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

Nobutaka Hattoria

Department of Neurology

Juntendo University School of Medicine

2-1-1 Hongo

Bunkyo

Japan

[email]@med.juntendo.ac.jp

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Neurology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo, Japan. 1998 - 2009

References

  1. Toxic effects of dopamine metabolism in Parkinson's disease. Hattoria, N., Wanga, M., Taka, H., Fujimura, T., Yoritaka, A., Kubo, S., Mochizuki, H. Parkinsonism Relat. Disord. (2009) [Pubmed]
  2. Animal models of Parkinson's disease: similarities and differences between the disease and models. Hattori, N., Sato, S. Neuropathology (2007) [Pubmed]
  3. Molecular mechanisms of nigral neurodegeneration in Park2 and regulation of parkin protein by other proteins. Hattori, N., Machida, Y., Sato, S., Noda, K., Iijima-Kitami, M., Kubo, S., Mizuno, Y. J. Neural Transm. Suppl. (2006) [Pubmed]
  4. Pathogenetic mechanisms of parkin in Parkinson's disease. Hattori, N., Mizuno, Y. Lancet (2004) [Pubmed]
  5. Familial Parkinson's disease: a hint to elucidate the mechanisms of nigral degeneration. Hattori, N., Kobayashi, H., Sasaki-Hatano, Y., Sato, K., Mizuno, Y. J. Neurol. (2003) [Pubmed]
  6. Appropriate dosing of pergolide in monotherapy and adjunctive therapy in Parkinson's disease. Hattori, N. Curr. Opin. Neurol. (2003) [Pubmed]
  7. Autosomal recessive juvenile parkinsonism: a key to understanding nigral degeneration in sporadic Parkinson's disease. Hattori, N., Shimura, H., Kubo, S., Kitada, T., Wang, M., Asakawa, S., Minashima, S., Shimizu, N., Suzuki, T., Tanaka, K., Mizuno, Y. Neuropathology (2000) [Pubmed]
  8. Importance of familial Parkinson's disease and parkinsonism to the understanding of nigral degeneration in sporadic Parkinson's disease. Hattori, N., Shimura, H., Kubo, S., Wang, M., Shimizu, N., Tanaka, K., Mizuno, Y. J. Neural Transm. Suppl. (2000) [Pubmed]
  9. Genotype in the 24-kDa subunit gene (NDUFV2) of mitochondrial complex I and susceptibility to Parkinson disease. Hattori, N., Yoshino, H., Tanaka, M., Suzuki, H., Mizuno, Y. Genomics (1998) [Pubmed]
  10. Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene. Hattori, N., Matsumine, H., Asakawa, S., Kitada, T., Yoshino, H., Elibol, B., Brookes, A.J., Yamamura, Y., Kobayashi, T., Wang, M., Yoritaka, A., Minoshima, S., Shimizu, N., Mizuno, Y. Biochem. Biophys. Res. Commun. (1998) [Pubmed]
 
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