The genomic structure and promoter region of the human Parkin gene

Biochemical and Biophysical Research Communications

Volumn 286, Issue 5, 2001, Pages 863-868

  Asakawa, S ^a   Tsunematsu, K I ^a   Takayanagi, A ^a   Sasaki, T ^a   Shimizu, A ^a   Shintani, A ^a   Kawasaki, K ^a   Mungall, A J ^b   Beck, S ^b   Minoshima, S ^a   Shimizu, N ^a  

^a KEIO UNIVERSITY   (Japan)

^b WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CPG ISLAND; DNA SEQUENCE; GENETIC TRANSCRIPTION; GENETIC TRANSFECTION; HUMAN; NEUROBLASTOMA CELL; PARKINSONISM; PRIORITY JOURNAL; PROMOTER REGION; REPORTER GENE; SEQUENCE ANALYSIS;

EID: 0034805921     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.2001.5490     Document Type: Article

References (16)

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3. Mutations in the Parkin gene cause autosomal recessive juvenile parkinsonism
4. Familial Parkinson disease gene product, Parkin, is a ubiquitin-protein ligase
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6. Parkin functions as an E2-dependent ubiquitin-protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1
7. An unfolding putative transmembrane polypeptide, which can lead to endoplasmic reticulum stress is a substrate of Parkin
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