|1.||Agrawal, Pankaj B: 4 articles (03/2015 - 01/2007)|
|2.||Joshi, Mugdha: 3 articles (03/2015 - 05/2012)|
|3.||Beggs, Alan H: 3 articles (01/2015 - 01/2007)|
|4.||Savic, Talia: 2 articles (01/2015 - 05/2012)|
|5.||Laing, Nigel G: 2 articles (09/2014 - 01/2007)|
|6.||Kuramitsu, Yasuhiro: 2 articles (09/2013 - 12/2011)|
|7.||Wang, Yufeng: 2 articles (09/2013 - 12/2011)|
|8.||Nakamura, Kazuyuki: 2 articles (09/2013 - 12/2011)|
|9.||Paolocci, Nazareno: 1 article (03/2015)|
|10.||Gianni, Davide: 1 article (03/2015)|
|2.||Nemaline Myopathies (Nemaline Myopathy)
09/01/2014 - "Novel cofilin-2 (CFL2) four base pair deletion causing nemaline myopathy."
05/15/2012 - "In humans, recessive cofilin-2 mutations have been associated with nemaline myopathy with minicores. "
01/01/2008 - "A homozygous mutation in CFL2, the gene for muscle cofilin, has been associated with nemaline myopathy in one family to date. "
03/31/2015 - "Aggregates in human myocardium were enriched for cofilin-2, an actin-depolymerizing protein known to participate in neurodegenerative diseases and nemaline myopathy. "
01/01/2007 - "Nemaline myopathy with minicores caused by mutation of the CFL2 gene encoding the skeletal muscle actin-binding protein, cofilin-2."
|3.||Muscular Diseases (Myopathy)
01/01/2015 - "Mutations in the gene for cofilin-2 (CFL2) have been identified in several families as a cause of congenital myopathy with nemaline bodies and cores. "
10/27/2014 - "Our findings also offer a rationale for why cofilin-2 mutations in humans lead to myopathies. "
01/01/2007 - "We report identification of a sixth gene, CFL2, encoding the actin-binding protein muscle cofilin-2, which is mutated in two siblings with congenital myopathy. "
|4.||Pancreatic Neoplasms (Pancreatic Cancer)
|5.||Neurodegenerative Diseases (Neurodegenerative Disease)
|1.||Proteins (Proteins, Gene)
|6.||Messenger RNA (mRNA)
|7.||Membrane Proteins (Integral Membrane Proteins)
|8.||Heat-Shock Proteins (Heat-Shock Protein)
|10.||Glutathione Transferase (Glutathione S-Transferase)