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394 related items for PubMed ID: 32029478
1. TNF receptor-associated factor 6 interacts with ALS-linked misfolded superoxide dismutase 1 and promotes aggregation. Semmler S, Gagné M, Garg P, Pickles SR, Baudouin C, Hamon-Keromen E, Destroismaisons L, Khalfallah Y, Chaineau M, Caron E, Bayne AN, Trempe JF, Cashman NR, Star AT, Haqqani AS, Durcan TM, Meiering EM, Robertson J, Grandvaux N, Plotkin SS, McBride HM, Vande Velde C. J Biol Chem; 2020 Mar 20; 295(12):3808-3825. PubMed ID: 32029478 [Abstract] [Full Text] [Related]
2. ALS-linked misfolded SOD1 species have divergent impacts on mitochondria. Pickles S, Semmler S, Broom HR, Destroismaisons L, Legroux L, Arbour N, Meiering E, Cashman NR, Vande Velde C. Acta Neuropathol Commun; 2016 Apr 27; 4(1):43. PubMed ID: 27121871 [Abstract] [Full Text] [Related]
3. Misfolding-Associated Exposure of Natively Buried Residues in Mutant SOD1 Facilitates Binding to TRAF6. Garg P, Semmler S, Baudouin C, Vande Velde C, Plotkin SS. J Mol Biol; 2022 Aug 30; 434(16):167697. PubMed ID: 35753527 [Abstract] [Full Text] [Related]
4. The molecular tweezer CLR01 inhibits aberrant superoxide dismutase 1 (SOD1) self-assembly in vitro and in the G93A-SOD1 mouse model of ALS. Malik R, Meng H, Wongkongkathep P, Corrales CI, Sepanj N, Atlasi RS, Klärner FG, Schrader T, Spencer MJ, Loo JA, Wiedau M, Bitan G. J Biol Chem; 2019 Mar 08; 294(10):3501-3513. PubMed ID: 30602569 [Abstract] [Full Text] [Related]
7. Endogenous macrophage migration inhibitory factor reduces the accumulation and toxicity of misfolded SOD1 in a mouse model of ALS. Leyton-Jaimes MF, Benaim C, Abu-Hamad S, Kahn J, Guetta A, Bucala R, Israelson A. Proc Natl Acad Sci U S A; 2016 Sep 06; 113(36):10198-203. PubMed ID: 27551074 [Abstract] [Full Text] [Related]
8. Mitochondrial damage revealed by immunoselection for ALS-linked misfolded SOD1. Pickles S, Destroismaisons L, Peyrard SL, Cadot S, Rouleau GA, Brown RH, Julien JP, Arbour N, Vande Velde C. Hum Mol Genet; 2013 Oct 01; 22(19):3947-59. PubMed ID: 23736301 [Abstract] [Full Text] [Related]
9. The metal cofactor zinc and interacting membranes modulate SOD1 conformation-aggregation landscape in an in vitro ALS model. Sannigrahi A, Chowdhury S, Das B, Banerjee A, Halder A, Kumar A, Saleem M, Naganathan AN, Karmakar S, Chattopadhyay K. Elife; 2021 Apr 07; 10():. PubMed ID: 33825682 [Abstract] [Full Text] [Related]
10. ALS-linked mutant SOD1 proteins promote Aβ aggregates in ALS through direct interaction with Aβ. Jang JY, Cho H, Park HY, Rhim H, Kang S. Biochem Biophys Res Commun; 2017 Nov 04; 493(1):697-707. PubMed ID: 28864422 [Abstract] [Full Text] [Related]
11. CNS-derived extracellular vesicles from superoxide dismutase 1 (SOD1)G93A ALS mice originate from astrocytes and neurons and carry misfolded SOD1. Silverman JM, Christy D, Shyu CC, Moon KM, Fernando S, Gidden Z, Cowan CM, Ban Y, Stacey RG, Grad LI, McAlary L, Mackenzie IR, Foster LJ, Cashman NR. J Biol Chem; 2019 Mar 08; 294(10):3744-3759. PubMed ID: 30635404 [Abstract] [Full Text] [Related]
12. Investigation of Anti-SOD1 Antibodies Yields New Structural Insight into SOD1 Misfolding and Surprising Behavior of the Antibodies Themselves. Atlasi RS, Malik R, Corrales CI, Tzeplaeff L, Whitelegge JP, Cashman NR, Bitan G. ACS Chem Biol; 2018 Sep 21; 13(9):2794-2807. PubMed ID: 30110532 [Abstract] [Full Text] [Related]
13. A copper-deficient form of mutant Cu/Zn-superoxide dismutase as an early pathological species in amyotrophic lateral sclerosis. Tokuda E, Nomura T, Ohara S, Watanabe S, Yamanaka K, Morisaki Y, Misawa H, Furukawa Y. Biochim Biophys Acta Mol Basis Dis; 2018 Jun 21; 1864(6 Pt A):2119-2130. PubMed ID: 29551730 [Abstract] [Full Text] [Related]
14. A human-derived antibody targets misfolded SOD1 and ameliorates motor symptoms in mouse models of amyotrophic lateral sclerosis. Maier M, Welt T, Wirth F, Montrasio F, Preisig D, McAfoose J, Vieira FG, Kulic L, Späni C, Stehle T, Perrin S, Weber M, Hock C, Nitsch RM, Grimm J. Sci Transl Med; 2018 Dec 05; 10(470):. PubMed ID: 30518612 [Abstract] [Full Text] [Related]
16. MIF inhibits the formation and toxicity of misfolded SOD1 amyloid aggregates: implications for familial ALS. Shvil N, Banerjee V, Zoltsman G, Shani T, Kahn J, Abu-Hamad S, Papo N, Engel S, Bernhagen J, Israelson A. Cell Death Dis; 2018 Jan 25; 9(2):107. PubMed ID: 29371591 [Abstract] [Full Text] [Related]
17. MS785-MS27 Reactive Misfolded/Non-Native Zn-Deficient SOD1 Species Exhibit Cytotoxicity and Adopt Heterozygous Conformations in Motor Neurons. Tokuda E, Sakashita Y, Tokoro N, Date A, Kosuge Y, Miyasaka T. Int J Mol Sci; 2024 May 21; 25(11):. PubMed ID: 38891791 [Abstract] [Full Text] [Related]
18. AAV2/9-mediated overexpression of MIF inhibits SOD1 misfolding, delays disease onset, and extends survival in mouse models of ALS. Leyton-Jaimes MF, Kahn J, Israelson A. Proc Natl Acad Sci U S A; 2019 Jul 16; 116(29):14755-14760. PubMed ID: 31262807 [Abstract] [Full Text] [Related]
19. Does wild-type Cu/Zn-superoxide dismutase have pathogenic roles in amyotrophic lateral sclerosis? Furukawa Y, Tokuda E. Transl Neurodegener; 2020 Aug 19; 9(1):33. PubMed ID: 32811540 [Abstract] [Full Text] [Related]
20. Amyotrophic lateral sclerosis is a non-amyloid disease in which extensive misfolding of SOD1 is unique to the familial form. Kerman A, Liu HN, Croul S, Bilbao J, Rogaeva E, Zinman L, Robertson J, Chakrabartty A. Acta Neuropathol; 2010 Mar 19; 119(3):335-44. PubMed ID: 20111867 [Abstract] [Full Text] [Related] Page: [Next] [New Search]