Showing 1 - 9 results of 9 for search 'Fricker, F', query time: 0.02s
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1
The role of neuregulin-1 in the response to nerve injury. by Fricker, F, Bennett, D
Published 2011Journal article -
2
Membrane metallo‐endopeptidase is dispensable for repair after nerve injury by Cervellini, I, Galino, J, Zhu, N, Fricker, F, Bao, L, Bennett, D
Published 2019Journal article -
3
Axonally derived neuregulin-1 is required for remyelination and regeneration after nerve injury in adulthood. by Fricker, F, Lago, N, Balarajah, S, Tsantoulas, C, Tanna, S, Zhu, N, Fageiry, S, Jenkins, M, Garratt, A, Birchmeier, C, Bennett, D
Published 2011Journal article -
4
RalGTPases contribute to Schwann cell repair after nerve injury via regulation of process formation by Galino, J, Cervellini, I, Zhu, N, Stöberl, N, Hütte, M, Fricker, F, Lee, G, McDermott, L, Lalli, G, Bennett, D
Published 2019Journal article -
5
Sensory axon-derived neuregulin-1 is required for axoglial signaling and normal sensory function but not for long-term axon maintenance. by Fricker, F, Zhu, N, Tsantoulas, C, Abrahamsen, B, Nassar, M, Thakur, M, Garratt, A, Birchmeier, C, McMahon, S, Wood, J, Bennett, D
Published 2009Journal article -
6
Neuregulin-1 controls an endogenous repair mechanism after spinal cord injury. by Bartus, K, Galino, J, James, N, Hernandez-Miranda, L, Dawes, J, Fricker, F, Garratt, A, McMahon, S, Ramer, MS, Birchmeier, C, Bennett, D, Bradbury, E
Published 2016Journal article -
7
Axonal neuregulin 1 is a rate limiting but not essential factor for nerve remyelination. by Fricker, F, Antunes-Martins, A, Galino, J, Paramsothy, R, La Russa, F, Perkins, J, Goldberg, R, Brelstaff, J, Zhu, N, McMahon, S, Orengo, C, Garratt, A, Birchmeier, C, Bennett, D
Published 2013Journal article -
8
AXONAL NEUREGULIN-1 IS RATE LIMITING BUT NOT ESSENTIAL FOR PERIPHERAL NERVE REMYELINATION by Fricker, F, Antunes-Martins, A, Galino, J, Paramsothy, R, La Russa, F, Perkins, J, Goldberg, R, Brelstaff, J, Zhu, N, McMahon, S, Orengo, C, Garratt, A, Birchmeier, C, Bennett, D
Published 2013Conference item -
9
A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome. by Kremeyer, B, Lopera, F, Cox, J, Momin, A, Rugiero, F, Marsh, S, Woods, C, Jones, N, Paterson, K, Fricker, F, Villegas, A, Acosta, N, Pineda-Trujillo, N, Ramírez, J, Zea, J, Burley, M, Bedoya, G, Bennett, D, Wood, J, Ruiz-Linares, A
Published 2010Journal article