ライフサイエンスコーパス: interaction with

1 Interactions with 34-nm long, S-shaped Atg17 complexes a

2 ome, we uncovered its specific and prevalent interaction with a large subset of primary microRNAs (pr

3 of a representative small-RNA precursor for interaction with a mRNA target.

4 kines in various biological matrices and its interaction with a natural receptor molecule has tremend

5 lack of interface specificity indicates that interaction with a particular ACh binding site is not th

6 Interaction with a second molecule of BF3 stabilizes the

7 he translational machinery is mediated by an interaction with a specific ribosomal protein, RACK1, an

8 it B-cell growth-promoting signals after its interaction with a still unknown receptor(s).

9 ves JAK isoform specificity through covalent interaction with a unique JAK3 residue Cys-909.

10 Moreover, this region coordinates interactions with a distributed network to support the f

11 powdery mildew colonization, but also affect interactions with a number of other phytopathogens.

12 tes herpes simplex virus (HSV) entry through interactions with a viral envelope glycoprotein.

13 nding sites of BSA play the main role in the interaction with acetate.

14 This direct interaction with actin suggests a new role of SPARC duri

15 tibility results from multiple pollen-pistil interactions with additive effects.

16 helial junctions are partially modulated via interaction with Ajuba, an actin binding and scaffolding

17 While interactions with and functions for MT motor proteins ar

18 Here, we show that ERG, through its physical interaction with androgen receptor, induces AR aggregati

19 transitions of the monomer, which facilitate interactions with another monomer that undergoes conform

20 struct such molecules and characterize their interaction with antigen.

21 Nef dimerization interface also reduced Nef interactions with AP-2 and CD4 and restored CD4 expressi

22 ranoanthocyanins led to an increase in their interaction with aPRPs.

23 ect events documented in vitro following IgG interaction with AQP4: AQP4 internalization, attenuated

24 eir fate in ecosystems, but its influence on interactions with aquatic plants is still unclear.

25 lants, including crops, engage in beneficial interactions with arbuscular mycorrhizal fungi.

26 We show that noncovalent interactions with associated benzene rings (a simple mod

27 r Drp1 in fed cells and in autophagy through interaction with Atg14L and other SNAREs in starved cell

28 cts mitochondrial ATP production through its interaction with ATP5alpha, whereas this relationship wa

29 6 more avidly, which in turn facilitates its interaction with AXL.

30 unts of dopamine and release it upon cognate interaction with B cells.

31 ition is further supported by its functional interaction with BasA (sphingolipid biosynthesis) and St

32 Correspondingly, CD177 ligation enhanced its interaction with beta2 integrins, as revealed by fluores

33 of time during their biogenesis and rely on interactions with binding partners to support proper fol

34 nd G3BP protein families, and only a lack of interaction with both protein families strongly affects

35 on HCA1, causing direct interference of HCA1 interaction with both the N-glycan and peptide-moiety of

36 to DNA double-strand breaks through bivalent interactions with both histone and DNA components of the

37 ctivity of each of these proteins depends on interactions with both ribosomal subunits, some portion

38 This work highlights that interactions with both S1-S2 and S3-S4 of NaV channels m

39 , CRIP1a can compete with beta-arrestins for interaction with C-terminal CB1R domains that could affe

40 lta1 averts its cell-surface expression, its interaction with CaValpha1, and modulation of CaV1.2 cur

41 ted with enabling protein trafficking to and interaction with cellular membranes.

42 ular motifs on xylan conformation and on the interaction with cellulose surfaces in Norway spruce (Pi

43 am of MeCP2 that influences neurogenesis via interactions with central molecular hubs linked to autis

44 W1L4L8 that is known to be important in the interaction with centrin.

45 ed surgery and to explore the effect surgery interaction with chemotherapy or radiation therapy on su

46 To analyze an RNA-dependent interaction with chromatin, we purified native nucleosom

47 We conclude that CD146/MCAM interactions with circulating galectin-3 may have an imp

48 we demonstrate a clear and rapidly emerging interaction with climate change.

49 C-terminal domains of TTP are involved in an interaction with CNOT9.

50 riptional activity despite unaltered protein interactions with co-activators and -repressors.

51 unknown to what degree diverse TCR-mediated interactions with cognate self-antigens are required for

52 We apply a global long-range Ising interaction with controllable strength and range, and me

53 c control of this process, including genetic interactions with crop quality parameters, is poorly und

54 re all risk factors for future relapse after interactions with CRTs.

55 he sequestration of soluble hematin or their interaction with crystal surfaces.

56 Thr(187)-Pro motif in p27 and reduces p27's interaction with cyclin A- or cyclin E-CDK2, leading to

57 pacting embryonic gene expression, and their interactions with developmental programs, remain largely

58 e phage genome via a mechanism that involves interaction with DNA and the bacterial RNAP.

59 mutants on its transcriptional activity and interactions with DNA, transcriptional cofactors and chr

60 in have profound and possible effects on the interaction with Dock7 and Vac14, respectively.

61 Le(X)) and display markedly greater adhesive interactions with E-selectin than do circulating lymphoc

62 PMN interaction with ECs induced the entry of Ca(2+) in ECs

63 associates with histone partially through an interaction with EIN2 nuclear-associated protein1 (ENAP1

64 binding regions are more accessible upon the interaction with EIN2, and more EIN3 proteins bind to th

65 Interaction with either of CheY's two binding partners,

66 Predefined subgroup analyses found no interaction with ejection fraction less than 30%, type o

67 microscopy, we observed the dynamics of GreB interactions with elongation complexes.

68 olysaccharide digestion, including microbial interactions with endogenous host glycans and the import

69 was observed in 5% O2, resulting in greater interaction with eNOS in response to histamine.

70 TMM interaction with ERL1 creates a binding pocket for recog

71 n, ethylenediamine) promotes a high-affinity interaction with exquisite selectivity for this sequence

72 ibutes to biofilm architecture through ionic interactions with extracellular DNA.

73 ation can explain how glycosylation enhances interactions with F-box proteins in cells.

74 horylation promotes RIPK1 activation and its interaction with FADD to mediate RIPK1-dependent apoptos

75 The interaction with FcepsilonRI is primarily responsible fo

76 l changes in the C3 domains that inhibit the interaction with FcRI.

77 rapment by carbon shells and strong chemical interaction with Fe3 O4 cores, this unique architecture

78 gesting that WRN recruitment and cooperative interaction with FEN1 during lagging-strand synthesis ma

79 ce and binding studies that the pneumococcal interaction with fibronectin is a non-human specific tra

80 In vivo, expanding vessel networks favor interactions with Flt1 mutant mouse endothelial cells.

81 over, mutation of this residue blocks PKD2's interaction with Focal Adhesion Kinase (FAK).

82 Understanding cold plasma interactions with food lipids and the critical parameter

83 bf4 is enriched at early origins through its interaction with forkhead transcription factors Fkh1 and

84 -GTPase Cdc42p promotes yeast fusion through interaction with Fus2p, a pheromone-induced amphiphysin-

85 ut mitral cells (MCs) appears to result from interactions with GABAergic granule cells (GCs), yet the

86 achment of individual nanoparticles, and the interaction with gas molecules plays a critical role, wh

87 In the absence of interaction with GIPC1, missorting of Plexin-D1 results

88 at are still not fully understood such as QD interactions with gold and other metal nanoparticles alo

89 AV1 scaffolding domain, indicating that CAV1 interaction with GRK2 is inversely regulated by endothel

90 that BAZ2B PHD-BRD establishes a polyvalent interaction with H3K14ac.

91 Lpl1 shows a synthetic genetic interaction with Hac1, the master regulator of a second

92 ortance of the Rev-erbbeta HRM in regulating interactions with heme and NCoR1 and advance our underst

93 n enhancing torsadogenic effects: oestradiol interaction with hERG mutations in the pore loop contain

94 ontrary to expectations based on known BECN1 interactions with heterologous partners.

95 iety of GRL-09510 forms strong hydrogen-bond-interactions with HIV-1 protease (PR) active-site amino

96 ediating uptake by immune cells, or blocking interaction with host cell receptors, making them a desi

97 he F-driven formation of VLPs occurs through interactions with host cell machinery, the cytoplasmic t

98 ability of the AIPL1 variants to mediate an interaction with HSP90 and modulate the rod cGMP PDE6 st

99 hilic, promiscuous pharmacophore and promote interaction with human nNOS-specific His342.

100 mperament than wolves, promoting cooperative interactions with humans and conspecifics.

101 ink between histamine-releasing factor (HRF) interactions with IgE and food allergy in a murine model

102 y to characterize the truncated NEMO protein interactions with IKK-alpha, IKK-beta, TNF receptor-asso

103 its depletion significantly reduces PapMV's interaction with immune cells.

104 y driven insight into the rise of ecological interactions, with implications for microbiome research

105 ape recognition can also be achieved by cell interaction with imprints that can be made into polymer

106 wn that MSC tumour residence and their close interactions with inflammatory factors are important fac

107 the regulation of insect development via the interaction with insect hormones, such as ecdysone and j

108 ooDSGCs leads to branch-specific homophilic interactions with interneurons.

109 of exogenous Lactobacillus plantarum and its interactions with intestinal bacteria in mice undergoing

110 nd contribution of single amino acids in OST interaction with its substrates.

111 eurulation induces NTDs by inhibiting folate interaction with its uptake systems.

112 recruitment of MAPKBP1 to the MSP and/or its interaction with JNK2 or WDR62.

113 ckening of the footpad epidermis through its interaction with K16.

114 at conformational changes in KCNQ1 alter its interaction with KCNE1.

115 mechanisms of RNA folding and unfolding, its interactions with ligands, and its functions.

116 el mitochondrial effectors in H. pylori-host interaction with links on gastric pathogenesis.

117 nistic knowledge of how it functions and its interactions with lipids are unknown or limited due to i

118 l targeting depends on co-expression of, and interaction with, LMBD1.

119 This interaction with LRP1 is direct, and is modulated by the

120 Screening the putative E3 ligases for interaction with LYK5 identified PLANT U-BOX13 (PUB13),

121 , our structural understanding of the MBS CC interaction with LZ PKG-1alpha has remained limited.

122 ontrol membrane curvature and to modify HA's interaction with M1 protein, while the stunting of fusio

123 annose Man9GlcNAc2 oligosaccharide exhibited interaction with Manalpha1-2Man on two different termini

124 toplasmic amino-terminus of iRhom2 alter its interaction with mature TACE, thereby licensing its prot

125 High-affinity interactions with MED25 are specific for the ETV1/4/5 su

126 as fluidity and charge that in turn modulate interactions with membrane-associated proteins.

127 n membranes: a precise understanding of RAS' interaction with membranes is essential to understand RA

128 of the beta2-adrenoceptor ligands and their interactions with membranes, we have investigated the lo

129 ave hypothesized to depend on the amygdala's interactions with memory systems.

130 e networks in circulating human cells, their interactions with metabolites, and their genetic control

131 hues in nature are not fully understood, but interactions with metal ions and phenolic compounds are

132 We propose that host interactions with microbes are critical for establishing

133 We found that interactions with microbes that do not directly enter le

134 tanding of the physics of surface structures interactions with microscale heat and mass transfer even

135 MinD-catalyzed ATP hydrolysis, stimulated by interactions with MinE's anti-MinCD domain.

136 ed by pharmacologic blockade of FcRn-albumin interactions with monoclonal antibodies or peptide mimet

137 ComplexViewer visualizes interactions with more than two participants and thereby

138 ain the specialized domains formed by axonal interaction with myelinating Schwann cells, such as clus

139 1 releases the autoinhibition, promoting its interaction with myosin VI.

140 Moreover, as interactions with natural stressors may cause underestim

141 he LIM domains of Rga1 are necessary for its interaction with Nba1, and loss of this interaction resu

142 SCs) with a DISC1 mutation that disrupts its interaction with Ndel1.

143 ipathic conformation, which allows increased interaction with negatively charged bacterial membranes.

144 cytes to (re)generate myelin and that failed interactions with neighboring cells or factors in the di

145 tes, control astrocyte morphogenesis through interactions with neuronal neurexins.

146 phology is sculpted by specific cell to cell interactions with neurons and each other.

147 ght to be strongly structured by competitive interactions, with niche partitioning of food resources

148 equisite role in tolerance induction through interactions with NKT cells.

149 hysiology of the tumor microenvironment, and interactions with non-cancer cells.

150 antileukemic effects of withaferin A and its interaction with NOTCH1 inhibition.

151 s maintained in a reduced state by substrate-interaction with NRX1, a process necessary for its H2O2-

152 imes, known as coherence times or T2, due to interactions with nuclear spins in the local environment

153 rminal domain of CrODA16 is required for the interaction with ODAs.

154 rk and default mode network strengthen their interaction with one another during episodic retrieval.

155 how RNA can remain soluble and available for interaction with other molecules in the cell despite the

156 ccoides subpopulations depend on synergistic interaction with other organohalide-respiring population

157 tinal absorption of mercury is influenced by interactions with other food components.

158 ultiple subunits, but how this regulates CPC interactions with other mitotic proteins remains unclear

159 ifferent sub-regions of the rVLPFC and their interactions with other motor-related brain regions.

160 interactions with proteases while preserving interactions with other proteins, such as target recepto

161 ight), increased illness (usually diarrhea), interactions with other trace elements such as copper an

162 ellular localization and result in decreased interactions with p210-selective interaction partners.

163 We propose that the cis interaction with P2Y2R provides allosteric resistance to

164 CI is directed to PDs through its interaction with P3N-PIPO.

165 n, Mdm2 deletion differed from blocking Mdm2 interaction with p53 family members, as Nutlin-3 induced

166 associated polymorphism does not abolish the interaction with p73alpha, indicating that oncosuppresso

167 infecting tomato as a system to dissect host interactions with pathogenic ncRNAs, using comprehensive

168 ponderance appear to have evolved from human interactions with pathogens in the microbial world.

169 enty hours of observation of nursing staff's interactions with patients and families was conducted, u

170 groups were asked to describe their typical interactions with patients, family members, doctors, and

171 P motif attenuate or abolish human MutLalpha interaction with PCNA, as well as PCNA-dependent activat

172 nsic motivation, social learning and natural interaction with peers, and embodiment.

173 ng ATGL lipid droplet translocation or ABHD5 interactions with perilipin proteins and ABHD5 ligands,

174 o alter apical membrane identity through its interactions with phosphatidylinositol 3-kinase (PI3K) a

175 th phospho-Thr4 in a manner analogous to its interaction with phospho-Ser2-modified CTD.

176 of the N-terminal amine further limited its interactions with phospholipid head-groups to facilitate

177 abled the design of mutants that disrupt Tau interactions with phospholipids without interfering with

178 RNA-protein interactions with physiological outcomes usually rely on

179 function is still unclear, and its possible interaction with PIP2 is unknown.

180 Rather, mutations that disrupted the pTRS1 interaction with PKR ablated the ability of pTRS1 to ant

181 pattern-triggered immunity induction through interaction with poly(A)-binding proteins.

182 ion has the potential to selectively perturb interactions with proteases while preserving interaction

183 resistant layer, which prevents nonspecific interactions with proteins and a layer containing the Ep

184 tric-based evidence to show that metallodrug interactions with proteins are considerably more complex

185 w similar overall rules of self-assembly and interactions with proteins, but that differences in the

186 quired for this effect, independently of the interaction with PTPdelta, but IL1RAPL1 mediates the act

187 structural and functional aspects of ligand interactions with purified P-gp and other ATP-binding ca

188 at is partially masked by its intramolecular interaction with R9.

189 and binding with alpha-helix formation upon interaction with RCD1, whereas peptides from ANAC013 and

190 modify the functionalities of starch through interactions with reactive species.

191 proteins (GlnB and GlnK), which orchestrate interactions with regulators of gene expression, transpo

192 shape deformations on filament stability and interactions with regulatory proteins, and analysis of s

193 icular and sperm function in adult males via interaction with relaxin/insulin-like family peptide rec

194 al role of the inflammatory response and its interactions with resident airway cells is critical to a

195 We sought to investigate potential interactions with respect to trace dominance, strengthen

196 ons in the RPA32 subunit of RPA that abolish interaction with RFWD3 also inhibit ICL repair, demonstr

197 of macronutrient deficiencies and symbiotic interactions with rhizobia and mycorrhiza were investiga

198 omain at multiple sites by TAK1 promotes its interaction with RIPK3 and necroptosis.

199 at the C-terminal end is responsible for the interaction with RNA polymerase.

200 Rca hexamer ring and analyzed its functional interaction with Rubisco.

201 verall shape complementarity and hydrophobic interactions with S372 and M368 on KCa3.1 and M72 on CaM

202 protein Lpd regulates actin dynamics through interactions with Scar/WAVE and Ena/VASP proteins to pro

203 However, most of our interactions with sensory information are in the context

204 The truncated NEMO interaction with SHANK-associated RH domain-interacting

205 The EF1a interaction with small and large subunits of ribosomes d

206 Overall, chloride and its interaction with sodium did not add clinically relevant

207 tau by immunodepletion, suggesting specific interactions with species involved in uptake.

208 concentration of receptor available for the interaction with specific targets, and thus has an impac

209 e presence of diarrhoea, location, and their interactions with specimen type.

210 n altered RNA structure that facilitates the interaction with SRSF3, an SR protein family member that

211 ngle-stranded DNA (ssDNA) is notable for its interactions with ssDNA binding proteins (SSBs) during f

212 yntheses using building blocks optimized for interactions with subtype-specific residues in the PPARd

213 mation-associated H443P mutant is altered in interaction with SUG1 and ubiquitinated proteins, trigge

214 ant p53 interacts with Rac1 and inhibits its interaction with SUMO-specific protease 1 (SENP1), which

215 ectrocatalytic behavior, mass transport, and interactions with surfaces.

216 tating properties of Kv2.1, specifically its interaction with syntaxin 1A, could lead to neuroprotect

217 data support a specific mode of TIA-1 RRM23 interaction with target oligonucleotides consistent with

218 llular matrix can direct and regulate vaspin interaction with target proteases or other proteins and

219 As (miRNAs) regulate gene expression through interactions with target sites within mRNAs, leading to

220 ic locus (nict-1) that mediates the phoretic interaction with terrestrial isopods.

221 binding kl-TSS that provides a long-distance interaction with the 5' end is unique.

222 dinates in a hitherto unreported monodentate interaction with the active site Fe(2+) ion, while the b

223 A paradigm for pneumococci is their interaction with the adhesive glycoprotein fibronectin,

224 Specifically, its initial interaction with the anionic microbial membrane is elect

225 ysis of tissue distribution reveals that the interaction with the antibody reduces the concentration

226 s, and computational docking to analyze GRK5 interaction with the beta2-adrenergic receptor (beta2AR)

227 s in ARTEMIS-deficient patients impaired the interaction with the C terminus and also affected protei

228 acting to polarize the peptide bond through interaction with the carbonyl oxygen atom.

229 elope glycoprotein in order to withstand the interaction with the cellular receptor during virus form

230 that confinement at the nanoscale and direct interaction with the charged interfaces produce anomalou

231 ty and cytokine secretion upon high-affinity interaction with the cognate CTLR keratinocyte-associate

232 ores in the nucleus of the host cells by its interaction with the conserved protein Spt4.

233 receptors 1 and 2 with significantly reduced interaction with the decoy TRAIL receptors 3 and 4.

234 hat this effect may be because of mechanical interaction with the dilated main pulmonary artery (MPA)

235 on the really interesting new gene (RING)-H2 interaction with the E2 enzyme UbcH5b in order to ligate

236 ination, and 3) binding via hydrogen-bonding interaction with the first-shell water molecules.

237 n in the Gal1 co-activator that disrupts the interaction with the Gal80 inhibitor specifically and co

238 in particular, the drug release kinetics and interaction with the gastrointestinal (GI) membrane.

239 HX MS revealed that interaction with the Hck SH3 or tandem SH3-SH2 domains i

240 Analyses of the interaction with the HEXIM protein confirm the importanc

241 e to this period of brain maturation and its interaction with the hormonal changes of pregnancy and p

242 understanding the life cycle of HCV and its interaction with the host cells.

243 amino acids in RRM1 likely to be involved in interaction with the i-motif DNA, and His24 and Arg26 we

244 heme binding protein (PhuS) is required for interaction with the iron-regulated heme oxygenase (HemO

245 rylation of ATR on S435 which promoted ATR's interaction with the key NER factor xeroderma pigmentosu

246 e is a rearrangement in the eag domain-CNBHD interaction with the kinetics, voltage-dependence, and A

247 has received much less attention because its interaction with the ligand induces no signaling.

248 coid (GC) downregulation of wound healing by interaction with the membrane bound GC receptor, followe

249 , additional epigenetic changes triggered by interaction with the microenvironment modulate cancer ce

250 regulation of mitochondrial dynamics through interaction with the mitochondrial fission factor Drp1 i

251 etabolism is needed to better understand its interaction with the motor symptoms of the disease.

252 Aha1-Hsp90 complex but prevents the specific interaction with the N-terminal domain of Hsp90 required

253 spatial orientation of tryptic peptides upon interaction with the negatively charged surface function

254 s cytoplasmic localization by increasing the interaction with the nuclear export factor CRM1.

255 ng to Rev-erbbeta indirectly facilitates its interaction with the nuclear receptor co-repressor (NCoR

256 N-terminal domain (NTD) on the Tudor domain interaction with the nucleosome.

257 early flooding stress, most likely in tight interaction with the other gases.

258 binding mechanisms and affinities for their interaction with the PRR of Itch.

259 cation but not Sabin-2 or Sabin-3 via direct interaction with the PV 5'UTR.

260 we have identified a key difference in their interaction with the ribosome, which correlates with the

261 by modulating YB-1 nuclear localization and interaction with the splicing factor U2AF65, which promo

262 etween 4 K and 340 K and the nature of their interaction with the surrounding inorganic cage using a

263 anslocated from the ER to the nucleus, where interaction with the WRKY29 transcription factor occurs.

264 he ligand to misalign the QA and form weaker interactions with the aromatic groups.

265 mational change that relieves autoinhibitory interactions with the ATPase motor, which selectively ac

266 hermore, sodium enhanced [(3)H]rauwolscine's interactions with the BiOctR, but not at a vertebrate al

267 pling and abundance of CaV2.1 through direct interactions with the CaV2.1 alpha1 subunit C-terminus a

268 imal face of the TCR, a region implicated in interactions with the CD3 co-receptor, suggests a possib

269 dered, yet utilizes transient intramolecular interactions with the DNA-recognition helix of the ETS d

270 R and extracellular environments and reduced interactions with the ER HSP70 chaperone BiP.

271 rgeted localization of proteins required for interactions with the extracellular matrix and for prote

272 y in the Vbeta8.1 segment mediated essential interactions with the GAP5040-48 peptide.

273 Upon anchorage, pi-stacking interactions with the graphene sheets provide further pi

274 g of these viruses and, in particular, their interactions with the host cell machinery.

275 molecules demonstrates that the non-covalent interactions with the host hardly affect the dihedral an

276 n CENP-N confers binding specificity through interactions with the L1 loop of CENP-A, stabilized by e

277 breast cancer patients, depend on tumor cell interactions with the mineralized bone extracellular mat

278 ore, G40 can also establish hydrogen bonding interactions with the nonbridging oxygen of the scissile

279 loop of CENP-A, stabilized by electrostatic interactions with the nucleosomal DNA.

280 , we have a localized particle with nonlocal interactions with the other slit.

281 ent interface are difficult to compensate by interactions with the protein or surrounding water molec

282 side chain, which establishes idiosyncratic interactions with the ribosomal RNA.

283 erent AAV serotypes have evolved distinctive interactions with the same receptor.IMPORTANCE Over the

284 ulate alternative splicing decisions through interactions with the splicing machinery.

285 we observe the translocon positioned through interactions with the SR in the vicinity of the ribosome

286 nd in some cases sequence-specific molecular interactions with the surface of carbon nanotubes that r

287 ules to adopt the conformations required for interaction with their target proteins.

288 ariance estimation approach, and assessed an interaction with time since eligibility.

289 alled corona which may strongly modify their interaction with tissues and cells relative to the bare

290 Following ligand interaction with TLRs, TIR serves to both initiate intra

291 c cochlin produces a qualitatively different interaction with TREK-1 compared to monomeric cochlin.

292 stalk movement and to understand its dynamic interactions with tRNA and other structural elements of

293 ciated with the replication fork through its interactions with two proteins, Proliferating Cell Nucle

294 et morphology to enzyme activity (host-guest interactions with uncaging and molecular cleavage).

295 YAP O-GlcNAcylation disrupts its interaction with upstream kinase LATS1, prevents its pho

296 ostatic activities of TrpRS by enhancing its interaction with vascular endothelial-cadherin.

297 ciency, strength, and stability of bacterial interactions with vascular surfaces.

298 ificantly disrupts its nuclear localization, interaction with VDR, intra-nuclear trafficking, and bin

299 his suggests that CTR-truncation disrupts an interaction with VLDLR (very low-density lipoprotein rec

300 ion of WASp at Y102 negatively regulates its interaction with Wiskott-Aldrich interacting protein and