Micronuclei, Chromosome-Defective

MeSH 搜索器

Micronuclei, Chromosome-Defective

Defective nuclei produced during the TELOPHASE of MITOSIS or MEIOSIS by lagging CHROMOSOMES or chromosome fragments derived from spontaneous or experimentally induced chromosomal structural changes.

推出的年份: 2005

副标题

chemically induced

classification

drug effects

embryology

radiation effects

statistics and numerical data

veterinary

树号: A11.284.430.106.570, A11.284.430.214.190.875.117.570, C23.550.210.570, G05.365.590.175.570

MeSH 单一 ID: D048629

进入的组:

Chromosome-Defective Micronucleus
Micronuclei, Chromosome Defective
Micronucleus, Chromosome-Defective
Micronucleus, Chromosome Defective
Chromosome-Defective Micronuclei
Chromosome Defective Micronuclei
Micronuclei, Genotoxicant-Induced
Genotoxicant-Induced Micronucleus
Micronuclei, Genotoxicant Induced
Micronucleus, Genotoxicant-Induced
Genotoxicant-Induced Micronuclei
Genotoxicant Induced Micronuclei

All MeSH Categories
- Anatomy Category
  - Cells [A11]
    - Cellular Structures [A11.284]
      - Intracellular Space [A11.284.430]
        
        Cell Nucleus [A11.284.430.106]
        
        Cell Nucleus Structures [A11.284.430.106.279] add_circle
        
        Macronucleus [A11.284.430.106.550]
        
        Micronuclei, Chromosome-Defective [A11.284.430.106.570]
        
        Micronucleus, Germline [A11.284.430.106.575]

All MeSH Categories
- Anatomy Category
  - Cells [A11]
    - Cellular Structures [A11.284]
      - Intracellular Space [A11.284.430]
        
        Cytoplasm [A11.284.430.214]
        
        Cytoplasmic Structures [A11.284.430.214.190]
        
        Organelles [A11.284.430.214.190.875]
        
        Cell Nucleus [A11.284.430.214.190.875.117]
        
        Macronucleus [A11.284.430.214.190.875.117.550]
        
        Micronuclei, Chromosome-Defective [A11.284.430.214.190.875.117.570]
        
        Micronucleus, Germline [A11.284.430.214.190.875.117.575]

All MeSH Categories
- Diseases Category
  - Pathological Conditions, Signs and Symptoms [C23]
    - Pathologic Processes [C23.550]
      - Chromosome Aberrations [C23.550.210]

All MeSH Categories
- Phenomena and Processes
  - Genetic Phenomena [G05]
    - Genetic Variation [G05.365]
      - Mutation [G05.365.590]
        
        Chromosome Aberrations [G05.365.590.175]
        
        Abnormal Karyotype [G05.365.590.175.024] add_circle
        
        Aneuploidy [G05.365.590.175.050] add_circle
        
        Chimerism [G05.365.590.175.125]
        
        Chromosomal Instability [G05.365.590.175.165] add_circle
        
        Chromosome Breakage [G05.365.590.175.175]
        
        Chromosome Duplication [G05.365.590.175.183] add_circle
        
        Chromosome Inversion [G05.365.590.175.190]
        
        Chromothripsis [G05.365.590.175.310]
        
        Isochromosomes [G05.365.590.175.430]
        
        Micronuclei, Chromosome-Defective [G05.365.590.175.570]
        
        Mosaicism [G05.365.590.175.595]
        
        Polyploidy [G05.365.590.175.677] add_circle
        
        Ring Chromosomes [G05.365.590.175.760]
        
        Sex Chromosome Aberrations [G05.365.590.175.815] add_circle
        
        Translocation, Genetic [G05.365.590.175.870] add_circle
        
        Uniparental Disomy [G05.365.590.175.935]

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MeSH 搜索器

Micronuclei, Chromosome-Defective

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