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相关概念视频

What is Genetic Engineering?00:49

What is Genetic Engineering?

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Overview
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CRISPR01:59

CRISPR

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Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced...
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Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

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Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
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Gene Therapy00:59

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Gene therapy is a technique where a gene is inserted into a person’s cells to prevent or treat a serious disease. The added gene may be a healthy version of the gene that is mutated in the patient, or it could be a different gene that inactivates or compensates for the patient’s disease-causing gene. For example, in patients with severe combined immunodeficiency (SCID) due to a mutation in the gene for the enzyme adenosine deaminase, a functioning version of the gene can be...
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In-vitro Mutagenesis01:16

In-vitro Mutagenesis

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To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.
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Homologous Recombination02:31

Homologous Recombination

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The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
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相关实验视频

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Establishment of Genome-edited Human Pluripotent Stem Cell Lines: From Targeting to Isolation
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第三代新技术用于基因编辑.

Pushpendra K Gupta1, Sourabh Kumar1

  • 1Department of Genetics and Plant Breeding, Chaudhary Charan Singh University, Meerut, India.

Trends in biotechnology
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概括
此摘要是机器生成的。

第三代基因编辑技术如seekRNA和bridgeRNA克服了CRISPR-Cas系统的局限性. 这些先进的工具解决了诸如protospacer相邻动图要求和双链断裂等问题,以改进基因编辑应用.

关键词:
这里是CAST CAST.克里斯普尔是什么意思?克里斯普尔是什么意思?这就是Cas3的情况.欧米茄 欧米茄 欧米茄 是一个.一个过时的过去.在过去,过去.基因编辑 基因编辑在searchRNA/bridgeRNA中找到

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科学领域:

  • 生物技术是生物技术.
  • 分子生物学分子生物学
  • 基因组学就是基因组学.

背景情况:

  • 克里斯普尔-卡斯系统被广泛用于作物和治疗中的基因编辑.
  • 现有的CRISPR-Cas方法有局限性,包括原空间子相邻动机依赖性和双链断裂生成.

研究的目的:

  • 审查第三代基因编辑技术.
  • 为了突出超越CRISPR-Cas,基础编辑器和主要编辑器的进步.

主要方法:

  • 关于基因编辑技术的科学文献的审查.
  • 专注于搜索RNA和桥梁RNA系统.

主要成果:

  • 第二代编辑 (基础编辑和主要编辑) 部分解决了CRISPR-Cas的局限性.
  • 第三代技术为基因编辑的剩余挑战提供了解决方案.

结论:

  • seekRNA和bridgeRNA代表了基因编辑的重大进展.
  • 这些新技术有望克服当前的基因编辑障碍.