ライフサイエンスコーパス: be impaired

1 ng memory loads, like transcoding zeros, can be impaired.

2 l13a1tm/tm mice in which ectodomain shedding is impaired.

3 e presence is attenuated and mating behavior is impaired.

4 e skeletal muscle of obese Zucker rats (OZR) is impaired.

5 ly because Argonaute2-catalyzed mRNA slicing is impaired.

6 SBVDeltaNoLS toward RNA Pol II transcription is impaired.

7 lls, but activation of the TNFalpha promoter is impaired.

8 mation is severely reduced and CSR frequency is impaired.

9 sting that ubiquitin-proteasomal degradation is impaired.

10 etions of ARL13b in which ARL3-GTP formation is impaired.

11 ing that the flexibility of guard cell walls is impaired.

12 re unable to re-polarize, and rice infection is impaired.

13 the ratio is disrupted, the seed development is impaired.

14 requires ErbB4 receptors in PV interneurons, is impaired.

15 n occur, activation of COX1 mRNA translation is impaired.

16 absence, contraction of smooth muscle cells is impaired.

17 formation around secondarily encountered ACs is impaired.

18 rtance of FBXL5 for regulating IRP1 when CIA is impaired.

19 ased and subsequent development of symbiosis is impaired.

20 of LMO2, the target site recognition of TAL1 is impaired.

21 dNGI survival and spatial pattern separation are impaired.

22 t tasks such as attention and working memory are impaired.

23 and bone morphogenetic protein (BMP) signals are impaired.

24 nd odour-induced attractive social responses are impaired.

25 nses against oral antigen and gut commensals are impaired.

26 n mice, in which BDNF processing and release are impaired.

27 s on apoA-IV gene expression and food intake are impaired.

28 y modalities are impaired, but not when both are impaired.

29 the GTPase activity of the mutated proteins was impaired.

30 xazolo[5,4-c]pyridine-3-ol) relative to GABA was impaired.

31 tive phenotype observed after let-7 function was impaired.

32 is normally present in wounds, wound healing was impaired.

33 re inhibited, both early- and late-phase LTP was impaired.

34 that of moDCs, Ag processing by CXCL4-moDCs was impaired.

35 s, functional recovery of mice following SCI was impaired.

36 Atalmt12, sulfate-triggered stomatal closure was impaired.

37 and MMC-induced monoubiquitination of FANCD2 was impaired.

38 ental activation by insulin and shear stress was impaired.

39 R accumulation near single growing axon tips was impaired.

40 itro were diminished and replication in vivo was impaired.

41 cellular equivalent of learning and memory, was impaired.

42 of smooth muscle, renin, and mesangial cells were impaired.

43 epressing complex on DNA-bound NF-kappaB/AP1 were impaired.

44 ired during hospitalization, and 11% (n=174) were impaired 1 month after discharge.

45 evere liver injury, hepatocyte proliferation is impaired-a feature of human chronic liver disease.

46 he results demonstrate that B cell responses are impaired across human and mouse obesity models and s

47 alterations in cognitive processes known to be impaired across psychiatric conditions.

48 complex auditory processing deficits, which are impaired after injury.

49 These aspects of daily life are known to be impaired after extended wake, yet, the underlying neu

50 t-time evidence in humans that cBF integrity is impaired after premature birth and links neonatal com

51 n synthase-like protein, and mycelial growth is impaired after treatment with a chitin-synthase inhib

52 tion in the perivascular astrocytic end feet was impaired after TBI, which was most prominent in the

53 Growth and K(+) nutrition were impaired along with stomatal behaviour, membrane tr

54 s such as synaptic tagging and capture (STC) were impaired already in presymptomatic mice.

55 n which the anterior-/ mid- cingulate cortex is impaired and fails to support the needed inhibition,

56 Our data indicate that barrier function is impaired and the localization of vascular endothelial

57 Subsequently, M2 polarization was impaired and macrophages were unable to sufficiently

58 tion of prions on follicular dendritic cells was impaired and oral prion disease susceptibility was r

59 er the sympathetic skin response of the foot was impaired and sweat gland innervation was reduced.

60 y, TLS density was similar, but GC formation was impaired and the prognostic value of TLS density was

61 onstrate that placental growth and structure were impaired and associated with reduced growth of alph

62 cluding mitochondrial Ca(2+) uptake capacity are impaired, and an increased resting level of free int

63 in cells in denser matrices, where migration is impaired, and it decreases in cells in aligned collag

64 epitopes by dispersed islet cells to T cells was impaired, and (iii) the development of autoimmune di

65 ntiation of sorted LPS-stimulated MZ B cells was impaired, and aged bumble mice were unable to respon

66 s upon FDC in Peyer's patches and the spleen was impaired, and disease susceptibility significantly r

67 ysmorphic, beta-cell maturation and function were impaired, and animals lost islet mass.

68 Moreover, whether such dynamic coupling is impaired as a consequence of brain aging in later lif

69 CE STATEMENT In amblyopia, vision in one eye is impaired as a result of abnormal early visual experie

70 After the lesion, mistuning detection was impaired, as indicated by decreased d' values, a shi

71 BT-IgSF, the functional integrity of the BTB was impaired, as revealed by injection of a BTB-impermea

72 that (1) at rest, endothelial function would be impaired at high altitude compared to sea level, (2)

73 iciently in canine cells at 33 degrees C but is impaired at temperatures of 37 to 39 degrees C and wa

74 observed that many spermatogenesis features were impaired at 160 microg/ml CSC.

75 In addition, Ehmt1(+/-) knockout mice were impaired at fear extinction and novel- and spatial

76 rane excitability and AP-evoked Ca(2+) entry were impaired at synapses and (2) AP propagation was sev

77 CgA-to-CST conversion in HF is impaired because of hyperglycosylation, which is asso

78 s when visual or chemical sensory modalities are impaired, but not when both are impaired.

79 al tasks of spatial learning and memory that are impaired by isoflurane exposure.

80 These interactions are impaired by the pathogenic p.C774R mutation.

81 prising prediction that motion detection can be impaired by "invisible" noise, i.e. noise at a spatia

82 the physiological performance of trees might be impaired by climatic changes.

83 L-type channel-dependent LTP is known to be impaired by hyaluronic acid digestion.

84 rotein in neurons whose function is known to be impaired by mutant Htt.

85 tein, also known as "genome guardian", might be impaired by the overexpression of its primary cellula

86 nding the molecular basis of the disease has been impaired by the lack of structural data.

87 apoptotic bodies by professional phagocytes is impaired by a limited understanding of the molecular

88 strated that stress-induced release of sCD93 is impaired by hyperglycemia.

89 KEY POINTS: Cognitive performance is impaired by hypoxia despite global cerebral oxygen de

90 hemical mechanism by which E3 ubiquitination is impaired by IKK-driven phosphorylation remains unclea

91 ome activation in response to L. amazonensis is impaired by inhibitors of NADPH oxidase, Syk, focal a

92 r localization of the MEF2 corepressor HDAC4 is impaired by Mrf4 knockdown, suggesting that MRF4 acts

93 odulates hippocampal synaptic plasticity and is impaired by predator scent stress, our results provid

94 ne is associated with rapid VGF translation, is impaired by reduced VGF expression, and as previously

95 oreover, LFA-1 affinity triggering by CXCL12 is impaired by SOS1, ARHGEF1, and DOCK2 downregulation.

96 vivo to investigate single molecule dynamics is impaired by the absence of an efficient way to chemic

97 GP signaling was impaired by altered paracrine signals from the knee

98 damage was enhanced if paracellular barrier was impaired by Ca2+ depletion, proinflammatory cytokine

99 in vitro correlated with RANK expression and was impaired by Denosumab-mediated disruption of the RAN

100 usal female mice, ventricular repolarization was impaired by Kcne4 deletion, and ventricular Kcne4 ex

101 that Treg cells recruitment by cancer-FOXP3 was impaired by neutralization of CCL5, thereby inhibiti

102 le membrane pre-existing at the surface, and was impaired by oxidation of cholesterol and inhibition

103 permeability of both materials to fluid flow was impaired by the presence of electric charges.

104 QoL was impaired by the presence of peri-implantitis with hi

105 n a coupled import-integration reaction that was impaired by the SECA inhibitor sodium azide.

106 Sleep was impaired by troublesome symptoms and nasal obstructi

107 The same parameters were impaired by a similar CSC concentration in vivo Fin

108 cells of patients with Muckle-Wells syndrome were impaired by ibrutinib.

109 When degradation is impaired, CAFs retain the capacity to induce invasion

110 Ola1(-/-) mouse embryonic fibroblasts (MEFs) is impaired due to defective cell cycle progression, ass

111 ycling cells, such as dendritic cells (DCs), is impaired due to limited availability of deoxynucleosi

112 experimental data suggest that efferocytosis is impaired during atherogenesis caused by dysregulation

113 However, vasorelaxation was impaired during hypoxia in the coronary circulation,

114 ne-tuned by miRNAs, and that this regulation is impaired either by the SNP c.*61 T > C or by diminish

115 se of [Ca(2+) ]i was larger when SR function was impaired either by making the ryanodine receptor lea

116 The most marked effect of the belt was impaired esophageal clearance of refluxed acid (medi

117 Observations that HIFalpha hydroxylation can be impaired even when oxygen is sufficient emphasise the

118 brain sensitivity to brief gaps in noise can be impaired even without a general loss of central audit

119 DEK-deficient cells were impaired for gammaH2AX phosphorylation and attenuat

120 IRF4-deficient DCs were impaired for Treg generation in vivo.

121 pression of meristem/tissue identity markers are impaired from the "symmetry-breaking" periclinal cel

122 Secondary outcomes were impaired functioning (measured by the WHO Disabilit

123 of blood flow after femoral artery ligation was impaired (>80%) in AMPKalpha2(-/-) versus wild-type

124 ses insulin-degrading enzyme and cathepsin D were impaired; hence insulin receptor activity increased

125 f-awareness and internal consciousness would be impaired if not abolished.

126 plotypes, only plants carrying group 1 ACQOS are impaired in acquired osmotolerance.

127 w that patients with cerebellar degeneration are impaired in adapting feedforward control of speech b

128 csp22 treatment, and NbCSPR-silenced plants are impaired in csp22-induced defense responses.

129 ch the mechanisms underlying scale selection are impaired in developmental dyslexia.

130 eparative functions of progenitor cells that are impaired in diabetes.

131 and associated auditory cortical plasticity are impaired in female Mecp2(het) mice, a model of Rett

132 iating leukocyte slow rolling and emigration are impaired in Gal-3(-/-) mice, which could be because

133 berculosis-specific CD4 T cell immunity that are impaired in HIV-infected individuals with LTBI, whic

134 rophils and inflammatory cytokine production are impaired in M-ILK-deficient mice, and activation of

135 ctin polymerization plays an important role, are impaired in MO-MDSCs.

136 e function and reward system neural activity are impaired in most psychiatric disorders, it is unknow

137 ates the expression of amino acid permeases, are impaired in multiple aspects of fungus-macrophage in

138 that telomere length and telomerase activity are impaired in primary lymphocyte subsets from patients

139 Mutants with reduced levels of ubiquitin are impaired in PSG formation.

140 A-MPK3/sid2 and CA-MPK3/ein2-50 lines, which are impaired in SA synthesis and ethylene signaling, res

141 mory, cognitive flexibility, and inhibition, are impaired in schizophrenia.

142 at developmental plasticity and connectivity are impaired in sensory systems in DS model mice, that s

143 percepts and decoding of integrated percepts are impaired in tandem, while leaving feedforward repres

144 Importantly, these cells are impaired in the morphological process of engulfment

145 ting that RNA polymerase V-related functions are impaired in the pkl mutant.

146 mouse model that NanA-deficient pneumococci are impaired in their ability to cause both nasal coloni

147 th more mature but still naive T cells, RTEs are impaired in their ability to perform aerobic glycoly

148 nt to the CD4(+)CD8(-) single-positive stage are impaired in Themis(-/-) mice, suggesting that Themis

149 Also, hit1 mutants are impaired in UV-B acclimation.

150 d mechanism for dendrite establishment might be impaired in a human genetic epilepsy syndrome, polyhy

151 Suicide attempters have been found to be impaired in decision-making; however, their specific

152 l role for tau in EB regulation, which might be impaired in neurodegenerative disorders.

153 Everyday visual search can be impaired in patients with common eye diseases like gl

154 eries of cognitive and social tasks known to be impaired in two different 16p11.2 deletion mouse mode

155 type in recycling membrane lipids to TAG but being impaired in additional de novo synthesis of TAG du

156 cked in the executer1executer2 mutant, which is impaired in (1) O2 signalling.

157 Furthermore, we show that GPNMB activity is impaired in a diabetic wound environment, which is as

158 limited to the abaxial side of the leaf, and is impaired in a few accessions.

159 ffinity between Sesn2 and AMPK upstream LKB1 is impaired in aged hearts during ischemia (P < 0.05 vs.

160 ytes is normal in the elderly, how lipolysis is impaired in ageing remains unknown.

161 lated by the Sesn2-AMPK complex in the heart-is impaired in aging that sensitizes the heart to ischem

162 Thus, SB-mediated iron acquisition is impaired in an sbnI mutant strain.

163 gnaling response in peripheral blood T cells is impaired in breast cancer patients and is associated

164 In human arterioles, H2O2-induced dilation is impaired in CAD, which is associated with a transitio

165 s integrin endocytosis and cell adhesion and is impaired in cancer and developmental diseases.

166 Mobilization is impaired in Chrm1(--) mice and rescued by parabiosis

167 c theories assume such metacognitive insight is impaired in compulsivity, though this is supported by

168 Bone healing is impaired in diabetes mellitus (DM) cases.

169 ed binding of the UBXD1 adaptor protein that is impaired in disease; this underlies the potential for

170 signaling in response to replication stress is impaired in DONSON-deficient cells, resulting in decr

171 rdia and cortical infection thread formation is impaired in epr3 mutants.

172 to the NER proteome and DNA excision repair is impaired in extracts prepared from FICZ/UVA-treated c

173 al maturation of auditory brainstem synapses is impaired in FXS.

174 after injury, endogenous thymic regeneration is impaired in GVHD.

175 ing the actin-related protein6 mutant, which is impaired in H2A.Z deposition, and by H2A.Z profiling

176 Cyclic nucleotide signaling is impaired in HD models, and PDE10 loss may represent a

177 Strain recovery is impaired in infarcted segments with intramyocardial h

178 spastic paraplegia mutant, ATL1-F151S, that is impaired in its nucleotide-hydrolysis cycle but can s

179 ese reasons, the growth of a DeltaICP0 virus is impaired in most cells, except cells of the human ost

180 hermore, we demonstrate that the in vivo HSR is impaired in mouse models of Huntington's disease but

181 HCM carrying MYBPC3 mutations, (2) autophagy is impaired in Mybpc3-targeted knockin mice, and (3) act

182 Activation of autophagy by HBB2 is impaired in NRF2-deficient cells, which have reduced

183 Shh signaling is impaired in null embryos and primary cilia are reduce

184 is reduced and sleep-dependent motor memory is impaired in older adults.

185 ulation when cytosolic Fe-S cluster assembly is impaired in order to maintain optimal iron levels for

186 Quality of life (QOL) is impaired in patients with food allergy and improves f

187 ) is a major airway host defence system that is impaired in patients with smoking-associated chronic

188 We hypothesized that cBF integrity is impaired in prematurely born individuals and mediates

189 ostatic regulation of intracellular chloride is impaired in pyramidal cells, yet how this dysregulati

190 This suggests that segmentation is impaired in readers with dyslexia but only on tasks c

191 Visuospatial working memory (vsWM), which is impaired in schizophrenia, requires information trans

192 ormal conditions as well as how this process is impaired in schizophrenia.

193 a key role in cognition, and working memory is impaired in several neurological and psychiatric diso

194 etes, and that mitochondrial BCAA management is impaired in skeletal muscle from T2D patients.

195 ucose production as well as how this process is impaired in T2D.

196 heterozygosity, and activated nuclear Notch is impaired in the miRNA mutant.

197 tenance of BRS and that BDNF/TrkB signalling is impaired in the NTS in the CHF state.

198 (MT)-associated protein of the EMAP family, is impaired in these mice.

199 n in wild-type VAO, suggesting deprotonation is impaired in these variants.

200 Here we show that B-cell lymphopoiesis is impaired in Treg-depleted mice, yet this reduced B-ce

201 suggest that retinoid metabolism in the eye is impaired in type 1 diabetes, which leads to deficient

202 Cell phagocytosis is impaired in type 2 diabetes and requires RvE1 for act

203 1K mutation, we show that hnRNP K expression is impaired in urea soluble extracts from mutant TDP-43

204 howed that a Xanthomonas strain lacking raxX is impaired in virulence.

205 Here we show that polarization of node cells is impaired in Wnt5a(-/-)Wnt5b(-/-) and Sfrp mutant embr

206 Cognition was impaired in 22q11DS, but it did not correlate with s

207 comparable control group, cognitive function was impaired in 4 of the 6 cognitive domains tested (med

208 neumococcal polysaccharide antibody response was impaired in 87% of patients (ie, antibody titer abov

209 ANK-associated RH domain-interacting protein was impaired in a male fetus with IP, leading to defecti

210 BCR-mediated canonical NF-kappaB signaling was impaired in all mature naive CVID-derived B cells.

211 OL or Bt2cAMP to induce neutrophil apoptosis was impaired in AnxA-knock-out mice.

212 y neurons from the ventromedial hypothalamus was impaired in BG4KO mice.

213 As expected, differentiation of Th17 cells was impaired in both cohorts.

214 Although viability of hybrid seeds was impaired in both directions of hybridization, the ca

215 cation fork stalling, as replication-restart was impaired in both SMI#9-pretreated and RAD6B-silenced

216 cGMP- and Ca(2+)-mediated inhibition of NHE3 was impaired in both the internal and the C-terminal PBM

217 Consistently, mGluR-LTD was impaired in calpain-1 KO mice, and the impairment co

218 Endothelium-dependent vasodilatation was impaired in coronary arterioles from aged rats (maxi

219 ound that fetal monocyte maturation into AMs was impaired in Cre(+)5(f/f) mice, and we also confirmed

220 FGF21 production was impaired in CREBH-deficient mice, and adenoviral ove

221 Tumor engraftment to lung was impaired in CXCR3(-/-) mice, and transient reconstit

222 ted enhanced sensitivity to deoxycholate and was impaired in DNA double strand break repair.

223 e response to adenosine receptor stimulation was impaired in eKO mice in single cells in patch clamp

224 uced formation of NEMO-containing structures was impaired in fibroblasts from patients with IP carryi

225 Oral tolerance induced by DNFB gavage was impaired in germ-free mice and TLR4-deficient mice.

226 d IFN-lambda1 antiviral activity against HCV was impaired in IL28B T/T infected hepatocytes compared

227 , capillarization of the infarct border zone was impaired in KO mice, and the animals developed large

228 Canonical Wnt signaling was impaired in LGR4-deficient breast cancer cells, and

229 Finally, spleen growth was impaired in mice lacking either cytochrome P450 26B1

230 The formation of these cells was impaired in mice lacking this self-antigen, while Tc

231 ary acidic protein in the hippocampus, which was impaired in Morris water maze-trained IL-4- and IL-1

232 In a community-based cohort, LA function was impaired in participants with prevalent HF, but ther

233 Endothelial function was impaired in patients with CP compared with healthy p

234 RA function was impaired in PH patients versus controls (P<0.001).

235 he circadian photoresponse to constant light was impaired in rh7 mutant flies, especially under dim l

236 Upregulation of Igkappa transcription was impaired in small pre-B cells from PU.1/Spi-B-defici

237 This IkappaBalpha(5xPEST) mutant was impaired in stripping NFkappaB from DNA and formed a

238 rformance in the single pellet reaching task was impaired in the AAV1/2-A53T-aSyn-injected stim-OFF g

239 rably reduced by phr1 and phl1 mutations and was impaired in the ABA-deficient aba2-3 and ABA-insensi

240 un time to exhaustion at various intensities was impaired in the KO rats.

241 IFN-alpha-induced signaling was impaired in the patient fibroblasts, as evidenced by

242 and population levels, but ecosystem process was impaired in the warmer scenarios.

243 the pro-apoptotic mediators CamkII and Stat1 was impaired in Trpc3-deficient M1 cells, gathering insi

244 approximately half had >/=3 comorbidities or were impaired in >/=1 aspect that significantly interfer

245 The patients were impaired in adapting their feedforward control syst

246 alcohol as wild-type animals; however, they were impaired in alcohol seeking during the motivation t

247 olor vision ability and contrast sensitivity were impaired in all patients.

248 ischemia-induced mobilization, of LSK cells were impaired in both models.

249 N-gamma production and microbicidal activity were impaired in individuals with diabetes mellitus (DM)

250 efective in TCR-dependent NFkappaB signaling were impaired in late expression of Pim-1, Eomes, and CD

251 These plastic changes were impaired in MMP-9 knockout mice.

252 that rats with contralateral PER-POR lesions were impaired in object-context recognition but not in c

253 1061I, suggesting that these mutant proteins were impaired in proteolytic processing.

254 IPS, attention and working memory were impaired in PwMS compared with PwCIS.

255 ptor 1/2 (TLR1/2), TLR2/6, and TLR4 agonists were impaired in the fibroblasts and leukocytes of all T

256 endent effects on some clock gene expression were impaired in the liver of mice deficient for BMAL1,

257 and macrophages lacking type I IFN signaling were impaired in their ability to promote IL-18 inductio

258 the recruitment of CD8+ T cells to the tumor is impaired, in part preventing containment or eliminati

259 A hallmark of type 2 diabetes is impaired insulin receptor (IR) signaling that results

260 In its absence, secretory vesicle formation is impaired, leading to accumulation of immature vesicle

261 strate that retrograde transport of retromer is impaired, leading to its significant reduction in the

262 showed that recycling of the TCR-CD3 complex was impaired, leading to increased lysosomal targeting a

263 rterial blood pressure (pressure reactivity) is impaired, leaving patients vulnerable to cerebral hyp

264 rs through multiple mechanisms, one of which is impaired lysosomal proteolytic activity.

265 HRQoL was impaired more after starting the course of therapy (

266 When metabolic effects of the knockout are impaired, NLRX1-deficient cells do not display signi

267 s, the formation of syncytiumlike structures was impaired not only by antibodies to gB or gH/gL but a

268 resistance and the increase in nitric oxide are impaired or absent in salt sensitivity, promoting an

269 nlargement of vessels when pericyte function is impaired or lost.

270 es the available evidence that this response is impaired or suboptimal.

271 The US swine industry has been impaired over the last 25 years by the far-reaching

272 tron-containing genes in cells lacking H2A.Z is impaired, particularly under suboptimal splicing cond

273 iac output and skeletal muscle O2 diffusion, were impaired relative to controls by an average of 27+/

274 growth from the chiasm toward their targets is impaired, resulting in a delay in RGC axons reaching

275 particularly when oxidative phosphorylation is impaired, such as in neurons treated with mitochondri

276 However, despite conscious access being impaired, the ability to decode the presence of in

277 When this pathway is impaired, the array can be robustly activated.

278 When this interaction is impaired, the intercellular movement of TuMV replicat

279 idate the mechanisms by which proton pumping is impaired, thus revealing key kinetic gating features

280 ty could be a plant strategy when glycolysis is impaired to achieve metabolic adjustment and optimize

281 ligands and capacity for antigen uptake but were impaired to induce Th1 and Th17 cells.

282 Patients were impaired to the same extent in the No-Rotation and

283 of c-Jun, whose cullin-mediated degradation is impaired under these circumstances.

284 ice), activation of AMPK signaling in muscle was impaired under starved conditions, while mTORC1 sign

285 cannot avoid it, their sensory responses may be impaired, unless the OSPW has received some remediati

286 The HBV permissiveness was impaired upon treatment with microtubule inhibitor n

287 creased gene expression, and both mechanisms are impaired when TET2 and nuclear factor kappaB are dow

288 arrier to bacterial proinflammatory products is impaired when biofilm lysine falls below the minimal

289 Resection of DNA breaks is impaired when either Sae2 activity is blocked, sugges

290 he survival or recovery of the mmpL11 mutant is impaired when it is incubated under conditions of nut

291 ociative learning depends on brain state and is impaired when the subject is sleepy or tired.

292 The TDB (located within the AIS) was impaired when AIS components (ankyrin G, EB1) were k

293 and insulin secretion in IRS2(5A)-beta mice were impaired when compared with IRS2(WT)-beta mice or t

294 th active and passive ventricular relaxation are impaired with advancing age.

295 However, UPR(ER) function is impaired with age, which, we propose, creates a permi

296 mice, suggesting that manganese elimination is impaired with Zip14 ablation.

297 at initiation of ocular dominance plasticity was impaired with reduced CS, using mice lacking a key C

298 B-cell development was impaired, with fewer memory cells, reduced class-swi

299 hat beta cell function and glucose tolerance were impaired within the first two days following treatm

300 ation that phonological processing abilities were impaired years after the stroke, suggests that othe