ライフサイエンスコーパス: expression levels of

1 The graded tuning of fast-spiking capacity by the absolute expression levels of specific ion channels provides a counter

2 Additionally, expression levels of eukaryotic translation initiation factor

3 n of mitochondria and decreased cell proliferation, altered expression levels of pyruvate dehydrogenase phosphatase (PDP)

4 ation by 1,25(OH)(2)-D(3) was independent of maturation and expression levels of microRNA-155 and PU.1 (as upstream regul

5 Immunoreactive-cells and expression-levels of spinal PAR-2, CGRP and c-Fos in the EA g

6 r evaluating ileitis at days 7 and 22, and distribution and expression-levels of PAR-2, CGRP and c-Fos on day 22.

7 ions were confirmed in studies of cell lines with different expression levels of signaling partners, and in experiments c

8 We investigated whether knocking down expression levels of HBV antigens in liver might increase the

9 on cells upon foxo knockdown was also confirmed by elevated expression levels of known ER stress markers.

10 mics analyses also revealed significant alterations in gene expression levels of key enzymatic regulators of biochemical

11 ivity of vitamin D in hPDLCs was assessed based on the gene expression levels of vitamin D receptor (VDR)-regulated genes

12 Owing to the high expression levels of HER2, combination therapies are currentl

13 Notably, the survival rate for the high expression levels of Lrp5, CSF1, and CD105 in tumor tissues w

14 gy compare to the more competitive G. androsaceus with high expression levels of keystone functional genes.

15 d maturation and activation over sCD40L evidenced by higher expression levels of CD83, CD86, HLA-DR and CD54, increased s

16 However, their observations are based on much higher expression levels of H-RasV12 than in our study and Liang et

17 disorders, and the adult cerebellum has one of the highest expression levels of CB1R, but little is known about CB1R in

18 red with their young adult counterparts when fold change in expression levels of GzmB, CD107a, IFN-gamma, and TNF was exa

19 he evolutionary age of genes, suggesting that divergence in expression levels of genes critical for cell function was res

20 that a challenge with LPS treatment significantly increased expression levels of alpha7nAChR in monocytes, alveolar and i

21 n granulocytes, monocytes and alveolar macrophages, and low expression levels of alpha7nAChR were detected in interstitia

22 cell growth via beta-catenin signaling in GSCs that had low expression levels of the transcription factor ASCL1.

23 In the intestinal epithelium of Hnf4alphagamma(DKO) mice, expression levels of FAO genes, FAO activity, and metabolites

24 type are observed, including alternative splicing, and mRNA expression levels of proto-oncogenes and tumor suppressors.

25 The mRNA expression levels of ST6GAL-I and SOX9 in human gastric epith

26 Native expression levels of Antarctic fish chaperomes showed very mo

27 e brain-the gene regulatory network (GRN)-that orchestrates expression levels of hundreds to thousands of genes in a beha

28 These intron retention events appear not to alter overall expression levels of the affected transcripts but rather the

29 to secrete a significant level of IL-1beta and had reduced expression levels of pro-IL-1beta in response to infection wi

30 Over-expressing miR-195 reduces expression levels of its top predicted target synaptojanin 1

31 d Il2rg (KO)/Rag1 (KO)/Tg(+) juveniles exhibited suppressed expression levels of Th2 markers, diminished MCM, suppressed

32 isms of OXPHOS exist in chRCC and renal oncocytoma and that expression levels of ETC complex subunits can serve as a diag

33 gar-producing accessions of Solanum pennellii revealed that expression levels of known and novel candidate genes (putativ

34 The expression levels of eotaxin, IFN-gamma, IL-6, IL-8, IL-16, M

35 Here we show that IGF1 alters the expression levels of a subset of lncRNAs.

36 gene, RPL10 (QM), in Nicotiana benthamiana We analyzed the expression levels of predicted intended-target and off-target

37 significantly reduced the level of ROS and H3K9me3, and the expression levels of IRE-1 and CHOP.

38 cancer centers (UM, USC, and KCCRI) were used to assess the expression levels of ER-associated proteins using immunohisto

39 We then compared the expression levels of those markers in PBMCs taken from ASD pa

40 Here, we introduce the APA-seq method to detect the expression levels of APA isoforms from 3'-end RNA-Seq data by

41 Here, we examined the expression levels of tau isoforms, their phosphorylation prof

42 ocation of bacterial resources, affecting, for example, the expression levels of proteins dedicated to metabolism and bio

43 Our results demonstrate that manipulating the expression levels of key sulfur assimilatory enzymes could be

44 wo decades, the scientific community is able to monitor the expression levels of tens of thousands of genes and proteins

45 d immune cell recruitment and cell motility by reducing the expression levels of the receptor for HA-mediated motility, R

46 We observed that the expression levels of GRP78 (p < 0.0001), ATF6 (p < 0.0001), a

47 tic outcomes of many cancer types have been linked with the expression levels of several of these architectural proteins.

48 nins in the potato cultivars correlated positively with the expression levels of the genes involved in the phenylpropanoi

49 rait loci analyses identified multiple SNPs associated with expression levels of post-GPI attachment to proteins 3, GSDMB

50 tion rates of S- and M-cones are negatively correlated with expression levels of FATP4 in the RPE of the KI, KI;Fatp4 (+/