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...
Κύριοι συγγραφείς: | Fernando, F, Conforti, L, Tosi, S, Smith, A, Coleman, M |
---|---|
Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
2002
|
Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
-
The progressive nature of Wallerian degeneration in wild-type and slow Wallerian degeneration (Wld<sup>S</sup>) nerves
ανά: Grumme Daniela S, κ.ά.
Έκδοση: (2005-02-01) -
Expression of the neuroprotective slow Wallerian degeneration (<it>Wld</it><sup><it>S</it></sup>) gene in non-neuronal tissues
ανά: Tsao Jack W, κ.ά.
Έκδοση: (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
ανά: Coleman Michael P, κ.ά.
Έκδοση: (2007-10-01) -
Wallerian degeneration
ανά: Tong HAN
Έκδοση: (2018-03-01) -
kwing_wld
ανά: Vincent, Regis
Έκδοση: (2011)