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  2. Human mitochondrial genetics - Wikipedia

    en.wikipedia.org/wiki/Human_mitochondrial_genetics

    the mitochondria within the fertilized oocyte is what the new life will have to begin with (in terms of mtDNA), the number of affected mitochondria varies from cell (in this case, the fertilized oocyte) to cell depending both on the number it inherited from its mother cell and environmental factors which may favor mutant or wildtype ...

  3. Paternal mtDNA transmission - Wikipedia

    en.wikipedia.org/wiki/Paternal_mtDNA_transmission

    In genetics, paternal mtDNA transmission and paternal mtDNA inheritance refer to the incidence of mitochondrial DNA (mtDNA) being passed from a father to his offspring. . Paternal mtDNA inheritance is observed in a small proportion of species; in general, mtDNA is passed unchanged from a mother to her offspring, [1] making it an example of non-Mendelian inh

  4. Extranuclear inheritance - Wikipedia

    en.wikipedia.org/wiki/Extranuclear_inheritance

    Uniparental inheritance occurs in extranuclear genes when only one parent contributes organellar DNA to the offspring. A classic example of uniparental gene transmission is the maternal inheritance of human mitochondria. The mother's mitochondria are transmitted to the offspring at fertilization via the egg. The father's mitochondrial genes are ...

  5. Mitochondrial DNA - Wikipedia

    en.wikipedia.org/wiki/Mitochondrial_DNA

    Mitochondrial DNA is the small circular chromosome found inside mitochondria. These organelles, found in all eukaryotic cells, are the powerhouse of the cell. [1] The mitochondria, and thus mitochondrial DNA, are passed exclusively from mother to offspring through the egg cell.

  6. Genetic genealogy - Wikipedia

    en.wikipedia.org/wiki/Genetic_genealogy

    DNA comparison may offer an alternative means of confirming family relationships of biological parents, but may be confused by adoption or when a mother conceals the identity of the father of her child. [49] While mitochondrial and Y-chromosome DNA matching offer the most definitive confirmation of ancestral relationships, the information from ...

  7. Heteroplasmy - Wikipedia

    en.wikipedia.org/wiki/Heteroplasmy

    Symptoms of severe heteroplasmic mitochondrial disorders do not usually appear until adulthood. Many cell divisions and a great deal of time are required for a cell to accumulate enough mutant mitochondria to cause symptoms. An example of this phenomenon is Leber optic atrophy. Generally, individuals with this condition do not experience vision ...

  8. Homoplasmy - Wikipedia

    en.wikipedia.org/wiki/Homoplasmy

    In almost every species, mitochondrial DNA is maternally inherited. [2] This means that all of the offspring of a female will have identical and homoplasmic mitochondrial DNA. It is very rare for females to pass on heteroplasmic or homoplasmic mutations because of the genetic bottleneck, where only a few out of many mitochondria actually are ...

  9. Genetic disorder - Wikipedia

    en.wikipedia.org/wiki/Genetic_disorder

    This type of inheritance, also known as maternal inheritance, is the rarest and applies to the 13 genes encoded by mitochondrial DNA. Because only egg cells contribute mitochondria to the developing embryo, only mothers (who are affected) can pass on mitochondrial DNA conditions to their children.