized motor neurons in neonatal rats further revealed that the conjugate retain

123 In neonatal rats, GLUT5 can be induced only by luminal fruc

124 has previously been studied by transfecting neonatal rat hair cells in culture with a beta-actin-GFP

125 Further, we found that LCS treated neonatal rats have higher intestinal expressions of Ki67

126 Studies in neonatal rats have shown that H-I acutely expands the nu

127 rdion-like honeycomb scaffolds with cultured neonatal rat heart cells demonstrated utility through: (

128 trically excitable grafts with multi-layered neonatal rat heart cells.

129 ardial delivery of the progenitor cells into neonatal rat hearts, in vivo incubation and analysis.

130 l as epicardium-derived cells) obtained from neonatal rat hearts.

131 epithelial cell lines but also explants from neonatal rat hearts.

132 Both cultured neonatal rat hippocampal neurons and differentiated olig

133 orted that neurotrophins induced survival of neonatal rat hippocampal neurons by promoting neural act

134 piratory pre-Botzinger complex (pre-BotC) of neonatal rat in vitro brainstem slice preparations.

135 gradely labeled with Ca(2+)-sensitive dye in neonatal rat in vitro brainstem slices.

136 vitro brainstem-spinal cord preparation from neonatal rat in which the respiratory and the locomotor

137 sion in the normal and the denervated PrV of neonatal rats in an in vitro brainstem preparation.

138 respiratory rhythm generation in slices from neonatal rats in vitro.

139 e same sequence is seen with OP exposures in neonatal rats, indicating that direct effects of these a

140 whether inflammatory insult to the colons of neonatal rats induced GHS in adult life.

141 Using neonatal rats intranasally colonized with pairs of marke

142 termine if E2-dependent PR expression in the neonatal rat is mediated through ERalpha and/or ERbeta.

143 transport of Nanogold-labeled Fc (Au-Fc) in neonatal rat jejunum, focusing on later aspects of trans

144 cal or mechanical irritation of the colon of neonatal rats leads to chronic visceral hypersensitivity

145 Human fetal and neonatal rat lungs contain ECFCs with robust proliferati

146 D1 inhibition in whole-cell recordings from neonatal rats may be mediated by a change in NMDA recept

147 l of the pre-Botzinger complex (pre-BotC) in neonatal rat medullary slices in vitro, and in the more

148 neuronal current-voltage (I-V) relations in neonatal rat medullary slices in vitro, we demonstrated

149 ed XII nerve activity in rhythmically active neonatal rat medullary slices.

150 ble to cause bacteremia or meningitis in the neonatal rat model and was significantly less virulent t

151 reviously that hypoxia-induced seizures in a neonatal rat model induce rapid phosphorylation of serin

152 ipotent Astrocytic Stem Cells (MASCs) into a neonatal rat model of hypoxia-ischemia (HI) and demonstr

153 A neonatal rat model of hypoxia-ischemia was used where ac

154 The neonatal rat model of rotavirus infection was used to de

155 In a neonatal rat model of unilateral hypoxia-ischaemia (HI),

156 human colonic carcinoma cell line Caco-2 and neonatal rat models.

157 Experiments in the fetal sheep or neonatal rat, mouse, or pig reveal dramatic effects of u

158 Neonatal rat myocyte monolayers were treated with media

159 We exposed cultured neonatal rat myocytes to a 10% cyclic mechanical stretch

160 and after VA supplementation.Sprague-Dawley neonatal rats (n = 104) were nursed by mothers fed a VA-

161 Neonatal rats of either sex (postal day 0-5) were expose

162 mined the expression and function of REST in neonatal rat oligodendrocyte precursor cells (OPCs).

163 amined in fibrous astrocytes within isolated neonatal rat optic nerve (RON) and in cultured cortical

164 olated by flow cytometry and cocultured with neonatal rat optic nerve cells in separate but media-con

165 A treatment of primary cortical neurons from neonatal rats or mice increases expression of phosphoryl

166 In neonatal rat organ of Corti, ALMS1 was localized to the

167 a, identified by differential display in the neonatal rat ovary.

168 ered vehicle, thyroxine (T4) or metformin to neonatal rats post FAE and rats were tested in the hippo

169 In a medullary slice preparation from neonatal rat (postnatal days 0-4) generating spontaneous

170 ry and metabolic response to hyperthermia in neonatal rats (postnatal age 2-4 days), pregnant dams we

171 tudied the effect of subplate removal in the neonatal rat primary somatosensory cortex (S1).

172 her mild chemical irritation of the colon of neonatal rats produced persistent changes in visceral se

173 Alcohol consumption in neonatal rats produces cerebellar damage and is widely u

174 We treated neonatal rat pups at postnatal day (P)2-3 with an intra-

175 n was cleared more rapidly from the lungs of neonatal rat pups compared with the wild-type strain, wh

176 Neonatal rat pups were chronically treated with nicotine

177 ental emergence of odor fear conditioning in neonatal rat pups, and examined synaptic plasticity of i

178 Survival of hippocampal neurons in neonatal rat requires spontaneous activity that depends

179 processing the plasma of the same cohort of neonatal rats revealed no difference in the same cytokin

180 the decreased survival of the mutant in the neonatal rat sepsis model of GBS infection.

181 increases the number of neurite outgrowth in neonatal rat SG in vitro.

182 cells in spinal slices from opiate-tolerant neonatal rats show an increase in miniature, spontaneous

183 ne (a synthetic glucocorticoid) treatment to neonatal rats showed a temporal decrease in Runx2 with a

184 Preclinical studies in neonatal rats showed that lactoferrin given orally befor

185 h frequency in experimental infection of the neonatal rat, significantly reduced the capacity of A192

186 In this study, neonatal rat skeletal myoblasts cultured within 3-dimens

187 stimulated glucose uptake by L6 myotubes and neonatal rat skeletal myoblasts.

188 anced by exposing the sacral segments of the neonatal rat spinal cord to the acetylcholinesterase inh

189 ombines patch-clamp recordings in the intact neonatal rat spinal cord with tract-tracing to demonstra

190 Using isolated preparations of the neonatal rat spinal cord, we explore the role of interve

191 in the lumbar ventral roots of the isolated neonatal rat spinal cord.

192 that in the whisker-related barrel cortex of neonatal rats, spontaneous whisker movements and passive

193 hat, in the whisker-related barrel cortex of neonatal rats, spontaneous whisker movements and passive

194 o adult levels (pH 5.0-5.5) over 5-6 days in neonatal rat stratum corneum (SC).

195 receptor currents in medium spiny neurons of neonatal rat striatum.

196 cells in vitro and in hippocampal neurons of neonatal rats subjected to cerebral hypoxia-ischemia in

197 etained efficiently in peripheral tissues of neonatal rats, suggesting that a more frequent, lower-do

198 nformatics analyses, we recently developed a neonatal rat system that enables maturation of PSC-deriv

199 It was previously found in neonatal rat that cyclic electrical stimulation of spina

200 Here, we present a systematic study in neonatal rats that charts the evolution of the cortical

201 We further evaluated mast cell activity in neonatal rats that display rapid expulsion.

202 LCS significantly decrease susceptibility of neonatal rats to oral E. coli K1 infection as reflected

203 blocked in perfused brain preparations from neonatal rats treated with selective antagonists of 5-HT

204 own to 0.5% O2) on mitochondrial function in neonatal rat type-1 cells.

205 n brain slices obtained from male and female neonatal rats, using voltage-clamp protocols designed to

206 cultures of myocytes and myofibroblasts from neonatal rat ventricles were optically mapped using a vo

207 so that it connected 2 independently beating neonatal rat ventricular cardiomyocyte monolayers; it ac

208 rotein levels were reduced by doxorubicin in neonatal rat ventricular cardiomyocytes (NRVC) and in mo

209 found that TRIM32 also degraded dysbindin in neonatal rat ventricular cardiomyocytes as well.

210 T-p27) was sufficient to induce autophagy in neonatal rat ventricular cardiomyocytes in vitro, under

211 Overexpression of KLF15 in neonatal rat ventricular cardiomyocytes inhibits cell si

212 Palmitate exposure to neonatal rat ventricular cardiomyocytes initially activa

213 The constructs were built by culturing neonatal rat ventricular cardiomyocytes on polydimethyls

214 from cryptophyte algae expressed in cultured neonatal rat ventricular cardiomyocytes produced inhibit

215 Neonatal rat ventricular cardiomyocytes were used to inv

216 d, in confirmation of the data obtained from neonatal rat ventricular cardiomyocytes, demonstrated in

217 Using neonatal rat ventricular cardiomyocytes, we further foun

218 tentials from hundreds of connected in vitro neonatal rat ventricular cardiomyocytes.

219 in, whereas TRIM24 promoted these effects in neonatal rat ventricular cardiomyocytes.

220 ation are also observed in palmitate-treated neonatal rat ventricular cardiomyocytes.

221 ligase, using gain- and loss-of-function in neonatal rat ventricular cardiomyocytes.

222 channels are regulated by aldosterone/MR in neonatal rat ventricular cardiomyocytes.

223 ace antigen, and mixed with freshly isolated neonatal rat ventricular cardiomyocytes.

224 of impulses in monolayers of well-polarized neonatal rat ventricular cardiomyocytes.We traced electr

225 monolayers of cocultured myofibroblasts and neonatal rat ventricular cells by inhibiting myofibrobla

226 We micropatterned cell pairs consisting of a neonatal rat ventricular myocyte (NRVM) coupled to an en

227 ability and electrophysiological property of neonatal rat ventricular myocyte (NRVM) cultures.

228 ion on reentry frequency, APD, CV, and WL in neonatal rat ventricular myocyte (NRVM) monolayers infec

229 Treatment of confluent neonatal rat ventricular myocyte (NRVM) monolayers with

230 Neonatal rat ventricular myocyte cultures subjected to h

231 induced MANF in an ATF6-dependent manner in neonatal rat ventricular myocyte cultures.

232 l fragment of PC-1 was sufficient to trigger neonatal rat ventricular myocyte hypertrophy.

233 Computer simulations using a realistic neonatal rat ventricular myocyte monolayer model provide

234 Optical imaging in neonatal rat ventricular myocyte monolayers demonstrated

235 Acute regional ischemia/reperfusion in neonatal rat ventricular myocyte monolayers recapitulate

236 reen fluorescent protein (GFP) expression in neonatal rat ventricular myocyte monolayers.

237 a simpler 2-dimensional geometry of cultured neonatal rat ventricular myocyte monolayers.

238 micropatterned strands (n=152) in which host neonatal rat ventricular myocytes (AP duration=153.2+/-2

239 all-optical system applied to monolayers of neonatal rat ventricular myocytes (NRVM).

240 ne the cellular location of NFAT in cultured neonatal rat ventricular myocytes (NRVMs) and adult feli

241 PHLPP-1 is expressed in neonatal rat ventricular myocytes (NRVMs) and in adult m

242 y, autophagic flux was increased in cultured neonatal rat ventricular myocytes (NRVMs) expressing a m

243 beta-AR stimulation of neonatal rat ventricular myocytes (NRVMs) or cardiac fib

244 growth, PLCepsilon protein was depleted from neonatal rat ventricular myocytes (NRVMs) using siRNA.

245 he level of transcription, HEK 293 cells and neonatal rat ventricular myocytes (NRVMs) were transfect

246 e developed a novel tissue model of cultured neonatal rat ventricular myocytes (NRVMs) with uniform o

247 The sensors were subsequently expressed in neonatal rat ventricular myocytes and acutely isolated a

248 and ROMK mRNA was confirmed to be present in neonatal rat ventricular myocytes and adult hearts.

249 In neonatal rat ventricular myocytes and H9c2 myoblasts, IS

250 ed IBZ by coculturing skeletal myotubes with neonatal rat ventricular myocytes and performed optical

251 y downregulated in Gq or by Gq expression in neonatal rat ventricular myocytes and reversed by CaMKII

252 GRK5 presented with the opposite results in neonatal rat ventricular myocytes as p65 and p50 were de

253 We engineered the shape of neonatal rat ventricular myocytes by culturing them on m

254 Human and porcine CDCs cocultured with neonatal rat ventricular myocytes exhibited biophysical

255 fness on cardiomyocyte maturation, we plated neonatal rat ventricular myocytes for 7 days on collagen

256 d overexpression of Fstl1 protected cultured neonatal rat ventricular myocytes from hypoxia/reoxygena

257 eduction, action potentials in Wnt3a-treated neonatal rat ventricular myocytes had a lower upstroke a

258 s of GDF11, showed that GDF11 did not reduce neonatal rat ventricular myocytes hypertrophy, but inste

259 ential, and cell death were recapitulated in neonatal rat ventricular myocytes infected with constitu

260 of native myocardium significantly enhances neonatal rat ventricular myocytes maturation.

261 In culture, neonatal rat ventricular myocytes mature to form striate

262 cal mapping of V(m) in patterned cultures of neonatal rat ventricular myocytes to assess the relation

263 We used cultured neonatal rat ventricular myocytes to examine how chronic

264 Exposing neonatal rat ventricular myocytes to hypo-osmotic medium

265 We used confluent monolayers of neonatal rat ventricular myocytes to investigate the use

266 We subjected neonatal rat ventricular myocytes to mechanical stretch

267 agation consisting of monolayers of cultured neonatal rat ventricular myocytes treated with anthopleu

268 lso observed in hERG-HEK cells as well as in neonatal rat ventricular myocytes treated with the musca

269 wn of endogenous Cav3 or Nedd4-2 in cultured neonatal rat ventricular myocytes using siRNA led to an

270 ssion of resistin using adenoviral vector in neonatal rat ventricular myocytes was associated with in

271 To eliminate neurohormonal influences, neonatal rat ventricular myocytes were subjected to cycl

272 Treatment of neonatal rat ventricular myocytes with either recombinan

273 Infection of 2D cultures of neonatal rat ventricular myocytes with WT and mutant cha

274 ioned media exerted antiapoptotic effects on neonatal rat ventricular myocytes, and proangiogenic eff

275 -resolution optical mapping in monolayers of neonatal rat ventricular myocytes, containing approximat

276 In vitro studies using phenylephrine-treated neonatal rat ventricular myocytes, to explore the putati

277 in-like growth factor 1 (IGF-1) treatment in neonatal rat ventricular myocytes, translocates to mitoc

278 In cultured neonatal rat ventricular myocytes, we compared the respo

279 a scrambled sequence) in primary cultures of neonatal rat ventricular myocytes.

280 on and reactive oxygen species generation in neonatal rat ventricular myocytes.

281 effect on myofibrillar proteins in isolated neonatal rat ventricular myocytes.

282 endogenous Cx43 colocalized with GFP-LC3 in neonatal rat ventricular myocytes.

283 latively high frequency after coculture with neonatal rat ventricular myocytes.

284 Scaffolds were first tested by seeding with neonatal rat ventricular myocytes.

285 acidification-induced uncoupling in pairs of neonatal rat ventricular myocytes.

286 hERG minigenes expressed in HEK293 cells or neonatal rat ventricular myocytes.

287 ted Hrd1 knockdown were examined in cultured neonatal rat ventricular myocytes.

288 d NF-kappaB DNA binding activity in cultured neonatal rat ventricular myocytes.

289 THODS AND Patch-clamp recordings of cultured neonatal rat ventricular myofibroblasts revealed that TG

290 ce glial differentiation in hypoxic ischemic neonatal rats via the hedgehog signaling pathway.

291 vitro brainstem-spinal cord preparation from neonatal rat, we report that the locomotor-related signa

292 Using rhythmic brainstem slices from neonatal rats, we microinjected AMPA into the pre-BotC o

293 ceptors, highly enriched ipRGC cultures from neonatal rats were generated using anti-melanopsin-media

294 Neonatal rats were intubated and infused with ethanol (E

295 Neonatal rats were isolated daily for 1 h from postnatal

296 Neonatal rats were normally reared or stressed-reared du

297 Infection of neonatal rats with Borna disease virus results in a char

298 Treating neonatal rats with decitabine, an inhibitor of DNA methy

299 Feeding LR17938 to neonatal rats with NEC increased the % of Foxp3(+) T cel

300 ncluding skin, brain, and adipose tissue, in neonatal rats without and after VA supplementation.Sprag