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相关概念视频

Epigenetic Regulation01:37

Epigenetic Regulation

3.0K
Epigenetic changes alter the physical structure of the DNA without changing the genetic sequence and often regulate whether genes are turned on or off. This regulation ensures that each cell produces only proteins necessary for its function. For example, proteins that promote bone growth are not produced in muscle cells. Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
X-chromosome...
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Genomic Imprinting and Inheritance02:30

Genomic Imprinting and Inheritance

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Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
34.3K
Nucleosome Remodeling02:54

Nucleosome Remodeling

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Nucleosomes are the basic units of chromatin compaction. Each nucleosome consists of the DNA bound tightly around a histone core, which makes the DNA inaccessible to DNA binding proteins such as DNA polymerase and RNA polymerase. Hence, the fundamental problem is to ensure access to DNA when appropriate, despite the compact and protective chromatin structure.
Nucleosome remodeling complex
Eukaryotic cells have specialized enzymes called ATP-dependent nucleosome remodeling enzymes. These enzymes...
9.1K
Histone Modification02:32

Histone Modification

13.2K
The histone proteins have a flexible N-terminal tail extending out from the nucleosome. These histone tails are often subjected to post-translational modifications such as acetylation, methylation, phosphorylation, and ubiquitination. Particular combinations of these modifications form “histone codes” that influence the chromatin folding and tissue-specific gene expression.
Acetylation
The enzyme histone acetyltransferase adds acetyl group to the histones. Another enzyme, histone...
13.2K
Human Genetics01:28

Human Genetics

556
Human genetics provides a profound framework for understanding the interplay between genetic predispositions and human psychology. At the heart of this discipline lies the study of how genes influence physical traits, behaviors, and susceptibility to diseases. Each person carries a unique genetic code that subtly or significantly shapes their psychological and behavioral landscape.
The complex relationship between genetics and psychology is observable through common biological components such...
556
Phase II Reactions: Methylation Reactions01:17

Phase II Reactions: Methylation Reactions

176
Methylation is a phase II biotransformation process involving the attachment of a methyl group to a substrate. Enzymes known as methyltransferases orchestrate this reaction.
The mechanism of methylation unfolds in two stages. The first stage sees a methyltransferase enzyme facilitating the transfer of a methyl group from S-adenosylmethionine (SAM) to the substrate, forming S-adenosylhomocysteine (SAH). The second stage involves further metabolism of SAH into homocysteine, which can be recycled...
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相关实验视频

Updated: Jun 22, 2025

Enhanced Reduced Representation Bisulfite Sequencing for Assessment of DNA Methylation at Base Pair Resolution
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Enhanced Reduced Representation Bisulfite Sequencing for Assessment of DNA Methylation at Base Pair Resolution

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人类疾病中的DNA甲基化.

Samareh Younesian1, Mohammad Hossein Mohammadi1, Ommolbanin Younesian2

  • 1Department of Hematology and Blood Banking, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, 1971653313 Iran.

Heliyon
|June 27, 2024
PubMed
概括

异常的DNA甲基化在疾病发展中至关重要. 了解DNA甲基化提供了新的诊断生物标记物和针对各种人类疾病的量身定制治疗方法.

关键词:
自身免疫性疾病是一种自身免疫性疾病.癌症 癌症 癌症 癌症通过DNA甲基化.代谢障碍 代谢障碍 代谢障碍单一的表观遗传性疾病 单一的表观遗传性疾病

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Continuous Fluorescence-Based Endonuclease-Coupled DNA Methylation Assay to Screen for DNA Methyltransferase Inhibitors
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Continuous Fluorescence-Based Endonuclease-Coupled DNA Methylation Assay to Screen for DNA Methyltransferase Inhibitors

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Methylated DNA Immunoprecipitation
21:24

Methylated DNA Immunoprecipitation

Published on: January 2, 2009

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相关实验视频

Last Updated: Jun 22, 2025

Enhanced Reduced Representation Bisulfite Sequencing for Assessment of DNA Methylation at Base Pair Resolution
13:47

Enhanced Reduced Representation Bisulfite Sequencing for Assessment of DNA Methylation at Base Pair Resolution

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Continuous Fluorescence-Based Endonuclease-Coupled DNA Methylation Assay to Screen for DNA Methyltransferase Inhibitors
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Methylated DNA Immunoprecipitation
21:24

Methylated DNA Immunoprecipitation

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科学领域:

  • 表观遗传学和分子生物学
  • 疾病病原和生物标志物

背景情况:

  • 异常的表观遗传修饰,特别是DNA甲基化,是人类疾病发展和进展的关键驱动因素.
  • DNA甲基化模式越来越被认为是影响细胞功能和疾病状态的关键因素.

研究的目的:

  • 阐明异常DNA甲基化在各种人类疾病的发病和进展中的作用.
  • 审查国际研究中关于疾病中DNA甲基化的原始数据.
  • 探索DNA甲基化作为各种疾病的诊断和预后生物标志物.

主要方法:

  • 对现有文献和原始研究数据的全面审查,重点是疾病中的DNA甲基化.
  • 对研究DNA甲基化在单一性疾病,自身免疫性疾病,代谢障碍,血液性瘤和固体瘤中的研究进行分析.
  • 检查针对DNA甲基化机制的制药方法.

主要成果:

  • 异常的DNA甲基化涉及广泛的人类疾病,包括遗传,自身免疫,代谢和瘤疾病.
  • 研究强调了DNA甲基化模式作为可靠的诊断和预后生物标志物的潜力.
  • DNA甲基化机制为开发新型治疗策略提供了有前途的途径.

结论:

  • 研究DNA甲基化机制为疾病机制提供了深刻的见解.
  • 异常的DNA甲基化作为发现新的诊断和预后生物标志物的宝贵来源.
  • 向DNA甲基化通路可以为患者提供个性化的治疗方法.