Human homologue of a gene mutated in the slow Wallerian degeneration (C57BL/Wld(s)) mouse.
The slow Wallerian degeneration mouse (C57BL/Wld(s)) is a mutant strain of mouse, with the unique phenotype of prolonged survival of the distal axon following axotomy. The causative mutation is an 85 kb tandem triplication on distal mouse chromosome 4. The dominant slow Wallerian degeneration phenot...
Prif Awduron: | Fernando, F, Conforti, L, Tosi, S, Smith, A, Coleman, M |
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Fformat: | Journal article |
Iaith: | English |
Cyhoeddwyd: |
2002
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Eitemau Tebyg
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The progressive nature of Wallerian degeneration in wild-type and slow Wallerian degeneration (Wld<sup>S</sup>) nerves
gan: Grumme Daniela S, et al.
Cyhoeddwyd: (2005-02-01) -
Expression of the neuroprotective slow Wallerian degeneration (<it>Wld</it><sup><it>S</it></sup>) gene in non-neuronal tissues
gan: Tsao Jack W, et al.
Cyhoeddwyd: (2009-12-01) -
Design of a novel quantitative PCR (QPCR)-based protocol for genotyping mice carrying the neuroprotective Wallerian degeneration slow (<it>Wld</it><sup><it>s</it></sup>) gene
gan: Coleman Michael P, et al.
Cyhoeddwyd: (2007-10-01) -
Wallerian degeneration
gan: Tong HAN
Cyhoeddwyd: (2018-03-01) -
kwing_wld
gan: Vincent, Regis
Cyhoeddwyd: (2011)