Research Paper on Huntington's Disease - 1268 Words.

Essay Huntington's Disease Huntington's disease, or Huntngton's chorea, is a genetic disease that causes selective neural cell death, which results in chorea, or irregular, jerking movements of the limbs caused by involuntary muscle contractions, and dementia. It can cause a lack of concentration and depression. It also may cause atrophy of the caudate nucleus, a part of the brain.

UCL Huntington’s Disease Centre strives to achieve this future by combining world-class scientific expertise and the highest quality multidisciplinary clinical care. Our research spans the full range from laboratory research to understand how the Huntington’s disease gene causes the disease and how it affects the living human brain, through to the development of innovative new treatments.

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Currently there is no cure for the disease but research is ongoing. The search for this disease’s cure is focused on genetic research. Following the discovery of the Huntington gene, a lot of research has been carried out (Miller). The gene has a section that is responsible for glutamine encoding. This code has its base pairs in a series of.

Our Huntington’s disease research team works to understand more about the disease and help patients from all over the UK. We are currently part of a large international study which aims to understand more about the natural course of Huntington’s disease and which factors, other than the Huntington’s disease gene, influence its onset, presentation and.

Topics: Huntington's disease,. After reading this paper and the subsequent ones to come, you surely will. According to PudMedHealth.com, “Huntington’s disease is a disorder passed down through families in which nerve cells in certain parts of the brain waste away or degenerate.” This can lead to many different complications to a person’s health. In most cases, the disease’s.

Category: essays research papers; Title: Huntingtons Disease. Huntingtons Disease Essay - Huntington's Disease Huntington's disease, or Huntngton's chorea, is a genetic disease that causes selective neural cell death, which results in chorea, or irregular, jerking movements of the limbs caused by involuntary muscle contractions, and dementia.

The research involved mice, who had been genetically altered to carry the Huntington’s mutation. In the mouse model it was shown that the electrical activity of the subthalamic nucleus was essentially gone. In addition, there was “impaired anomalous receptor signaling, leading to defective energy metabolism and accumulation of damaging oxidants.” What all this means is that a new region.

This publication provides in-depth information about Huntington's disease, including common symptoms, diagnosis, and available therapies. Also discussed is NINDS-funded research to increase scientific understanding of Huntington's disease. Sources of additional information are included. Related resource: Huntington's Disease Information Page.

A mind-boggling and ever-expanding range of topics run the gamut from basic and clinical to translational research. Basic research provides a fundamental understanding of molecules and mechanisms that, without offering any apparent practical avenue for patient treatment, involves identifying cellular processes and genetic mutations and revealing breakdowns in cellular communication associated.

Human brain cells showing aspects of Huntington's Disease have been developed, opening up new research pathways for treating the fatal disorder. An international consortium, including scientists from the School of Biosciences, has taken cells from Huntington's Disease patients and generated human brain cells that develop aspects of the disease in the laboratory.