Cellular distribution of torsin A and torsin B in normal human brain

Archives of Neurology

Volumn 58, Issue 6, 2001, Pages 921-927

  Konakova, Marina ^a   Huynh, Duong P ^a   Yong, William ^b   Pulst, Stefan M ^a,b  

^a BURNS AND ALLEN RESEARCH INSTITUTE   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BRAIN PROTEIN; POLYCLONAL ANTIBODY; TORSIN A; TORSIN B; UNCLASSIFIED DRUG;

ARTICLE; BRAIN; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; NEUROCHEMISTRY; PRIORITY JOURNAL; PROTEIN DETERMINATION; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; TISSUE DISTRIBUTION; WESTERN BLOTTING;

EID: 0034970023     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.58.6.921     Document Type: Article

References (25)

1. Human gene for torsion dystonia located on chromosome 9q32-q34
2. Strong, allelic association between the torsion dystonia gene (DYT1) and loci on chromosome 9q34 in Ashkenazi Jews
3. The early-onset dystonia gene (DYT1) encodes an ATP-binding protein
4. Dopa-responsive dystonia: A syndrome of selective nigrostriatal dopamine deficiency
5. Dopa-responsive dystonia: A clinical and molecular genetic study
6. The gene (DYT1) for early-onset torsion dystonia encodes a novel protein related to the CIp protease/heat shock family
7. Distribution of the mRNAs encoding torsin A and torsin B in the normal adult human brain
8. Immunohistochemical localization and distribution of torsin A in normal human and rat brain
9. Torsin A and its torsion dystonia-associated mutant forms are lumenal glycoproteins that exhibit distinct subcellular localizations
10. Expression of ataxin-2 in brains from normal individuals and patients with Alzheimer's disease and spinocerebellar ataxia 2
11. Cleavage of structural proteins during the assembly of the head of bacteriophage T4
12. Mutant torsin A, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells
13. Functional brain networks in DYT1 dystonia
14. Hsp100/CIp proteins: A common mechanism explains diverse functions
15. Molecular chaperones
16. +: A class of chaperone-like ATPases associated with the assembly, operation, and disassembly of protein complexes
17. The AAA team: Related ATPases with diverse functions
18. Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia
19. Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders
20. A common PEX1 frameshift mutation in patients with disorders of peroxisome biogenesis correlates with the severe Zellweger syndrome phenotype
21. Disruption of a PEX1-PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease
22. The Vps4p AAA ATPase regulates membrane association of a Vps protein complex required for normal endosome function
23. Cloning, characterization, and functional expression of the Mus musculus SKD1 gene in yeast demonstrates that the mouse SKD1 and the yeast VPS4 genes are orthologues and involved in intracellular protein trafficking
24. The mouse SKD1, a homologue of yeast Vps4p, is required for normal endosomal trafficking and morphology in mammalian cells
25. Parkin is associated with actin filaments in neuronal and nonneuronal cells