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Taiwan-Ea-Ea Κατάλογοι Εταιρεία
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Εταιρικά Νέα :
- Huntingtin - Wikipedia
Huntingtin (Htt) is the protein coded for in humans by the HTT gene, also known as the IT15 ("interesting transcript 15") gene [5] Mutated HTT is the cause of Huntington's disease (HD), and has been investigated for this role and also for its involvement in long-term memory storage
- Hereditary hemorrhagic telangiectasia - Symptoms and causes
Hereditary hemorrhagic telangiectasia (tuh-lan-jee-uk-TAY-zhuh) is a condition that's passed through families, called inherited It causes atypical links between arteries and veins called arteriovenous malformations (AVMs) The most common sites AVMs affect are the skin, nose, digestive system, lungs, brain and liver AVMs may get larger over time
- HTT huntingtin [Homo sapiens (human)] - Gene - NCBI
Huntingtin is a disease gene linked to Huntington's disease, a neurodegenerative disorder characterized by loss of striatal neurons This is thought to be caused by an expanded, unstable trinucleotide repeat in the huntingtin gene, which translates as a polyglutamine repeat in the protein product
- Huntington Disease | Learn Science at Scitable - Nature
HD is a rare, adult-onset, autosomal dominant, progressive neurodegenerative disease George Huntington (Figure 1) was the first person to provide a comprehensive description of adult-onset HD
- The HTT Gene: Function, Mutation, and Huntington’s Disease
The HTT gene, or huntingtin gene, holds the instructions for creating a protein called huntingtin This protein is produced in cells throughout the body but is most active within the brain The huntingtin protein is necessary for the normal development of an embryo before birth and is particularly active in nerve cells, known as neurons
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