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Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophy.
Neurology. 2012 May 29;78(22):1714-20. doi: 10.1212/WNL.0b013e3182556c05. Epub 2012 Mar 28.
Neurology. 2012.
PMID: 22459677
Free PMC article.
Mitofusin2 mutations disrupt axonal mitochondrial positioning and promote axon degeneration.
Misko AL, Sasaki Y, Tuck E, Milbrandt J, Baloh RH.
Misko AL, et al.
J Neurosci. 2012 Mar 21;32(12):4145-55. doi: 10.1523/JNEUROSCI.6338-11.2012.
J Neurosci. 2012.
PMID: 22442078
Free PMC article.
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Myofibrillar disruption and RNA-binding protein aggregation in a mouse model of limb-girdle muscular dystrophy 1D.
Bengoechea R, Pittman SK, Tuck EP, True HL, Weihl CC.
Bengoechea R, et al. Among authors: tuck ep.
Hum Mol Genet. 2015 Dec 1;24(23):6588-602. doi: 10.1093/hmg/ddv363. Epub 2015 Sep 11.
Hum Mol Genet. 2015.
PMID: 26362252
Free PMC article.
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Roles of membrane trafficking in nerve repair and regeneration.
Tuck E, Cavalli V.
Tuck E, et al.
Commun Integr Biol. 2010 May;3(3):209-14. doi: 10.4161/cib.3.3.11555.
Commun Integr Biol. 2010.
PMID: 20714395
Free PMC article.
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