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Home › Research › Topics › myopathy

myopathy

2 studies tagged myopathy, dated 2010-07-05 to 2015-07-24. Bibliography: BibTeX (.bib) · RIS (.ris)

Newest in this topic

  1. SQSTM1 splice site mutation in distal myopathy with rimmed vacuoles 2015-07-24
  2. Enhanced ATPase activities as a primary defect of mutant valosin-containing proteins that cause inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia 2010-07-05

Studies

2 studies carry this tag.

Date range

2010 to 2015

Top journals

  • Genes to cells : devoted to molecular & cellular mechanisms 1
  • Neurology 1

Newest first, then by address. Each study has a usefulness score out of 100 (rubric version 4.0); tap a score to see what makes it up. Tags were assigned automatically from each study's title and summary. The same studies as a filter in the library.

  1. SQSTM1 splice site mutation in distal myopathy with rimmed vacuoles

    ✓ Peer-reviewed alzhub usefulness score 45 out of 100. Neurology 2015-07-24 Genetics

    SQSTM1 is an autophagic adaptor that shuttles aggregated and ubiquitinated proteins to the autophagosome for degradation via its C-terminal UBA domain.

  2. Enhanced ATPase activities as a primary defect of mutant valosin-containing proteins that cause inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia

    ✓ Peer-reviewed alzhub usefulness score 36 out of 100. Genes to cells : devoted to molecular & cellular mechanisms 2010-07-05 Brain scans and imaging

    Valosin-containing protein (VCP) has been shown to colocalize with abnormal protein aggregates, such as nuclear inclusions of Huntington disease and Machado-Joseph disease, Lewy bodies in Parkinson disease.

All topic tags with their study counts