Transcript Abundances(성적표 풍부)란 무엇입니까?
Transcript Abundances 성적표 풍부 - Metabolite and transcript abundances for the upregulation of flavone and flavonol biosynthesis under prolonged heat stress were closely correlated. [1] The transcript abundances of known anion transporters were determined and a family of putative B transporters was associated with the Cl- exclusion phenotype. [2] Clinical parameters between patient groups were compared, and several bioinformatic tools were used to assess differences in transcript abundances and cellular composition. [3] In future acidified oceanic conditions, dramatic oscillation with >10-fold change between nighttime (high) and daytime (low) transcript abundances of the antiporter was associated with increased resilience of T. [4] Real-time polymerase chain reaction and Western blotting were performed to determine the transcript abundances and protein expressions of TRIM66, HP1γ, AR, c-Myc, and GAPDH. [5] In the CuNP treatment, on the other hand, the transcript abundances of cell junction compositions, except adherens junction, were upregulated. [6] To understand how glial cells promoted neuronal maturation, we studied the association of transcript abundances in glial cells to gene expression in neurons. [7] However, long protein half-lives dampen this oscillation of transcript abundances, and putative functions remain elusive. [8] Nitrogen fertilization rate had a stronger influence on diazotroph population size and activity (determined by nifH gene and transcript abundances) and community composition (determined by nifH gene amplicon sequencing) than agricultural season or grass species. [9] We performed whole transcriptome sequencing and assessed sexually dimorphic changes in transcript abundances (transcriptional niches) associated with each gene-edited genotype. [10] However, transcript abundances (TA) in these cell mixture samples are confounded by proportions of the component leukocyte subpopulations. [11] The exceptions are the LOV-domain transcription factors with peaks in transcript abundances at different times and putative phototaxis photoreceptors transcribed throughout the day. [12] The transcript abundances of genes that regulate OsABI5, e. [13] The completeness of the resulting environmental eukaryotic taxonomic bins was assessed, and 48 genera were further evaluated for diel patterns in transcript abundances. [14] Changes in transcript abundances in the RNase P mutant also correlated with changes in their half-lives. [15] 0), was used to quantify gene and transcript abundances from 22 RNA-seq experiments, covering 843 separate samples. [16] RNA extracted from representative strains of each serovar grown to late exponential phase in Luria-Bertani (LB) broth showed that transcript abundances of core genes were significantly higher (p<0. [17] RA and RAn were positively correlated with transcript abundances of amoA and hzsB genes, respectively, rather than gene abundances. [18] Analysis of transcript abundances in excised inflorescences during an extended night suggested an intricate relationship among sugar starvation, senescence and SL biosynthesis and signalling. [19] Determination of the transcript abundances of lignocellulolytic enzyme genes reveals significant upregulation of multiple α-l-arabinofuranosidase genes and downregulation of some cellulolytic and xylanolytic enzyme genes in the engineered strain relative to its parent. [20] Moveover, salt and drought stresses can regulate the transcript abundances of BnaPHT1s, as well as phytohormones including auxin and cytokinin. [21] qPCR analysis indicated that transcript abundances of DkZF1/4 were significantly upregulated during AHCA treatment (1% O2 and 95% CO2) at day 1, DkZF2/5 at both day 1 and 2, while DkZF3 at day 2. [22] In addition, drought-responsive cis-elements were observed in peach NF-Y promoters, and 9 peach NF-Y genes were shown to distinctly increase their transcript abundances under drought stress. [23] To explore the expression patterns of CsPAP genes in response to excessive Fe supply, RNA-sequencing (RNA-seq) analyses were performed to compare their transcript abundances between tea plants that are grown under normal and high iron conditions, respectively. [24] Furthermore, transcript abundances of the alcoholic fermentation-related genes ADH1-1, ADH1-2, ADH1-3, PDC1, and PDC2 were reduced in PhERF2-silenced plants, but increased in PhERF2-overexpressing plants following exposure to 12-h waterlogging. [25] MnEIL3 overexpression in Arabidopsis significantly upregulated the transcript abundances of ethylene biosynthetic genes. [26] While no differences were detected for transcript abundances of the assessed ovarian HSP, the protein abundance of specific HSP was influenced by stressors during the follicular and luteal phases. [27] Transcript abundances are estimated from equivalence classes (ECs), which determine the transcripts that any given read is compatible with. [28] The transcript abundances of nine highly abundant candidate transcripts, as well as of two additional genes previously known to be involved in reproduction, cyp19 (p450 aromatase) and foxl2, were assessed in the individual samples by qRT-PCR. [29] Here we found that total carotenoid content continued to be elevated along the course of banana ripening and peaked at the ripening stage followed by a decrease, which is presumably caused by the transcript abundances of carotenoid biosynthetic genes MaLCYB1. [30] Upon TDIF treatment, the DR5:GUS poplar leaves revealed a higher GUS activity and in TDIF-overexpressing leaves, the transcript abundances of several PIN genes, especially that of PIN1, were increased, which implied an integration of TDIF and auxin in mediating this process. [31] Two candidate elicitors (designated as tetranin1 (Tet1) and tetranin2 (Tet2)) triggered early leaf responses (cytosolic calcium influx and membrane depolarization) and increased the transcript abundances of defense genes in the leaves, eventually resulting in reduced survivability of T. [32] Current expression quantification methods suffer from a fundamental but under-characterized type of error: the most likely estimates for transcript abundances are not unique. [33] The expression profile analysis indicated that BrCB5s were differentially expressed in different tissues, and the transcript abundances were significantly different under various abiotic stresses and plant hormone treatments. [34] Transcript abundances for cellular lineage markers (KRT18 and VIM), oestrogen receptor (ESR1), interferon α/beta receptor 1 (IFNAR1), and prostaglandin G/H synthase 1 (PTGS1) and 2 (PTGS2) were evaluated by real-time quantitative PCR. [35] The described approach, named AAV-bcTuD screening, offers a new alternative for in vivo assessment of rAAV that can accurately quantify vector genomes and transcript abundances in tissues, as exampled by the demonstration in liver and brain infections. [36] Results of the reverse transcription-polymerase chain reaction (RT-PCR) showed that transcript abundances of nitrate reductase (narG), nitrite reductase (nirS), and perchlorate reductase (pcrA) increased when the perchlorate and nitrate concentrations were higher. [37] The transcript abundances of these corresponding genes were analyzed by qRT-PCR. [38] Transcript abundances of genes encoding 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4 (PFKFB4), lactate dehydrogenase-A (LDHA), and phosphorylase kinase beta subunit (PHKB) were increased in heavy-WS but decreased in heavy-WS+WB. [39] Transcript abundances were analyzed by group means parameterization, controlling the false discovery rate below 0. [40] Finally, we detected a negative relationship between changes in transcript abundances in response to the solvent and phenanthrene. [41] High levels of transcript abundances were not confined to genes associated with the distinct walls of grasses but also of those associated with xyloglucan and pectin synthesis. [42] We also investigated the relative expression levels of six genes related to K+ and Na+ transport in roots of diploid and tetraploid by qRT-PCR method, and found that BvHKT1;1, BvNHX1, BvSKOR, and BvSOS1 were induced by additional 50 mM NaCl, and their transcript abundances in tetraploid were relatively higher than those in diploid. [43] Transcript abundances are estimated from equivalence classes (ECs), which determine the transcripts that any given read is compatible with. [44] In the ovary, transcript abundances of fshr and lhr gradually increased during previtellogenic follicle growth, but markedly and significantly increased thereafter. [45] While genetic effects on transcript abundances were generally transmitted to the protein level, we found a significant uncoupling of the transcript-protein relationship for certain protein classes, such as subunits of protein complexes. [46]장기간 열 스트레스 하에서 플라본 및 플라보놀 생합성의 상향 조절에 대한 대사 산물 및 전사체 풍부도는 밀접한 상관 관계가 있었습니다. [1] 알려진 음이온 수송체의 전사체 풍부도가 결정되었고 추정되는 B 수송체 패밀리가 Cl-배제 표현형과 연관되었다. [2] 환자 그룹 간의 임상 매개변수를 비교하고 여러 생물정보학 도구를 사용하여 전사체 풍부와 세포 구성의 차이를 평가했습니다. [3] 미래의 산성화된 해양 조건에서 안티포터의 전사체 풍부도가 야간(높음)과 낮(낮음) 사이에 >10배 변화하는 극적인 진동은 T. [4] TRIM66, HP1γ, AR, c-Myc 및 GAPDH의 전사체 풍부도 및 단백질 발현을 결정하기 위해 실시간 중합효소 연쇄 반응 및 웨스턴 블로팅을 수행했습니다. [5] 반면에 CuNP 처리에서는 부착 접합부를 제외한 세포 접합 조성물의 전사체 풍부도가 상향 조절되었다. [6] glial 세포가 신경 성숙을 촉진하는 방법을 이해하기 위해 우리는 glial 세포의 전사체 풍부와 뉴런의 유전자 발현의 연관성을 연구했습니다. [7] 그러나 긴 단백질 반감기는 이러한 전사체 풍부함의 진동을 약화시키고 추정 기능은 파악하기 어려운 상태로 남아 있습니다. [8] 질소 시비율은 농경기나 풀 종보다 디아조영양체 개체군 크기 및 활동(nifH 유전자 및 전사체 풍부도로 결정됨) 및 군집 구성(nifH 유전자 앰플리콘 시퀀싱으로 결정됨)에 더 강한 영향을 미쳤습니다. [9] 우리는 전체 transcriptome 시퀀싱을 수행하고 각 유전자 편집 유전자형과 관련된 전사체 풍부(전사 틈새)의 성적 이형 변화를 평가했습니다. [10] 그러나 이러한 세포 혼합물 샘플의 전사체 풍부도(TA)는 구성 요소 백혈구 하위 집단의 비율에 의해 혼동됩니다. [11] 예외는 다른 시간에 전사체 풍부가 피크를 갖는 LOV-도메인 전사 인자와 하루 종일 전사되는 추정 광주성 광수용체입니다. [12] OsABI5를 조절하는 유전자의 전사체 풍부, e. [13] 생성된 환경 진핵 생물 분류학적 빈의 완전성이 평가되었고, 48개의 속이 전사체 풍부도의 디엘 패턴에 대해 추가로 평가되었습니다. [14] RNase P 돌연변이체의 전사체 풍부도의 변화는 또한 반감기의 변화와 상관관계가 있었습니다. [15] 0)은 843개의 개별 샘플을 포함하는 22개의 RNA-seq 실험에서 유전자 및 전사체 풍부함을 정량화하는 데 사용되었습니다. [16] Luria-Bertani(LB) 브로스에서 후기 지수기까지 성장한 각 혈청형의 대표 균주에서 추출한 RNA는 핵심 유전자의 전사체 풍부도가 유의하게 더 높은 것으로 나타났습니다(p<0. [17] RA 및 RAn은 각각 유전자 풍부도보다는 amoA 및 hzsB 유전자의 전사체 풍부도와 양의 상관관계가 있었다. [18] 연장된 밤 동안 절제된 꽃차례의 전사체 풍부도 분석은 설탕 기아, 노화, SL 생합성 및 신호 전달 사이의 복잡한 관계를 시사했습니다. [19] 리그노셀룰로스 분해 효소 유전자의 전사체 풍부함의 측정은 다수의 α-1-아라비노푸라노시다제 유전자의 상당한 상향 조절 및 그 모체에 비해 조작된 균주에서 일부 셀룰로스 분해 및 자일라놀 분해 효소 유전자의 하향 조절을 나타낸다. [20] 이동, 염분 및 가뭄 스트레스는 BnaPHT1의 전사체 풍부함과 옥신 및 사이토키닌을 포함한 식물 호르몬을 조절할 수 있습니다. [21] qPCR 분석은 DkZF1/4의 전사체 풍부가 1일째에 AHCA 처리(1% O2 및 95% CO2) 동안, 1일 및 2일 모두에서 DkZF2/5, 2일째에 DkZF3에서 유의하게 상향조절되었음을 나타내었다. [22]