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Characterising the human epitranscriptome using catalysis-dependent RIP-Seq approaches

Characterising the human epitranscriptome using catalysis-dependent RIP-Seq approaches
使用催化依赖性 RIP-Seq 方法表征人类表观转录组
批准号:
BB/N000749/1
负责人:
Shobbir Hussain
金额:
$42.83万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2016
资助国家:
英国
项目状态:
已结题
起止时间:
2016 至 --

项目摘要

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中文摘要
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英文摘要
It has for decades been known that the building blocks, known as bases, within DNA and RNA molecules can be chemically modified. In DNA, the occurrence and biological function of such modifications has been a fundamentally important area of biosciences research with far-reaching impact. In stark contrast, the progress for research into RNA modifications has been very disappointing which is especially unfortunate as these modifications are actually known to be more prevalent and chemically complex than in DNA; and many of the enzymes that catalyse the RNA modifications have been linked with human disease, suggesting important biological roles. The primary reason for this slow progress has been due to the fact that similar detailed studies of RNA modifications have been technically very difficult. However in recent years, major advances in DNA/RNA sequencing techniques have been made that has allowed RNA modifications to be identified in the detail required to elucidate biological function. The first such studies were described in 2012 and indeed we are just now beginning to realise the potential scope offered by such investigations in biosciences research. The research field is however still in its very early stages and a massive concerted effort is required between laboratories in order to provide detailed maps of these RNA modifications, with preferably information regarding which cellular enzymes catalyse the modifications. The studies proposed here will provide major contributions to the field in this regard.
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会议论文
Robust long-read native DNA sequencing using the ONT CsgG Nanopore system
使用 ONT CsgG Nanopore 系统进行稳健的长读长天然 DNA 测序
DOI: 10.12688/wellcomeopenres.11246.2
发表时间: 2017
期刊: Wellcome Open Research
影响因子: --
作者: [Carter J]
通讯作者: Carter J
DOI: 10.12688/wellcomeopenres.11246.3
发表时间: 2017-04-06
期刊: Wellcome open research
影响因子: --
作者: [Carter JM, Hussain S]
通讯作者: Hussain S
DOI: 10.1093/nar/gkaa1193
发表时间: 2021-01-25
期刊: Nucleic acids research
影响因子: 14.9
作者: [Selmi T, Hussain S, Dietmann S, Heiß M, Borland K, Flad S, Carter JM, Dennison R, Huang YL, Kellner S, Bornelöv S, Frye M]
通讯作者: Frye M
Shaping and Reshaping Transcriptome Plasticity during Evolution.
进化过程中转录组可塑性的塑造和重塑。
DOI: 10.1016/j.tibs.2017.06.009
发表时间: 2017
期刊: Trends in biochemical sciences
影响因子: 13.8
作者: [Hussain S]
通讯作者: Hussain S
Long-read Nanopore sequencing to identify isoform-specific patterns of mRNA methylation
  • 批准号:
    BB/R006431/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $15.51万
  • 财政年份:
    2018
  • 负责人:
    Shobbir Hussain
  • 依托单位:
国内基金
海外基金
靶向Human ZAG蛋白的降糖小分子化合物筛选以及疗效观察
  • 批准号:
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2025
  • 负责人:
    胡文静
  • 依托单位:
新型小分子蛋白—人肝细胞生长因子三环域(hHGFK1)抑制破骨细胞及治疗小鼠骨质疏松的疗效评估与机制研究
  • 批准号:
    82370885
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    姚晨
  • 依托单位:
自闭症相关基因CHD8在非人灵长类大脑发育中的作用
HBV S-Human ESPL1融合基因在慢性乙型肝炎发病进程中的分子机制研究
  • 批准号:
    81960115
  • 项目类别:
    地区科学基金项目
  • 资助金额:
    34.0万元
  • 批准年份:
    2019
  • 负责人:
    江建宁
  • 依托单位: