ライフサイエンスコーパス: expressed at

1 te response, especially CA12g05030, which was 700-fold more expressed at 96 HPI compared to control plants.

2 rally regulated and likely influenced by additional factors expressed at a given developmental stage.

3 Prmt1v2 was expressed at a higher level compared to Prmt1v1 in hepatic ti

4 ural activity expressed during perceptual experience are re-expressed at a later time, a putative neural marker of memory

5 a monomeric, glycan-engineered RBD protein fragment that is expressed at a purified yield of 214 mg/l in unoptimized, mam

6 ntified genes that were uniquely or commonly differentially expressed at all three time points.

7 n the present study, we found TMPRSS13 to be differentially expressed at both the transcript and protein levels in human

8 Odd-paired (Opa), a zinc-finger transcription factor expressed at cellularization, controls the transition of gene

9 oid aberrant aggregation, and hence they are expected to be expressed at concentrations safely below their solubility lim

10 , whereas PCs that potentially could provide redundancy are expressed at considerably lower levels.

11 Ibsp, Phex, and Loxl4 were expressed at decreased levels in the ossification region in t

12 The detection of biomarkers expressed at early onset of carcinogenesis, hold promise for

13 We show here that transient exposure to a single microRNA, expressed at early stages during normal development, improves

14 A wide range of cytokines were expressed at high levels both in the blood and in the lungs,

15 gnaling is dependent on four Wnts (Wg, Wnt5, 6,10) that are expressed at high levels in arrested tracheoblasts and are do

16 In the developing teeth, BSP-GFPtpz was expressed at high levels in cementoblasts but not in odontobl

17 The recombinant cannabinoid CB(2) receptor was expressed at high yield in Expi293F mammalian cell cultures,

18 The results show that although Pcdh-gammaC4 is expressed at higher levels in the embryo and earlier postnata

19 ith obesity or type 2 diabetes mellitus, AGO1 and THBS1 are expressed at higher levels than the healthy controls, support

20 Pol IV is expressed at increased levels in E. coli cells exposed to exo

21 opsins; 2) most of the long-wavelength photoreceptive units expressed at least one middle-wavelength-sensitive opsin tran

22 r zinc sensor probing zinc release, supported that Z-LTD is expressed, at least in part, via reductions in presynaptic zi

23 the RRF/EF-G pair are functionally interchangeable, HflX is expressed at low levels and is dispensable under normal growt

24 or an abundance of biosynthetic gene clusters, but most are expressed at low levels and need to be activated for characte

25 Also, SSP-coding small open reading frames are often expressed at low levels or only under specific conditions, an

26 Despite these global changes, NMD targets and mRNAs expressed at low levels with short half-lives were enriched i

27 t antigenically silent, and viral proteins are sporadically expressed at low levels without full virion production.

28 Most of these covalently linked transcripts are expressed at low levels, but some accumulate to higher levels

29 K61Q-actin inhibit INF2-mediated actin polymerization when expressed at low levels.

30 s highly enriched in neurons, whereas Tet1(FL) is generally expressed at lower levels and more abundant in glia, suggesti

31 We used Ci variants expressed at physiological levels to investigate the contribu

32 Here, we demonstrate that SULT4A1 is highly expressed at postsynaptic sites where it sequesters Pin1, pre

33 Subsequent experiments validated that YY1 is expressed at protein and mRNA levels for MCF10A and 184A1, re

34 s, miR-146a is a known tumor suppressor commonly deleted or expressed at reduced levels in human myeloid leukemia.

35 entified to function in interference with virus entry, were expressed at significantly higher levels in HepG2 cells.

36 t is up-regulated by hepatocytes during liver injury but is expressed at significantly lower levels in mice with hepatocy

37 e found that upon U. maydis infection of Z. mays, KWL1-b is expressed at significantly lower levels than KWL1 and exhibit

38 1 expression levels, with both mutant and wild-type alleles expressed at similar levels.

39 e and mutant retinas, suggesting that the mutant protein is expressed at some level in mutant retinal cells.

40 We integrated allometric scaling laws expressed at static and ontogenetic levels into genetic mappi

41 intrinsic functional activity observed when the channel is expressed at the cell surface.

42 een different neuropsychiatric diseases and heterogeneously expressed at the level of each individual patient.

43 inding cassette subfamily C member 1 [ABCC1]) is abundantly expressed at the lung epithelial barrier, where it may influe

44 SHEATH1 (NS1) is a WUSCHEL-related homeobox3 (WOX3) homolog expressed at the margins of leaf primordia, and is required f

45 widely expressed in beta-cells, absent in alpha-cells, and expressed at the mRNA, but not protein, level in delta-cells.

46 the level of Per2AS, a novel non-coding transcript that is expressed at the Period 2 locus, was also linearly correlated

47 tter extracts contain a similar activity, and the enzyme is expressed at the surface of cultured human astrocytic cells a

48 ially expressed genes (DEGs) was 2.5-times lower than those expressed at unrestricted oxygen.

49 native splicing of mRNA, which allows exons of a gene to be expressed at varying levels across different cell types.

50 These alternate transcripts were expressed at very low levels in the wild-type mice and were s