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In line with this repressive role, previous studies indicate that reduced Mecp2 activity leads to increased Tbr1 transcription

Inflammation and disruption of the mucosal architecture in claudin-7-deficient mice

ChREBP deficiency alleviates apoptosis by inhibiting TXNIP/oxidative stress in diabetic nephropathy

The study of Lysosomal Storage Disorders Muccopolysaccharidosis Type III (Sanfilippo Syndrome) Mucopolysaccharidosis type III (MPS III) is a multisystemic lysosomal storage disease characterized by progressive neurodegeneration characterized by severe developmental regression, intellectual disability, autism, and other behavioral problems