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

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Mariz Vainzof

Dept of Genetics and Evolutionary Biology

University of Sao Paulo

Sao Paulo

Brasil

[email]@usp.br

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Dept of Genetics and Evolutionary Biology, University of Sao Paulo, Sao Paulo, Brasil. 2008
  • Centro de Estudos do Genoma Humano, Instituto de Biociências, Universidade de São Paulo, R. do Matão, Brazil. 2000 - 2003
  • Center for the Study of the Human Genome, IBUSP, São Paulo, Brazil. 2000 - 2002
  • Departamento de Neurologia, FMUSP, São Paulo, Brazil. 1999
  • Departamento de Neurologia, Centro de Investigações em Neurologia, Faculdade de Medicina, Universidade de São Paulo, Brazil. 1999

References

  1. Animal models for genetic neuromuscular diseases. Vainzof, M., Ayub-Guerrieri, D., Onofre, P.C., Martins, P.C., Lopes, V.F., Zilberztajn, D., Maia, L.S., Sell, K., Yamamoto, L.U. J. Mol. Neurosci. (2008) [Pubmed]
  2. Protein defects in neuromuscular diseases. Vainzof, M., Zatz, M. Braz. J. Med. Biol. Res. (2003) [Pubmed]
  3. Telethonin protein expression in neuromuscular disorders. Vainzof, M., Moreira, E.S., Suzuki, O.T., Faulkner, G., Valle, G., Beggs, A.H., Carpen, O., Ribeiro, A.F., Zanoteli, E., Gurgel-Gianneti, J., Tsanaclis, A.M., Silva, H.C., Passos-Bueno, M.R., Zatz, M. Biochim. Biophys. Acta (2002) [Pubmed]
  4. Dysferlin protein analysis in limb-girdle muscular dystrophies. Vainzof, M., Anderson, L.V., McNally, E.M., Davis, D.B., Faulkner, G., Valle, G., Moreira, E.S., Pavanello, R.C., Passos-Bueno, M.R., Zatz, M. J. Mol. Neurosci. (2001) [Pubmed]
  5. Partial alpha-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D family. Vainzof, M., Moreira, E.S., Canovas, M., Anderson, L.V., Pavanello, R.C., Passos-Bueno, M.R., Zatz, M. Muscle. Nerve (2000) [Pubmed]
  6. Does the A3333G mutation in the CACNL1A3 gene, detected in malignant hyperthermia, also occur in central core disease?. Vainzof, M., Muniz, V.P., Tsanaclis, A.M., Silva, H.C., Rusticci, M.S. Genet. Test. (2000) [Pubmed]
  7. Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complex. Vainzof, M., Moreira, E.S., Ferraz, G., Passos-Bueno, M.R., Marie, S.K., Zatz, M. Eur. J. Hum. Genet. (1999) [Pubmed]
  8. Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population. Vainzof, M., Passos-Bueno, M.R., Pavanello, R.C., Marie, S.K., Oliveira, A.S., Zatz, M. J. Neurol. Sci. (1999) [Pubmed]
 
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