1 Here we show a strong association between low circulating pla
2 Here we show by in vivo fluorescence and MR imaging, that LN
3 Here we show how dualities can enhance the symmetries of a dy
4 Here we show that beta-cells express abundant Kindlin-2 and d
5 Here we show that beta4*nAChRs also are involved in non-nicot
6 Here we show that depletion of transforming growth factor-bet
7 Here we show that dynamically growing somatosensory neurons i
8 Here we show that Dysf(-/-) mice develop adverse LV remodelin
9 Here we show that heterotypic multicomponent interactions dom
10 Here we show that keratin intermediate filaments directly reg
11 Here we show that North America warmed at the rate of 0.02 de
12 Here we show that primary mouse and human T cells engage in m
13 otide polymorphisms can affect RNA secondary structure, and
here we show that single nucleotide polymorphisms can affect
14 Here we show that this problem can be circumvented by assembl
15 Here we show that this system exhibits physiology-dependent t
16 Here we show that transcription factor EB (TFEB), a master re
17 Here we show that using prior knowledge to facilitate learnin
18 Here we show that Wdp modulates the Hedgehog (Hh) pathway.
19 Here we show that, although the N-terminal region of RNF4 bea
20 Here, we show a molecular mechanism of how plants can sense p
21 Here, we show an N. gonorrhoeae diagnostic workflow for analy
22 Here, we show that adrenergic stimulation of BAT activates a
23 Here, we show that adult animals respond to ascarosides produ
24 Here, we show that Agd3 deacetylates GAG in a metal-dependent
25 Here, we show that although structurally clustered mutations
26 Here, we show that an AT-hook motif-containing nuclear locali
27 Here, we show that constrained 31-residue-peptides ('msR4Ms')
28 Here, we show that cytotoxic chemotherapies induce dynamic ch
29 Here, we show that efficiency of these processes is enhanced,
30 Here, we show that expression of a fusion protein combining w
31 Here, we show that GAGA factor (GAF), a Drosophila pioneer-li
32 Here, we show that histone H4 lysine 16 acetylation (H4K16ac)
33 Here, we show that intestinal epithelial cells expressing IRE
34 Here, we show that LDs induced by the yeast triacylglycerol (
35 Here, we show that macrophages not only fail to efficiently k
36 Here, we show that melanoma cells can adapt to targeted thera
37 Here, we show that mice in which alpha2-Na/K ATPase is condit
38 Here, we show that phosphatidylethanolamine (PE) synergizes w
39 Here, we show that resistance to glyphosate in the studied po
40 Here, we show that SOX11 confers distinct features to ER-nega
41 Here, we show that Syrian hamsters, in contrast to mice, are
42 Here, we show that the MA region is required for nuclear impo
43 Here, we show that the microcephalin 1/BRCT-repeats inhibitor
44 Here, we show that the three major classes of LCCBs activate
45 Here, we show that this differentiation becomes possible by a
46 e replication of intravacuolar pathogens such as Salmonella
Here, we show that this mechanism requires aconitate decarbox
47 Here, we show that this toughness design approach can be appl
48 Here, we show that tree mortality concomitant with drought ha
49 Here, we show that TRYPTOPHAN AMINOTRANSFERASE OF ARABIDOPSIS
50 Here, we show with a reversible knockout model that re-expres