These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
292 related articles for article (PubMed ID: 22578008)
1. 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. PubMed ID: 22578008 [TBL] [Abstract][Full Text] [Related]
2. 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; 285(33):25372-81. PubMed ID: 20538597 [TBL] [Abstract][Full Text] [Related]
3. Laforin-malin complex degrades polyglucosan bodies in concert with glycogen debranching enzyme and brain isoform glycogen phosphorylase. Liu Y; Zeng L; Ma K; Baba O; Zheng P; Liu Y; Wang Y Mol Neurobiol; 2014 Apr; 49(2):645-57. PubMed ID: 24068615 [TBL] [Abstract][Full Text] [Related]
4. Laforin prevents stress-induced polyglucosan body formation and Lafora disease progression in neurons. Wang Y; Ma K; Wang P; Baba O; Zhang H; Parent JM; Zheng P; Liu Y; Minassian BA; Liu Y Mol Neurobiol; 2013 Aug; 48(1):49-61. PubMed ID: 23546741 [TBL] [Abstract][Full Text] [Related]
5. 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; 287(30):25650-9. PubMed ID: 22669944 [TBL] [Abstract][Full Text] [Related]
6. Impaired malin expression and interaction with partner proteins in Lafora disease. Skurat AV; Segvich DM; Contreras CJ; Hu YC; Hurley TD; DePaoli-Roach AA; Roach PJ J Biol Chem; 2024 May; 300(5):107271. PubMed ID: 38588813 [TBL] [Abstract][Full Text] [Related]
7. 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; 4(6):e5907. PubMed ID: 19529779 [TBL] [Abstract][Full Text] [Related]
8. Suppression of leptin signaling reduces polyglucosan inclusions and seizure susceptibility in a mouse model for Lafora disease. Rai A; Mishra R; Ganesh S Hum Mol Genet; 2017 Dec; 26(24):4778-4785. PubMed ID: 28973665 [TBL] [Abstract][Full Text] [Related]
9. The phosphatase activity of laforin is dispensable to rescue Epm2a-/- mice from Lafora disease. Gayarre J; Duran-Trío L; Criado Garcia O; Aguado C; Juana-López L; Crespo I; Knecht E; Bovolenta P; Rodríguez de Córdoba S Brain; 2014 Mar; 137(Pt 3):806-18. PubMed ID: 24430976 [TBL] [Abstract][Full Text] [Related]
10. Protein degradation and quality control in cells from laforin and malin knockout mice. Garyali P; Segvich DM; DePaoli-Roach AA; Roach PJ J Biol Chem; 2014 Jul; 289(30):20606-14. PubMed ID: 24914213 [TBL] [Abstract][Full Text] [Related]
12. Loss of laforin or malin results in increased Drp1 level and concomitant mitochondrial fragmentation in Lafora disease mouse models. Upadhyay M; Agarwal S; Bhadauriya P; Ganesh S Neurobiol Dis; 2017 Apr; 100():39-51. PubMed ID: 28063983 [TBL] [Abstract][Full Text] [Related]