1 Aiming at a simplification of dosimetry,
we analyzed the accuracy of a theoretically substantiated app
2 We analyzed the adaptation of avian influenza viruses to a ma
3 We analyzed the association of common and rare genetic varian
4 Using a census of 121 villages in rural Mali,
we analyzed the association of community latrine coverage (de
5 In a cohort of 1,596 breast cancer patients,
we analyzed the associations of 33 laboratory variables with
6 Here
we analyzed the clonality of HIV-1-infected cells using high-
7 We analyzed the distribution of EPSPS copies in the genome of
8 fic projections from the lateral hypothalamus and midbrain,
we analyzed the distribution of projections labeled with anti
9 To better understand the role of His-50,
we analyzed the effect of DHA on aS-derived species: a natura
10 Using the Caenorhabditis elegans touch receptor neurons,
we analyzed the effects of 67 tubulin missense mutations on n
11 Here
we analyzed the effects of a set of distinct formin fragments
12 tested these models in two EEG experiments in humans where
we analyzed the effects of prestimulus alpha power on visual
13 We analyzed the effects of SH2 domain overexpression on prote
14 We analyzed the effects of SNVs on enzyme active sites, ligan
15 To examine potential mechanisms,
we analyzed the expression of key fibrinolytic molecules in e
16 We analyzed the fidelity of nascent RNAs from all actively tr
17 We analyzed the flows of N and P through the processes of cul
18 We analyzed the frequency of tacrolimus trough levels below a
19 Here
we analyzed the genomes of 119 strains of the marine actinomy
20 We analyzed the impact of 4 specific DTN time reduction strat
21 Here
we analyzed the impact of aPC on inflammasome activity in myo
22 We analyzed the impact of mainly biogas (as well as electric
23 Here,
we analyzed the intravasation of invasive human breast cancer
24 and to gain insight into the pathogenesis of the disorder,
we analyzed the localization of EXTL3 in fibroblasts derived
25 We analyzed the mechanisms of these dysfunctions and their re
26 We analyzed the modulation of mitochondrial and chlororespira
27 We analyzed the morphology of melanopsin-immunopositive ORDs
28 In this study,
we analyzed the mutability of each residue using an approach
29 We analyzed the outcome of infection of C3H/HeJ mice with Lep
30 To gain insights into the function of the SUFB protein,
we analyzed the phenotypes of two SUFB mutants, laf6 and hmc1
31 We analyzed the presence of Golgi-associated genes using sing
32 To demonstrate practical utility,
we analyzed the proteomes of 10 human pancreatic cancer cell
33 We analyzed the recognition of normal lymphocytes by SLAMF7-C
34 In this study,
we analyzed the requirement of endogenous Kras to maintain su
35 evels of mRNA and active protein translation, respectively,
we analyzed the responses of host cells to vaccinia virus inf
36 Herein,
we analyzed the role of exosomes in the differentiation of HT
37 In this study,
we analyzed the role of lipid droplets during the interaction
38 Here,
we analyzed the role of PLC2 in plant immunity using an artif
39 Herein,
we analyzed the role of transforming growth factor (TGF)-beta
40 Here
we analyzed the roles of translesion synthesis (TLS) Pols in
41 We analyzed the spectrum of the neural activity while listeni
42 In this study,
we analyzed the status of TMPRSS2-ERG fusion genes and inters
43 We analyzed the structure of recombinant CLEC3A by SDS-PAGE a
44 In an accompanying paper (Hartenstein et al., ),
we analyzed the systems of fiber tracts and secondary lineage
45 We analyzed the timing of river floods in Europe over the pas
46 We analyzed the transcriptome of the intron-rich eukaryote Pa
47 In this study
we analyzed the transcriptomes of Brassica napus parental lin
48 biogenesis and identify putative cuticle-associated genes,
we analyzed the transcriptomes of peels from ripe and overrip
49 Herein,
we analyzed the ultrastructure of the accumulated lipids in e
50 Using a blinded approach,
we analyzed the value of quantitative automated pupillometry