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Chlorure de phosphoryle
Déficit combiné de la phosphorylation oxydative type 15
Déficit combiné de la phosphorylation oxydative type 7
Déficit combiné de la phosphorylation oxydative type 8
Glycéride phosphorylé d'ammonium
Oxychlorure de phosphore
Phosphorilation
Phosphorylation
Phosphoryler
Phosphorylisation
Sel d'ammonium de glycéride phosphorylé

Translation of "phosphoryler " (French → English) :

TERMINOLOGY
see also In-Context Translations below
phosphoryler

phosphorylate, to
IATE - Natural and applied sciences
IATE - Natural and applied sciences


sel d'ammonium de glycéride phosphorylé [ glycéride phosphorylé d'ammonium ]

ammonium salt of phosphorylated glyceride
Industrie de l'alimentation
Food Industries


oxychlorure de phosphore | chlorure de phosphoryle

phosphorus oxychloride
chimie
chimie


phosphorylation

phosphorylation
biologie > biochimie
biologie > biochimie


oxychlorure de phosphore [ chlorure de phosphoryle ]

phosphorus oxychloride [ phosphoryl chloride ]
Additifs alimentaires
Food Additives


chlorure de phosphoryle | oxychlorure de phosphore

phosphorus oxychloride
IATE - Chemistry
IATE - Chemistry


phosphorilation | phosphorylation | phosphorylisation

phosphorylation
IATE - Natural and applied sciences
IATE - Natural and applied sciences


ficit combiné de la phosphorylation oxydative type 8

A mitochondrial disease due to a defect in mitochondrial protein synthesis resulting in deficiency of respiratory chain complexes I, III and IV in the cardiac and skeletal muscle and brain. The disease has characteristics of severe hypertrophic cardi
SNOMEDCT-BE (disorder) / 733600007
SNOMEDCT-BE (disorder) / 733600007


ficit combiné de la phosphorylation oxydative type 15

A rare mitochondrial disease due to a defect in mitochondrial protein synthesis with onset in infancy or early childhood of muscular hypotonia, gait ataxia, mild bilateral pyramidal tract signs, developmental delay (affecting mostly speech and coordi
SNOMEDCT-BE (disorder) / 763203009
SNOMEDCT-BE (affecting mostly speech and coordi / 763203009


ficit combiné de la phosphorylation oxydative type 7

A rare mitochondrial disease due to a defect in mitochondrial protein synthesis with a variable phenotype that includes onset in infancy or early childhood of failure to thrive and psychomotor regression (after initial normal development), as well as
SNOMEDCT-BE (disorder) / 763204003
SNOMEDCT-BE (after initial normal development), as well as / 763204003
IN-CONTEXT TRANSLATIONS
(C) sels d’ammonium de glycérides phosphorylés,

(C) ammonium salts of phosphorylated glycerides,


(C) sels d’ammonium de glycérides phosphorylés,

(C) ammonium salts of phosphorylated glycerides,


(C) sels d’ammonium de glycérides phosphorylés.

(C) ammonium salts of phosphorylated glycerides.


k) de la lécithine ou du sel d’ammonium de glycéride phosphorylé;

(k) lecithin or ammonium salt of phosphorylated glyceride;


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Le glucose et le fructose sont phosphorylés par l'adénosine-triphosphate (ATP) au cours d'une réaction enzymatique catalysée par l'hexokinase (HK) et donnent du glucose-6-phosphate (G6P) et du fructose-6-phosphate (F6P):

Glucose and fructose are phosphorylated by adenosine triphosphate (ATP) during an enzymatic reaction catalysed by hexokinase (HK), and produce glucose 6-phosphate (G6P) and fructose 6-phosphate (F6P):




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phosphoryler

Date index:2024-03-23 -

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