1 Here,
we show an N. gonorrhoeae diagnostic workflow for analysis of
2 Here
we show by in vivo fluorescence and MR imaging, that LN parac
3 omeric receptors that contain binding-impaired subunits, as
we show for both kainate and GluA2 AMPA receptors.
4 We show here that at low doses these SCFAs directly impact B
5 Using monkey and human electrophysiology data,
we show here that attractor dynamics that control neural spik
6 We show here that RAD50-deficient fibroblasts exhibit a marke
7 We show in awake behaving mice that the onset of tremor is co
8 We show that 21-plex DiLeu tags generate strong reporter ions
9 Here,
we show that adrenergic stimulation of BAT activates a PKA-de
10 Here,
we show that adult animals respond to ascarosides produced un
11 Here,
we show that an AT-hook motif-containing nuclear localized (A
12 Here
we show that beta-cells express abundant Kindlin-2 and deleti
13 Here
we show that beta4*nAChRs also are involved in non-nicotine-m
14 We show that chemometric analysis of peanut leaflet spectra p
15 Here,
we show that constrained 31-residue-peptides ('msR4Ms') desig
16 We show that CSB forms a stable complex with Pol II and acts
17 Here,
we show that cytotoxic chemotherapies induce dynamic changes
18 Here
we show that dynamically growing somatosensory neurons in the
19 We show that epimutations arise spontaneously at a rate appro
20 We show that exposure of leukemia cells to daunorubicin activ
21 Here,
we show that expression of a fusion protein combining wheat G
22 well-known oncoprotein overexpressed in most human cancers,
we show that FBXL16 stabilizes C-MYC by antagonizing FBW7-med
23 We show that glycolysis is required to maintain the plasma me
24 Here
we show that keratin intermediate filaments directly regulate
25 Here,
we show that LDs induced by the yeast triacylglycerol (TAG)-s
26 ing the melanoma lineage survival oncogene MITF as a model,
we show that low-affinity binding sites act as a competitive
27 We show that mantis shrimp rely on navigational strategies cl
28 We show that neutral evolution and nucleotide substitution ra
29 We show that NVP was readily taken up by dendritic cells (DCs
30 e and an ensemble approach to CNN parameter interpretation,
we show that our trained network ("AI-TAC") does so by redisc
31 In addition,
we show that phosphorylation of Ser(3) may be an additional m
32 Here
we show that primary mouse and human T cells engage in macrop
33 y integrating multiple sources of genetic and genomic data,
we show that putative G-quadruplex forming sequences (pG4) in
34 We show that Rho can prematurely terminate transcription of b
35 variation in media markets for 771 matched rural counties,
we show that rural residents are more likely to practice soci
36 polymorphisms can affect RNA secondary structure, and here
we show that single nucleotide polymorphisms can affect RNA-p
37 Here,
we show that SOX11 confers distinct features to ER-negative D
38 Here,
we show that Syrian hamsters, in contrast to mice, are highly
39 We show that the increased cytokinin signaling in ARR1 gain-o
40 Here, using focal trans-synaptic anterograde tracing,
we show that the motor-action-related topographical organizat
41 We show that the non-canonical tubulin Tuba8, transiently exp
42 Using ChIP,
we show that the occurrence of G4 structures peaks at the lat
43 We show that the phosphorylation of the RNA-DNA binding prote
44 Here,
we show that the three major classes of LCCBs activate STIM/O
45 We show that these dendrites develop by retrograde extension,
46 ication of intravacuolar pathogens such as Salmonella Here,
we show that this mechanism requires aconitate decarboxylase
47 stems-encompassing plants, protists, and algae with grazers-
we show that this method predicts the results of unobserved e
48 Here,
we show that tree mortality concomitant with drought has led
49 Here
we show that using prior knowledge to facilitate learning is
50 We show two applications using Primo to examine the molecular