Creatine deficiency syndromes and the importance of creatine synthesis in the brain - Wikidata - awgldk - TriplyDB

Creatine deficiency syndromes and the importance of creatine synthesis in the brain

Creatine deficiency syndromes and the importance of creatine synthesis in the brain

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A buffered form of creatine does not promote greater changes in muscle creatine content, body composition, or training adaptations than creatine monohydrate Creatine supplementation with specific view to exercise/sports performance: an update The effect of the creatine analogue beta-guanidinopropionic acid on energy metabolism: a systematic review Patterns of brain injury in inborn errors of metabolism Understanding pyrroline-5-carboxylate synthetase deficiency: clinical, molecular, functional, and expression studies, structure-based analysis, and novel therapy with arginine Ammonia toxicity to the brain.Inborn errors of creatine metabolism and epilepsy.International Society of Sports Nutrition position stand: safety and efficacy of creatine supplementation in exercise, sport, and medicine γ-Aminobutyric acid transporter 2 mediates the hepatic uptake of guanidinoacetate, the creatine biosynthetic precursor, in rats.The role of dietary creatine.Creatine, Glutamine plus Glutamate, and Macromolecules Are Decreased in the Central White Matter of Premature Neonates around Term.Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms Unchanged mitochondrial organization and compartmentation of high-energy phosphates in creatine-deficient GAMT-/- mouse hearts.Creatine and guanidinoacetate transport at blood-brain and blood-cerebrospinal fluid barriers.X-linked creatine transporter deficiency: clinical aspects and pathophysiology.New insights into the trophic and cytoprotective effects of creatine in in vitro and in vivo models of cell maturation.Creatine synthesis and exchanges between brain cells: What can be learned from human creatine deficiencies and various experimental models?A mouse model for creatine transporter deficiency reveals early onset cognitive impairment and neuropathology associated with brain aging.Creatine transporter deficiency leads to increased whole body and cellular metabolism.Creatine and guanidinoacetate content of human milk and infant formulas: implications for creatine deficiency syndromes and amino acid metabolism.Laboratory diagnosis of creatine deficiency syndromes: a technical standard and guideline of the American College of Medical Genetics and Genomics.Does brain creatine content rely on exogenous creatine in healthy youth? A proof-of-principle study.In memory of Professor Eric Helmer Hultman.Involvement of hippocampal CAMKII/CREB signaling in the spatial memory retention induced by creatine.Downregulation of the creatine transporter SLC6A8 by JAK2.Dodecyl creatine ester and lipid nanocapsule: a double strategy for the treatment of creatine transporter deficiency.A simple screening method using ion chromatography for the diagnosis of cerebral creatine deficiency syndromes.Effects of creatine supplementation on cognitive function of healthy individuals: A systematic review of randomized controlled trials

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P2860

Creatine deficiency syndromes and the importance of creatine synthesis in the brain

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2011 nî lūn-bûn

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2011 թուականի Մարտին հրատարակուած գիտական յօդուած

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2011 թվականի մարտին հրատարակված գիտական հոդված

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2011年の論文

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Creatine deficiency syndromes and the importance of creatine synthesis in the brain

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Elidie Béard

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Hugues Henry

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Joséphine Uldry

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Olivier Braissant

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P2860

Intracellular compartmentation, structure and function of creatine kinase isoenzymes in tissues with high and fluctuating energy demands: the 'phosphocreatine circuit' for cellular energy homeostasis

X-linked creatine-transporter gene (SLC6A8) defect: a new creatine-deficiency syndrome.

High prevalence of SLC6A8 deficiency in X-linked mental retardation

Arginine:glycine amidinotransferase deficiency: the third inborn error of creatine metabolism in humans

Creatine synthesis and transport during rat embryogenesis: spatiotemporal expression of AGAT, GAMT and CT1.

Neuron-specific expression of cationic amino acid transporter 3 in the adult rat brain

Creatine depletion in a new case with AGAT deficiency: clinical and genetic study in a large pedigree

Inhibition of arginine-glycine amidinotransferase by ornithine. A possible mechanism for the muscular and chorioretinal atrophies in gyrate atrophy of the choroid and retina with hyperornithinemia

Early time course of N-acetylaspartate, creatine and phosphocreatine, and compounds containing choline in the brain after acute stroke. A proton magnetic resonance spectroscopy study

The putative rat choline transporter CHOT1 transports creatine and is highly expressed in neural and muscle-rich tissues

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