ライフサイエンスコーパス: be required for

1 Intensive care unit admission was required for 27 patients (8.8%) during delivery.

2 We show that VEGFA from the epithelium is required for a distinct endothelial cell (EC) populat

3 Neither T-type VGCC isoform was required for ACh-induced inhibition of contraction,

4 based or community-wide treatment strategies are required for achieving the EPHP goal.

5 The catalytic activity of the protease MALT1 is required for adaptive immune responses and regulatory

6 encoding starch branching enzyme IIb, which is required for amylopectin synthesis in the endosperm.

7 Two class I TCP transcription factors are required for an efficient elongation of hypocotyls i

8 Our results indicate that TCP14 and TCP15 are required for an efficient elongation response to aux

9 the PGC family of transcriptional activators is required for angiogenic responses.

10 lation and SIRT3-mediated oxidant scavenging are required for anoikis resistance in vitro following m

11 Moreover, BRI1 is required for another function of RLP44: the control o

12 Selective V2 receptor agonism is required for anti-DI activity and we hypothesised tha

13 a GTPase-activating protein for FgRab8 which is required for apical secretion-mediated growth and pat

14 Surprisingly, IRX3/5 are required for appropriate cell cycle progression and

15 We conclude that KMT2D is required for appropriate cranial NCC differentiation

16 lular but not magnocellular oxytocin pathway is required for autism-relevant social reward behavior.

17 omplexes regulate key trafficking events and are required for autophagy.

18 infiltration of macrophages and neutrophils is required for autoreactive CD4 T cell-mediated skin di

19 We showed that SnRK2.8 was required for AvrPtoB virulence functions, including

20 havior indicating its intracellular delivery was required for behavioral effect.

21 d by an aspartate residue in type P(O) SadP, was required for binding to Gb4 and, strikingly, was als

22 tivities are down-regulated by acylation but are required for biofilm formation, thus providing a def

23 s in intercellular aggregation, while groEL1 was required for biofilm maturation in M. smegmatis.

24 ntestinal lysosome-related organelles (LROs) is required for biosynthesis of most modular ascarosides

25 in vitro, and the DNA-binding ability of CST is required for blocking MRE11-mediated nascent-strand d

26 nes involved in apicoplast carbon metabolism are required for blood-stage parasite survival and organ

27 tified near RA target genes already known to be required for body axis and limb formation, thus valid

28 y, we showed that acidified amebic lysosomes are required for both amebic trogocytosis and phagocytos

29 ular evidence that transient phosphorylation is required for CAP1 functions in both actin filament tu

30 nslated RNA (scoutRNA), together with crRNA, is required for Cas12d-catalyzed DNA cutting.

31 Extracellular virions are required for cell-to-cell spread and pathogenesis.

32 the cell wall architecture, suggesting GPI7 is required for cell wall biogenesis.

33 Interestingly, MNT was required for cell proliferation even in the absence

34 thetic pathway are crucial host factors that are required for cellular entry by hepatoviruses.

35 M was found to engage part of Na(V) 1.5 that is required for channel inactivation with high affinity.

36 tion (FDA) emergency use authorization (EUA) is required for clinical application of SARS-CoV-2 molec

37 Cul5, different determinants in the MVV Vif are required for cofactor binding and stabilization of t

38 Identifying molecular processes that are required for cognition and are altered during old ag

39 and cohesin and demonstrate that while CTCF is required for cohesin binding to KSHV, they have very

40 rmogenesis-promoting neurons in the DMH that is required for cold defense and fever.

41 tly activates the myf5 and myod genes, which are required for commitment to myogenesis.

42 RIN, ET and other factors are required for completion of the full fruit-ripening p

43 nd direct it to a subset of viral genes that are required for completion of the viral replication cyc

44 Such simulations are required for comprehensive river modeling, where a s

45 text-responding vCA1 neurons, whose activity was required for contextual fear learning and synaptic p

46 Visceral adipose NLRP3 was required for deficits in long-term potentiation (LTP

47 Our results show that macrophages are required for dental pulp stem cell activation and ap

48 re-T-cell receptor (TCR) signal transduction is required for developing thymocytes to differentiate f

49 dMtmr6, which is required for development and viability in Drosophila,

50 iscovered that the E3 ubiquitin ligase Nedd4 is required for developmental myelination through stabil

51 1 (DGAT1) synthesizes triacylglycerides and is required for dietary fat absorption and fat storage i

52 t eight cell divisions in vivo, with BLIMP-1 being required for differentiation at division eight.

53 Our data support a model in which flotillins are required for direct control of membrane fluidity rat

54 hat RAB13-RABIF association at the periphery is required for directing RAB13 GTPase activity to promo

55 the epidermal growth factor receptor (EGFR) is required for directing STING to endosomes, where it i

56 pressing interneurons, the activity of which is required for discrimination.

57 TL-1 Hypo control of pulmonary infection but are required for dissemination control.

58 Spermathecal gene products are required for Drosophila sperm storage and sperm viab

59 Curli expression is required for E. coli to exacerbate alphaSyn-induced b

60 ic muscle, or that an innate immune response is required for effective donor cell engraftment.

61 he distribution and magnitude of earthquakes is required for effective earthquake forecasting.

62 een cytotoxic T lymphocytes and tumour cells is required for effective immunotherapy.

63 ith the composite Phactr1/PP1 surface, which are required for efficient dephosphorylation.

64 t different chromatin remodelling activities are required for efficient repair in specific genomic co

65 is is associated with increased sleep, which is required for efficient active zone removal after inju

66 t of RAD51AP1 in FANCD2 deubiquitination, it is required for efficient HR-mediated chromosome damage

67 heparan sulfate, we show that this activity is required for efficient infection by SBV.

68 e show that in Caenorhabditis elegans COQ-2e is required for efficient RQ synthesis and survival in c

69 P2RX7 was required for efficient re-expression of the receptor

70 ev1 protein, but not its catalytic activity, was required for efficient TLS.

71 ous inward and outward lactate fluxes, which were required for efficient utilization of glucose by be

72 n of Tyr(297), Tyr(246), and Tyr(336) of Shb is required for EphB2-ephrinB1 boundary formation, as we

73 DGK4 are essential during gametogenesis and are required for ER-localized phospholipid metabolism in

74 Here we show that that the lPBN is required for escape behaviors and aversive learning t

75 ents, a pole of Nodal signaling emerges that is required for explant elongation via the planar cell p

76 rotein synthesis; however, protein synthesis was required for expression of Fibromodulin and Adamtsl2

77 ypothesized that a flexible vimentin network is required for fast amoeboid migration.

78 alibration free point-of-care testing device is required for fast screening to rule-in and rule-out A

79 nacidin A, an additional ketoreductase RslO8 is required for formation of the main products rishirili

80 of multiple myc mutants confirmed that MYCs are required for full expression of red (R) light-regula

81 its ability to associate with membranes, but is required for full activation of the GTPase and for ef

82 observed that this cytoplasmic translocation is required for full activation of the JNK pathway and t

83 response to acute stress and that ATF6alpha is required for full activation of XBP1 targets, but XBP

84 nt challenge, suggesting that serratiochelin is required for full S. marcescens pathogenesis in the b

85 omprehensive, high-quality reference genomes are required for functional characterization and taxonom

86 ions according to biological characteristics is required for further BTMs validation and appropriate

87 n RNAPII reaches the middle of RDH genes and is required for further RNAPII elongation and 3'-end pro

88 gulated by transcription factor AP2-G, which is required for gametocytogenesis.

89 l input, likely via neuron-supplied factors, is required for generation of differentiated taste cells

90 protoporphyrin IX in order to form heme that is required for growth stimulation and survival in vivo

91 major quinone of Pseudomonas aeruginosa and is required for growth under anaerobic respiration (i.e.

92 However, lower concentrations of agonist were required for half-maximum inhibition of dopamine-in

93 d SMRT deacetylase-activating domains, which are required for HDAC3's enzymatic function, permit norm

94 d clonal analysis, we demonstrate that Ift20 is required for HF-SC migration and their contribution t

95 Farnesylation at the C-terminus is required for hGBP1's activity against microbial patho

96 ribute to mitochondrial iron homeostasis and are required for high-affinity iron import during active

97 e demonstrate that the degradation of PTPN14 is required for high-risk HPV18 E7 to extend keratinocyt

98 independent of Notch activation, the latter was required for high NKp80 expression and a stage 4B-li

99 The stringent response regulator SpoT is required for HipA-mediated antibiotic persistence, bu

100 nriched at telomeres during the G2 phase and is required for histone H3.3 deposition and telomere DNA

101 Jun N-terminal kinases (JNKs) and p38s that are required for host immune response, whereas extracell

102 as the sentinel for ribosome collisions and is required for immediate early activation of both SAPK

103 pi7 mutant, indicating GPI-anchored proteins are required for immune evasion.

104 This distance is required for improving rituximab recognition, and in

105 We also show that ET-1 is required for increased neural stem cell and OPC proli

106 e calcineurin catalytic A-subunit (CaNAbeta) is required for induction of pathological myocyte hypert

107 ings suggest that Plc2, but not Plc1 or Plc3 are required for infection of host cells.

108 t studies revealed that actin polymerization is required for initiation of myelination whereas actin

109 enes, and found that only galactosylated WTA is required for InlB surface presentation and function,

110 Such output is required, for instance, for larval zebrafish to learn

111 Interestingly, PAK1 has been suggested to be required for insulin-stimulated glucose transporter 4

112 The TBC1D4-RAB10 signaling module is required for insulin-stimulated GLUT4 translocation t

113 In contrast, glucose was required for insulin to increase mitochondrial oxida

114 s) contribute to erythrocyte homeostasis and are required for iron recycling.

115 he pleckstrin homology (PH) domain of P-Rex1 is required for its activation in cells.

116 tion signal (NLS) that binds to importin and is required for its function during cytokinesis.

117 in binding of human ISG15 to LFA-1 in vitro were required for its adjuvant effect in vivo.

118 me pathways, multiple domains of the protein were required for its function, whereas in other pathway

119 says, we show that both HEPN nuclease motifs are required for Las1 nuclease activity and fidelity.

120 s IIa histone deacetylases (HDAC4 and HDAC5) are required for loading-induced Sost suppression and bo

121 glycan-retaining peptide fragments would not be required for localization.

122 The EACBE is required for long-distance regulation of the Ealpha o

123 , and a spermathecal-derived heme peroxidase is required for long-term Anopheles gambiae fertility.

124 Sustained P2RX7 signaling was required for long-term Trm cell maintenance, indicat

125 Simplified diagnostics are required for low-resource settings and difficult-to-

126 rafficking and synaptic targeting of AMPARs, is required for LTP and learning and memory.

127 ow that the lipid-droplet-related gene Fitm2 is required for maintaining cell fitness after exposure

128 man acute myeloid leukemia (AML), and ALKBH5 is required for maintaining leukemia stem cell (LSC) fun

129 gain of prefrontal GABAergic function, which is required for maintaining proper excitatory-inhibitory

130 ive to rapid turning off of the receptor and is required for maintaining RhoA-mediated transcription

131 ng the primary host infection cycle but also is required for maintenance in a host population.

132 However, bound ligand is required for maximal activity.

133 ty, explaining why catalytically active Fig4 is required for maximal PI(3,5)P(2) production by PIKfyv

134 zation, which suggests that T3SS1 repression is required for maximal virulence.

135 cted zinc-binding residues, Asp87 and His88, are required for MBLAC2 hydrolase activity.

136 hrough OCA-B-MED1 interactions, this complex is required for Mediator association with the BCL6 promo

137 ressed at the margins of leaf primordia, and is required for mediolateral outgrowth.

138 el states that the secreted substrate ESAT-6 is required for membrane permeabilization and that a sub

139 gy, and here, we investigated whether Ca(2+) is required for MERS-CoV fusion by screening a mutant ar

140 ter Tap1 and the aminopeptidase Erap1, which are required for MHC-I trafficking to the cell surface.

141 The N-terminal coiled-coil CC1 domain is required for microtubule localization, while the C-te

142 Our findings demonstrate that RTEL1 is required for MiDAS and suggest that RTEL1 maintains g

143 export occurs in the absence of Fzo1, which is required for mitochondrial dynamics/respiration.

144 Mechanistically, PGAM5 is required for mitochondrial fission through dephosphor

145 Our findings reveal that human METTL15 is required for mitochondrial function, delineate the ev

146 rones, HSP60 and HSP10, suggesting that Akt3 is required for mitochondrial homeostasis.

147 or of atypical mitosis in the gametogony and is required for mosquito transmission.

148 -1, MTV1 interacts with AP-4, whose function is required for MTV1 recruitment.

149 sed by Muller glia following neuronal death, is required for Muller glia to progress through the cell

150 We demonstrate that MMP14 is required for NC delamination.

151 em cells, we further demonstrated that MCM10 is required for NK cell terminal maturation and acquisit

152 ese data demonstrate that both AMPK and ATF1 are required for normal hematoma resolution.

153 This stage-specific HIF suppression is required for normal B cell development because geneti

154 nding protein that regulates translation and is required for normal cognition.

155 Thus, LOXL1 expression is required for normal IOP control, while ablation resul

156 uggest that SIRT1 in mPFC excitatory neurons is required for normal neuronal excitability and synapti

157 oles together with ESCRT-mediated remodeling is required for nuclear closure.

158 Here, we show that the MA region is required for nuclear import of Gag through the TNPO3

159 ental second messenger in all cell types and is required for numerous essential cellular functions, i

160 cn-Cre(+) dDG neurons identified BDNF, which was required for Ocn-Cre(+) dDG neurons mediated antianx

161 ng cell migration toward oncogenic cells and is required for oncogenic cell extrusion.

162 ate that cell-intrinsic adrenergic signaling is required for optimal adaptive NK cell responses.

163 irect orchestration of their cross-talk that is required for optimal anti-tumour immunity.

164 These results show that Hdac3 is required for optimal bone healing and osteoclast fusi

165 e processing, immunohistology and microscopy is required for optimal results.

166 lobal operation of thiol redox switches that is required for optimal usage of energy stores by the mi

167 onal insights into an essential protein that is required for organelle-specific trafficking and brain

168 HopO1-1 is required for P. syringae to spread locally to neighbo

169 Replication-dependent histones (RDH) are required for packaging of newly synthetized DNA into

170 s including endocytosis of hemoglobin, which is required for parasite growth and artemisinin activati

171 in with uncompromised DNA-binding activities is required for PARPi-induced innate immune response.

172 ell cytotoxicity early during activation and is required for persistence of activated CD8 T cells fol

173 ssion of the cell cycle regulatory gene CDK6 is required for Philadelphia-positive (Ph+) acute lympho

174 the CTS of Bim directly interacts with Bax, is required for physiological concentrations of Bim to a

175 tein SUMO and the SUMO E3 ligase Su(var)2-10 are required for piRNA-guided deposition of repressive c

176 that the MHC-II antigen presentation pathway is required for PIV-mediated protection against C. burne

177 PDXK kinase activity is required for PLP production and AML cell proliferatio

178 ments in vivo or in cellulo indicate that it is required for Pnr- and Srp-dependent gene expression,

179 This interaction is required for polarised growth.

180 Phosphorylation at other sites is required for PopP2 but not AvrRps4 responsiveness and

181 c analysis we show that intact SA-signalling is required for potato defences against the necrotrophic

182 intact SA signalling, and not JA signalling, is required for potato defences against the necrotrophic

183 hat the kinetochore proteins KNL-1 and KNL-3 are required for preanaphase chromosome stretching, sugg

184 ing and the presence of an OSRE1 in intron 1 are required for precise enhancement of hyperosmotic glu

185 X-ray clock transitions(8,12) in HCIs, which are required for precision studies of fundamental physic

186 smic reticulum (ER) aminopeptidase 1 (ERAP1) is required for processing of the signal peptide, the me

187 were expressed upon IS maturation, and OVCH2 was required for processing of the sperm surface protein

188 class of siRNAs known as WAGO-class 22G-RNAs are required for proper expression of spermatogenic and

189 ly reported that Roundabout (Robo) receptors are required for proper islet morphogenesis.

190 ic force microscopy reveals the Y269 residue is required for proper DNA bending by APE1, providing ev

191 rain axons traversing the midbrain, and this is required for proper GABAergic neuronal migration into

192 tight balance in the Wnt-Adamts19-Klf2 axis is required for proper valve maturation and maintenance.

193 of enriched PM fractions revealed that EPS1 was required for proper PM abundance of a discrete subse

194 e expression of prostacyclin synthase, which is required for prostacyclin production after lipopolysa

195 conserved set of peroxin (Pex) proteins that are required for protein import, peroxisomal growth, and

196 Notably, FAM134B is required for protein secretion in chondrocytes, and c

197 utations, which indicates that SOS1 and SOS2 are required for PUT3 transport activity.

198 upling between distant electron spins, which is required for quantum error correction, presents a cha

199 evaluation with improved benchmark datasets is required for reaching a definite conclusion.

200 ed in <10 mus, which is far better than what is required for real-time performance, and with low erro

201 many iMCD patients, but additional therapies are required for refractory cases.

202 ransition from quiescence to activation that is required for regeneration, but it remains unknown if

203 the expression of genes required for FAO and are required for renewal of ISCs.

204 Not4-mediated monoubiquitination of eS7A was required for resistance to tunicamycin, whereas E3 l

205 To test whether Tregs are required for resolution of atherosclerotic inflammat

206 d by both chaperones revealed that while Hfq is required for RNA sponge-mediated downregulation of th

207 Pathway dissection revealed that Mkt1 is required for RNAi-mediated post-transcriptional silen

208 in line with the notion that mitotic arrest is required for ROS buildup and oxidation of the nucleot

209 The conserved SAM domain was required for SAMD14 to increase colony-forming activ

210 iation for 5 h); thus, only a picomolar dose is required for sentinel LNs detection.

211 miR-206 is required for skeletal muscle regeneration in vivo.

212 fractory blood cancers, but further advances are required for solid tumor CAR therapy.

213 Spc110 domains that are required for SPB localization and toxicity include i

214 ng of the sperm surface protein ADAM3, which is required for sperm fertilizing ability.

215 e show that spindle-periphery localized FMN2 is required for spindle migration.

216 rom Caulobacter crescentus and show that CTP is required for spreading.

217 The initiation of MSCI is required for stage progression, which enables crossov

218 in of unknown biochemical function, TMEM127, are required for SteD-dependent ubiquitination of mMHCII

219 vascular endothelial growth factor D (VEGFD) is required for structural integrity of dendrites and co

220 nsitive allele (Sac1(ts)), we show that Sac1 is required for structural integrity of the Drosophila r

221 The catalytic activity of CTK-1 is required for such a response.

222 Here we show that Foxm1 is required for survival, quiescence and self-renewal of

223 x components in multivesicular bodies (MVBs) is required for sustained canonical Wnt signaling.

224 fusion machinery component syntaxin18, which is required for SV40-arrival to the ER.

225 We have previously shown that TBX1 is required for systemic lymphatic vessel development in

226 wnt1 was required for tail expansion after mob4 inhibition an

227 than just activation of PHAS transcription, are required for targeting increased CHH methylation at

228 ll differentiation, while their decommission is required for TCRA locus activation and enforced alpha

229 e, we show that 4 bp of core-enclosing helix is required for telomerase to be active in vitro and to

230 The shelterin protein TPP1 is required for telomere stability and elongation, but i

231 We demonstrated that MKP5 was required for TGF-beta1 signaling in muscle and that

232 DGFRbeta-initiated phosphorylation of PRAS40 is required for TGFbeta-induced mesangial cell hypertrop

233 key structural components of this matrix and are required for the assembly and architecture of biofil

234 t hypotheses suggest that flotillin proteins are required for the formation of complexes of membrane

235 nments strongly influence, and in some cases are required for the growth and fructification of cultiv

236 We demonstrate that IL-4/13A and IL-4/13B are required for the maintenance of a Th2-like phenotype

237 onging to the direct (striatonigral) pathway are required for the motor-impairing activity of Delta(9

238 n sorting (HOPS)-mediated vesicle tethering, are required for the phosphorylation of Vac17 in its Myo

239 he transcription factor AP-2beta is shown to be required for the differentiation of distal tubule pre

240 we show that this trait, which is thought to be required for the tolerance of abiotic stress, is not

241 s five CCCH zinc fingers (ZFs), with ZF2-ZF3 being required for the recognition of the AAUAAA poly(A)

242 a novel mitochondrial micropeptide Mm47 that is required for the activation of the Nlrp3 inflammasome

243 We found that PML is required for the ALT mechanism, and that this necessi

244 rosomal triglyceride transfer protein (MTP), is required for the biosynthesis of these lipoproteins,

245 c interaction indicates that functional MLH1 is required for the CAG repeat destabilizing effect of F

246 en together, our data demonstrate that Cdc23 is required for the chromosome segregation through regul

247 Taken together, our results show that Padi2 is required for the citrullination of histones within a

248 entified SMALL LEAF AND BUSHY1 (SLB1), which is required for the control of organ size and lateral br

249 pper transcription factor ATF-like 3 (BATF3) is required for the development of conventional type 1 d

250 It has long been known that glucose is required for the development of pre-implantation mous

251 Bcl6 is required for the development of T follicular helper c

252 se requires Asc as a reductant; thereby, Asc is required for the energy-dependent component of nonpho

253 r virus and demonstrate that the full capsid is required for the essential interaction with its GAG r

254 mycobacteria but absent in Escherichia coli, is required for the EsxA:B separation.

255 Lastly, ST2 is required for the exacerbated allergic airway inflamma

256 n, and that unhindered replisome progression is required for the faithful propagation of DNA methylat

257 Co-expression of Yin Yang 1 (YY1) is required for the full function of the transcription f

258 this study, we sought to test whether DOCK8 is required for the function and maintenance of ILC subs

259 Thus, Coq10 is required for the function of Q(6) in respiration and

260 This confirmed that OTX2 is required for the generation of photoreceptors, but al

261 Therefore, activation in these regions is required for the improvement in recognition of childr

262 , we have demonstrated that the 5-HT(3A)-ICD is required for the interaction between 5-HT(3A) and the

263 PQM-1 is required for the longevity of insulin signaling mutan

264 SirE located in the sir gene cluster is required for the maturation of SirA, but not NrfA.

265 G protein-coupled receptor signaling is required for the navigation of immune cells along che

266 Our results indicate that MFSD7c is required for the normal growth of CNS blood vessels a

267 We hypothesize that VF coalescence is required for the reassortment of the Birnaviridae Thi

268 nd proteolytic site (S2'), cleavage of which is required for the release of the fusion peptide(11,12)

269 results indicate that the endosomal pathway is required for the signaling cascade initiated by BDNF

270 In addition, we find that EIPR1 is required for the stability of the EARP complex subuni

271 coordination of multiple signaling pathways is required for the successful formation of a complete o

272 njugated and inhibited thermolysin, His-1084 was required for the conjugation and inhibition of acety

273 ohesion in HCT116 and HeLa cells, whereas it was required for the dissociation of cohesin from chroma

274 Mechanistically, talin1 was required for the formation of preassembled TLR compl

275 TRAF6 E3 ubiquitin ligase activity was required for the former but was dispensable for the

276 Time-lapse microscopy showed that HuR was required for the promotion of cell motility in migra

277 caspase activation, and that Akt1 and dCIZ1 are required for their survival and overgrowth.

278 s compared to controls suggests that cohesin is required for their full integrity.

279 Normally, accessibility to DNA is required for their function.

280 strates that ubiquitination of ciliary GPCRs is required for their regulated exit from cilia.

281 t1l and its H3K79 methyltransferase activity is required for thermogenic gene program.

282 aize chlorotic mottle virus (MCMV) infection is required for this disease.

283 phila melanogaster Vasa intronic gene (VIG), is required for this process.

284 sary for ZNF165 transcriptional activity and is required for TNBC tumor growth in vivo using an ortho

285 and whether its histone-modifying activities are required for transcriptional repression remains cont

286 MUT-2) is a ribonucleotidyltransferase that is required for transposon silencing and RNA interferenc

287 itis and pancreatic tumor development and to be required for tumor development and progression in mic

288 in and the UBF1 Ser-412 phosphorylation site are required for UBF1-mediated ECT2 recruitment to rDNA,

289 s) into densely aligned evenly spaced arrays is required for ultrascaled technology nodes.

290 d that the T cell receptor (TCR):CD3 complex is required for USSN-induced T cell activation, and that

291 eatment, however future prospective analysis is required for validation.

292 Although the presence of gRNA in virions is required for viral infectivity, in its absence, Gag c

293 ccumulation of other rotavirus proteins that are required for viroplasm formation and that NSP5 hyper

294 formation and that NSP5 hyperphosphorylation is required for viroplasm assembly.

295 ipathic helix and its amphipathic properties were required for virus restriction.

296 Adipocyte DICER is required for whole-body metabolic adaptations to aero

297 In scales, actin bundles are required for width formation.

298 on in the field-whether receptor endocytosis is required for Wnt signal transduction.

299 poprotein receptor-related protein 5 (Lrp5), is required for Wnt3-Fzd1 interaction.

300 of Plasmodium yoelii and identify that GEP1 is required for XA-stimulated gametogenesis.