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Items: 1 to 20 of 60

1.

What are Neurotransmitter Release Sites and Do They Interact?

Ge D, Noakes PG, Lavidis NA.

Neuroscience. 2020 Jan 15;425:157-168. doi: 10.1016/j.neuroscience.2019.11.017. Epub 2019 Nov 30. Review.

PMID:
31790671
2.

Size-Dependent Vulnerability of Lumbar Motor Neuron Dendritic Degeneration in SOD1G93A Mice.

Fogarty MJ, Mu EWH, Lavidis NA, Noakes PG, Bellingham MC.

Anat Rec (Hoboken). 2019 Sep 11. doi: 10.1002/ar.24255. [Epub ahead of print]

PMID:
31509351
3.

The Role of Altered BDNF/TrkB Signaling in Amyotrophic Lateral Sclerosis.

Pradhan J, Noakes PG, Bellingham MC.

Front Cell Neurosci. 2019 Aug 13;13:368. doi: 10.3389/fncel.2019.00368. eCollection 2019. Review.

4.

Revisiting the role of the innate immune complement system in ALS.

Parker SE, Hanton AM, Stefanou SN, Noakes PG, Woodruff TM, Lee JD.

Neurobiol Dis. 2019 Jul;127:223-232. doi: 10.1016/j.nbd.2019.03.003. Epub 2019 Mar 6. Review.

PMID:
30849511
5.

Seasonal comparison of the neuromuscular junction morphology of Bufo marinus.

Ge D, Noakes PG, Lavidis NA.

J Comp Neurol. 2019 Aug 15;527(12):1931-1939. doi: 10.1002/cne.24661. Epub 2019 Feb 25.

PMID:
30737989
6.

Complement components are upregulated and correlate with disease progression in the TDP-43Q331K mouse model of amyotrophic lateral sclerosis.

Lee JD, Levin SC, Willis EF, Li R, Woodruff TM, Noakes PG.

J Neuroinflammation. 2018 Jun 1;15(1):171. doi: 10.1186/s12974-018-1217-2.

7.

Defects in synaptic transmission at the neuromuscular junction precede motor deficits in a TDP-43Q331K transgenic mouse model of amyotrophic lateral sclerosis.

Chand KK, Lee KM, Lee JD, Qiu H, Willis EF, Lavidis NA, Hilliard MA, Noakes PG.

FASEB J. 2018 May;32(5):2676-2689. doi: 10.1096/fj.201700835R. Epub 2018 Jan 2.

PMID:
29295857
8.

Investigating Methodological Differences in the Assessment of Dendritic Morphology of Basolateral Amygdala Principal Neurons-A Comparison of Golgi-Cox and Neurobiotin Electroporation Techniques.

Klenowski PM, Wright SE, Mu EWH, Noakes PG, Lavidis NA, Bartlett SE, Bellingham MC, Fogarty MJ.

Brain Sci. 2017 Dec 19;7(12). pii: E165. doi: 10.3390/brainsci7120165.

9.

Regulated Alternative Splicing of Drosophila Dscam2 Is Necessary for Attaining the Appropriate Number of Photoreceptor Synapses.

Kerwin SK, Li JSS, Noakes PG, Shin GJ, Millard SS.

Genetics. 2018 Feb;208(2):717-728. doi: 10.1534/genetics.117.300432. Epub 2017 Dec 5.

10.

Motor Areas Show Altered Dendritic Structure in an Amyotrophic Lateral Sclerosis Mouse Model.

Fogarty MJ, Mu EWH, Lavidis NA, Noakes PG, Bellingham MC.

Front Neurosci. 2017 Nov 1;11:609. doi: 10.3389/fnins.2017.00609. eCollection 2017.

11.

Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.

Benyamin B, He J, Zhao Q, Gratten J, Garton F, Leo PJ, Liu Z, Mangelsdorf M, Al-Chalabi A, Anderson L, Butler TJ, Chen L, Chen XD, Cremin K, Deng HW, Devine M, Edson J, Fifita JA, Furlong S, Han YY, Harris J, Henders AK, Jeffree RL, Jin ZB, Li Z, Li T, Li M, Lin Y, Liu X, Marshall M, McCann EP, Mowry BJ, Ngo ST, Pamphlett R, Ran S, Reutens DC, Rowe DB, Sachdev P, Shah S, Song S, Tan LJ, Tang L, van den Berg LH, van Rheenen W, Veldink JH, Wallace RH, Wheeler L, Williams KL, Wu J, Wu X, Yang J, Yue W, Zhang ZH, Zhang D, Noakes PG, Blair IP, Henderson RD, McCombe PA, Visscher PM, Xu H, Bartlett PF, Brown MA, Wray NR, Fan D.

Nat Commun. 2017 Sep 20;8(1):611. doi: 10.1038/s41467-017-00471-1.

12.

Complement C5a-C5aR1 signalling drives skeletal muscle macrophage recruitment in the hSOD1G93A mouse model of amyotrophic lateral sclerosis.

Wang HA, Lee JD, Lee KM, Woodruff TM, Noakes PG.

Skelet Muscle. 2017 Jun 1;7(1):10. doi: 10.1186/s13395-017-0128-8.

13.

Functional decline at the aging neuromuscular junction is associated with altered laminin-α4 expression.

Lee KM, Chand KK, Hammond LA, Lavidis NA, Noakes PG.

Aging (Albany NY). 2017 Mar 14;9(3):880-899. doi: 10.18632/aging.101198.

14.

Pharmacological inhibition of complement C5a-C5a1 receptor signalling ameliorates disease pathology in the hSOD1G93A mouse model of amyotrophic lateral sclerosis.

Lee JD, Kumar V, Fung JN, Ruitenberg MJ, Noakes PG, Woodruff TM.

Br J Pharmacol. 2017 Apr;174(8):689-699. doi: 10.1111/bph.13730. Epub 2017 Mar 3.

15.

A rat model of ataxia-telangiectasia: evidence for a neurodegenerative phenotype.

Quek H, Luff J, Cheung K, Kozlov S, Gatei M, Lee CS, Bellingham MC, Noakes PG, Lim YC, Barnett NL, Dingwall S, Wolvetang E, Mashimo T, Roberts TL, Lavin MF.

Hum Mol Genet. 2017 Jan 1;26(1):109-123. doi: 10.1093/hmg/ddw371.

PMID:
28007901
16.

Loss of laminin-α4 results in pre- and postsynaptic modifications at the neuromuscular junction.

Chand KK, Lee KM, Lavidis NA, Noakes PG.

FASEB J. 2017 Apr;31(4):1323-1336. doi: 10.1096/fj.201600899R. Epub 2016 Dec 20.

PMID:
27998908
17.

Alterations in hypoglossal motor neurons due to GAD67 and VGAT deficiency in mice.

Fogarty MJ, Kanjhan R, Yanagawa Y, Noakes PG, Bellingham MC.

Exp Neurol. 2017 Mar;289:117-127. doi: 10.1016/j.expneurol.2016.12.004. Epub 2016 Dec 10.

PMID:
27956032
18.

Cortical synaptic and dendritic spine abnormalities in a presymptomatic TDP-43 model of amyotrophic lateral sclerosis.

Fogarty MJ, Klenowski PM, Lee JD, Drieberg-Thompson JR, Bartlett SE, Ngo ST, Hilliard MA, Bellingham MC, Noakes PG.

Sci Rep. 2016 Nov 29;6:37968. doi: 10.1038/srep37968.

19.

Rats with a missense mutation in Atm display neuroinflammation and neurodegeneration subsequent to accumulation of cytosolic DNA following unrepaired DNA damage.

Quek H, Luff J, Cheung K, Kozlov S, Gatei M, Lee CS, Bellingham MC, Noakes PG, Lim YC, Barnett NL, Dingwall S, Wolvetang E, Mashimo T, Roberts TL, Lavin MF.

J Leukoc Biol. 2017 Apr;101(4):927-947. doi: 10.1189/jlb.4VMA0716-316R. Epub 2016 Nov 28.

PMID:
27895165
20.

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