Search Results - "te Morsche, Rene H. M" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Whole-exome sequencing reveals LRP5 mutations and canonical Wnt signaling associated with hepatic cystogenesis

Whole-exome sequencing reveals LRP5 mutations and canonical Wnt signaling associated with hepatic cystogenesis

by 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.
Published in Proceedings of the National Academy of Sciences - PNAS (08.04.2014)

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Novel GANAB variants associated with polycystic liver disease

Novel GANAB variants associated with polycystic liver disease

by van de Laarschot, Liyanne F M, Te Morsche, René H M, Hoischen, Alexander, Venselaar, Hanka, Roelofs, Hennie M, Cnossen, Wybrich R, Banales, Jesus M, Roepman, Ronald, Drenth, Joost P H
Published in Orphanet journal of rare diseases (23.10.2020)

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Influence of Curcumin, Quercetin, and Eicosapentaenoic Acid on the Expression of Phase II Detoxification Enzymes in the Intestinal Cell Lines HT-29, Caco-2, HuTu 80, and LT97

Influence of Curcumin, Quercetin, and Eicosapentaenoic Acid on the Expression of Phase II Detoxification Enzymes in the Intestinal Cell Lines HT-29, Caco-2, HuTu 80, and LT97

by Odenthal, Julia, van Heumen, Bjorn W. H, Roelofs, Hennie M. J, te Morsche, Rene H. M, Marian, Brigitte, Nagengast, Fokko M, Peters, Wilbert H. M
Published in Nutrition and cancer (01.08.2012)

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Cyclooxygenase-2 polymorphisms and the risk of esophageal adeno- or squamous cell carcinoma

Cyclooxygenase-2 polymorphisms and the risk of esophageal adeno- or squamous cell carcinoma

by 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
Published in World journal of gastroenterology : WJG (28.07.2009)

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The functional -765G→C polymorphism of the COX-2 gene may reduce the risk of developing crohn's disease

The functional -765G→C polymorphism of the COX-2 gene may reduce the risk of developing crohn's disease

by de Vries, Hilbert S, te Morsche, Rene H M, van Oijen, Martijn G H, Nagtegaal, Iris D, Peters, Wilbert H M, de Jong, Dirk J
Published in PloS one (24.11.2010)

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Infliximab Exerts No Direct Hepatotoxic Effect on HepG2 Cells In Vitro

Infliximab Exerts No Direct Hepatotoxic Effect on HepG2 Cells In Vitro

by de Vries, Hilbert S., de Heij, Tineke, Roelofs, Henie M. J., te Morsche, Rene H. M., Peters, Wilbert H. M., de Jong, Dirk J.
Published in Digestive diseases and sciences (01.06.2012)

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Common variants in glyoxalase I do not increase chronic pancreatitis risk

Common variants in glyoxalase I do not increase chronic pancreatitis risk

by Kaune, Tom, Hollenbach, Marcus, Keil, Bettina, Chen, Jian-Min, Masson, Emmanuelle, Becker, Carla, Damm, Marko, Ruffert, Claudia, Grützmann, Robert, Hoffmeister, Albrecht, Te Morsche, Rene H M, Cavestro, Giulia Martina, Zuppardo, Raffaella Alessia, Saftoiu, Adrian, Malecka-Panas, Ewa, Głuszek, Stanislaw, Bugert, Peter, Lerch, Markus M, Weiss, Frank Ulrich, Zou, Wen-Bin, Liao, Zhuan, Hegyi, Peter, Drenth, Joost Ph, Riedel, Jan, Férec, Claude, Scholz, Markus, Kirsten, Holger, Tóth, Andrea, Ewers, Maren, Witt, Heiko, Griesmann, Heidi, Michl, Patrick, Rosendahl, Jonas
Published in PloS one (29.10.2019)

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Over-expression of COX-2 mRNA in colorectal cancer

Over-expression of COX-2 mRNA in colorectal cancer

by Roelofs, Hennie M J, Te Morsche, Rene H M, van Heumen, Bjorn W H, Nagengast, Fokko M, Peters, Wilbert H M
Published in BMC gastroenterology (02.01.2014)

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COX-2 polymorphisms and the risk for head and neck cancer in white patients

COX-2 polymorphisms and the risk for head and neck cancer in white patients

by Peters, Wilbert H. M., Lacko, Martin, te Morsche, Rene H. M., Voogd, Adri C., Oude Ophuis, Michael B., Manni, Johannes J.
Published in Head & neck (01.07.2009)

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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

Functional profiles of SCN9A variants in dorsal root ganglion neurons and superior cervical ganglion neurons correlate with autonomic symptoms in small fibre neuropathy

by 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
Published in Brain (London, England : 1878) (01.09.2012)

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Polymorphisms in the insulin-like growth factor axis are associated with gastrointestinal cancer

Polymorphisms in the insulin-like growth factor axis are associated with gastrointestinal cancer

by 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
Published in PloS one (07.03.2014)

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COX-2 polymorphisms -765G-->C and -1195A-->G and colorectal cancer risk

COX-2 polymorphisms -765G-->C and -1195A-->G and colorectal cancer risk

by 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
Published in World journal of gastroenterology : WJG (28.09.2009)

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Genetic polymorphisms in the tobacco smoke carcinogens detoxifying enzyme UGT1A7 and the risk of head and neck cancer

Genetic polymorphisms in the tobacco smoke carcinogens detoxifying enzyme UGT1A7 and the risk of head and neck cancer

by Lacko, Martin, Roelofs, Hennie M. J., te Morsche, Rene H. M., Voogd, Adri C., Ophuis, Michael B. Oude, Peters, Wilbert H. M., Manni, Johannes J.
Published in Head & neck (01.10.2009)

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GST Theta null genotype is associated with an increased risk for ulcerative colitis: a case-control study and meta-analysis of GST Mu and GST Theta polymorphisms in inflammatory bowel disease

GST Theta null genotype is associated with an increased risk for ulcerative colitis: a case-control study and meta-analysis of GST Mu and GST Theta polymorphisms in inflammatory bowel disease

by Broekman, Mark M T J, Bos, Caro, Te Morsche, René H M, Hoentjen, Frank, Roelofs, Hennie M J, Peters, Wilbert H M, Wanten, Geert J A, de Jong, Dirk J
Published in Journal of human genetics (01.10.2014)

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SCN9A Mutations Define Primary Erythermalgia as a Neuropathic Disorder of Voltage Gated Sodium Channels

SCN9A Mutations Define Primary Erythermalgia as a Neuropathic Disorder of Voltage Gated Sodium Channels

by Drenth, Joost P.H., te Morsche, Rene H.M., Guillet, Gerard, Taieb, Alain, Lee Kirby, R., Jansen, Jan B.M.J.
Published in Journal of investigative dermatology (01.06.2005)

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Genetic polymorphism in the conjugating enzyme UGT1A1 and the risk of head and neck cancer

Genetic polymorphism in the conjugating enzyme UGT1A1 and the risk of head and neck cancer

by 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.
Published in International journal of cancer (15.12.2010)

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Heterozygosity of ALG9 in Association with Autosomal Dominant Polycystic Liver Disease

Heterozygosity of ALG9 in Association with Autosomal Dominant Polycystic Liver Disease

by Boerrigter, Melissa M, Duijzer, Renée, te Morsche, René H. M, Drenth, Joost P. H
Published in Genes (01.09.2023)

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Alternative splicing may contribute to time-dependent manifestation of inherited erythromelalgia

Alternative splicing may contribute to time-dependent manifestation of inherited erythromelalgia

by 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.
Published in Brain (London, England : 1878) (01.06.2010)

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NaV1.7 Gain-of-Function Mutations as a Continuum: A1632E Displays Physiological Changes Associated with Erythromelalgia and Paroxysmal Extreme Pain Disorder Mutations and Produces Symptoms of Both Disorders

NaV1.7 Gain-of-Function Mutations as a Continuum: A1632E Displays Physiological Changes Associated with Erythromelalgia and Paroxysmal Extreme Pain Disorder Mutations and Produces Symptoms of Both Disorders

by 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
Published in The Journal of neuroscience (22.10.2008)

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Loss of heterozygosity is present in SEC63 germline carriers with polycystic liver disease

Loss of heterozygosity is present in SEC63 germline carriers with polycystic liver disease

by Janssen, Manoe J, Salomon, Jody, Te Morsche, René H M, Drenth, Joost P H
Published in PloS one (28.11.2012)

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