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Results: 1 to 20 of 127

1.

Cannabinol delays symptom onset in SOD1 (G93A) transgenic mice without affecting survival.

Weydt P, Hong S, Witting A, Möller T, Stella N, Kliot M.

Amyotroph Lateral Scler Other Motor Neuron Disord. 2005 Sep;6(3):182-4.

PMID:
16183560
[PubMed - indexed for MEDLINE]
2.

Amyotrophic lateral sclerosis: delayed disease progression in mice by treatment with a cannabinoid.

Raman C, McAllister SD, Rizvi G, Patel SG, Moore DH, Abood ME.

Amyotroph Lateral Scler Other Motor Neuron Disord. 2004 Mar;5(1):33-9.

PMID:
15204022
[PubMed - indexed for MEDLINE]
3.

Therapeutic immunization with a glatiramer acetate derivative does not alter survival in G93A and G37R SOD1 mouse models of familial ALS.

Haenggeli C, Julien JP, Mosley RL, Perez N, Dhar A, Gendelman HE, Rothstein JD.

Neurobiol Dis. 2007 Apr;26(1):146-52. Epub 2006 Dec 30.

PMID:
17276077
[PubMed - indexed for MEDLINE]
4.

In vivo quantification of spinal and bulbar motor neuron degeneration in the G93A-SOD1 transgenic mouse model of ALS by T2 relaxation time and apparent diffusion coefficient.

Niessen HG, Angenstein F, Sander K, Kunz WS, Teuchert M, Ludolph AC, Heinze HJ, Scheich H, Vielhaber S.

Exp Neurol. 2006 Oct;201(2):293-300. Epub 2006 Jun 5.

PMID:
16740261
[PubMed - indexed for MEDLINE]
5.

Pyruvate slows disease progression in a G93A SOD1 mutant transgenic mouse model.

Park JH, Hong YH, Kim HJ, Kim SM, Kim MJ, Park KS, Sung JJ, Lee KW.

Neurosci Lett. 2007 Feb 21;413(3):265-9. Epub 2006 Dec 13.

PMID:
17174029
[PubMed - indexed for MEDLINE]
6.

Overexpression of Abeta is associated with acceleration of onset of motor impairment and superoxide dismutase 1 aggregation in an amyotrophic lateral sclerosis mouse model.

Li QX, Mok SS, Laughton KM, McLean CA, Volitakis I, Cherny RA, Cheung NS, White AR, Masters CL.

Aging Cell. 2006 Apr;5(2):153-65.

PMID:
16626394
[PubMed - indexed for MEDLINE]
7.

Vacuolization correlates with spin-spin relaxation time in motor brainstem nuclei and behavioural tests in the transgenic G93A-SOD1 mouse model of ALS.

Bucher S, Braunstein KE, Niessen HG, Kaulisch T, Neumaier M, Boeckers TM, Stiller D, Ludolph AC.

Eur J Neurosci. 2007 Oct;26(7):1895-901. Epub 2007 Sep 14.

PMID:
17868365
[PubMed - indexed for MEDLINE]
8.

Metabolic progression markers of neurodegeneration in the transgenic G93A-SOD1 mouse model of amyotrophic lateral sclerosis.

Niessen HG, Debska-Vielhaber G, Sander K, Angenstein F, Ludolph AC, Hilfert L, Willker W, Leibfritz D, Heinze HJ, Kunz WS, Vielhaber S.

Eur J Neurosci. 2007 Mar;25(6):1669-77.

PMID:
17432958
[PubMed - indexed for MEDLINE]
9.

AM1241, a cannabinoid CB2 receptor selective compound, delays disease progression in a mouse model of amyotrophic lateral sclerosis.

Kim K, Moore DH, Makriyannis A, Abood ME.

Eur J Pharmacol. 2006 Aug 7;542(1-3):100-5. Epub 2006 May 20.

PMID:
16781706
[PubMed - indexed for MEDLINE]
10.

Background and gender effects on survival in the TgN(SOD1-G93A)1Gur mouse model of ALS.

Heiman-Patterson TD, Deitch JS, Blankenhorn EP, Erwin KL, Perreault MJ, Alexander BK, Byers N, Toman I, Alexander GM.

J Neurol Sci. 2005 Sep 15;236(1-2):1-7.

PMID:
16024047
[PubMed - indexed for MEDLINE]
11.

Over-expression of Hsp27 does not influence disease in the mutant SOD1(G93A) mouse model of amyotrophic lateral sclerosis.

Krishnan J, Vannuvel K, Andries M, Waelkens E, Robberecht W, Van Den Bosch L.

J Neurochem. 2008 Sep;106(5):2170-83. doi: 10.1111/j.1471-4159.2008.05545.x. Epub 2008 Jul 4.

PMID:
18624915
[PubMed - indexed for MEDLINE]
12.

Vascular endothelial growth factor prolongs survival in a transgenic mouse model of ALS.

Zheng C, Nennesmo I, Fadeel B, Henter JI.

Ann Neurol. 2004 Oct;56(4):564-7.

PMID:
15389897
[PubMed - indexed for MEDLINE]
13.

Memantine prolongs survival in an amyotrophic lateral sclerosis mouse model.

Wang R, Zhang D.

Eur J Neurosci. 2005 Nov;22(9):2376-80.

PMID:
16262676
[PubMed - indexed for MEDLINE]
14.

Sex-specific behavioural effects of environmental enrichment in a transgenic mouse model of amyotrophic lateral sclerosis.

Stam NC, Nithianantharajah J, Howard ML, Atkin JD, Cheema SS, Hannan AJ.

Eur J Neurosci. 2008 Aug;28(4):717-23. doi: 10.1111/j.1460-9568.2008.06374.x.

PMID:
18702691
[PubMed - indexed for MEDLINE]
15.

Recombinant human erythropoietin suppresses symptom onset and progression of G93A-SOD1 mouse model of ALS by preventing motor neuron death and inflammation.

Koh SH, Kim Y, Kim HY, Cho GW, Kim KS, Kim SH.

Eur J Neurosci. 2007 Apr;25(7):1923-30.

PMID:
17439481
[PubMed - indexed for MEDLINE]
16.

Human mesenchymal stromal cells ameliorate the phenotype of SOD1-G93A ALS mice.

Zhao CP, Zhang C, Zhou SN, Xie YM, Wang YH, Huang H, Shang YC, Li WY, Zhou C, Yu MJ, Feng SW.

Cytotherapy. 2007;9(5):414-26.

PMID:
17786603
[PubMed - indexed for MEDLINE]
17.

Protective effects of heat shock protein 27 in a model of ALS occur in the early stages of disease progression.

Sharp PS, Akbar MT, Bouri S, Senda A, Joshi K, Chen HJ, Latchman DS, Wells DJ, de Belleroche J.

Neurobiol Dis. 2008 Apr;30(1):42-55. doi: 10.1016/j.nbd.2007.12.002. Epub 2007 Dec 23.

PMID:
18255302
[PubMed - indexed for MEDLINE]
18.

Muscle-derived but not centrally derived transgene GDNF is neuroprotective in G93A-SOD1 mouse model of ALS.

Li W, Brakefield D, Pan Y, Hunter D, Myckatyn TM, Parsadanian A.

Exp Neurol. 2007 Feb;203(2):457-71. Epub 2006 Oct 10.

PMID:
17034790
[PubMed - indexed for MEDLINE]
19.

Thalidomide and lenalidomide extend survival in a transgenic mouse model of amyotrophic lateral sclerosis.

Kiaei M, Petri S, Kipiani K, Gardian G, Choi DK, Chen J, Calingasan NY, Schafer P, Muller GW, Stewart C, Hensley K, Beal MF.

J Neurosci. 2006 Mar 1;26(9):2467-73.

PMID:
16510725
[PubMed - indexed for MEDLINE]
Free Article
20.

Immunosuppressant FK506 does not exert beneficial effects in symptomatic G93A superoxide dismutase-1 transgenic mice.

Anneser JM, Gmerek A, Gerkrath J, Borasio GD, Heumann R.

Neuroreport. 2001 Aug 28;12(12):2663-5.

PMID:
11522944
[PubMed - indexed for MEDLINE]

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