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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1984 2
1985 3
1986 13
1987 6
1988 7
1989 11
1990 11
1991 25
1992 12
1993 18
1994 23
1995 20
1996 18
1997 19
1998 33
1999 38
2000 37
2001 32
2002 20
2003 23
2004 16
2005 11
2006 18
2007 15
2008 8
2009 4
2010 9
2011 20
2012 22
2013 13
2014 19
2015 17
2016 27
2017 15
2018 25
2019 13
2020 0
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589 results
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Page 1
Novel mutations in dystonin provide clues to the pathomechanisms of HSAN-VI.
Manganelli F, Parisi S, Nolano M, Tao F, Paladino S, Pisciotta C, Tozza S, Nesti C, Rebelo AP, Provitera V, Santorelli FM, Shy ME, Russo T, Zuchner S, Santoro L. Manganelli F, et al. Neurology. 2017 May 30;88(22):2132-2140. doi: 10.1212/WNL.0000000000003992. Epub 2017 May 3. Neurology. 2017. PMID: 28468842 Free PMC article.
Cellular and molecular biology of neuronal dystonin.
Ferrier A, Boyer JG, Kothary R. Ferrier A, et al. Int Rev Cell Mol Biol. 2013;300:85-120. doi: 10.1016/B978-0-12-405210-9.00003-5. Int Rev Cell Mol Biol. 2013. PMID: 23273860 Review.
Dystonin is essential for maintaining neuronal cytoskeleton organization.
Dalpé G, Leclerc N, Vallée A, Messer A, Mathieu M, De Repentigny Y, Kothary R. Dalpé G, et al. Mol Cell Neurosci. 1998 Apr;10(5-6):243-57. doi: 10.1006/mcne.1997.0660. Mol Cell Neurosci. 1998. PMID: 9604204
Transgenic expression of neuronal dystonin isoform 2 partially rescues the disease phenotype of the dystonia musculorum mouse model of hereditary sensory autonomic neuropathy VI.
Ferrier A, Sato T, De Repentigny Y, Gibeault S, Bhanot K, O'Meara RW, Lynch-Godrei A, Kornfeld SF, Young KG, Kothary R. Ferrier A, et al. Hum Mol Genet. 2014 May 15;23(10):2694-710. doi: 10.1093/hmg/ddt663. Epub 2013 Dec 30. Hum Mol Genet. 2014. PMID: 24381311 Free PMC article.
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