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BMC Neuroscience|March 10, 2011
Endosomal accumulation of APP in wobbler motor neurons reflects impaired vesicle trafficking: implications for human motor neuron diseaseRalf Palmisano, Panagiota Golfi, Peter Heimann, et al.
Stem Cells and Development|April 7, 2011
Schwann cells can be reprogrammed to multipotency by cultureDarius Widera, Peter Heimann, Christin Zander, et al.
Prehospital and Disaster Medicine|February 25, 2006
Panel 2.9: repair and recovery of health systemsBjorn Melgaard, Maria Cristina Profili, Peter Heimann, et al.
Human Molecular Genetics|December 3, 2014
Ataxia is the major neuropathological finding in arylsulfatase G-deficient mice: similarities and dissimilarities to Sanfilippo disease (mucopolysaccharidosis type III)Björn Kowalewski, Peter Heimann, Theresa Ortkras, et al.
Stem Cell Reviews and Reports|June 6, 2012
Generation of Schwann cell-derived multipotent neurospheres isolated from intact sciatic nerveIna Martin, The Duy Nguyen, Vivien Krell, et al.
Small (Weinheim an Der Bergstrasse, Germany)|October 6, 2015
Helium Ion Microscopy Visualizes Lipid Nanodomains in Mammalian CellsMatthias Schürmann, Natalie Frese, André Beyer, et al.
Scientific Reports|October 4, 2018
Primary rat LSECs preserve their characteristic phenotype after cryopreservationViola Mönkemöller, Hong Mao, Wolfgang Hübner, et al.
Frontiers in Cellular Neuroscience|August 1, 2020
Absence of Plekhg5 Results in Myelin Infoldings Corresponding to an Impaired Schwann Cell Autophagy, and a Reduced T-Cell Infiltration Into Peripheral NervesPatrick Lüningschrör, Carsten Slotta, Peter Heimann, et al.
International Journal of Molecular Sciences|May 28, 2013
Loss of vps54 function leads to vesicle traffic impairment, protein mis-sorting and embryonic lethalityPáll Karlsson, Aida Droce, Jakob M Moser, et al.
Nature Genetics|October 26, 2005
Mutation of Vps54 causes motor neuron disease and defective spermiogenesis in the wobbler mouseThomas Schmitt-John, Carsten Drepper, Anke Mussmann, et al.
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