Polymorphisms in gene encoding TRPV1-receptor involved in pain perception are unrelated to chronic pancreatitis von van Esch, Aura A J, Lamberts, Mark P, te Morsche, René H M, van Oijen, Martijn G H, Jansen, Jan B M J, Drenth, Joost P H

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Cyclooxygenase-2 polymorphisms and the risk of esophageal adeno- or squamous cell carcinoma von Kristinsson, Jón O, van Westerveld, Paul, te Morsche, Rene H M, Roelofs, Hennie M J, Wobbes, T, Witteman, Ben J M, Tan, Adriaan C I T L, van Oijen, Martijn G H, Jansen, Jan B M J, Peters, Wilbert H M

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Short mucin 6 alleles are associated with H pylori infection von Nguyen, Thai V, Janssen, Jr, Marcel, Gritters, Paulien, te Morsche, René H M, Drenth, Joost P H, van Asten, Henri, Laheij, Robert J F, Jansen, Jan B M J

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LRP5 variants may contribute to ADPKD von Cnossen, Wybrich R, te Morsche, René H M, Hoischen, Alexander, Gilissen, Christian, Venselaar, Hanka, Mehdi, Soufi, Bergmann, Carsten, Losekoot, Monique, Breuning, Martijn H, Peters, Dorien J M, Veltman, Joris A, Drenth, Joost P H

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Over-expression of COX-2 mRNA in colorectal cancer von Roelofs, Hennie M J, Te Morsche, Rene H M, van Heumen, Bjorn W H, Nagengast, Fokko M, Peters, Wilbert H M

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Whole-exome sequencing reveals LRP5 mutations and canonical Wnt signaling associated with hepatic cystogenesis von Cnossen, Wybrich R., te Morsche, René H. M., Hoischen, Alexander, Gilissen, Christian, Chrispijn, Melissa, Venselaar, Hanka, Mehdi, Soufi, Bergmann, Carsten, Veltman, Joris A., Drenth, Joost P. H.

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COX-2 polymorphisms -765G-->C and -1195A-->G and colorectal cancer risk von Hoff, Juliët H, te Morsche, Rene H M, Roelofs, Hennie M J, van der Logt, Elise M J, Nagengast, Fokko M, Peters, Wilbert H M

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Heterozygous variant of CYP2C83 is a protective factor for developing post-ERCP pancreatitis von de Jong, Mike Jp, Kuipers, Romy N, Drenth, Joost Ph, Te Morsche, René Hm, van Delft, Foke, Siersema, Peter D

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Severe Polycystic Liver Disease Is Not Caused by Large Deletions of the PRKCSH Gene von Cnossen, Wybrich R., Maurits, Jake S.F., Salomon, Jody, te Morsche, René H.M., Waanders, Esmé, Drenth, Joost P. H.

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Compound Heterozygosity in Sodium Channel Nav1.7 in a Family with Hereditary Erythermalgia von Samuels, Mark E, Morsche, Rene HM te, Lynch, Mary E, Drenth, Joost PH

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Polymorphisms in alcohol-metabolizing enzymes and esophageal carcinoma susceptibility: a Dutch Caucasian case-control study von Dura, Polat, Berkers, Tineke, van Veen, Elke M, Salomon, Jody, te Morsche, Rene H M, Roelofs, Hennie M J, Kristinsson, Jon O, Wobbes, Theo, Witteman, Ben J M, Tan, Adriaan C I T L, Drenth, Joost P H, Peters, Wilbert H M

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Pain perception is altered by a nucleotide polymorphism in SCN9A von Reimann, Frank, Cox, James J, Belfer, Inna, Diatchenko, Luda, Zaykin, Dmitri V, McHale, Duncan P, Drenth, Joost P.H, Dai, Feng, Wheeler, Jerry, Sanders, Frances, Wood, Linda, Wu, Tian-Xia, Karppinen, Jaro, Nikolajsen, Lone, Männikkö, Minna, Max, Mitchell B, Kiselycznyk, Carly, Poddar, Minakshi, te Morsche, Rene H.M, Smith, Shad, Gibson, Dustin, Kelempisioti, Anthi, Maixner, William, Gribble, Fiona M, Woods, C. Geoffrey

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Celecoxib and tauro-ursodeoxycholic acid co-treatment inhibits cell growth in familial adenomatous polyposis derived LT97 colon adenoma cells von van Heumen, Bjorn W.H., Roelofs, Hennie M.J., te Morsche, René H.M., Marian, Brigitte, Nagengast, Fokko M., Peters, Wilbert H.M.

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Duodenal mucosal risk markers in patients with familial adenomatous polyposis: effects of celecoxib/ursodeoxycholic acid co-treatment and comparison with patient controls von van Heumen, Bjorn W H, Roelofs, Hennie M J, te Morsche, René H M, Nagengast, Fokko M, Peters, Wilbert H M

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Chymotrypsin C (CTRC) variants that diminish activity or secretion are associated with chronic pancreatitis von Nickel, Renate, Sahin-Tóth, Miklós, Ózsvári, Béla, Gress, Thomas M, Truninger, Kaspar, Macek, Milan, Landt, Olfert, Büning, Carsten, Berg, Thomas, Witt, Heiko, Kovacs, Peter, Puhl, Gero, Pfützer, Roland, Groneberg, David Alexander, Kage, Andreas, Hegyi, Péter, Wiedenmann, Bertram, Bhatia, Eesh, Blüher, Matthias, Schmidt, Hartmut, te Morsche, René HM, Bödeker, Hans, Stumvoll, Michael, Teich, Niels, Schulz, Hans-Ulrich, Szmola, Richárd, Ockenga, Johann, Mössner, Joachim, Keim, Volker, Rosendahl, Jonas, Löhr, Matthias, Choudhuri, Gourdas, Drenth, Joost PH, Witt, Ulrike

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Functional profiles of SCN9A variants in dorsal root ganglion neurons and superior cervical ganglion neurons correlate with autonomic symptoms in small fibre neuropathy von CHONGYANG HAN, HOEIJMAKERS, Janneke G. J, WAXMAN, Stephen G, SHUJUN LIU, GERRITS, Monique M, TE MORSCHE, Rene H. M, LAURIA, Giuseppe, DIB-HAJJ, Sulayman D, DRENTH, Joost P. H, FABER, Catharina G, MERKIES, Ingemar S. J

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SCN9A Mutations Define Primary Erythermalgia as a Neuropathic Disorder of Voltage Gated Sodium Channels von Drenth, Joost P.H., te Morsche, Rene H.M., Guillet, Gerard, Taieb, Alain, Lee Kirby, R., Jansen, Jan B.M.J.

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Alternative splicing may contribute to time-dependent manifestation of inherited erythromelalgia von Choi, Jin-Sung, Cheng, Xiaoyang, Foster, Edmund, Leffler, Andreas, Tyrrell, Lynda, te Morsche, Rene H. M., Eastman, Emmanuella M., Jansen, Henry J., Huehne, Kathrin, Nau, Carla, Dib-Hajj, Sulayman D., Drenth, Joost P. H., Waxman, Stephen G.

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Autosomal dominant polycystic liver disease in a family without polycystic kidney disease associated with a novel missense protein kinase C substrate 80K-H mutation von Peces, Ramón, Drenth, Joost P H, Te Morsche, Rene H M, González, Pedro, Peces, Carlos

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Infliximab Exerts No Direct Hepatotoxic Effect on HepG2 Cells In Vitro von de Vries, Hilbert S., de Heij, Tineke, Roelofs, Henie M. J., te Morsche, Rene H. M., Peters, Wilbert H. M., de Jong, Dirk J.

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