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Items: 1 to 20 of 41

1.

The Endoplasmic Reticulum Chaperone GRP78/BiP Modulates Prion Propagation in vitro and in vivo.

Park KW, Eun Kim G, Morales R, Moda F, Moreno-Gonzalez I, Concha-Marambio L, Lee AS, Hetz C, Soto C.

Sci Rep. 2017 Mar 23;7:44723. doi: 10.1038/srep44723.

2.

From structure to redox: The diverse functional roles of disulfides and implications in disease.

Bechtel TJ, Weerapana E.

Proteomics. 2017 Mar;17(6). doi: 10.1002/pmic.201600391. Review.

3.

Emerging roles of extracellular vesicles in neurodegenerative disorders: focus on HIV-associated neurological complications.

Hu G, Yang L, Cai Y, Niu F, Mezzacappa F, Callen S, Fox HS, Buch S.

Cell Death Dis. 2016 Nov 24;7(11):e2481. doi: 10.1038/cddis.2016.336. Review.

4.

Misfolding leads the way to unraveling signaling pathways in the pathophysiology of prion diseases.

Puig B, Altmeppen HC, Glatzel M.

Prion. 2016 Nov;10(6):434-443.

PMID:
27870599
5.

Secretory pathway retention of mutant prion protein induces p38-MAPK activation and lethal disease in mice.

Puig B, Altmeppen HC, Ulbrich S, Linsenmeier L, Krasemann S, Chakroun K, Acevedo-Morantes CY, Wille H, Tatzelt J, Glatzel M.

Sci Rep. 2016 Apr 27;6:24970. doi: 10.1038/srep24970.

6.

Interplay of endoplasmic reticulum stress and autophagy in neurodegenerative disorders.

Cai Y, Arikkath J, Yang L, Guo ML, Periyasamy P, Buch S.

Autophagy. 2016;12(2):225-44. doi: 10.1080/15548627.2015.1121360. Review.

7.

ERp57 as a novel cellular factor controlling prion protein biosynthesis: Therapeutic potential of protein disulfide isomerases.

Sepulveda M, Rozas P, Hetz C, Medinas DB.

Prion. 2016;10(1):50-6. doi: 10.1080/19336896.2015.1129485.

8.

PDIA3 Knockdown Exacerbates Free Fatty Acid-Induced Hepatocyte Steatosis and Apoptosis.

Zhang XQ, Pan Y, Yu CH, Xu CF, Xu L, Li YM, Chen WX.

PLoS One. 2015 Jul 27;10(7):e0133882. doi: 10.1371/journal.pone.0133882. eCollection 2015.

9.

The Protein-disulfide Isomerase ERp57 Regulates the Steady-state Levels of the Prion Protein.

Torres M, Medinas DB, Matamala JM, Woehlbier U, Cornejo VH, Solda T, Andreu C, Rozas P, Matus S, Muñoz N, Vergara C, Cartier L, Soto C, Molinari M, Hetz C.

J Biol Chem. 2015 Sep 25;290(39):23631-45. doi: 10.1074/jbc.M114.635565. Epub 2015 Jul 13.

10.

Prion degradation pathways: Potential for therapeutic intervention.

Goold R, McKinnon C, Tabrizi SJ.

Mol Cell Neurosci. 2015 May;66(Pt A):12-20. doi: 10.1016/j.mcn.2014.12.009. Epub 2015 Jan 10. Review.

11.

Metabolism of minor isoforms of prion proteins: Cytosolic prion protein and transmembrane prion protein.

Song Z, Zhao D, Yang L.

Neural Regen Res. 2013 Oct 25;8(30):2868-78. doi: 10.3969/j.issn.1673-5374.2013.30.009. Review.

12.

Stress protein expression in early phase spinal cord ischemia/reperfusion injury.

Zhang S, Wu D, Wang J, Wang Y, Wang G, Yang M, Yang X.

Neural Regen Res. 2013 Aug 25;8(24):2225-35. doi: 10.3969/j.issn.1673-5374.2013.24.002.

13.

A molecular web: endoplasmic reticulum stress, inflammation, and oxidative stress.

Chaudhari N, Talwar P, Parimisetty A, Lefebvre d'Hellencourt C, Ravanan P.

Front Cell Neurosci. 2014 Jul 29;8:213. doi: 10.3389/fncel.2014.00213. eCollection 2014. Review.

14.

ER stress-induced clearance of misfolded GPI-anchored proteins via the secretory pathway.

Satpute-Krishnan P, Ajinkya M, Bhat S, Itakura E, Hegde RS, Lippincott-Schwartz J.

Cell. 2014 Jul 31;158(3):522-33. doi: 10.1016/j.cell.2014.06.026.

15.

The essential biology of the endoplasmic reticulum stress response for structural and computational biologists.

Wakabayashi S, Yoshida H.

Comput Struct Biotechnol J. 2013 Sep 3;6:e201303010. doi: 10.5936/csbj.201303010. eCollection 2013. Review.

16.

Disulfide bonding in neurodegenerative misfolding diseases.

Mossuto MF.

Int J Cell Biol. 2013;2013:318319. doi: 10.1155/2013/318319. Epub 2013 Aug 1.

17.

ER stress-mediated autophagy promotes Myc-dependent transformation and tumor growth.

Hart LS, Cunningham JT, Datta T, Dey S, Tameire F, Lehman SL, Qiu B, Zhang H, Cerniglia G, Bi M, Li Y, Gao Y, Liu H, Li C, Maity A, Thomas-Tikhonenko A, Perl AE, Koong A, Fuchs SY, Diehl JA, Mills IG, Ruggero D, Koumenis C.

J Clin Invest. 2012 Dec;122(12):4621-34. doi: 10.1172/JCI62973. Epub 2012 Nov 12.

18.

Overexpression of the Hspa13 (Stch) gene reduces prion disease incubation time in mice.

Grizenkova J, Akhtar S, Hummerich H, Tomlinson A, Asante EA, Wenborn A, Fizet J, Poulter M, Wiseman FK, Fisher EM, Tybulewicz VL, Brandner S, Collinge J, Lloyd SE.

Proc Natl Acad Sci U S A. 2012 Aug 21;109(34):13722-7. doi: 10.1073/pnas.1208917109. Epub 2012 Aug 6.

19.

The impact of the unfolded protein response on human disease.

Wang S, Kaufman RJ.

J Cell Biol. 2012 Jun 25;197(7):857-67. doi: 10.1083/jcb.201110131. Review.

20.

Altered Prion protein expression pattern in CSF as a biomarker for Creutzfeldt-Jakob disease.

Torres M, Cartier L, Matamala JM, Hernández N, Woehlbier U, Hetz C.

PLoS One. 2012;7(4):e36159. doi: 10.1371/journal.pone.0036159. Epub 2012 Apr 27.

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