336 related articles for article (PubMed ID: 26546463)
1. Ubiquitin conjugating enzyme E2-N and sequestosome-1 (p62) are components of the ubiquitination process mediated by the malin-laforin E3-ubiquitin ligase complex.
Sánchez-Martín P; Romá-Mateo C; Viana R; Sanz P
Int J Biochem Cell Biol; 2015 Dec; 69():204-14. PubMed ID: 26546463
[TBL] [Abstract][Full Text] [Related]
2. Regulation of the autophagic PI3KC3 complex by laforin/malin E3-ubiquitin ligase, two proteins involved in Lafora disease.
Sanchez-Martin P; Lahuerta M; Viana R; Knecht E; Sanz P
Biochim Biophys Acta Mol Cell Res; 2020 Feb; 1867(2):118613. PubMed ID: 31758957
[TBL] [Abstract][Full Text] [Related]
3. The laforin/malin E3-ubiquitin ligase complex ubiquitinates pyruvate kinase M1/M2.
Viana R; Lujan P; Sanz P
BMC Biochem; 2015 Oct; 16():24. PubMed ID: 26493215
[TBL] [Abstract][Full Text] [Related]
4. 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; 102(24):8501-6. PubMed ID: 15930137
[TBL] [Abstract][Full Text] [Related]
5. Lafora disease E3-ubiquitin ligase malin is related to TRIM32 at both the phylogenetic and functional level.
Romá-Mateo C; Moreno D; Vernia S; Rubio T; Bridges TM; Gentry MS; Sanz P
BMC Evol Biol; 2011 Jul; 11():225. PubMed ID: 21798009
[TBL] [Abstract][Full Text] [Related]
6. 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; 17(5):667-78. PubMed ID: 18029386
[TBL] [Abstract][Full Text] [Related]
7. The laforin-malin complex, involved in Lafora disease, promotes the incorporation of K63-linked ubiquitin chains into AMP-activated protein kinase beta subunits.
Moreno D; Towler MC; Hardie DG; Knecht E; Sanz P
Mol Biol Cell; 2010 Aug; 21(15):2578-88. PubMed ID: 20534808
[TBL] [Abstract][Full Text] [Related]
8. 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; 16(7):753-62. PubMed ID: 17337485
[TBL] [Abstract][Full Text] [Related]
9. Endocytosis of the glutamate transporter 1 is regulated by laforin and malin: Implications in Lafora disease.
Perez-Jimenez E; Viana R; Muñoz-Ballester C; Vendrell-Tornero C; Moll-Diaz R; Garcia-Gimeno MA; Sanz P
Glia; 2021 May; 69(5):1170-1183. PubMed ID: 33368637
[TBL] [Abstract][Full Text] [Related]
10. Glycogenic activity of R6, a protein phosphatase 1 regulatory subunit, is modulated by the laforin-malin complex.
Rubio-Villena C; Garcia-Gimeno MA; Sanz P
Int J Biochem Cell Biol; 2013 Jul; 45(7):1479-88. PubMed ID: 23624058
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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; 18(4):688-700. PubMed ID: 19036738
[TBL] [Abstract][Full Text] [Related]
14. Lafora Disease: A Ubiquitination-Related Pathology.
García-Gimeno MA; Knecht E; Sanz P
Cells; 2018 Jul; 7(8):. PubMed ID: 30050012
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Lafora disease proteins laforin and malin negatively regulate the HIPK2-p53 cell death pathway.
Upadhyay M; Gupta S; Bhadauriya P; Ganesh S
Biochem Biophys Res Commun; 2015 Aug; 464(1):106-11. PubMed ID: 26102034
[TBL] [Abstract][Full Text] [Related]
17. Malin decreases glycogen accumulation by promoting the degradation of protein targeting to glycogen (PTG).
Worby CA; Gentry MS; Dixon JE
J Biol Chem; 2008 Feb; 283(7):4069-76. PubMed ID: 18070875
[TBL] [Abstract][Full Text] [Related]
18. Interdependence of laforin and malin proteins for their stability and functions could underlie the molecular basis of locus heterogeneity in Lafora disease.
Mittal S; Upadhyay M; Singh PK; Parihar R; Ganesh S
J Biosci; 2015 Dec; 40(5):863-71. PubMed ID: 26648032
[TBL] [Abstract][Full Text] [Related]
19. P-Rex1 is a novel substrate of the E3 ubiquitin ligase Malin associated with Lafora disease.
Kumarasinghe L; Garcia-Gimeno MA; Ramirez J; Mayor U; Zugaza JL; Sanz P
Neurobiol Dis; 2023 Feb; 177():105998. PubMed ID: 36638890
[TBL] [Abstract][Full Text] [Related]
20. Loss of malin, but not laforin, results in compromised autophagic flux and proteasomal dysfunction in cells exposed to heat shock.
Jain N; Rai A; Mishra R; Ganesh S
Cell Stress Chaperones; 2017 Mar; 22(2):307-315. PubMed ID: 27975203
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
