ライフサイエンスコーパス: bipartite

1 and a less-characterized NLS2, thought to be bipartite.

2 The bipartite adhesion G protein-coupled receptor CD97 shows

3 The avian tail embodies a bipartite anatomy, with the proximal separate caudal ver

4 us contributions, ranging from local, global bipartite and global tripartite, which characterize the

5 ral feature in a pre-mRNA can be targeted by bipartite antisense molecules designed to hybridize with

6 RNase protection assays, we demonstrate that bipartite antisense molecules designed to simultaneously

7 This general bipartite antisense strategy could be employed to modula

8 The RNA-binding region has a bipartite architecture composed of ROQ and HEPN domains,

9 We also discovered that TprC has a bipartite architecture consisting of a soluble N-termina

10 The structure reveals a bipartite architecture of Core Factor and its recognitio

11 print and the eRNA initiation cores-define a bipartite architecture of enhancers, inform enhancer fun

12 This simplified, bipartite architecture offers a new framework to underst

13 provides insight into how a riboswitch with bipartite architecture uses dynamics to modulate express

14 Herein, we show that TprI also possesses bipartite architecture, trimeric structure, and porin fu

15 There was oedema at the bipartite area in 35 patients.

16 This configuration suggests that a bipartite arrangement is primitive and reinforces the vi

17 TprI represent a new class of dual function, bipartite bacterial OMP.

18 Each bipartite bar is identified as being respectively equiva

19 ature is the branchial area with an array of bipartite bars.

20 n of TYLCV with ToLCB and the legume adapted bipartite begomovirus MYMIV co-infecting tomato.

21 st closely related to DNA-A components of NW bipartite begomoviruses.

22 The structures reveal that PEA-15 uses a bipartite binding mode, occupying two key docking sites

23 ively support an integrative structure and a bipartite binding model, wherein the TAR central loop en

24 cetylated tails of both histones 3 and 4 via bipartite binding pockets on the DPF2 surface.

25 binding affinity by a factor of 2,500 for a bipartite binding site on myosin-VI.

26 intracellular substrates are recruited to a bipartite binding site when the transporter rests in an

27 ese structures show that by forming a single bipartite binding site, MRP1 can recognize a spectrum of

28 . occasionally overlapping the 3'-end of the bipartite binding site.

29 cterize both interfaces and demonstrate that bipartite binding to both USP7 domains is required for e

30 ated genome editing to functionally define a bipartite boundary element critical for neuron-specific

31 ble eIF2 trimers bind and align with eIF2B's bipartite catalytic centers to catalyze nucleotide excha

32 h a H3.1 peptide shows that ATXR5 contains a bipartite catalytic domain that specifically "reads" ala

33 a tethering function tailored to the unique bipartite centrosome in the Apicomplexa.

34 Thus, the N- and C-terminal halves of this bipartite channel may interact with other viral and host

35 This bipartite character explains why the SP1 spacer is a cri

36 ronized environmental proxy records reveal a bipartite climate response in the Black Sea region at th

37 n health systems performing CABG (SD for the bipartite clustering coefficient was 0.09).

38 To test whether teamwork (assessed with the bipartite clustering coefficient) among these physicians

39 hysician teamwork in these networks with the bipartite clustering coefficient.

40 Bipartite co-occurrence networks were constructed for ea

41 in E9 is ideal for its function as it allows bipartite complex affinity, whereby the stable colicin:i

42 The virus is bipartite, containing two double-stranded RNA (dsRNA) se

43 They involve bipartite cooperation via the exchange of goods or servi

44 The bipartite correlations of the two N-V centers and the tw

45 Inactivation of the bipartite cyclinA2-CDK-binding site in the SAMHD1 C term

46 d displacing Cdc20 to disrupt formation of a bipartite D-box receptor with the APC/C subunit Apc10.

47 We identified a novel bipartite degradation signal in the N-terminal domain of

48 d by the CBC:HapX protein complex comprise a bipartite DNA binding site 5'-CSAATN12RWT-3' and an addi

49 -binding complex (CBC) to cooperatively bind bipartite DNA motifs; however, the mode of HapX-DNA reco

50 The unusual assembly explains the basis of bipartite DNA recognition at hAT transposon ends, provid

51 nant computational framework outlined only a bipartite, dorsal/ventral, division of striatum.

52 miRNA and target form a bipartite duplex with an unpaired flexible linker.

53 over a mechanistically important role of the bipartite Dvl DEP domain and C terminal region (DEP-C) i

54 2, TAL1, E47, GATA1 and LDB1 that recognizes bipartite E-box-GATA1 sites on target genes.

55 Our results reveal a juxtaposed bipartite electrostatic interaction utilized by the nucl

56 mRNA to the Ire1 focus requires a cis-acting bipartite element (3'BE) located at the 3' untranslated

57 sponsive expression of both genes requires a bipartite enhancer whose activity declines during L3.

58 ccumulation generated using a GAL4-dependent bipartite enhancer-trap system confirmed that PPhiB or p

59 standing open question of whether every pure bipartite entangled state is self-testable.

60 Bipartite entangled states of identical particles have b

61 rk of an intronic splicing silencer (ISS), a bipartite exonic splicing silencer (ESS3a/b), and an exo

62 that SbMATE transcription is controlled in a bipartite fashion, primarily in cis but also in trans Mu

63 ut down sleep-active neurons, thus forming a bipartite flip-flop switch.

64 de Association Study allows us to identify a bipartite food-nutrient network, highlighting which food

65 te patella, oedema around the synchondrosis, bipartite fragment height (FH), distance between the fra

66 Fifty-nine of the bipartite fragments were located at the superolateral qu

67 Our studies highlight how the bipartite function of Tolloid CUB domains, in substrate

68 ticipates in the function, albeit CCP2 has a bipartite function.

69 ion, we characterize how ketamine impacts on bipartite functional interactions between neural subsyst

70 oligomeric state of gB with mutations in the bipartite fusion loops were similarly altered despite th

71 ture (YSS) in the 3' terminal regions of the bipartite genome of Lettuce chlorosis virus (LCV), a mem

72 The bipartite genome of Vibrio cholerae harbors sporadic and

73 Some appear to have had a bipartite genome organization, a unique characteristic a

74 is a positive-sense RNA insect virus with a bipartite genome.

75 ses) with origins in the New World (NW) have bipartite genomes composed of a DNA-A and DNA-B componen

76 viral infection, yet their importance in the bipartite genomes of the picorna-like, plant-infecting c

77 viruses are positive-sense RNA viruses with bipartite genomes that are most closely related to nodav

78 pe is located in the internal segment of the bipartite GPC fusion peptide, which also contains four c

79 he genes with which they are associated as a bipartite graph and then uses the modular structure of t

80 tite graph is then transformed into weighted bipartite graph by considering the interaction strength

81 In this study, we propose BiFusion, a bipartite graph convolution network model for DR through

82 h models interdomain information fusion with bipartite graph convolution operation.

83 On a large-scale bipartite graph derived from the Internet Movie Database

84 We model the problem as a semi-bipartite graph in which we are able to use drug-drug an

85 Then a bipartite graph is constructed from the collected CSC ge

86 The bipartite graph is then transformed into weighted bipart

87 The proposed learning model on semi-bipartite graph model, can integrate drug-drug and prote

88 ariational Bayes method, and then building a bipartite graph on the generated modules using sparse re

89 er scores than interactions connected in the bipartite graph representation.

90 hieved through an innovative exploitation of bipartite graph structure, and through computational red

91 by analyzing its genomic content network - a bipartite graph that links microbes to the genes in thei

92 rately well connected as a compound graph or bipartite graph, and poorly connected as a hypergraph (w

93 The model is represented as a probabilistic bipartite graph, which can handle highly complex network

94 f the similarities is provided by means of a bipartite graph, whose layout is heuristically optimized

95 We applied our bipartite graph-based functional module discovery algori

96 We use a bipartite graph-theoretic representation called a drug-e

97 bed that produces all maximal bicliques in a bipartite graph.

98 reads from different technologies through a bipartite-graph-based clustering algorithm, our approach

99 tionalization of a single sub-lattice of the bipartite graphene structure.

100 rticular, the embedding for general complete bipartite graphs and logical disjunctions may be of broa

101 nts disease-disease associations in terms of bipartite graphs and provides International Classificati

102 almost any applications environment in which bipartite graphs can be used to model relationships betw

103 Bipartite graphs can be useful for representing relation

104 ls and statistical tests for this purpose to bipartite graphs, and introduces a new significance scor

105 mplete graphs with broken links and complete bipartite graphs, in particular, the star graph.

106 s in biological networks when represented by bipartite graphs.

107 inhibited during interphase by the essential bipartite GTPase-activating protein Byr4-Cdc16.

108 PKA)-dependent phosphorylation of Dock180, a bipartite guanine nucleotide exchange factor (GEF) for R

109 ator of cytokinesis 180 (Elmo1/Dock180) is a bipartite guanine nucleotide exchange factor for the mon

110 ts of a Cupin domain, a helical hairpin, and bipartite helix-turn-helix motif.

111 sing a dual complementation system involving bipartite HIV-1 gRNA, we observed that gRNA packaging is

112 ns at least 8 imprinted genes regulated by a bipartite imprinting center (IC) associated with the SNR

113 sequences common to these deletions define a bipartite imprinting center for the AS-PWS locus.

114 (PWS/AS) imprinted domain is regulated by a bipartite imprinting control center (IC) composed of a s

115 t range from 4.6 kb (monopartite) to 5.3 kb (bipartite) in size.

116 s ability to block replicative complexes via bipartite, independent, and additive N-terminal domains.

117 lent linkage of GE to a rifamycin provides a bipartite inhibitor having very high potency and very lo

118 we describe the rational design of a potent bipartite inhibitor of NFAT-calcineurin interaction, MCV

119 osite and the active site are engaged by the bipartite inhibitors.

120 This novel F-box-protein-substrate bipartite interaction is susceptible to disruption by bo

121 We propose a binding model consisting of a bipartite interaction mode in which the largely disorder

122 We propose a bipartite interaction model in which the previously iden

123 n intrinsically disordered domain containing bipartite interaction motifs and provide valuable insigh

124 Bipartite interactions that affect agriculture as well a

125 at NEK7 bridges adjacent NLRP3 subunits with bipartite interactions to mediate the activation of the

126 S results also suggested the presence of the bipartite, legume-adapted begomovirus Mungbean yellow mo

127 ndicating that TPR3 and the C-helix define a bipartite localization determinant that is both necessar

128 S/G(2) phase cyclin, cyclin A2 (CCNA2), in a bipartite manner.

129 led Coverage Sensitive many-to-many min-cost bipartite Matching (CSM).

130 neralizes the standard (one-to-one) weighted bipartite matching problem, and can be solved using netw

131 We therefore propose a bipartite mechanism controlling leaf movement: ethylene

132 Our findings define a bipartite mechanism for stretch-induced actin remodeling

133 eplication initiation and elongation using a bipartite mechanism involving N-terminal exons lost in c

134 EcRppH interacts with RNA by a bipartite mechanism involving specific recognition of th

135 es, and Chlamydia trachomatis have developed bipartite metabolism within their hosts.

136 Interestingly, on a bipartite microtubule consisting of tyrosinated and dety

137 This unique bipartite microtubule-binding structure may mediate the

138 light of our results, a universal eukaryotic bipartite mode of binding to eIF4E is proposed.

139 Recent studies have uncovered a bipartite mode of cytosolic DNA recognition, in which th

140 this phosphorylation is enabled by a unique bipartite mode of ERK2 engagement by Ets-1 and involves

141 NA and Zn2-DNA structures establish a novel, bipartite mode of sequence-independent DNA interaction t

142 Together, these data establish a new bipartite mode of USP7 substrate binding.

143 HAT-C convex surface binds USP15 in a novel bipartite mode.

144 Our results support a bipartite model in which core first requires DGAT1 to ga

145 d PrsS, when expressed ectopically, act as a bipartite module to trigger a self-recognition:self-dest

146 ) of the scaffolding protein Sin3A through a bipartite motif comprising a helix and an adjacent exten

147 This bipartite motif in A36 is required for kinesin-1-depende

148 hnRNP A1 can bind simultaneously to a single bipartite motif of the human intronic splicing silencer

149 icate that a mechanism involving a conserved bipartite motif that is predicted to bind a homeodomain

150 engages the scaffolding protein Sin3A, via a bipartite motif within the Sin3 interaction domain (SID)

151 x-homology (PX) domain of SNX5 or SNX6 and a bipartite motif, termed SNX-BAR-binding motif (SBM), in

152 lity is negatively affected by nestedness in bipartite mutualistic networks.

153 cornavirales, we have taken advantage of the bipartite nature of a plant-infecting member of this ord

154 Thanks to the bipartite nature of the CPMV genome, which allows the ma

155 Furthermore, the bipartite nature of the ribosome is presumed to be essen

156 ed SBUs drives an MOF-to-MOF conversion into bipartite nets compatible with the connectivity of the o

157 ification and genome annotation tool using a bipartite network algorithm.

158 Phylogeny-based bipartite network analysis showed that Nerodia erythroga

159 of the ports as the one-mode projection of a bipartite network composed of ports and ship routes.

160 We constructed a bipartite network of archaeal viruses that includes two

161 Here we trace domain history onto a bipartite network of elementary functional loop sequence

162 Starting with a bipartite network of known OD and OD-causing mutant gene

163 We analyze the temporal bipartite network of the leading Irish companies and the

164 ys regulatory interactions in the model as a bipartite network, and (iii) a tunable compression pipel

165 ethod, a genomic dataset is represented as a bipartite network, to which Markov chain updates (switch

166 o the end of 2013, but can be applied to any bipartite network.

167 is obtained by the one-mode projection of a bipartite network.

168 or negative) between users from the original bipartite network.

169 rformance is better for tripartite than with bipartite networks and (iii) the measure of similarity u

170 nternational trade, typically represented as bipartite networks in which connections can be establish

171 trait locus (eQTL) analyses, we constructed bipartite networks in which edges represent significant

172 In particular, by using bipartite networks methodology from Complex Network Theo

173 Using bipartite networks, we compute a measure of topic simila

174 With six bipartite networks, we investigate the stabilities of fi

175 Building on our previous work about rewiring bipartite networks, we propose a method for rewiring any

176 can be applied to undirected, directed, and bipartite networks, yielding valuable insights into the

177 duces to the problem of rewiring two induced bipartite networks.

178 asets, and other data that can be modeled as bipartite networks.

179 to more complex circuitries of composite and bipartite networks.

180 method that follows from a basic property of bipartite networks: large dominant eigenvalues are assoc

181 We designed a bipartite NFAT inhibitor that is more potent than VIVIT

182 : an N-terminal monopartite NLS and a unique bipartite NLS closer to the C terminus.

183 localization elements defined a new form of bipartite NLS consisting of a triplet of basic residues

184 EBP, identifying it as an extended classical bipartite NLS encompassing minimally residues 158-190.

185 dant import receptor, KPNA2, which binds the bipartite NLS in Tpr with nanomolar affinity.

186 We propose NLS1 and NLS2 form a bipartite NLS in trans, which ensures high avidity for i

187 t import of FlbB into the nucleus requires a bipartite NLS, that FlbB localization at the tip require

188 jacent basic section defining the motif as a bipartite NLS.

189 p8 location in the nucleolus is linked to a bipartite NoLS.

190 We show that, for a bipartite non zero-sum game, input local quantum correla

191 In this contribution, we investigate the bipartite non-classical correlations (NCCs) of a system

192 show that MRTF-A contains an unusually long bipartite nuclear localisation signal (NLS), comprising

193 d that the WH2 cluster overlaps an atypical, bipartite nuclear localization sequence (NLS) and contro

194 the APC/C binding of Cdh1 but inactivated a bipartite nuclear localization sequence (NLS) and thereb

195 ion sites included three Lys residues on the bipartite nuclear localization sequence (NLS) and two Ly

196 A) in the cytoplasm and that RSK1 contains a bipartite nuclear localization sequence that is necessar

197 ct in which a kinase substrate is fused to a bipartite nuclear localization signal (bNLS) and nuclear

198 vity by releasing importin alpha/beta from a bipartite nuclear localization signal (NLS) located in t

199 SAP11 contains a bipartite nuclear localization signal (NLS) that targets

200 this study, we report that Nurr1 contains a bipartite nuclear localization signal (NLS) within its D

201 undescribed function of PHLPP1 depends on a bipartite nuclear localization signal in its unique N-te

202 protein, referred to as pUL31, containing a bipartite nuclear localization signal, an intrinsically

203 Nuclear entry of dreCmas1 was mediated by a bipartite nuclear localization signal, which seemed irre

204 clear localization of RBM45 is mediated by a bipartite nuclear-localization sequence (NLS) located at

205 ignificantly bends its DNA substrate using a bipartite, nucleolytic center formed at an N-terminal di

206 terize this entanglement by treating it as a bipartite one between a single mode of phonons and a sin

207 ral way with Rubidium and Caesium atoms in a bipartite optical lattice involving laser-dressed Rydber

208 This bipartite or two-signal mechanism has likely evolved to

209 Limited proteolysis reveals a bipartite organization consisting of an N-terminal ATPas

210 The discovery of a novel bipartite organization in the parasite centrosome that s

211 Oomycete genomes display a strongly bipartite organization in which conserved housekeeping g

212 c chromatin contacts, we discover a specific bipartite organization of the mouse inactive X chromosom

213 e p130(cas) carboxyl terminus, adjacent to a bipartite p130(cas) Src-binding domain (SBD) and induces

214 magnetic resonance imaging (MRI) features of bipartite patella and evaluate the association with clin

215 Bipartite patella is a rare developmental variation of t

216 n showing that the symptomatic occurrence of bipartite patella is statistically higher in young patie

217 ipartite variant were evaluated for types of bipartite patella, oedema around the synchondrosis, bipa

218 the knee is highly accurate in evaluation of bipartite patella.

219 These studies identify a unique bipartite pathway for activation of beta-cell proliferat

220 space during cocultivation with seedlings in bipartite Petri dishes, and (35)S was assimilated from t

221 Finally, pulldown assays reveal a bipartite physical interaction between hpol eta and WRN

222 mathematical modelling and data from eleven bipartite plant-pollinator networks observed along a lan

223 Instead, bipartite PML I binding domains located in the N-termina

224 These substrates share a bipartite polybasic recognition determinant (BPR) flanki

225 ntains a site of palmitoylation as well as a bipartite polybasic region.

226 Daz interacting protein 1 (Dzip1) has bipartite positive and negative functions in the Hh path

227 Bean pod mottle virus (BPMV) is a bipartite, positive-sense (+) RNA plant virus in the Sec

228 aenorhabditis elegans or any nematode, has a bipartite, positive-sense RNA genome.

229 TRV is a bipartite, positive-strand RNA virus with the TRV1 and T

230 it emerged from the DNA-A component of a NW bipartite progenitor via convergent evolution and recomb

231 A bipartite protein complex of LptD and LptE assembles LPS

232 Cut12 harbors a bipartite protein phosphatase 1 (PP1) docking domain.

233 The zona pellucida (ZP) domain is a bipartite protein structural element comprised of ZP-N a

234 emonstrates that, besides specifying SI, the bipartite PrpS-PrsS module can trigger growth arrest and

235 s a superconducting two-level system and the bipartite quantum channel is a microwave photonic entang

236 For a bipartite quantum state, the classical correlation is th

237 xperimental approach, we have identified the bipartite RCD1-binding SLiM as (DE)X(1,2)(YF)X(1,4)(DE)L

238 didate REs, we showed that a strong intronic bipartite RE selectively governs Cacna1g expression in t

239 The two distinct motifs form a bipartite recycling signal recognized by the retromer su

240 Our study reveals a bipartite regulation of presynaptic activity by endolyso

241 everal known NLRP3 activators, demonstrating bipartite regulatory potential of pH on the activity of

242 We infer that the vertebrate Hox bipartite regulatory system is an evolutionary novelty g

243 partitioning system to equal segregation is bipartite- replication-independent and replication-depen

244 To address this, first we create a bipartite representation and generate a multidimensional

245 A bipartite representation of trade, however, inevitably n

246 We find that bipartite resource competition networks are better predi

247 Quantum discord is the minimal bipartite resource which is needed for a secure quantum

248 eptor-mediated adaptation to indole caused a bipartite response-wild-type cells were attracted to reg

249 gy) domains of ZBP1 specifically recognize a bipartite RNA element comprised of a 5' element (CGGAC)

250 STAR proteins function as dimers and bind to bipartite RNA sequences; however, the structural and fun

251 The structure reveals a bipartite RNA-binding motif on the distal face that is c

252 In this study, we have identified the bipartite role of Hsp90 in chaperoning CRAF kinase.

253 tetramer by BldD is selective and requires a bipartite RXD-X8-RXXD signature.

254 horacic or lumbar rib, os centrale carpi and bipartite scaphoid, tripartite patella, left foot anomal

255 ORC (origin recognition complex) binds to a bipartite sequence consisting of an 11 bp ACS element an

256 f PML isoforms II, IV, and VI, while using a bipartite sequence flanking the RING domain to degrade P

257 RNAs in vitro, and we biochemically define a bipartite sequence motif that is necessary and sufficien

258 he 5' and 3' stem-loops forming an essential bipartite signal.

259 Heterologous, ectopic expression of a plant bipartite signaling module in plants has not been shown

260 al step in HIV-1 assembly, is facilitated by bipartite signals within the matrix (MA) domain: N-termi

261 bsite on PACS-1 and PACS-2 interacted with a bipartite site on Nef formed by the EEEE(65) acidic clus

262 PTF1 binds two canonical bipartite sites within a 0.7-kb transcriptional enhancer

263 ructural La member crystallizes in the cubic bipartite sodalite structure (Type-VII clathrate) with L

264 n triangular and kagome lattices compared to bipartite (square and honeycomb) lattices.

265 e, where we verify the inseparability of the bipartite state and fully characterize its logarithmic n

266 e conclude that the pointed-end complex is a bipartite structural domain that stabilizes dynactin and

267 The holocomplex is a hexamer of a bipartite structure composed of a membrane-proximal ATPa

268 HypX has a bipartite structure composed of an N-terminal module sim

269 The apicomplexan centrosome has a unique bipartite structure comprising an inner and outer core r

270 east interphase spindle pole body (SPB) is a bipartite structure in which a bulky cytoplasmic domain

271 that SiRTAs on chromosomes V and IX share a bipartite structure in which a core sequence (Core) is d

272 study in Toxoplasma gondii revealed a unique bipartite structure of the centrosome, which coordinates

273 MOC began to strengthen mid-YDS, producing a bipartite structure of the YDS in records from continent

274 at the inactive murine X chromosome adopts a bipartite structure using a novel 3C protocol, termed in

275 he FokI restriction enzyme (which revealed a bipartite structure with a separable DNA-binding domain

276 e find that the networks possess a two-level bipartite structure: common competing endogenous network

277 (OMPs) revealed that seven have an Msp-like bipartite structure; phylogenetic analysis revealed that

278 n of polyacetylene chains is captured by the bipartite sublattice structure of the SSH model, emblema

279 ansferrin binding proteins (Tbps) comprise a bipartite system for iron acquisition from human transfe

280 The bipartite system is treated as two black boxes, with no

281 ternal failures the model is equivalent to a bipartite system, which can be useful to model a financi

282 al import pathways: whereas preproteins with bipartite targeting sequences are imported within second

283 Here we apply bipartite tetracysteine display to demonstrate that DM a

284 and block coiled coil formation as judged by bipartite tetracysteine display.

285 ters of jawed vertebrates are organized into bipartite three-dimensional chromatin structures that se

286 erred by Ty-1 was also effective against the bipartite tomato severe rugose begomovirus, where a simi

287 prI localize to the outer membrane, adopting bipartite topologies, whereas TprF is periplasmic.

288 ron microscopy (cryo-EM) structure of CDT, a bipartite toxin comprised of the proteins CDTa and CDTb.

289 ty (FC) algorithm to measure centrality in a bipartite trade network, which aims to represent the 'Fi

290 We here uncover that the proteins share a bipartite transactivation mechanism, whereby a transacti

291 We now show that a bipartite tryptophan-based kinesin-1 binding motif, orig

292 Bioinformatic analysis reveals that related bipartite tryptophan-based motifs are present in over 45

293 shoe-shaped lophophore, supported by a lower bipartite tubular attachment structure with a long pedic

294 nd biochemical analyses that Prp3 contains a bipartite U4/U6 di-snRNA-binding region comprising an ex

295 MRI exams of 61 patients with bipartite variant were evaluated for types of bipartite

296 other birds, while the internal structure is bipartite with songbird-like anatomical features, includ

297 The p53TAD is bipartite, with two interaction motifs, termed AD1 and A

298 We have explored the evolution of the bipartite World Trade Web (WTW) across the years 1995-20

299 at 3.5 angstrom resolution, comprised of the bipartite zona pellucida (ZP) module in a helical arrang

300 Via its bipartite zona pellucida module (ZP-N/ZP-C), UMOD forms