150 related articles for article (PubMed ID: 28697486)
21. Neuromuscular electrical stimulation improves skeletal muscle regeneration through satellite cell fusion with myofibers in healthy elderly subjects.
Di Filippo ES; Mancinelli R; Marrone M; Doria C; Verratti V; Toniolo L; Dantas JL; Fulle S; Pietrangelo T
J Appl Physiol (1985); 2017 Sep; 123(3):501-512. PubMed ID: 28572500
[TBL] [Abstract][Full Text] [Related]
22. Weakness of whole muscles in mice deficient in Cu, Zn superoxide dismutase is not explained by defects at the level of the contractile apparatus.
Larkin LM; Hanes MC; Kayupov E; Claflin DR; Faulkner JA; Brooks SV
Age (Dordr); 2013 Aug; 35(4):1173-81. PubMed ID: 22696118
[TBL] [Abstract][Full Text] [Related]
23. Ts65Dn, a mouse model of Down syndrome, exhibits increased GABAB-induced potassium current.
Best TK; Siarey RJ; Galdzicki Z
J Neurophysiol; 2007 Jan; 97(1):892-900. PubMed ID: 17093127
[TBL] [Abstract][Full Text] [Related]
24. Involvement of Potassium and Cation Channels in Hippocampal Abnormalities of Embryonic Ts65Dn and Tc1 Trisomic Mice.
Stern S; Segal M; Moses E
EBioMedicine; 2015 Sep; 2(9):1048-62. PubMed ID: 26501103
[TBL] [Abstract][Full Text] [Related]
25. Neonatal mice of the Down syndrome model, Ts65Dn, exhibit upregulated VIP measures and reduced responsiveness of cortical astrocytes to VIP stimulation.
Sahir N; Brenneman DE; Hill JM
J Mol Neurosci; 2006; 30(3):329-40. PubMed ID: 17401158
[TBL] [Abstract][Full Text] [Related]
26. Elevated expression of the G-protein-activated inwardly rectifying potassium channel 2 (GIRK2) in cerebellar unipolar brush cells of a Down syndrome mouse model.
Harashima C; Jacobowitz DM; Stoffel M; Chakrabarti L; Haydar TF; Siarey RJ; Galdzicki Z
Cell Mol Neurobiol; 2006; 26(4-6):719-34. PubMed ID: 16783527
[TBL] [Abstract][Full Text] [Related]
27. Intracellular oxidant activity, antioxidant enzyme defense system, and cell senescence in fibroblasts with trisomy 21.
Rodríguez-Sureda V; Vilches Á; Sánchez O; Audí L; Domínguez C
Oxid Med Cell Longev; 2015; 2015():509241. PubMed ID: 25852816
[TBL] [Abstract][Full Text] [Related]
28. Disruption of bone development and homeostasis by trisomy in Ts65Dn Down syndrome mice.
Blazek JD; Gaddy A; Meyer R; Roper RJ; Li J
Bone; 2011 Feb; 48(2):275-80. PubMed ID: 20870049
[TBL] [Abstract][Full Text] [Related]
29. Decreased cell proliferation and higher oxidative stress in fibroblasts from Down Syndrome fetuses. Preliminary study.
Gimeno A; García-Giménez JL; Audí L; Toran N; Andaluz P; Dasí F; Viña J; Pallardó FV
Biochim Biophys Acta; 2014 Jan; 1842(1):116-25. PubMed ID: 24184606
[TBL] [Abstract][Full Text] [Related]
30. Adaptive changes in structure of skeletal muscles from adult Sod1 homozygous knockout mice.
Kostrominova TY; Pasyk KA; Van Remmen H; Richardson AG; Faulkner JA
Cell Tissue Res; 2007 Mar; 327(3):595-605. PubMed ID: 17109119
[TBL] [Abstract][Full Text] [Related]
31. Reactive oxygen intermediates during programmed cell death induced in the thymus of the Ts(1716)65Dn mouse, a murine model for human Down's syndrome.
Paz-Miguel JE; Flores R; Sánchez-Velasco P; Ocejo-Vinyals G; Escribano de Diego J; López de Rego J; Leyva-Cobián F
J Immunol; 1999 Nov; 163(10):5399-410. PubMed ID: 10553065
[TBL] [Abstract][Full Text] [Related]
32. Role of reactive oxygen species in contraction-mediated glucose transport in mouse skeletal muscle.
Sandström ME; Zhang SJ; Bruton J; Silva JP; Reid MB; Westerblad H; Katz A
J Physiol; 2006 Aug; 575(Pt 1):251-62. PubMed ID: 16777943
[TBL] [Abstract][Full Text] [Related]
33. Upregulation of beta-catenin expression in down syndrome model Ts65Dn mouse brain.
Ramakrishna N; Meeker HC; Li S; Brown WT; Rao R; El Idrissi A
Neuroscience; 2009 Jun; 161(2):451-8. PubMed ID: 19328224
[TBL] [Abstract][Full Text] [Related]
34. Double Knockout of Peroxiredoxin 4 (Prdx4) and Superoxide Dismutase 1 (Sod1) in Mice Results in Severe Liver Failure.
Homma T; Kurahashi T; Lee J; Nabeshima A; Yamada S; Fujii J
Oxid Med Cell Longev; 2018; 2018():2812904. PubMed ID: 30050648
[TBL] [Abstract][Full Text] [Related]
35. 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; 37(2):412-22. PubMed ID: 19879358
[TBL] [Abstract][Full Text] [Related]
36. Abnormal expression of the G-protein-activated inwardly rectifying potassium channel 2 (GIRK2) in hippocampus, frontal cortex, and substantia nigra of Ts65Dn mouse: a model of Down syndrome.
Harashima C; Jacobowitz DM; Witta J; Borke RC; Best TK; Siarey RJ; Galdzicki Z
J Comp Neurol; 2006 Feb; 494(5):815-33. PubMed ID: 16374808
[TBL] [Abstract][Full Text] [Related]
37. The transcriptional coregulator PGC-1β controls mitochondrial function and anti-oxidant defence in skeletal muscles.
Gali Ramamoorthy T; Laverny G; Schlagowski AI; Zoll J; Messaddeq N; Bornert JM; Panza S; Ferry A; Geny B; Metzger D
Nat Commun; 2015 Dec; 6():10210. PubMed ID: 26674215
[TBL] [Abstract][Full Text] [Related]
38. Long-term running alleviates some behavioral and molecular abnormalities in Down syndrome mouse model Ts65Dn.
Kida E; Rabe A; Walus M; Albertini G; Golabek AA
Exp Neurol; 2013 Feb; 240():178-89. PubMed ID: 23201095
[TBL] [Abstract][Full Text] [Related]
39. Ts65Dn mouse, a Down syndrome model, exhibits elevated myo-inositol in selected brain regions and peripheral tissues.
Shetty HU; Siarey RJ; Galdzicki Z; Stoll J; Rapoport SI
Neurochem Res; 2000 Apr; 25(4):431-5. PubMed ID: 10823574
[TBL] [Abstract][Full Text] [Related]
40. The effect of peripheral nerve injury on disease progression in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
Sharp PS; Dick JR; Greensmith L
Neuroscience; 2005; 130(4):897-910. PubMed ID: 15652988
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]