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5. The intermediate filament protein peripherin is the specific interaction partner of mouse BPAG1-n (dystonin) in neurons. Leung CL, Sun D, Liem RK. J Cell Biol; 1999 Feb 08; 144(3):435-46. PubMed ID: 9971739 [Abstract] [Full Text] [Related]
12. Disruption in the autophagic process underlies the sensory neuropathy in dystonia musculorum mice. Ferrier A, De Repentigny Y, Lynch-Godrei A, Gibeault S, Eid W, Kuo D, Zha X, Kothary R. Autophagy; 2015 Feb 08; 11(7):1025-36. PubMed ID: 26043942 [Abstract] [Full Text] [Related]
13. Impaired fast axonal transport in neurons of the sciatic nerves from dystonia musculorum mice. De Repentigny Y, Deschênes-Furry J, Jasmin BJ, Kothary R. J Neurochem; 2003 Aug 08; 86(3):564-71. PubMed ID: 12859670 [Abstract] [Full Text] [Related]
14. Dystonin expression in the developing nervous system predominates in the neurons that degenerate in dystonia musculorum mutant mice. Bernier G, Brown A, Dalpé G, De Repentigny Y, Mathieu M, Kothary R. Mol Cell Neurosci; 1995 Dec 08; 6(6):509-20. PubMed ID: 8742268 [Abstract] [Full Text] [Related]
18. Developmental expression of BPAG1-n: insights into the spastic ataxia and gross neurologic degeneration in dystonia musculorum mice. Dowling J, Yang Y, Wollmann R, Reichardt LF, Fuchs E. Dev Biol; 1997 Jul 15; 187(2):131-42. PubMed ID: 9242412 [Abstract] [Full Text] [Related]