1 We analysed 1218 P. falciparum clinical isolates, and the res
2 We analysed 400 consecutive treatment-naive HBV-monoinfected
3 From March 18, to April 26, 2020,
we analysed 800 patients with a diagnosis of cancer and sympt
4 We analysed a prospective cohort dataset of 201 individuals w
5 We analysed a widely used barcode, the V9 region of the 18S r
6 We analysed all data together and separately for marsupials a
7 Therefore,
we analysed archaeal communities from in situ hypersaline bri
8 Finally,
we analysed brain-wide rearrangements of the vasculature in a
9 We analysed data from 16 countries in sub-Saharan Africa wher
10 We analysed data from two large multimorbidity studies to det
11 We analysed data on hospital admissions in England for types
12 We analysed directly obtained and imputed genotypes, and foll
13 We analysed funding by donor for the 20 largest donors, by re
14 l processes that give selective advantage to mutant clones,
we analysed genotyping data from the blood-derived DNA of 482
15 expand the molecular knowledge governing virion maturation,
we analysed HCMV virions using proteomics, and identified a s
16 To test for MeCP2 binding to these motifs in vivo,
we analysed human neuronal cells using ChIP-seq and ATAC-seq
17 In this study,
we analysed iron, zinc and phosphorus in cabbage, broccoli, p
18 In this study,
we analysed key genes and pathways involved in KIRC from an a
19 We analysed linked data from the BiB study-an ongoing, multi-
20 ola in the dozens of generations before the individuals who
we analysed lived.
21 We analysed meerkat (Suricata suricatta) movements of a total
22 We analysed physiological and activity data from 32 individua
23 To investigate the role of PIEZO1 in gliomas,
we analysed PIEZO1 gene expression at the transcriptome level
24 To inform the development of insect-based foods,
we analysed selected minerals (Fe-Mn-Zn-Cu-Mg) in wild-harves
25 In this retrospective study, performed on 417 participants,
we analysed serum NfL and p-Tau(181) concentrations with an u
26 Therefore,
we analysed the allelic sequence variation in three Sub1 gene
27 We analysed the association between histopathology, duration
28 Using two-sample Mendelian randomization
we analysed the association of genetically elevated levels of
29 Here,
we analysed the association of street tree density and specie
30 As the predictor,
we analysed the collective testosterone of males within each
31 We analysed the dynamics of these two modules alone and in mi
32 Using phylogenetic generalized linear mixed models,
we analysed the effect of diversification rate, different geo
33 g natural seawater samples at three different temperatures,
we analysed the effect of experimental warming on the abundan
34 Finally,
we analysed the effect of three clinical missense mutations (
35 We analysed the effect of tumour subtype and patient demograp
36 Here
we analysed the expression of exl1 by Pectobacterium brasilie
37 Here, using age/region-matched sub-sets,
we analysed the gut microbiome differences across five major
38 Here,
we analysed the influences of metabolites that are differenti
39 We analysed the intention-to-treat (ITT) population, adjusted
40 We analysed the mitochondrial COI gene of 84 butterfly specie
41 about the role of SASH1 in the pathogenesis of the disease,
we analysed the prognostic value of SASH1 in non-small cell l
42 Here,
we analysed the RNA virome from approximately 10 l water from
43 Here,
we analysed the semantic neighbourhoods of 1,010 meanings in
44 We analysed the skeletal intracrystalline amino acids of mass
45 In this study,
we analysed the spatial responses of a resident large herbivo
46 We analysed the sterol profile of four beetle species reared
47 In this study,
we analysed the transcriptomic profile of P. aeruginosa cells
48 We analysed these with maximum likelihood, Bayesian inference
49 Here,
we analysed transcriptomic and metabolite responses of two cu
50 We analysed VO(2max), respiratory exchange ratio and test dur