Results 1 to 10 of about 336,760 (258)

Ketotic hypoglycemia in patients with Down syndrome

open access: yesJIMD Reports, 2021
Background Ketotic hypoglycemia (KH) without an identifiable underlying metabolic or hormonal disease is historically named idiopathic KH. The prevalence is unknown, but idiopathic KH is considered the most frequent cause of hypoglycemia beyond the ...
Danielle Drachmann   +4 more
doaj   +1 more source

Manipulation of glycogen and sucrose synthesis increases photosynthetic productivity in cyanobacteria

open access: yesFrontiers in Microbiology, 2023
Photosynthetic productivity is limited by low energy conversion efficiency in naturally evolved photosynthetic organisms, via multiple mechanisms that are not fully understood.
Michael Cantrell   +6 more
doaj   +1 more source

Does the Nutritional Composition of Dairy Milk Based Recovery Beverages Influence Post-exercise Gastrointestinal and Immune Status, and Subsequent Markers of Recovery Optimisation in Response to High Intensity Interval Exercise?

open access: yesFrontiers in Nutrition, 2021
This study aimed to determine the effects of flavored dairy milk based recovery beverages of different nutrition compositions on markers of gastrointestinal and immune status, and subsequent recovery optimisation markers.
Isabella Russo   +6 more
doaj   +1 more source

Dynamics of training and acute exercise-induced shifts in muscular glucose transporter (GLUT) 4, 8, and 12 expression in locomotion versus posture muscles in healthy horses

open access: yesFrontiers in Physiology, 2023
Important changes in glucose transporter (GLUT) expression should be expected if the glucose influx plays a pivotal role in fuelling or connecting metabolic pathways that are upregulated in response to exercise.
Carmen Vidal Moreno de Vega   +13 more
doaj   +1 more source

The Action of Recombinant Human Lysosomal α-Glucosidase (rhGAA) on Human Liver Glycogen: Pathway to Complete Degradation

open access: yesInternational Journal of Translational Medicine, 2021
Glycogen is present in all tissues, but it is primarily stored in the liver and in muscle. As a branched chain carbohydrate, it is broken down by phosphorylase and debrancher enzymes, which are cytoplasmic.
Allen K. Murray
doaj   +1 more source

Role of Astrocytes in the Pathophysiology of Lafora Disease and Other Glycogen Storage Disorders

open access: yesCells, 2023
Lafora disease is a rare disorder caused by loss of function mutations in either the EPM2A or NHLRC1 gene. The initial symptoms of this condition are most commonly epileptic seizures, but the disease progresses rapidly with dementia, neuropsychiatric ...
Jordi Duran
doaj   +1 more source

Liver Glycogen Phosphorylase Deficiency Leads to Profibrogenic Phenotype in a Murine Model of Glycogen Storage Disease Type VI

open access: yesHepatology Communications, 2019
Mutations in the liver glycogen phosphorylase (Pygl) gene are associated with the diagnosis of glycogen storage disease type VI (GSD‐VI). To understand the pathogenesis of GSD‐VI, we generated a mouse model with Pygl deficiency (Pygl−/−).
Lane H. Wilson   +8 more
doaj   +1 more source

Dynamics of morphometric parameters and the glycogen content in rat hearts after аntenatal antigen influence

open access: yesPatologìâ, 2013
Cardiovascular pathology may be formed on the background of the heart morphogenesis disturbances during fetal development. There is a high prevalence of pathological pregnancy, intrauterine infections of different etiology, accompanied by dysfunction of ...
A. N. Lebedinets
doaj   +1 more source

Sleep and Wake Affect Glycogen Content and Turnover at Perisynaptic Astrocytic Processes

open access: yesFrontiers in Cellular Neuroscience, 2018
Astrocytic glycogen represents the only form of glucose storage in the brain, and one of the outcomes of its breakdown is the production of lactate that can be used by neurons as an alternative energetic substrate.
Michele Bellesi   +5 more
doaj   +1 more source

Changes of gangliosides and other lipids in skeletal muscle from rabbits with experimental dystrophy

open access: yesJournal of Lipid Research, 1974
Comparison of the skeletal muscles from vitamin E-deficient and control rabbits showed that the muscles from the deficient animals had lower contents of protein and glycogen but more water and lipid.
I. Albarracín, F.E. Lassaga, R. Caputto
doaj   +1 more source

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