Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 116

Similar articles for PubMed (Select 18782598)


Low Ca2+ buffering in hypoglossal motoneurons of mutant SOD1 (G93A) mice.

von Lewinski F, Fuchs J, Vanselow BK, Keller BU.

Neurosci Lett. 2008 Nov 21;445(3):224-8. doi: 10.1016/j.neulet.2008.08.084. Epub 2008 Sep 3.


SOD1 silencing in motoneurons or glia rescues neuromuscular function in ALS mice.

Dirren E, Aebischer J, Rochat C, Towne C, Schneider BL, Aebischer P.

Ann Clin Transl Neurol. 2015 Feb;2(2):167-84. doi: 10.1002/acn3.162. Epub 2015 Jan 15.


Homeostatic dysregulation in membrane properties of masticatory motoneurons compared with oculomotor neurons in a mouse model for amyotrophic lateral sclerosis.

Venugopal S, Hsiao CF, Sonoda T, Wiedau-Pazos M, Chandler SH.

J Neurosci. 2015 Jan 14;35(2):707-20. doi: 10.1523/JNEUROSCI.1682-14.2015.


Early intrinsic hyperexcitability does not contribute to motoneuron degeneration in amyotrophic lateral sclerosis.

Leroy F, Lamotte d'Incamps B, Imhoff-Manuel RD, Zytnicki D.

Elife. 2014 Oct 14;3. doi: 10.7554/eLife.04046.


Soma size and Cav1.3 channel expression in vulnerable and resistant motoneuron populations of the SOD1G93A mouse model of ALS.

Shoenfeld L, Westenbroek RE, Fisher E, Quinlan KA, Tysseling VM, Powers RK, Heckman CJ, Binder MD.

Physiol Rep. 2014 Aug 7;2(8). pii: e12113. doi: 10.14814/phy2.12113. Print 2014 Aug 1.


Mutant SOD1-expressing astrocytes release toxic factors that trigger motoneuron death by inducing hyperexcitability.

Fritz E, Izaurieta P, Weiss A, Mir FR, Rojas P, Gonzalez D, Rojas F, Brown RH Jr, Madrid R, van Zundert B.

J Neurophysiol. 2013 Jun;109(11):2803-14. doi: 10.1152/jn.00500.2012. Epub 2013 Mar 13.


Selective mitochondrial Ca2+ uptake deficit in disease endstage vulnerable motoneurons of the SOD1G93A mouse model of amyotrophic lateral sclerosis.

Fuchs A, Kutterer S, Mühling T, Duda J, Schütz B, Liss B, Keller BU, Roeper J.

J Physiol. 2013 May 15;591(Pt 10):2723-45. doi: 10.1113/jphysiol.2012.247981. Epub 2013 Feb 11.


Talampanel reduces the level of motoneuronal calcium in transgenic mutant SOD1 mice only if applied presymptomatically.

Paizs M, Tortarolo M, Bendotti C, Engelhardt JI, Siklós L.

Amyotroph Lateral Scler. 2011 Sep;12(5):340-4. doi: 10.3109/17482968.2011.584627. Epub 2011 May 30.


Altered postnatal maturation of electrical properties in spinal motoneurons in a mouse model of amyotrophic lateral sclerosis.

Quinlan KA, Schuster JE, Fu R, Siddique T, Heckman CJ.

J Physiol. 2011 May 1;589(Pt 9):2245-60. doi: 10.1113/jphysiol.2010.200659. Epub 2011 Feb 28.


Downregulation of the potassium chloride cotransporter KCC2 in vulnerable motoneurons in the SOD1-G93A mouse model of amyotrophic lateral sclerosis.

Fuchs A, Ringer C, Bilkei-Gorzo A, Weihe E, Roeper J, Schütz B.

J Neuropathol Exp Neurol. 2010 Oct;69(10):1057-70. doi: 10.1097/NEN.0b013e3181f4dcef.


Hypoglossal motor neurons display a reduced calcium increase after axotomy in mice with upregulated parvalbumin.

Paizs M, Engelhardt JI, Katarova Z, Siklós L.

J Comp Neurol. 2010 Jun 1;518(11):1946-61. doi: 10.1002/cne.22312.


The proinflammatory action of microglial P2 receptors is enhanced in SOD1 models for amyotrophic lateral sclerosis.

D'Ambrosi N, Finocchi P, Apolloni S, Cozzolino M, Ferri A, Padovano V, Pietrini G, Carrì MT, Volonté C.

J Immunol. 2009 Oct 1;183(7):4648-56. doi: 10.4049/jimmunol.0901212. Epub 2009 Sep 4.


Intra-bone marrow-bone marrow transplantation slows disease progression and prolongs survival in G93A mutant SOD1 transgenic mice, an animal model mouse for amyotrophic lateral sclerosis.

Ohnishi S, Ito H, Suzuki Y, Adachi Y, Wate R, Zhang J, Nakano S, Kusaka H, Ikehara S.

Brain Res. 2009 Nov 3;1296:216-24. doi: 10.1016/j.brainres.2009.08.012. Epub 2009 Aug 15.


Dysregulation of intracellular copper trafficking pathway in a mouse model of mutant copper/zinc superoxide dismutase-linked familial amyotrophic lateral sclerosis.

Tokuda E, Okawa E, Ono S.

J Neurochem. 2009 Oct;111(1):181-91. doi: 10.1111/j.1471-4159.2009.06310.x. Epub 2009 Jul 27.


Cytosolic TDP-43 expression following axotomy is associated with caspase 3 activation in NFL-/- mice: support for a role for TDP-43 in the physiological response to neuronal injury.

Moisse K, Mepham J, Volkening K, Welch I, Hill T, Strong MJ.

Brain Res. 2009 Nov 3;1296:176-86. doi: 10.1016/j.brainres.2009.07.023. Epub 2009 Jul 18.


Disease-dependent reciprocal phosphorylation of serine and tyrosine residues of c-Met/HGF receptor contributes disease retardation of a transgenic mouse model of ALS.

Kadoyama K, Funakoshi H, Ohya-Shimada W, Nakamura T, Matsumoto K, Matsuyama S, Nakamura T.

Neurosci Res. 2009 Oct;65(2):194-200. doi: 10.1016/j.neures.2009.06.016. Epub 2009 Jul 10.


Familial amyotrophic lateral sclerosis-linked mutant SOD1 aberrantly interacts with tubulin.

Kabuta T, Kinugawa A, Tsuchiya Y, Kabuta C, Setsuie R, Tateno M, Araki T, Wada K.

Biochem Biophys Res Commun. 2009 Sep 11;387(1):121-6. doi: 10.1016/j.bbrc.2009.06.138. Epub 2009 Jul 1.


Impairment of mitochondrial calcium handling in a mtSOD1 cell culture model of motoneuron disease.

Jaiswal MK, Zech WD, Goos M, Leutbecher C, Ferri A, Zippelius A, Carrì MT, Nau R, Keller BU.

BMC Neurosci. 2009 Jun 22;10:64. doi: 10.1186/1471-2202-10-64.


Immunohistochemical localization of insulin-like growth factor binding protein 2 in the central nervous system of SOD1(G93A) transgenic mice.

Sim SE, Chung YH, Jeong JH, Yun SW, Lim HS, Kim D, Kim SS, Lee WB, Cha CI.

J Mol Histol. 2009 Apr;40(2):157-63. doi: 10.1007/s10735-009-9219-0. Epub 2009 May 26.


Pre-symptomatic alterations in subcellular betaCGRP distribution in motor neurons precede astrogliosis in ALS mice.

Ringer C, Weihe E, Schütz B.

Neurobiol Dis. 2009 Aug;35(2):286-95. doi: 10.1016/j.nbd.2009.05.011. Epub 2009 May 22.

Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk