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1137 related items for PubMed ID: 26298469
1. Rab1-dependent ER-Golgi transport dysfunction is a common pathogenic mechanism in SOD1, TDP-43 and FUS-associated ALS. Soo KY, Halloran M, Sundaramoorthy V, Parakh S, Toth RP, Southam KA, McLean CA, Lock P, King A, Farg MA, Atkin JD. Acta Neuropathol; 2015 Nov; 130(5):679-97. PubMed ID: 26298469 [Abstract] [Full Text] [Related]
2. Ataxin-2 interacts with FUS and intermediate-length polyglutamine expansions enhance FUS-related pathology in amyotrophic lateral sclerosis. Farg MA, Soo KY, Warraich ST, Sundaramoorthy V, Blair IP, Atkin JD. Hum Mol Genet; 2013 Feb 15; 22(4):717-28. PubMed ID: 23172909 [Abstract] [Full Text] [Related]
3. Shared Molecular Mechanisms in Alzheimer's Disease and Amyotrophic Lateral Sclerosis: Neurofilament-Dependent Transport of sAPP, FUS, TDP-43 and SOD1, with Endoplasmic Reticulum-Like Tubules. Muresan V, Ladescu Muresan Z. Neurodegener Dis; 2016 Feb 15; 16(1-2):55-61. PubMed ID: 26605911 [Abstract] [Full Text] [Related]
4. ERp57 is protective against mutant SOD1-induced cellular pathology in amyotrophic lateral sclerosis. Parakh S, Jagaraj CJ, Vidal M, Ragagnin AMG, Perri ER, Konopka A, Toth RP, Galper J, Blair IP, Thomas CJ, Walker AK, Yang S, Spencer DM, Atkin JD. Hum Mol Genet; 2018 Apr 15; 27(8):1311-1331. PubMed ID: 29409023 [Abstract] [Full Text] [Related]
5. Extracellular wildtype and mutant SOD1 induces ER-Golgi pathology characteristic of amyotrophic lateral sclerosis in neuronal cells. Sundaramoorthy V, Walker AK, Yerbury J, Soo KY, Farg MA, Hoang V, Zeineddine R, Spencer D, Atkin JD. Cell Mol Life Sci; 2013 Nov 15; 70(21):4181-95. PubMed ID: 23765103 [Abstract] [Full Text] [Related]
6. Mutant SOD1 inhibits ER-Golgi transport in amyotrophic lateral sclerosis. Atkin JD, Farg MA, Soo KY, Walker AK, Halloran M, Turner BJ, Nagley P, Horne MK. J Neurochem; 2014 Apr 15; 129(1):190-204. PubMed ID: 24134191 [Abstract] [Full Text] [Related]
7. Aberrant localization of FUS and TDP43 is associated with misfolding of SOD1 in amyotrophic lateral sclerosis. Pokrishevsky E, Grad LI, Yousefi M, Wang J, Mackenzie IR, Cashman NR. PLoS One; 2012 Apr 15; 7(4):e35050. PubMed ID: 22493728 [Abstract] [Full Text] [Related]
8. Protein disulphide isomerase (PDI) is protective against amyotrophic lateral sclerosis (ALS)-related mutant Fused in Sarcoma (FUS) in in vitro models. Parakh S, Perri ER, Vidal M, Sultana J, Shadfar S, Mehta P, Konopka A, Thomas CJ, Spencer DM, Atkin JD. Sci Rep; 2021 Sep 02; 11(1):17557. PubMed ID: 34475430 [Abstract] [Full Text] [Related]
10. RNA and Protein Interactors with TDP-43 in Human Spinal-Cord Lysates in Amyotrophic Lateral Sclerosis. Volkening K, Keller BA, Leystra-Lantz C, Strong MJ. J Proteome Res; 2018 Apr 06; 17(4):1712-1729. PubMed ID: 29513014 [Abstract] [Full Text] [Related]
11. FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosis. Deng HX, Zhai H, Bigio EH, Yan J, Fecto F, Ajroud K, Mishra M, Ajroud-Driss S, Heller S, Sufit R, Siddique N, Mugnaini E, Siddique T. Ann Neurol; 2010 Jun 06; 67(6):739-48. PubMed ID: 20517935 [Abstract] [Full Text] [Related]
12. TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy. Turner BJ, Bäumer D, Parkinson NJ, Scaber J, Ansorge O, Talbot K. BMC Neurosci; 2008 Oct 28; 9():104. PubMed ID: 18957104 [Abstract] [Full Text] [Related]
13. Lack of TDP-43 abnormalities in mutant SOD1 transgenic mice shows disparity with ALS. Robertson J, Sanelli T, Xiao S, Yang W, Horne P, Hammond R, Pioro EP, Strong MJ. Neurosci Lett; 2007 Jun 13; 420(2):128-32. PubMed ID: 17543992 [Abstract] [Full Text] [Related]
14. FUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosis. Kabashi E, Bercier V, Lissouba A, Liao M, Brustein E, Rouleau GA, Drapeau P. PLoS Genet; 2011 Aug 13; 7(8):e1002214. PubMed ID: 21829392 [Abstract] [Full Text] [Related]
15. Pathological Modification of TDP-43 in Amyotrophic Lateral Sclerosis with SOD1 Mutations. Jeon GS, Shim YM, Lee DY, Kim JS, Kang M, Ahn SH, Shin JY, Geum D, Hong YH, Sung JJ. Mol Neurobiol; 2019 Mar 13; 56(3):2007-2021. PubMed ID: 29982983 [Abstract] [Full Text] [Related]
16. TDP-43 or FUS-induced misfolded human wild-type SOD1 can propagate intercellularly in a prion-like fashion. Pokrishevsky E, Grad LI, Cashman NR. Sci Rep; 2016 Mar 01; 6():22155. PubMed ID: 26926802 [Abstract] [Full Text] [Related]
17. Co-aggregation of RNA binding proteins in ALS spinal motor neurons: evidence of a common pathogenic mechanism. Keller BA, Volkening K, Droppelmann CA, Ang LC, Rademakers R, Strong MJ. Acta Neuropathol; 2012 Nov 01; 124(5):733-47. PubMed ID: 22941224 [Abstract] [Full Text] [Related]
18. Protein Disulfide Isomerase Endoplasmic Reticulum Protein 57 (ERp57) is Protective Against ALS-Associated Mutant TDP-43 in Neuronal Cells. Parakh S, Perri ER, Vidal M, Takalloo Z, Jagaraj CJ, Mehta P, Yang S, Thomas CJ, Blair IP, Hong Y, Atkin JD. Neuromolecular Med; 2024 Jun 11; 26(1):23. PubMed ID: 38861223 [Abstract] [Full Text] [Related]
19. Superoxide dismutase 1 mutants related to amyotrophic lateral sclerosis induce endoplasmic stress in neuro2a cells. Oh YK, Shin KS, Yuan J, Kang SJ. J Neurochem; 2008 Feb 11; 104(4):993-1005. PubMed ID: 18233996 [Abstract] [Full Text] [Related]
20. Mislocalization of TDP-43 in the G93A mutant SOD1 transgenic mouse model of ALS. Shan X, Vocadlo D, Krieger C. Neurosci Lett; 2009 Jul 17; 458(2):70-4. PubMed ID: 19379791 [Abstract] [Full Text] [Related] Page: [Next] [New Search]