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Degradation of salicylhydroxamic acid in mineral beneficiation wastewater by dielectric barrier discharge and La-Fe3O4-doped activated carbon: Parametric optimization, kinetics, activation process, and transformation pathway

Arabian journal of chemistry, 2023-09, Vol.16 (9), p.105048, Article 105048

2023

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RAB-10 Promotes EHBP-1 Bridging of Filamentous Actin and Tubular Recycling Endosomes

PLoS genetics, 2016-06, Vol.12 (6), p.e1006093-e1006093

2016

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Ppp1r3d deficiency preferentially inhibits neuronal and cardiac Lafora body formation in a mouse model of the fatal epilepsy Lafora disease

Journal of neurochemistry, 2021-06, Vol.157 (6), p.1897-1910

2021

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An EHBP-1-SID-3-DYN-1 axis promotes membranous tubule fission during endocytic recycling

PLoS genetics, 2020-05, Vol.16 (5), p.e1008763-e1008763

2020

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Skeletal Muscle Glycogen Chain Length Correlates with Insolubility in Mouse Models of Polyglucosan-Associated Neurodegenerative Diseases

Cell reports (Cambridge), 2019-04, Vol.27 (5), p.1334-1344.e6

2019

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Glycogen synthase downregulation rescues the amylopectinosis of murine RBCK1 deficiency

Brain (London, England : 1878), 2022-07, Vol.145 (7), p.2361-2377

2022

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Laforin targets malin to glycogen in Lafora progressive myoclonus epilepsy

Disease models & mechanisms, 2023-01, Vol.16 (1)

2023

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PTG protein depletion rescues malin-deficient Lafora disease in mouse

Annals of neurology, 2014-03, Vol.75 (3), p.442-446

2014

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Study on the Polymer Morphology and Electro-Optical Performance of Acrylate/Epoxy Resin-Based Polymer-Stabilized Liquid Crystals Based on Stepwise Photopolymerization

Polymers, 2024-08, Vol.16 (17), p.2446

2024

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Lafora disease in miniature Wirehaired Dachshunds

PloS one, 2017-08, Vol.12 (8), p.e0182024-e0182024

2017

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Abnormal glycogen chain length pattern, not hyperphosphorylation, is critical in Lafora disease

EMBO molecular medicine, 2017-07, Vol.9 (7), p.906-917

2017

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Early-onset Lafora body disease

Brain (London, England : 1878), 2012-09, Vol.135 (Pt 9), p.2684-2698

2012

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PTG depletion removes Lafora bodies and rescues the fatal epilepsy of Lafora disease

PLoS genetics, 2011-04, Vol.7 (4), p.e1002037-e1002037

2011

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Glycogen hyperphosphorylation underlies lafora body formation

Annals of neurology, 2010-12, Vol.68 (6), p.925-933

2010

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Ghrelin Through GHSR1a and OX1R Heterodimers Reveals a Gαs-cAMP-cAMP Response Element Binding Protein Signaling Pathway in Vitro

Frontiers in molecular neuroscience, 2018-07, Vol.11, p.245-245

2018

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Canine Lafora Disease: An Unstable Repeat Expansion Disorder

Life (Basel, Switzerland), 2021-07, Vol.11 (7), p.689

2021

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Increased Laforin and Laforin Binding to Glycogen Underlie Lafora Body Formation in Malin-deficient Lafora Disease

The Journal of biological chemistry, 2012-07, Vol.287 (30), p.25650-25659

2012

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Correction to: Nationwide genetic testing towards eliminating Lafora disease from Miniature Wirehaired Dachshunds in the United Kingdom

Canine medicine and genetics, 2021-12, Vol.8 (1), p.14-14, Article 14

2021

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Degrading hazardous benzohydroxamic acid in the industrial beneficiation wastewater by dielectric barrier discharge reactor

Separation and purification technology, 2022-10, Vol.299, p.121644, Article 121644

2022

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GYS1 or PPP1R3C deficiency rescues murine adult polyglucosan body disease

Annals of clinical and translational neurology, 2020-11, Vol.7 (11), p.2186-2198

2020

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Fast Bayesian modal identification with known seismic excitations

Earthquake engineering & structural dynamics, 2024-09, Vol.53 (11), p.3439-3468

2024

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POU Homeodomain Protein Oct-1 Functions as a Sensor for Cyclic AMP

The Journal of biological chemistry, 2009-09, Vol.284 (39), p.26456-26465

2009

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Preparation and thermal properties of colloidal mixtures of capric acid and Na2HPO4·12H2O as a phase change material for energy storage

Solar energy materials and solar cells, 2020-09, Vol.215, p.110636, Article 110636

2020

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Oct-1 functions as a sensor for metabolic and stress signals

Islets, 2010-01, Vol.2 (1), p.46-48

2010

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Heterodimerization of apelin and opioid receptor-like 1 receptors mediates apelin-13-induced G protein biased signaling

Life sciences (1973), 2023-09, Vol.328, p.121892-121892, Article 121892

2023

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Degradation of salicylhydroxamic acid in mineral beneficiation wastewater by dielectric barrier discharge and La-Fe3O4-doped activated carbon: Parametric optimization, kinetics, activation process, and transformation pathway

RAB-10 Promotes EHBP-1 Bridging of Filamentous Actin and Tubular Recycling Endosomes

Ppp1r3d deficiency preferentially inhibits neuronal and cardiac Lafora body formation in a mouse model of the fatal epilepsy Lafora disease

An EHBP-1-SID-3-DYN-1 axis promotes membranous tubule fission during endocytic recycling

Skeletal Muscle Glycogen Chain Length Correlates with Insolubility in Mouse Models of Polyglucosan-Associated Neurodegenerative Diseases

Glycogen synthase downregulation rescues the amylopectinosis of murine RBCK1 deficiency

Laforin targets malin to glycogen in Lafora progressive myoclonus epilepsy

PTG protein depletion rescues malin-deficient Lafora disease in mouse

Study on the Polymer Morphology and Electro-Optical Performance of Acrylate/Epoxy Resin-Based Polymer-Stabilized Liquid Crystals Based on Stepwise Photopolymerization

Lafora disease in miniature Wirehaired Dachshunds

Abnormal glycogen chain length pattern, not hyperphosphorylation, is critical in Lafora disease

Early-onset Lafora body disease

PTG depletion removes Lafora bodies and rescues the fatal epilepsy of Lafora disease

Glycogen hyperphosphorylation underlies lafora body formation

Ghrelin Through GHSR1a and OX1R Heterodimers Reveals a Gαs-cAMP-cAMP Response Element Binding Protein Signaling Pathway in Vitro

Canine Lafora Disease: An Unstable Repeat Expansion Disorder

Increased Laforin and Laforin Binding to Glycogen Underlie Lafora Body Formation in Malin-deficient Lafora Disease

Correction to: Nationwide genetic testing towards eliminating Lafora disease from Miniature Wirehaired Dachshunds in the United Kingdom

Degrading hazardous benzohydroxamic acid in the industrial beneficiation wastewater by dielectric barrier discharge reactor

GYS1 or PPP1R3C deficiency rescues murine adult polyglucosan body disease

Fast Bayesian modal identification with known seismic excitations

POU Homeodomain Protein Oct-1 Functions as a Sensor for Cyclic AMP

Preparation and thermal properties of colloidal mixtures of capric acid and Na2HPO4·12H2O as a phase change material for energy storage

Oct-1 functions as a sensor for metabolic and stress signals

Heterodimerization of apelin and opioid receptor-like 1 receptors mediates apelin-13-induced G protein biased signaling

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