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Journal Abstract Search
211 related items for PubMed ID: 22606355
1. Dihydrotestosterone ameliorates degeneration in muscle, axons and motoneurons and improves motor function in amyotrophic lateral sclerosis model mice. Yoo YE, Ko CP. PLoS One; 2012; 7(5):e37258. PubMed ID: 22606355 [Abstract] [Full Text] [Related]
7. A Novel Iron Chelator-Radical Scavenger Ameliorates Motor Dysfunction and Improves Life Span and Mitochondrial Biogenesis in SOD1G93A ALS Mice. Golko-Perez S, Amit T, Bar-Am O, Youdim MB, Weinreb O. Neurotox Res; 2017 Feb; 31(2):230-244. PubMed ID: 27826939 [Abstract] [Full Text] [Related]
8. Mechano-growth factor, an IGF-I splice variant, rescues motoneurons and improves muscle function in SOD1(G93A) mice. Riddoch-Contreras J, Yang SY, Dick JR, Goldspink G, Orrell RW, Greensmith L. Exp Neurol; 2009 Feb; 215(2):281-9. PubMed ID: 19038252 [Abstract] [Full Text] [Related]
9. Neuroprotective effects of glial cell line-derived neurotrophic factor mediated by an adeno-associated virus vector in a transgenic animal model of amyotrophic lateral sclerosis. Wang LJ, Lu YY, Muramatsu S, Ikeguchi K, Fujimoto K, Okada T, Mizukami H, Matsushita T, Hanazono Y, Kume A, Nagatsu T, Ozawa K, Nakano I. J Neurosci; 2002 Aug 15; 22(16):6920-8. PubMed ID: 12177190 [Abstract] [Full Text] [Related]
10. Axonal degeneration, distal collateral branching and neuromuscular junction architecture alterations occur prior to symptom onset in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis. Clark JA, Southam KA, Blizzard CA, King AE, Dickson TC. J Chem Neuroanat; 2016 Oct 15; 76(Pt A):35-47. PubMed ID: 27038603 [Abstract] [Full Text] [Related]
12. Epothilone D accelerates disease progression in the SOD1G93A mouse model of amyotrophic lateral sclerosis. Clark JA, Blizzard CA, Breslin MC, Yeaman EJ, Lee KM, Chuckowree JA, Dickson TC. Neuropathol Appl Neurobiol; 2018 Oct 15; 44(6):590-605. PubMed ID: 29380402 [Abstract] [Full Text] [Related]
15. Bisperoxovanadium promotes motor neuron survival and neuromuscular innervation in amyotrophic lateral sclerosis. Wang J, Tierney L, Mann R, Lonsway T, Walker CL. Mol Brain; 2021 Oct 11; 14(1):155. PubMed ID: 34635126 [Abstract] [Full Text] [Related]
16. Progressive impairment of CaV1.1 function in the skeletal muscle of mice expressing a mutant type 1 Cu/Zn superoxide dismutase (G93A) linked to amyotrophic lateral sclerosis. Beqollari D, Romberg CF, Dobrowolny G, Martini M, Voss AA, Musarò A, Bannister RA. Skelet Muscle; 2016 Oct 11; 6():24. PubMed ID: 27340545 [Abstract] [Full Text] [Related]
17. The anabolic/androgenic steroid nandrolone exacerbates gene expression modifications induced by mutant SOD1 in muscles of mice models of amyotrophic lateral sclerosis. Galbiati M, Onesto E, Zito A, Crippa V, Rusmini P, Mariotti R, Bentivoglio M, Bendotti C, Poletti A. Pharmacol Res; 2012 Feb 11; 65(2):221-30. PubMed ID: 22178654 [Abstract] [Full Text] [Related]
19. Intranasal delivery of insulin and a nitric oxide synthase inhibitor in an experimental model of amyotrophic lateral sclerosis. Martinez JA, Francis GJ, Liu WQ, Pradzinsky N, Fine J, Wilson M, Hanson LR, Frey WH, Zochodne D, Gordon T, Toth C. Neuroscience; 2008 Dec 10; 157(4):908-25. PubMed ID: 18951954 [Abstract] [Full Text] [Related]
20. Functional over-load saves motor units in the SOD1-G93A transgenic mouse model of amyotrophic lateral sclerosis. Gordon T, Tyreman N, Li S, Putman CT, Hegedus J. Neurobiol Dis; 2010 Feb 10; 37(2):412-22. PubMed ID: 19879358 [Abstract] [Full Text] [Related] Page: [Next] [New Search]