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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Nigel G. Laing

Centre for Medical Research

University of Western Australia

Western Australian Institute for Medical Research

QEII Medical Centre

Australia

[email]@cyllene.uwa.edu.au

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Centre for Medical Research, University of Western Australia, Western Australian Institute for Medical Research, QEII Medical Centre, Australia. 2005 - 2009
  • Centre for Neuromuscular and Neurologic Disorders, Australian Neuromuscular Research Institute and Centre for Medical Research, University of Western Australia, QEII Medical Centre, Australia. 2005
  • Centre for Neuromuscular and Neurological Disorders, Australia. 2004
  • Australian Neuromuscular Research Institute, Centre for Neuromuscular and Neurological Disorders, University of Western Australia, Nedlands, Australia. 1999
  • University of Western Australia, QEII Medical Centre, Nedlands, Australia. 1999

References

  1. Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1). Laing, N.G., Dye, D.E., Wallgren-Pettersson, C., Richard, G., Monnier, N., Lillis, S., Winder, T.L., Lochmüller, H., Graziano, C., Mitrani-Rosenbaum, S., Twomey, D., Sparrow, J.C., Beggs, A.H., Nowak, K.J. Hum. Mutat. (2009) [Pubmed]
  2. 161st ENMC International Workshop on nemaline myopathy and related disorders, Newcastle upon Tyne, 2008. Laing, N.G., Wallgren-Pettersson, C. Neuromuscul. Disord. (2009) [Pubmed]
  3. Multiplicity of experimental approaches to therapy for genetic muscle diseases and necessity for population screening. Laing, N.G. J. Muscle Res. Cell. Motil. (2008) [Pubmed]
  4. Congenital myopathies. Laing, N.G. Curr. Opin. Neurol. (2007) [Pubmed]
  5. More surprises in sarcomeric protein diseases. Laing, N.G. Brain (2007) [Pubmed]
  6. Myosin storage myopathy: slow skeletal myosin (MYH7) mutation in two isolated cases. Laing, N.G., Ceuterick-de Groote, C., Dye, D.E., Liyanage, K., Duff, R.M., Dubois, B., Robberecht, W., Sciot, R., Martin, J.J., Goebel, H.H. Neurology (2005) [Pubmed]
  7. When contractile proteins go bad: the sarcomere and skeletal muscle disease. Laing, N.G., Nowak, K.J. Bioessays (2005) [Pubmed]
  8. Actin mutations are one cause of congenital fibre type disproportion. Laing, N.G., Clarke, N.F., Dye, D.E., Liyanage, K., Walker, K.R., Kobayashi, Y., Shimakawa, S., Hagiwara, T., Ouvrier, R., Sparrow, J.C., Nishino, I., North, K.N., Nonaka, I. Ann. Neurol. (2004) [Pubmed]
  9. Inherited disorders of sarcomeric proteins. Laing, N.G. Curr. Opin. Neurol. (1999) [Pubmed]
  10. Inherited skeletal muscle disorders. Laing, N.G., Mastaglia, F.L. Ann. Hum. Biol. (1999) [Pubmed]
 
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