Greensmith L - Search Results

1

HDAC4-myogenin axis as an important marker of HD-related skeletal muscle atrophy.

Mielcarek M, Toczek M, Smeets CJ, Franklin SA, Bondulich MK, Jolinon N, Muller T, Ahmed M, Dick JR, Piotrowska I, Greensmith L, Smolenski RT, Bates GP. Mielcarek M, et al. Among authors: greensmith l. PLoS Genet. 2015 Mar 6;11(3):e1005021. doi: 10.1371/journal.pgen.1005021. eCollection 2015 Mar. PLoS Genet. 2015. PMID: 25748626 Free PMC article.

2

Blocking of NMDA receptors during a critical stage of development reduces the effects of nerve injury at birth on muscles and motoneurones.

Dick J, Greensmith L, Vrbova G. Dick J, et al. Among authors: greensmith l. Neuromuscul Disord. 1995 Sep;5(5):371-82. doi: 10.1016/0960-8966(94)00088-q. Neuromuscul Disord. 1995. PMID: 7496171

3

Induction of transmitter release at the neuromuscular junction prevents motoneuron death after axotomy in neonatal rats.

Greensmith L, Dick J, Emanuel AO, Vrbová G. Greensmith L, et al. Neuroscience. 1996 Mar;71(1):213-20. doi: 10.1016/0306-4522(95)00446-7. Neuroscience. 1996. PMID: 8834403

4

Manipulating transmitter release at the neuromuscular junction of neonatal rats alters the expression of ChAT and GAP-43 in motoneurons.

Sharp PS, Dekkers J, Dick JR, Greensmith L. Sharp PS, et al. Among authors: greensmith l. Brain Res Dev Brain Res. 2003 Dec 19;146(1-2):29-38. doi: 10.1016/j.devbrainres.2003.09.005. Brain Res Dev Brain Res. 2003. PMID: 14643009

5

Over-expression of parvalbumin in transgenic mice rescues motoneurons from injury-induced cell death.

Dekkers J, Bayley P, Dick JR, Schwaller B, Berchtold MW, Greensmith L. Dekkers J, et al. Among authors: greensmith l. Neuroscience. 2004;123(2):459-66. doi: 10.1016/j.neuroscience.2003.07.013. Neuroscience. 2004. PMID: 14698753

6

Treatment with arimoclomol, a coinducer of heat shock proteins, delays disease progression in ALS mice.

Kieran D, Kalmar B, Dick JR, Riddoch-Contreras J, Burnstock G, Greensmith L. Kieran D, et al. Among authors: greensmith l. Nat Med. 2004 Apr;10(4):402-5. doi: 10.1038/nm1021. Epub 2004 Mar 21. Nat Med. 2004. PMID: 15034571

7

The effect of peripheral nerve injury on disease progression in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.

Sharp PS, Dick JR, Greensmith L. Sharp PS, et al. Among authors: greensmith l. Neuroscience. 2005;130(4):897-910. doi: 10.1016/j.neuroscience.2004.09.069. Neuroscience. 2005. PMID: 15652988

8

A mutation in dynein rescues axonal transport defects and extends the life span of ALS mice.

Kieran D, Hafezparast M, Bohnert S, Dick JR, Martin J, Schiavo G, Fisher EM, Greensmith L. Kieran D, et al. Among authors: greensmith l. J Cell Biol. 2005 May 23;169(4):561-7. doi: 10.1083/jcb.200501085. J Cell Biol. 2005. PMID: 15911875 Free PMC article.

9

Increasing cannabinoid levels by pharmacological and genetic manipulation delay disease progression in SOD1 mice.

Bilsland LG, Dick JR, Pryce G, Petrosino S, Di Marzo V, Baker D, Greensmith L. Bilsland LG, et al. Among authors: greensmith l. FASEB J. 2006 May;20(7):1003-5. doi: 10.1096/fj.05-4743fje. Epub 2006 Mar 29. FASEB J. 2006. PMID: 16571781

10

Mechano-growth factor, an IGF-I splice variant, rescues motoneurons and improves muscle function in SOD1(G93A) mice.

Riddoch-Contreras J, Yang SY, Dick JR, Goldspink G, Orrell RW, Greensmith L. Riddoch-Contreras J, et al. Among authors: greensmith l. Exp Neurol. 2009 Feb;215(2):281-9. doi: 10.1016/j.expneurol.2008.10.014. Epub 2008 Nov 7. Exp Neurol. 2009. PMID: 19038252

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