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Abbreviation : LBs
Long Form : Lafora bodies
No. Year Title Co-occurring Abbreviation
2018 Astrocytes and neurons produce distinct types of polyglucosan bodies in Lafora disease. LD, PGBs, PTGOE, SAMP8
2018 Astrocytes: new players in progressive myoclonus epilepsy of Lafora type. GFAP, LD
2018 Diabetes Mellitus in a Patient With Lafora Disease: Possible Links With Pancreatic beta-Cell Dysfunction and Insulin Resistance. LD
2018 Lafora Disease: A Ubiquitination-Related Pathology. PME
2017 Abnormal glycogen chain length pattern, not hyperphosphorylation, is critical in Lafora disease. LD
2017 Pathogenesis of Lafora Disease: Transition of Soluble Glycogen to Insoluble Polyglucosan. ---
2016 Genetics of Lafora progressive myoclonic epilepsy: current perspectives. GS, LD
2016 Pharmacological Interventions to Ameliorate Neuropathological Symptoms in a Mouse Model of Lafora Disease. AMPK
2015 Structural mechanism of laforin function in glycogen dephosphorylation and lafora disease. LD
10  2014 Neuronal glycogen synthesis contributes to physiological aging. CA
11  2013 Inhibiting glycogen synthesis prevents Lafora disease in a mouse model. LD
12  2013 Laforin prevents stress-induced polyglucosan body formation and Lafora disease progression in neurons. LD
13  2012 Lafora bodies and neurological defects in malin-deficient mice correlate with impaired autophagy. LD
14  2012 Malin knockout mice support a primary role of autophagy in the pathogenesis of Lafora disease. LD
15  2012 Ontogeny of Lafora bodies and neurocytoskeleton changes in Laforin-deficient mice. LD
16  2011 Laforin, a dual specificity phosphatase involved in Lafora disease, is present mainly as monomeric form with full phosphatase activity. LD
17  2011 Neurodegeneration and functional impairments associated with glycogen synthase accumulation in a mouse model of Lafora disease. GS, KO, LD
18  2009 Conservation of the glucan phosphatase laforin is linked to rates of molecular evolution and the glucan metabolism of the organism. LD
19  2007 The phosphatase laforin crosses evolutionary boundaries and links carbohydrate metabolism to neuronal disease. LD, SEX4
20  2005 Novel glycogen synthase kinase 3 and ubiquitination pathways in progressive myoclonus epilepsy. GS, GSK-3
21  2004 Laforin preferentially binds the neurotoxic starch-like polyglucosans, which form in its absence in progressive myoclonus epilepsy. ER, LD
22  1991 Early detection of skin and muscular involvement in Lafora disease. LD