Mutations
Mutations are changes in the DNA sequence of an organism's genome and can have varying effects. While some mutations may be harmless or even beneficial, particularly when they contribute to genetic diversity and adaptation, others can disrupt essential cellular functions or regulatory mechanisms. Such detrimental mutations may lead to genetic disorders or increase the risk of diseases like cancer. For example, mutations causing cystic fibrosis, sickle cell disease, or Huntington's disease can result in severe health conditions. Additionally, as cells divide, mutations can accumulate, particularly in rapidly dividing cells like those in the skin or gastrointestinal tract. This accumulation can disrupt normal cell growth and division, potentially leading to cancer. Despite their potential negative effects, mutations are a natural part of biological processes and crucial for evolution. Ongoing research aims to understand their roles in health and disease, and to develop strategies for managing or treating genetic disorders.
Related Conference of Mutations
December 10-11, 2024
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Dubai, UAE
January 30-31, 2025
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June 16-17, 2025
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Mutations Conference Speakers
Recommended Sessions
- Advancements in Vaccines and Therapeutics
- Antigen-Antibody Reactions
- Bacterial Infections and Diseases
- Biofertilizers
- COVID-19
- Fungal Infections
- Gene Expression
- Infectious Diseases and Cancer
- Mutations
- Parasitic Infections
- Prion Diseases
- Probiotics and Prebiotics
- Sexually Transmitted Diseases (STDs) and Infections (STIs)
- Veterinary Infectious Diseases
- Viral Infections and Diseases
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