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International Archives of Allergy and Applied Immunology|January 1, 1989
Human Fc epsilon R II and IgE-binding factorsG Delespesse, M Sarfati, H Hofstetter, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 20, 2000
Uncoupling of myelin assembly and schwann cell differentiation by transgenic overexpression of peripheral myelin protein 22S Niemann, M W Sereda, U Suter, et al.
Nature Genetics|November 1, 1995
Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient miceK Adlkofer, R Martini, A Aguzzi, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|March 29, 1991
Molecular approaches to nerve regenerationA A Welcher, U Suter, M De Leon, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 1991
A myelin protein is encoded by the homologue of a growth arrest-specific geneA A Welcher, U Suter, M De Leon, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 15, 1992
The rat trk protooncogene product exhibits properties characteristic of the slow nerve growth factor receptorS O Meakin, U Suter, C C Drinkwater, et al.
Journal of Neuroscience Research|December 15, 1995
Widespread expression of the peripheral myelin protein-22 gene (PMP22) in neural and non-neural tissues during murine developmentD Baechner, T Liehr, H Hameister, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 15, 1997
Heterozygous peripheral myelin protein 22-deficient mice are affected by a progressive demyelinating tomaculous neuropathyK Adlkofer, R Frei, D H Neuberg, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 5, 1999
Transport of Trembler-J mutant peripheral myelin protein 22 is blocked in the intermediate compartment and affects the transport of the wild-type protein by direct interactionA R Tobler, L Notterpek, R Naef, et al.
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