Drenth JP - Search Results

1

Polycystic liver: clinical characteristics of patients with isolated polycystic liver disease compared with patients with polycystic liver and autosomal dominant polycystic kidney disease.

Hoevenaren IA, Wester R, Schrier RW, McFann K, Doctor RB, Drenth JP, Everson GT. Hoevenaren IA, et al. Among authors: drenth jp. Liver Int. 2008 Feb;28(2):264-70. doi: 10.1111/j.1478-3231.2007.01595.x. Epub 2007 Oct 9. Liver Int. 2008. PMID: 17927714

2

Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease.

Drenth JP, te Morsche RH, Smink R, Bonifacino JS, Jansen JB. Drenth JP, et al. Nat Genet. 2003 Mar;33(3):345-7. doi: 10.1038/ng1104. Epub 2003 Feb 10. Nat Genet. 2003. PMID: 12577059

3

Abnormal hepatocystin caused by truncating PRKCSH mutations leads to autosomal dominant polycystic liver disease.

Drenth JP, Tahvanainen E, te Morsche RH, Tahvanainen P, Kääriäinen H, Höckerstedt K, van de Kamp JM, Breuning MH, Jansen JB. Drenth JP, et al. Hepatology. 2004 Apr;39(4):924-31. doi: 10.1002/hep.20141. Hepatology. 2004. PMID: 15057895

4

Polycystic liver disease is a disorder of cotranslational protein processing.

Drenth JP, Martina JA, van de Kerkhof R, Bonifacino JS, Jansen JB. Drenth JP, et al. Trends Mol Med. 2005 Jan;11(1):37-42. doi: 10.1016/j.molmed.2004.11.004. Trends Mol Med. 2005. PMID: 15649821 Review.

5

Extensive mutational analysis of PRKCSH and SEC63 broadens the spectrum of polycystic liver disease.

Waanders E, te Morsche RH, de Man RA, Jansen JB, Drenth JP. Waanders E, et al. Among authors: drenth jp. Hum Mutat. 2006 Aug;27(8):830. doi: 10.1002/humu.9441. Hum Mutat. 2006. PMID: 16835903

6

Biochemical and biophysical assessment of MTX-induced liver fibrosis in psoriasis patients: Fibrotest predicts the presence and Fibroscan predicts the absence of significant liver fibrosis.

Berends MA, Snoek J, de Jong EM, Van Krieken JH, de Knegt RJ, van Oijen MG, van de Kerkhof PC, Drenth JP. Berends MA, et al. Among authors: drenth jp. Liver Int. 2007 Jun;27(5):639-45. doi: 10.1111/j.1478-3231.2007.01489.x. Liver Int. 2007. PMID: 17498249

7

Laparoscopic fenestration of liver cysts in polycystic liver disease results in a median volume reduction of 12.5%.

van Keimpema L, Ruurda JP, Ernst MF, van Geffen HJ, Drenth JP. van Keimpema L, et al. Among authors: drenth jp. J Gastrointest Surg. 2008 Mar;12(3):477-82. doi: 10.1007/s11605-007-0376-8. Epub 2007 Oct 24. J Gastrointest Surg. 2008. PMID: 17957434

8

Cysts of PRKCSH mutated polycystic liver disease patients lack hepatocystin but express Sec63p.

Waanders E, Croes HJ, Maass CN, te Morsche RH, van Geffen HJ, van Krieken JH, Fransen JA, Drenth JP. Waanders E, et al. Among authors: drenth jp. Histochem Cell Biol. 2008 Mar;129(3):301-10. doi: 10.1007/s00418-008-0381-3. Epub 2008 Jan 26. Histochem Cell Biol. 2008. PMID: 18224332

9

Aspiration-sclerotherapy results in effective control of liver volume in patients with liver cysts.

van Keimpema L, de Koning DB, Strijk SP, Drenth JP. van Keimpema L, et al. Among authors: drenth jp. Dig Dis Sci. 2008 Aug;53(8):2251-7. doi: 10.1007/s10620-007-0121-x. Epub 2008 Feb 26. Dig Dis Sci. 2008. PMID: 18299984 Free PMC article. Clinical Trial.

10

Hepatocystin is not secreted in cyst fluid of hepatocystin mutant polycystic liver patients.

Waanders E, Lameris AL, Op den Camp HJ, Pluk W, Gloerich J, Strijk SP, Drenth JP. Waanders E, et al. Among authors: drenth jp. J Proteome Res. 2008 Jun;7(6):2490-5. doi: 10.1021/pr8000282. Epub 2008 Apr 18. J Proteome Res. 2008. PMID: 18419150

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