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相关概念视频

Nondisjunction01:29

Nondisjunction

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During meiosis, chromosomes occasionally separate improperly. This occurs due to failure of homologous chromosome separation during meiosis I or failed sister chromatid separation during meiosis II. In some species, notably plants, nondisjunction can result in an organism with an entire additional set of chromosomes, which is called polyploidy. In humans, nondisjunction can occur during male or female gametogenesis and the resulting gametes possess one too many or one too few chromosomes.
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Karyotyping

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Overview
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Mismatch Repair01:20

Mismatch Repair

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Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
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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...
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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...
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Meiosis I01:49

Meiosis I

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Meiosis is a carefully orchestrated set of cell divisions, the goal of which—in humans—is to produce haploid sperm or eggs, each containing half the number of chromosomes present in somatic cells elsewhere in the body. Meiosis I is the first such division, and involves several key steps, among them: condensation of replicated chromosomes in diploid cells; the pairing of homologous chromosomes and their exchange of information; and finally, the separation of homologous chromosomes by...
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相关实验视频

Updated: Jul 5, 2025

Interphase Fluorescence in situ Hybridization of Bone Marrow Smears of Multiple Myeloma
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Interphase Fluorescence in situ Hybridization of Bone Marrow Smears of Multiple Myeloma

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多发性骨髓瘤中的染色体缺陷

Sarah E Clarke1, Kathryn A Fuller2, Wendy N Erber3

  • 1School of Biomedical Sciences, The University of Western Australia (M504), Crawley, WA 6009, Australia; Department of Haematology, PathWest Laboratory Medicine WA, Fiona Stanley Hospital, Murdoch, WA 6150, Australia.

Blood reviews
|January 11, 2024
PubMed
概括

多发性骨髓瘤涉及染色体异常,对预后至关重要. 目前的测试如FISH和SNP-array在检测低级克隆方面存在局限性,需要先进的方法来进行准确的评估.

关键词:
染色体是一种染色体.细胞遗传学 细胞遗传学光在现场混合化中的光.多发性骨髓瘤是一种多发性骨髓瘤.

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Chromosome Preparation From Cultured Cells
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Last Updated: Jul 5, 2025

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科学领域:

  • 血液学 血液学 血液学
  • 在瘤学瘤学.
  • 遗传学 遗传学 是一个

背景情况:

  • 多发性骨髓瘤是一种由特定染色体事件驱动的血细胞癌症.
  • 检测这些异常对于患者的预后和治疗选择至关重要.

研究的目的:

  • 审查多发性骨髓瘤中初级和二级细胞遗传异常.
  • 讨论当前和新兴的技术进行评估.

主要方法:

  • 对多发性骨髓瘤中细胞遗传检测现有文献的综述.
  • 讨论相间光在位杂交 (FISH),SNP阵列和下一代测序 (NGS).

主要成果:

  • FISH和SNP-array是标准的,但对低级克隆的敏感性有限.
  • 新型海水系统和新型FISH技术显示出改善检测和监测的前景.

结论:

  • 精确检测染色体异常对于管理多发性骨髓瘤至关重要.
  • 分子技术的进步正在改善诊断灵敏度和治疗指导.