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References from Molecular dynamics analysis of superoxide dismutase 1 mutations suggests decoupling between mechanisms underlying ALS onset and progression. Local targets link to admitted publications; unresolved targets remain external evidence.
10.1038/35097565
10.1038/35097565 · External reference
10.1016/j.neuron.2006.09.018
10.1016/j.neuron.2006.09.018 · External reference
10.1080/14737159.2020.1779060
10.1080/14737159.2020.1779060 · External reference
10.1110/ps.041256705
10.1110/ps.041256705 · External reference
10.1074/jbc.m509496200
10.1074/jbc.m509496200 · External reference
10.1073/pnas.0602048103
10.1073/pnas.0602048103 · External reference
ALSoD: a user‐friendly online bioinformatics tool for amyotrophic lateral sclerosis genetics
10.1002/humu.22157 · 2012 · External reference
ALSOD: the amyotrophic lateral sclerosis online database
10.1080/17482960802146106 · 2008 · External reference
The biophysics of superoxide dismutase-1 and amyotrophic lateral sclerosis
10.1017/s003358351900012x · 2019 · External reference
Structural properties and interaction partners of familial ALS-associated SOD1 mutants
10.3389/fneur.2019.00527 · 2019 · External reference
10.1074/jbc.m115.683763
10.1074/jbc.m115.683763 · External reference
Current hypotheses for the underlying biology of amyotrophic lateral sclerosis
10.1002/ana.21543 · 2009 · External reference
Metal-free superoxide dismutase forms soluble oligomers under physiological conditions: a possible general mechanism for familial ALS
10.1073/pnas.0704307104 · 2007 · External reference
Loss of metal ions, disulfide reduction and mutations related to familial ALS promote formation of amyloid-like aggregates from superoxide dismutase
10.1371/journal.pone.0005004 · 2009 · External reference
10.1021/bi030246r
10.1021/bi030246r · External reference
A prion-like mechanism for the propagated misfolding of SOD1 from in silico modeling of solvated near-native conformers
10.1371/journal.pone.0177284 · 2017 · External reference
10.1073/pnas.1102645108
10.1073/pnas.1102645108 · External reference
10.1073/pnas.1312245111
10.1073/pnas.1312245111 · External reference
10.1212/01.wnl.0000343509.76828.2a
10.1212/01.wnl.0000343509.76828.2a · External reference
10.1007/s11910-996-0008-9
10.1007/s11910-996-0008-9 · External reference
Sporadic amyotrophic lateral sclerosis and breast cancer: hyaline conglomerate inclusions lead to identification of SOD1 mutation
10.1016/j.jns.2005.11.016 · 2006 · External reference
H46R SOD1 mutation is consistently associated with a relatively benign form of amyotrophic lateral sclerosis with slow progression
10.1080/21678421.2016.1199698 · 2016 · External reference
Slowly progressing amyotrophic lateral sclerosis caused by H46R SOD1 mutation
10.1159/000102170 · 2007 · External reference
10.1007/s00401-003-0763-5
10.1007/s00401-003-0763-5 · External reference
Genetics of amyotrophic lateral sclerosis: seeking therapeutic targets in the era of gene therapy
2022 · External reference
10.1146/annurev.biochem.72.121801.161647
10.1146/annurev.biochem.72.121801.161647 · External reference
10.1074/jbc.m112087200
10.1074/jbc.m112087200 · External reference
10.1073/pnas.0730423100
10.1073/pnas.0730423100 · External reference
Superoxide dismutase is an abundant component in cell bodies, dendrites, and axons of motor neurons and in a subset of other neurons
10.1073/pnas.92.4.954 · 1995 · External reference
Cu/Zn-superoxide dismutase and wild-type like fALS SOD1 mutants produce cytotoxic quantities of H2O2 via cysteine-dependent redox short-circuit
10.1038/s41598-019-47326-x · 2019 · External reference
10.1016/j.jmb.2006.09.048
10.1016/j.jmb.2006.09.048 · External reference
Decreased stability and increased formation of soluble aggregates by immature superoxide dismutase do not account for disease severity in ALS
10.1073/pnas.0913021108 · 2011 · External reference
Probing the free energy landscapes of ALS disease mutants of SOD1 by NMR spectroscopy
10.1073/pnas.1611418113 · 2016 · External reference
The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration
10.1038/s41467-022-34620-y · 2022 · External reference
10.1080/07391102.1996.10508874
10.1080/07391102.1996.10508874 · External reference
Essential dynamics of proteins
10.1002/prot.340170408 · 1993 · External reference
Essential dynamics of DNA containing a cis. syn cyclobutane thymine dimer lesion
10.1093/nar/26.8.1939 · 1998 · External reference
Unresolved reference
2022 · External reference
10.1016/j.bbrc.2016.08.172
10.1016/j.bbrc.2016.08.172 · External reference
10.1021/acs.jpclett.9b02868
10.1021/acs.jpclett.9b02868 · External reference
A common property of amyotrophic lateral sclerosis-associated variants: destabilization of the copper/zinc superoxide dismutase electrostatic loop
10.1074/jbc.m109.023945 · 2009 · External reference
Superoxide dismutase 1 encoding mutations linked to ALS adopts a spectrum of misfolded states
10.1186/1750-1326-6-77 · 2011 · External reference
Molecular mechanisms underlying the impact of mutations in SOD1 on its conformational properties associated with amyotrophic lateral sclerosis as revealed with molecular modelling
10.1186/s12900-018-0080-9 · 2018 · External reference
10.1016/j.jmgm.2021.108026
10.1016/j.jmgm.2021.108026 · External reference
The G93C mutation in superoxide dismutase 1: clinicopathologic phenotype and prognosis
10.1001/archneur.63.2.262 · 2006 · External reference
10.1371/journal.pgen.1007682
10.1371/journal.pgen.1007682 · External reference
10.1093/brain/awt097
10.1093/brain/awt097 · External reference
10.1093/brain/awz182
10.1093/brain/awz182 · External reference
10.1056/nejmoa2204705
10.1056/nejmoa2204705 · External reference
Comprehensive analysis to explain reduced or increased SOD1 enzymatic activity in ALS patients and their relatives
10.1080/21678421.2017.1301481 · 2017 · External reference
10.1093/nar/28.1.235
10.1093/nar/28.1.235 · External reference
10.1002/0471250953.bi0506s15
10.1002/0471250953.bi0506s15 · External reference
Unresolved reference
1993 · External reference
10.1093/bioinformatics/btt055
10.1093/bioinformatics/btt055 · External reference
10.1016/j.softx.2015.06.001 · Admitted local publication
Improved side‐chain torsion potentials for the Amber ff99SB protein force field
10.1002/prot.22711 · 2010 · External reference
10.1063/1.328693
10.1063/1.328693 · External reference
10.1002/(sici)1096-987x(199709)18:12<1463::aid-jcc4>3.0.co;2-h
10.1002/(sici)1096-987x(199709)18:12<1463::aid-jcc4>3.0.co;2-h · External reference
10.1063/1.470117
10.1063/1.470117 · External reference
PyMod 2.0: improvements in protein sequence-structure analysis and homology modeling within PyMOL
10.1093/bioinformatics/btw638 · 2017 · External reference
10.1016/0263-7855(96)00018-5
10.1016/0263-7855(96)00018-5 · External reference
10.1038/s41592-019-0686-2
10.1038/s41592-019-0686-2 · External reference
10.1093/bioinformatics/bty1011
10.1093/bioinformatics/bty1011 · External reference
Simulated epidemics in 3d protein structures to detect functional properties
10.1021/acs.jcim.9b01027 · 2020 · External reference
Inferring the stabilization effects of SARS-CoV-2 variants on the binding with ACE2 receptor
10.1038/s42003-021-02946-w · 2022 · External reference
10.1038/s41431-018-0177-4
10.1038/s41431-018-0177-4 · External reference