1 We identified 1044 patients, among whom 460 (44.1%) received
2 Through RNA-Seq analyses,
we identified 137 genes that are missing in chicken, includin
3 Using mass spectrometry approaches,
we identified 16 VTPs of the CyHV-3 FL strain.
4 of Transplant Recipients data from June 2013 to June 2015,
we identified 1768 DD livers exported to regional candidates
5 However,
we identified 2 or more missense variants predicted to be del
6 In the combined meta-analysis,
we identified 22 loci associated at genome-wide significance,
7 We identified 26 ancient and more recent polyploidy events di
8 We identified 265 specimens to species or genus using DNA bar
9 We identified 3 mechanisms underlying local progression in th
10 We identified 31 cases of PTLD during the study period.
11 We identified 4 host gene expression profiles, among which ca
12 We identified 57 longitudinal studies exploring the associati
13 We identified 79 associations influencing 13 primary and 19 s
14 We identified 89,790 incident PD cases and 118,095 comparable
15 We identified a causal mutation in 1 of 14 genes in 50% (353/
16 (MAbs) that recognize known major antigenic sites in MeV-H,
we identified a D4 genotype variant that escapes neutralizati
17 We identified a feedback loop within the NANCI (Nkx2.1-associ
18 Moreover, by using mutated promoter constructs,
we identified a NF-kappaB site as critical in this activation
19 In summary,
we identified a novel pathway for regulation of beta-catenin
20 We identified a novel splice mutation in IKBKG (c.518+2T>G, r
21 Previously,
we identified a potent neutralizing antitoxin against BoNT/A1
22 Overall,
we identified a small number of immunodominant regions, which
23 Instead,
we identified a specific set of markers associated with the c
24 After a meta-analysis including >300,000 European samples,
we identified an additional nine novel loci.
25 We identified an atherosclerosis-associated single-nucleotide
26 By cDNA library screening,
we identified an immune cell-specific, co-stimulatory recepto
27 Here,
we identified an orphan protein (Plu2236) from Photorhabdus l
28 pendent technology called CANE developed in our laboratory,
we identified and selectively labeled noxious-stimulus-activa
29 Last,
we identified and studied three novel patient XIAP mutations
30 We identified Arabidopsis pex6 and pex26 mutants by screening
31 We identified autophagy as a pivotal cell response determinin
32 We identified BRPF1 deletions or point mutations in six addit
33 We identified compounds that match the pharmacophore of the k
34 Furthermore,
we identified conserved miRNA-targets regulations in the cont
35 We identified few horizontally transferred genes, but some of
36 We identified heavy smokers that were resistant (n = 65) or s
37 Here we investigate the role of two gtr operons that
we identified in the S Typhi genome.
38 Previously,
we identified increased translocation of the fatty acid trans
39 We identified low but escalating risk of severe M. chimaera i
40 Unexpectedly,
we identified PABPN1-dependent ALYREF binding near the 3' end
41 We identified pathogenic mutations in 36 of 204 (17.6%) patie
42 -complete response to PD-1 blockade in a mesenchymal tumor,
we identified PTEN mutations and reduced expression of genes
43 Here,
we identified seven unrelated individuals affected with an ap
44 In particular,
we identified several arginine residues that interact with th
45 We identified significant group differences in striatal dopam
46 We identified single-point mutations in the Fc domain (e.g.,
47 Among others,
we identified sites catalyzed at faster rates with potential
48 Here,
we identified the conserved NK-2 homeobox gene ceh-24 to be c
49 We identified the following variables as unfavourable predict
50 In this study,
we identified the proliferating cell nuclear antigen (PCNA) a