Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 54


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.


Hyperexcitability in synaptic and firing activities of spinal motoneurons in an adult mouse model of amyotrophic lateral sclerosis.

Jiang MC, Adimula A, Birch D, Heckman CJ.

Neuroscience. 2017 Oct 24;362:33-46. doi: 10.1016/j.neuroscience.2017.08.041. Epub 2017 Aug 24.


Changes in the Excitability of Neocortical Neurons in a Mouse Model of Amyotrophic Lateral Sclerosis Are Not Specific to Corticospinal Neurons and Are Modulated by Advancing Disease.

Kim J, Hughes EG, Shetty AS, Arlotta P, Goff LA, Bergles DE, Brown SP.

J Neurosci. 2017 Sep 13;37(37):9037-9053. doi: 10.1523/JNEUROSCI.0811-17.2017. Epub 2017 Aug 17.


Calretinin and Neuropeptide Y interneurons are differentially altered in the motor cortex of the SOD1G93A mouse model of ALS.

Clark RM, Blizzard CA, Young KM, King AE, Dickson TC.

Sci Rep. 2017 Mar 15;7:44461. doi: 10.1038/srep44461.


An ALS-Associated Mutant SOD1 Rapidly Suppresses KCNT1 (Slack) Na+-Activated K+ Channels in Aplysia Neurons.

Zhang Y, Ni W, Horwich AL, Kaczmarek LK.

J Neurosci. 2017 Feb 22;37(8):2258-2265. doi: 10.1523/JNEUROSCI.3102-16.2017. Epub 2017 Jan 24.


Increased Synaptic Excitation and Abnormal Dendritic Structure of Prefrontal Cortex Layer V Pyramidal Neurons following Prolonged Binge-Like Consumption of Ethanol.

Klenowski PM, Fogarty MJ, Shariff M, Belmer A, Bellingham MC, Bartlett SE.

eNeuro. 2016 Dec 23;3(6). pii: ENEURO.0248-16.2016. doi: 10.1523/ENEURO.0248-16.2016. eCollection 2016 Nov-Dec.


Gamma motor neurons survive and exacerbate alpha motor neuron degeneration in ALS.

Lalancette-Hebert M, Sharma A, Lyashchenko AK, Shneider NA.

Proc Natl Acad Sci U S A. 2016 Dec 20;113(51):E8316-E8325. doi: 10.1073/pnas.1605210113. Epub 2016 Dec 7.


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.


Axonal Excitability in Amyotrophic Lateral Sclerosis : Axonal Excitability in ALS.

Park SB, Kiernan MC, Vucic S.

Neurotherapeutics. 2017 Jan;14(1):78-90. doi: 10.1007/s13311-016-0492-9. Review.


Voltage-gated calcium channels are abnormal in cultured spinal motoneurons in the G93A-SOD1 transgenic mouse model of ALS.

Chang Q, Martin LJ.

Neurobiol Dis. 2016 Sep;93:78-95. doi: 10.1016/j.nbd.2016.04.009. Epub 2016 May 2.


INaP selective inhibition reverts precocious inter- and motorneurons hyperexcitability in the Sod1-G93R zebrafish ALS model.

Benedetti L, Ghilardi A, Rottoli E, De Maglie M, Prosperi L, Perego C, Baruscotti M, Bucchi A, Del Giacco L, Francolini M.

Sci Rep. 2016 Apr 15;6:24515. doi: 10.1038/srep24515.


Mutant SOD1 protein increases Nav1.3 channel excitability.

Kubat Öktem E, Mruk K, Chang J, Akin A, Kobertz WR, Brown RH Jr.

J Biol Phys. 2016 Jun;42(3):351-70. doi: 10.1007/s10867-016-9411-x. Epub 2016 Apr 12. Erratum in: J Biol Phys. 2016 Jun;42(3):371.


Modeling ALS with motor neurons derived from human induced pluripotent stem cells.

Sances S, Bruijn LI, Chandran S, Eggan K, Ho R, Klim JR, Livesey MR, Lowry E, Macklis JD, Rushton D, Sadegh C, Sareen D, Wichterle H, Zhang SC, Svendsen CN.

Nat Neurosci. 2016 Apr;19(4):542-53. doi: 10.1038/nn.4273. Review.


Inducing Chronic Excitotoxicity in the Mouse Spinal Cord to Investigate Lower Motor Neuron Degeneration.

Blizzard CA, Lee KM, Dickson TC.

Front Neurosci. 2016 Mar 2;10:76. doi: 10.3389/fnins.2016.00076. eCollection 2016.


Emerging Roles of Filopodia and Dendritic Spines in Motoneuron Plasticity during Development and Disease.

Kanjhan R, Noakes PG, Bellingham MC.

Neural Plast. 2016;2016:3423267. doi: 10.1155/2016/3423267. Epub 2015 Dec 30. Review.


Is hyperexcitability really guilty in amyotrophic lateral sclerosis?

Leroy F, Zytnicki D.

Neural Regen Res. 2015 Sep;10(9):1413-5. doi: 10.4103/1673-5374.165308. No abstract available.


Developmental changes in the morphology of mouse hypoglossal motor neurons.

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

Brain Struct Funct. 2016 Sep;221(7):3755-86. doi: 10.1007/s00429-015-1130-8. Epub 2015 Oct 17.


Reactive oxygen species trigger motoneuron death in non-cell-autonomous models of ALS through activation of c-Abl signaling.

Rojas F, Gonzalez D, Cortes N, Ampuero E, Hernández DE, Fritz E, Abarzua S, Martinez A, Elorza AA, Alvarez A, Court F, van Zundert B.

Front Cell Neurosci. 2015 Jun 9;9:203. doi: 10.3389/fncel.2015.00203. eCollection 2015.


Postactivation depression of the Ia EPSP in motoneurons is reduced in both the G127X SOD1 model of amyotrophic lateral sclerosis and in aged mice.

Hedegaard A, Lehnhoff J, Moldovan M, Grøndahl L, Petersen NC, Meehan CF.

J Neurophysiol. 2015 Aug;114(2):1196-210. doi: 10.1152/jn.00745.2014. Epub 2015 Jun 17.

Supplemental Content

Support Center