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1 cells to a duct-like phenotype, providing an explanation for how a characteristically ductal tumor ca
2        These observations provide a possible explanation for how a linear bacterial chromosome can ex
3 ening of the cytoplasmic gate and provide an explanation for how a missense mutation in the transport
4                             The conventional explanation for how a morphogen patterns a tissue holds
5                 And, there is now a testable explanation for how a protein can fold so quickly: A pro
6        These observations offer a harmonious explanation for how a single TAK1 kinase can mediate the
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
10                         Our work provides an explanation for how AIDA-1 dysfunction might contribute
11                   This mechanism provides an explanation for how an agonist-bound nuclear receptor ca
12          More broadly, our study provides an explanation for how and why eccentricity emerges as a do
13                  Still needed is a synthetic explanation for how and why growth rates vary as body si
14                       These results offer an explanation for how and why unmethylated microsatellite
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
17               Our results provide a possible explanation for how autophagy is regulated by MPP7 and M
18 production by cDCs and provides one possible explanation for how bacterial infection might precipitat
19                    These findings provide an explanation for how beta-catenin localizes to the nucleu
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
28             The results provide one possible explanation for how chirality arises in nature by provid
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
33             This study provides a structural explanation for how CobT can phosphoribosylate most of t
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
36        This regular distribution provides an explanation for how complete chromosome replication can
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
41            These results offer a mechanistic explanation for how different detyrosinated alpha-tubuli
42 is finding is that it provides a mechanistic explanation for how different types (strains) of rhinovi
43               Information theory has offered explanations for how different types of neurons can maxi
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
46                                One potential explanation for how divergent circuits have evolved is t
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
50                       Our results provide an explanation for how DNA replication is linked to sister
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
53      In summary, NTA provides a parsimonious explanation for how excitatory-inhibitory co-tuning and
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
63  LPL's large basic patch, providing a likely explanation for how GPIHBP1 stabilizes LPL.
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
71         These observations provide a partial explanation for how homogenization of centromere DNA seq
72                    These findings provide an explanation for how human cancers, which are often assoc
73                     Here, we provide a novel explanation for how human time perception might be accom
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.
79 n the absence of ring stacking, providing an explanation for how it can reset the clock.
80 eviously appreciated and provide a molecular explanation for how it moves actin at fast speeds.
81 ular organisms, we hope to uncover proximate explanations for "how" it causes disease in humans.
82          These results provide a mechanistic explanation for how ketamine used for the treatment of d
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
86                        These data provide an explanation for how low levels of Beclin 1 facilitate tu
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
91       This nucleation mechanism provides one explanation for how mercury may be immobilized, and even
92        In addition, we provide a mechanistic explanation for how mesangial cells in primary culture a
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
95          We provide a possible physiological explanation for how microgravity can cause symptoms simi
96                     These results provide an explanation for how mitotic HSF2 sumoylation is regulate
97            These results provide a molecular explanation for how Mtb impairs the adaptive immune resp
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
102 d nucleoporin Nup160 at the NE, providing an explanation for how Ndc1 controls NPC number.
103            Our results provide a mechanistic explanation for how Nde1 and Lis1 synergistically activa
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
106       Economic efficiency has been a popular explanation for how networks self-organize within the de
107 Altogether, these data provide a mechanistic explanation for how newborns may cope with an immunosupp
108             Our findings provide a molecular explanation for how newly assembled dyneins are packaged
109             Our model provides a mechanistic explanation for how nucleotides regulate the p97-ataxin3
110                   These findings provide one explanation for how obesity worsens cancer outcomes and
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
115                         They also provide an explanation for how pathologically increased TGF-beta si
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
118        Together, these mechanisms provide an explanation for how phenologically variable annual plant
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
121           Our findings provide a mechanistic explanation for how plants appropriately respond to tiss
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
125             These data provide a mechanistic explanation for how PPARgamma activation facilitates amy
126 -B at Ser(523) provides a possible molecular explanation for how pressor hormones inhibit CNP signali
127                  Our results provide a novel explanation for how primates uniquely concentrate xantho
128           These results therefore provide an explanation for how proteins can misfold into soluble co
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
132                   They also give a molecular explanation for how rising CO(2) concentrations elicit i
133                     This can provide a novel explanation for how risk influences action selection and
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
136                   In this paper, we offer an explanation for how selectivity for orientation could be
137                  Our data suggest compelling explanations for how senescent cells persist in dormancy
138  during the cell cycle, thereby providing an explanation for how 'silent' heterochromatin can be tran
139         These findings provide a mechanistic explanation for how Smk1 activity thresholds are generat
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
146                       Our results provide an explanation for how structurally similar spectrin-like r
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
150                           Here we provide an explanation for how Tax induces some Chk2 activities but
151                        Our findings offer an explanation for how telomerase is recruited to telomeres
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
154                                We provide an explanation for how the AMO may drive physical changes i
155      This deformation pattern may provide an explanation for how the Arabidopsis leaf maintains a rel
156           Our findings provide a mechanistic explanation for how the brain assembles spatial represen
157  and network theories to offer a mechanistic explanation for how the brain moves between cognitive st
158        These results provide a new and novel explanation for how the calpain/calpastatin network is o
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
161                This provides one mechanistic explanation for how the epithelial-mesenchymal transitio
162 gnment of order, the JCI is now requiring an explanation for how the first-author position is determi
163       These findings offer a molecular-level explanation for how the HCM mutation cTnI-R145G reduces
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
170                               Missing was an explanation for how the movements of these domains are c
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
177                          Our data provide an explanation for how the stromal ECM encodes architectura
178             These data provide a mechanistic explanation for how the SUMOylation status of Drp1 acts
179                       Our results provide an explanation for how the unique domain architecture of JA
180 emical shift mapping results also suggest an explanation for how the unstable dnaQ49 mutator phenotyp
181                   Systems neuroscience seeks explanations for how the brain implements a wide variety
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
187                             The evolutionary explanation for how these polymorphisms are maintained h
188        The results challenge the traditional explanation for how these rapidly oscillating structures
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
191 nd the cell surface and provide a functional explanation for how this association occurs.
192 , the 'ABC model' is a simple and satisfying explanation for how this conserved floral architecture i
193                   It also provides the first explanation for how this increased potassium current ind
194                         They also provide an explanation for how this small molecule can direct diver
195          These studies provide a mechanistic explanation for how this therapeutic strategy can select
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
198              This study provides a molecular explanation for how Twist1-induced dissemination works a
199           Our results provide a long-awaited explanation for how Ubx controls morphogenetic transform
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
202            Our results provide a theoretical explanation for how virus antigenic evolution can be hig
203 P RBD RNA structure provides an atomic-level explanation for how ZAP selectively targets foreign, CG-

 
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