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DNA joinase
DNA ligase
DNA sealase
Deoxyribonucleic acid ligase
Kinase
Ligase
MAP kinase
MAPK
Mitogen activated protein kinase
Mitogen-activated protein kinase
PKA
Polydeoxyribonucleotide synthetase
Polynucleotide kinase
Polynucleotide ligase
Polynucleotide synthetase
Protein kinase

Translation of "Polynucleotide kinase " (English → French) :

polynucleotide kinase

polynucléotide kinase
biologie > génétique | biologie > enzyme
biologie > génétique | biologie > enzyme


Polynucleotide kinase

polynucléotide kinase
génie génétique | génétique moléculaire
génie génétique > génétique moléculaire


polynucleotide kinase

polynucléotide kinase
IATE - Health
IATE - Health


polynucleotide kinase

polynucléotide kinase
IATE - Health | Natural and applied sciences
IATE - Health | Natural and applied sciences


mitogen activated protein kinase | MAPK | mitogen-activated protein kinase | MAP kinase

protéine kinase activée par des agents mitogènes | MAP kinase | kinase MAP | MAPK
biologie > enzyme
biologie > enzyme


DNA ligase | deoxyribonucleic acid ligase | DNA joinase | DNA sealase | polynucleotide synthetase | polydeoxyribonucleotide synthetase | polynucleotide ligase | ligase

ADN ligase | ADN-ligase | polynucléotide ligase | DNA ligase | ligase
biologie > enzyme
biologie > enzyme


kinase | protein kinase | PKA [Abbr.]

kinase | protéine-kinase
IATE - Health | Chemistry
IATE - Health | Chemistry


This syndrome is characterized by psychomotor delay and severe myopathy (hypotonia, absent tendon reflexes and delayed myelination) from birth, associated with hypermethioninemia and elevated serum creatine kinase levels. It has been described in thr

retard psychomoteur par déficit en S-adénosylhomocystéine hydrolase
SNOMEDCT-BE (hypotonia, absent tendon reflexes and delayed myelination) from birth, associated with hypermethioninemia and elevated serum creatine kinase levels. It has been described in thr / 724039002
SNOMEDCT-BE (disorder) / 724039002


A rare metabolic myopathy with characteristics of muscle cramping and/or stiffness after exercise (especially during heat exposure), post-exertional rhabdomyolysis and myoglobinuria and elevation of serum creatine kinase. Caused by mutation in the SL

myopathie métabolique par défaut de transport du lactate
SNOMEDCT-BE (especially during heat exposure), post-exertional rhabdomyolysis and myoglobinuria and elevation of serum creatine kinase. Caused by mutation in the SL / 766715000
SNOMEDCT-BE (disorder) / 766715000


A rare, very severe form of mevalonate kinase deficiency with characteristics of dysmorphic features, failure to thrive, psychomotor delay, ocular involvement, hypotonia, progressive ataxia, myopathy, and recurrent inflammatory episodes.

acidurie mévalonique
SNOMEDCT-BE (disorder) / 718558008
SNOMEDCT-BE (disorder) / 718558008




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'Polynucleotide kinase'

Date index:2023-04-14 -

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