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

Volltext

Barrett associated MHC and FOXF1 variants also increase esophageal carcinoma risk von Dura, Polat, Veen, Elke M., Salomon, Jody, 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.

Volltext

Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease von Drenth, Joost P.H, te Morsche, Rene H.M, Smink, Renate, Bonifacino, Juan S, Jansen, Jan B.M.J

Volltext

ddPCR enables rapid detection of bloodstream infections in patients on home parenteral nutrition: A prospective cohort study von Gillis, Veerle E.L.M., Dalloyaux, Daisy, te Morsche, Rene H.M., van Ingen, Jakko, Sir, Özcan, Rovers, Chantal P., Wouters, Yannick, Wanten, Geert J.A.

Volltext

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.

Volltext

Genetic polymorphism 609C>T in NAD(P)H:quinone oxidoreductase 1 enhances the risk of proximal colon cancer von Freriksen, Jolien J M, Salomon, Jody, Roelofs, Hennie M J, Te Morsche, Rene H M, van der Stappen, Jos W J, Dura, Polat, Witteman, Ben J M, Lacko, Martin, Peters, Wilbert H M

Volltext

Tropical calcific pancreatitis and its association with CTRC and SPINK1 (p.N34S) variants von Derikx, Monique H.M, Szmola, Richard, te Morsche, Rene H.M, Sunderasan, Santhosh, Chacko, Ashok, Drenth, Joost P.H

Volltext

Combined polymorphisms in UDP-glucuronosyltransferases 1A1 and 1A6: implications for patients with Gilbert's syndrome von Peters, Wilbert H.M, te Morsche, Rene H.M, Roelofs, Hennie M.J

Volltext

Common single nucleotide polymorphisms in transient receptor potential melastatin type 6 increase the risk for proton pump inhibitor-induced hypomagnesemia: a case–control study von Hess, Mark W, de Baaij, Jeroen H.F, Broekman, Mark M.T.J, Bisseling, Tanya M, Haarhuis, Bertram J.T, Tan, Adriaan C.I.T.L, te Morsche, René H.M, Hoenderop, Joost G.J, Bindels, René J.M, Drenth, Joost P.H

Volltext

Secondary, Somatic Mutations Might Promote Cyst Formation in Patients With Autosomal Dominant Polycystic Liver Disease von Janssen, Manoe J, Waanders, Esmé, te Morsche, René H.M, Xing, Ruoyu, Dijkman, Henry B.P.M, Woudenberg, Jannes, Drenth, Joost P.H

Volltext

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

Volltext

Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis von Rosendahl, Jonas, Kirsten, Holger, Hegyi, Eszter, Kovacs, Peter, Weiss, Frank Ulrich, Laumen, Helmut, Lichtner, Peter, Ruffert, Claudia, Chen, Jian-Min, Masson, Emmanuelle, Beer, Sebastian, Zimmer, Constantin, Seltsam, Katharina, Algül, Hana, Bühler, Florence, Bruno, Marco J, Bugert, Peter, Burkhardt, Ralph, Cavestro, Giulia Martina, Cichoz-Lach, Halina, Farré, Antoni, Frank, Josef, Gambaro, Giovanni, Gimpfl, Sebastian, Grallert, Harald, Griesmann, Heidi, Grützmann, Robert, Hellerbrand, Claus, Hegyi, Péter, Hollenbach, Marcus, Iordache, Sevastitia, Jurkowska, Grazyna, Keim, Volker, Kiefer, Falk, Krug, Sebastian, Landt, Olfert, Leo, Milena Di, Lerch, Markus M, Lévy, Philippe, Löffler, Markus, Löhr, Matthias, Ludwig, Maren, Macek, Milan, Malats, Nuria, Malecka-Panas, Ewa, Malerba, Giovanni, Mann, Karl, Mayerle, Julia, Mohr, Sonja, te Morsche, Rene H M, Motyka, Marie, Mueller, Sebastian, Müller, Thomas, Nöthen, Markus M, Pedrazzoli, Sergio, Pereira, Stephen P, Peters, Annette, Pfützer, Roland, Real, Francisco X, Rebours, Vinciane, Ridinger, Monika, Rietschel, Marcella, Rösmann, Eva, Saftoiu, Adrian, Schneider, Alexander, Schulz, Hans-Ulrich, Soranzo, Nicole, Soyka, Michael, Simon, Peter, Skipworth, James, Stickel, Felix, Strauch, Konstantin, Stumvoll, Michael, Testoni, Pier Alberto, Tönjes, Anke, Werner, Lena, Werner, Jens, Wodarz, Norbert, Ziegler, Martin, Masamune, Atsushi, Mössner, Joachim, Férec, Claude, Michl, Patrick, P H Drenth, Joost, Witt, Heiko, Scholz, Markus, Sahin-Tóth, Miklós

Volltext

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

Volltext

NaV1.7 Gain-of-Function Mutations as a Continuum: A1632E Displays Physiological Changes Associated with Erythromelalgia and Paroxysmal Extreme Pain Disorder Mutations and Produces... von Estacion, M, Dib-Hajj, S. D, Benke, P. J, te Morsche, Rene H. M, Eastman, E. M, Macala, L. J, Drenth, J. P. H, Waxman, S. G

Volltext

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.

Volltext

Polymorphisms in the insulin-like growth factor axis are associated with gastrointestinal cancer von Ong, Jennie, Salomon, Jody, te Morsche, Rene H M, Roelofs, Hennie M J, Witteman, Ben J M, Dura, Polat, Lacko, Martin, Peters, Wilbert H M

Volltext

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.

Volltext

Analysis of GPRC6A variants in different pancreatitis etiologies von Kaune, Tom, Ruffert, Claudia, Hesselbarth, Nico, Damm, Marko, Krug, Sebastian, Cardinal von Widdern, Julian, Masson, Emmanuelle, Chen, Jian-Min, Rebours, Vinciane, Buscail, Louis, Férec, Claude, Grützmann, Robert, te Morsche, Rene H.M., Drenth, Joost PH, Cavestro, Giulia Martina, Zuppardo, Raffaella Alessia, Saftoiu, Adrian, Malecka-Panas, Ewa, Głuszek, Stanislaw, Bugert, Peter, Lerch, Markus M., Sendler, Matthias, Weiss, Frank Ulrich, Zou, Wen-Bin, Deng, Shun-Jiang, Liao, Zhuan, Scholz, Markus, Kirsten, Holger, Hegyi, Peter, Witt, Heiko, Michl, Patrick, Griesmann, Heidi, Rosendahl, Jonas

Volltext

Genetic polymorphism in the conjugating enzyme UGT1A1 and the risk of head and neck cancer von Lacko, Martin, Roelofs, Hennie M.J., te Morsche, Rene H.M., Voogd, Adri C., Ophuis, Michel B. Oude, Peters, Wilbert H.M., Manni, Johannes J.

Volltext

High enzyme activity UGT1A1 or low activity UGT1A8 and UGT2B4 genotypes increase esophageal cancer risk von DURA, Polat, 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

Volltext