Publications by authors named "A G Murzin"

Biondi bodies are filamentous amyloid inclusions of unknown composition in ependymal cells of the choroid plexuses, ependymal cells lining cerebral ventricles and ependymal cells of the central canal of the spinal cord. Their formation is age-dependent and they are commonly associated with a variety of neurodegenerative conditions, including Alzheimer's disease and Lewy body disorders. Here, we show that Biondi bodies are strongly immunoreactive with TMEM239, an antibody specific for inclusions of transmembrane protein 106B (TMEM106B).

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Neurodegenerative diseases are characterized by the abnormal filamentous assembly of specific proteins in the central nervous system. Human genetic studies have established a causal role for protein assembly in neurodegeneration. However, the underlying molecular mechanisms remain largely unknown, which is limiting progress in developing clinical tools for these diseases.

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Chloride perovskites are semiconductors with a near-ultraviolet bandgap that are promising for applications in optoelectronics and photonics. One of the most studied representatives of this family is the methylammonium lead chloride MAPbCl (MA = CHNH). Low-temperature luminescence spectroscopy of this material demonstrates a complex emission structure.

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Article Synopsis
  • Mutations in the tau gene can cause a type of brain disease called frontotemporal dementia and parkinsonism, leading to changes in behavior and thinking.
  • The study focused on two specific mutations, P301L and P301T, found in different people, revealing unique structures of tau proteins in their brains.
  • The researchers suggest that these mutations create special kinds of tau-related brain diseases that should be treated differently in research studies about similar conditions.
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Neurodegenerative diseases are characterised by the abnormal filamentous assembly of specific proteins in the central nervous system . Human genetic studies established a causal role for protein assembly in neurodegeneration . However, the underlying molecular mechanisms remain largely unknown, which is limiting progress in developing clinical tools for these diseases.

View Article and Find Full Text PDF