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1 tastatic cancer, even in the same patient or experimental model.
2 nce of subsequent cardiac vasculitis in this experimental model.
3  to develop an alternative, non-select agent experimental model.
4  and chose Pacific oyster Magallana gigas as experimental model.
5 ons in liver function and structure using an experimental model.
6 uids (with and without nicotine) on the same experimental model.
7 h improved pathophysiologic properties as an experimental model.
8  image pancreatic inflammation in a relevant experimental model.
9 the procedure provides a unique clinical and experimental model.
10 oped and analyzed an integrated mathematical-experimental model.
11 GC projection depends on the duration of the experimental model.
12 e also shown endocrine-disrupting effects in experimental models.
13 nct effects on virus phenotypes in different experimental models.
14 o enhanced metastasis and chemoresistance in experimental models.
15 rted by clinical data and the translation to experimental models.
16 in atherosclerosis is based on findings from experimental models.
17 regarding senescence in the human kidney and experimental models.
18 ll pathology and acute pancreatitis in mouse experimental models.
19  disciplines, encompassing human studies and experimental models.
20 liver fibrosis but also vessel remodeling in experimental models.
21 coactivators, are drivers of tumor growth in experimental models.
22 at autoimmune and inflammatory conditions in experimental models.
23 ble vascular scaffold [BVS]) using different experimental models.
24 ed informatics or can only be used in single experimental models.
25 sm of the virus and the paucity of tractable experimental models.
26 of various modes of cell death in a range of experimental models.
27 valuated for its anti-inflammatory action in experimental models.
28 ecrease mortality and morbidity after ICH in experimental models.
29 nd anti-senescence responses in a variety of experimental models.
30 s on using human tissues and supplemented by experimental models.
31 y have been hampered by a paucity of in vivo experimental models.
32 ide (NO)-dependent vasodilator properties in experimental models.
33   Both aspects are challenging to capture in experimental models.
34 d the functional role of CST was explored in experimental models.
35 , various prion strains can be propagated in experimental models.
36  effects of altered fatty acid metabolism in experimental models.
37  modulation of spinal networks in accessible experimental models.
38 cific anatomical environments, functions and experimental models.
39 fts we constructed dedicated classifiers for experimental models.
40 eptor modulators regulate podocyte injury in experimental models.
41 extensively studied in cancer cell lines and experimental models.
42 suitable for studying neutrophil function in experimental models.
43 e due to the absence of truly representative experimental models.
44 cardioprotective effects in a broad range of experimental models.
45  have been found to reduce neuronal death in experimental models.
46                                           In experimental models a number of epigenetic mechanisms ha
47 Using the mouse tyrosinase (Tyr) locus as an experimental model, a gene whose mutations are associate
48                                      In this experimental model, Acute Respiratory Distress Syndrome
49            To address this, we have used two experimental models, administering alpha-naphtylisocyana
50                  As cmo disease in mice, the experimental model analogous to human CRMO, is mediated
51                     We relied on a wild boar experimental model, analysing 24 wild-born specimens rai
52                        Thus, we establish an experimental model and use genetic, thermogenetic, and l
53              By employing a simple coculture experimental model and using single-molecule imaging, we
54 plex electrophysiology datasets from diverse experimental models and acquisition modalities.
55 anti-BP180 IgE has been suggested in various experimental models and by the successful use of omalizu
56 ion of HDAC6 improved established PAH in two experimental models and can be safely given in combinati
57  interference with tumor detection; however, experimental models and clinical studies have shown a co
58                     Innovative research with experimental models and exploitation of the geographical
59 nding off-target impacts of IL-2C regimes in experimental models and for considering how IL-2 may con
60 gated tagraxofusp resistance in patients and experimental models and found that it was not associated
61                                   We present experimental models and human data that support the conc
62 ecular mediator of plexiform lesions in both experimental models and human disease.
63 developed to narrow the gap between in vitro experimental models and human pathophysiology.
64 uantify occurrence of extracellular traps in experimental models and human samples.
65                                   Studies in experimental models and humans have identified 9 highly
66                                   Studies in experimental models and humans showed that the major fun
67 atient data and advances in imaging methods, experimental models and multiomics-generated big data.
68                        Based on data in both experimental models and patient samples, NUP98 fusion on
69 emain elusive due to the lack of appropriate experimental models and precise molecular mechanisms.
70 ntify knowledge gaps, appraise the available experimental models and propose future directions for th
71                                              Experimental models and retrospective studies have sugge
72 as a theoretical framework to bridge between experimental models and scales, with the aim of separati
73 tudies in humans and genetically manipulated experimental models and that exploit awareness of the lo
74 d in human thyroid cancer and thyroid cancer experimental models and their effects on Pax8 and Bcl2 w
75 tation of research data generated in various experimental models and to promote cross-disciplinary co
76 rular endothelial cells (MGECs) were used as experimental models, and GYY4137 as H2S donor.
77 f infection has been hampered by the lack of experimental models, and until now, a mouse roseolovirus
78 es that the ferret is a potentially valuable experimental model animal for understanding the evolutio
79  also highlights the strengths of a combined experimental-modeling approach to unambiguously understa
80                   Here, we present a coupled experimental/modeling approach to establish an in vitro
81  expression in single cells using a combined experimental/modeling approach.
82    In this review, we will discuss how these experimental models are carving a way for understanding
83 , which result in high rates of lethality in experimental models, are thought to include multicellula
84               Interference with autophagy in experimental models, but also during the pathological va
85         These findings were confirmed in the experimental model by showing that only CMR-MaR values f
86                                              Experimental models carrying these mutations facilitate
87                              Through such an experimental-modeling cycle, we predict how the auxin mi
88     Indeed, planarian flatworms were used as experimental models decades before Caenorhabditis elegan
89                         We then developed an experimental model demonstrating that holoHC is transpor
90                                           In experimental models, diffuse axonal injury triggers post
91                                           In experimental models, dry eye disease is associated with
92  are difficult to observe due to the lack of experimental models easily combined with theoretical mod
93             Here we demonstrate that a novel experimental model employing thermoneutral housing, as o
94 e maximum modulatory effects observed in all experimental models evaluated in this study.
95  (BPA) is known to be biologically active in experimental models even at low levels of exposure.
96                                      In both experimental models, Fam20C becomes overactive when asso
97  This study evaluated cardiac function in an experimental model following exposure to e-cigarettes.
98 astoid cell lines (LCLs), which represent an experimental model for EBV-associated cancers.
99              The metal complex can act as an experimental model for graphene-supported nickel single-
100 ing that CREM transgenic mice are a valuable experimental model for human AF pathophysiology.
101 metic co-culture systems provide a promising experimental model for investigating the functional role
102 cted to oxygen-glucose deprivation (OGD), as experimental model for ischemic conditions, were treated
103 onhuman primates currently serve as the best experimental model for Lyme disease because of their clo
104 Cs) in the Drosophila ovary are an important experimental model for the study of epithelial stem cell
105         The crab Neohelice is an established experimental model for the study of neurons involved in
106 inogeniculate synapse, has become a powerful experimental model for understanding how circuits in the
107                   In particular, the lack of experimental models for a process that largely occurs du
108                                              Experimental modeling further suggests that upfront dual
109                                           In experimental models, growth factor stimulation and/or on
110                                              Experimental modeling has defined a cooperative role of
111 xtensively studied, but the absence of valid experimental models has hampered our understanding of th
112                        Evidence, mostly from experimental models, has accumulated, indicating that mo
113                                        While experimental models have been used to investigate some m
114 dge of their driving defects and the lack of experimental models have impaired clinical successes.
115                                    Using our experimental model, impact of adaptive immunity on S. au
116 ll as for numerous application, e.g. for the experimental modelling in a lab of natural processes.
117                                              Experimental models in mice and human epithelial cells s
118                                 Canonically, experimental models in mice have been designed to ascert
119 in modulation of vascular function and BP in experimental models in vivo and in humans.
120 ultiple developmental contexts, the range of experimental models in which each of the steps can be ex
121            We combined these approaches with experimental models in which gck was genetically deleted
122 tegration of epidemiology-based data with an experimental model increases the evidence that prenatal
123 n to occur in response to Plasmodium spp. in experimental model infections, and in human malaria.
124                                As such, this experimental model may be adopted to examine vicarious s
125  better understanding of EV-D68 infection in experimental models may allow for better prevention and
126 gh eNOS derangement has been demonstrated in experimental models, no studies have directly shown that
127 ture represents, to our knowledge, the first experimental model of a G-protein-coupled receptor-G-pro
128                                   We used an experimental model of ACD (ie, contact hypersensitivity
129 l to their medication can be explained in an experimental model of acetylcholine receptor deficiency,
130                                        In an experimental model of acquired epilepsy, we show that pr
131 the renoprotective effects of puerarin in an experimental model of advanced DN and provide a molecula
132                                     Using an experimental model of ALK positive NSCLC, we explored th
133 ut genetic and environmental confounders, an experimental model of allergic asthma in mice was used.
134                                      In this experimental model of allergic asthma, matched bronchoal
135 h epicardial remodeling was reproduced in an experimental model of atrial cardiomyopathy in rat and i
136                                        In an experimental model of cardiac fibrosis, cardiac pressure
137 sults show that the bile duct ligation (BDL) experimental model of cholestasis leads to rapid and sig
138                Due to the lack of a standard experimental model of coincident disease, the underlying
139 rrelated with increased susceptibility to an experimental model of colitis.
140 med in vivo two-photon calcium imaging in an experimental model of Dravet syndrome (Scn1a+/- mice)-a
141                                     Using an experimental model of elevated hematocrit in healthy mic
142 eractions by water-soluble CORM-401 using an experimental model of endotoxemia in vitro.
143 TMEV) infection induces a well-characterized experimental model of epilepsy in C57BL/6 mice.
144                   To guide investigation, an experimental model of genital tract infection has been d
145                                           An experimental model of glaucoma has been established by e
146  importance of the IL-6-STAT3 pathway in our experimental model of group 2 PH and human patients.
147          Collectively, these data provide an experimental model of how NPCs can facilitate fast passa
148                 They also introduce a robust experimental model of human leukemogenesis to further el
149 1 mutations in patient samples as well as an experimental model of inducible expression.
150                                        In an experimental model of inflammatory lung injury, deletion
151 nteraction between sex and weight gain in an experimental model of lung allergic inflammation induced
152 e ability for early metastatic seeding in an experimental model of lung metastasis, indicating that h
153 ung squamous cell carcinoma (LSCC) and in an experimental model of lung TLS induction.
154 patients, a finding that we confirmed in the experimental model of lung TLS induction.
155 hese observations has been extended using an experimental model of multiple sclerosis [experimental a
156 al of the generated cells was assessed in an experimental model of myocardial infarction.
157 his question, we developed a virtual reality experimental model of neighborhood disadvantage and affl
158 uction, and airway hyperresponsiveness in an experimental model of OVA-induced asthma.
159                              We show that an experimental model of PI in mice can promote lymph node
160 Ts and EVTs in vitro thereby establishing an experimental model of primate placentation.
161 78 drive TF-mediated tumor progression in an experimental model of prostate cancer.
162 proarthritogenic, bone erosive pathway in an experimental model of RA.
163 a survival advantage to photoreceptors in an experimental model of retinal detachment.
164              These findings describe a novel experimental model of severe PH that provides insight in
165 ve undergone partial nephrectomy serve as an experimental model of uremic cardiomyopathy.
166 n and establish a proof of principle whereby experimental modelling of a disorder can help mechanisti
167                                              Experimental modelling of the pathogenic human mutations
168  late phases of the inflammatory response in experimental models of acute and chronic renal IRI using
169                                              Experimental models of allergic disease, basic mechanism
170                                              Experimental models of allergic disease, basic mechanism
171                                              Experimental models of allergic disease, basic mechanism
172                         Incorporation of the experimental models of and psi into the backbone of an o
173                                   Studies in experimental models of anti-MPO GN suggest that, after A
174 erimental Psychopathology approach, based on experimental models of anxiety in healthy subjects, can
175                           Recent advances in experimental models of anxiety in humans, such as threat
176 downstream messengers of the AC-cAMP axis in experimental models of ARDS.
177 t that IL-17a promotes behavioral changes in experimental models of autism and aggregation behavior i
178 tion, and inhibits inflammation in different experimental models of autoimmune diseases.
179 o reverse or slowdown disease progression in experimental models of autoimmune encephalomyelitis-, SO
180 ffect of the human ILT3.Fc protein in murine experimental models of autoimmunity and cancer.
181                                        Thus, experimental models of BDV infection may provide new too
182      GHRH and its receptors are expressed in experimental models of BPH, in which antagonists of GHRH
183                              Here, using two experimental models of breast cancer, we reinforced the
184  energetic metabolism, was found elevated in experimental models of cancer, starvation, diabetes, and
185 ity and how their functions are regulated in experimental models of cancer.
186 mprove myocardial remodeling and function in experimental models of cardiovascular disease.
187  catheter-induced clotting assays and rabbit experimental models of catheter occlusion and arterioven
188 he known neuroreparative actions of IL-33 in experimental models of central nervous system (CNS) inju
189 om patients with cholestatic disease, in two experimental models of cholestasis, as well as in human
190 s in hippocampal and neocortical circuits in experimental models of chronic temporal lobe epilepsy.
191 ced expression of noncanonical WNT-5A in two experimental models of COPD and increased posttranslatio
192                                           In experimental models of diabetes, phenyl sulfate administ
193 n may confound understanding alloimmunity in experimental models of diabetes.
194 dpoints, provide quantitative endorsement of experimental models of disease, and could be incorporate
195                                   In in vivo experimental models of disseminated candidiasis, C. auri
196 ficial effects of GLP-1R analogs reported in experimental models of DR.
197                                              Experimental models of dys-/demyelination are characteri
198 hown to suppress seizures both in humans and experimental models of epilepsy.
199 cessary and sufficient to drive tauopathy in experimental models of familial AD.
200 ms of pathology, both clinically and in many experimental models of FGR, impaired uteroplacental vasc
201 s were also tumorigenic and prometastatic in experimental models of HCC, and eight of these mapped to
202                                       We use experimental models of house dust mite- or ovalbumin-ind
203 , the use of Nox1(-/-) and Nox1(+/+) mice as experimental models of human responses demonstrated a cr
204 e 2 diabetes (T2D), and cognitive decline in experimental models of IH patterned after O2 profiles se
205 Here, we used theoretical considerations and experimental models of immune responses in vitro and in
206 and conditionally delete C5aR2 expression in experimental models of inflammation.
207  and conditionally delete C3aR expression in experimental models of inflammation.
208 haracterized T(RM) cells in human IBD and in experimental models of intestinal inflammation.
209                                              Experimental models of malaria have shown that infection
210 ned cell lines constitute a resource of live experimental models of mutational processes, which poten
211 icacy of mitochondrial-targeted therapies in experimental models of neurodegenerative disease and CNS
212 and anti-inflammatory properties in numerous experimental models of neuroinflammation.
213 d neurorestorative effects across a range of experimental models of neuronal degeneration, and, recen
214                                       In two experimental models of PAH (i.e., monocrotaline and Su54
215 ation, oxidative damage, and fibrosis in the experimental models of PAH and lung fibrosis.
216 deleted mice and their WT littermates in two experimental models of pancreatitis.
217 t on alphaSyn misfolding and transmission in experimental models of Parkinson's disease.
218 tion and evidence of immune dysregulation in experimental models of PD.
219  strategy for pulmonary hypertension (PH) in experimental models of PH.
220  is frequently targeted by autoantibodies in experimental models of prostatic autoimmunity.
221 inical features, termed the "PTEN-opathies." Experimental models of PTEN pathway disruption uncover t
222 eutic potential for lung regeneration in two experimental models of pulmonary fibrosis.
223     Intricate lineage-tracing strategies and experimental models of regenerative stress have revealed
224 arians, flatworms from order Tricladida, are experimental models of stem cell biology and tissue rege
225                                              Experimental models of the human brain are needed for ba
226  antithrombotic effects of such nutrients in experimental models of thrombosis or analyzed biomarkers
227                                              Experimental models of thrombotic stroke induced by eith
228 ased BKIs are effective in acute and chronic experimental models of toxoplasmosis.
229                                           In experimental models of tumor progression and metastasis,
230                      Their beneficial use in experimental models of ulcerative colitis and lung allog
231                    We emphasize the need for experimental models of wound healing that better approxi
232 the success of a few wild tobacco species as experimental model organisms have resulted in growing kn
233                                     Using an experimental model, permitting exposure of developing bl
234                                     Based on experimental models, polyamine concentrations may be als
235 otein synthesis and breakdown with two basic experimental models, primed-dose continuous tracer infus
236              Development of population-based experimental models provide a potential approach to fill
237                     In a normotensive animal experimental model, reducing Na(+) intake for 2 weeks in
238 80s, avoidance had fallen out of favor as an experimental model relevant to fear and anxiety.
239                         Drug combinations in experimental models restore crenolanib sensitivity.
240 iled assessments of tumor growth in subtyped experimental models revealed that a highly invasive grow
241 chedules within the STAR Methods section and Experimental Models section of the Key Resource Table.
242                  On the basis of a number of experimental models, several alternative cell types have
243                                              Experimental models show that the brain monoaminergic sy
244                       In stable patients and experimental models, statins favor the elevation of glyc
245                                         This experimental-modeling study suggests that (1) inner-ear
246       Recent studies using human samples and experimental modeling suggest that glutathione redox met
247 e events have been unsuccessful; findings in experimental models suggest that CD8+ T cells drive dise
248               These patterns observed in our experimental models suggest that iron exerts its effects
249 silicon photoanodes and photocathodes as the experimental model system and described a systematic ana
250 this study, we developed a computational and experimental model system to address this challenge and
251                          Here, we develop an experimental model system using in vitro lineage tracing
252  by taking advantage of a well-characterized experimental model system, in which auxotrophic genotype
253 on has allowed for a wide range of different experimental model systems designed to explore different
254                                              Experimental model systems have been instrumental in rap
255 alysis of multiple samples, or for non-human experimental model systems with no reliable databases of
256  atomistic interpretation of the behavior of experimental model systems, such as the degree of lipid
257 iciently high yields to be routinely used as experimental model systems.
258   Thus, ALX receptor deficiency serves as an experimental model that defines multiple cellular and mo
259 e sulfonic acid (DNBS)-induced colitis is an experimental model that mimics Crohn's disease.
260 te how ZIKV leads to microcephaly in a novel experimental model that mimics early brain development.
261                             Here, we used an experimental model that reproduces olanzapine-induced hy
262 ephalomyelitis in nonobese diabetic mice, an experimental model that resembles several aspects of SPM
263 he bioaccessibility of polyphenols, using an experimental model that simulates human gastrointestinal
264 umans to mosquitoes, and have established an experimental model that will accelerate the development
265 ogression, which requires the development of experimental models that aid better deconstruction of th
266 oals in mind, we discuss the need to develop experimental models that better capture the contexts tha
267 nologies to better target ILC2s and engaging experimental models that better manifest both acute infe
268  the appearance of any disease symptoms, yet experimental models that can be used to examine clonal a
269                       However, the number of experimental models that can be used to explore collecti
270 gates in purified properdin preparations and experimental models that do not allow discrimination bet
271 coring the importance of developing improved experimental models that holistically encompass the meta
272 ytosing RPE cells, utilizing three different experimental models: the human-derived RPE-like cell lin
273       However, due to the lack of accessible experimental models, their functional properties and the
274            Given Oncopeltus's strength as an experimental model, these new sequence resources bolster
275                                              Experimental models thus highlight dual effects of sepsi
276                        We developed a murine experimental model to facilitate the study of IDV pathog
277     This organoid culture system provides an experimental model to investigate human placental develo
278  in the bee gut and that holds promise as an experimental model to study bacteria-phage dynamics in n
279  enabled by ODC1 interference provides a new experimental model to study mechanisms and consequences
280   This novel cell culture system provides an experimental model to understand how telomerase is regul
281 n in mice provides an efficient cause-effect experimental model to understand the mechanisms of direc
282 cific populations, and how we have developed experimental models to decipher the interactions between
283 hythmic strategy warrants further testing in experimental models to evaluate its clinical potential.
284 y in multiple clinical contexts, and we used experimental models to identify mechanisms by which suPA
285 on are incompletely understood, with limited experimental models to investigate the mechanisms drivin
286                                           In experimental models, treatment of old donor animals with
287     In vitro cancer cell cultures are facile experimental models used widely for research and drug de
288 theter mitral valve replacement system in an experimental model was feasible and safe.
289 w how information from related and unrelated experimental models was translated to a clinical setting
290                                          The experimental model we describe provides a system to furt
291 ription polymerase of T7 bacteriophage as an experimental model, we identify hundreds of new replicat
292 ia isolated from an HIV/AIDS patient, as our experimental model, we show that the proteins are ATP an
293 veloping a classification system tailored to experimental models, we have uncovered subtype-specific
294                         We have developed an experimental model where genetically identical, co-house
295                                   Our unique experimental model which incorporates genetic effect, na
296 major obstacle is the lack of an appropriate experimental model which incorporates genetic susceptibi
297 n the ability to reproduce already existing 'experimental models', which in turn, have an unclear acc
298            Further investigation in relevant experimental models will elucidate the mechanisms by whi
299              Here, using the epidermis as an experimental model with the RNA sequencing approach, we
300                           In pregnant sheep, experimental models with a small, defective placenta tha

 
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