Mutation Databases

Mutation databases are a type of digital repository that stores data related to genetic mutations. They provide a comprehensive collection of information about genetic variants and their effects on cellular function. The data in these databases is used to inform research in the fields of genomics and genetics, enabling scientists to study the influence of genetic variations on cellular organisms and the development of new treatments. Mutation databases provide essential resources for identifying novel disease-causing genes and for understanding the molecular mechanisms of disease development and progression. In addition, they are invaluable for helping to unravel the mechanisms of drug resistance in cancer and infectious diseases. By providing a comprehensive repository of genetic variations, mutation databases can significantly advance medical research and help to improve patient care.

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Related Articles

15 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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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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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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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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