Degradation of survival motor neuron (SMN) protein is mediated via the ubiquitin/proteasome pathway

This publication has 30 references indexed in Scilit:

• Mechanisms controlling EGF receptor endocytosis and degradation
  Biochemical Society Transactions, 2003
• Proteasome inhibitors as new anticancer drugs
  Current Opinion in Oncology, 2002
• Degradation of p27 at the G0-G1 Transition Mediated by a Skp2-independent Ubiquitination Pathway
  Journal of Biological Chemistry, 2001
• Aclarubicin treatment restores SMN levels to cells derived from type I spinal muscular atrophy patients
  Human Molecular Genetics, 2001
• Treatment of spinal muscular atrophy by sodium butyrate
  Proceedings of the National Academy of Sciences, 2001
• The ubiquitin-mediated proteolytic pathway: Mode of action and clinical implications
  Journal of Cellular Biochemistry, 2000
• Differential SMN2 expression associated with SMA severity
  Nature Genetics, 1998
• Molecular analysis of survival motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) genes of spinal muscular atrophy patients and their parents
  Human Genetics, 1997
• The SMN–SIP1 Complex Has an Essential Role in Spliceosomal snRNP Biogenesis
  Cell, 1997
• Population frequencies of inherited neuromuscular diseases—A world survey
  Neuromuscular Disorders, 1991