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Most familial cases of both ALS (~40%) and FTD (25%) are associated with hexanucleotide (G4C2) expansions in the Chromosome 9 open reading frame 72 (C9orf72) gene (Dejesus-Hernandez et al., 2011

However, the GSTP1 genotype was not associated with prothrombin time, which might have been due to a small sample size in this group (n=5) [91]

Targeting strategies for bone diseases: signaling pathways and clinical studies

24) using red fluorophore-labeled CuSAE (RF@CuSAE)

[DOI] [PMC free article] [PubMed] [Google Scholar] 26.Lucke-Wold BP, Nguyen L, Turner RC, Logsdon AF, Chen YW, Smith KE, et al
