安裝中文字典英文字典辭典工具!
安裝中文字典英文字典辭典工具!
|
- 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
- HTT Gene - GeneCards | HD Protein | HD Antibody
HTT (Huntingtin) is a Protein Coding gene Diseases associated with HTT include Huntington Disease and Lopes-Maciel-Rodan Syndrome Among its related pathways are Gene expression (Transcription) and Transcriptional Regulation by MECP2
- Htt Gene: Functions, Disorders, and Therapeutic Strategies - Genetics
The Htt gene encodes a protein called huntingtin, which plays a role in various cellular processes, including neuronal development and vesicular trafficking
- The HTT Gene - Huntingtons Victoria – Huntington’s Victoria
The HTT gene, located on Chromosome 4, provides instructions for producing a vital protein called huntingtin While the precise role of this protein remains unclear, it holds significance in nerve cells (neurons) within the brain and is crucial for normal development before birth
- Entry - *613004 - HUNTINGTIN; HTT - OMIM - (OMIM. ORG)
HGNC Approved Gene Symbol: HTT The HTT gene encodes huntingtin, a ubiquitously expressed nuclear protein that binds to a number of transcription factors to regulate transcription
- The biological function of the Huntingtin protein and its relevance to . . .
Huntington’s Disease (HD) is a progressive and disabling neurodegenerative disorder of the central nervous system, affecting approximately 1 in 10,000 individuals [1] Patients suffer from motor, cognitive, and behavioural disturbances arising at a mean age of 35 years
|
|
|