Schwarz, Petra
University Hospital Zurich
7 papers on CoChatORCID 0000-0003-1686-8624
Most cited papers
- Verified
A neuroprotective role for microglia in prion diseases
Zhu, C., Herrmann, U. S., Falsig, J., Abakumova, I., Nuvolone, M., Schwarz, P., Frauenknecht, K., Rushing, E. J., & Aguzzi, A. (2016) · Journal of Experimental Medicine
Prion Diseases and Protein MisfoldingNeuroinflammation and Neurodegeneration Mechanisms
Cited by 134
- Verified
Engulfment of cerebral apoptotic bodies controls the course of prion disease in a mouse strain–dependent manner
Kranich, J., Krautler, N. J., Falsig, J., Ballmer, B., Li, S., Hutter, G., Schwarz, P., Moos, R., Julius, C., Miele, G., et al. (2010) · Journal of Experimental Medicine
Prion Diseases and Protein MisfoldingNeuroinflammation and Neurodegeneration Mechanisms
Cited by 110
- Verified
Prion pathogenesis in the absence of Toll-like receptor signalling
Prinz, M., Heikenwalder, M., Schwarz, P., Takeda, K., Akira, S., & Aguzzi, A. (2003) · The EMBO Reports
Prion Diseases and Protein MisfoldingNeuroinflammation and Neurodegeneration Mechanisms
Cited by 85
- Verified
Ribosomal profiling during prion disease uncovers progressive translational derangement in glia but not in neurons
Scheckel, C., Imeri, M., Schwarz, P., & Aguzzi, A. (2020) · eLife
Prion Diseases and Protein MisfoldingRNA and protein synthesis mechanisms
Cited by 57
- Verified
Triggering receptor expressed on myeloid cells-2 is involved in prion-induced microglial activation but does not contribute to prion pathogenesis in mouse brains
Zhu, C., Herrmann, U. S., Li, B., Abakumova, I., Moos, R., Schwarz, P., Rushing, E. J., Colonna, M., & Aguzzi, A. (2015) · Neurobiology of Aging
Prion Diseases and Protein MisfoldingNeuroinflammation and Neurodegeneration Mechanisms
Cited by 44
- Verified
Prion Pathogenesis in the Absence of NLRP3/ASC Inflammasomes
Nuvolone, M., Sorce, S., Schwarz, P., & Aguzzi, A. (2015) · PLOS ONE
Prion Diseases and Protein MisfoldingInflammasome and immune disorders
Cited by 39
- Verified
Glial activation in prion diseases is selectively triggered by neuronal PrPSc
Lakkaraju, A. K. K., Sorce, S., Senatore, A., Nuvolone, M., Guo, J., Schwarz, P., Moos, R., Pelczar, P., & Aguzzi, A. (2022) · Brain Pathology
Prion Diseases and Protein MisfoldingNeuroinflammation and Neurodegeneration Mechanisms
Cited by 34
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