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Results: 1 to 20 of 113

Similar articles for PubMed (Select 23408434)

1.

Neuronatin-mediated aberrant calcium signaling and endoplasmic reticulum stress underlie neuropathology in Lafora disease.

Sharma J, Mukherjee D, Rao SN, Iyengar S, Shankar SK, Satishchandra P, Jana NR.

J Biol Chem. 2013 Mar 29;288(13):9482-90. doi: 10.1074/jbc.M112.416180. Epub 2013 Feb 13.

2.

Lafora disease ubiquitin ligase malin promotes proteasomal degradation of neuronatin and regulates glycogen synthesis.

Sharma J, Rao SN, Shankar SK, Satishchandra P, Jana NR.

Neurobiol Dis. 2011 Oct;44(1):133-41. doi: 10.1016/j.nbd.2011.06.013. Epub 2011 Jun 25.

PMID:
21742036
3.

Lafora disease proteins malin and laforin are recruited to aggresomes in response to proteasomal impairment.

Mittal S, Dubey D, Yamakawa K, Ganesh S.

Hum Mol Genet. 2007 Apr 1;16(7):753-62. Epub 2007 Mar 2.

4.

Increased endoplasmic reticulum stress and decreased proteasomal function in lafora disease models lacking the phosphatase laforin.

Vernia S, Rubio T, Heredia M, Rodríguez de Córdoba S, Sanz P.

PLoS One. 2009 Jun 16;4(6):e5907. doi: 10.1371/journal.pone.0005907.

5.

Sequestration of chaperones and proteasome into Lafora bodies and proteasomal dysfunction induced by Lafora disease-associated mutations of malin.

Rao SN, Maity R, Sharma J, Dey P, Shankar SK, Satishchandra P, Jana NR.

Hum Mol Genet. 2010 Dec 1;19(23):4726-34. doi: 10.1093/hmg/ddq407. Epub 2010 Sep 21.

6.

Deciphering the role of malin in the lafora progressive myoclonus epilepsy.

Romá-Mateo C, Sanz P, Gentry MS.

IUBMB Life. 2012 Oct;64(10):801-8. doi: 10.1002/iub.1072. Epub 2012 Jul 20. Review.

7.

Genetic depletion of the malin E3 ubiquitin ligase in mice leads to lafora bodies and the accumulation of insoluble laforin.

DePaoli-Roach AA, Tagliabracci VS, Segvich DM, Meyer CM, Irimia JM, Roach PJ.

J Biol Chem. 2010 Aug 13;285(33):25372-81. doi: 10.1074/jbc.M110.148668. Epub 2010 Jun 10.

8.

Early-onset Lafora body disease.

Turnbull J, Girard JM, Lohi H, Chan EM, Wang P, Tiberia E, Omer S, Ahmed M, Bennett C, Chakrabarty A, Tyagi A, Liu Y, Pencea N, Zhao X, Scherer SW, Ackerley CA, Minassian BA.

Brain. 2012 Sep;135(Pt 9):2684-98. doi: 10.1093/brain/aws205.

9.

Co-chaperone CHIP stabilizes aggregate-prone malin, a ubiquitin ligase mutated in Lafora disease.

Rao SN, Sharma J, Maity R, Jana NR.

J Biol Chem. 2010 Jan 8;285(2):1404-13. doi: 10.1074/jbc.M109.006312. Epub 2009 Nov 5.

10.

Increased laforin and laforin binding to glycogen underlie Lafora body formation in malin-deficient Lafora disease.

Tiberia E, Turnbull J, Wang T, Ruggieri A, Zhao XC, Pencea N, Israelian J, Wang Y, Ackerley CA, Wang P, Liu Y, Minassian BA.

J Biol Chem. 2012 Jul 20;287(30):25650-9. doi: 10.1074/jbc.M111.331611. Epub 2012 Jun 5.

11.

Laforin is required for the functional activation of malin in endoplasmic reticulum stress resistance in neuronal cells.

Zeng L, Wang Y, Baba O, Zheng P, Liu Y, Liu Y.

FEBS J. 2012 Jul;279(14):2467-78. doi: 10.1111/j.1742-4658.2012.08627.x. Epub 2012 Jun 8.

12.

The malin-laforin complex suppresses the cellular toxicity of misfolded proteins by promoting their degradation through the ubiquitin-proteasome system.

Garyali P, Siwach P, Singh PK, Puri R, Mittal S, Sengupta S, Parihar R, Ganesh S.

Hum Mol Genet. 2009 Feb 15;18(4):688-700. doi: 10.1093/hmg/ddn398. Epub 2008 Nov 25.

13.

Insights into Lafora disease: malin is an E3 ubiquitin ligase that ubiquitinates and promotes the degradation of laforin.

Gentry MS, Worby CA, Dixon JE.

Proc Natl Acad Sci U S A. 2005 Jun 14;102(24):8501-6. Epub 2005 Jun 1.

14.

Regulation of glycogen synthesis by the laforin-malin complex is modulated by the AMP-activated protein kinase pathway.

Solaz-Fuster MC, Gimeno-Alcañiz JV, Ros S, Fernandez-Sanchez ME, Garcia-Fojeda B, Criado Garcia O, Vilchez D, Dominguez J, Garcia-Rocha M, Sanchez-Piris M, Aguado C, Knecht E, Serratosa J, Guinovart JJ, Sanz P, Rodriguez de Córdoba S.

Hum Mol Genet. 2008 Mar 1;17(5):667-78. Epub 2007 Nov 20.

15.

Laforin preferentially binds the neurotoxic starch-like polyglucosans, which form in its absence in progressive myoclonus epilepsy.

Chan EM, Ackerley CA, Lohi H, Ianzano L, Cortez MA, Shannon P, Scherer SW, Minassian BA.

Hum Mol Genet. 2004 Jun 1;13(11):1117-29. Epub 2004 Apr 21.

16.

Lafora progressive myoclonus epilepsy: NHLRC1 mutations affect glycogen metabolism.

Couarch P, Vernia S, Gourfinkel-An I, Lesca G, Gataullina S, Fedirko E, Trouillard O, Depienne C, Dulac O, Steschenko D, Leguern E, Sanz P, Baulac S.

J Mol Med (Berl). 2011 Sep;89(9):915-25. doi: 10.1007/s00109-011-0758-y. Epub 2011 Apr 20.

17.

The laforin-malin complex negatively regulates glycogen synthesis by modulating cellular glucose uptake via glucose transporters.

Singh PK, Singh S, Ganesh S.

Mol Cell Biol. 2012 Feb;32(3):652-63. doi: 10.1128/MCB.06353-11. Epub 2011 Nov 28.

18.

PTG protein depletion rescues malin-deficient Lafora disease in mouse.

Turnbull J, Epp JR, Goldsmith D, Zhao X, Pencea N, Wang P, Frankland PW, Ackerley CA, Minassian BA.

Ann Neurol. 2014 Mar;75(3):442-6. doi: 10.1002/ana.24104. Epub 2014 Mar 7.

PMID:
24419970
19.

Dysfunctions in endosomal-lysosomal and autophagy pathways underlie neuropathology in a mouse model for Lafora disease.

Puri R, Suzuki T, Yamakawa K, Ganesh S.

Hum Mol Genet. 2012 Jan 1;21(1):175-84. doi: 10.1093/hmg/ddr452. Epub 2011 Sep 30.

20.

Advances in lafora progressive myoclonus epilepsy.

Delgado-Escueta AV.

Curr Neurol Neurosci Rep. 2007 Sep;7(5):428-33. Review.

PMID:
17764634
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