ライフサイエンスコーパス: exaggerate

1 e of IM in timing and quality, were never as exaggerated.

2 A2;1, the hyponastic growth response becomes exaggerated.

3 fects on low-status or low-performing groups exaggerated?

4 the 45-55 Hz activity, the amplitude of the exaggerated 29-36 Hz rhythm in the STN was modulated by

5 Pain perception temporarily exaggerates abrupt thermal stimulus changes revealing a

6 gly, ChREBP-dependent effects were due to an exaggerated activation of the proapoptotic arms of the e

7 1 and M2 NK-cell subsets in association with exaggerated activation, apoptosis, and autophagy.

8 e their innate immune properties to limit an exaggerated adaptive immune response.

9 that APOL1 risk alleles are associated with exaggerated age-related nephron loss, probably decaying

10 ung DCs, and blockade of Ccl24 prevented the exaggerated airway eosinophilia and lung inflammation in

11 This bias was exaggerated among individuals with a more anxious dispos

12 Studies suggest that exaggerated amygdala reactivity is a vulnerability facto

13 esvirus-driven germinal center expansion was exaggerated and lost its transient nature in the absence

14 bstrate and Akt phosphorylation demonstrated exaggerated and more rapid HFD-induced insulin resistanc

15 In contrast, young infants display exaggerated and uncoordinated limb reflexes [2].

16 is a term that has been used to describe the exaggerated and unrealistic fear of fever expressed by p

17 t IL-18 production from monocytes is greatly exaggerated, and depletion of monocytes in vivo prevents

18 antages of nanoformulations were drastically exaggerated, and the assumptions used in nanomedicine an

19 An exaggerated anti-incretin effect could contribute to ins

20 Exaggerated antibody responses in mice depleted of CD301

21 vocal tract and laryngeal allometry thereby exaggerating apparent body size.

22 creasing microtubule depolymerization causes exaggerated asymmetric spindle positioning.

23 ow brain volumes observed in VPT infants are exaggerated at 7 years.

24 n response to nitrate as ckx3 phenotypes are exaggerated at increased nitrate levels.

25 Loss of NUB1L exaggerated atypical neddylation, whereas NUB1L overexpr

26 Thirty-seven percent admitted to sometimes exaggerating Banff i in the presence of tubulitis, to re

27 CF AMs exhibited exaggerated basal and LPS-induced production of tumor ne

28 Exaggerated basal ganglia beta activity (13-35 Hz) is co

29 a to an immune challenge, thereby preventing exaggerated behavioral and neuroinflammatory responses f

30 tor deficits correlate with the emergence of exaggerated beta frequency (15-30 Hz) oscillations throu

31 lso particularly prone to being recruited to exaggerated beta oscillations.

32 l medial thalamus in the propagation of this exaggerated beta range oscillatory activity and the sequ

33 evalent during SWA partly generalized to the exaggerated beta-frequency (15-30 Hz) oscillations arisi

34 onic subjects, trigger sounds elicit greatly exaggerated blood-oxygen-level-dependent (BOLD) response

35 for males to lower frequency components and exaggerate body size in reproductive contexts, this hypo

36 acidic protein-expressing astrocytes induced exaggerated body weight gain and glucose intolerance in

37 In conclusion, young adults who show exaggerated brain processing underlying whether to 'stop

38 inhibitor into murine airways abrogated the exaggerated bronchoconstriction induced by allergen sens

39 These changes were exaggerated by anti-Tie2 antibody, inhibition of PI3K si

40 These mechanisms are exaggerated by chronic stress exposure, where architectu

41 g tympanoplasty, which appears to be further exaggerated by corticosteroids.

42 action, but this mechanism may be altered or exaggerated by disease states.

43 impairment of protein translation, which was exaggerated by drug treatment.

44 his anatomical difference in DA signaling is exaggerated by intravenous infusion of cocaine.

45 that a small fraction of peroxisomal Pex15, exaggerated by overexpression, is turned over by Msp1.

46 arison with open repair, which may have been exaggerated by patient selection.

47 a conformational change of the motor domain exaggerated by the lever arm.

48 Patients with stable asthma exhibited exaggerated capsaicin-evoked cough responses consistent

49 abin-deficient (Carabin(-/-)) mice developed exaggerated cardiac hypertrophy and displayed a strong d

50 Sirt2 knockout markedly exaggerated cardiac hypertrophy and fibrosis and decreas

51 ely 50% increase in cardiomyocyte number and exaggerated cardiac hypertrophy, as indicated by increas

52 ges interacts in pressure wave transmission, exaggerates cardiac, brain and kidney damage, and lead t

53 rome, group I mGluR-activated translation is exaggerated causing enhanced seizure propensity.

54 Exaggerated CD4(+) T helper 2-specific cytokine producin

55 D patients and siblings that manifests in an exaggerated CD4(+)Tem response and shutdown by apoptosis

56 studies are required to understand how this exaggerated CD4(+)Tem response fits within the pathomech

57 tial for preventing loss of Paneth cells and exaggerated cell death in animal models of virally trigg

58 broad LP region and display correspondingly exaggerated centripetal flow.

59 ated by reduced elevations in heart rate and exaggerated changes in femoral vascular conductance and

60 ulation of IL-17-induced gene expression and exaggerated chemokine production in vitro and overt psor

61 primed in the degenerating brain to produce exaggerated chemokine responses to acute stimulation wit

62 d cell function in disease may be related to exaggerated chemotactic responses.

63 to inhibit epithelial apoptosis but exhibit exaggerated CHI3L1-driven fibroproliferation, which toge

64 ccumulation, photoreceptor degeneration, and exaggerated choroidal neovascularization similar to AMD.

65 Exaggerated claims about inaccuracy and downplaying vera

66 It is, therefore, of concern that exaggerated claims about side-effect rates with statin t

67 unter the adverse effect on public health of exaggerated claims about statin-related side-effects.

68 ulfate (DSS), Tfeb (DeltaIEC) mice exhibited exaggerated colitis.

69 and/or improved insulin sensitivity, with an exaggerated counter-regulatory response for glucagon sec

70 his manifests in brain surface recordings as exaggerated coupling between the phase of the beta rhyth

71 Exaggerated cranial structures such as crests and horns,

72 ging and discusses the mechanisms underlying exaggerated CVD and aging induced by prelamin A and prog

73 l-like receptor agonists, such as LPS, drive exaggerated cytokine responses on this background.

74 y C. rodentium, prolonged pathogen shedding, exaggerated cytokine responses, and greater tissue injur

75 tors of flg22-induced genes often to prevent exaggerated defense responses.

76 Exaggerated dendritic protein synthesis resulting from l

77 -state response levels, but the latter shows exaggerated depression.

78 Mice lacking adiponectin mounted an exaggerated dermal fibrotic response, while transgenic m

79 ke, and energy expenditure but results in an exaggerated diabetic phenotype when challenged with a hi

80 was not protective, and was associated with exaggerated disuse-induced cancellous bone loss.

81 a may demonstrate phenotypes consistent with exaggerated dopaminergic signaling, including alteration

82 e the function of these structures, using an exaggerated dorsal fin to generate lift by swimming roll

83 he colon and its ablation in mice results in exaggerated DSS-induced colitis and disruption of epithe

84 Finally, exaggerated emotional memory and BLA synaptic plasticity

85 Exaggerated endothelial activation, altered blood flow,

86 Our results show that TRPC4 underlies an exaggerated endothelial permeability response in PAH.

87 e conditionally deficient in Muc5b displayed exaggerated eosinophilic inflammation in response to int

88 a severe asthma subtype, is characterized by exaggerated eosinophilic respiratory inflammation and re

89 ents with severe eosinophilic asthma have an exaggerated eosinophilopoeitic process in their airways.

90 at reactive oxygen species (ROS) mediate the exaggerated EPR associated with PAD.

91 with peripheral artery disease (PAD) show an exaggerated EPR, sometimes report pain when walking and

92 in mutant iPSC-derived cardiomyocytes showed exaggerated ER stress induced CHOP and apoptotic signatu

93 del for peripheral artery disease, causes an exaggerated exercise pressor reflex in response to muscl

94 We found that exaggerated expression of DCC and reduced levels of miR-

95 By contrast, exaggerated expression of mst reduced intestine diameter

96 c stress disorder (PTSD) is characterized by exaggerated fear expression and impaired fear extinction

97 ockade of CXCL12 with AMD3100 attenuated the exaggerated fibrosis observed in Twist1-null mice.

98 on result in an ataxic gait characterized by exaggerated flexion movements and marked alterations to

99 reflex' (CSAR) critically contributes to the exaggerated global sympathetic tone in chronic heart fai

100 Despite the markedly exaggerated GLP-1 response after RYGB, changes in postpr

101 nstrated increased glucose effectiveness and exaggerated glycosuria relative to wild-type littermate

102 All four PTHS mouse models demonstrated exaggerated hippocampal long-term potentiation (LTP), co

103 Although exaggerated host immune responses have been implicated i

104 d exposure is mediated in part by initiating exaggerated host innate immune responses.

105 Here we investigate whether exaggerated HPA axis responses associated with chronic v

106 The T-DNA insertion mutant of MSRB8 exaggerates HR-associated and UV-induced cell death and

107 hy and fibrosis following MI, accompanied by exaggerated HSPC activity and impaired macrophage phenot

108 rogen-excess pregnancies (P = 0.045), and an exaggerated, hyperinsulinaemic response to glucose chall

109 apability to promote cell growth and thereby exaggerating hyperoxia-induced lung epithelial cell deat

110 ng Index (RI) that was designed to detect an exaggerated hypertrophic response to hypertension and te

111 d cardiac elevation of GRK5 in mice leads to exaggerated hypertrophy and early heart failure after tr

112 Arabidopsis (Arabidopsis thaliana) line with exaggerated hyponasty.

113 Codon re-engineering of dosR exaggerates hypoxia-induced changes in codon-biased DosR

114 normal responses to hypoxia, as evidenced by exaggerated hypoxic pulmonary hypertension that is rever

115 with history of EH, viral signals induce an exaggerated IDO1 expression and activity.

116 w levels of bacterial LPS, giving rise to an exaggerated IL-1beta response.

117 that filarial infection induces Ag-specific, exaggerated IL-4 responses in distinct T cell memory com

118 Peripheral immune stimuli cause exaggerated immune responses in the aged brain, which li

119 me (WAS) often suffer from poorly understood exaggerated immune responses that result in autoimmunity

120 Aim2(-/-) mice showed similarly exaggerated immune responses to IAV.

121 ulation with typically rare fungi results in exaggerated immune responses, suggesting that fungal col

122 is amplified Tem phenotype also exhibited an exaggerated immune shutdown with heightened sensitivity

123 As an adaptive response to this exaggerated immune state, affected tissue typically deve

124 (RSV) infection, and its inhibition leads to exaggerated immunopathology.

125 ereby wearing hospital pyjamas results in an exaggerated impression of severity).

126 buminuric effects are preserved, and perhaps exaggerated in chronic kidney disease.

127 zed network oscillations that are abnormally exaggerated in cortical-basal ganglia circuits in parkin

128 vity, locomotor activity and stereotypy were exaggerated in DRD mice in response to the D1-dopamine r

129 l-dependent spatial learning and memory were exaggerated in E4 mice.

130 vasculature is not only preserved, but also exaggerated in hypertension.

131 l-mediated bronchoconstriction is presumably exaggerated in patients with aspirin-exacerbated respira

132 e compared with alteplase, benefits possibly exaggerated in patients with baseline computed tomograph

133 t mechanism] that regulate startle, which is exaggerated in PTSD.

134 er during winter, and these differences were exaggerated in smaller lakes.

135 These effects are exaggerated in spontaneously hypertensive rats (SHRs), r

136 LR11 plays an energy conserving role that is exaggerated in states of obesity.

137 These findings were exaggerated in Tecta(C1509G/C1509G) mice, where the tect

138 ent and inflammatory factors, which are most exaggerated in the ARMS2/HTRA1 lines.

139 terminal branching and neurotransmission was exaggerated in the Col13a1tm/tm mice, the transmembrane

140 impaired in ECSHIP2(Delta/+) mice, which was exaggerated in the presence of a superoxide dismutase/ca

141 sulted in increased RGC apoptosis, which was exaggerated in the presence of CXCL10.

142 This trend is exaggerated in unresectable, locally invasive or metasta

143 circuits that is caused by a combination of exaggerated incentive salience and habit formation, rewa

144 r MI through defective mitophagy, associated exaggerated inflammasome activation, cell death, and IL-

145 ded activation raises the risk of developing exaggerated inflammation and autoimmunity.

146 her system may lead-often synergistically-to exaggerated inflammation and host tissue injury.

147 trated increased intestinal permeability and exaggerated inflammation during dextran sodium sulfate-i

148 immune deficiency states, and modulation of exaggerated inflammation in autoinflammatory diseases.

149 es support the contribution of dysregulated, exaggerated inflammation in scar formation.

150 lung disease is characterized by chronic and exaggerated inflammation in the airways.

151 xisting diabetes by a mechanism unrelated to exaggerated inflammation or coagulation.

152 ay a beneficial role in sepsis by mitigating exaggerated inflammation through a novel mechanism.

153 (-/-)) C57BL/6 mice had intact ear swelling, exaggerated inflammation, and higher levels of dinitrofl

154 en the microbiota and the host, resulting in exaggerated inflammation.

155 tested the hypothesis that ANX-A1-deficiency exaggerates inflammation, haematopoietic stem progenitor

156 uperoxide dismutase mimetic, ameliorated the exaggerated inflammatory response and prevented developm

157 aling (34% on day 4) but did not resolve the exaggerated inflammatory response in HO-2(-/-) mice.

158 nstrates that BMPR-II deficiency promotes an exaggerated inflammatory response in vitro and in vivo,

159 anced nuclear factor-kappaB signaling and an exaggerated inflammatory response on stimulation with li

160 ngtin, whereby basal dysfunction leads to an exaggerated inflammatory response once a stimulus is enc

161 nt mice display a counterintuitive transient exaggerated inflammatory response to cutaneous and perit

162 iency in uterine GR signaling resulted in an exaggerated inflammatory response to induced decidualiza

163 myeloid-specific loss of Phd2 resulted in an exaggerated inflammatory response to Streptococcus pneum

164 layed impaired efferocytosis associated with exaggerated inflammatory response, poor angiogenesis, an

165 collateral damage to the lungs because of an exaggerated inflammatory response.

166 dary infection in the aged are not due to an exaggerated inflammatory response.

167 Exaggerated inflammatory responses dictated by persisten

168 Exaggerated inflammatory responses during influenza A vi

169 addition, knocking ADAR1 down in hepatocytes exaggerates inflammatory signaling to dsRNA or endotoxin

170 The exaggerated influence of the medial prefrontal cortex on

171 In HNF-4gamma knockout mice, we detect an exaggerated insulin peak and improvement in glucose tole

172 ontent, impaired somatostatin secretion, and exaggerated insulin release, and that these defects are

173 These findings suggest that an exaggerated interferon response to viral infection by ai

174 ting transcription factor 4 (Atf4) showed an exaggerated ISR and greater loss of endogenous hydrogen

175 Roquin-1/2-deficient NKT17 cells show exaggerated lineage-specific expression of nearly all NK

176 Stat5 in CD11c(+) cells was associated with exaggerated LPS-induced inflammatory responses and vascu

177 of Elk1 causes enhanced Itgb6 expression and exaggerated lung fibrosis in an in vivo model of fibrosi

178 We further showed that AM pyroptosis exaggerates lung inflammation.

179 ly different between groups with and without exaggerated LV after LPI.

180 Deletion of Nox4 rescued the exaggerated LV remodeling in FYN-deficient mice.

181 Exaggerated LV, defined as LV greater than one-third of

182 of these findings, we suggest that tics are exaggerated, maladaptive, and persistent motor habits re

183 inhibition in coelomocytes may represent an exaggerated manifestation of the elongate mother filamen

184 that LC degeneration in Ts65Dn mice leads to exaggerated memory loss and neuronal degeneration.

185 resulting in liver tumorigenesis through an exaggerated mesenchymal phenotype with prominent Twist1-

186 model (Fmr1(-/y)) hippocampus, which exhibit exaggerated mGlu1/5-induced long-term synaptic depressio

187 -/y), including excessive protein synthesis, exaggerated mGluR-LTD, and audiogenic seizures.

188 ice lacking Mef2C in microglia results in an exaggerated microglial response and has an adverse effec

189 iable reduced anterior prefrontal cortex and exaggerated midbrain engagement occurred in unaffected s

190 Moreover, Tregs with exaggerated miR-27-mediated gene regulation exhibited di

191 the head, both demonstrating the presence of exaggerated morphogenesis early among stem-group ants.

192 ions that mitigate any costs associated with exaggerated morphology are central in the evolution of s

193 Using a novel assay, we discovered exaggerated motor responses to whisker stimulation in yo

194 with aberrant storage material organized as exaggerated multilamellar whorls, striated belts and 'fi

195 rolled attention tasks, but they demonstrate exaggerated neural responses in order to do so, which ma

196 e (FXS), which is considered to be caused by exaggerated neuronal translation and is the most frequen

197 ild-type or p110delta(D910A) Tregs abrogated exaggerated neutrophil activity, increased neutrophil ap

198 Mice lacking PTX3 have exaggerated neutrophilic/eosinophilic lung inflammation,

199 isolated from HMGB-1-treated rats expressed exaggerated NLRP3 and proinflammatory cytokine expressio

200 The basal ganglia motor circuit exhibits exaggerated oscillatory and coherent activity patterns i

201 ls treated with IL-4 followed by ADMA showed exaggerated oxo-nitrative stress and potent induction of

202 ssive accumulation of sleep debt and also to exaggerated pain responses, both of which are rescued af

203 improved recovery of function by normalizing exaggerated perilesional alpha5-GABAAR-dependent tonic i

204 le increase in cardiac contractility with an exaggerated peripheral vasoconstriction in the CHF state

205 lity in isolated lungs, and found that TRPC4 exaggerated permeability responses to thapsigargin in Su

206 on permits the establishment of the markedly exaggerated, persistent elevation of the stress response

207 implemented in the treatment of infants with exaggerated physiologic and pathologic jaundice but adap

208 a moderate riluzole effect, and the risk for exaggerated placebo responses was mitigated.

209 We observed no exaggerated placental hypoxia or oxidative stress associ

210 Contributing factors appear to be exaggerated polycythemia and hypoxemia, and lower and sl

211 Industry funding of surgical trials leads to exaggerated positive reporting of outcomes.

212 Abdominal obesity and exaggerated postprandial lipemia are independent risk fa

213 ES demonstrated an exaggerated postprandial satiety gut hormone response th

214 After esophagectomy, patients demonstrate an exaggerated postprandial satiety gut hormone response, w

215 These dissociable reduced and exaggerated prefrontal and subcortical circuit functions

216 iron, a superoxide scavenger, attenuated the exaggerated pressor reflex and reduced reactive oxygen s

217 e oxygen species with respect to causing the exaggerated pressor response to contraction seen in rats

218 by TSP4 or peripheral nerve injury promotes exaggerated presynaptic excitatory input and evoked sens

219 ERFVII) RAP2.12, as rap2.12-1 seedlings show exaggerated primary root bending.

220 , clinicians are now describing infants with exaggerated primitive reflexes, epilepsy, acquired hydro

221 find that rats expressing G2019S LRRK2 have exaggerated pro-inflammatory responses and subsequent ne

222 portion of memory CD4 T cells in part due to exaggerated production of effector cytokines.

223 Moreover, obese VEGF(Deltamyel) mice exhibit exaggerated progression of cognitive decline and neuroin

224 This was accompanied by an exaggerated proinflammatory cytokine profile and increas

225 regnant women, monocytes and pDCs exhibit an exaggerated proinflammatory immune response to 2 strains

226 tes the innate immune response, producing an exaggerated proinflammatory reaction to viral infection.

227 areful regulation during fetal life to avoid exaggerated proinflammatory responses.

228 modynamic signs of PH, which were related to exaggerated proliferation of pulmonary artery endothelia

229 le other conditions can occasionally produce exaggerated prolongation of the QT interval on the elect

230 e mRNA translational repressor FMRP leads to exaggerated protein synthesis downstream of metabotropic

231 iated phenotypes in FXS model mice including exaggerated protein synthesis, inappropriate social beha

232 g enzyme SMP30 in C57/BL6J-betaENaC-Tg mice, exaggerated pulmonary phenotypes.

233 increased ammonia production as a result of exaggerated purine degradation.

234 n (BV) IXbeta tetrapyrrole(s) and results in exaggerated reactive oxygen species accumulation as a pu

235 Furthermore, Klf3-/- mice displayed exaggerated recovery from anemic stress and persistent c

236 pulmonary ECs from iPAH, contributing to an exaggerated recruitment of peripheral blood mononuclear

237 eft ventricular wall thickness of >/=1.0 cm, exaggerated reduction in E/A, and lateral e' of <14 cm/s

238 Further studies in T cells with exaggerated regulation by individual members of the miR-

239 e that a combination of failed clearance and exaggerated release of glutamate by glial cells during i

240 he human COMT-Val gene (COMT-Val-tg) present exaggerated remote memories (>50 days) while having unal

241 anulomatous disease presumably reflecting an exaggerated response to an unknown antigen, celiac disea

242 Hyperalgesia is an exaggerated response to noxious stimuli produced by peri

243 Prdm16-deficient adipose displays an exaggerated response to type I IFN, including higher STA

244 Anxious subjects' exaggerated response to uncertainty leads to a suboptima

245 nhibition of their recruitment prevented the exaggerated response.

246 (large and bold individuals) showed the most exaggerated responses in several social measures.

247 with impaired TH17 cell differentiation and exaggerated responsiveness to type I and II interferons.

248 ISO treatment exaggerated ROS generation, p38 MAPK activation but down

249 assumption that paranoia is mainly due to an exaggerated sense of personalised threat and suggests in

250 Photosensitization, an exaggerated sensitivity to harmless light, occurs geneti

251 released from miR-223-KO MSCs significantly exaggerated sepsis-induced injury.

252 e linear scaling and can therefore invert or exaggerate sex and SCA effects on subcortical anatomy.

253 Here we review the evolutionary allometry of exaggerated sexual traits (for example, antlers, horns,

254 riments on peacocks and demonstrate that the exaggerated sexually selected train does not compromise

255 emoval of Siglec-E causes the development of exaggerated signs of aging at the molecular, structural,

256 We found that exaggerated skin inflammation was absent in DeltaLC x CX

257 yet significant reduction in baseline BP and exaggerated sodium sensitivity in mice.

258 Postprandial dysmetabolism-an exaggerated spike in triglycerides, glucose, and insulin

259 romotes PTSD, which has been associated with exaggerated startle and deficient sensorimotor gating.

260 a rare clinical syndrome characterized by an exaggerated startle in response to trivial tactile or ac

261 on, hyperekplexia, which is characterised by exaggerated startle reflexes, muscle hypertonia and apno

262 ysiological response magnitude and levels of exaggerated startle responses in daily life in PTSD part

263 yperphagia, impaired learning and memory and exaggerated startle responses.

264 ) trafficking, increased basal ER stress and exaggerated susceptibility to inducers of ER stress.

265 Lack of Jak3 also resulted in exaggerated symptoms of metabolic syndrome by western hi

266 Furthermore, movement leads to exaggerated synchronization in the low beta band specifi

267 n inhibitory loop in the basal ganglia yield exaggerated synchrony and locking to beta oscillations,

268 ine substitutions in the viral genome caused exaggerated syncytium formation, reduced VZV titers (-1.

269 Sepsis, an exaggerated systemic inflammatory response, remains a ma

270 clearance in blood, spleen, and liver and an exaggerated systemic inflammatory response.

271 ated that global deletion of Pdpn results in exaggerated T cell responses and spontaneous experimenta

272 It may also have implications in the exaggerated tactile sensations induced by recreational d

273 An uncontrolled exaggerated Th17 response can drive the onset of autoimm

274 cillator model of AI, the latter is found to exaggerate the antiaromaticity of true and potential 4n

275 ebs formed after axon transection, which may exaggerate the passive propagation of somatic depolariza

276 results from gain-of-function mutations that exaggerate the signal output of the fibroblast growth fa

277 the hypoxia-induced heart rate elevation and exaggerated the blood pressure decrease in response to h

278 estigated if weaning onto an obesogenic diet exaggerated the detrimental effects of maternal diet-ind

279 at satellite cell-specific deletion of Traf6 exaggerates the dystrophic phenotype in the mdx (a mouse

280 ng cochlear compression associated with SNHL exaggerates the perceived fluctuations in intensity in a

281 t weakening the interaction between G blocks exaggerates the resistance oscillations.

282 hronic hypercapnia in COPD patients does not exaggerate this response.

283 raumatic stress disorder is characterized by exaggerated threat response, and theoretical accounts to

284 Hz) oscillations that become pathologically exaggerated throughout basal ganglia circuits in parkins

285 bs' to act as keystone species may have been exaggerated to date.

286 ory pathways likely to underlie each type of exaggerated trait.

287 Many exaggerated traits represent an additional mechanical lo

288 Exaggerated traits, like the peacock train, are recogniz

289 We review insect examples of exaggerated traits, such as the mandibles of stag beetle

290 We found that this exaggerated transport of the human receptor is mediated

291 siological mechanisms that cause persistent, exaggerated, upper airway inflammation rather than acute

292 In order to identify a mechanism of the exaggerated uterine infection in HFD-fed atERalphaKO mic

293 Experimental evidence, including exaggerated ventilatory responses to CO2 and prolonged c

294 nts have high circulating viral loads and an exaggerated virus-induced immune response involving both

295 rritable bowel syndrome, are associated with exaggerated visceral nociceptive actions that may involv

296 nesia, but DA replacement therapy can elicit exaggerated voluntary and involuntary behaviors that hav

297 obesity-risk in FTO carriers and lead to an exaggerated weight gain over time.

298 tion and prevented enhanced inflammation and exaggerated weight loss.

299 th targeting unmodified cytosine are further exaggerated when deaminating mC.

300 s, Nf2 (Merlin) and WWC1 (Kibra), leading to exaggerated YAP function.