Muscle Glycogen Remodeling and Glycogen Phosphate Metabolism following Exhaustive Exercise of Wild Type and Laforin Knockout Mice

PTG protein depletion rescues malin-deficient Lafora disease in mouse

(2014) Julie Turnbull et al.   ANNALS OF NEUROLOGY

Glycogen accumulation underlies neurodegeneration and autophagy impairment in Lafora disease

(2014) J. Duran et al.   HUMAN MOLECULAR GENETICS

Protein Degradation and Quality Control in Cells from Laforin and Malin Knockout Mice

(2014) Punitee Garyali et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Glycogen Phosphomonoester Distribution in Mouse Models of the Progressive Myoclonic Epilepsy, Lafora Disease

(2014) Anna A. DePaoli-Roach et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Hyperphosphorylation of Glucosyl C6 Carbons and Altered Structure of Glycogen in the Neurodegenerative Epilepsy Lafora Disease

(2013) Felix Nitschke et al.   Cell Metabolism

Autophagy defects in Lafora disease

(2012) Rajat Puri et al.   Autophagy

Glycogen and its metabolism: some new developments and old themes

(2012) Peter J. Roach et al.   BIOCHEMICAL JOURNAL

Exercise-induced AMPK activity in skeletal muscle: Role in glucose uptake and insulin sensitivity

(2012) Martin Friedrichsen et al.   MOLECULAR AND CELLULAR ENDOCRINOLOGY

Exercise-induced BCL2-regulated autophagy is required for muscle glucose homeostasis

(2012) Congcong He et al.   NATURE

Hexokinase 2, Glycogen Synthase and Phosphorylase Play a Key Role in Muscle Glycogen Supercompensation

(2012) José M. Irimia et al.   PLoS One

Phosphate Incorporation during Glycogen Synthesis and Lafora Disease

(2011) Vincent S. Tagliabracci et al.   Cell Metabolism

Laforin and malin knockout mice have normal glucose disposal and insulin sensitivity

(2011) Anna A. DePaoli-Roach et al.   HUMAN MOLECULAR GENETICS

Human skeletal muscle glycogen utilization in exhaustive exercise: role of subcellular localization and fibre type

(2011) Joachim Nielsen et al.   JOURNAL OF PHYSIOLOGY-LONDON

Regulation of glucose and glycogen metabolism during and after exercise

(2011) Thomas E. Jensen et al.   JOURNAL OF PHYSIOLOGY-LONDON

PTG Depletion Removes Lafora Bodies and Rescues the Fatal Epilepsy of Lafora Disease

(2011) Julie Turnbull et al.   PLoS Genetics

The regulation of muscle glycogen: the granule and its proteins

(2010) T. E. Graham et al.   Acta Physiologica

Starch: Its Metabolism, Evolution, and Biotechnological Modification in Plants

(2010) Samuel C. Zeeman et al.   Annual Review of Plant Biology

Impaired autophagy in Lafora disease

(2010) Erwin Knecht et al.   Autophagy

Laforin, the most common protein mutated in Lafora disease, regulates autophagy

(2010) Carmen Aguado et al.   HUMAN MOLECULAR GENETICS

Starch Binding Domain-containing Protein 1/Genethonin 1 Is a Novel Participant in Glycogen Metabolism

(2010) Sixin Jiang et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Genetic Depletion of the Malin E3 Ubiquitin Ligase in Mice Leads to Lafora Bodies and the Accumulation of Insoluble Laforin

(2010) Anna A. DePaoli-Roach et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Lafora disease: insights into neurodegeneration from plant metabolism

(2009) Matthew S. Gentry et al.   TRENDS IN BIOCHEMICAL SCIENCES

Suppression of autophagy in skeletal muscle uncovers the accumulation of ubiquitinated proteins and their potential role in muscle damage in Pompe disease

(2008) N. Raben et al.   HUMAN MOLECULAR GENETICS

Abnormal Metabolism of Glycogen Phosphate as a Cause for Lafora Disease

(2008) Vincent S. Tagliabracci et al.   JOURNAL OF BIOLOGICAL CHEMISTRY