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

4 ealed that: i) thymic and bone marrow output was impaired in 4 out 5 patients at the time of PML deve

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

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

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

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

9 ctions in response to environmental changes, is impaired in a number of neuropsychiatric conditions,

10 eration of 11-cis-retinal and visual pigment is impaired in a type 1 diabetes animal model, which neg

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

12 In the older transgenic mice, however, LTP was impaired in a way that occluded further reduction by

13 5xFAD mice of the same age were impaired in a hippocampal-dependent memory task.

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

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

16 The patients were impaired in adapting their feedforward control syst

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

18 MJ aging although its structure and function are impaired in aged animals.

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

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

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

22 lly, using OUL, we show that memory updating is impaired in aging, 18-m.o.

23 lly, using OUL, we show that memory updating is impaired in aging, 18-m.o. mice.

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

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

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

27 ing why adult hippocampal neurogenesis (AHN) is impaired in Alzheimer's disease (AD) is essential for

28 ut adult life, their morphology and function is impaired in Alzheimer's disease (AD).

29 ypothalamic reactivity to glucose metabolism is impaired in AN.METHODSTwenty-four participants with A

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

31 Postprandial repression of Cyp7a1 was impaired in Areg(-/-) mice, and recombinant AREG dow

32 responses during allergic inflammation, but is impaired in asthma.

33 r of corticothalamic communication which may be impaired in autism, non-convulsive seizures and other

34 nal model when voltage-gated sodium currents were impaired in basket cells (BCs).

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

36 efrontal cortex (PFC)-striatal circuitry and is impaired in both manifest and premanifest Huntington'

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

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

39 GU function was impaired in both groups after surgery.

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

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

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

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

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

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

46 OVERLY SENSITIVE1 and Na(+)/H(+) ANTIPORTER, was impaired in camta6 mutants.

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

48 plasticity, motor control and learning that are impaired in CB(1) receptor knockout (CB (1) -KO) mic

49 This innate vasoprotective mechanism is impaired in certain chronic clinical conditions, whic

50 learance during the first hours of infection was impaired in CF human Airway Surface Liquid (ASL) bec

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

52 and mitochondrial fitness of CD8(+) T cells are impaired in CLL.

53 o, we recently showed that sulfide oxidation is impaired in Coenzyme Q10 (CoQ10) deficiency.

54 rventions during their lifetime and survival is impaired in comparison with the age- and sex-matched

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

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

57 Iron efflux was impaired in Cp KO astrocytes and Heph KO oligodendro

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

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

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

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

62 show that its genotoxin-induced degradation is impaired in ddi1.

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

64 However, hookworm-infected hamsters were impaired in detecting a displaced object.

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

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

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

68 This counterregulatory mechanism is impaired in diabetes.

69 nitor cells (HSPC) from the bone marrow (BM) is impaired in diabetes.

70 Pol II processivity is impaired in diauxic cells, but strains with reduced p

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

72 LV global circumferential strain was impaired in DM (coefficient [95% CI]: 0.38% [0.01 to

73 We have isolated mutant UAF1 variants that are impaired in DNA binding and tested them together wit

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

75 l tolerance to oxazolone, mediated by Tregs, was impaired in Dock8(-/-) mice.

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

77 t that both facial and vocal recognition may be impaired in DP.

78 than that of WT, suggesting that the mutant was impaired in drought-induced gene expression.

79 m reabsorption that offset acute rises in BP are impaired in early type 1 diabetes, and this impairme

80 roliferation and invasion regulated by ACTN4 is impaired in early onset preeclampsia.

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

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

83 l tension, we show that chromosome alignment is impaired in extra-soft mouse oocytes, despite normal

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

85 lease at newly formed dyads, dyadic function was impaired in failing cells despite similar organizati

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

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

88 De novo serine biosynthesis was impaired in fibroblasts with GOT2 mutations and GOT2

89 factor beta-1 signaling and SMAD3 activation were impaired in fibroblasts depleted of the primary cil

90 Both processes were impaired in fibroblasts from children with HGPS and

91 These patterns are impaired in FoxP mutant flies, which present an alte

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

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

94 Moreover, proximal TCR signaling was impaired in galectin-9-deficient T cells, and prolif

95 te endosomes and degradation of its receptor were impaired in GBA knockout cells.

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

97 Shh signaling was impaired in gigaxonin-null zebrafish and was correct

98 t a virus lacking the UL48 gene (vDeltaUL48) is impaired in growth in cell culture and has diminished

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

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

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

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

103 tude of mismatch negativity and, critically, is impaired in healthy people who report more psychotic-

104 nction and fatty acid and glucose metabolism were impaired in HF-patients compared with HC (P<0.05).

105 responsible for raising exercise heart rate are impaired in HFpEF is unknown.

106 rther assessed whether coupling of MBF to EW is impaired in HFpEF and associated with compensatory in

107 ling of MVO(2) to EW (mechanical efficiency) was impaired in HFpEF.

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

109 ar immune responses to influenza vaccination being impaired in HIV-infected individuals with a CD4+ T

110 romotes antifungal immunity in the CNS; this is impaired in human deficiency in CARD9, which leads to

111 Spatial learning is impaired in humans with preclinical Alzheimer's disea

112 metry assays revealed that condensin complex is impaired in HyperD-ALL cells, leading to chromosome h

113 t the ETBR-mediated diuresis and natriuresis are impaired in hypertension with unknown mechanism.

114 sion: The nutrient-stimulated FGF19 response is impaired in ICU patients, which is mechanistically li

115 at KC-mediated mature neutrophil recruitment is impaired in IL-36gamma(-/-) mice.

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

117 Attention and memory may be impaired in individuals at-risk for Alzheimer's disea

118 nse to maintain normal glucose tolerance but is impaired in individuals with T2DM.

119 whether the internal monitoring of movements is impaired in individuals with Tourette syndrome, relat

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

121 in the cerebellum with advancing PMA, which was impaired in infants with brain injury on MRI and may

122 Strain recovery is impaired in infarcted segments with intramyocardial h

123 The GLP-1 system is known to be impaired in insulin-resistant conditions, and we soug

124 lin in skeletal muscle and PAK1/2 signalling is impaired in insulin-resistant mouse and human skeleta

125 the fatty acid synthesis genes FASN and ACC1 is impaired in IQGAP1-null mice.

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

127 The Deltahda-2 strain was impaired in its ability to colonize Arabidopsis root

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

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

130 ed monkeys received fornix transection, they were impaired in learning new visuospatial discriminatio

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

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

133 Patients with VMF damage were impaired in making choices when value was uniquely

134 nt formation with a primary caregiver, which is impaired in many children with childhood maltreatment

135 This mechanism was impaired in Mcoln1 (-/-) mice, which showed diminish

136 Mitochondrial function was impaired in mdKO mice, but energy charge was preserv

137 wever, TCPOBOP-induced cell cycle activation was impaired in [MET KO + EGFRi] mice due to defective i

138 hing process of store-operated calcium entry was impaired in MFN2 knockdown cells, whereas DRP1-DN-pr

139 show that the development of bone lymphatics is impaired in mice that lack osteoclasts.

140 Liver regeneration is impaired in mice with hepatocyte-specific deficiencie

141 keletal muscle, as well as cutaneous wounds, is impaired in mice with myeloid-specific deficiency of

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

143 onsistent with these findings, wound healing was impaired in mice lacking IL-6 or GPR39.

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

145 Conversely, fibroblast activation was impaired in mice with a fibroblast-specific deletion

146 genic resolution after CCl(4) administration was impaired in mice with Alb-Cre-mediated L-Fabp deleti

147 Evoked vascular reactivity was impaired in mice with CAA, which corresponded to slo

148 However, IFN-gamma responsiveness was impaired in microglia/macrophages irrespective of si

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

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

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

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

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

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

155 n a behavioural paradigm of active-avoidance was impaired in MT mice, strengthening the conclusion th

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

157 tal circumstances, or cognitive flexibility, is impaired in multiple psychiatric conditions, includin

158 Dynamic turnover of dendritic spines is impaired in mutant mice and is accompanied by an incr

159 omains and tethering to the nuclear envelope were impaired in mutant cells.

160 c pulses of glycine onto outside-out patches were impaired in mutant receptors, as deactivation was a

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

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

163 Perception of the Kanizsa illusory contours is impaired in neurodevelopmental disorders such as schi

164 Synaptic transmission was impaired in neurons expressing mutant variants, whic

165 significant repertoire remodeling, which may be impaired in nonresponders because of the preexisting

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

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

168 myocardial energetics and diastolic function are impaired in obesity, systolic function is usually pr

169 RC1 as an important metabolic regulator that is impaired in obesity, leading to altered MAIT cell res

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

171 Each of these steps may be impaired in older adults.

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

173 nstrate that reflex cutaneous vasodilatation is impaired in older hypercholesterolaemic adults but no

174 lthy remodeling in Abdsc and these processes are impaired in Om.

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

176 s, such as ASH1L, DYRK1A, MED13, and SHANK3, was impaired in our Drosophila models.

177 S-competent cells promoted cell survival, it was impaired in OXPHOS-defective cells because of inhibi

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

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

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

181 n error-based learning-even when this system is impaired in patients with cerebellar disease.

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

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

184 In conclusion, CA during thrombolysis was impaired in patients who did not respond to therapy.

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

186 All 3 strain indices were impaired in patients with MACE (all P<0.001).

187 vely regulate our emotions has been shown to be impaired in people with depression.

188 Thermoregulatory ability is impaired in persons with elevated serum cholesterol,

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

190 In contrast, the propagation of icPEDV-EnUmt was impaired in porcine epithelial cells (LLC-PK1), wher

191 hypothesis that entorhinal-based navigation is impaired in pre-dementia Alzheimer's disease.

192 In summary, proNGF maturation is impaired in preclinical and clinical AD while mature

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

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

195 hibitory TIM-3/Gal-9 pathway, in particular, is impaired in primary progressive MS (PPMS).

196 ex vivo-cultured Ral-deficient Schwann cells were impaired in process extension and the formation of

197 1061I, suggesting that these mutant proteins were impaired in proteolytic processing.

198 Microgliosis was impaired in PS2APP;Trem2(ko) mice, with Trem2-defici

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

200 the balance between the two decision systems is impaired in psychiatric disorders such as compulsion

201 ction errors benefits learning in health and is impaired in psychosis.

202 Working memory (WM) is impaired in psychotic disorders and linked to functio

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

204 ggest specific facets of response inhibition are impaired in PWSICdel mice and that abnormal 5-HT2CR

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

206 Working memory was impaired in rats with mEC lesions, but the occurrenc

207 This release of ATP is impaired in RBCs from older adults, but the underlyin

208 This ATP release is impaired in RBCs from older vs. young adults, but the

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

210 nate novel object-context configurations but are impaired in recognition of novel object-place-contex

211 However, expansion and Th1 differentiation was impaired in response to UV-inactivated virus (UV-HSV

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

213 to-cell movement of its replication vesicles are impaired in rhd3 This defect can be tracked to a del

214 response, the protective epidermal function was impaired in Ric(EKO) mice, as revealed by increased

215 Modulation of activity duration is impaired in rLG, confirming the role of reflex feedba

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

217 increases in left medial temporal lobe (mTL) are impaired in schizophrenia, as is theta phase couplin

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

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

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

221 hanisms, synaptic tagging and capture (STC), was impaired in SD mice at cellular and behavioral level

222 d HSF1 nuclear localization and distribution were impaired in senescence.

223 ng the activity of the TGF-beta pathway that was impaired in senescent cells.

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

225 n integral role in human social dynamics and is impaired in several neurodevelopmental disorders.

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

227 This ability is impaired in several psychiatric disorders, such as au

228 ytis cinerea Furthermore, bsk5 mutant plants were impaired in several immune responses induced by the

229 Our study shows that outcome is impaired in sickle cell disease patients receiving ex

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

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

232 ncluded that early steps of phloem formation are impaired in smxl4;smxl5 double mutants and that the

233 us mechanisms of compensatory plasticity may be impaired in some individuals with sleep apnoea, and t

234 ibe a novel route to imitation that may also be impaired in some patients with apraxia.

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

236 pressive function of Tregs from DeltaDC mice was impaired in T cell cocultures.

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

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

239 tants of the BON1 gene family, bon1bon2bon3, are impaired in the induction of gene expression and ABA

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

241 fector functions and to identify those which are impaired in the obesity setting.

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

243 We therefore hypothesized that ODP would be impaired in the absence of C1q, and that V1b developm

244 While proton transfer appears to be impaired in the oxidized state (Hox), the presented d

245 Additionally, we found that ORF24 expression is impaired in the absence of a stable vTA complex.

246 n the drought-tolerant variety, but recovery is impaired in the drought-sensitive sorghum variety.

247 In contrast, the pathway is impaired in the glioma stem-like cells resulting in t

248 Here we provide evidence that mitophagy is impaired in the hippocampus of AD patients, in induce

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 tion in response to exogenous RGF1 treatment is impaired in the rgi1/2/3/4/5 quintuple, yda single, a

252 duction of lysosomal biogenesis and function is impaired in the RPE from miR-211(-/-) mice that show

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

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

255 sequent evasion of degradative lysosomes, it was impaired in the ability to replicate, with that defe

256 ecycling via the retromer and WASH complexes was impaired in the absence of ARPC1B.

257 Alanine transport was impaired in the cycA mutant, and this correlated wit

258 inward-rectifying K(+) (K(+) (in) ) channels was impaired in the guard cells of cipk23 mutants, where

259 Moreover, interoceptive performance was impaired in the HHD group.

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

261 longation of hypocotyls in response to auxin was impaired in the mutant.

262 Insulin signaling at the level of Akt2 was impaired in the nonexercised muscle on the exercise

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

264 tiation of the temporoammonic pathway to CA1 was impaired in the postictal period, but only when seve

265 activity of TAM, M1-like TAM differentiation was impaired in the s.c. tumor microenvironment of mTORC

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

267 Although control LTP was impaired in the young transgenic mice, it was not TN

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

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

270 Both functions were impaired in the patient group.

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

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

273 a result, hnRNP A2 is displaced, and BC RNAs are impaired in their ability to reach synapto-dendritic

274 mmadelta T cells lacking both S1PR2 and CD69 are impaired in their maintenance within the dermis.

275 te immune activation is not due to SACC-PHHs being impaired in their ability to induce interferon sti

276 ELA animals were impaired in their ability to develop appropriate bi

277 , and parasites carrying a single APX allele were impaired in their ability to infect macrophages and

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

279 Although some MxA super-restrictors of THOV were impaired in their restriction of H5N1 influenza A v

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

281 al synaptic plasticity, learning, and memory are impaired in these mutant mice.

282 asts, we show that oxidative phosphorylation is impaired in these cells when given glucose and pyruva

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

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

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

286 ow that a PLY-deficient S. pneumoniae mutant was impaired in triggering human neutrophil transepithel

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

288 the ventral tegmental area following mating was impaired in TRPM8(-/-) males.

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

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

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

292 Stimulus-evoked release but not SV priming, was impaired in unc-10 mutants deficient for C2A/RIM het

293 1K mutation, we show that hnRNP K expression is impaired in urea soluble extracts from mutant TDP-43

294 Mitochondrial import of USP30 substrates is impaired in USP30 knockout (KO) cells, suggesting tha

295 F. nucleatum unable to consume sialic acids was impaired in vaginal colonization.

296 In vitro Th17 differentiation was impaired in VHL-deficient T cells.

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

298 Lyn(-/-) cells are impaired in virus release and are rescued when recon

299 Angiogenesis and remodeling are impaired in vivo in endothelium-specific CNP(-/-) an

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