The Shortest Isoform of Dystrophin (Dp40) Interacts with a Group of Presynaptic Proteins to Form a Presumptive Novel Complex in the Mouse Brain-Reference-Cited by-同舟云学术

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The Shortest Isoform of Dystrophin (Dp40) Interacts with a Group of Presynaptic Proteins to Form a Presumptive Novel Complex in the Mouse Brain

Published:2012-01-19 Issue:2 Volume:45 Page:287-297
ISSN:0893-7648
Container-title:Molecular Neurobiology
language:en
Short-container-title:Mol Neurobiol

Author:

Tozawa Takenori,Itoh Kyoko,Yaoi Takeshi,Tando So,Umekage Masafumi,Dai Hongmei,Hosoi Hajime,Fushiki Shinji

Publisher

Springer Science and Business Media LLC

Subject

Neuroscience (miscellaneous),Cellular and Molecular Neuroscience,Neurology

Link

http://www.springerlink.com/index/pdf/10.1007/s12035-012-8233-5

Reference35 articles.

1. Emery AEH (1987) Central nervous system. In: Motulsky AG (ed) Duchenne muscular dystrophy 2. Oxford University Press, New York, p 99

2. Bresolin N, Castelli E, Comi GP et al (1994) Cognitive impairment in Duchenne muscular dystrophy. Neuromuscul Disord 4:359–369

3. Wicksell RK, Kihlgren M, Melin L, Eeg-Olofsson O (2004) Specific cognitive deficits are common in children with Duchenne muscular dystrophy. Dev Med Child Neurol 46:154–159

4. Billard C, Gillet P, Signoret JL et al (1992) Cognitive functions in Duchenne muscular dystrophy: a reappraisal and comparison with spinal muscular atrophy. Neuromuscul Disord 2:371–378

5. Lederfein D, Levy Z, Augier N et al (1992) A 71-kilodalton protein is a major product of the Duchenne muscular dystrophy gene in brain and other nonmuscle tissues. Proc Natl Acad Sci USA 89:5346–5350

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2. Dystrophin- and Utrophin-Based Therapeutic Approaches for Treatment of Duchenne Muscular Dystrophy: A Comparative Review;BioDrugs;2023-11-02

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4. Ion Channels of the Sarcolemma and Intracellular Organelles in Duchenne Muscular Dystrophy: A Role in the Dysregulation of Ion Homeostasis and a Possible Target for Therapy;International Journal of Molecular Sciences;2023-01-23

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