Reverse Mutation

Reverse mutation is a term used to describe a genetic change that reverses the effects of an earlier mutation, resulting in a return to the original appearance and function of the gene. This phenomenon is used in genetic studies to understand the role of a certain gene in a given condition. Reverse mutation can also be used to potentially correct genetic diseases caused by other mutation events. When this process is successfully applied, it provides hope to those affected by genetic disorders. Reverse mutation research is ongoing and is becoming an increasingly potent tool in the development of new treatments and cures.

← Journal of Genetic Engineering

Related Articles

19 article(s) found

Branch Retinal Vein Occlusion in Factor V Leiden Mutation

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

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The Identification of Somatic Mutations in Interferon-G Signal Molecules in Human Uterine Leiomyosarcoma

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Recurrent branch retinal arterial occlusions associated with plasminogen activator inhibitor-1 mutation

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Melanoma of the Breast with Smoothened (SMO) Mutation: Case Report and review of the Literature

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A Rare Cause of Fever of Unknown Origin: Reverse Shapiro’s Syndrome

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Docking Studies of HIV-1 Reverse Transcriptase and HIV-1 Protease with Phytocompounds of Carissa Carandas L.

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Transmutation of Sweat Glands - Eccrine Porocarcinoma

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Characterization of rpoB Gene Mutations Associated with Rifampicin Resistance in Multidrug Resistant Tuberculosis Patients Co-infected with HIV from Southern India.

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Genetic-Mathematical Modelling of Mutational Processes in a Population

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Nucleoside and Nucleotide Reverse Transcriptase Inhibitors Induce Aging by Inhibiting Telomerase Function

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An Algorithm to Predict the Possible SARS-CoV-2 Mutations

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A New Gene Mutation of PRKAR1A was found in a Carney Complex Case

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Stem Cell Differentiation Stage Factors (SCDSFs) Taken from Zebrafish Embryo during Organogenesis and their Role as Epigenetics Regulators able to Reverse Neurosensory Hearing Loss

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Targeting Mutational Landscape of TP53 in patients diagnosed with Oral Cancer living in Senegal

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Prolonged survival of Diamond-Blackfan anemia and RPS19 mutation: an observation in Togo

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A Trio Study Showing Novel Gene Mutation In LAMB3 Causing Junctional Epidermolysis Bullosa (Intermediate/ Severe)

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Understanding Inherited Bleeding Disorders: Genetic Mutations in Blood Coagulation Factors and Regulatory Proteins

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Disruption of Hydrogen Bonding Network Decreases Catalytic Diversity of Chloroperoxidase via Abolishing Both Chlorination and Dismutation Activities

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