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1 mature mouse hearts that were otherwise non-regenerative.
2 resources provide a platform to leverage the regenerative abilities of neonatal skin to develop clini
4 hed conditioning significantly increases the regenerative ability of dorsal root ganglia (DRG) sensor
5 e studies provide a paradigm that drives the regenerative ability of sensory neurons offering a poten
9 whereas the fast events represent intrinsic regenerative activity, the slow events reflect the elect
11 r plasmonic nanoantenna-based biosensors are regenerative, allowing multiple measurements using the s
13 ase of high economic impact and the reported regenerative and antibacterial effects of mesenchymal st
15 enic properties, which, in turn, facilitates regenerative and hypertrophic processes that restore str
24 injury are critical for our understanding of regenerative biology, and might facilitate the identific
25 espite its importance in human fertility and regenerative biology, our understanding of this unique t
27 itive manufacturing processes used to create regenerative bone tissue engineered implants are not bio
28 annels play a critical role in mediating the regenerative Ca(2+) oscillations induced by physiologica
29 mice, which may contribute to the different regenerative capabilities of MG from fish and mammals.
30 lthough the mammalian retina has no inherent regenerative capabilities, fish have robust regeneration
32 rian worms, which due to their extraordinary regenerative capability can experimentally result in phe
34 entral nervous system (CNS) has very limited regenerative capability, and injury at the cellular and
39 rganisms replace lost or damaged tissue, and regenerative capacity can vary greatly among species, ti
41 s in animal species with substantial cardiac regenerative capacity dominantly comprise diploid cardio
42 hanosensitive Hippo pathway, correlates with regenerative capacity in acceleration-sensing utricles o
43 de that polyploid hepatocytes have extensive regenerative capacity in situ and routinely undergo redu
48 nsplantation therapy relies on the life-long regenerative capacity of haematopoietic stem cells (HSCs
49 a requirement for the intrinsic clock in the regenerative capacity of insulin-producing cells followi
53 d decline in the levels of neurogenesis, the regenerative capacity of the hippocampus also subsided w
54 stinal stem cells in vitro recapitulates the regenerative capacity of the intestinal epithelium(1,2).
56 e polyploidy was not associated with altered regenerative capacity or tissue fitness, changes in gene
61 unction, diminished pulmonary remodeling and regenerative capacity, and increased susceptibility to a
63 of cellular senescence can promote impaired regenerative capacity, chronic inflammation, and tumorig
65 nervous system axons have intrinsically poor regenerative capacity, so axonal injury has permanent co
73 rates, but should not be to the detriment of regenerative cell populations, primarily mesenchymal ste
74 residual disease (RD) expressed an alveolar-regenerative cell signature suggesting a therapy-induced
75 papillary fibroblasts that form a transient regenerative cell type that promotes healthy skin regene
76 inomas are characterized by the emergence of regenerative cell types, typically seen in response to l
79 otent BSCs can reactivate multipotency under regenerative conditions and upon oncogene expression(3,9
80 iotic molecules as well as a multistep, self-regenerative cycle of iminodiacetic acid were validated
82 This review presents a model for age-related regenerative decline in the fly intestine and discusses
83 n, O-GlcNAc, as a key molecular regulator of regenerative decline underlying an age-related NSC fate
85 cytes, that are hyperproliferative, yet have regenerative deficits and are shifted towards a de-diffe
87 ent inflammation is a feature of age-related regenerative deficits, yet the underlying mechanisms are
88 marked variation in tissue architecture and regenerative demands, SCs often follow similar paradigms
89 Perspective, we discuss the rise of the CNS regenerative drugs, the main biological techniques used
95 apable of dual drug release are designed for regenerative engineering and drug delivery applications.
101 the cellular and molecular logic behind the regenerative failure of injured RGC axons in adult mamma
102 es the genuine state at a young age, causing regenerative failure of muscle, as occurs in geriatric m
103 egulating myeloid cell cycle, maturation and regenerative function of the epithelial niche in ST2(-/-
111 fect is guided by microchannel size-specific regenerative macrophage polarization with the consequent
112 thesized chaperone ApoM as a circulating pro-regenerative mediator that is deficient in aging and mit
117 oaches to direct cellular behaviour for many regenerative medicine applications including those for p
119 d as a novel tool for cellular and acellular regenerative medicine approaches for osteoarthritis (OA)
120 nant of RPE phenotype, with implications for regenerative medicine approaches that utilise stem cell-
123 vitro tissue models, tissue engineering, and regenerative medicine are provided to further motivate f
124 caffolds unveils great potential not only in regenerative medicine but also in drug testing and disea
125 n induced pluripotent stem cell (iPSC)-based regenerative medicine can be applied; however, mass prod
126 n of Wnt signaling has untapped potential in regenerative medicine due to its essential functions in
127 efficacy of mesenchymal stem cells (MSCs) in regenerative medicine has been documented in many clinic
129 tors the location of SPIO-labelled cells for regenerative medicine of the knee with MRI, histology, a
131 her development, this approach may provide a regenerative medicine solution to uterine factor inferti
132 f non-collagenous matrix and suggesting that regenerative medicine strategies should change focus fro
133 f applications including neural engineering, regenerative medicine, multi-functional sensors and actu
134 mmes has been proposed as a new paradigm for regenerative medicine, therefore, a complete understandi
135 genome editing easier, and may be useful in regenerative medicine, unravelling heterogeneity in dise
167 s has important potential in biomedicine and regenerative medicine; however, it often requires comple
168 m cells as a prerequisite for harnessing the regenerative-medicine potential of these cells in the cl
170 without reducing the development of the pro-regenerative microenvironment required for ductular rege
171 educe scar formation while maintaining a pro-regenerative microenvironment will be essential in devel
172 neurons offering a potential redox-dependent regenerative model for mechanistic and therapeutic disco
173 cues and modulating secretion of instructive regenerative molecules in response to dynamic signaling
184 lutionized DPSCs significantly shortened the regenerative period of periodontal defects by enhancing
185 rated that chick fetal wound healing shows a regenerative phenotype regarding the cellular and molecu
186 nipulated to adopt a neuroprotective and pro-regenerative phenotype that can aid repair and alleviate
187 ology, as well as comparison of scarring and regenerative phenotypes to uncover master regulators of
192 ous axon growth through the injury, but this regenerative potential diminishes with maturity until it
193 in zebrafish may provide cues to unlock the regenerative potential in the mammalian nervous system.
194 We investigated the vasculoprotective and regenerative potential of a newly identified PPARgamma-p
195 an shed significant light on the quality and regenerative potential of cultivated human corneal epith
197 acing in BAC-transgenic mice, we confirm the regenerative potential of intestinal stem cells (ISCs) b
200 The study thus revealed an unappreciated regenerative potential of the young DG and suggests hipp
202 (ER) cell survival, exit from quiescence and regenerative potential upon gamma radiation-induced inju
203 that inactivation of Drp1 causes loss of HSC regenerative potential while maintaining HSC quiescence.
204 e arrest, resulting in impaired homeostasis, regenerative potential, and gradual functional decline i
205 to a pro-fibrotic phenotype, expanding their regenerative potential, and improving healing in a compl
209 rate in capturing the overall benefit of the regenerative procedure and (2) to better identify which
214 Heterotopic ossification (HO) is an aberrant regenerative process with ectopic bone induction in resp
217 reactivate nerve-dependent developmental and regenerative processes to promote their growth and survi
220 raising the hypothesis as to the presence of regenerative progenitor-like populations in the adult pa
221 terocytes show basal induction of the Clu(+) regenerative program and a fetal gene expression signatu
223 ablished an inducible PPARgamma-p53 mediated regenerative program regulating 19 genes involved in lun
224 s inhibitory Hippo signaling and facilitates regenerative proliferation in nonmammalian utricles, whe
225 cell nuclei in chicken utricles and promoted regenerative proliferation, but YAP remained cytoplasmic
226 elops as repair Schwann cells lose their pro-regenerative properties and inhibitory factors such as C
230 el blood-derived embolic material (BEM) with regenerative properties, that can achieve instant and du
232 anscriptional programs spanning stem-like to regenerative pulmonary epithelial progenitor states.
233 able various biomedical applications such as regenerative repair in medicine and biosensing in bioeng
236 -specific ablation of Ptger4 misdirected the regenerative reprogramming of stem cells and prevented S
237 The molecular mechanisms that mediate the regenerative response and its blockade in later life are
239 We showed that LOXL2 is elevated in the regenerative response during fracture healing in mice an
240 intestinal (GI) syndrome, elucidation of the regenerative response following radiation-induced gut in
242 ed P2RX7 and P1R participation in the retina regenerative response induced by photoreceptor damage ca
244 dystrophies, little is known about whether a regenerative response is regularly elicited in FSHD musc
246 epithelial-mesenchymal transition (EMT)-like regenerative response manifested by cytoskeletal remodel
247 Our findings suggest that Runx1 controls the regenerative response of multiple cardiac cell types and
248 in chondrocytes, and restoration of youthful regenerative response to aged, human muscle stem cells,
249 h1 intracellular domain (N1ICD) and impaired regenerative response to injury in comparison to young (
251 f adult limb joints in mice by stimulating a regenerative response using microfracture (MF) surgery.
252 roliferation in vitro, possibly reflecting a regenerative response, but is dispensable for chondrocyt
257 nd knee joint, induces chondroprotective and regenerative responses, and attenuates NF-kB signaling.
261 turation, (d) recent insights related to the regenerative role of the subpopulation of CMs that are n
265 Identification of molecular signatures and regenerative signaling pathways for each surgical proced
272 studies provide encouraging evidence that a regenerative strategy for patients will be available in
273 racing strategies and experimental models of regenerative stress have revealed a degree of plasticity
274 Cs) have been the focus of developmental and regenerative studies, yet our understanding of the signa
275 ive benefits of Er:YAG laser irradiation for regenerative surgical therapy of peri-implantitis-associ
277 ther distinguish the analgesic mechanisms of regenerative therapies from those of cellular replacemen
278 therapeutic options are urgently needed, but regenerative therapies have remained an unfulfilled prom
279 e development of characterization assays for regenerative therapies that could be integrated into a g
285 ng laser irradiation during peri-implantitis regenerative therapy may aid in better probing PD reduct
286 ealth with a reduced support, whereas, after regenerative therapy, a successful outcome was described
287 eveal a reciprocal interdependence between a regenerative tissue and its niche at different stages an
290 s osteochondral defect model, the quality of regenerative tissues in both chondral and subchondral la
291 ophic myofibers and uncover degenerative and regenerative transcriptional pathways underlying DMD pat
292 However, in mice with injury alone this regenerative transcriptome is downregulated after two we
294 T) motor neurons in mice, to identify their 'regenerative transcriptome' after spinal cord injury and
297 papilla preservation (EPP) technique in the regenerative treatment of isolated deep intrabony defect