Neuroprotection

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Neuroprotection: A Simple Solution for Spinocerebellar ataxia

Spinocerebellar ataxia is a neurodegenerative disease. It is associated with mutation of the DNA repair enzyme tyrosyl-DNA phosphodiesterase 1 (TDP1). It's been shown that oxidative damage and ionizing radiation lead to a pronounced defect in the repair of chromosomal single-strand breaks leading to progressive cerebellar atrophy. This links the inability to repair DNA damage and the onset of neurodegeneration while highlighting the importance of TDP1 in this process.

What can we do with this information in terms of treatment options? In DNA Reprogramming we commonly clear for DNA damage repair genes and proteins. In this case the mutated repair enzyme has been identified. All that is necessary is to use DNA Reprogramming to clear for TDP1 and the ability to repair DNA damage and mitigate the progress of neurodegeneration should be alleviated.
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1

Neuroprotection: A Simple Solution for Spinocerebellar ataxia

Spinocerebellar ataxia is a neurodegenerative disease. It is associated with mutation of the DNA repair enzyme tyrosyl-DNA phosphodiesterase 1 (TDP1). It's been shown that oxidative damage and ionizing radiation lead to a pronounced defect in the repair of chromosomal single-strand breaks leading to progressive cerebellar atrophy. This links the inability to repair DNA damage and the onset of neurodegeneration while highlighting the importance of TDP1 in this process.

What can we do with this information in terms of treatment options? In DNA Reprogramming we commonly clear for DNA damage repair genes and proteins. In this case the mutated repair enzyme has been identified. All that is necessary is to use DNA Reprogramming to clear for TDP1 and the ability to repair DNA damage and mitigate the progress of neurodegeneration should be alleviated.
2

A Simple Solution for Spinocerebellar ataxia

Spinocerebellar ataxia is a neurodegenerative disease. It is associated with mutation of the DNA repair enzyme tyrosyl-DNA phosphodiesterase 1 (TDP1). It's been shown that oxidative damage and ionizing radiation lead to a pronounced defect in the repair of chromosomal single-strand breaks leading to progressive cerebellar atrophy. This links the inability to repair DNA damage and the onset of neurodegeneration while highlighting the importance of TDP1 in this process.

What can we do with this information in terms of treatment options? In DNA Reprogramming we commonly clear for DNA damage repair genes and proteins. In this case the mutated repair enzyme has been identified. All that is necessary is to use DNA Reprogramming to clear for TDP1 and the ability to repair DNA damage and mitagate the progress of neurodegeneration should be alleviated.

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