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As a modified fragment of human growth hormone, it provides a model system for studying how specific peptide domains influence receptor interaction and downstream signaling

Huntingtons disease HD is caused by the abnormal elongation of CAG trinucleotide repeats in the Huntington ( HTT ) gene, resulting in mutations in the HTT protein, which causes the gradual development of this fatal hereditary neurodegenerative disease

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This rate is approximately 11 times lower than that observed with the FeSe 2 nanospheres

[DOI] [PMC free article] [PubMed] [Google Scholar] Mauro T., Bench G., Sidderas-Haddad E., Feingold K., Elias P., Cullander C

Ruopp NF, Cockrill BA