ライフサイエンスコーパス: neonatal rat

1 ng organotypic hippocampal slice cultures of neonatal rat.

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

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

4 role of cytokine regulation following TBI in neonatal rats.

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

6 was reported to disrupt myelin formation in neonatal rats.

7 I(Kr) in ventricular myocytes isolated from neonatal rats.

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

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

10 in ventricular cardiomyocytes isolated from neonatal rats.

11 ortex and ventral midline thalamic nuclei of neonatal rats.

12 rotavirus strain, CDC-9, in Caco-2 cells and neonatal rats.

13 spontaneous activity in the visual system of neonatal rats.

14 the ventilatory response to hyperthermia 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 l and/or genetically manipulate cells in the neonatal rat and mouse brain.

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

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

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

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

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

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

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

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

27 Neonatal rat atrial cardiomyocyte cultures and intact at

28 METHODS AND Neonatal rat atrial cardiomyocyte monolayers expressing

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

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

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

32 Exposing the neonatal rat brain to propofol induces acute neurotrophi

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

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

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

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

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

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

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

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

41 Neonatal rat cardiac fibroblasts, myocytes, and adult fi

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

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

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

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

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

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

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

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

50 chronotrope with low nanomolar activity in a neonatal rat cardiomyocyte (NRCM) arrhythmia model.

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

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

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

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

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

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

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

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

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

60 Neonatal rat cardiomyocytes (NRCMs) transduced with GFP

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

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

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

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

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

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

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

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

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

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

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

72 In neonatal rat cardiomyocytes induced to hypertrophy with

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

74 Neonatal rat cardiomyocytes plated on PPy-chitosan showe

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

76 novirus-mediated overexpression of Tsg101 in neonatal rat cardiomyocytes resulted in cell hypertrophy

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

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

79 CryAB overexpression in cultured neonatal rat cardiomyocytes significantly attenuated adr

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

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

82 Neonatal rat cardiomyocytes were treated with DEHP at a

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

84 Using cultured neonatal rat cardiomyocytes with adenoviral gene deliver

85 We treated neonatal rat cardiomyocytes with an inhibitory erbB2 ant

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

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

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

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

90 In neonatal rat cardiomyocytes, NN and NRG induced similar

91 In neonatal rat cardiomyocytes, TrpC4alpha, but not TrpC4be

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

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

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

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

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

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

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

99 protection against DOX toxicity in cultured neonatal rat cardiomyocytes.

100 glucose-induced mitochondrial dysfunction in neonatal rat cardiomyocytes.

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

102 Similar results were obtained with primary neonatal rat cardiomyocytes.

103 ation calorimetry and sorting experiments in neonatal rat cardiomyocytes.

104 In neonatal rats, CDC-9 P45 showed reduced rotavirus sheddi

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

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

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

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

109 e used primary OPCs in culture isolated from neonatal rat cortices of both sexes and young male and f

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

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

112 Few days after SCI, neonatal rats developed behavioral signs of spasticity w

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

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

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

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

117 he contribution of Tff2 to protection of the neonatal rat from E. coli K1 bacteremia and tissue invas

118 ling in semi-intact cochlear preparations in neonatal rats from both sexes.

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

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

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

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

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

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

125 Here, we investigated the interaction of neonatal rat heart cells with engineered spider silk pro

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

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

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

129 Both cultured neonatal rat hippocampal neurons and differentiated olig

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

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

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

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

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

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

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

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

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

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

140 ulation of I(NaP) and KCC2, respectively, in neonatal rat lumbar motoneurons.

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

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

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

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

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

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

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

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

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

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

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

152 Neonatal rat myocyte monolayers were treated with media

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

169 Neonatal rat pups were chronically treated with nicotine

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

193 els in Vero cells and attenuated and safe in neonatal rats; thus, the study supports clinical develop

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

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

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

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

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

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

200 bly, electrophysiology, and contractility of neonatal rat ventricular cardiomyocytes (NRVCMs) culture

201 Our results in primary neonatal rat ventricular cardiomyocytes (NRVCs) show tha

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

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

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

205 Palmitate exposure to neonatal rat ventricular cardiomyocytes initially activa

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

207 nd increased apoptosis were also observed in neonatal rat ventricular cardiomyocytes overexpressing t

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

209 Neonatal rat ventricular cardiomyocytes were infected wi

210 Neonatal rat ventricular cardiomyocytes were used to inv

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

212 Using neonatal rat ventricular cardiomyocytes, we further foun

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

214 sed Ki67 and BrdU staining in cultured fresh neonatal rat ventricular cardiomyocytes.

215 ion in CryAB(WT) and CryAB(R120G)-expressing neonatal rat ventricular cardiomyocytes.

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

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

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

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

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

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

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

223 In vitro studies with neonatal rat ventricular CMscorroborated the in vivo fin

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

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

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

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

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

229 C2C12 skeletal myoblast differentiation and neonatal rat ventricular myocyte hypertrophy are inhibit

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

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

232 Optical imaging in neonatal rat ventricular myocyte monolayers demonstrated

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

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

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

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

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

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

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

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

241 Mechanistically, MANF knockdown in cultured neonatal rat ventricular myocytes (NRVMs) impaired prote

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

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

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

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

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

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

248 In neonatal rat ventricular myocytes and H9c2 myoblasts, IS

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

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

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

252 Mechanistically, knockdown of ATF6 in neonatal rat ventricular myocytes blocked phenylephrine-

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

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

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

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

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

258 culturing Kv1.5-expressing HEK 293 cells and neonatal rat ventricular myocytes in low osmolarity (LO)

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 of-function ETV1 RNA sequencing dataset from neonatal rat ventricular myocytes transduced with Etv1 s

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

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

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

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

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

273 Treatment of neonatal rat ventricular myocytes with either recombinan

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

275 model of ACM (expression of JUP(2157del2) in neonatal rat ventricular myocytes) and a robust murine m

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

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

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

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

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

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

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

283 ine 293 (HEK293) cells and I(Kr) in isolated neonatal rat ventricular myocytes.

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

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

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

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

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

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

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

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

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

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

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

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

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

297 Neonatal rats were normally reared or stressed-reared du

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