282 related articles for article (PubMed ID: 24131995)
1. Activation of serum/glucocorticoid-induced kinase 1 (SGK1) underlies increased glycogen levels, mTOR activation, and autophagy defects in Lafora disease.
Singh PK; Singh S; Ganesh S
Mol Biol Cell; 2013 Dec; 24(24):3776-86. PubMed ID: 24131995
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 22124153
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. Abnormal glycogen chain length pattern, not hyperphosphorylation, is critical in Lafora disease.
Nitschke F; Sullivan MA; Wang P; Zhao X; Chown EE; Perri AM; Israelian L; Juana-López L; Bovolenta P; Rodríguez de Córdoba S; Steup M; Minassian BA
EMBO Mol Med; 2017 Jul; 9(7):906-917. PubMed ID: 28536304
[TBL] [Abstract][Full Text] [Related]
7. Laforin, the most common protein mutated in Lafora disease, regulates autophagy.
Aguado C; Sarkar S; Korolchuk VI; Criado O; Vernia S; Boya P; Sanz P; de Córdoba SR; Knecht E; Rubinsztein DC
Hum Mol Genet; 2010 Jul; 19(14):2867-76. PubMed ID: 20453062
[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. 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]
10. 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]
11. 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]
12. FoxO3a-mediated autophagy is down-regulated in the laforin deficient mice, an animal model for Lafora progressive myoclonus epilepsy.
Jain N; Mishra R; Ganesh S
Biochem Biophys Res Commun; 2016 May; 474(2):321-327. PubMed ID: 27107699
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Muscle glycogen remodeling and glycogen phosphate metabolism following exhaustive exercise of wild type and laforin knockout mice.
Irimia JM; Tagliabracci VS; Meyer CM; Segvich DM; DePaoli-Roach AA; Roach PJ
J Biol Chem; 2015 Sep; 290(37):22686-98. PubMed ID: 26216881
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Laforin targets malin to glycogen in Lafora progressive myoclonus epilepsy.
Mitra S; Chen B; Wang P; Chown EE; Dear M; Guisso DR; Mariam U; Wu J; Gumusgoz E; Minassian BA
Dis Model Mech; 2023 Jan; 16(1):. PubMed ID: 36511140
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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. PubMed ID: 21505799
[TBL] [Abstract][Full Text] [Related]
20. Trehalose Ameliorates Seizure Susceptibility in Lafora Disease Mouse Models by Suppressing Neuroinflammation and Endoplasmic Reticulum Stress.
Sinha P; Verma B; Ganesh S
Mol Neurobiol; 2021 Mar; 58(3):1088-1101. PubMed ID: 33094475
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
