Similar articles for PMID: 20498711

Year	Number of Results
1995	1
1996	1
1999	1
2000	4
2001	4
2002	1
2003	3
2004	2
2005	3
2006	6
2007	3
2008	5
2009	8
2010	10
2011	3
2012	9
2013	14
2014	9
2015	5
2016	7
2017	5
2018	3
2019	2
2020	5
2021	4
2022	8
2023	3
2024	0

1

Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosis.

Chia R, Tattum MH, Jones S, Collinge J, Fisher EM, Jackson GS. Chia R, et al. PLoS One. 2010 May 13;5(5):e10627. doi: 10.1371/journal.pone.0010627. PLoS One. 2010. PMID: 20498711 Free PMC article.

2

Prion-like propagation of mutant SOD1 misfolding and motor neuron disease spread along neuroanatomical pathways.

Ayers JI, Fromholt SE, O'Neal VM, Diamond JH, Borchelt DR. Ayers JI, et al. Acta Neuropathol. 2016 Jan;131(1):103-14. doi: 10.1007/s00401-015-1514-0. Epub 2015 Dec 9. Acta Neuropathol. 2016. PMID: 26650262 Free PMC article.

3

Human Cu/Zn superoxide dismutase (SOD1) overexpression in mice causes mitochondrial vacuolization, axonal degeneration, and premature motoneuron death and accelerates motoneuron disease in mice expressing a familial amyotrophic lateral sclerosis mutant SOD1.

Jaarsma D, Haasdijk ED, Grashorn JA, Hawkins R, van Duijn W, Verspaget HW, London J, Holstege JC. Jaarsma D, et al. Neurobiol Dis. 2000 Dec;7(6 Pt B):623-43. doi: 10.1006/nbdi.2000.0299. Neurobiol Dis. 2000. PMID: 11114261

4

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. Li QX, et al. Aging Cell. 2006 Apr;5(2):153-65. doi: 10.1111/j.1474-9726.2006.00200.x. Aging Cell. 2006. PMID: 16626394 Free article.

5

Lysine acylation in superoxide dismutase-1 electrostatically inhibits formation of fibrils with prion-like seeding.

Rasouli S, Abdolvahabi A, Croom CM, Plewman DL, Shi Y, Ayers JI, Shaw BF. Rasouli S, et al. J Biol Chem. 2017 Nov 24;292(47):19366-19380. doi: 10.1074/jbc.M117.805283. Epub 2017 Oct 3. J Biol Chem. 2017. PMID: 28974578 Free PMC article.

6

Amyloid precursor protein (APP) contributes to pathology in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.

Bryson JB, Hobbs C, Parsons MJ, Bosch KD, Pandraud A, Walsh FS, Doherty P, Greensmith L. Bryson JB, et al. Hum Mol Genet. 2012 Sep 1;21(17):3871-82. doi: 10.1093/hmg/dds215. Epub 2012 Jun 7. Hum Mol Genet. 2012. PMID: 22678056

7

Mutant superoxide dismutase aggregates from human spinal cord transmit amyotrophic lateral sclerosis.

Ekhtiari Bidhendi E, Bergh J, Zetterström P, Forsberg K, Pakkenberg B, Andersen PM, Marklund SL, Brännström T. Ekhtiari Bidhendi E, et al. Acta Neuropathol. 2018 Dec;136(6):939-953. doi: 10.1007/s00401-018-1915-y. Epub 2018 Oct 3. Acta Neuropathol. 2018. PMID: 30284034 Free PMC article.

8

Chan PK, Chattopadhyay M, Sharma S, Souda P, Gralla EB, Borchelt DR, Whitelegge JP, Valentine JS. Chan PK, et al. Proc Natl Acad Sci U S A. 2013 Jul 2;110(27):10934-9. doi: 10.1073/pnas.1309613110. Epub 2013 Jun 18. Proc Natl Acad Sci U S A. 2013. PMID: 23781106 Free PMC article.

9

Distinct conformers of transmissible misfolded SOD1 distinguish human SOD1-FALS from other forms of familial and sporadic ALS.

Ayers JI, Diamond J, Sari A, Fromholt S, Galaleldeen A, Ostrow LW, Glass JD, Hart PJ, Borchelt DR. Ayers JI, et al. Acta Neuropathol. 2016 Dec;132(6):827-840. doi: 10.1007/s00401-016-1623-4. Epub 2016 Oct 4. Acta Neuropathol. 2016. PMID: 27704280 Free PMC article.

10

Transcriptional profiling in the lumbar spinal cord of a mouse model of amyotrophic lateral sclerosis: a role for wild-type superoxide dismutase 1 in sporadic disease?

D'Arrigo A, Colavito D, Peña-Altamira E, Fabris M, Dam M, Contestabile A, Leon A. D'Arrigo A, et al. J Mol Neurosci. 2010 Jul;41(3):404-15. doi: 10.1007/s12031-010-9332-2. Epub 2010 Feb 23. J Mol Neurosci. 2010. PMID: 20177826

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