A brain-specific decrease of the tyrosine hydroxylase protein in sepiapterin reductase-null mice—as a mouse model for Parkinson’s disease-Reference-Cited by-同舟云学术

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A brain-specific decrease of the tyrosine hydroxylase protein in sepiapterin reductase-null mice—as a mouse model for Parkinson’s disease

Published:2008-03 Issue:4 Volume:367 Page:787-792
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Takazawa Chisato,Fujimoto Kengo,Homma Daigo,Sumi-Ichinose Chiho,Nomura Takahide,Ichinose Hiroshi,Katoh Setsuko

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference24 articles.

1. Progress in familial Parkinson’s disease;Mizuno;J. Neural Transm. (Suppl.),2006

2. Hereditary Parkinson disease: report of 3 families with dominant autosomal inheritance;Wszolek;Nervenarzt,1993

3. Western Nebraska family (family D) with autosomal dominant parkinsonism;Wszolek;Neurology,1995

4. A susceptibility locus for Parkinson’s disease maps to chromosome 2p13;Gasser;Nature Genet.,1998

5. Sepiapterin reductase from horse liver: purification and properties of the enzyme;Katoh;Arch. Biochem. Biophys.,1971

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