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Items: 1 to 20 of 177

1.

Potential effect of S-nitrosylated protein disulfide isomerase on mutant SOD1 aggregation and neuronal cell death in amyotrophic lateral sclerosis.

Jeon GS, Nakamura T, Lee JS, Choi WJ, Ahn SW, Lee KW, Sung JJ, Lipton SA.

Mol Neurobiol. 2014 Apr;49(2):796-807. doi: 10.1007/s12035-013-8562-z.

PMID:
24091828
2.

Induction of the unfolded protein response in familial amyotrophic lateral sclerosis and association of protein-disulfide isomerase with superoxide dismutase 1.

Atkin JD, Farg MA, Turner BJ, Tomas D, Lysaght JA, Nunan J, Rembach A, Nagley P, Beart PM, Cheema SS, Horne MK.

J Biol Chem. 2006 Oct 6;281(40):30152-65.

3.

Protein disulphide isomerase protects against protein aggregation and is S-nitrosylated in amyotrophic lateral sclerosis.

Walker AK, Farg MA, Bye CR, McLean CA, Horne MK, Atkin JD.

Brain. 2010 Jan;133(Pt 1):105-16. doi: 10.1093/brain/awp267.

PMID:
19903735
4.

S-nitrosylated protein disulfide isomerase contributes to mutant SOD1 aggregates in amyotrophic lateral sclerosis.

Chen X, Zhang X, Li C, Guan T, Shang H, Cui L, Li XM, Kong J.

J Neurochem. 2013 Jan;124(1):45-58. doi: 10.1111/jnc.12046.

5.

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;104(4):993-1005. doi: 10.1111/j.1471-4159.2007.05053.x.

6.

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;70(21):4181-95. doi: 10.1007/s00018-013-1385-2.

PMID:
23765103
7.

Reticulon-4A (Nogo-A) redistributes protein disulfide isomerase to protect mice from SOD1-dependent amyotrophic lateral sclerosis.

Yang YS, Harel NY, Strittmatter SM.

J Neurosci. 2009 Nov 4;29(44):13850-9. doi: 10.1523/JNEUROSCI.2312-09.2009.

8.

Familial amyotrophic lateral sclerosis (FALS)-linked SOD1 mutation accelerates neuronal cell death by activating cleavage of caspase-4 under ER stress in an in vitro model of FALS.

Koyama Y, Hiratsuka T, Matsuzaki S, Yamagishi S, Kato S, Katayama T, Tohyama M.

Neurochem Int. 2010 Dec;57(7):838-43. doi: 10.1016/j.neuint.2010.08.023.

PMID:
20816908
9.

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;129(1):190-204. doi: 10.1111/jnc.12493.

10.

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. doi: 10.1007/s00401-015-1468-2.

PMID:
26298469
11.

Protein disulfide isomerase in ALS mouse glia links protein misfolding with NADPH oxidase-catalyzed superoxide production.

Jaronen M, Vehviläinen P, Malm T, Keksa-Goldsteine V, Pollari E, Valonen P, Koistinaho J, Goldsteins G.

Hum Mol Genet. 2013 Feb 15;22(4):646-55. doi: 10.1093/hmg/dds472.

PMID:
23118353
12.

Protein disulfide isomerase-immunopositive inclusions in patients with amyotrophic lateral sclerosis.

Honjo Y, Kaneko S, Ito H, Horibe T, Nagashima M, Nakamura M, Fujita K, Takahashi R, Kusaka H, Kawakami K.

Amyotroph Lateral Scler. 2011 Nov;12(6):444-50. doi: 10.3109/17482968.2011.594055.

PMID:
21745122
13.

Transglutaminase 2 accelerates neuroinflammation in amyotrophic lateral sclerosis through interaction with misfolded superoxide dismutase 1.

Oono M, Okado-Matsumoto A, Shodai A, Ido A, Ohta Y, Abe K, Ayaki T, Ito H, Takahashi R, Taniguchi N, Urushitani M.

J Neurochem. 2014 Feb;128(3):403-18. doi: 10.1111/jnc.12441.

14.

The small heat shock protein B8 (HspB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS).

Crippa V, Sau D, Rusmini P, Boncoraglio A, Onesto E, Bolzoni E, Galbiati M, Fontana E, Marino M, Carra S, Bendotti C, De Biasi S, Poletti A.

Hum Mol Genet. 2010 Sep 1;19(17):3440-56. doi: 10.1093/hmg/ddq257.

PMID:
20570967
15.

Impaired extracellular secretion of mutant superoxide dismutase 1 associates with neurotoxicity in familial amyotrophic lateral sclerosis.

Turner BJ, Atkin JD, Farg MA, Zang DW, Rembach A, Lopes EC, Patch JD, Hill AF, Cheema SS.

J Neurosci. 2005 Jan 5;25(1):108-17.

17.

S-nitrosylated protein-disulphide isomerase links protein misfolding to neurodegeneration.

Uehara T, Nakamura T, Yao D, Shi ZQ, Gu Z, Ma Y, Masliah E, Nomura Y, Lipton SA.

Nature. 2006 May 25;441(7092):513-7.

PMID:
16724068
19.

Accumulation of misfolded SOD1 in dorsal root ganglion degenerating proprioceptive sensory neurons of transgenic mice with amyotrophic lateral sclerosis.

Sábado J, Casanovas A, Tarabal O, Hereu M, Piedrafita L, Calderó J, Esquerda JE.

Biomed Res Int. 2014;2014:852163. doi: 10.1155/2014/852163.

20.

Palmitoylation of superoxide dismutase 1 (SOD1) is increased for familial amyotrophic lateral sclerosis-linked SOD1 mutants.

Antinone SE, Ghadge GD, Lam TT, Wang L, Roos RP, Green WN.

J Biol Chem. 2013 Jul 26;288(30):21606-17. doi: 10.1074/jbc.M113.487231.

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