ライフサイエンスコーパス: be necessary for

1 into four functional categories: those that are necessary for (1) glycosylase activity (C146 and C25

2 ave access to sufficient and nutritious food is necessary for a healthy life and the core tenet of fo

3 g neurons and visual projection neurons, and is necessary for a male to pursue a female during courts

4 f leukocytes to sites of damage or infection is necessary for a productive immune response.

5 nd optogenetic activation, we show that LC11 is necessary for a visual object-induced stopping behavi

6 ng and that this astrocyte-mediated response is necessary for A1R-mediated LTD.

7 and kallikrein by soybean trypsin inhibitor was necessary for abolishing RBC-MV-induced TG in normal

8 Eradicating food insecurity is necessary for achieving global health goals.

9 chanisms exhibit clear daily variation which is necessary for achieving the homeostatic osmolality.

10 d that glycosylation of Asn-471 and Asn-1030 is necessary for ACLP secretion and identified a specifi

11 These data indicate that the primate ACC is necessary for acquisition of prosocial preferences fr

12 s IRONMAN1 and IRONMAN2 In addition, bHLH121 is necessary for activating the expression of transcript

13 mploying highly reactive intermediates which are necessary for activations of most stable chemical bo

14 show that activity of the NAc to VTA pathway is necessary for adaptive inhibition of food intake in r

15 o investigate whether the presence of a cost is necessary for adaptive therapy to extend the time to

16 serotonin receptors with G(s) heterotrimers is necessary for agonist-induced signaling.

17 y bulb to the posterior medial amygdala-that is necessary for all behavioural responses to darcin.

18 Both properties are necessary for an Ede1-dependent autophagy pathway fo

19 se findings confirm that attentional control is necessary for an association between attentional bias

20 Furthermore, ovarian-derived hormones were necessary for and sufficient to restore (R,S)-ketam

21 y provides direct genetic evidence that Sox2 is necessary for androgen ablation-induced neuroendocrin

22 We showed that Flvcr2 was necessary for angiogenic sprouting in the brain, but

23 cemia through hepatic gluconeogenesis, which is necessary for anticipating and fueling "fight or flig

24 not support the conclusion that dissociation is necessary for antidepressant response to ketamine.

25 ses (HATs) and histone deacetylases (HDACs), is necessary for appropriate gene expression and neurona

26 e demonstrate that reactivation-induced hPAC is necessary for avoidance memory destabilization, and t

27 This interaction is necessary for B-cell maturation and oncogenesis by E2

28 ll glycerophospholipids and cholesterol that are necessary for bacterial proliferation.

29 ammation triggered by pneumococcal infection is necessary for bacterial clearance but must be spatial

30 The beta(ps)-integrin Myospheroid, which is necessary for basal cell adhesion, is mislocalized in

31 egree of conformational dynamics of ECD that is necessary for binding GLP-1.

32 MSeq may be necessary for biomarker development in these heteroge

33 HELLS is recruited to hot spots by PRDM9 and is necessary for both histone modifications and DNA acce

34 conformational flexibility of the KFRR motif are necessary for cardio-physiological activity.

35 associated with monocyte recruitment, IRAK-M was necessary for CCR2 upregulation following bleomycin

36 depends on the Xrp1 DNA binding domains and is necessary for cell competition.

37 on in swimming direction, mediated by CheY3, is necessary for cells to escape from the porous biofilm

38 amplifies p190A-mediated LATS activation and is necessary for CIP.

39 uggesting that cell-autonomous PTN signaling was necessary for CML disease evolution.

40 5b functions as a dopamine-induced gene that is necessary for cocaine reward memory and DRD1-mediated

41 g matrix detachment, and both SIRT3 and SOD2 are necessary for colonization of the peritoneal cavity

42 chosen stimulus, and reward outcomes, which are necessary for computing the value of novel and famil

43 Accurate molecular diagnostic tests are necessary for confirming a diagnosis of coronavirus

44 ampal CA1 (vCA1) projections to the amygdala are necessary for contextual fear memory.

45 cation between the VH and PL during training is necessary for contextual fear memory, but not for tra

46 receptor complex CLAVATA2/CORYNE (CLV2/CRN) is necessary for continuous flower outgrowth during infl

47 ANCE STATEMENT The transcription factor Gli3 is necessary for correct development of the olfactory sy

48 cating that the synapse formation/maturation is necessary for creating infantile memories.

49 dition, formation of microtubule (MT) arrays was necessary for cytolysis and was accompanied by chang

50 iron which co-localizes with DA vesicles and is necessary for DA synthesis, was assessed across the s

51 We determined whether Bmal1 function is necessary for daily molecular oscillations in skin fi

52 Precise assessment of the corneal condition is necessary for deciding which type of keratoplasty (i.

53 r receptor protein NR5A1 (also known as SF1) are necessary for defensive responses to predators in mi

54 Consequently, rapid ABHD4 downregulation is necessary for delaminated daughter neuroblasts to esc

55 This distinction is necessary for determining the net impact of disturban

56 xidation and mitochondrial uncoupling, which are necessary for development of functional beige adipoc

57 of transient transcriptional repression that is necessary for development.

58 of whether local neuronal inhibition in NAc is necessary for DNQX microinjections to produce either

59 Enteric bacteria and/or their products are necessary for doxorubicin (DXR)-induced small intest

60 to knock out CD21, we demonstrated that CD21 is necessary for EBV entry into the Jurkat T-cell line.

61 gative regulator of Ras signaling in EC that is necessary for EC export of collagen IV, thus permitti

62 ole in sleep physiology, which may, in turn, be necessary for efficacious episodic memory.

63 Both MTA and TGH are necessary for efficient colocalization of the Microp

64 hylation and obscuring epigenetic marks that are necessary for efficient DNA repair.

65 Moreover, we report that FUS is necessary for efficient stalling of translation becau

66 Helical cell shape is necessary for efficient stomach colonization by Helic

67 a relatively stable HA protein (pH 5.5-5.6) was necessary for efficient replication and airborne tra

68 Both of these residues were necessary for efficient 14-3-3 protein binding.

69 Drainage of exudative retinal detachment may be necessary for either therapeutic or diagnostic purpos

70 -1-dependent microglia-endothelia cross talk is necessary for eliciting this spinal cord microglia ph

71 ultimate death, and detail how this journey is necessary for epidermal function.

72 The Human Silencing Hub (HUSH) complex is necessary for epigenetic repression of LINE-1 element

73 e conclusive evidence that miR-31 expression is necessary for ESCC development.

74 Such studies are necessary for establishing developmental trajectorie

75 Although MID is necessary for establishing the posterior fate of the

76 Subcellular compartmentalisation is necessary for eukaryotic cell function.

77 Transition to the second state is necessary for exhaustion.

78 ng that the AHR-ARNT transcriptional complex is necessary for expression of MMP1 in OFs.

79 ed growth factor A (Adgf-A) from enterocytes is necessary for extracellular adenosine to activate Ado

80 xperience with faces nor fovea-biased inputs is necessary for face-selectivity to arise in the latera

81 Both Anr and Mhr were necessary for fitness in lasR+ and lasR mutant stra

82 Although AUX1 is necessary for full actin rearrangements in response t

83 nd its predicted protein interaction domains are necessary for function.

84 between different configurations, which may be necessary for function.

85 ases play in amide-assisted NP syntheses and were necessary for Ge incorporation.

86 est that the INR region of the GLI2 promoter is necessary for GLI2 repression.

87 mucosa, moreover, we discovered that Ascl-1 is necessary for GnRH-1 ontogeny.

88 The posterior dorsomedial striatum (pDMS) is necessary for goal-directed action; however, the role

89 e beta-glucoside salicin; however, only bglP was necessary for growth in other non-beta-glucoside PTS

90 bute to cartilage compression resistance and are necessary for healthy joint function.

91 E Transition from latency to the lytic phase is necessary for herpesvirus-mediated pathology as well

92 signaling is high in tracheoblasts and this is necessary for high levels of activated (phosphorylate

93 ortholog to the yeast HMP-P synthase (Thi5) was necessary for HMP synthesis in Legionella pneumophil

94 te balance among primate prefrontal networks is necessary for homeostasis and behavioral flexibility.

95 We present evidence that the SAGA complex is necessary for homeostatic plasticity, demonstrating i

96 dent on a specific L-type Ca(2+) channel and is necessary for homeostatic sleep rebound.

97 tin receptor expression in Nav1.8(+) neurons was necessary for hyperalgesic priming in female, but no

98 Here, we show that NP-Ct is necessary for IB formation when NP is expressed alone

99 1 (HSV-1) immediate early (IE) promoters and is necessary for IE gene expression, viral DNA replicati

100 CD8+ T cell responses are necessary for immune control of simian immunodeficie

101 ence map of all cell types in the human body is necessary for improving our understanding of fundamen

102 ods, technologies, and analytical approaches are necessary for in situ plastic-type identification an

103 racts with the p22phox subunit of NOX, which is necessary for increased ROS-mediated RA pathogenesis.

104 The orbitofrontal cortex (OFC) is necessary for inferring value in tests of model-based

105 glycolysis and mitochondrial oxidation that is necessary for insulin secretion.

106 In muscle, LRP2 is necessary for insulin-dependent IR internalization, a

107 horyl group positioned at carbon 5 of PIP(2) is necessary for interaction with ENaC.

108 t binds beclin1 and controls neurovirulence, are necessary for interactions with PGAM5, KEAP1, and ot

109 ays that result in elevated serum PCT levels is necessary for interpretation and subsequent clinical

110 Results suggest five areas of understanding are necessary for interpreting spectra, and progress in

111 downstream of the Toll and Imd pathways and is necessary for iron relocation from the hemolymph to t

112 whether ketamine's dissociative side effects are necessary for its antidepressant effects remains unc

113 protein, and nuclear localization of AFFL-2 is necessary for its role in heat shock response.

114 the C-terminal edge of the second DCX domain is necessary for KLHL15-mediated ubiquitination of DCX a

115 Yet we find that it is necessary for larval development in D. melanogaster.

116 indicate that cross-area population dynamics are necessary for learned motor skills.

117 alization of the aqueous space within a cell is necessary for life.

118 mmadeltaT cells up-regulate both CD1d, which is necessary for lipid-based antigens presentation, and

119 nscriptional sites in the MMT1 promoter that are necessary for low-iron- or oxidant-mediated MMT1 exp

120 atal stimulation and this astrocyte response is necessary for LTD.

121 ERK activation downstream of C-Raf is necessary for maintaining ongoing depolarization and

122 ely suppress female (pistil) development and are necessary for male (anther) development.

123 e alpha-chymotrypsin-based cleavage reaction is necessary for manufacturing peptides using rDNA techn

124 pain after diagnosis of MBC will continue to be necessary for many patients.

125 Gle1 oligomerization is necessary for many, but not all aspects of Gle1A and

126 HIV-1 Vpr is necessary for maximal HIV infection and spread in mac

127 Selective depletion demonstrated that Tregs were necessary for maximal apoptotic cell-directed enhan

128 e DCN improves EBC learning, but intact PNNs are necessary for memory retention.

129 on of DNA methylation in postmitotic neurons is necessary for memory formation and other adaptive beh

130 Our findings demonstrate that SETD6 is necessary for memory-related nuclear factor-kappaB RE

131 These signal transducing systems are necessary for metabolic regulation, resistance to an

132 d wet) and a maximum of 4km(2) spatial scale is necessary for minimizing uncertainties (<10%) in regi

133 atalyzed by dynamin-related protein 1 (Drp1) is necessary for mitochondrial biogenesis and maintenanc

134 Our data suggests that miRNAs are necessary for modulating the shift in cellular metab

135 strated that expression of BM-derived IRAK-M was necessary for monocyte trafficking into the lung and

136 ing that none of these interference proteins are necessary for naive adaptation.

137 he hypothesis that VitE, not just alpha-TTP, is necessary for nervous system development, adult 5D st

138 a functional blood-brain barrier (BBB) that is necessary for neuronal survival and activity.

139 tion of nitric oxide (NO) with the P450 heme are necessary for NO to trigger ubiquitination and prote

140 nteract with each other in cardiogenesis and are necessary for normal heart formation.

141 medial prefrontal cortex (mPFC) is known to be necessary for normal avoidance in the EPM.

142 demonstrate that orbitofrontal cortex (OFC) is necessary for normal behavior in this task, but a cau

143 ate that Adar adenosine deamination activity is necessary for normal locomotion and prevents age-depe

144 m through both lactate production and OXPHOS is necessary for normal osteoclastogenesis.

145 show that embryonic photosynthetic activity is necessary for normal skoto- and photomorphogenesis in

146 Here we show that ILK is necessary for normal trafficking of melanosomes along

147 Activation of Cx43 hemichannels was necessary for nuclear localization of Yap/Taz and in

148 re, the intact structure of the retinal ring is necessary for obtaining the excitonic interaction.

149 type transition, signaling through PPARdelta is necessary for obtaining the M2-biased phenotype.

150 gomers suggest structural rearrangement that is necessary for oligomers with an antiparallel beta-she

151 Several of the 11 classical HDAC enzymes are necessary for optimal Treg function while others are

152 ity in how the AAA+ ring docks with ClpP may be necessary for optimal function.

153 , therefore tuning its electronic properties is necessary for optimal performance.

154 positively controls Sox2 mRNA stability and is necessary for optimal SOX2 mRNA and protein levels in

155 The Origin Recognition Complex (ORC) is necessary for orchestrating the initiation process by

156 enes, in their proper genomic context, which is necessary for overlapping expression data with other

157 Phospholipase Cbeta is necessary for OXTR-mediated excitation of CeL neurons

158 We also found that PABPN1 is necessary for p63alpha translation by modulating the

159 Knockdown of DHHC5 showed that this enzyme is necessary for palmitoylation of Galphas, Galphai, and

160 ient to drive PD-L1 and PD-L2 expression and is necessary for PD-L2 expression.

161 ies, we show that PI3K recruitment of ZC3H14 is necessary for PDGF-induced neuroprotection and that t

162 Thus, although early visual cortex is necessary for perceptual object constancy, it is unne

163 ic inhibition along with synaptic plasticity is necessary for place field stabilization.

164 The channels are necessary for postengulfment FS gene expression, whi

165 y of natural metal-(hydr)oxide nanoparticles is necessary for predicting ion adsorption phenomena in

166 I-A and III-B), only the I-B system and Cas3 were necessary for priming.

167 ERK3 is necessary for production of several cellular factors

168 NRF2 hyperactivation was necessary for proliferation and survival in lung tum

169 acid aggregation-prone region, both of which are necessary for proper Gle1 oligomerization.

170 LXR alpha/beta, expressed in sensory neurons are necessary for proper peripheral nerve function.

171 s, where tight regulation of Pol II activity is necessary for proper ESC differentiation.

172 Correspondingly, deletion of Ccr2 in MPs is necessary for proper fusion into regenerating aged mu

173 The intrinsic lymphatic contractile activity is necessary for proper lymph transport.

174 We conclude that Mn is necessary for proper maintenance of the intestinal ba

175 Lastly, we demonstrate that the alarmones are necessary for protecting GTP homeostasis against exc

176 Although high antibody levels are necessary for protection, our study suggests that on

177 ly, FGF21 signaling in glutamatergic neurons is necessary for protection against body weight gain and

178 ly showed that the autophagy protein ATG16L1 is necessary for protection against MRSA strains encodin

179 Further, we demonstrate that Sox2 3'UTR AREs are necessary for RBM24-based elevation of Sox2 mRNA hal

180 tain two bromodomains (BD; BD1 and BD2) that are necessary for recognition of acetylated lysine resid

181 thaliana) cyclin-dependent kinase G1 (CDKG1) is necessary for recombination and synapsis during male

182 o protein-coding genes (Hnrnph1, Rufy1) that was necessary for reduced methamphetamine-induced locomo

183 Smad3 was necessary for regulation of Fibromodulin and Adamtsl

184 e evolution of intraspecific trait variation is necessary for reliable, long-term species and climate

185 bolic strategies in consumer-resource models is necessary for reproducing experimental growth curves

186 nding of (18)F-FGln pharmacokinetics and may be necessary for response assessment to targeted therapi

187 Thus, we propose that both proteins are necessary for retinal lipidome membrane organization

188 idence that the mushroom body vertical lobes are necessary for retrieving visual memories for success

189 Cmi is necessary for robust H3K4 monomethylation and H3K27 a

190 fically, the separation of plasma from blood is necessary for routine health assessments such as comp

191 single-cell RNA-sequencing (scRNA-seq) data are necessary for samples containing a mixture of genoty

192 Prescreening of CP may be necessary for selecting donors with high titers of ne

193 ivation showed that the somatosensory cortex was necessary for sequence discrimination.

194 All UHRF1 reader and writer domains were necessary for silencing and DNMT3B was identified a

195 or the frequent treatment regimen that would be necessary for siRNA-induced gene silencing.

196 tion of both growth and cell-division timing is necessary for size control in animal cells, and this

197 lamic spindles, an interregional dialog that is necessary for sleep-dependent memory consolidation.

198 We report that TMC-1 is necessary for sodium attraction, but not aversion in

199 actor tyrosine kinase substrate (HRS), which was necessary for sorting surface receptors to intralumi

200 onstrate that another sperm protein, TMEM95, is necessary for sperm-egg interaction.

201 ive memory, it is not yet known whether SWRs are necessary for such memories.

202 This process is necessary for T enhancement of GSIS.

203 ymerization of NM myosin in airway SM, which is necessary for tension development.

204 he neuroeffector junction (NEJ) is likely to be necessary for terminating inhibitory neurotransmissio

205 her, these data indicate that forebrain DORs are necessary for the action of DOR agonists in relievin

206 ishing human-origin and swine-origin viruses are necessary for the continued surveillance of influenz

207 To test whether fast-spiking interneurons are necessary for the development of compulsive ethanol

208 actions posited to occur during neurogenesis are necessary for the formation of the characteristic la

209 1 DNA-binding activity and BRG1 reexpression are necessary for the gene and protein expression of epi

210 o on to identify cell envelope proteins that are necessary for the import of PyoG and its killing act

211 y and specific geometry of GM1 binding sites are necessary for the induction of membrane curvature.

212 n of matrix metalloproteinases (MMPs), which are necessary for the invasive and metastatic phenotype.

213 y whether visual inputs to the intact retina are necessary for the LPZ responses, here, we measured B

214 ors, which interact in the late endosome(9), are necessary for the membrane fusion and delivery of RN

215 hy adult mouse brain, we show that microglia are necessary for the normal functional development of a

216 the importin proteins IMPalpha-1, -2 and -3 are necessary for the nuclear import of LHP1.

217 h experimental features or model assumptions are necessary for the observed continual evolution to em

218 manner and demonstrate that ovarian hormones are necessary for the prophylactic efficacy of (R,S)-ket

219 ting that factors such as adhesion molecules are necessary for the stabilization of the CAR-Env inter

220 We find that rotation is necessary for the accumulation of DNA writhe and for

221 rite-free electrodeposition of lithium metal is necessary for the adoption of high energy-density rec

222 These findings indicate that the HCND is necessary for the cell-surface expression of HCN chan

223 MT5 expression in recently activated T cells is necessary for the cholesterol biosynthesis metabolic

224 at the integrity of CA activity in the brain is necessary for the consolidation of fear extinction me

225 While early experience with moving stimuli is necessary for the development of direction selectivit

226 The homeobox transcription factor PROX1 is necessary for the development of lymphatic vessels, l

227 ated in development and DNA damage 1 (REDD1) is necessary for the development of oxidative stress in

228 2 interfered with TGF-beta1 signaling, which is necessary for the development of T(H)17 and regulator

229 e results suggest that optimization of MP135 is necessary for the development of therapeutics that su

230 han SRPX2(-/Y) mice, which indicates that C3 is necessary for the effect of SRPX2 on synapse eliminat

231 itro, and observed that membrane association is necessary for the efficient transfer of acyl-phosphat

232 estion that maintenance of critical dynamics is necessary for the emergence of consciousness and comp

233 utaryl reductase degradation protein 1), and is necessary for the ERAD activity of the Sel1L-Hrd1 com

234 e hypothalamic paraventricular nucleus (PVN) is necessary for the expression of binge-eating behavior

235 during and shortly after the critical period is necessary for the expression of LTP at PV-IN output s

236 gulator, and it is well-described that KIF11 is necessary for the formation and maintenance of the bi

237 in brain nuclei in response to an experience is necessary for the formation of long-term memories.

238 The polar organizing protein Z (PopZ) is necessary for the formation of three-dimensional micr

239 Accurate regulation of innate immunity is necessary for the host to efficiently respond to inva

240 gVH and/or VL regions of RA synovial B cells is necessary for the immunoreactivity to NET-Ags.

241 Staphylococcus aureus fatty acid kinase FakA is necessary for the incorporation of exogenous fatty ac

242 RNAi triggered by mitochondrial dysfunction is necessary for the increase in longevity that is induc

243 The microbiota is necessary for the induction of intestinal immunoglobu

244 LSV ex vivo, demonstrating that this pathway is necessary for the induction of the acute arterial WSS

245 bitory neurons in the centrolateral amygdala is necessary for the inhibition of a conditioned respons

246 bitory neurons in the centrolateral amygdala is necessary for the long-term storage of conditioned-th

247 e with a mutation in MSK1, we show that MSK1 is necessary for the majority of gene expression changes

248 Collectively, our findings suggest that ACC is necessary for the mitigation of competing inputs and

249 NCOA4, the autophagic receptor for ferritin, is necessary for the mobilization of liver iron stores d

250 mewhat unexpectedly, the autophagy machinery is necessary for the normal formation and compartmentali

251 r, our results demonstrate that the mouse SC is necessary for the normal performance of voluntary vis

252 Our data show that amnesiac is necessary for the PKA activation process that results

253 Here, we demonstrate that CDKG1 is necessary for the processing of recombination interme

254 Thus, AHR is necessary for the proliferation of MYC-overexpressing

255 FA-like phenotypes, we establish that BRCA2 is necessary for the protection of DNA at ICLs.

256 We conclude that human CA3 is necessary for the retrieval of episodic memories long

257 nal evidence that Wnt/beta-catenin signaling is necessary for the specification of dorsal cell fate i

258 Nuclear RNA helicase A (DHX9/RHA) is necessary for the translation of the mRNAs of JUND (J

259 is sufficient, and TrkB receptor activation is necessary, for the transsynaptic trophic effect exert

260 Nevertheless, low GATA3 expression was necessary for the generation of functionally mature

261 hetic polymer coating prevented fibrosis and was necessary for the long-term function of the device.

262 uced translation during the day in vitro and was necessary for the rhythmic synthesis of select prote

263 occurred with Pam(3)CSK(4) stimulation, and were necessary for the early priming events to occur.

264 ed genes influencing the IgE response, eight were necessary for the response, while 12 repressed IgE.

265 targets because a three-dimensional assembly is necessary for their formation.

266 aQ, suggesting that the SPA1 kinase activity is necessary for thermomorphogenesis.

267 gem-Dialkyl activation is necessary for these reactions to occur, as unactivate

268 we demonstrate that a Thi5-dependent pathway is necessary for thiamine biosynthesis in Legionella pne

269 on, and confirm that core promoter sequences are necessary for this activity.

270 unknown whether early visual cortical areas are necessary for this improvement.

271 to date, no study has demonstrated that ACC is necessary for this form of behavioral flexibility, no

272 and that K-Ras(G12V)-driven MEK/ERK activity is necessary for this lethality.

273 To test if inflammation was necessary for this effect, we treated melanoma trans

274 sistant to Thr repletion, showing that TARS2 is necessary for Thr-dependent mTORC1 activation.

275 omain of p150(Glued), thus explaining why H2 is necessary for tight binding.

276 Adaptive angiogenesis is necessary for tissue repair, however, it may also be

277 ing CD8(+) T cell sensing of TGF-beta, which was necessary for tissue residency.

278 n in seasonal changes in reproduction, which is necessary for traits to evolve via natural selection.

279 volutionarily conserved regions of ZIC3 that are necessary for trans-activation.

280 rthermore, we find that a minimum of two 3Bs is necessary for trans replication of FMDV replicons, wh

281 Both complexes are necessary for transcriptional regulation but through

282 remotor cortex, and the primary motor cortex is necessary for transforming visual information into gr

283 Complete live viruses are necessary for transmission, not the fragments identi

284 This restriction is necessary for trap formation, because ectopic adaxial

285 However, it is unclear why a functional ETC is necessary for tumour growth in vivo.

286 mitochondrial electron transport chain (ETC) is necessary for tumour growth(1-6) and its inhibition h

287 f how effectively these movements shift gaze is necessary for understanding their functions and is he

288 tification of differentially expressed genes is necessary for unraveling disease pathogenesis.

289 SPN transmodulation across the striatum that is necessary for updating previous goal-directed learnin

290 f OFC to test whether these correlates might be necessary for value inference during later probe test

291 ort for the first time that VEGF-C signaling is necessary for valve morphogenesis.

292 that physiological levels of AMPK activation are necessary for vasodilatation in healthy pregnancy.

293 lpha (HIF-1alpha) in CNS respiratory centres is necessary for ventilatory acclimatization to hypoxia

294 Furthermore, we showed that this induction is necessary for vIL-6-mediated cell adhesion and angiog

295 ude that association of E2 with the Brd4 CTM is necessary for viral genome replication and suggest th

296 eins, becoming internalized with CD63, which is necessary for virus production.

297 We found that partial feedback is necessary for VPL of calcifications, whereas detailed

298 rthermore, detailed feedback during training is necessary for VPL of distortion and calcification les

299 naling targets of N-oleoylethanolamide (OEA) were necessary for weight loss, metabolic improvements,

300 Importantly, we find that TRIM27 alone is necessary for ZNF165 transcriptional activity and is