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

Kimberlee Michals Matalon

Department of Pediatrics

University of Texas Medical Branch at Galveston

USA

[email]@utmb.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Pediatrics, University of Texas Medical Branch at Galveston, USA. 1999 - 2007
  • Department of Pediatrics, Galveston, Texas 77555-0359, USA. 2003
  • Department of Pediatrics and Human Biological Chemistry and Genetics, Children's Hospital, Galveston, TX 77555-0359, USA. 2002

References

  1. Double blind placebo control trial of large neutral amino acids in treatment of PKU: effect on blood phenylalanine. Matalon, R., Michals-Matalon, K., Bhatia, G., Burlina, A.B., Burlina, A.P., Braga, C., Fiori, L., Giovannini, M., Grechanina, E., Novikov, P., Grady, J., Tyring, S.K., Guttler, F. J. Inherit. Metab. Dis. (2007) [Pubmed]
  2. Canavan disease: studies on the knockout mouse. Matalon, R., Michals-Matalon, K., Surendran, S., Tyring, S.K. Adv. Exp. Med. Biol. (2006) [Pubmed]
  3. Large neutral amino acids in the treatment of phenylketonuria (PKU). Matalon, R., Michals-Matalon, K., Bhatia, G., Grechanina, E., Novikov, P., McDonald, J.D., Grady, J., Tyring, S.K., Guttler, F. J. Inherit. Metab. Dis. (2006) [Pubmed]
  4. Hyaluronidase increases the biodistribution of acid alpha-1,4 glucosidase in the muscle of Pompe disease mice: an approach to enhance the efficacy of enzyme replacement therapy. Matalon, R., Surendran, S., Campbell, G.A., Michals-Matalon, K., Tyring, S.K., Grady, J., Cheng, S., Kaye, E. Biochem. Biophys. Res. Commun. (2006) [Pubmed]
  5. Response of patients with phenylketonuria in the US to tetrahydrobiopterin. Matalon, R., Michals-Matalon, K., Koch, R., Grady, J., Tyring, S., Stevens, R.C. Mol. Genet. Metab. (2005) [Pubmed]
  6. Adeno-associated virus-mediated aspartoacylase gene transfer to the brain of knockout mouse for canavan disease. Matalon, R., Surendran, S., Rady, P.L., Quast, M.J., Campbell, G.A., Matalon, K.M., Tyring, S.K., Wei, J., Peden, C.S., Ezell, E.L., Muzyczka, N., Mandel, R.J. Mol. Ther. (2003) [Pubmed]
  7. Future role of large neutral amino acids in transport of phenylalanine into the brain. Matalon, R., Surendran, S., Matalon, K.M., Tyring, S., Quast, M., Jinga, W., Ezell, E., Szucs, S. Pediatrics (2003) [Pubmed]
  8. Canavan disease prenatal diagnosis and genetic counseling. Matalon, R., Matalon, K.M. Obstet. Gynecol. Clin. North Am. (2002) [Pubmed]
  9. Spongy degeneration of the brain, Canavan disease: biochemical and molecular findings. Matalon, R.M., Michals-Matalon, K. Front. Biosci. (2000) [Pubmed]
  10. Knock-out mouse for Canavan disease: a model for gene transfer to the central nervous system. Matalon, R., Rady, P.L., Platt, K.A., Skinner, H.B., Quast, M.J., Campbell, G.A., Matalon, K., Ceci, J.D., Tyring, S.K., Nehls, M., Surendran, S., Wei, J., Ezell, E.L., Szucs, S. J. Gene. Med (2000) [Pubmed]
  11. Biochemistry and molecular biology of Canavan disease. Matalon, R., Michals-Matalon, K. Neurochem. Res. (1999) [Pubmed]
  12. Prenatal diagnosis of Canavan disease. Matalon, R., Michals-Matalon, K. Prenat. Diagn. (1999) [Pubmed]
 
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