ライフサイエンスコーパス: regeneration

1 of natural killer T cells in impaired liver regeneration.

2 that DRP1 has a vital role in injured tissue regeneration.

3 Bungner's bands, which are indispensable for regeneration.

4 or the study of ectodermal organ renewal and regeneration.

5 ghts into therapeutic pathways for beta cell regeneration.

6 in the column setup were observed during the regeneration.

7 nificantly more hygroscopic particles during regeneration.

8 ntial use of dTBs for functional whole tooth regeneration.

9 promising therapeutic for pediatric cardiac regeneration.

10 mmation in the skin and promoting melanocyte regeneration.

11 al muscle development, postnatal growth, and regeneration.

12 tudies of positional memory during appendage regeneration.

13 ion of extracellular proteases in late stage regeneration.

14 s may serve as a powerful system for cardiac regeneration.

15 ng in loss of adult NSCs and defective V-SVZ regeneration.

16 l proliferation during heart development and regeneration.

17 ntial off-the-shelf scaffold for whole tooth regeneration.

18 anti CD1d antibodies exhibited reduced liver regeneration.

19 s are a source of IL-13, which promotes lung regeneration.

20 ypothesis that macrophages are necessary for regeneration.

21 e fusion of myoblasts during development and regeneration.

22 g the astonishing biological process of limb regeneration.

23 an essential role in tissue development and regeneration.

24 subsequently for proper and complete tissue regeneration.

25 ecific diagnostics, therapeutics, and tissue regeneration.

26 romote blood vessel growth and hematopoietic regeneration.

27 evelop new insights for achieving myocardial regeneration.

28 egulated in oligodendrocytes during RGC axon regeneration.

29 such as axon guidance, injury signaling and regeneration.

30 ty, suggesting that epigenetic factors limit regeneration.

31 on injuries heal via scar tissue rather than regeneration.

32 itor cells are involved in tissue repair and regeneration.

33 in (hOPN) in plants for inducing dental bone regeneration.

34 ll cultures, and even stem cell-based tissue regeneration.

35 ivision to epithelial tissue homeostasis and regeneration.

36 s in full-length root canals for dental pulp regeneration.

37 utic target identification, drug testing and regeneration.

38 ncile conflicting data on GSK3-mediated axon regeneration.

39 ppo signaling-a central regulator of cardiac regeneration.

40 o treat vasculopathies and to promote tissue regeneration.

41 /c-Kit signaling, which promotes erythrocyte regeneration.

42 that normal aging processes impose on tissue regeneration.

43 ic attributes such as metabolic zonation and regeneration.

44 entually lead to better approaches for heart regeneration.

45 , but significantly, compromised optic nerve regeneration.

46 deal candidates for drug delivery and tissue regeneration.

47 requirement of active CRMP2 for optic nerve regeneration.

48 tivation, with very limited spontaneous axon regeneration.

49 ges are known to play a major role in tissue regeneration.

50 f these cells before, during, and after tail regeneration.

51 microRNA-mRNA target pairs expressed during regeneration.

52 the source of positional information guiding regeneration.

53 mRNAs related to protein synthesis and nerve regeneration.

54 o differentiation stages on peripheral nerve regeneration.

55 n (PRF) has recently been applied in osseous regeneration.

56 d, high food availability favored whole-body regeneration.

57 ) as a mediator of muscle atrophy and muscle regeneration.

58 eptor and sensory fiber function after nerve regeneration.

59 dox-mediated cathode is demonstrated for Cl2 regeneration.

60 ntribution of non-hepatocytes to parenchymal regeneration.

61 own to mediate immune suppression and tissue regeneration.

62 ocyte polyploidization and compromised heart regeneration.

63 defects in inflammatory cell recruitment and regeneration.

64 of natural stem cells in therapeutic cardiac regeneration.

65 ought to impair osteogenic and hematopoietic regeneration.

66 its heat-shock (HS) inducible impaired heart regeneration.

67 s are a major contributor to oligodendrocyte regeneration.

68 s with potential applications to adult liver regeneration.

69 s, predominantly of the collecting duct, and regeneration.

70 pmental myelination as well as during myelin regeneration.

71 ulated HSPC cell cycle and quiescence during regeneration.

72 crotic debris and for coordination of tissue regeneration.

73 strate their value for promoting hard tissue regeneration.

74 ing a prominent role of DA in effective bone regeneration.

75 ions during cardiac development, repair, and regeneration.

76 he steatosis that normally accompanies liver regeneration.

77 enuate remodeling while promoting repair and regeneration.

78 tion dynamics and subsequently muscle tissue regeneration.

79 ogical repair phenotype that promotes axonal regeneration.

80 on of CRMP2 in RGCs and improved optic nerve regeneration.

81 er sorption performance, with notably facile regeneration ability and structural integrity.

82 ially involved in RGC degeneration or axonal regeneration after acute CNS injury.SIGNIFICANCE STATEME

83 minate a previously unknown program of liver regeneration after acute injury and allow for exploratio

84 utant neoplastic ductal cells and pancreatic regeneration after acute pancreatitis.

85 y has revealed a novel role of GSK3 in liver regeneration after APAP overdose and identified GSK3 as

86 otential therapeutic target to improve liver regeneration after APAP-induced ALF.

87 Functional regeneration after axonal injury requires transected axo

88 ole of GAGs in neural development and axonal regeneration after CNS injury.

89 gated the process of axon regrowth and nerve regeneration after complete transection of the Octopus p

90 Various mouse models of liver regeneration after extended partial hepatectomy and port

91 and the cellular sources that contribute to regeneration after injury are largely unknown in many ti

92 Adult mammalian cardiomyocyte regeneration after injury is thought to be minimal.

93 irective molecules known for inhibiting axon regeneration after injury.

94 EDHB selectively augmented liver regeneration after partial hepatectomy and portal vein l

95 stration just after injury similarly hinders regeneration and compromises muscle strength.

96 dentify Dkk1 as a regulator of hematopoietic regeneration and demonstrate paracrine cross-talk betwee

97 Hoip(Deltahep) mice displayed enhanced liver regeneration and DNA damage.

98 ion studies may propel improvements in nerve regeneration and draw critical parallels to mechanisms o

99 These insights will guide vascular regeneration and engineering.

100 ecreted Wnt proteins are critical for tissue regeneration and frequently contribute to cancer.

101 nervous system (CNS) pose barriers to axonal regeneration and functional recovery following injury.

102 ng therapeutic strategies that improve nerve regeneration and functional recovery.

103 lts uncover a new inducer of mammalian heart regeneration and highlight fundamental roles of the extr

104 ls (CPCs) have been shown to promote cardiac regeneration and improve heart function.

105 erapeutic approaches to improve blood vessel regeneration and increase survival and hematopoietic rec

106 opment, under homeostatic conditions, and in regeneration and liver pathology.

107 in the lesion site, thereby promoting axonal regeneration and locomotor function recovery.

108 eads to divergent effects on epithelial cell regeneration and lung repair during fibrosis.

109 cated mechanism that orchestrates epithelial regeneration and maintenance of tissue integrity.

110 ting factors and cytokines that promote bone regeneration and maturation of soft tissue.

111 ethyl-3,4-dihydroxybenzoate (EDHB) on liver regeneration and metastatic tumor growth.

112 late to pyruvate and are essential for NADPH regeneration and reactive oxygen species homeostasis.

113 ch reflexes are permanently lost, even after regeneration and reinnervation of muscle by motor and se

114 Here, we review research on regeneration and repair of the optic system.

115 several processes, including visual pigment regeneration and retinal attachment to the RPE.

116 gnaling has been linked to accelerated liver regeneration and several chronic inflammatory pathologie

117 ificant increase in corneal epithelial nerve regeneration and substance P-positive nerve density in b

118 known about the potential functions of C3 on regeneration and survival of injured neurons after SCI.

119 proteomics to identify key players in liver regeneration and the importance of posttranslational reg

120 vivo, with potential applications to tissue regeneration and the suppression of metastasis.

121 er T cells is markedly elevated during liver regeneration and their activation under different condit

122 or growth factor receptors involved in liver regeneration and their downstream mitogenic signaling.

123 esults establish an exciting model of tendon regeneration and uncover a novel cellular mechanism unde

124 r upwelling allowing for more cycles of iron regeneration and uptake.

125 uld bridge the gap between cell/tissue-scale regeneration and whole organ-scale technology needed to

126 onding to 91% purity of the gas stream after regeneration), and reached 97 at ultralow CO2 partial pr

127 Analysis of liver function, hepatic regeneration, and comprehensive genomic and metabolic pr

128 uscle and cardiac pathology, improves muscle regeneration, and extends the lifespan.

129 s direct stress-dependent versus homeostatic regeneration, and highlight the importance of postmitoti

130 tion, skeletal tissue differentiation during regeneration, and homeostatic regeneration of intact lim

131 al activator with a critical role in cancer, regeneration, and organ size control.

132 with closely linked phases of inflammation, regeneration, and remodeling.

133 NAD availability is limiting during liver regeneration, and supplementation with precursors such a

134 ding with declines in tree species richness, regeneration, and survival of the dominant tree species,

135 have been associated with liver development, regeneration, and tumorigenesis.

136 Whole tooth regeneration approaches currently are limited by our ina

137 Implications of GSK3 activity for axon regeneration are often inconsistent, if not controversia

138 l cells (MSCs) could be used for bone tissue regeneration as tissue engineered periosteum in a femora

139 s current understanding in wound healing and regeneration as two distinct aspects of cellular self-re

140 ation on follicular and epidermal melanocyte regeneration as well as skin and hair hyperpigmentation.

141 mmalian embryogenesis, stem cell biology and regeneration, as revealed by studies of animal models.

142 aling to regulate intestinal homeostasis and regeneration, as well as adenoma formation.

143 that regulate development, homeostasis, and regeneration, as well as the mechanisms of disease.

144 A demethylation and upregulation of multiple regeneration-associated genes in a Tet3- and thymine DNA

145 le traditionally viewed as a barrier to axon regeneration, beneficial functions of the glial scar hav

146 ng of reciprocal dynamics of portal flow and regeneration between the graft and native liver along wi

147 dvances that relate to central objectives of regeneration biologists researching different tissues an

148 ta-Cat, Axin2 and Dkk1 also increased during regeneration but more notably in AhR-null livers.

149 a well-established model for studying heart regeneration, but due to its tissue opaqueness, repair h

150 ), has been shown to stimulate corneal nerve regeneration, but the mechanisms involved are unclear.

151 ct electron transfer in comparison to enzyme regeneration by NADPH.

152 that is a key regulator of axonal growth and regeneration by promoting microtubule dynamics for reorg

153 nd migration responses that are critical for regeneration by targeting proregenerative P2Y2 nucleotid

154 -type-specific regulatory programs of tissue regeneration can be revealed by genome-wide H3.3 profili

155 of 120 mouse strains have identified a heart regeneration candidate gene that modulates the contracti

156 and multiple imaging sessions to observe the regeneration capabilities of their axons post-injury.

157 e, decline in muscle satellite cell-mediated regeneration coincides with activation of DNA damage res

158 sually mediated behaviors are restored after regeneration, consistent with recovery of retinal functi

159 in satellite cell homeostasis during muscle regeneration could help inform research efforts to treat

160 es of nerve repair, resulting in slowed axon regeneration, cutaneous reinnervation, and functional re

161 olecules needed for growth may contribute to regeneration decline.

162 pithelium (OE) for lifelong neurogenesis and regeneration depends on the persistence of neurocompeten

163 nmental heterogeneity and how its effects on regeneration dynamics play out in long-term stand dynami

164 As such, the contribution of regeneration emissions from a growing fleet of diesel ve

165 ption, large CO2 removal capacities, and low regeneration energies are needed to achieve these separa

166 1 (cKO), an endocytic protein crucial for SV regeneration, enhances PTP in cKO over control.

167 not significantly sensitive to the number of regeneration facilities.

168 though this is a key reason for the frequent regeneration failures in humans, the transcriptional mec

169 Venom Factor (CVF) result in impaired muscle regeneration following cardiotoxin-induced injury in mic

170 current genetic modification methods require regeneration from tissue culture, involving complicated,

171 alian brain, the possibility of brain tissue regeneration has captured the minds of scientists, clini

172 r ability to give rise to myelin cells after regeneration has not been demonstrated directly, althoug

173 For in vivo bone regeneration, HCCS-PDA or HCCS particulates with or with

174 This provides a simple model for tissue regeneration, implicating cellular reprogramming as an e

175 overexpression supported long-term epidermal regeneration in 3D organotypic cultures, and resulted in

176 APAP, resulted in early initiation of liver regeneration in a dose-dependent manner, without modifyi

177 dissect cell fate transitions during colonic regeneration in a mouse dextran sulfate sodium (DSS) col

178 sor cell differentiation and improved muscle regeneration in a separate, toxin-induced model of injur

179 L1 peptides conjugated to FHs promote tissue regeneration in a wound-healing model of mouse submandib

180 gle administration of agrin promotes cardiac regeneration in adult mice after myocardial infarction,

181 elopment, promotes long-distance optic nerve regeneration in adult rats of both sexes.

182 resources have limited our understanding of regeneration in adult salamanders.

183 erent growth-promoting interventions promote regeneration in distinct neuronal types.

184 We propose that spinal cord regeneration in geckos represents a truncation of the re

185 The role of PDGF-BB in muscle regeneration in humans has not been studied.

186 Regeneration in many organisms involves the formation of

187 Here, we investigated bone turnover and regeneration in mice lacking either C5aR1 or C5aR2 in a

188 is a negative regulator of tissue repair and regeneration in multiple organs.

189 d drive sensing of integrity and response by regeneration in other materials as well.

190 could be an effective way of promoting bone regeneration in patients with diabetes.

191 Brain regeneration in planarians is mediated by precise spatio

192 s membrane supports corneal endothelial cell regeneration in rabbits after endothelial injury.

193 ontrol the balance between muscle growth and regeneration in response to oxygen fluctuations, and hyp

194 he door to molecular analysis of single-cell regeneration in Stentor.

195 ults highlight significant decreases in tree regeneration in the 21st century.

196 d by active DNA demethylation to permit axon regeneration in the adult mammalian nervous system.

197 lels to mechanisms of nerve degeneration and regeneration in the CNS and in the context of peripheral

198 st confirmed that PEDF + DHA increased nerve regeneration in the mouse cornea.

199 key role in spontaneous lizard retinal axon regeneration in the presence of Nogo-A.

200 er did not prevent death or promote vascular regeneration in Tnfr1(-/-); Tnfr2(-/-) mice.

201 tosis, we report evidence of striated muscle regeneration in vivo in mice by human MiPs.

202 actions, stimulates axon growth in vitro and regeneration in vivo.

203 em has recently been shown to promote tissue regeneration in which classic wound-healing responses pr

204 We propose a model for eye regeneration in which eye tissue production by planarian

205 immediately after PH (priming phase of liver regeneration) in control mice, but this effect was delay

206 partial amputation culminates in a localized regeneration instead of global hypertrophy and prolifera

207 Concomitant hepatocyte apoptosis and regeneration is a hallmark of chronic liver diseases (CL

208 Regeneration is a process that restores structure and fu

209 t that the spontaneous endothelial cell (EC) regeneration is a slow and insufficient process, it is o

210 Efficient cardiac regeneration is closely associated with the ability of c

211 Pigment regeneration is critical for the function of cone photor

212 lopment and that contrary to mammals, muscle regeneration is normal without functional Pax7 gene.

213 the vasculature during organ development and regeneration is of considerable interest for application

214 Aerosol emitted during filter regeneration is significantly more CCN active and hygros

215 rative pathways become activated when normal regeneration is thwarted and trigger the appearance of "

216 fied and how different muscle subsets affect regeneration is unknown.

217 est c-Jun elevation, which is beneficial for regeneration, is well tolerated during Schwann cell deve

218 blation of the EP4 receptor in MuSCs impairs regeneration, leading to decreased muscle force.

219 of residual bacteria on the outcome of pulp regeneration mediated by a tissue-engineered construct a

220 Our work provides an organ regeneration model through de novo root formation, stati

221 Methods to augment heart regeneration now have potential to counteract the high m

222 Liver regeneration occurs in a hypoxic environment.

223 After liver injury, regeneration occurs through self-replication of hepatocy

224 on of any other organ is followed with local regeneration of a limited degree, but it never attempts

225 ulfated polysaccharide heparin, and promoted regeneration of bone in the spine with a protein dose th

226 did not appear to contribute appreciably to regeneration of cardiac endothelium.

227 ombined with stem cell therapy could enhance regeneration of cartilaginous tissue and serve as a pote

228 and functional repair mechanisms, including regeneration of cerebral white matter and improvement in

229 Regeneration of CNS myelin involves differentiation of o

230 These results show that targeted regeneration of deprived neighborhoods can improve menta

231 nctionally, Tet3 is required for robust axon regeneration of DRG neurons and behavioral recovery.

232 ency of the copolymer was tested in vivo for regeneration of dystrophin in the muscle of mdx mouse th

233 iation of cultured myoblasts and impairs the regeneration of injured muscles.

234 reatment strategies for long-term repair and regeneration of injured or diseased tissues and organs.

235 ion of many cell types; hence, it may affect regeneration of injured skeletal muscle.

236 tiation during regeneration, and homeostatic regeneration of intact limbs.

237 ic stem and progenitor cell numbers, reduced regeneration of leukemic long-term hematopoietic stem ce

238 more complex binding pathway determines the regeneration of mammalian green cone opsin with chromoph

239 5(Creert2)/Met(fl/fl)/LacZ mice had impaired regeneration of MET-deficient ISCs.

240 s also required to support the synthesis and regeneration of nicotinamide adenine dinucleotide phosph

241 The regeneration of organ morphology and function following

242 ectively as a reversible redox agent for the regeneration of the dye.

243 Here we find in zebrafish that regeneration of the epicardium, the mesothelial covering

244 heart disease and are under development for regeneration of the injured heart.

245 ing the ablation protocol, enabling complete regeneration of the oocyte pool.

246 mal stem cells (PDLMSCs) are responsible for regeneration of the periodontium that is lost due to per

247 Here, we show that the lack of regeneration of these populations began ca. 165 ya (arou

248 ions do not create suitable openings for the regeneration of these species, whereas deforestation deg

249 of immune responses to hepatic infection and regeneration of tissue.

250 ircumstances, such as developmental changes, regeneration of tissues, cell divisions, aging, and path

251 ans, positional control genes (PCGs) control regeneration outcomes and are regionally expressed predo

252 enhancers that revise H3.3 occupancy during regeneration, overlaid upon a genome-wide reduction of H

253 on of tissue-engineered constructs for wound regeneration, perhaps the most significant hurdle remain

254 We observed a similar regeneration phenotype with cwn-1 mutation in ALM neuron

255 trate that macrophages are essential for the regeneration process.

256 de transdifferentiation of denervated SCs to regeneration-promoting repair SCs.

257 Regeneration rates of ABOi grafts were not significantly

258 we report a complete energy diagram for the regeneration reaction of rhodopsin.

259 ynamics of this reaction, also known as the "regeneration reaction".

260 te that damaged lobes underwent multilineage regeneration, reforming a lobe often indistinguishable f

261 at control cell-cycle dynamics during tissue regeneration require elucidation.

262 Regeneration requires cells to regulate proliferation an

263 Tissue regeneration requires dynamic cellular adaptation to the

264 Successful regeneration requires that progenitors of different line

265 tility of zebrafish in organ development and regeneration research and might be applicable to other m

266 model organism in developmental biology and regeneration research, genetic techniques enabling condi

267 n, the recruitment of immune cells, and bone regeneration, resulting in delayed fracture healing.

268 ionally, burn injury induced skeletal muscle regeneration, satellite cell proliferation and fusion.

269 ch cells can transform to myelin cells after regeneration.SIGNIFICANCE STATEMENT After injury to peri

270 ion of skeletal patterning during epimorphic regeneration, skeletal tissue differentiation during reg

271 thus inspiring the development of new tissue regeneration strategies.

272 However, nerve regeneration studies require long-term recovery of the a

273 pital" allows us to perform the entire nerve regeneration studies, including on-chip axotomy, post-su

274 d availability affect self-repair choice and regeneration success in cydippid larvae of M. leidyi.

275 highlights strategies for stem cell-mediated regeneration that may be conserved in other adult stem c

276 e, which is important for cytoplasmic NAD(+) regeneration that sustains rapid glucose breakdown throu

277 ed an emerging mammalian model of epimorphic regeneration, the African spiny mouse, to examine cell-b

278 vide signals and spatial clues for promoting regeneration, the clinical outcome after nerve damage is

279 yte proliferation in cardiac development and regeneration, the mechanisms that promote cardiomyocyte

280 Body regeneration through formation of new organs is a major

281 ntion for their ability to guide bone tissue regeneration through structural and biological cues.

282 or active DNA demethylation in allowing axon regeneration to occur in the mature nervous system follo

283 However, knowledge of the structure of these regeneration tracks has not advanced for decades and the

284 s in abnormal morphology of repair cells and regeneration tracks, and failure to sustain expression o

285 tree, providing proof of principle for organ regeneration using human primary cholangiocytes expanded

286 histicated genetic studies on stem cells and regeneration using M. lignano as a model organism.

287 VBA was performed via guided bone regeneration using titanium mesh and allografts.

288 reduced HMGB1 orchestrates muscle and liver regeneration via CXCR4, whereas disulfide HMGB1 and its

289 mice reportedly accelerates peripheral nerve regeneration via increased MAP1B phosphorylation and con

290 , reduction of pain, and promotion of tissue regeneration via novel mechanisms.

291 Failure of regeneration was associated with increased retraction af

292 Similarly, optic nerve regeneration was completely unaffected, although repopul

293 Membrane regeneration was conducted by first dissembling the exis

294 In line with in vitro results, muscle regeneration was stimulated, and muscle fiber size decre

295 innate immune cells play during retinal cell regeneration, we used intravital microscopy to visualize

296 a depletion, spontaneous and LI-induced axon regeneration were unaffected by PLX5622 treatment or per

297 echanism linking C5aR and C5L2 in pulp nerve regeneration, which may be useful in future dentin-pulp

298 role of claudin-1 and occludin in epidermal regeneration with potential clinical importance.

299 hanisms responsible for this action, pigment regeneration with this locked retinal analogue requires

300 n GSK3(S/A) RGCs further boosted optic nerve regeneration, with axons reaching the optic chiasm withi