1 We further confirmed a role for Ogn in the in vivo regulation
2 We further confirmed by site-directed mutagenesis and mass sp
3 We further confirmed CYC is a target of miR-34a by a dural lu
4 We further confirmed directly in living pancreas slices that
5 We further confirmed E2-dependant engulfment of LCs by real-t
6 Using these assays,
we further confirmed frequent CpG island methylation in the o
7 In addition, a novel mutation V158I was identified, and
we further confirmed its resistance to boceprevir in protease
8 We further confirmed our observation using exome sequence dat
9 We further confirmed specific and robust dCas9VPR on-target e
10 We further confirmed that 5S rRNA percent and 5S/18S rRNA rat
11 In a mouse model with a DG knockout of the GRIN1 gene,
we further confirmed that a selective decrease in DG GluN1 is
12 We further confirmed that at least two PTPS-2-producing speci
13 We further confirmed that cullin 4 may interact with Hsp90bet
14 By studying diverse human tissues and mouse models,
we further confirmed that developmentally programmed 3' CGI m
15 Through siRNA silencing approach,
we further confirmed that DPP8 but not DPP9 is a key molecule
16 We further confirmed that extracellular vesicles could transf
17 We further confirmed that hypermethylated RAB25 is inversely
18 We further confirmed that hyperoxia up-regulates the levels o
19 As this finding predicted,
we further confirmed that loneliness was associated with diff
20 We further confirmed that our phenotypic analysis of IgG-SCs
21 We further confirmed that podoplanin(+) cells exist in small
22 By using in vivo imaging and transfusion experiments,
we further confirmed that senescent erythrocytes that are ret
23 Using an H3K4su-H4 tetramer as a substrate,
we further confirmed that Sirt5 is an active histone desuccin
24 We further confirmed that some ASD risk genes (NLGN1, STAG1,
25 We further confirmed that the local density of hydrate-formin
26 We further confirmed that the observed deficit in vestibular
27 We further confirmed that the remaining wild-type Bap1 allele
28 In addition,
we further confirmed that the TBG promoter confers transgene
29 We further confirmed that the Treg-DC-mediated skewed CD4(+)
30 We further confirmed that the unexpected binding mode targets
31 We further confirmed that Top2alpha inhibition was due to a c
32 We further confirmed that tumor regression upon infection was
33 We further confirmed that, in vivo, CG was required for the e
34 We further confirmed the consequences of beta-arrestin1 regul
35 We further confirmed the effects of Ces3 inhibition in vivo b
36 We further confirmed the functionality of NES2 by a heterokar
37 We further confirmed the identity of the uPFCAs by imposing h
38 We further confirmed the immunogenicity of frameshift peptide
39 Here, using chemical peptide synthesis,
we further confirmed the importance of the balance between hy
40 We further confirmed the importance of this complex in vivo u
41 We further confirmed the isoform-specific differential expres
42 We further confirmed the presence of proline-rich proteins, l
43 We further confirmed the results of the primary screen in IR4
44 We further confirmed the role of (199)KxGxYR(204) as a TGN re
45 We further confirmed the role of SLP-76 in HIV-1 infection by
46 We further confirmed the utility of this method by quantifyin
47 -interacting component using a yeast two-hybrid screen, and
we further confirmed this interaction by the glutathione S-tr
48 We further confirmed this negative regulation of Nrf2 by Hrd1
49 We further confirmed this unexpected finding using a photogra
50 We further confirmed via immunohistochemistry that gene expre