J. Fogh
发表
T. Braulke,
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Mahmoud A. Bassal,
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Autophagy.
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Orphanet Journal of Rare Diseases.
R. D'Hooge,
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Human molecular genetics.
V. Gieselmann,
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Experimental Neurology.
H. R. Stensland,
F. Wibrand,
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Orphanet Journal of Rare Diseases.
H. C. Beck,
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Journal of Inherited Metabolic Disease.
C. Wessig,
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C. Möller,
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Human molecular genetics.
T. Andersen,
J. Fogh,
T. Andersen,
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Journal of human nutrition and dietetics : the official journal of the British Dietetic Association.
R. D'Hooge,
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Human molecular genetics.
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The Journal of Biological Chemistry.
R. D'Hooge,
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Molecular medicine.
V. Gieselmann,
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U. Matzner,
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Journal of Molecular Medicine.
R. D'Hooge,
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Molecular therapy : the journal of the American Society of Gene Therapy.
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Neurobiology of Disease.
H. C. Beck,
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Annals of clinical and translational neurology.
R. D'Hooge,
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Molecular and Cellular Biology.
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Human molecular genetics.
L. de Meirleir,
D. Ardigò,
A. Lund,
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Journal of Inherited Metabolic Disease.
P. Nilsson,
B. Oesch,
J. Fogh,
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Biochemistry.
A. Lund,
C. Dali,
K. J. Olsen,
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Journal of Inherited Metabolic Disease.
Recombinant pro-CTSD (cathepsin D) enhances SNCA/α-Synuclein degradation in α-Synucleinopathy models
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Analytical and Bioanalytical Chemistry.
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