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4.9 Ferroptosis in Huntingtons disease HD is an autosomal dominant neurodegenerative disorder caused by CAG repeat expansions in the HTT gene, which encodes mutant huntingtin (mHTT) proteins containing elongated polyglutamine (polyQ) tracts
The transcriptome of Arabidopsis thaliana during systemic acquired resistance
Its important to note that having vitamin B12 levels too high doesnt usually cause symptoms on its own, but it can be a marker for other medical concerns that need attention
Furthermore, it is not affected by tachyphylaxis
Studies in other fungal pathogens have shown the potential for modulation of glutathione for biocontrol
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