Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Claudia Mistl"'
Autor:
Rusudan Okujava, Patrick Guye, Yun-Yueh Lu, Claudia Mistl, Florine Polus, Muriel Vayssier-Taussat, Cornelia Halin, Antonius G Rolink, Christoph Dehio
Publikováno v:
PLoS Pathogens, Vol 10, Iss 6, p e1004187 (2014)
Numerous bacterial pathogens secrete multiple effectors to modulate host cellular functions. These effectors may interfere with each other to efficiently control the infection process. Bartonellae are Gram-negative, facultative intracellular bacteria
Externí odkaz:
https://doaj.org/article/dfc71ebe1dfc4046aa5dac5c1cb18c31
Autor:
Maxime Québatte, Michael Kosoy, Alexander Harms, Pablo Manfredi, Claudia Mistl, Bruno B Chomel, Jonas Körner, Christoph Dehio, Soichi Maruyama, Philipp Engel, Francisca H. I. D. Segers
Publikováno v:
Genome Biology and Evolution, 9 (3)
Genome Biology and Evolution, vol. 9, no. 3, pp. 761-776
Genome Biology and Evolution
Genome Biology and Evolution, vol. 9, no. 3, pp. 761-776
Genome Biology and Evolution
The α-proteobacterial genus Bartonella comprises a group of ubiquitous mammalian pathogens that are studied as a model for the evolution of bacterial pathogenesis. Vast abundance of two particular phylogenetic lineages of Bartonella had been linked
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e67d54c8824d5d6d4f91ecdfaefa81e3
https://edoc.unibas.ch/57505/
https://edoc.unibas.ch/57505/
Publikováno v:
Cellular Microbiology. 13:419-431
Summary The vasculotropic pathogen Bartonella henselae (Bh) intimately interacts with human endothelial cells (ECs) and subverts multiple cellular functions. Here we report that Bh specifically interferes with vascular endothelial growth factor (VEGF
Autor:
S Kafmann, Will P.J.M Spooren, P Caromi, Katja Hofele, Graeme Bilbe, Claudia Mistl, M Tolnay, Markus A. Rüegg, Bernd Sommer, Karl-Heinz Wiederhold, Simone Danner, Alphonse Probst, Samuel Barbieri, H van der Putten, Sabine Kauffmann
Publikováno v:
Experimental Gerontology. 35:1389-1403
The discovery of two missense mutations (A53T and A30P) in the gene encoding the presynaptic protein alpha-synuclein (alphaSN) that are genetically linked to rare familial forms of Parkinson's disease and its accumulation in Lewy bodies and Lewy neur
Publikováno v:
Mechanisms of Development. 93(1-2):83-93
Protein phosphatase 2A (PP2A) plays central roles in development, cell growth and transformation. Inactivation of the gene encoding the PP2A catalytic subunit Calpha by gene targeting generates a lethal embryonic phenotype. No mesoderm is formed in C
Publikováno v:
Neuropathology and Applied Neurobiology. 24:53-59
Braak's argyrophilic grains (ArGs) are spindle-shaped neuropil structures originally found in patients afflicted with adult onset dementia. We recently observed that tau protein is hyperphosphorylated in most nerve cells in areas rich in ArGs, sugges
Autor:
Matthias Staufenbiel, Christine Sturchler-Pierrat, Birgit Ledermann, Dorothee Abramowski, Claudia Mistl, Michael E. Calhoun, Paolo Paganetti, Kurt Bürki, Karl-Heinz Wiederhold, Caroline Waridel, Mathias Jucker, Mairead Duke, Sabin Rothacher, Bernd Sommer, Alphonse Probst, Peter Frey
Publikováno v:
Proceedings of the National Academy of Sciences. 94:13287-13292
Mutations in the amyloid precursor protein (APP) gene cause early-onset familial Alzheimer disease (AD) by affecting the formation of the amyloid β (Aβ) peptide, the major constituent of AD plaques. We expressed human APP 751 containing these mutat
Autor:
Willibrordus Spooren, Samuel Barbieri, Sabine Kauffmann, Simone Danner, Alphonse Probst, Bernd Sommer, Herman van der Putten, Graeme Bilbe, Claudia Mistl, M Tolnay, Katja Hofele, Karl-Heinz Wiederhold
Publikováno v:
Alzheimer's Disease: Advances in Etiology, Pathogenesis and Therapeutics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb1c860d6fd1caa6b98ff79539cf3b99
https://doi.org/10.1002/0470846453.ch61
https://doi.org/10.1002/0470846453.ch61
Publikováno v:
ResearcherID
A number of pathological changes have been reported in relation to CA1 pyramidal cells in Alzheimer's disease (AD), among them hyperphosphorylation of tau protein followed by the formation of filamentous tau lesions, granulovacuolar degeneration (GVD
Autor:
H van der Putten, Sabine Kauffmann, M Tolnay, Claudia Mistl, Will P.J.M Spooren, Graeme Bilbe, Katja Hofele, Karl-Heinz Wiederhold, Bernd Sommer, Samuel Barbieri, Simone Danner, Alphonse Probst
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9781461354611
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d7625398f282ae479fe365c83dfb9cc
https://doi.org/10.1007/978-1-4615-1249-3_13
https://doi.org/10.1007/978-1-4615-1249-3_13