Tìm thấy 20+ kết quả cho từ khóa "Long non-coding RNAs"
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Genome-wide identification of long non-coding RNA genes and their association with insecticide resistance and metamorphosis in diamondback moth, Plutella xylostella. Genome-wide identification of long non-coding RNAs and their regulatory networks involved in Apis mellifera ligustica response to Nosema ceranae infection. Unique features of long non-coding RNA biogenesis and function. On the classification of long non-coding RNAs.
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Genome-wide identification and functional prediction of long non-coding RNAs involved in the heat stress response in Metarhizium robertsii. Characteristics of long non-coding RNAs in the Brown Norway rat and alterations in the Dahl salt-sensitive rat. Non-coding RNAs turn up the heat: an emerging layer of novel regulators in the mammalian heat shock response. Immobilization of proteins in the nucleolus by ribosomal intergenic spacer noncoding RNA.
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Systematic Identification and Characterization of Long Non-Coding RNAs in the Silkworm, Bombyx mori. BmncRNAdb: a comprehensive database of non-coding RNAs in the silkworm, Bombyx mori. Identification and comparison of long non-coding RNAs in the silk gland between domestic and wild silkworms. An antisense lncRNA functions in alternative splicing of Bmdsx in the silkworm, Bombyx mori.
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Transcriptome-wide N6-methyladenosine modification profiling of long non-coding RNAs during replication of Marek ’ s disease virus in vitro. Long non-coding RNAs (lncRNAs) participate in Marek ’ s disease virus (MDV) replication but how m 6 A modifications in lncRNAs are affected during MDV infection is currently unknown. We report for the first time profiling of the alterations in transcriptome-wide m 6 A modification in lncRNAs of MDV-infected CEF cells..
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Genome-wide analysis of long non-coding RNAs affecting roots development at an early stage in the rice response to cadmium stress.. Long Non-Coding RNAs Responsive to Salt and Boron Stress in the Hyper-Arid Lluteno Maize from Atacama Desert. Research on plant abiotic stress responses in the post-genome era: past, present and future. Novel signals in the regulation of Pi starvation responses in plants: facts and promises.
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Long non-coding RNAs responsive to salt and boron stress in the hyper-arid Lluteno maize from Atacama Desert. Wang A, Hu J, Gao C, et al. Genome-wide analysis of long non-coding RNAs unveils the regulatory roles in the heat tolerance of Chinese cabbage (Brassica rapa ssp. Qin T, Zhao H, Cui P, et al. Swiezewski S, Liu F, Magusin A, et al. Wang Z, Zhai X, Cao Y, et al. Cui J, Luan Y, Jiang N, et al. Cui J, Jiang N, Meng J, et al. Zhang L, Wang M, Li N, et al. Xin M, Wang Y, Yao Y, et al.
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Of the 95,523 assembled tran- scripts, CPC2 annotation identified 31,967 non-coding transcripts (CPC2 score <. Additional file 1: Fig. of the total . Most (61%, or 9341 of 15,312) TE- lncRNAs showed similarity to TEs over ≥90% of their length (Fig. Hereafter we refer to lncRNAs with se- quence similarity to TEs as “TE-lncRNAs”.. We further investigated the superfamily of TEs that were similar to the 15,312 TE-lncRNAs.
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Differentially expressed non-coding RNAs induced by transmissible gastroenteritis virus potentially regulate inflammation and NF-kappaB pathway in porcine intestinal epithelial cell line. BMC Genomics. BMC Genomics Page 13 of 13
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Analyses of histological and transcriptome differences in the skin of short-hair and long- hair rabbits. Inhibition of bmp signaling affects growth and differentiation in the anagen hair follicle. Notch signaling in bulge stem cells is not required for selection of hair follicle fate. The secret life of the hair follicle. Integrated analysis of coding genes and non-coding RNAs during hair follicle cycle of cashmere goat ( Capra hircus.
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Systematic Analysis of Non-coding RNAs Involved in the Angora Rabbit (Oryctolagus cuniculus) Hair Follicle Cycle by RNA Sequencing. The seasonal development dynamics of the yak hair cycle transcriptome. Systematic analysis of long noncoding RNAs in the senescence-accelerated mouse prone 8 brain using RNA sequencing. Comparative expression dynamics of Intergenic long noncoding RNAs in the genus drosophila. Whales originated from aquatic artiodactyls in the Eocene epoch of India
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Molecular Functions of Long Non-Coding RNAs in Plants. Joung J, Engreitz JM, Konermann S, Abudayyeh OO, Verdine VK, Aguet F, Gootenberg JS, Sanjana NE, Wright JB, Fulco CP, et al. Long Non-Coding RNAs Responsive to Salt and Boron Stress in the Hyper-Arid Lluteno Maize from Atacama Desert. Zhao T, Tao X, Feng S, Wang L, Hong H, Ma W, Shang G, Guo S, He Y, Zhou B, et al. Hu Y, Chen J, Fang L, Zhang Z, Ma W, Niu Y, Ju L, Deng J, Zhao T, Lian J, et al.
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Transcriptome sequencing to detect the potential role of long non-coding RNAs in bovine mammary gland during the dry and lactation period. Systematic analysis of Long non-coding RNAs and mRNAs in the ovaries of Duroc pigs during different follicular stages using RNA sequencing. Systematic identification and characterization of Long non-coding RNAs in the silkworm, Bombyx mori
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Of the 40 lncRNA contigs for which a high-confidence ortholog gene could be identified, the ortholog annota- tions included 16 long noncoding RNA genes, 12 non- coding antisense RNAs, ten noncoding isoforms of protein-coding genes, and two sense-overlapping RNAs (Table 3).
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However, by fractionating nuclei using a high urea buffer contain- ing salts and detergent, RNAs that are tightly bound to chromatin can be separated from RNAs that are soluble in the nucleoplasm, enabling the characterization of several thousand lncRNAs enriched in the insoluble chromatin fraction, as im- plemented in human cell lines and mouse macro- phages [30, 31]..
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The datasets also reveal a rich network of long non-coding RNAs expressed in the de- veloping Mullerian duct. Duct formation commences in the chicken between embryonic day (E) 4.0–4.5 (Hamburger and Hamilton stage . At this stage, Müllerian progenitors are specified in the coel- omic epithelium and undergo invagination at the anter- ior pole of the mesonephric kidney (Fig.
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The expression of non-coding RNAs (ncRNAs) in cells is closely related to the stage of virus infection [13]. RNA libraries establishment and lncRNA identification Total RNA was extracted from 36 h post-infected HD11 cells (Exp 1, 2, and 3) and mock-infected cells (CK 1, 2, and 3). 1 Indirect immunofluorescence assay (IFA) of HD11 cells infected by IBV.
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A nucleus-localized long non- coding RNA enhances drought and salt stress tolerance. Identification of Gossypium hirsutum long non-coding RNAs (lncRNAs) under salt stress. Identification and characterization of long non-coding RNAs involved in osmotic and salt stress in Medicago truncatula using genome-wide high-throughput sequencing. plants under salt stress. Potential of duckweed (Lemna minor) for removal of nitrogen and phosphorus from water under salt stress.
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Exon-intron circular RNAs regulate transcription in the nucleus. Identification of long non-coding RNAs in the immature and mature rat anterior pituitary. Effects of a controlled heat stress during late gestation, lactation, and after weaning on thermoregulation, metabolism, and reproduction of primiparous sows. Integrating miRNA and mRNA expression profiles in response to heat stress- induced injury in rat small intestine.
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Lncatlas database for subcellular localization of long noncoding rnas.. The lncLocator: a subcellular localization predictor for long non-coding RNAs based on a stacked ensemble classifier. https://doi.org/. Prediction of microrna subcellular localization by using a sequence-to-sequence model.
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Regulation of spermatogenesis by small non-coding RNAs: role of the germ granule. A 5 ′ UTR-overlapping LncRNA activates the male- determining gene doublesex1 in the crustacean Daphnia magna. Long non-coding RNAs potentially function synergistically in the cellular reprogramming of SCNT embryos. Crosstalk among lncRNAs, microRNAs and mRNAs in the muscle 'degradome' of rainbow trout. Transcription of CYP19A1 is directly regulated by SF-1 in the theca cells of ovary follicles in chicken