L-threo-dihydroxyphenylserine corrects neurochemical abnormalities in a Menkes disease mouse model
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Mottled Mice and Non-Mammalian Models of Menkes DiseaseTranslational research investigations on ATP7A: an important human copper ATPaseMolecular basis of neurodegeneration and neurodevelopmental defects in Menkes diseaseMolecular and biochemical characterization of Mottled-dappled, an embryonic lethal Menkes disease mouse modelAutonomous requirements of the Menkes disease protein in the nervous system.Peptidylglycine α-amidating monooxygenase heterozygosity alters brain copper handling with region specificity.
P2860
L-threo-dihydroxyphenylserine corrects neurochemical abnormalities in a Menkes disease mouse model
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name
L-threo-dihydroxyphenylserine ...... n a Menkes disease mouse model
@ast
L-threo-dihydroxyphenylserine ...... n a Menkes disease mouse model
@en
type
label
L-threo-dihydroxyphenylserine ...... n a Menkes disease mouse model
@ast
L-threo-dihydroxyphenylserine ...... n a Menkes disease mouse model
@en
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L-threo-dihydroxyphenylserine ...... n a Menkes disease mouse model
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L-threo-dihydroxyphenylserine ...... n a Menkes disease mouse model
@en
P2093
P2860
P356
P1433
P1476
L-threo-dihydroxyphenylserine ...... n a Menkes disease mouse model
@en
P2093
David S Goldstein
Lauren R Brinster
Patricia Sullivan
Stephen G Kaler
P2860
P304
P356
10.1002/ANA.23787
P577
2012-12-07T00:00:00Z