Chromosome Inactivation

Chromosome inactivation is a process by which a cell prevents the expression of certain genes within one of its two copies of a chromosome. This process, which is typically found in female mammals, is essential for preserving the correct amount of proteins produced from the two copies of a particular chromosome. It is also essential for maintaining genetic balance or homeostasis during the early stages of embryonic development. As a result, this process serves a key role in the effective functioning of mammalian cells. Chromosome inactivation also has implications for stem cell research, cancer research, and gene therapy research.

← Journal of Chromosomes

Related Articles

7 article(s) found

Skeletal Muscle Calcium Channel Mutation R528G: Enhanced Channel Inactivation and Omega-Current at Hyperpolarization Contribute to Hypokalemic Periodic Paralysis.

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Pericentric Inversion in Chromosome 10 in a Girl, Inherited from a Phenotypically Normal Mother: Case Report and Literature Review

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Humans Chromosome 1 Fractal Periods Signature is Highly Correlated with Intelligence and Brain Evolution

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Intriguing Humans and Primates chromosomes 4

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An Inherited Balanced Translocation Between Chromosomes 4 and 6 in Recurrent Pregnancy Loss: A Case Report

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A Patient with Monoclonal Gammopathy of Undetermined Significance and Detected Philadelphia Chromosome

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The Chromosomes of Dictyostelium Giganteum

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