Greensmith L - Search Results

1

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.

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

Integrins at the neuromuscular junction are important for motoneuron survival.

Wong KC, Meyer T, Harding DI, Dick JR, Vrbová G, Greensmith L. Wong KC, et al. Among authors: greensmith l. Eur J Neurosci. 1999 Sep;11(9):3287-92. doi: 10.1046/j.1460-9568.1999.00749.x. Eur J Neurosci. 1999. PMID: 10510192

5

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

6

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

7

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

8

Inhibition of calpains, by treatment with leupeptin, improves motoneuron survival and muscle function in models of motoneuron degeneration.

Kieran D, Greensmith L. Kieran D, et al. Among authors: greensmith l. Neuroscience. 2004;125(2):427-39. doi: 10.1016/j.neuroscience.2004.01.046. Neuroscience. 2004. PMID: 15062985

9

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

10

The SOD1 transgene in the G93A mouse model of amyotrophic lateral sclerosis lies on distal mouse chromosome 12.

Achilli F, Boyle S, Kieran D, Chia R, Hafezparast M, Martin JE, Schiavo G, Greensmith L, Bickmore W, Fisher EM. Achilli F, et al. Among authors: greensmith l. Amyotroph Lateral Scler Other Motor Neuron Disord. 2005 Jun;6(2):111-4. doi: 10.1080/14660820510035351. Amyotroph Lateral Scler Other Motor Neuron Disord. 2005. PMID: 16036435

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