Regional and cellular expression of the parkin gene in the rat cerebral cortex

European Journal of Neuroscience

Volumn 12, Issue 10, 2000, Pages 3583-3588

  D'Agata, Velia ^a,b   Grimaldi, Maurizio ^c   Pascale, Alessia ^c   Cavallaro, Sebastiano ^a,b  

^a CNR   (Italy)

^b OASI RESEARCH INSTITUTE IRCCS   (Italy)

^c NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

Author keywords

Autosomal recessive juvenile parkinsonism; Cortex; Neurons; Parkinson's disease; Type I astrocytes

Indexed keywords

MESSENGER RNA;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BRAIN CORTEX; CELLULAR DISTRIBUTION; CONFOCAL MICROSCOPY; FETUS; GENE EXPRESSION; GENE MUTATION; IMMUNOFLUORESCENCE; IN SITU HYBRIDIZATION; MOLECULAR WEIGHT; NONHUMAN; PARKINSON DISEASE; PRIORITY JOURNAL; RAT; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

ANIMALS; ASTROCYTES; CELL SIZE; CELLS, CULTURED; CEREBRAL CORTEX; GENE EXPRESSION REGULATION; LIGASES; NEURONS; PARKINSONIAN DISORDERS; PROTEINS; RATS; RATS, SPRAGUE-DAWLEY; RATS, WISTAR; RNA, MESSENGER; UBIQUITIN-PROTEIN LIGASES;

EID: 0033783617     PISSN: 0953816X     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1460-9568.2000.00244.x     Document Type: Article

References (18)

1. A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease
2. A rapid and sensitive method for the quantification of micrograms quantities of proteins utilizing the principle of protein dye binding
3. The primary structure of rat ribosomal protein S18
4. Cloning and distribution of the rat parkin mRNA
5. Functional and molecular diversity of PACAP/VIP receptors in cortical neurons and type I astrocytes
6. Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in the Parkin gene in affected individuals
7. Point mutations (Thr240Arg and Ala311Stop) in the Parkin gene
8. Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonism
9. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
10. Deletions in the Parkin gene and genetic heterogeneity in a Greek family with early onset Parkinson's disease
11. Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Group
12. Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.5-27
13. A novel transactivation domain in parkin
14. Functional impairment in protein kinase C by RACK1 (Receptor for Activated C Kinase 1) deficiency in aged rat brain cortex
15. Familial juvenile parkinsonism: Clinical and pathologic study in a family
16. Polymorphism in the parkin gene in sporadic Parkinson's disease
17. Paralysis agitans of early onset with marked diurnal fluctuation of symptoms
18. Early-onset parkinsonism with diurnal fluctuation-clinical and pathological studies