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1925, University of Toronto studies. Physiological series, Volume no. 97, 22-35
Book
Clinical Neurophysiology, ISSN 1388-2457, 07/2019, Volume 130, Issue 7, pp. e31 - e31
Micro-EMG is a novel multi-electrode system that samples EMG signal from 64 electrodes along the surface of the needle in order to localise the muscle fibres... 
Glycogen
Journal Article
Nutrition and cancer, 02/2019, p. 1
Capsaicin (trans-8-methyl-n-vanillyl-6-nonenamide) is the main pungent component found in hot peppers. In this study, we investigated the effect of capsaicin... 
Journal Article
BBA - Bioenergetics, ISSN 0005-2728, 08/2016, Volume 1857, pp. e98 - e98
Journal Article
La Revue de medecine interne, ISSN 0248-8663, 03/2017, Volume 38, Issue 3, p. 201
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1016/j.revmed.2016.05.001 La... 
Glycogen
Journal Article
Toxicology, ISSN 0300-483X, 09/2017, Volume 390, pp. 146 - 158
Lead (Pb) is an environmental neurotoxin which particularly affects the developing brain but the molecular mechanism of its neurotoxicity still needs... 
Glycogen phosphorylase brain isoform (PYGB) | Glycogen phosphorylase muscle isoform (PYGM) | Brain glycogen metabolism | Lead (Pb) neurotoxicity | Glycogen synthase (Gys1) | Glycogen phosphorylase kinase (PHKB) | OXIDATIVE-STRESS | GAP-JUNCTION HEMICHANNELS | AUTISM SPECTRUM DISORDER | TAU PHOSPHORYLATION | LOW-LEVEL LEAD | CEREBROSPINAL FLUID BARRIER | PHARMACOLOGY & PHARMACY | TOXICOLOGY | RAT-BRAIN | ENERGY-METABOLISM | NF-KAPPA-B | PARKINSONS-DISEASE | Neurons - pathology | Prenatal Exposure Delayed Effects | Age Factors | Rats, Wistar | Glycogen Synthase - metabolism | Astrocytes - pathology | Lead Poisoning, Nervous System, Childhood - metabolism | Glycogen Phosphorylase, Brain Form - genetics | Lead Poisoning, Nervous System, Childhood - pathology | RNA, Messenger - metabolism | Brain - metabolism | Glycogen - metabolism | Female | Lead Poisoning, Nervous System, Childhood - etiology | Neurons - metabolism | Neurons - drug effects | Animals, Newborn | Astrocytes - drug effects | Glycogen Synthase - genetics | Organometallic Compounds - toxicity | Connexin 43 - metabolism | RNA, Messenger - genetics | Glycogen Phosphorylase, Brain Form - metabolism | Lead Poisoning, Nervous System, Childhood - genetics | Gestational Age | Phosphorylase Kinase - genetics | Brain - drug effects | Pregnancy | Animals | Phosphorylase Kinase - metabolism | Cell Communication - drug effects | Brain - pathology | Glucose - metabolism | Energy Metabolism - drug effects | Astrocytes - metabolism | Infants (Newborn) | Physiological aspects | Glucose metabolism | Synthesis | Neurons | Glycogen | Analysis | Glucose | Gene expression | Dextrose | Index Medicus
Journal Article
Journal Article
Molecular Therapy, ISSN 1525-0016, 03/2018, Volume 26, Issue 3, pp. 890 - 901
Glycogen storage disease type III (GSDIII) is an autosomal recessive disorder caused by a deficiency of glycogen-debranching enzyme (GDE), which results in... 
dual AAV vectors | acid-alpha-glucosidase | neuromuscular disease | gene therapy | glycogen storage disease type III | glycogenosis | Cori disease | adeno-associated vector | MEDICINE, RESEARCH & EXPERIMENTAL | EFFICACY | ADENOASSOCIATED VIRUS | TRANSDUCTION | GENOME | THERAPY | GLYCOGEN-STORAGE-DISEASE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | AAV | MOUSE MODEL | IN-VIVO | GENETICS & HEREDITY | VECTORS | Dependovirus - genetics | Glycogen Storage Disease Type III - metabolism | Genetic Vectors - administration & dosage | Male | Muscle, Skeletal - metabolism | Hepatocytes - metabolism | Glycogen - metabolism | Glycogen Debranching Enzyme System - genetics | Disease Models, Animal | Gene Transfer Techniques | Gene Expression | Glycogen Storage Disease Type III - therapy | Glycogen Debranching Enzyme System - metabolism | Glycogen Storage Disease Type III - diagnosis | Liver - metabolism | Blood Glucose | Organ Specificity | Genetic Vectors - genetics | Glycogen Storage Disease Type III - genetics | Mice, Knockout | Phenotype | Animals | Biomarkers | Mice | Enzyme Activation | Genetic Therapy - methods | Enzymes | Phenotypes | Statistical analysis | Gene transfer | Glycogen | Cardiomyopathy | Liver | Glucose | Gene expression | Hypoglycemia | Metabolism | Vectors (Biology) | Hereditary diseases | Storage diseases | Consortia | Glucose metabolism | Musculoskeletal system | Biopsy | Gene therapy | Age | Index Medicus | Original
Journal Article
Journal of Equine Veterinary Science, ISSN 0737-0806, 05/2015, Volume 35, Issue 5, pp. 408 - 409
Journal Article
BBA - General Subjects, ISSN 0304-4165, 01/2017, Volume 1861, Issue 1, pp. 3388 - 3398
Journal Article
Genetics in Medicine, ISSN 1098-3600, 04/2019, Volume 21, Issue 4, pp. 772 - 789
Journal Article
Journal Article
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 1126 - 15
Journal Article