1 Here,
we show by blue-native gel electrophoresis and stable isotope
2 Here
we show competition between defensive (to avoid predatory det
3 In summary,
we show here that Rap1 contains an AD required for Rap1-depen
4 In these situations,
we show how errors in positions can be corrected essentially
5 Here, using in situ electron microscopy,
we show how gold and silver nanocrystals nucleate from supers
6 We show how myocardial region-specific heterogeneity in cell
7 Herein
we show in a diverse array of human cancer cells that IMP2 ov
8 Here
we show,
in the context of near-field planar ultra-thin Therm
9 By utilizing these novel structures
we show that (i) the detection limit for dopamine can be impr
10 Here
we show that a microfluidic system supports murine ovarian fo
11 of these enhanced sgRNAs (e-sgRNA) and mRNA encoding Cas9,
we show that a single intravenous injection into mice induces
12 Further,
we show that an rpsA polymorphism previously identified in a
13 Using Aspergillus nidulans,
we show that AP-2 has a clathrin-independent essential role i
14 Here
we show that assumption ii is not valid, due to strong intraa
15 Here,
we show that both 2009 pandemic H1N1 influenza A (H1N1) virus
16 Therefore,
we show that both habit-like attention and goal-directed proc
17 In this article,
we show that CXCL8 expression, prior to proliferation, is com
18 Here
we show that drugs that inhibit important kinases in the BCR
19 Here
we show that ER-localized THBS1 is cytoprotective to rat, mou
20 We show that HSP22E and HSP22F are major chloroplast-targeted
21 Here
we show that in mice DND1 binds a UU(A/U) trinucleotide motif
22 Here, we directly monitor RNA proof-reading by RIG-I and
we show that it is controlled by a set of conserved amino aci
23 Finally,
we show that knockdown of EmMBD2/3 expression disrupts normal
24 Here,
we show that knockdown of Hop in the germ line nurse cells (G
25 Here,
we show that lamin A/C expressing cells can form an actin cap
26 Here
we show that mice with an adipose-tissue-specific knockout of
27 Here,
we show that modeling of neural sound representations in term
28 Here,
we show that mutation of the mouse orthologue of GPSM2 affect
29 Despite this high baseline rate,
we show that NAGC slows down as duplicate sequences diverge-u
30 Here,
we show that NKT-specific deletion of Hdac3 results in a seve
31 We show that OnGuard2 faithfully reproduces the kinetics of s
32 Using the Xenopus system,
we show that RARbeta2 plays a specific role in somite number
33 Here
we show that ripple bursts in CA1 and medial entorhinal corte
34 NF54 wild-type parasites at multiple stages of development,
we show that sexually committed, AP2-G(+) mature schizonts sp
35 We show that signalling through the TrpA1 thermo-sensor is re
36 We show that SiO2 first undergoes a change in Si-O coordinati
37 We show that such a framework is consistent with the stationa
38 Here,
we show that the cytokine activin-A instructs the generation
39 We show that the expression of many miRNAs is dramatically re
40 We show that the line-shape of the measured resonant elastic
41 ee mice with the cecal contents of neonatal and adult mice,
we show that the neonatal microbiota is unable to prevent col
42 We show that the photoacids can be used as fluorescent marker
43 We show that the photochemical reaction mechanisms for alpha-
44 ement learning simulations, and behavioral experimentation,
we show that the resolution to this tension-and the adaptatio
45 process to nanotubes presorted by surfactant-based methods,
we show that the resulting DNA-wrapped carbon nanotubes can b
46 We show that the same as for genes SPAD follows a beta distri
47 Using three mouse infection models,
we show that the SIP signaling pathway is active during infec
48 Here,
we show that Tomt/Comt2, the murine ortholog of LRTOMT, has a
49 We show that TSRI estimators with modified standard errors ha
50 Here,
we show using functional GFP reconstitution experiments that