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.
2. 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]
3. 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]
4. Lafora progressive myoclonus epilepsy: recent insights into cell degeneration. Spuch C; Ortolano S; Navarro C Recent Pat Endocr Metab Immune Drug Discov; 2012 May; 6(2):99-107. PubMed ID: 22369717 [TBL] [Abstract][Full Text] [Related]
7. Lafora disease: from genotype to phenotype. Parihar R; Rai A; Ganesh S J Genet; 2018 Jul; 97(3):611-624. PubMed ID: 30027899 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. Lafora disease: Current biology and therapeutic approaches. Mitra S; Gumusgoz E; Minassian BA Rev Neurol (Paris); 2022 Apr; 178(4):315-325. PubMed ID: 34301405 [TBL] [Abstract][Full Text] [Related]
12. 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. PubMed ID: 22815132 [TBL] [Abstract][Full Text] [Related]
13. Laforin in autophagy: a possible link between carbohydrate and protein in Lafora disease? Puri R; Ganesh S Autophagy; 2010 Nov; 6(8):1229-31. PubMed ID: 20818153 [TBL] [Abstract][Full Text] [Related]
15. Lafora disease in the Indian population: EPM2A and NHLRC1 gene mutations and their impact on subcellular localization of laforin and malin. Singh S; Satishchandra P; Shankar SK; Ganesh S Hum Mutat; 2008 Jun; 29(6):E1-12. PubMed ID: 18311786 [TBL] [Abstract][Full Text] [Related]