Manuela Pfammatter
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Explore the profile of Manuela Pfammatter including associated specialties, affiliations and a list of published articles.
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7
Citations
114
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Recent Articles
1.
Heinzer D, Avar M, Pfammatter M, Moos R, Schwarz P, Buhmann M, et al.
PLoS One
. 2024 Jun;
19(6):e0304603.
PMID: 38870196
Iatrogenic transmission of prions, the infectious agents of fatal Creutzfeldt-Jakob disease, through inefficiently decontaminated medical instruments remains a critical issue. Harsh chemical treatments are effective, but not suited for routine...
2.
Sorce S, Nuvolone M, Russo G, Chincisan A, Heinzer D, Avar M, et al.
PLoS Pathog
. 2020 Jun;
16(6):e1008653.
PMID: 32598380
The clinical course of prion diseases is accurately predictable despite long latency periods, suggesting that prion pathogenesis is driven by precisely timed molecular events. We constructed a searchable genome-wide atlas...
3.
Zhu C, Li Z, Li B, Pfammatter M, Hornemann S, Aguzzi A
Neurobiol Aging
. 2019 Feb;
76:208-213.
PMID: 30743056
Progression of prion diseases is driven by the accumulation of prions in the brain. Ablation of microglia or deletion of the eat-me-signal, milk-fat globule epidermal growth factor VIII (Mfge8), accelerates...
4.
Gang H, Galvagnion C, Meisl G, Muller T, Pfammatter M, Buell A, et al.
Anal Chem
. 2018 Jan;
90(5):3284-3290.
PMID: 29313342
Elucidation of the fundamental interactions of proteins with biological membranes under native conditions is crucial for understanding the molecular basis of their biological function and malfunction. Notably, the large surface...
5.
Meisl G, Rajah L, Cohen S, Pfammatter M, Saric A, Hellstrand E, et al.
Chem Sci
. 2017 Nov;
8(10):7087-7097.
PMID: 29147538
The formation of filaments from naturally occurring protein molecules is a process at the core of a range of functional and aberrant biological phenomena, such as the assembly of the...
6.
Pfammatter M, Andreasen M, Meisl G, Taylor C, Adamcik J, Bolisetty S, et al.
Anal Chem
. 2017 Oct;
89(22):12306-12313.
PMID: 28972786
The self-replicating properties of proteins into amyloid fibrils is a common phenomenon and underlies a variety of neurodegenerative diseases. Because propagation-active fibrils are chemically indistinguishable from innocuous aggregates and monomeric...
7.
Frontzek K, Pfammatter M, Sorce S, Senatore A, Schwarz P, Moos R, et al.
PLoS One
. 2016 Sep;
11(9):e0163601.
PMID: 27684562
Prions are the infectious agents causing transmissible spongiform encephalopathies (TSE), progressive, inexorably lethal neurological diseases. Antibodies targeting the globular domain (GD) of the cellular prion protein PrPC trigger a neurotoxic...