Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 115


Subcellular Localization of Matrin 3 Containing Mutations Associated with ALS and Distal Myopathy.

Gallego-Iradi MC, Clare AM, Brown HH, Janus C, Lewis J, Borchelt DR.

PLoS One. 2015 Nov 3;10(11):e0142144. doi: 10.1371/journal.pone.0142144. eCollection 2015.


Endoplasmic Reticulum Stress Interacts With Inflammation in Human Diseases.

Cao SS, Luo KL, Shi L.

J Cell Physiol. 2016 Feb;231(2):288-94. doi: 10.1002/jcp.25098. Review.


In vivo kinetic approach reveals slow SOD1 turnover in the CNS.

Crisp MJ, Mawuenyega KG, Patterson BW, Reddy NC, Chott R, Self WK, Weihl CC, Jockel-Balsarotti J, Varadhachary AS, Bucelli RC, Yarasheski KE, Bateman RJ, Miller TM.

J Clin Invest. 2015 Jul 1;125(7):2772-80. doi: 10.1172/JCI80705. Epub 2015 Jun 15.


Emerging mechanisms of molecular pathology in ALS.

Peters OM, Ghasemi M, Brown RH Jr.

J Clin Invest. 2015 May;125(5):1767-79. doi: 10.1172/JCI71601. Epub 2015 May 1. Review. Erratum in: J Clin Invest. 2015 Jun;125(6):2548.


Macrophage migration inhibitory factor as a chaperone inhibiting accumulation of misfolded SOD1.

Israelson A, Ditsworth D, Sun S, Song S, Liang J, Hruska-Plochan M, McAlonis-Downes M, Abu-Hamad S, Zoltsman G, Shani T, Maldonado M, Bui A, Navarro M, Zhou H, Marsala M, Kaspar BK, Da Cruz S, Cleveland DW.

Neuron. 2015 Apr 8;86(1):218-32. doi: 10.1016/j.neuron.2015.02.034. Epub 2015 Mar 19.


Metal-deficient SOD1 in amyotrophic lateral sclerosis.

Hilton JB, White AR, Crouch PJ.

J Mol Med (Berl). 2015 May;93(5):481-7. doi: 10.1007/s00109-015-1273-3. Epub 2015 Mar 11.


Low-frequency magnetic fields do not aggravate disease in mouse models of Alzheimer's disease and amyotrophic lateral sclerosis.

Liebl MP, Windschmitt J, Besemer AS, Schäfer AK, Reber H, Behl C, Clement AM.

Sci Rep. 2015 Feb 26;5:8585. doi: 10.1038/srep08585.


Impaired bone homeostasis in amyotrophic lateral sclerosis mice with muscle atrophy.

Zhu K, Yi J, Xiao Y, Lai Y, Song P, Zheng W, Jiao H, Fan J, Wu C, Chen D, Zhou J, Xiao G.

J Biol Chem. 2015 Mar 27;290(13):8081-94. doi: 10.1074/jbc.M114.603985. Epub 2015 Feb 3.


Direct and indirect mechanisms for wild-type SOD1 to enhance the toxicity of mutant SOD1 in bigenic transgenic mice.

Xu G, Ayers JI, Roberts BL, Brown H, Fromholt S, Green C, Borchelt DR.

Hum Mol Genet. 2015 Feb 15;24(4):1019-35. doi: 10.1093/hmg/ddu517. Epub 2014 Oct 9.


Copper-based pulsed dipolar ESR spectroscopy as a probe of protein conformation linked to disease states.

Merz GE, Borbat PP, Pratt AJ, Getzoff ED, Freed JH, Crane BR.

Biophys J. 2014 Oct 7;107(7):1669-74. doi: 10.1016/j.bpj.2014.07.068.


Early detection of motor dysfunction in the SOD1G93A mouse model of Amyotrophic Lateral Sclerosis (ALS) using home cage running wheels.

Bennett EJ, Mead RJ, Azzouz M, Shaw PJ, Grierson AJ.

PLoS One. 2014 Sep 30;9(9):e107918. doi: 10.1371/journal.pone.0107918. eCollection 2014.


Analysis of mutant SOD1 electrophoretic mobility by Blue Native gel electrophoresis; evidence for soluble multimeric assemblies.

Brown HH, Borchelt DR.

PLoS One. 2014 Aug 14;9(8):e104583. doi: 10.1371/journal.pone.0104583. eCollection 2014.


Altered thiol chemistry in human amyotrophic lateral sclerosis-linked mutants of superoxide dismutase 1.

Solsona C, Kahn TB, Badilla CL, Álvarez-Zaldiernas C, Blasi J, Fernandez JM, Alegre-Cebollada J.

J Biol Chem. 2014 Sep 26;289(39):26722-32. doi: 10.1074/jbc.M114.565333. Epub 2014 Aug 4.


Protein charge ladders reveal that the net charge of ALS-linked superoxide dismutase can be different in sign and magnitude from predicted values.

Shi Y, Abdolvahabi A, Shaw BF.

Protein Sci. 2014 Oct;23(10):1417-33. doi: 10.1002/pro.2526. Epub 2014 Aug 7.


Spinal cord pathology is ameliorated by P2X7 antagonism in a SOD1-mutant mouse model of amyotrophic lateral sclerosis.

Apolloni S, Amadio S, Parisi C, Matteucci A, Potenza RL, Armida M, Popoli P, D'Ambrosi N, Volonté C.

Dis Model Mech. 2014 Sep;7(9):1101-9. doi: 10.1242/dmm.017038. Epub 2014 Jul 18.


Metal-deficient aggregates and diminished copper found in cells expressing SOD1 mutations that cause ALS.

Bourassa MW, Brown HH, Borchelt DR, Vogt S, Miller LM.

Front Aging Neurosci. 2014 Jun 16;6:110. doi: 10.3389/fnagi.2014.00110. eCollection 2014.


Dimerization, oligomerization, and aggregation of human amyotrophic lateral sclerosis copper/zinc superoxide dismutase 1 protein mutant forms in live cells.

Kim J, Lee H, Lee JH, Kwon DY, Genovesio A, Fenistein D, Ogier A, Brondani V, Grailhe R.

J Biol Chem. 2014 May 23;289(21):15094-103. doi: 10.1074/jbc.M113.542613. Epub 2014 Apr 1.


Superoxide dismutases and superoxide reductases.

Sheng Y, Abreu IA, Cabelli DE, Maroney MJ, Miller AF, Teixeira M, Valentine JS.

Chem Rev. 2014 Apr 9;114(7):3854-918. doi: 10.1021/cr4005296. Epub 2014 Apr 1. Review. No abstract available.


Microglia and motor neurons during disease progression in the SOD1G93A mouse model of amyotrophic lateral sclerosis: changes in arginase1 and inducible nitric oxide synthase.

Lewis KE, Rasmussen AL, Bennett W, King A, West AK, Chung RS, Chuah MI.

J Neuroinflammation. 2014 Mar 23;11:55. doi: 10.1186/1742-2094-11-55.


ALS-linked SOD1 in glial cells enhances ß-N-Methylamino L-Alanine (BMAA)-induced toxicity in Drosophila.

Islam R, Kumimoto EL, Bao H, Zhang B.

F1000Res. 2012 Nov 9;1:47. doi: 10.12688/f1000research.1-47.v1. eCollection 2012.

Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk