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Karyotyping01:17

Karyotyping

69.4K
Overview
69.4K
Meiosis I01:49

Meiosis I

220.9K
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...
220.9K
The Retinoblastoma Gene01:20

The Retinoblastoma Gene

4.9K
Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
4.9K
Nondisjunction01:29

Nondisjunction

82.9K
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.
82.9K
Nondisjunction01:21

Nondisjunction

5.4K
Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate correctly and move to the opposite poles of the cells. This produces daughter cells with abnormal chromosome numbers.  Nondisjunction is common during anaphase I or anaphase II of meiosis.  Mutations in synaptonemal complex proteins that attach homologous chromosomes increase the chances of nondisjunction in anaphase I of meiosis I. In contrast, mutations in topoisomerases and condensins that hold...
5.4K
Alternative RNA Splicing02:18

Alternative RNA Splicing

25.5K
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...
25.5K

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相关实验视频

Updated: Mar 7, 2026

FISH for Pre-implantation Genetic Diagnosis
07:34

FISH for Pre-implantation Genetic Diagnosis

Published on: February 23, 2011

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家庭罗伯逊转位,rob(14;21),患唐氏综合征的风险很高.

Anna Rajab, Heidemarie Neitzel, Jenny Jalali

    Cytogenetic and genome research
    |March 5, 2026
    PubMed
    概括

    这项研究揭示了罗伯茨的14·21转位家族中中性重组的一个不寻常的模式,导致转位三位症21后代的高率. 在第一个介质分裂期间发生了非分裂,观察到明显的交叉模式.

    科学领域:

    • 遗传学 是一个遗传学.
    • 人类遗传学 人类遗传学
    • 生殖遗传学 生殖遗传学

    背景情况:

    • 罗伯茨的转位是常见的染色体重排.
    • 女携带罗伯逊14·21转位的女性携带者有患三发症21后代的风险较高.
    • 了解转位遗传背后的机制对于遗传咨询至关重要.

    研究的目的:

    • 在一个庞大的阿曼家庭中调查异常高的转位三位症21发病率的遗传基础.
    • 分析具有罗伯逊14·21转位的个体中介性重组模式.
    • 识别可能导致非离合事件的潜在遗传变异.

    主要方法:

    • 对14号和21号染色体进行微卫星标记分析,以研究介质性重组.
    • 载体母体的全基因组测序 (WGS).
    • 与一个表现为自由三发症21的家庭进行比较分析.

    主要成果:

    • 核心家庭中21型三位症转移后代的风险显著增加.
    • 在所有受影响的病例中,在第一个介质分裂 (MI) 期间发生了非离合.
    • 在21号染色体上观察到不寻常的交叉模式,包括双重交叉,与自由三症21例不同.
    • WGS没有识别出与介质功能障碍相关的已知致病变体.

    更多相关视频

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    Generation of Induced Pluripotent Stem Cells from Turner Syndrome 45XO Fetal Cells for Downstream Modelling of Neurological Deficits Associated with the Syndrome

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    In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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    In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila

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    相关实验视频

    Last Updated: Mar 7, 2026

    FISH for Pre-implantation Genetic Diagnosis
    07:34

    FISH for Pre-implantation Genetic Diagnosis

    Published on: February 23, 2011

    38.0K
    Generation of Induced Pluripotent Stem Cells from Turner Syndrome 45XO Fetal Cells for Downstream Modelling of Neurological Deficits Associated with the Syndrome
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    Generation of Induced Pluripotent Stem Cells from Turner Syndrome 45XO Fetal Cells for Downstream Modelling of Neurological Deficits Associated with the Syndrome

    Published on: December 4, 2021

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    In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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    In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila

    Published on: August 20, 2019

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    结论:

    • 该研究报告了染色体传播比率扭曲的一个新例.
    • 在转位染色体和自由染色体21之间观察到一种非典型的介质重组模式.
    • 需要进一步的研究来阐明这种现象背后的确切机制.