Torsin A and Its Torsion Dystonia-associated Mutant Forms Are Lumenal Glycoproteins That Exhibit Distinct Subcellular Localizations
Open Access
- 1 September 2000
- journal article
- Published by Elsevier BV in Journal of Biological Chemistry
- Vol. 275 (36), 27933-27939
- https://doi.org/10.1074/jbc.m910025199
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Functional brain networks in DYT1 dystoniaAnnals of Neurology, 1998
- Molecular chaperones: Clamps for the Clps?Current Biology, 1998
- Molecular Properties of ClpAP Protease of Escherichia coli: ATP-Dependent Association of ClpA and ClpPBiochemistry, 1998
- The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding proteinNature Genetics, 1997
- Molecular characterization of an enzyme that degrades neuromodulatory fatty-acid amidesNature, 1996
- Spread of symptoms in idiopathic torsion dystoniaMovement Disorders, 1995
- Dystonia in Ashkenazi Jews: Clinical characterization of a founder mutationAnnals of Neurology, 1994
- BiP (GRP78), an essential hsp70 resident protein in the endoplasmic reticulumCellular and Molecular Life Sciences, 1994
- Enzyme asymmetry in hepatic microsomal vesicles. Criteria for localization of lumenal enzymes with proteasesBiochimica et Biophysica Acta (BBA) - Biomembranes, 1980
- Structural aspects of the membrane of the endoplasmic reticulumBiochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1975