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相关概念视频

RNA Splicing01:32

RNA Splicing

56.5K
Splicing is the process by which eukaryotic RNA is edited before its translation into protein. The RNA strand transcribed from eukaryotic DNA is called the primary transcript. The primary transcripts that become mRNAs are called precursor messenger RNAs (pre-mRNAs). Eukaryotic pre-mRNA contains alternating sequences of exons and introns. Exons are nucleotide sequences that code for proteins, whereas introns are the non-coding regions. In RNA splicing, introns are removed and exons are bonded...
56.5K
Alternative RNA Splicing02:18

Alternative RNA Splicing

21.2K
Alternative RNA splicing is the regulated splicing of exons and introns to produce different mature mRNAs from a single pre-mRNA. Unlike in constitutive splicing where a single gene produces a single type of mRNA, alternative splicing allows an organism to produce multiple proteins from a single gene and plays an important role in protein diversity.
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...
21.2K
Cancers Originate from Somatic Mutations in a Single Cell02:21

Cancers Originate from Somatic Mutations in a Single Cell

12.0K
Cancer arises from mutations in the critical genes that allow healthy cells to escape cell cycle regulation and acquire the ability to proliferate indefinitely. Though originating from a single mutation event in one of the originator cells, cancer progresses when the mutant cell lines continue to gain more and more mutations, and finally, become malignant. For example, chronic myelogenous leukemia (CML) develops initially as a non-lethal increase in white blood cells, which progressively...
12.0K
Abnormal Proliferation02:23

Abnormal Proliferation

4.6K
Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the...
4.6K
Translation01:31

Translation

14.9K
Translation is the process of synthesizing proteins from the genetic information carried by messenger RNA (mRNA). Following transcription, it constitutes the final step in the expression of genes. This process is carried out by ribosomes, complexes of protein and specialized RNA molecules. Ribosomes, transfer RNA (tRNA), and other proteins produce a chain of amino acids—the polypeptide—as the end product of translation.
Translation Produces the Building Blocks of Life
Proteins are...
14.9K
Pre-mRNA Processing: RNA Splicing01:36

Pre-mRNA Processing: RNA Splicing

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相关实验视频

Updated: Jul 15, 2025

Detection of Alternative Splicing During Epithelial-Mesenchymal Transition
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Detection of Alternative Splicing During Epithelial-Mesenchymal Transition

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[由异常拼接驱动的血液恶性瘤]

Weijia Zang1,2, Wataru Saika1,3, Yumi Aoyama1,2

  • 1Department of Hematology-Oncology, Institute of Biomedical Research and Innovation, Foundation for Biomedical Research and Innovation at Kobe.

[Rinsho ketsueki] The Japanese journal of clinical hematology
|October 4, 2023
PubMed
概括

RNA拼接对于基因表达至关重要,但它的调节失调会导致血癌,如骨髓质疏松综合征和急性骨髓性白血病. 本综述探讨了癌症和潜在疗法中的拼接因子突变.

科学领域:

  • 分子生物学分子生物学
  • 遗传学 遗传学 是一个
关键词:
较小的内子在mRNA前拼接.在SF3B1中.这就是ZRSR2的原因.

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Engineering Artificial Factors to Specifically Manipulate Alternative Splicing in Human Cells
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Engineering Artificial Factors to Specifically Manipulate Alternative Splicing in Human Cells

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Using RNA-sequencing to Detect Novel Splice Variants Related to Drug Resistance in In Vitro Cancer Models
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相关实验视频

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Using RNA-sequencing to Detect Novel Splice Variants Related to Drug Resistance in In Vitro Cancer Models
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  • 在瘤学瘤学.
  • 背景情况:

    • RNA剪接对于将前mRNA转化为成熟的mRNA至关重要,调节基因表达.
    • 异常RNA拼接与造血性恶性瘤有关,包括骨髓质疏松症候群 (MDS) 和急性骨髓性白血病 (AML).
    • 拼接因子突变越来越多地被认为是这些血液癌症的驱动因素.

    结论:

    • 剪接因子突变是MDS和AML病变发生的关键驱动因素.
    • 对异常拼接机制的进一步研究可以揭示新的治疗点.
    • 基于机制的治疗策略对治疗拼接驱动的血液恶性瘤具有前景.