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1                                                             We identify 1434 protein-coding genes and 39,806 noncoding re
2                                  From 832 high-LD variants, we identify 39 candidate functional variants from 14 loci dis
3                                                             We identify 48 genes (25 newly reported) showing significant
4                     Using bioinformatics, mutation and NMR, we identify a 7-residue sequence, named P1 (residues 36-42),
5                                                       Here, we identify a family of over 30 enzymes, which are homologous
6      Using RNA-seq profiling of the intima of lesions, here we identify a macrophage-specific lncRNA MAARS (Macrophage-As
7                                                       Here, we identify a neuronal circuit in the nematode Caenorhabditis
8                                                        Here we identify a novel and critical function of IKK2 and its co-
9                                                    Finally, we identify a novel group of CA1 neurons that robustly encode
10                                                             We identify a pH-sensitive electrostatic interaction between
11       Through intravital imaging of NSCs and their progeny, we identify a population of Gli1-targeted NSCs showing long-t
12                                                      Herein we identify a previously unrecognized connection between thes
13 ely terminate transcription of bacterial CRISPR arrays, and we identify a widespread antitermination mechanism that antag
14                                                        Here we identify an adaptive circuit-based mechanism that enables
15                                                Furthermore, we identify an allele of the GTPase obgE that is syntheticall
16                                                             We identify an ATS pertaining to which drug add-ons to recomm
17                                                       Here, we identify and functionally validate a CRC 'trio' constitute
18                                                             We identify binding sites for substrate K(+) and Cl(-) ions,
19                                                       Here, we identify BRCA2 and MEILB2-associating protein 1 (BRME1), w
20                                                             We identify candidate members of the gut microbiome that elic
21                                 Beyond these known subsets, we identify CD4(-)CD8(-)TCRalphabeta(+), double-negative (DN)
22                                                             We identify convergence of antibody sequences across SARS-CoV
23 ions attributed to particular cell size control mechanisms, we identify dependencies that point to potentially new mechan
24                                                       Here, we identify disordered micrometer-size organic phases rather
25 h a combination of proteomics and gene expression analysis, we identify enzymes involved in carbohydrate metabolism as tr
26                                              In this study, we identify Fgl2 as a soluble TFR cell effector molecule thro
27                                                             We identify five new colonies, and 21 additional colonies pre
28                                                Furthermore, we identify genes involved in cellular transport, including c
29                                                        Here we identify globally distributed haplotypes from 15,789 SARS-
30 partment composed of novel fibril-like substructures, which we identify here by three-dimensional single-molecule superre
31 roduces highly contiguous, chromosome-length scaffolds, and we identify hundreds of TE insertions that were missed by Ill
32                                                             We identify indicator micropollutants for further studies: be
33               Central to the adaptation-enhancing principle we identify is the ability of noise to mitigate population bo
34 gether with an in vitro site-directed mutagenesis approach, we identify loss of STAT3 O-GlcNAc at Threonine 717 as a driv
35  genome-wide profiling of the H3K27ac histone modification, we identify neuron-subtype-specific regulatory elements that
36                                                      Hence, we identify new therapeutic targets and putative therapeutic
37  of large curated datasets from human cancer RNA-Seq, where we identify novel putative biomarker genes in different tumor
38                                                             We identify outstanding questions and methodological challeng
39                       In the highly interconnected network, we identify pathway communities and hundreds of previously un
40                    Using a CRISPR-mediated knockout screen, we identify SLC35B2 and myosin-7B (MYO7B) as critical endocyt
41                                                             We identify that a fusion of the catalytic domain of TET1 to
42                                                             We identify that ARID1A inactivating mutations are present at
43                                                     Herein, we identify the CBP/p300-interacting transactivator with glut
44                                                       Here, we identify the conditions and substrates that decouple the c
45                                                      Herein we identify the dual function cytokine IL-33 as an orchestrat
46                                                        Here we identify the nuclear receptor peroxisome proliferator-acti
47 al characterization of the knot region by NMR spectroscopy, we identify the SAM-binding region and observe changes in the
48                                              In this study, we identify the vesicular soluble N-ethylmaleimide-sensitive
49                                                             We identify these intertwined density waves as being Fermi su
50                   Within posts made by users in our sample, we identify topics that appear more often within users' socia