Pub. Date : 2014 Jul 11
PMID : 24858692
7 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | Spinocerebellar Ataxia Type1 (SCA1) is a dominantly inherited neurodegenerative disease and belongs to polyglutamine expansion disorders. | polyglutamine | ataxin 1 | Homo sapiens |
| 2 | Spinocerebellar Ataxia Type1 (SCA1) is a dominantly inherited neurodegenerative disease and belongs to polyglutamine expansion disorders. | polyglutamine | ataxin 1 | Homo sapiens |
| 3 | The polyglutamine expansion in Ataxin-1 (ATXN1) is responsible for SCA1 pathology. | polyglutamine | ataxin 1 | Homo sapiens |
| 4 | The polyglutamine expansion in Ataxin-1 (ATXN1) is responsible for SCA1 pathology. | polyglutamine | ataxin 1 | Homo sapiens |
| 5 | The polyglutamine expansion in Ataxin-1 (ATXN1) is responsible for SCA1 pathology. | polyglutamine | ataxin 1 | Homo sapiens |
| 6 | The wild-type ATXN1 dominantly forms a complex with CIC and the polyglutamine expanded form of ATXN1 favors to form a complex with RBM17. | polyglutamine | ataxin 1 | Homo sapiens |
| 7 | The wild-type ATXN1 dominantly forms a complex with CIC and the polyglutamine expanded form of ATXN1 favors to form a complex with RBM17. | polyglutamine | ataxin 1 | Homo sapiens |