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IGF-I stimulates muscle growth by suppressing protein breakdown and expression of atrophy-related ubiquitin ligases, atrogin-1 and MuRF1

506 A specific form of ASD, known as Rett syndrome (clinically manifested with microcephaly, loss of motor coordination, stereotypic hand wringing, ataxia, seizures, and sleep disturbances) is caused by a loss of function mutation of the methyl-CpG-binding protein 2 or MECP2 gene, expressed in both neurones and neuroglia

Understanding the pleiotropic effects of CXCL10/IP-10 in the immunopathogenesis of inflammatory rheumatic diseases: implications for better understanding disease mechanisms

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