1 We performed 3 meta-analyses each for CD, UC, and IBD (CD and
2 To evaluate the performance of this scheme,
we performed a cgMLST analysis of 92 newly sequenced genomes,
3 To determine direct targets,
we performed a chromatin immunoprecipitation against Lmx1b in
4 olution of gene transcription in and between plant species,
we performed a comparative transcriptomic and genomic analysi
5 Here,
we performed a correlative gene-expression microarray and in
6 We performed a cost-effectiveness analysis to assess diagnosi
7 We performed a cross-sectional study of matrix turnover in HI
8 We performed a discrete event simulation to forecast patient
9 We performed a double-blind crossover challenge of 59 individ
10 Additionally,
we performed a genome-wide scan and identified one SNP with s
11 We performed a genomewide association study in a discovery se
12 Following lab validation,
we performed a human validation by collecting fingerprick who
13 METHODS AND
We performed a meta-analysis of available studies comparing d
14 We performed a meta-analysis of randomised controlled trials
15 We performed a meta-analysis to examine miRNA diagnostic valu
16 We performed a multicenter prospective study of 226 patients
17 In this study,
we performed a novel drug-repurposing screening to identify F
18 We performed a parallel-arm randomized controlled trial to te
19 We performed a prospective, observational clinical study to d
20 We performed a retrospective cohort study using inpatient and
21 To identify the endogenous receptor for PGE2-G,
we performed a subtractive screening approach where mRNA from
22 We performed a whole-transcriptomic analysis of blood samples
23 ar mechanisms of Lrp4 function in modulating Wnt signaling,
we performed an array of genetic analyses in murine tooth dev
24 Using region-specific mouse reporter strains,
we performed an RNA-seq screen, identifying tip- and stalk-en
25 We performed an unbiased analysis of transcriptional heteroge
26 tigate the accuracy of low-titer positive CrAg LFA results,
we performed chart reviews for all patients with positive CrA
27 Here,
we performed clonal multicolor lineage tracing of skeletal mu
28 Here,
we performed epigenetic profiling of human resting naive, cen
29 ysbiosis of the gut microbiome impacts honeybee health, and
we performed experiments to determine whether antibiotic expo
30 We performed expression quantitative trait locus (eQTL) analy
31 We performed fragment-based and high-throughput screens again
32 To investigate the molecular basis of TAD formation,
we performed Hi-C experiments on cells depleted for the Forkh
33 Here,
we performed marker analysis, cell proliferation assays, and
34 Here,
we performed molecular dynamics simulations of GLIC in the ab
35 We performed multimodal immunomonitoring to assess allergen-s
36 We performed multinomial logistic regression analysis to asse
37 In this prospective cohort study,
we performed multiregion whole-exome sequencing on 100 early-
38 In this study,
we performed optic nerve injury in adult naked mole-rats, the
39 have anti-eIF2α-P activity suitable for clinical use,
we performed phenotypic screens on a NINDS small molecule lib
40 Here
we performed quantitative trait locus analysis, utilizing RNA
41 We performed RNA-seq on purified peripheral afferent neurons,
42 Here,
we performed scans for regions of high relative divergence (F
43 We performed screening visual fields using a calibrated iPad
44 To characterize plasma cell-free eccDNAs,
we performed sequencing analysis in 26 libraries from three b
45 We performed studies of mice with disruption of Sirt1 specifi
46 To test the non-tumor cell microenvironment role of RAGE,
we performed syngeneic studies with orthotopically injected b
47 We performed the first genome-wide association study for mola
48 In parallel,
we performed the same study of 29 healthy individuals (contro
49 We performed whole exome sequencing on six out of nine member
50 We performed whole-exome sequencing on individuals with histo