All Relations between huntingtin and htt
| Publication | Sentence | Publish Date | Extraction Date | Species |
|---|---|---|---|---|
| L M Mende-Mueller, T Toneff, S R Hwang, M F Chesselet, V Y Hoo. Tissue-specific proteolysis of Huntingtin (htt) in human brain: evidence of enhanced levels of N- and C-terminal htt fragments in Huntington's disease striatum. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 21. issue 6. 2001-06-07. PMID:11245667. | tissue-specific proteolysis of huntingtin (htt) in human brain: evidence of enhanced levels of n- and c-terminal htt fragments in huntington's disease striatum. | 2001-06-07 | 2023-08-12 | human |
| S Holbert, I Denghien, T Kiechle, A Rosenblatt, C Wellington, M R Hayden, R L Margolis, C A Ross, J Dausset, R J Ferrante, C Nér. The Gln-Ala repeat transcriptional activator CA150 interacts with huntingtin: neuropathologic and genetic evidence for a role in Huntington's disease pathogenesis. Proceedings of the National Academy of Sciences of the United States of America. vol 98. issue 4. 2001-04-19. PMID:11172033. | huntington's disease (hd) is a neurodegenerative disease caused by polyglutamine expansion in the protein huntingtin (htt). | 2001-04-19 | 2023-08-12 | human |
| B R Leavitt, C L Wellington, M R Hayde. Recent insights into the molecular pathogenesis of Huntington disease. Seminars in neurology. vol 19. issue 4. 2000-03-30. PMID:10716661. | huntington disease (hd) is a neurodegenerative disorder caused by a cag repeat expansion in the hd gene resulting in expression of an uninterrupted polyglutamine stretch within the n-terminus of its protein product huntingtin (htt). | 2000-03-30 | 2023-08-12 | mouse |