1 ology showed evidence of intracellular storage, and genetic
analysis confirmed a GLA A gene mutation (p.Asn215Ser) in all
2 A bootstrapping
analysis confirmed a significant increase in R(2) for the mod
3 Change-point
analysis confirmed a temporal association of high-frequency P
4 Qualitative
analysis confirmed cerebrocerebellar diaschisis in all gliobl
5 Single-cell RNAseq
analysis confirmed CHX10(+) cells within the differentiated p
6 TM thinning with collapse of Schlemm's canal; and proteomic
analysis confirmed downregulation of metabolic and structural
7 Chromatin immunoprecipitation assays and PCR
analysis confirmed HNF-1beta binding to the Ppargc1a promoter
8 validation cohort (mean age, 62 years; range, 27-86 years),
analysis confirmed improvement in specificity (from 17% to 33
9 Functional
analysis confirmed inactivating CYLD mutations as drivers for
10 Metabolomic
analysis confirmed no change in cellular metabolic response t
11 Stomach content
analysis confirmed predation on cnidarians and gelatinous org
12 Moreover, In-silico
analysis confirmed probable binding polar and non-polar regio
13 Our trans-ethnic meta-
analysis confirmed recent findings implicating the KLB and GC
14 Glycan array
analysis confirmed selective binding of the CRD to glycans th
15 Kinetic and mutational
analysis confirmed several features seen in the crystal struc
16 Conjunction
analysis confirmed significant differences in the bilateral A
17 Gene-based
analysis confirmed strong interaction between COL5A3 and MMP9
18 Accordingly, DNase I footprinting
analysis confirmed that AbrB bound to the promoter region of
19 Multivariable
analysis confirmed that ATLG was associated with inferior PFS
20 Chromatin immunoprecipitation
analysis confirmed that clofibrate abrogates the binding of n
21 iles using multiple V regions validated by quantitative PCR
analysis confirmed that distinct bacterial taxa dominate in d
22 Multivariable regression
analysis confirmed that high-burden hospitals were more likel
23 Mutation
analysis confirmed that JZTx-27 bound to S3-4 linker of NsVBa
24 RNAseq
analysis confirmed that many of these loci are expressed.
25 Live-cell bioenergetic flux
analysis confirmed that mensacarcin disturbs energy productio
26 ChIP
analysis confirmed that PGR proteins were recruited on proges
27 Critically, effective connectivity
analysis confirmed that reduced amygdala activity was not mer
28 Second, western blot and immunohistochemical
analysis confirmed that Sal-1 suppressed iNOS expression in v
29 Western blotting and immunostaining
analysis confirmed that ShcA is expressed in podocytes.
30 was significantly associated with fertility and functional
analysis confirmed that sperm from bulls possessing the haplo
31 Behavioral
analysis confirmed that the 14-day social defeat sessions res
32 X-ray crystallography, HDX-MS and SPR
analysis confirmed that the CDR regions of VHH6 interact simu
33 Protein BLAST
analysis confirmed that the chosen peptide markers were uniqu
34 Moreover, RT-PCR
analysis confirmed that the expression of the RNAi apparatus
35 In addition, the PCA-MLR
analysis confirmed that the industrial sections; cutting, shi
36 Further mass spectrometry
analysis confirmed that the isolated FaEO consists in the alr
37 c extracts were able to inhibit fungal amylase, and the PCA
analysis confirmed that the relation between the chlorogenic
38 Marker
analysis confirmed that the two cell phenotypes were mutually
39 idgut protein vesicles showed weak binding, and ligand blot
analysis confirmed the binding specificity.
40 r NOTAs was still functional; (iii) circular dichroism (CD)
analysis confirmed the complexation of unmodified and NOTA-mo
41 the influence of combustion parameters and the sensitivity
analysis confirmed the dominating influence of hydrocarbon fr
42 qRT-PCR
analysis confirmed the microarray results, that KIR2DL4, IL6
43 esence of NEIL1 and DNA, while small-angle X-ray scattering
analysis confirmed the NEIL1 mediated PCNA trimer dissociatio
44 Patch-clamp
analysis confirmed the neuron-like electrophysiological profi
45 The immunological and histological
analysis confirmed the positive radiological performance with
46 Quantitative
analysis confirmed the positive visual findings in (15)O-wate
47 Multivariate
analysis confirmed the predictive value of baseline LV SUV fo
48 Scanning electron microscopy
analysis confirmed the presence of AuNP on the surface of PPD
49 CLRN1 minigene-based
analysis confirmed the splicing of an aberrant exon due to us
50 We conclude that metabolic network
analysis confirmed the validity of the thermodynamic constrai