The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Editor

Share

Personal info

View

Links

Table of contents

About

Terms

 

Joost P. H. Drenth

Department of Gastroenterology and Hepatology

Radboud University Nijmegen Medical Center

Nijmegen

Netherlands

[email]@cs.com

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Gastroenterology and Hepatology, Radboud University Nijmegen Medical Center, Nijmegen, Netherlands. 2001 - 2012
  • Cell Biology and Metabolism Branch, National Institute of Child Health and Human Development, National Institutes of Health, Building 18T, USA. 2004

References

  1. Rationale and design of the RESOLVE trial: lanreotide as a volume reducing treatment for polycystic livers in patients with autosomal dominant polycystic kidney disease. Gevers, T.J., Chrispijn, M., Wetzels, J.F., Drenth, J.P. BMC. Nephrol (2012) [Pubmed]
  2. Hepatitis C virus infection management in 2012. Van Gulick, J.J., Lamers, M.H., Drenth, J.P. Panminerva. Med (2012) [Pubmed]
  3. Primary erythermalgia as a sodium channelopathy: screening for SCN9A mutations: exclusion of a causal role of SCN10A and SCN11A. Drenth, J.P., Te Morsche, R.H., Mansour, S., Mortimer, P.S. Arch. Dermatol (2008) [Pubmed]
  4. Mutations in sodium-channel gene SCN9A cause a spectrum of human genetic pain disorders. Drenth, J.P., Waxman, S.G. J. Clin. Invest. (2007) [Pubmed]
  5. Do COX-2 inhibitors give enough gastrointestinal protection?. Drenth, J.P., Verheugt, F.W. Lancet (2007) [Pubmed]
  6. Chronic pancreatitis resulting from genetic mutations in trypsin and trypsin inhibitors. Drenth, J.P. Neth. J. Med (2007) [Pubmed]
  7. Polycystic liver disease is a disorder of cotranslational protein processing. Drenth, J.P., Martina, J.A., van de Kerkhof, R., Bonifacino, J.S., Jansen, J.B. Trends. Mol. Med (2005) [Pubmed]
  8. SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels. Drenth, J.P., te Morsche, R.H., Guillet, G., Taieb, A., Kirby, R.L., Jansen, J.B. J. Invest. Dermatol. (2005) [Pubmed]
  9. Abnormal hepatocystin caused by truncating PRKCSH mutations leads to autosomal dominant polycystic liver disease. Drenth, J.P., Tahvanainen, E., te Morsche, R.H., Tahvanainen, P., Kääriäinen, H., Höckerstedt, K., van de Kamp, J.M., Breuning, M.H., Jansen, J.B. Hepatology (2004) [Pubmed]
  10. Molecular characterization of hepatocystin, the protein that is defective in autosomal dominant polycystic liver disease. Drenth, J.P., Martina, J.A., Te Morsche, R.H., Jansen, J.B., Bonifacino, J.S. Gastroenterology (2004) [Pubmed]
  11. Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease. Drenth, J.P., te Morsche, R.H., Smink, R., Bonifacino, J.S., Jansen, J.B. Nat. Genet. (2003) [Pubmed]
  12. Genetic aspects of chronic pancreatitis, and the exploration of an association with keratin 8/18. Drenth, J.P., Verlaan, M. Dig. Liver. Dis (2003) [Pubmed]
  13. Mutations in serine protease inhibitor Kazal type 1 are strongly associated with chronic pancreatitis. Drenth, J.P., te Morsche, R., Jansen, J.B. Gut (2002) [Pubmed]
  14. Reduced diffusion in liver cirrhosis is related to impairment of protein liver synthesis. Drenth, J.P., Jansen, J.B., Dekhuijzen, P.N. Scand. J. Gastroenterol. (2002) [Pubmed]
  15. The primary erythermalgia-susceptibility gene is located on chromosome 2q31-32. Drenth, J.P., Finley, W.H., Breedveld, G.J., Testers, L., Michiels, J.J., Guillet, G., Taieb, A., Kirby, R.L., Heutink, P. Am. J. Hum. Genet. (2001) [Pubmed]
  16. Hereditary periodic fever. Drenth, J.P., van der Meer, J.W. N. Engl. J. Med. (2001) [Pubmed]
 
WikiGenes - Universities