ライフサイエンスコーパス: be impaired in

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

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

3 In this study, we find that adipogenesis is impaired in 3T3-L1 preadipocytes stably transfected w

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

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

6 g that pre-BCR signaling and B cell survival are impaired in a BclxL-independent manner.

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

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

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

10 Further, the TLR-induced IgM response is impaired in a type I and type II IFN-independent mann

11 ngencies is an essential survival skill that is impaired in a variety of psychiatric disorders.

12 GIPR, GLP-1-mediated GLP-1R internalization was impaired in a GIPR concentration-dependent manner.

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

14 tion and secretion of SBT3 in vivo Secretion was impaired in a propeptide-deletion mutant but could b

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

16 SAI is impaired in AD and shows a strong association with th

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

18 The patients were impaired in adapting their feedforward control syst

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

20 defects and communication with immune cells are impaired in aged keratinocytes, diminishing their ef

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

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

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

24 opic glutamate receptor-dependent plasticity is impaired in AIDA-1 cKO mice, further supporting a rol

25 tory demonstrate that OFC-mediated behaviors are impaired in alcohol-dependent animals.

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

27 Insulin secretion from pancreatic beta-cells is impaired in all forms of diabetes.

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

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

30 Furthermore, repression of cryptic exons was impaired in ALS-FTD cases, suggesting that this spli

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

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

33 diated ubiquitination and degradation, which is impaired in approximately 6% of diffuse large B-cell

34 ystem, regulating synaptic strength that may be impaired in ASD.

35 tioning studies revealed that remobilization is impaired in atg12 plants, which significantly decreas

36 wound healing with and without Cu treatment is impaired in Atox1(-/-) mice.

37 matin and identified mutants of cohesin that are impaired in ATPase activity but remarkably confer ro

38 ed for cell fission and infectivity, BB0323, is impaired in BbhtrA mutants grown at 37 degrees C, whi

39 genous autoantigen and diabetogenic function were impaired in BDC-Idd9.905 CD4(+) T cells.

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

41 phospho-mimetic residue Asp at this position is impaired in both signalling and Myddosome assembly.

42 to increase vulnerability to drug addiction-was impaired in both adolescent mice and adult mice with

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

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

45 r (mGluR)-induced dendritic spine regulation was impaired in both Fmr1(-/y) and Cyfip2(+/-) cortical

46 Microstructural integrity was impaired in both hippocampi in patients.

47 A pglA deletion mutant was impaired in both pathogenesis and gut persistence in

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

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

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

51 Patients with SHD were impaired in both phases of this task.

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

53 ate to terminate inflammation, and which may be impaired in C1q-deficient patients with autoimmune di

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

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

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

57 activation of insulin, and PI3K-Akt pathways were impaired in CCR5 and CCL5 deficient hypothalamus.

58 f-ubiquitination and proteasomal degradation is impaired in Cd28(-/-) T cells, the defective developm

59 orphology in response to anti-CD40 plus IL-4 were impaired in Cdc42-deficient B cells compared with W

60 undly attenuated in orally infected mice and were impaired in cell-to-cell spread in vitro.

61 y, immunoglobulin junctional diversification is impaired in cells.

62 Imitation, which is impaired in children with autism spectrum disorder (A

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

64 pacitance decay following strong stimulation is impaired in cKO; the rapid capacitance changes immedi

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

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

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

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

69 king the type I IFN signaling molecule STAT2 are impaired in cross-presenting tumor Ags to CD8(+) T c

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

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

72 innate defense mechanism in airways, and it is impaired in cystic fibrosis (CF) and other obstructiv

73 maturation and that phagosomal acidification was impaired in DCs in which the gene encoding TFEB was

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

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

76 We show in vivo that autophagy is impaired in dGBA-deficient fly brains.

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

78 This work demonstrates that PKA signaling is impaired in diabetes and suggests that treating hyper

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

80 Wound healing is impaired in diabetes, resulting in significant morbid

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

82 understood transient brain oscillation that is impaired in disorders such as Alzheimer's disease and

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

84 docytosis of the thrombopoietin receptor Mpl was impaired in Dnm2-null platelets, causing constitutiv

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

86 irical evidence, RPE signaling is thought to be impaired in drug addiction.

87 in cognitive control that has been shown to be impaired in early mild AD.

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

89 al and distal ends of the dorsal hippocampus was impaired in epileptic rats.

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

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

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

93 Excitatory presynaptic differentiation is impaired in Fgfr2b and Fgfr1b mutant mice; however, i

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

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

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

97 DC migration toward peripheral lymph nodes was impaired in Gata1-KO(DC) mice.

98 While IR is impaired in GDM-placenta, it is unaffected in GDM-pla

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

100 found that T cell and iNKT cell development are impaired in germline-deficient animals.

101 chore component and the cohesin subunit SMC3 is impaired in gip1gip2.

102 tissue factor-triggered thrombin generation was impaired in GPVI-deficient patients and reduced by t

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

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

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

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

107 that proBNP1-108 processing and degradation are impaired in HF patients ex vivo.

108 Adaptive thermogenesis of BAT was impaired in HFD offspring at weaning.

109 dy-state glucose-induced Ca(2+) oscillations were impaired in HFD-fed S2HET islets.

110 triguingly, the function of this zinc finger is impaired in high-altitude-adapted Tibetans, suggestin

111 Endothelium-dependent vasodilatation was impaired in high compared with normal phosphate in r

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

113 Neurogenesis is impaired in HIV-infected individuals.

114 rmatogenesis and we provide evidence that it is impaired in human male fertility.

115 ses (DUBs), including USP8, USP15 and USP30, are impaired in hydrolyzing phosphoUb chains.

116 Moreover, CD4 T cells but not CD8 T cells were impaired in IFN-gamma production.

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

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

119 Strain recovery is impaired in infarcted segments with intramyocardial h

120 to maintain skeletal muscle mass appears to be impaired in insulin-resistant conditions, such as typ

121 A C-terminally truncated SNAP-47 was impaired in interaction with VAMPs and affected thei

122 plants grown under iron-deficient conditions was impaired in iron-regulated transporter1 and ferric c

123 lucosyl-transferase, STARCH SYNTHASE 4 (SS4) is impaired in its ability to initiate starch granules;

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

125 ts of crude total lipids revealed that roc40 was impaired in its ability to increase the accumulation

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

127 o demonstrate that expression of HLA-DRalpha was impaired in KSHV de novo infection.

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

129 ts with combined manipulation of OFC and NAC were impaired in learning to use environmental cues to w

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

131 Consequently, the mutant mice were impaired in locomotor activity and spatial memory a

132 Nevertheless, hippocampal neuroplasticity was impaired in LV-IRAS-treated rats.

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

134 sponse and the migration of dendritic cells, were impaired in M ganglia.

135 y we found that invitro efferocytosis of ACM was impaired in macrophages from db/db (diabetic) mice.

136 plication of the PF74-resistant HIV-1 mutant was impaired in macrophages, likely owing to altered int

137 T cells activated without CD4(+) T-cell help are impaired in memory expansion.

138 In turn, mice lacking SynCAM 1 were impaired in memory tasks involving CA3.

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

140 We found that glutamate release in the brain was impaired in mice lacking low-density lipoprotein rec

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

142 and thus initiation of liver tumorigenesis, were impaired in mice harboring a MYC mutant unable to a

143 ) mice), we show that long-term potentiation is impaired in MKP-2(-/-) mice compared with MKP-2(+/+)

144 MMP-14(Sf-/-) mice, but resolution over time was impaired in MMP-14(Sf-/-) mice.

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

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

147 However, patients were impaired in modulating their decisions in response

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

149 ke receptor (TLR) 9-induced B-cell responses are impaired in most patients with common variable immun

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

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

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

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

154 Furthermore, capillary formation was impaired in murine aortic tissue rings or Matrigel p

155 anelle that is essential for the Hh pathway, was impaired in mutant dermal condensate cells, suggesti

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

157 of HIV-1 entry receptors, particularly CCR5, is impaired in Nef clones from elite controllers.

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

159 ortex (mPFC) serves executive functions that are impaired in neuropsychiatric disorders and pain.

160 otor functions and cognitive processing that are impaired in neuropsychiatric disorders such as Parki

161 We show that TGFbeta2 signaling is impaired in NF-kappaB-deficient and Lhx2 knockout emb

162 PtdOH delivery to the ER is impaired in Nir2-depleted cells, leading to limited P

163 Endothelial function is impaired in nonsevere and severe vivax malaria, is as

164 Similarly, insulin secretion was impaired in normal mouse and human islets that were

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

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

167 GLUT4 function is impaired in obesity and type 2 diabetes leading to hy

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

169 ory innervation of mesenteric arteries (MAs) is impaired in Old ( approximately 24 months) versus You

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

171 Reflex cutaneous vasoconstriction is impaired in older adults; however, the relative roles

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

173 -dependent secretion of BDNF in the vitreous is impaired in P301S mice.

174 RA reservoir and passive conduit functions are impaired in PAH, independent of RA size and pressure

175 the principal cellular degradative pathway, is impaired in pancreatitis, but it is unknown whether i

176 specific networks that support cognition and are impaired in Parkinson's disease.

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

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

179 Antibacterial immune responses are impaired in patients with AAH.

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

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

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

183 on healing and quality of life (QOL), which is impaired in patients with VLUs.

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

185 e-containing precursors and carrier proteins is impaired in PC-deficient mitochondria.

186 itial precursor binding to the TIM23 complex is impaired in PC-deficient mitochondria.

187 B'theta knockout mutants were impaired in peroxisomal beta-oxidation as shown by

188 ial mechanism for why RBV antiviral activity is impaired in persistently HCV-infected cell cultures a

189 stomatosis virus-induced IL-1beta secretion was impaired in Pgam5(-/-) bone marrow-derived macrophag

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

191 or spoIIIAH mutants that complete engulfment are impaired in post-engulfment, forespore and mother ce

192 Functionality of mono-macs is impaired in pregnant ALF-E patients compared to AVH-E

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

194 n and long-term potentiation-like plasticity were impaired in presymptomatic carriers, compared to he

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

196 he BCR, BAFFR, CXCR4, CXCR5, CD40, and TLR4, were impaired in promoting CD19 co-receptor activation a

197 Endothelial function was impaired in proportion to disease severity (median R

198 shment of systemic acquired resistance (SAR) is impaired in proteasome mutants, suggesting that the p

199 1061I, suggesting that these mutant proteins were impaired in proteolytic processing.

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

201 This communication is impaired in psychiatric disease, and ongoing studies

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

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

204 Moreover, oral tolerance was impaired in Rag2(R229Q) mice, and transfer of wild-t

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

206 t patients who received anterior cingulotomy were impaired in recognizing negative facial affect expr

207 domain produces channels that bind Hax-1 but are impaired in recruiting Arp2/3 to the plasma membrane

208 Viruses with an M split segment were impaired in replication at nonpermissive high tempe

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

210 n of the hypo-methylated nrpe1 mutant, which is impaired in RNA-directed DNA methylation, and the hyp

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

212 Regulation of renal microvascular tone is impaired in salt-sensitive (SS) hypertension-induced

213 ive processes, such as working memory, which are impaired in schizophrenia.

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

215 Control-related gamma power is impaired in schizophrenia, and an understudied treatm

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

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

218 tic plasticity, and memory that are known to be impaired in SCZ.

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

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

221 is a core aspect of cognition, and one that is impaired in several neuropsychiatric diseases, includ

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

223 In addition, mitochondrial mobility was impaired in SMA disease conditions, with decreased r

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

225 the first to show that immune tolerance may be impaired in spaceflight, leading to excessive inflamm

226 tiation into plasma cells and IgM production are impaired in Stat1(-/-) MZ B cells.

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

228 he hypothesis that gliovascular interactions are impaired in subjects with high burdens of white matt

229 ing, MMN, and P300 have been demonstrated to be impaired in subjects clinically at risk of developing

230 and N-SA groups, but this suppressive effect was impaired in subjects with SA.

231 from patients with CF or from Cftr(-/-) mice were impaired in suppressing conventional T cells, an ef

232 In agreement, mossy fiber refinement in CA3 was impaired in SynCAM 1 KO mice.

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

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

235 Recall responses by memory CD8 T cells are impaired in the absence of CD4 T cells.

236 ate and adaptive antibacterial host defenses are impaired in the context of preceding influenza virus

237 Miz1DeltaPOZ mice are impaired in the maintenance of myelinated fibers and

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

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

240 ived from patients with Ruijs-Aalfs syndrome are impaired in the resolution of covalent DPCs in vivo.

241 activity) of identified midbrain DA neurons are impaired in the ventral tegmental area (VTA), but no

242 Ischemic AMPK activation was found to be impaired in the Sestrin2 KO hearts.

243 -CSF-induced neutrophil and HSC mobilization is impaired in the absence of autophagy.

244 d the recruitment of NuA4 to these promoters is impaired in the absence of its Eaf1p component.

245 fG1-4, whereas secretion of the inhibitor(s) is impaired in the biofilm-forming mutant, leading to sy

246 ein Tau, because its microtubule interaction is impaired in the course of Alzheimer's disease and sev

247 The observation that the BDNF/TrkB pathway is impaired in the dmNTS during CHF provides a novel mec

248 Imprint establishment at hIC1 is impaired in the male germ line, which is associated w

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

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

251 st prominent during conflict learning, which is impaired in the X-irradiated mice.

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

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

254 and evasion of lysosomal fusion, the mutant was impaired in the ability to initiate replication betw

255 of immunity by the type I-E and I-F systems was impaired in the absence of QS signaling.

256 5 mus in the wild-type cytochrome c oxidase) was impaired in the Asp372Ile variant.

257 Moreover, this process was impaired in the autophagy-deficient liver and kidney

258 ere initially decreased, whereas DF function was impaired in the beta2ARag-treated porcine wound bed.

259 -4-isoxazolepropionic acid receptor subunits was impaired in the GluD1 knockout mice.

260 Our results showed that auxin signaling was impaired in the gsnor1-3 mutant as revealed by signi

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

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

263 Antithrombin inactivation of thrombin was impaired in the presence of the sulfated coumarins s

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

265 script cleavage and translational repression were impaired in the AGO3 mutant background, indicating

266 mmitment and oligodendrocyte differentiation were impaired in the corpus callosum of Olig1-null mice,

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

268 c degranulation and proliferative capacities were impaired in the HIV-infected group.

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

270 ight ventricular effective refractory period were impaired in the mutant mice, whereas sinus nodal fu

271 region or arm-like P-domain of calreticulin are impaired in their abilities to induce apoptotic cell

272 e formation of antibody-toxin complexes that are impaired in their ability to access host cell recept

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

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

275 om subjects with established type 1 diabetes were impaired in their ability to produce CCL3 and CCL4.

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

277 gs deficient for expression of CCL3 and CCL4 were impaired in their ability to suppress experimental

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

279 We show here that patients with PD are impaired in these across-trial decision threshold ad

280 ther two sites and that lymphoid development is impaired in these animals.

281 stimulation revealed that insulin signaling is impaired in these animals.

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

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

284 Insulin secretion was impaired in these mice under basal and high-glucose

285 logous cells, whereas TREM2 disease variants were impaired in this activity.

286 may explain how peripheral immune tolerance is impaired in tissues under autoimmune attack, includin

287 5R components, we found that IL-25 responses were impaired in Traf4 (-/-) cells.

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

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

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

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

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

293 nced, and its inhibition by low-dose aspirin is impaired in type 2 diabetes mellitus.

294 vesicle endocytosis and membrane trafficking were impaired in Ub(G76V)-GFP-Syb2 mice.

295 1K mutation, we show that hnRNP K expression is impaired in urea soluble extracts from mutant TDP-43

296 A new study shows that Parkinson patients are impaired in using their prior knowledge leading to s

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

298 ogical sensory attenuation has been shown to be impaired in various patient groups, so understanding

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

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