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European Journal of Biochemistry
|
December 15, 1996
Structure/function relationships in human phenylalanine hydroxylase. Effect of terminal deletions on the oligomerization, activation and cooperativity of substrate binding to the enzyme
P M Knappskog, T Flatmark, J M Aarden, et al.
Human Genetics
|
February 1, 1995
The PKU mutation S349P causes complete loss of catalytic activity in the recombinant phenylalanine hydroxylase enzyme
P M Knappskog, H G Eiken, A Martinez, et al.
European Journal of Biochemistry
|
January 1, 1980
Electron paramagnetic resonance of the copper in dopamine beta-monooxygenase. Rapid reduction by ascorbate, the steady-state redox level, chelation with EDTA, and reactivation of the apoenzyme by added copper
T Skotland, L Petersson, D Bäckström, et al.
The Journal of Biological Chemistry
|
December 15, 1988
Resonance Raman studies on the blue-green-colored bovine adrenal tyrosine 3-monooxygenase (tyrosine hydroxylase). Evidence that the feedback inhibitors adrenaline and noradrenaline are coordinated to iron
K K Andersson, D D Cox, L Que, et al.
Carcinogenesis
|
September 1, 1986
Relation between induction of ornithine decarboxylase and specific gene expression in rat liver in response to the tumor promoter agent clofibrate
M H Fukami, T S Eikhom, R Ekanger, et al.
Advances in Experimental Medicine and Biology
|
March 10, 2000
Metabolic effects of 3-thia fatty acid in cancer cells
K J Tronstad, K Berge, R Bjerkvig, et al.
Nature Structural Biology
|
December 24, 1997
Crystal structure of the catalytic domain of human phenylalanine hydroxylase reveals the structural basis for phenylketonuria
H Erlandsen, F Fusetti, A Martinez, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1993
Characterization of the iron environment in recombinant human tyrosine hydroxylase, using Mössbauer and EPR-spectroscopy
J Haavik, E Bill, M Lengen, et al.
FEBS Letters
|
April 7, 1997
Crystallization and preliminary diffraction analysis of a truncated homodimer of human phenylalanine hydroxylase
H Erlandsen, A Martinez, P M Knappskog, et al.
Human Mutation
|
January 1, 1996
PKU mutation (D143G) associated with an apparent high residual enzyme activity: expression of a kinetic variant form of phenylalanine hydroxylase in three different systems
P M Knappskog, H G Eiken, A Martínez, et al.
Page
of 17
Search research articles
Search
Showing results (141-150 of 169) with videos related to
Sort By:
Page
of 17
European Journal of Biochemistry
|
December 15, 1996
Structure/function relationships in human phenylalanine hydroxylase. Effect of terminal deletions on the oligomerization, activation and cooperativity of substrate binding to the enzyme
P M Knappskog, T Flatmark, J M Aarden, et al.
Human Genetics
|
February 1, 1995
The PKU mutation S349P causes complete loss of catalytic activity in the recombinant phenylalanine hydroxylase enzyme
P M Knappskog, H G Eiken, A Martinez, et al.
European Journal of Biochemistry
|
January 1, 1980
Electron paramagnetic resonance of the copper in dopamine beta-monooxygenase. Rapid reduction by ascorbate, the steady-state redox level, chelation with EDTA, and reactivation of the apoenzyme by added copper
T Skotland, L Petersson, D Bäckström, et al.
The Journal of Biological Chemistry
|
December 15, 1988
Resonance Raman studies on the blue-green-colored bovine adrenal tyrosine 3-monooxygenase (tyrosine hydroxylase). Evidence that the feedback inhibitors adrenaline and noradrenaline are coordinated to iron
K K Andersson, D D Cox, L Que, et al.
Carcinogenesis
|
September 1, 1986
Relation between induction of ornithine decarboxylase and specific gene expression in rat liver in response to the tumor promoter agent clofibrate
M H Fukami, T S Eikhom, R Ekanger, et al.
Advances in Experimental Medicine and Biology
|
March 10, 2000
Metabolic effects of 3-thia fatty acid in cancer cells
K J Tronstad, K Berge, R Bjerkvig, et al.
Nature Structural Biology
|
December 24, 1997
Crystal structure of the catalytic domain of human phenylalanine hydroxylase reveals the structural basis for phenylketonuria
H Erlandsen, F Fusetti, A Martinez, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1993
Characterization of the iron environment in recombinant human tyrosine hydroxylase, using Mössbauer and EPR-spectroscopy
J Haavik, E Bill, M Lengen, et al.
FEBS Letters
|
April 7, 1997
Crystallization and preliminary diffraction analysis of a truncated homodimer of human phenylalanine hydroxylase
H Erlandsen, A Martinez, P M Knappskog, et al.
Human Mutation
|
January 1, 1996
PKU mutation (D143G) associated with an apparent high residual enzyme activity: expression of a kinetic variant form of phenylalanine hydroxylase in three different systems
P M Knappskog, H G Eiken, A Martínez, et al.
Page
of 17