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The TGF-/SMAD signaling pathway as a mediator of NK cell dysfunction and immune evasion in Myelodysplastic Syndrome

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Each rabbit was observed individually in a controlled ground area for 20 minutes daily at a set time

The mutations in certain genes such as PTEN , fragile X mental retardation 1 ( FMR1 ), chromodomain helicase DNA binding protein 7 ( CHD7 ), and tuberous sclerosis 1 and 2 ( TSC1 and TSC2 ) are associated with the ASD [208,209,210,211,212]