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

Ruben Vidal

1Department of Pathology and Laboratory Medicine

Indiana University School of Medicine

635 Barnhill Dr. MSB A136

Indianapolis

USA

[email]@iupui.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • 1Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, 635 Barnhill Dr. MSB A136, Indianapolis, USA. 2003 - 2012
  • Pathology and Laboratory Medicine, Indiana Alzheimer Disease Center, Indianapolis, Indiana 46202, USA. 2008
  • New York University School of Medicine, Department of Pathology, New York, USA. 2001

References

  1. The Psen1-L166P-knock-in mutation leads to amyloid deposition in human wild-type amyloid precursor protein YAC transgenic mice. Vidal, R., Sammeta, N., Garringer, H.J., Sambamurti, K., Miravalle, L., Lamb, B.T., Ghetti, B. FASEB J. (2012) [Pubmed]
  2. Abnormal iron metabolism in fibroblasts from a patient with the neurodegenerative disease hereditary ferritinopathy. Barbeito, A.G., Levade, T., Delisle, M.B., Ghetti, B., Vidal, R. Mol. Neurodegener (2010) [Pubmed]
  3. Cerebral amyloid angiopathy and parenchymal amyloid deposition in transgenic mice expressing the Danish mutant form of human BRI2. Vidal, R., Barbeito, A.G., Miravalle, L., Ghetti, B. Brain Pathol. (2009) [Pubmed]
  4. Expression of a mutant form of the ferritin light chain gene induces neurodegeneration and iron overload in transgenic mice. Vidal, R., Miravalle, L., Gao, X., Barbeito, A.G., Baraibar, M.A., Hekmatyar, S.K., Widel, M., Bansal, N., Delisle, M.B., Ghetti, B. J. Neurosci. (2008) [Pubmed]
  5. Intracellular ferritin accumulation in neural and extraneural tissue characterizes a neurodegenerative disease associated with a mutation in the ferritin light polypeptide gene. Vidal, R., Ghetti, B., Takao, M., Brefel-Courbon, C., Uro-Coste, E., Glazier, B.S., Siani, V., Benson, M.D., Calvas, P., Miravalle, L., Rascol, O., Delisle, M.B. J. Neuropathol. Exp. Neurol. (2004) [Pubmed]
  6. Neurodegeneration caused by proteins with an aberrant carboxyl-terminus. Vidal, R., Delisle, M.B., Ghetti, B. J. Neuropathol. Exp. Neurol. (2004) [Pubmed]
  7. Hereditary ferritinopathy. Vidal, R., Delisle, M.B., Rascol, O., Ghetti, B. J. Neurol. Sci. (2003) [Pubmed]
  8. Sequence, genomic structure and tissue expression of Human BRI3, a member of the BRI gene family. Vidal, R., Calero, M., Révész, T., Plant, G., Ghiso, J., Frangione, B. Gene (2001) [Pubmed]
 
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