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

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Gerard T. Berry

Department of Pediatrics

Division of Human Genetics and Molecular Biology and the Metabolic Research Laboratory

University of Pennsylvania School of Medicine

The Children's Hospital of Philadelphia

USA

[email]@jefferson.edu

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Affiliations

  • Department of Pediatrics, Division of Human Genetics and Molecular Biology and the Metabolic Research Laboratory, University of Pennsylvania School of Medicine, The Children's Hospital of Philadelphia, USA. 2004 - 2005
  • Department of Pediatrics, University of Pennsylvania School of Medicine, The Children's Hospital of Philadelphia, Philadelphia, USA. 2003 - 2004
  • Children's Research Institute, Children's National Medical Center, Department of Pediatrics, George Washington University School of Medicine and Health Sciences, USA. 2004

References

  1. Elements of diabetic nephropathy in a patient with GLUT 2 deficiency. Berry, G.T., Baynes, J.W., Wells-Knecht, K.J., Szwergold, B.S., Santer, R. Mol. Genet. Metab. (2005) [Pubmed]
  2. The rate of de novo galactose synthesis in patients with galactose-1-phosphate uridyltransferase deficiency. Berry, G.T., Moate, P.J., Reynolds, R.A., Yager, C.T., Ning, C., Boston, R.C., Segal, S. Mol. Genet. Metab. (2004) [Pubmed]
  3. Phosphoinositide deficiency due to inositol depletion is not a mechanism of lithium action in brain. Berry, G.T., Buccafusca, R., Greer, J.J., Eccleston, E. Mol. Genet. Metab. (2004) [Pubmed]
  4. Extended [13C]galactose oxidation studies in patients with galactosemia. Berry, G.T., Reynolds, R.A., Yager, C.T., Segal, S. Mol. Genet. Metab. (2004) [Pubmed]
  5. Loss of murine Na+/myo-inositol cotransporter leads to brain myo-inositol depletion and central apnea. Berry, G.T., Wu, S., Buccafusca, R., Ren, J., Gonzales, L.W., Ballard, P.L., Golden, J.A., Stevens, M.J., Greer, J.J. J. Biol. Chem. (2003) [Pubmed]
 
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