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1 cells to a duct-like phenotype, providing an explanation for how a characteristically ductal tumor ca
3 ening of the cytoplasmic gate and provide an explanation for how a missense mutation in the transport
7 t model provides an attractive and plausible explanation for how a typical antigen presenting cell, e
8 tabolite-initiated amyloidogenesis offers an explanation for how Abeta aggregation could occur at phy
9 orepressor, HPr-Ser46-P, provide a molecular explanation for how adjunct corepressors G6P and FBP enh
15 These results provide a simple evolutionary explanation for how ankyrin-B and ankyrin-G have acquire
16 ights into the function of ATDC and offer an explanation for how ATDC promotes cancer cell proliferat
18 production by cDCs and provides one possible explanation for how bacterial infection might precipitat
20 amin A production and provides a mechanistic explanation for how both genetics and diet can affect th
21 a loss of protein motion may also provide an explanation for how calcium-ion-binding affinity is incr
22 of karyokinesis and cytokinesis provides an explanation for how cell cycle flexibility is achieved i
23 degeneration in SCA7 and thus may provide an explanation for how cell-type specificity is achieved in
24 Regulated tip growth provides an attractive explanation for how cells are able to synthesise very lo
25 h a multimodal assembly platform provides an explanation for how cells build a powerful yet transient
26 on-condensation dynamics creates mechanistic explanation for how cells properly respond to variable l
27 known about NP function, there is no obvious explanation for how changes in NP can selectively modula
29 neage specification, and suggest mechanistic explanations for how CIC mutations may impact the pathog
30 We believe that our data provide a molecular explanation for how circadian phases, such as wake-sleep
31 hese results provide a plausible mechanistic explanation for how closely related species exhibit quan
32 n of the coactivator and suggest a molecular explanation for how coactivators increase the transcript
34 hieve distinct cohesin functions provides an explanation for how cohesin mutations can specifically l
35 eurodevelopmental disorders, and provided an explanation for how common risk alleles persist in the p
37 pithelial differentiation, and they offer an explanation for how decreased levels of GLI1 are likely
38 al states of SERCA and provides a structural explanation for how dephosphorylated PLB decreases Ca(2+
39 fense (PATHOS-D) hypothesis provides a novel explanation for how depression can be nonadaptive in the
40 3 function as a PRROS provides a mechanistic explanation for how diastolic Ca(2+) influx specifically
42 is finding is that it provides a mechanistic explanation for how different types (strains) of rhinovi
44 ese findings provide a potential mechanistic explanation for how disruption of LINC complex may contr
45 re of these interactions provide a molecular explanation for how distinct SNX-BAR-decorated tubules a
47 be mutually fruitful, e.g., by providing an explanation for how diverse ecological communities can a
48 ansfer rates.Our results provides a testable explanation for how diversity can be maintained by gene-
49 ction by pDCs in mice, providing a potential explanation for how DMPA impairs innate antiviral immuni
51 oss promotes tumor progression, providing an explanation for how E-cadherin loss increases metastasis
52 for GMP-PCP-bound Cdc42, provides a possible explanation for how effectors can distinguish between th
54 ream effector of Sema3E-PlexinD1 provides an explanation for how extracellular signals are translated
55 ds to the 36-bp DNA fragment and provides an explanation for how FitB enhances the DNA binding affini
56 nctional compartmentalization may provide an explanation for how fluid flows are managed in an open c
57 a-2, and provide a comprehensive mechanistic explanation for how functional synaptic phenotypes contr
58 tibody was employed to provide a mechanistic explanation for how fundamental alloantibody biology inf
59 lpha/GPR-1/2 signaling pathway, providing an explanation for how Galpha-dependent force is regulated
60 These findings provide a strong biochemical explanation for how genetically driven alterations in ci
61 n the PBN, providing a potential mechanistic explanation for how GIPR agonist treatment reduces PYY-i
62 read among neuronal cells and may provide an explanation for how glucocerebrosidase mutations increas
64 he Antarctic green algae and offer potential explanations for how green plants adapt to extreme envir
65 ilize range boundaries and provide a general explanation for how groups of widely divergent sizes can
66 These results further provide a molecular explanation for how >50 mutations in BAP1 and ASXL1 foun
67 They also may provide a refined biochemical explanation for how H3K36me3 loss leads to genomic insta
68 hobic face of the epitope, thus providing an explanation for how HCV isolates bearing mutations at As
69 hromatin proteins and provides a mechanistic explanation for how Hmgb2 regulates gene expression and
70 ucleator TPX2 along the neurite, offering an explanation for how HMMR contributes to the promotion of
74 to BCAA catabolism, providing a mechanistic explanation for how increased BCAA catabolic flux can ca
75 calcium entry pathways provided a plausible explanation for how inflammatory [Ca2+]i mediators may d
76 III by the DnaX complex provides a molecular explanation for how initiation complexes form when suppo
77 l via IRS1/PI3K/Akt2 activation, a potential explanation for how insulin is retarding the progression
78 to alter the Ab paratope, thus providing an explanation for how isotype can affect Ab specificity.
83 al constraints but also provide a mechanical explanation for how large-scale interactions through cel
84 igomerize syt II offers a possible molecular explanation for how lead interferes with calcium-evoked
85 opeptidase access is determined and offer an explanation for how longer peptides may be displayed at
87 Together these results provide a plausible explanation for how male and female moths, and maybe oth
88 ovel hypothesis provides the first plausible explanation for how marine animals can navigate to natal
89 ion, the mechanism proposed here provides an explanation for how MDA5 uses filament assembly and disa
90 t on magnesium affinity provides a plausible explanation for how mechanical strain can alter this act
93 tion and this mechanism provides a plausible explanation for how metal binding controls the DtxR repr
94 ia throughout the mouse lifespan provides an explanation for how microglial priming early in life can
98 hread-width imbalance provides a mechanistic explanation for how multithread channels develop on Eart
99 nt kinetics in both cell types, providing an explanation for how mutations in the ubiquitously expres
100 alpha control provides a potential molecular explanation for how N-terminal Rb loss-of-function delet
101 is as well as recent evidence that offers an explanation for how NADPH required by the redox system m
104 e measured orientation provides a structural explanation for how neck surface residues enhance proces
105 a clear framework and biological mechanistic explanation for how neighborhood disadvantage affects ca
107 Altogether, these data provide a mechanistic explanation for how newborns may cope with an immunosupp
111 although not necessarily mutually exclusive, explanation for how oncogenes initiate and sustain tumor
112 he cyclin-binding motif of p21, providing an explanation for how p21 is found associated with active
113 ycle checkpoint is activated and provides an explanation for how p53 is protected from degradation in
114 Our findings provide an elegant molecular explanation for how PAS sequences are recognized for mRN
116 recision of beliefs and provides a potential explanation for how patients could simultaneously show o
117 weight of evidence by providing a plausible explanation for how PCBs can cause NHL through immune dy
119 se interdomain contacts provide a functional explanation for how PIP(2) binding and tyrosine phosphor
120 ses lamina dynamics, providing a mechanistic explanation for how PKC activity influences nuclear size
122 ty of natural small molecules represents one explanation for how plants may rapidly recruit enzymes f
123 g in the short term and provides a plausible explanation for how plastic neural codes remain integrat
124 , with the dynein motor complex may offer an explanation for how poliovirus hijacks the cellular tran
126 -B at Ser(523) provides a possible molecular explanation for how pressor hormones inhibit CNP signali
129 s psychologically and biologically plausible explanations for how psychological factors might influen
130 we use computational modeling to provide an explanation for how pulsatile stimulation affects axonal
131 ural and biochemical results thus provide an explanation for how receptor recognition, phospholipid b
134 ments, this structure provides a mechanistic explanation for how S1 regulates formation of an inhibit
135 eins localized only at the OMM, providing an explanation for how select mitochondrial proteins are in
138 during the cell cycle, thereby providing an explanation for how 'silent' heterochromatin can be tran
140 These findings suggest a possible structural explanation for how so many commonly used medications bl
141 ystems, wall deficiency provides a plausible explanation for how some bacteria may hide in their host
142 propose that normalization provides a simple explanation for how spatial and feature attention could
143 standing this link may provide a mechanistic explanation for how species can adapt to changing climat
144 ound apolipoprotein A-I which may provide an explanation for how specific domains of apolipoprotein A
145 These studies provide a simple mechanistic explanation for how stromal cell signals regulate both t
147 Our results provide mechanistic insight and explanation for how subthalamic stimulation modulates mo
148 aureus entry into the dermis and provide an explanation for how such dermal dysbiosis results in inc
149 hoto-alteration of DOM provide a mechanistic explanation for how sunlight exposure of terrigenous DOM
152 In this paper, we develop a theoretical explanation for how temperature robustness can emerge fr
153 nding and specificity, providing a molecular explanation for how the activin class accommodates low-a
155 This deformation pattern may provide an explanation for how the Arabidopsis leaf maintains a rel
157 and network theories to offer a mechanistic explanation for how the brain moves between cognitive st
159 ptosis in thymocytes and provide a molecular explanation for how the cAMP stimulators, including the
160 nt ABC transporter activities and provide an explanation for how the comparable transporter in native
162 gnment of order, the JCI is now requiring an explanation for how the first-author position is determi
164 H production provide a tentative mechanistic explanation for how the inhalation of PM2.5 induces oxid
165 This study represents the first detailed explanation for how the islet facilitates inhibitory act
166 eased by light, thereby providing a possible explanation for how the long-short Tim polymorphism adap
167 t serves to protect the genome, providing an explanation for how the loss of a survival pathway leads
168 The Nse1-Nse3-Nse4 structure provides an explanation for how the lung disease immunodeficiency an
169 (OCT2), a dopamine transporter, providing an explanation for how the membrane-impermeant dopamine acc
171 at a peripheral location, which provides an explanation for how the NAT protein structure is not sig
172 ctivities in homologues of OSBS and a likely explanation for how the OSBS from Amycolaptosis also can
173 r protease recognition provides a compelling explanation for how the oxidation-induced conformational
174 cognition specificity provides a mechanistic explanation for how the same effector function can be us
175 s (scleractinian corals) provides a possible explanation for how the site of gastrulation has changed
176 omewhat cross-reactive, thereby providing an explanation for how the specific recognition of a limite
180 emical shift mapping results also suggest an explanation for how the unstable dnaQ49 mutator phenotyp
182 lated receptors by Nef is rising, so are the explanations for how their downregulation could contribu
183 nic in geothermal systems, offer a molecular explanation for how these algae tolerate arsenic in thei
184 ave been well characterized, a network-level explanation for how these changes lead to loss of consci
185 e of the two compounds provided a structural explanation for how these compounds are able to effectiv
186 yl)propane 1-phosphate provided a structural explanation for how these compounds are able to effectiv
189 ped strand displacement model as a potential explanation for how these stutter products are generated
190 tory and excitatory CIN pathways and suggest explanations for how these pathways maintain alternating
192 , the 'ABC model' is a simple and satisfying explanation for how this conserved floral architecture i
196 on of the skin-homing receptor, providing an explanation for how thymic selection is coordinated with
197 may help resolve the debate by proposing an explanation for how training in rhythmic skills can impr
200 conformational ensemble model, providing an explanation for how VDR and possibly the estrogen recept
201 cancer cells, providing a direct mechanistic explanation for how VEGF-C expression is upregulated in
203 P RBD RNA structure provides an atomic-level explanation for how ZAP selectively targets foreign, CG-