戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (right1)

通し番号をクリックするとPubMedの該当ページを表示します
1 ence for effects on splicing even of mutations in genes not expressed in accessible tissue.
2 fect was caused by acid activation of these cation channels expressed in airway sensory nerves.
3                                                        When expressed in an Escherichia coli strain deficient in sulfite
4               Nearly two-thirds of the transcripts that are expressed in anatomically similar tendons were different betw
5                                            PVN LepR are not expressed in astroglia and rarely in microglia; instead, glut
6                                             Pcdh-gammaC4 is expressed in both neurons and astrocytes.
7 ered in the human genome and whether APE2 is differentially expressed in cancer patients.
8 )) when restricting to LOF variants located in exons highly expressed in cardiac tissue (TTN(LOF)).
9 e adhesion G protein-coupled receptor family, is abundantly expressed in cells of the developing cerebral cortex, includi
10 RICH3 mRNA transcripts and protein isoforms that are highly expressed in central nervous system cells.
11   We show that the non-canonical tubulin Tuba8, transiently expressed in cortical progenitors, drives differentiation of
12 significant excess of loss-of-function DNMs in genes highly expressed in craniofacial tissues, as well as genes associate
13                                        Genes differentially expressed in depression were identified with the TWAS FUSION
14 l damage even when spliced into a heterologous receptor and expressed in heterologous cells.
15                            However, here we found that when expressed in human cells, two highly homologous HSP70s, HSPA1
16 , and to confirm its agonist activity on rat P2X2 receptors expressed in human cells.
17 LA-E, with nearly complete identity between the two alleles expressed in humans, HLA-E*01:01 and HLA-E*01:03, can lead to
18  types such as the immune-related genes that were similarly expressed in immune cells (hemocytes) and ovarian somatic cel
19 enzyme required for 15-Oxo-ETE synthesis, was predominantly expressed in mast cells and localized near 15-LO(+) epitheliu
20                                        ORF8b was abundantly expressed in MERS-CoV-infected Huh-7 cells.
21 ctively our results suggest that, although T-type VGCCs are expressed in mouse lymphatic smooth muscle, they do not play
22                                   Yet, lncRNA LINP1 is over-expressed in multiple cancers and confers resistance to ioniz
23             Several of these AD risk genes are specifically expressed in myeloid cells, whereas others are ubiquitously e
24                                            LIN28B is highly expressed in neuroblastoma and promotes tumorigenesis, at lea
25 rf72 and SMCR8 both contain longin and DENN (differentially expressed in normal and neoplastic cells) domains(7), and WDR
26 TSG-6 and heavy-chain protein-hyaluronan are constitutively expressed in normal skin and increase post-wounding but are c
27 nist of estrogen receptor (ERalpha), a transcription factor expressed in over 50% of breast cancers.
28                        Here we report that Slit ligands are expressed in overlapping and distinct patterns in both endocr
29 hesis that gene expression profiles of protein-coding genes expressed in peripheral white blood cells (PWBCs), and circul
30                                       We report that HuR is expressed in postmitotic projection neurons during mouse brai
31 vel candidate gene (ILDR1), which encodes a receptor highly expressed in prostate tissue and is related to the B7/CD28 fa
32                      The transcription factor JUN is highly expressed in pulmonary fibrosis.
33 xisome proliferator-activated receptor alpha (PPARalpha) is expressed in retinal Muller cells, endothelial cells, and in
34                                Although NUCB2/nesfatin-1 is expressed in reward-related brain areas, its role in regulati
35 ranscripts from 125 genes were significantly differentially expressed in ribeye muscle between the highest and lowest REA
36 families of transcription factors (TFs) were differentially expressed in root system during plant development.
37  Many of the identified susceptibility genes for asthma are expressed in the airway epithelium, supporting the notion tha
38  a class-A orphan G-protein-coupled receptor that is highly expressed in the brain and represents a promising therapeutic
39                       While both LASP1 and LASP2 are highly expressed in the brain, little is currently known about their
40 ase that is highly conserved across species and extensively expressed in the brain.
41                                       We show that Wnt3a is expressed in the caudal embryo in a dorsal-ventral (DV) gradi
42 alpha2, alpha5, beta2, beta3, gamma2, and delta were highly expressed in the dentate molecular layer, whereas alpha1, alp
43 ohol use was enriched in gene sets that were preferentially expressed in the DLPFC and was associated with replicable dif
44 LF-likes (i.e., MiRALF1 and MiRALF3) from M. incognita were expressed in the esophageal gland with high expression during
45 emonstrated that integrin alpha5beta1 and Fn1 (fibronectin) expressed in the Isl1 lineages regulate PAA formation.
46             Here we report that multiple MYO7A isoforms are expressed in the mouse cochlea.
47      The mouse alkaline ceramidase 2 gene (Acer2) is highly expressed in the placenta between embryonic day (E) 9.5 and E
48 se findings suggest that when TRP channels and GPCRs are co-expressed in the same tissues, many of these channels can inh
49 xpressed across mouse branchial arches, and HOXA2, which is expressed in the second and more posterior branchial arches.
50                                                    PD-L1 is expressed in tumor cells and its interaction with PD-1 plays