ライフサイエンスコーパス: be necessary for

1 NK mitogen activated protein kinases (MAPKs) is necessary for 2-OHE2 - and 4-OHE2 -induced P-UAEC pro

2 A program longer than 6 months might be necessary for a longer lasting intervention effect.

3 Recalibration may be necessary for accurate risk assessment.

4 cervical and mandibular musculatures, which is necessary for accurately positioning lethal bites on

5 w that genes regulated by METTL3 in this way are necessary for acute myeloid leukaemia.

6 ltogether, this study demonstrates that SOX4 is necessary for adult beta-cell replication through dir

7 ophylls into chlorophyll a and chlorophyll b is necessary for advanced monitoring of plant growth.

8 TSG-6 is necessary for AHR in allergic asthma, because it faci

9 In conclusion, TSG-6 is necessary for AHR in response to ozone or sHA, in par

10 ting complex/cyclosome (APC/C), whose action is necessary for anaphase initiation.

11 em and progenitor cells demonstrated that it is necessary for and specifically regulates CEBPA expres

12 s9, we demonstrated that residue 172 in Arf1 is necessary for AP-1 activation and is required for the

13 f a transcription factor that we demonstrate is necessary for appressorial formation.

14 Moreover, subsets of autophagy genes were necessary for asexual/sexual differentiation and de

15 Clarifying this central concept is necessary for assessing Burkart et al.'s proposal tha

16 e models are inconclusive on whether B cells are necessary for asthma development.

17 itamin D status beginning in early pregnancy is necessary for asthma/recurrent wheeze prevention in e

18 2a1a/b and deposition of Collagen XII, which is necessary for axons to actively navigate the non-neur

19 the secreted protein netrin 1 (Ntn1), which is necessary for basement membrane breakdown, although t

20 These data indicate that SFK activity is necessary for BDNF-mediated suppression of cocaine-se

21 It is unknown whether it is necessary for beta-adrenergic signaling-promoted canc

22 nternalization of the PAR4-P2Y12 heterodimer is necessary for beta-arrestin recruitment to endosomes

23 s established that histone acetylation marks are necessary for both hot spot activity and crossover r

24 S-induced p38 MAPK and NF-kappaB activations were necessary for both IL-33 production and PGE2 genera

25 lex required for transport (ESCRT) machinery is necessary for budding of many enveloped viruses.

26 eptor C-type 1 (MRC1), suggesting that PRMT1 is necessary for c-Myc function in M2 macrophage differe

27 We found that PRMT1 activity was necessary for c-Myc binding to the acetyltransferase

28 We found that Ca(2+) influx through TRPV1 is necessary for capsaicin-induced ablation of nocicepti

29 hat control signal transduction pathways and are necessary for cellular homeostasis.

30 uired for the viral life cycle and might not be necessary for cellular transformation, yet HPV integr

31 ndent on the C. elegans PINK1 homolog, which is necessary for cellular resistance to chronic malfunct

32 Strikingly, PIKfyve is necessary for chemotaxis, ROS production, and stimula

33 s demonstrate that amygdala-OFC interactions are necessary for choices among actions based on the upd

34 damaged tissues upon acute sterile injuries is necessary for clearance of necrotic debris and for co

35 Intracellular H2O is necessary for CO2/HCO3(-) conversion.

36 e kinase B (TrkB) receptors in NACsh neurons is necessary for cocaine-induced dendritic spine formati

37 body of the central complex, are reported to be necessary for complex visual tasks such as pattern re

38 Larger studies are necessary for confirmation.

39 PG synthesis at the cell division septum is necessary for constructing new poles of progeny cells

40 erefore, interaction between the POR and PER is necessary for context-guided exploratory behavior but

41 As in macaques, human lOFC and mOFC/vmPFC are necessary for contingent learning and value-guided d

42 y networks and identify nodes whose override is necessary for control in the general case but not in

43 uired five upstream adenylates, and H4a/Psi3 was necessary for cooperative association of two other h

44 e that this evolutionarily conserved protein is necessary for Cox15 oligomerization and function.

45 provide evidence that the mPFC-->NAc pathway is necessary for cue-induced reinstatement of alcohol se

46 ny undesired effect on lactic bacteria which are necessary for development of aroma and chemical prop

47 Dpp in the developing fly wing and that this is necessary for developmental signaling.

48 rvation of the impact of respiration on flow is necessary for diagnostics; (c) cardiopulmonary imagin

49 inding affinity, suggesting that all domains are necessary for directing recombination.

50 aDG) and anterior CA2/CA3 (aCA2/CA3) of mice are necessary for discrimination of social, but not non-

51 Furthermore, STRA6 is necessary for diurnal rhythmicity of insulin action a

52 ignaling axis and investigated whether STRA6 is necessary for diurnal variations in insulin sensitivi

53 annabinoid type-1 receptor (CB1R) activation is necessary for E2 to potentiate reinstatement.

54 uman, we show that cullin E3-ligase activity is necessary for each step of the muscle cell differenti

55 Glycolysis is necessary for early gene transcription, while glutami

56 rly gene transcription, while glutaminolysis is necessary for early gene translation but not transcri

57 d with breast cancer brain metastasis (BCBM) is necessary for early identification and evaluation of

58 Knowledge of population density is necessary for effective management and conservation o

59 y regulator of the cellular ESCRT machinery, is necessary for efficient entry and egress of Autograph

60 energy bias toward native interactions that is necessary for efficient folding.

61 lular metabolic profiling revealed that PknG is necessary for efficient metabolic adaptation during h

62 Estrogen is necessary for embryo transport in mammals; however, t

63 These results indicate that NUMB is necessary for establishing polarity in CE cells, and

64 search based on accumulated prospective data is necessary for evidencing specific pathways.

65 hat homozygous variants in WNT7A and SMARCA4 are necessary for expression of TH and selection against

66 an ortholog of the plant protein Ycf4, which is necessary for expression of proteins of the photosynt

67 ement of alcohol seeking and neither pathway is necessary for extinction of responding.

68 ram cells in the basolateral amygdala, which were necessary for fear memory, were maintained.

69 hat conversion of ARF6 to its GDP-bound form is necessary for final stabilization of the hair bundle.

70 ith both S1-S2 and S3-S4 of NaV channels may be necessary for functional modulation, and that targeti

71 at is, qudits, with D > 2) and their control are necessary for fundamental investigations of quantum

72 , the positive charge of the lysine residues was necessary for fusion regulation, as alanine substitu

73 g spin-lattice relaxation time-both of which are necessary for future clinical investigations.

74 Importantly, functional STING was necessary for GCV to inhibit inflammation in culture

75 LOG2 ubiquitin ligase activity is necessary for GDU1-dependent tolerance to exogenous a

76 ate in this study that mitochondrial fission is necessary for glucose-stimulated insulin secretion in

77 e cross talk between microbes and host cells is necessary for health, survival, and regulation of phy

78 ed repopulation ability, indicating that Erf is necessary for hematopoietic stem cell maintenance or

79 llagen mRNAs regulates their translation and is necessary for high type I collagen expression.

80 Understanding ACP population diversity is necessary for HLB regulatory practices aimed at reduc

81 Platelets are necessary for host defense and prevention of hemorrh

82 A PAT-perturbed microbial community is necessary for host effects and sufficient to transfer

83 Parasite motility is necessary for host-cell invasion and virulence, but s

84 oreover, the region of DnaK that we found to be necessary for Hsp90Ec binding includes residues that

85 Moreover, CD2AP is necessary for ICAM-1-induced Rac1 recruitment and act

86 of ciliary beating and mucociliary transport is necessary for identifying new receptor targets to sti

87 by which IL-4(+)IL-13(+) invariant NKT cells are necessary for IL-4Ralpha signaling that regulates th

88 the pyroptosis regulator gasdermin D (GSDMD) was necessary for IL-1beta secretion from living macroph

89 Regulation of cell proliferation is necessary for immune responses, tissue repair, and up

90 subsets, plasmacytoid and myeloid DCs (mDCs) was necessary for increased chemokine and IFN-alpha secr

91 asolateral nucleus of the amygdala (BLA) and was necessary for increased phosphorylation of the GluA1

92 indicating that the INS-membrane interaction is necessary for increasing activity of pvLAAD.

93 nsion, and IL-33-driven mast cell activation are necessary for induction of type 2 immunopathology an

94 Better understanding of LOS is necessary for informed consent and discharge planning

95 maintain triplet microtubules and that these are necessary for inheritance of centrioles from one cel

96 The carboxyl terminus of p17 is necessary for interaction with CDK2 and for induction

97 ot to be essential for particle assembly but is necessary for interactions with the transmission vect

98 The LIM domains of Rga1 are necessary for its interaction with Nba1, and loss of

99 CLY phosphorylation and nuclear localization are necessary for its role in promoting BRCA1 recruitmen

100 ore, Nedd8 binding site in Smurf is shown to be necessary for its ubiquitin ligase activity towards t

101 ectly and a PKA phosphorylation site in TCF4 is necessary for its transcriptional activity in culture

102 ted whether Dam1, a known substrate of Mps1, was necessary for its critical meiotic role.

103 omain had a mutation in the HPD motif, which is necessary for J-protein-Hsp70 interactions, suggestin

104 ipts, and RNAs present at active centromeres are necessary for kinetochore assembly and cell-cycle pr

105 esion studies showing that cortical circuits are necessary for learning, but that subcortical circuit

106 de stability to the C-terminal domain, which is necessary for lethal toxicity against lepidopteran in

107 SLC38A9 is necessary for leucine generated via lysosomal proteol

108 Nutrients are necessary for life, as they are a crucial requiremen

109 iologically relevant concentrations of Abeta are necessary for long-term potentiation (LTP) and memor

110 NA) is a conserved Rhadinovirus protein that is necessary for long-term chronic infection by these vi

111 lial stem cell quiescence and exhaustion and is necessary for long-term maintenance of the mammary gl

112 The abundant synaptic protein CaMKII is necessary for long-term potentiation (LTP) and memory

113 Its postsynaptic displacement is necessary for loss of AMPARs during homeostatic scali

114 further identified that GABAB(1a) receptors are necessary for maintaining contextual memory precisio

115 ppropriate methods of post-harvest treatment are necessary for maintaining these bioactive phytochemi

116 Finally, we showed that CHD7 is necessary for maintaining an open, accessible chromat

117 These results argue that TbSmee1 is necessary for maintaining HC morphology, which is imp

118 Importantly, dose adjustments for tacrolimus were necessary for maintaining sufficient trough levels.

119 regulator of a chromatin-based pathway that is necessary for maintenance of the leukaemic state and

120 5/MLL2/AR epigenetic circuit drives CRPC and is necessary for maintenance of the malignant state.

121 n, signaling, and logical programming, which are necessary for making enclosed, hierarchical structur

122 hrocytes by Plasmodium falciparum merozoites is necessary for malaria pathogenesis and is therefore a

123 ed that the cytoplasmic juxtamembrane domain is necessary for maximal FERONIA activity, whereas the t

124 Furthermore, lysine 9 on histone H3 is necessary for maximal pol II pause release through SE

125 ly, we show that the nucleosome acidic patch is necessary for maximum activity of all ISWI remodeller

126 ts demonstrated that the first two cysteines are necessary for McpM to inhibit susceptible cells.

127 of Foxp1 during embryonic brain development is necessary for mediating proper interactions between F

128 an steroid/Meth responsive cells in the MePD are necessary for Meth-induced facilitation of proceptiv

129 ory receptors control NK-cell activation and are necessary for MHC-I-dependent education, we investig

130 ially derived reactive oxygen species, which are necessary for microbial killing.

131 exible and scalable energy storage solutions are necessary for mitigating fluctuations of renewable e

132 We also found that FDXR was necessary for mitochondrial iron homeostasis and pro

133 of cell cycle regulators and that the KDM5s are necessary for mitotic clonal expansion in 3T3-L1 cel

134 MKII mRNA with a long 3'-untranslated region is necessary for modulating spontaneous neurotransmissio

135 Accurate amyloid PET quantification is necessary for monitoring amyloid-beta accumulation an

136 g infection and transmission dynamics, which is necessary for more effective treatment strategies.

137 tatory (E) and inhibitory (I) spinal neurons are necessary for motor behavior, but the influence of r

138 The stress response and cell survival are necessary for normal pancreatic beta-cell function,

139 pressed in the adult, JAK2 is also likely to be necessary for normal organ function.

140 In addition, cpsA is necessary for normal asexual and sexual development.

141 immediately after unreinforced lever presses is necessary for normal extinction of cocaine seeking, s

142 metabolic labeling, we found that TbPSS2 (i) is necessary for normal growth of procyclic trypanosomes

143 ndicate that the function of ppk29 in muscle is necessary for normal postsynaptic responsivity to neu

144 ediated by L-VGCCs in oligodendroglial cells is necessary for normal remyelination and is an essentia

145 tential to release both 5-HT and substance P is necessary for normal respiratory dynamics, perhaps vi

146 These studies demonstrate that DDR2 is necessary for normal TMJ condyle development and home

147 of SoxF function revealed that these factors are necessary for NOTCH1 and notch1b enhancer activity a

148 Molecules that are necessary for ocular hypersensitivity reactions incl

149 These results suggest that pUL33 is necessary for one of the two viral DNA cleavage event

150 biochemical and physical component, and both are necessary for optimal barrier restoration.

151 In moderation, however, neutrophils are necessary for optimal viral control.

152 in hPSC culture and 3D organoid systems may be necessary for optimal results.

153 that TLR4 expression on hematopoietic cells was necessary for oral tolerance induction.

154 atory circuit and show that D2 cell activity is necessary for orexin-dependent innate risk-avoidance

155 t serine hydroxymethyl transferase 1 (SHMT1) was necessary for ovarian cancer tumor growth and cell m

156 pulse-labeling experiments showed that RAD6 is necessary for overcoming cisplatin-induced replicatio

157 the situation when the permutation procedure is necessary for p-value calculation.

158 m of the CK5 transcriptional start site that is necessary for P4 activation and contains a putative p

159 f palatal medial edge epithelial (MEE) cells were necessary for palatal adhesion.

160 ntified the GLASSY HAIR 1 (GLH1) gene, which is necessary for papillae formation.

161 t the SIN1 5'UTR, suggesting that Sin1 5'UTR is necessary for Pdcd4 to inhibit Sin1 translation.

162 at activation of focal adhesion kinase (FAK) is necessary for PE-stimulated autophagy suppression and

163 ANTXR1 is necessary for permissivity in vitro and in vivo.

164 Subsequently, the TP domain is necessary for pgRNA packaging into viral nucleocapsid

165 e FLI1 and depends on tyrosine residues that are necessary for phase transitions of the EWSR1 prion-l

166 ivation of Src within endothelial cells that is necessary for phosphorylation of VE-cadherin and for

167 s of zebrafish and mice and that the exocyst is necessary for photoreceptor ciliogenesis and retinal

168 Though REC phosphorylation is necessary for PhyR function in vivo, we did not detec

169 This result suggested that both PiTs are necessary for Pi signaling.

170 hat Ezrin links CFTR and TLR4 signaling, and is necessary for PI3K/AKT signaling induction in respons

171 (FR) light-coupled jasmonate (JA) signaling is necessary for plant defense and development.

172 l of MCT8 deficiency, and we found that MCT8 was necessary for polarized influx of the active form of

173 ons by state of origin (source-state), which is necessary for policy makers to determine efficient st

174 difications to the characteristic time scale is necessary for porous electrodes.

175 LAP1 does not impair myogenesis but that it is necessary for postnatal skeletal muscle growth.

176 sed tendon thickness, indicating that mTORC1 is necessary for postnatal tendon development.

177 cs workflows, and new informatics approaches are necessary for processing the associated data.

178 s and a minimal fusogenic peptide motif that is necessary for promoting cell-cell fusion with myomake

179 indicate that Tcf1-beta-catenin interaction is necessary for promoting thymocyte survival to maintai

180 ella motility, Rab11, and actin coordination are necessary for proper abscission.

181 teraction with the RNA binding protein STAU2 are necessary for proper transport and local translation

182 ver formation between homologous chromosomes is necessary for proper chromosome disjunction during me

183 priate time and location in polarizing cells is necessary for proper establishment of epithelial pola

184 ro and in vivo studies have shown that NECL4 is necessary for proper peripheral nerve myelination.

185 we found that miR-155 expression by T cells is necessary for proper tumor-associated macrophage expr

186 noble metals with unique surface structures are necessary for prospective applications.

187 odies (NAbs) targeting distinct epitopes may be necessary for protective immunity.

188 These truncations demonstrated that SL3 is necessary for Pxr function in the defective strain.

189 ensity of Na(+) channels at nodes of Ranvier is necessary for rapid and efficient action potential pr

190 ns that do not have structural templates, it is necessary for reconstruction studies to focus on hard

191 n and tested the hypothesis that macrophages are necessary for regeneration.

192 These specific characteristics may be necessary for regulation of allosteric structural tra

193 The VTA is necessary for reward behavior with dopamine cells cri

194 Controlled human feeding studies are necessary for robust nutritional biomarker developme

195 [8, 9], we hypothesized that M-cell activity was necessary for S-start generation.

196 However, it is not known whether the VP is necessary for salt appetite in terms of seeking out s

197 We identified that PLCepsilon1 was necessary for SDF-1alpha-induced adhesion using shea

198 s are consumed, and 3) the surrogate L chain is necessary for selection of productive IgH gene rearra

199 that cooperation between miRNA target sites is necessary for silencing in vivo in the C. elegans emb

200 ls with detailed membrane potential dynamics are necessary for simulation studies where sub-neuronal

201 Remarkably, NTS(HSD2) neurons are necessary for sodium appetite, and with concurrent A

202 by target-derived nerve growth factor (NGF) is necessary for soma-to-axon transcytosis of TrkA recep

203 However, this information may not be necessary for some applications.

204 We find that systemic pools of TIMP2 are necessary for spatial memory in young mice, while tr

205 Integration of reproduction and metabolism is necessary for species survival.

206 s and trans interactions between ParB dimers is necessary for spreading.

207 a highly conserved amino acid, Gly449, that is necessary for Src activation.

208 The nuclear receptor LXR is necessary for Srebf-1c transcription.

209 f p53, modulates p53-dependent apoptosis and is necessary for steroidogenesis and biogenesis of iron-

210 Experiments in rodents are necessary for studying the mechanisms of brain funct

211 lso novel was the finding that this adhesion was necessary for subsequent ROS production and apoptosi

212 ach based on knowledge of local epidemiology is necessary for success.

213 induced increases in ripple-spindle coupling are necessary for successful memory consolidation has no

214 ressed in the Bvg positive (Bvg+) phase that are necessary for successful respiratory tract infection

215 toxic T lymphocytes upon antigen stimulation is necessary for successful antiviral, and antitumor imm

216 curate community-level surgical epidemiology is necessary for surgical health systems planning.

217 with an abundance of virulence factors that are necessary for survival within a host, including the

218 on behavior (carrier animal-hitchhiking) and are necessary for switching from repulsion to CO2 (a car

219 Notably, Matrigel mattress was necessary for T-tubule formation.

220 put neuron type, we identified which neurons are necessary for T4 directional selectivity and ON moti

221 Wnt, BMPs, Notch, and Hh signaling pathways are necessary for taste cell proliferation, differentiat

222 subunits, largely dispensable early in life, are necessary for terminating contraction (systole) in a

223 ic ductal adenocarcinoma (PDAC) PAR2 protein is necessary for TGF-beta1-dependent cell motility.

224 l variation in nutrient and food consumption are necessary for the development and validation of robu

225 pression by Sox2 in retinal progenitor cells are necessary for the differential growth of the corresp

226 Ms) and membrane electrode assemblies (MEAs) are necessary for the evaluation of advanced electrocata

227 loop and the N-terminal cytoplasmic segment are necessary for the functional interaction between the

228 e expression and/or repression of genes that are necessary for the initiation of gametocyte developme

229 Hence, SPA proteins are necessary for the light-controlled change in COP1 su

230 strates that dopaminergic spinal projections are necessary for the maintenance of a chronic pain stat

231 relationships in fitness-related traits, (3) are necessary for the maintenance of sexual dimorphism,

232 further demonstrate that both Chd7 and Top2b are necessary for the transcription of a set of long neu

233 n experiments in aged mice revealed TIMP2 to be necessary for the cognitive benefits conferred by cor

234 Race-specific normative data may not be necessary for the deployment of BMO-MRW in AD patient

235 MT3-MMP, a membrane-bound zinc protease, to be necessary for the development of excitatory synapses

236 Bcp1 has been shown to be necessary for the export of Mss4, a phosphatidylinosi

237 Therefore, experience must be necessary for the formation (or maintenance) of face

238 olipid transporter activity of ALA1/ALA2 may be necessary for the formation of similar invaginations

239 cating activity, although such a species may be necessary for the process.

240 ivotal role in chloroplast redox regulation, being necessary for the activity of diverse Trxs with un

241 rst evidence that the VP or any brain region is necessary for the ability to use contextual cues to g

242 Remarkably, although Smad4 is necessary for the activation of the mineralization-re

243 ivity-dependent BDNF release within the mPFC is necessary for the antidepressant actions of scopolami

244 the neuron A03a5, which together with Wave, is necessary for the backward locomotion touch response.

245 ction between P. gingivalis and S. cristatus is necessary for the cell-cell communication.

246 f note, we found that cell cycle progression is necessary for the DDR-resistant MYOD mutant to revers

247 tanding the gas adsorption behavior on shale is necessary for the design of optimal gas recovery and

248 Mechanical loading is necessary for the development and maintenance of the

249 of the mechanisms that regulate DAT function is necessary for the development of clinical interventio

250 Visual experience is necessary for the development of direction selectivit

251 Sensory experience is necessary for the development of some receptive field

252 molecular mechanisms governing neurogenesis is necessary for the development of translational strate

253 R is sufficient but does not show whether it is necessary for the effects of exogenous GLP-1R agonist

254 IRF1 is necessary for the expression of type III IFNs (IFNLs

255 -trial fluctuations in outcomes, whereas BLA is necessary for the facilitation of learning in respons

256 s, in which Bmpr1a signaling in chondrocytes is necessary for the formation of a pool or niche of ost

257 rstanding of the regulation of A1R signaling is necessary for the future design of therapeutic agents

258 Vitamin D is necessary for the healthy growth and development of b

259 emonstrated that cholinergic neuroplasticity is necessary for the induction of persistent AHR after n

260 ut not GATOR2, to the lysosomal surface; and is necessary for the interaction of GATOR1 with its subs

261 ion of stem cell factor (SCF) by these cells is necessary for the maintenance of differentiated melan

262 Human chorionic gonadotropin (hCG) is necessary for the maintenance of early pregnancy and

263 ase changes, and stimuli-response behaviors, is necessary for the most basic functions of life, and o

264 , an auto-activation loop on the buffer node is necessary for the NFBL class.

265 nd a later phase whose successful completion is necessary for the normal expression of LTM.

266 howing that prolactin action on MPOA neurons is necessary for the normal expression of postpartum mat

267 f appropriate beta-catenin-mediated Wnt tone is necessary for the orderly differentiation of cortical

268 Interaction with AtMIA40 is necessary for the phosphatase activity of AtSLP2 and

269 , it was not clear whether p25/Cdk5 activity is necessary for the progression of these pathological c

270 Neuronal survival is necessary for the proper function of cochlear prosthe

271 Regulated mesoderm migration is necessary for the proper morphogenesis and organ form

272 s of nanoparticles (NPs) with serum proteins is necessary for the rational development of nanocarrier

273 ggesting that the enzymatic activity of PARN is necessary for the release of 18S-E from Bystin-associ

274 ffelmacher et al. (2017) show that autophagy is necessary for the release of free fatty acids from in

275 ity and cell composition prior to the injury is necessary for the repair macrophage phenotypic transi

276 Thus, the expression of Ifnlr1 by IECs is necessary for the response to both endogenous and exo

277 tiation, timely repression of their activity is necessary for the self-renewal and maintenance of mus

278 e endoplasmic reticulum (ER) and peroxisomes is necessary for the synthesis and catabolism of lipids,

279 rabinosylates MtCLE12, and this modification is necessary for the transport and/or reception of the A

280 e divergence of sponges and eumetazoans, and was necessary for the evolution of animal multicellulari

281 PDZD8 was necessary for the formation of ER-mitochondria conta

282 found that minimal trial-and-error learning was necessary for the participants to solve the new soci

283 In addition, TA localized to TAN lines and was necessary for the proper mobility of EGFP-mini-nespr

284 It was necessary for the radiotherapy dose to be as high as

285 Slack channel expression at the DRG membrane is necessary for their characteristic firing accommodati

286 d diacidic motif (Asp-Glu) in these proteins is necessary for their export.

287 functional evidence that only seven enzymes are necessary for this process.

288 m, the debate on whether an active mechanism is necessary for this asymmetry remains unsolved.

289 routine reporting in the public domain will be necessary for tracking progress towards the 90-90-90

290 Cadherin-mediated homophilic adhesion is necessary for trans-endocytosis, and adhesive junctio

291 number of Cdx target genes, and both factors are necessary for transcriptional regulation of such tar

292 Sensory receptor hair cells (HCs) are necessary for transducing mechanical inputs and stim

293 hat modulate epithelial resistance to injury is necessary for understanding intestinal homeostasis an

294 binuclear cluster transcription factor CLR-1 is necessary for utilization of cellulose, a major, reca

295 Our results suggest that shuttling is necessary for viability of embryos from mothers with

296 A dynamic actin cytoskeleton is necessary for viral entry, intracellular migration, a

297 network, and its attention-control function, are necessary for virtually all volitional motor acts wh

298 0 that allow its binding to co-receptors and is necessary for virus entry to establish infection.

299 gBcyt regulation is necessary for VZV pathogenesis, as the hyperfusogenic

300 MEI-S332 is necessary for Wdb localization, but, additionally, bo