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Proceedings of the National Academy of Sciences of the United States of America|November 13, 2013
Unexpected gain of function for the scaffolding protein plectin due to mislocalization in pancreatic cancerSoo J Shin, Jeffrey A Smith, Günther A Rezniczek, et al.
The American Journal of Pathology|October 5, 2010
Host defense mechanisms in secondary syphilitic lesions: a role for IFN-gamma-/IL-17-producing CD8+ T cells?Georg Stary, Irene Klein, Marie-Charlotte Brüggen, et al.
European Journal of Cell Biology|October 7, 2025
Consequences of plectin ablation on the various intermediate filament systems in skeletal muscleMarta Rocha, Jonas Petsch, Dorothea Schultheis, et al.
Experimental Cell Research|March 30, 2007
Ferritin associates with marginal band microtubulesAnthony A Infante, Dzintra Infante, Muh-Chun Chan, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 19, 2013
Mechanosensing through focal adhesion-anchored intermediate filamentsMartin Gregor, Selma Osmanagic-Myers, Gerald Burgstaller, et al.
Frontiers in Cellular Neuroscience|December 5, 2015
Schwann Cell Expressed Nogo-B Modulates Axonal Branching of Adult Sensory Neurons Through the Nogo-B Receptor NgBRChristoph Eckharter, Nina Junker, Lilli Winter, et al.
Methods in Enzymology|January 19, 2016
Functional and Genetic Analysis of Epiplakin in Epithelial CellsSandra Szabo, Karl L Wögenstein, Peter Fuchs
European Journal of Pediatrics|February 14, 2004
Severe mucous membrane involvement in epidermolysis bullosa simplex with muscular dystrophy due to a novel plectin gene mutationUlrike Schara, Jens Tücke, Wilhelm Mortier, et al.
The Journal of Cell Biology|February 9, 2022
Plectin-mediated cytoskeletal crosstalk controls cell tension and cohesion in epithelial sheetsMagdalena Prechova, Zuzana Adamova, Anna-Lena Schweizer, et al.
The Journal of Investigative Dermatology|February 20, 2002
A site-specific plectin mutation causes dominant epidermolysis bullosa simplex Ogna: two identical de novo mutationsDörte Koss-Harnes, Bjørn Høyheim, Ingrun Anton-Lamprecht, et al.
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