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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
Figure 3 4.3 Non-classical effects of HO-1 Recent studies have demonstrated that, in addition to its enzymatic function, HO-1 performs several non-canonical roles, including proteinprotein interactions, subcellular localization (e.g., secretion into the extracellular space), and regulation of cellular metabolism ( Initially discovered in the endoplasmic reticulum, HO-1 has also been detected in mitochondria, nuclei, and follicles in subsequent studies
Efficient and rapid generation of induced pluripotent stem cells from human keratinocytes
* Correspondence: Tao Liu, [email protected]
In vitro studies have shown that strains such as Lactobacillus salivarius LS03, along with Lactococcus and S
Figure 2: Changes in the histolopathological scores amongst the four experimental treatment groups
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