copy and paste this google map to your website or blog!
Press copy button and paste into your blog or website.
(Please switch to 'HTML' mode when posting into your blog. Examples: WordPress Example, Blogger Example)
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 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 | Huntingtons 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
Regulation of HTT mRNA Biogenesis: The Norm and Pathology - MDPI In this review, we discuss the features of transcriptional regulation and processing that lead to the formation of various HTT mRNA variants, each of which may uniquely contribute to the progression of the disease
What does HTT stand for? - Abbreviations. com Find out what is the full meaning of HTT on Abbreviations com! 'Human Touch Technology' is one option -- get in to view more @ The Web's largest and most authoritative acronyms and abbreviations resource
The Biology of Huntingtin: Neuron - Cell Press Huntington’s disease (HD) is a genetically inherited autosomal dominant neurodegenerative disorder, with a mean age at onset of 40 years (Ross and Tabrizi, 2011) It is a rare disorder with a prevalence of 5–10 individuals per 100,000 in the Caucasian population Some juvenile forms exist but are rare, accounting for 5% of the cases