Literature DB >> 7374955

An allele of the mouse mutant dystonia musculorum exhibits lesions in red nucleus and striatum.

A Messer, N L Strominger.   

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Year:  1980        PMID： 7374955     DOI： 10.1016/0306-4522(80)90051-2

Source DB:  PubMed          Journal:  Neuroscience        ISSN： 0306-4522            Impact factor:   3.590


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  8 in total

1.  Axonopathy in the Central Nervous System Is the Hallmark of Mice with a Novel Intragenic Null Mutation of Dystonin.

Authors:  Frauke Seehusen; Kirsten Kiel; Stefano Jottini; Peter Wohlsein; Andre Habierski; Katharina Seibel; Tanja Vogel; Henning Urlaub; Martin Kollmar; Wolfgang Baumgärtner; Ulrike Teichmann
Journal:  Genetics       Date:  2016-07-08       Impact factor: 4.562

Review 2.  Animal models of generalized dystonia.

Authors:  Robert S Raike; H A Jinnah; Ellen J Hess
Journal:  NeuroRx       Date:  2005-07

Review 3.  Animal models for dystonia.

Authors:  Bethany K Wilson; Ellen J Hess
Journal:  Mov Disord       Date:  2013-06-15       Impact factor: 10.338

4.  Segmental demyelination in the peripheral nerves of mice affected by a hereditary neuropathy (dystonia musculorum).

Authors:  T H Moss
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088

5.  Motor unit abnormalities in Dystonia musculorum mice.

Authors:  Yves De Repentigny; Andrew Ferrier; Scott D Ryan; Tadasu Sato; Rashmi Kothary
Journal:  PLoS One       Date:  2011-06-15       Impact factor: 3.240

6.  Neuronal dystonin isoform 2 is a mediator of endoplasmic reticulum structure and function.

Authors:  Scott D Ryan; Andrew Ferrier; Tadasu Sato; Ryan W O'Meara; Yves De Repentigny; Susan X Jiang; Sheng T Hou; Rashmi Kothary
Journal:  Mol Biol Cell       Date:  2011-12-21       Impact factor: 4.138

7.  Untethering the nuclear envelope and cytoskeleton: biologically distinct dystonias arising from a common cellular dysfunction.

Authors:  Nadia A Atai; Scott D Ryan; Rashmi Kothary; Xandra O Breakefield; Flávia C Nery
Journal:  Int J Cell Biol       Date:  2012-05-06

8.  Diverse dystonin gene mutations cause distinct patterns of Dst isoform deficiency and phenotypic heterogeneity in Dystonia musculorum mice.

Authors:  Nozomu Yoshioka; Yudai Kabata; Momona Kuriyama; Norihisa Bizen; Li Zhou; Dang M Tran; Masato Yano; Atsushi Yoshiki; Tatsuo Ushiki; Thomas J Sproule; Riichiro Abe; Hirohide Takebayashi
Journal:  Dis Model Mech       Date:  2020-05-21       Impact factor: 5.758
  8 in total

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