Researchers at Ruhr University Bochum discovered that a lipid anchor on nerve cell membranes stabilizes prion protein folding ...
Protein aggregation is typical of neurodegenerative diseases such as Alzheimer's, Parkinson's and prion diseases such as ...
The answer lies in a membrane structure called ... abnormalities that affect glial cells. Regardless of its cause, myelin loss causes remarkable nerve dysfunction because nerve conduction can ...
The process may someday be used in humans with spinal cord injuries to minimize or reverse the damage to nerve cells that results in paralysis, says Richard B. Borgens, professor of developmental ...
This takes place when molecules diffuse across the cell membrane by travelling through ... cells and potassium into the cells. This helps nerve cells to transmit nerve impulses.
Protein aggregation is typical of various neurodegenerative diseases such as Alzheimer’s, Parkinson’s and prion diseases such ...
nerve cells, muscle cells, ciliated cells, and villi. Get it, lark? Anyone…? Okay let's move on. An animal cell is made of three main parts a nucleus, cell membrane and cytoplasm, which holds ...
A lipid anchor on nerve cell membranes stabilizes prion proteins (PrPC) and prevents their pathological aggregation into forms linked to prion diseases.
Protein aggregation is typical of various neurodegenerative diseases such as Alzheimer's, Parkinson's and prion diseases such as Creutzfeld-Jakob disease. A research team has now used new in vitro and ...
Researchers have gained valuable insight into the development of prion diseases of the brain.Protein aggregation is typical of various ...
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