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1 -4-CLP36 complex in podocytes and provide an explanation as to how alpha-actinin-4 deficiency or muta
2 ace of the T3 channel, providing a plausible explanation as to how BCL9 co-factors binding to Pygo PH
4 ivity and might begin to provide a molecular explanation as to how E2 modulates dendritic spine plast
6 rogen bonding in the active site suggests an explanation as to how in the wild-type and H98N mutated
8 s of intracellular Na+ and hence provides an explanation as to how KNa channel can control normal neu
12 experimental evidence for its presence or an explanation as to how such a polar molecule could exit t
13 methylation in cis and provide a mechanistic explanation as to how these loci impact upon OA suscepti
14 ing pathway, and provide a first mechanistic explanation as to how upregulation of CD44 may constitut
18 dy to cause pathogenicity and may provide an explanation as to why apparently similar auto-antibodies
19 p53 to maintain hepatic CSCs and provide an explanation as to why autophagy is required to promote h
20 ipose tissue and also represents a plausible explanation as to why brown adipocytes ultimately specia
24 ng the optic nerves, could be an alternative explanation as to why glaucoma develops in patients with
26 W loci in (NZB x NZW)F1 mice and provides an explanation as to why H2(d/z) heterozygosity is required
30 f Slc30a8 deletion, though the physiological explanation as to why impaired insulin secretion is not
32 l expansion of this population, providing an explanation as to why Mir155 deletion impairs affinity m
33 ery common, but to date there is no complete explanation as to why one out of two people systematical
35 urthermore, our findings provide a plausible explanation as to why P[6] RV strains are more common in
39 tractility, and ECM stiffness and provide an explanation as to why stiffer environments result in enh
40 of the R(61,2)C adduct provides a potential explanation as to why that adduct does not induce A -->
41 vivo, and they provide a potential molecular explanation as to why the developmental impact of these
43 perimental regioselectivities and provide an explanation as to why the hydrogen is transferred from t
45 y Hsp70/40 chaperones, providing a molecular explanation as to why the N domain is dispensable for pr
48 ural communication signals, but also a novel explanation as to why these preferentially occur on top
49 heir bacterial homologues, thus providing an explanation as to why this novel chloroplast SRP pathway
50 mine transporter, and provides an intriguing explanation as to why use of these compounds, unlike coc
52 These experimental results offer possible explanations as to why Juliette is perceived to have a s
53 g merlin, Falco columbarius, and alternative explanations as to why observed behaviours should differ
55 d the acquisition/loss of mutations, to give explanations as to why there is a discrepancy in pharmac
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