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How can mutations in different genes contribute to the development of a single disease?
Mutations in different genes can contribute to the development of a single disease by affecting various biological pathways or processes that are involved in the disease. These mutations can interact with each other or with environmental factors to disrupt normal cellular functions, leading to the manifestation of the disease.
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What are the factors that contribute to the development of breast cancer in females?
Several factors contribute to the development of breast cancer in females, including genetic mutations, family history of the disease, hormonal factors, lifestyle choices such as diet and exercise, and exposure to certain environmental factors like radiation. Regular screenings and early detection can help in managing the risk of breast cancer.
What are the factors that can cause breast cancer?
Several factors can contribute to the development of breast cancer, including genetic mutations, family history of the disease, hormonal factors, lifestyle choices such as alcohol consumption and lack of physical activity, and exposure to certain environmental factors like radiation.
Cancer is a disease of which of these genes DNA hormones?
Cancer emerges by DNA mutations. DNA = genes. The mutations lead to protein aberations in the cell. But, some proteins are hormones as well and some of these can cause cancer. To summarize it, let's say that cancer is a disease of genes and DNA in 95% cases and cancer is a disease of hormons in 5% cases. (very roughly, but it is true)
What happens to the CFTR gene in cystic fibrosis and how does it contribute to the development of the disease?
In cystic fibrosis, mutations in the CFTR gene cause it to produce a faulty protein. This protein is unable to regulate the flow of salt and fluids in and out of cells, leading to the buildup of thick, sticky mucus in various organs. This mucus clogs the airways, digestive system, and other organs, causing breathing difficulties, digestive problems, and other symptoms characteristic of the disease.
What are the most commonly mutated genes in cancer and how do they contribute to the development and progression of the disease?
The most commonly mutated genes in cancer are TP53, KRAS, and PIK3CA. These mutations can lead to uncontrolled cell growth, resistance to cell death, and increased ability to spread to other parts of the body. This contributes to the development and progression of cancer by allowing the cancer cells to grow and divide uncontrollably, evade the immune system, and invade surrounding tissues.
What is marked degenerative arthritis and disc disease mean?
Degenerative disk disease and arthritis are different conditions conditions.The cause of degenerative disk disease at this point is not understood, however having arthritis can contribute to its development.
What are the factors that contribute to the development of breast cancer in females?
Several factors contribute to the development of breast cancer in females, including genetic mutations, family history of the disease, hormonal factors, lifestyle choices such as diet and exercise, and exposure to certain environmental factors like radiation. Regular screenings and early detection can help in managing the risk of breast cancer.
Is maple syrup urine disease cause by a mutation?
Yes, there are several different mutations that can cause it.
What is the mutated gene of the Charcot-Marie-Tooth disease?
CMT is caused by mutations in genes that produce proteins involved in the structure and function of either the peripheral nerve axon or the myelin sheath. Although different proteins are abnormal in different forms of CMT disease, all of the mutations affect the normal function of the peripheral nerves. The gene mutations in CMT disease are usually inherited.
Can chrohn's disease be sexually transmitted?
No. Recent research suggests hereditary, genetics, and/or environmental factors contribute to the development of Crohn’s Disease.
An inherited disease or disorder that is caused by a mutation in a gene or by a chromosomal defect?
There are many thousands of different mutations.
What are the factors that can cause breast cancer?
Several factors can contribute to the development of breast cancer, including genetic mutations, family history of the disease, hormonal factors, lifestyle choices such as alcohol consumption and lack of physical activity, and exposure to certain environmental factors like radiation.
Cancer is a disease of which of these genes DNA hormones?
Cancer emerges by DNA mutations. DNA = genes. The mutations lead to protein aberations in the cell. But, some proteins are hormones as well and some of these can cause cancer. To summarize it, let's say that cancer is a disease of genes and DNA in 95% cases and cancer is a disease of hormons in 5% cases. (very roughly, but it is true)
Which genetic disease affects cerebral cortex?
One example of a genetic disease that affects the cerebral cortex is lissencephaly. This condition is characterized by smooth brain surfaces due to abnormal neuronal migration during development, leading to intellectual disabilities, developmental delays, and seizures. It is often caused by mutations in genes involved in brain development.
What happens to the CFTR gene in cystic fibrosis and how does it contribute to the development of the disease?
In cystic fibrosis, mutations in the CFTR gene cause it to produce a faulty protein. This protein is unable to regulate the flow of salt and fluids in and out of cells, leading to the buildup of thick, sticky mucus in various organs. This mucus clogs the airways, digestive system, and other organs, causing breathing difficulties, digestive problems, and other symptoms characteristic of the disease.
What type of disease can occur from mutations that can disrupt the control of cell reproduction?
Cancer is a disease that can occur from mutations that disrupt the control of cell reproduction. Mutations in genes involved in cell cycle regulation and growth can lead to uncontrolled cell division and the formation of tumors.
An example of all human cells and mutations?
Sickle-cell disease
