Search Results - "Te Morsche, R H M"

UGT1A7 polymorphisms in chronic pancreatitis: an example of genotyping pitfalls by te Morsche, R H M, Drenth, J P H, Truninger, K, Schulz, H-U, Kage, A, Landt, O, Verlaan, M, Rosendahl, J, Macek, M, Jansen, J B M J, Witt, H

“…UDP-glucuronosyltransferases (UGT) catalyze the glucuronidation of various compounds and thus inactivate toxic substrates. Genetic variations reducing the…”
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Long-term olive oil-based parenteral nutrition sustains innate immune function in home patients without active underlying disease by Olthof, E.D, Roelofs, H.M.J, Versleijen, M.W.J, te Morsche, R.H.M, Simonetti, E.R, Hermans, P.W.M, Wanten, G.J.A

“…Summary Background & aims It remains unclear whether impaired host defenses contribute to the increased risk for infectious complications seen in patients on…”
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Catechol-O-methyltransferase (COMT) gene variants and pain in chronic pancreatitis by VAN ESCH, A. A. J, DE VRIES, E, TE MORSCHE, R. H. M, VAN OIJEN, M. G. H, JANSEN, J. B. M. J, DRENTH, J. P. H

“…Pain is the major symptom of chronic pancreatitis. The role of genetics in pancreatic pain is unclear. Catechol-O-methyltransferase (COMT) regulates enkephalin…”
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Prevalence of hepatitis C in the general population in the Netherlands by SLAVENBURG, S, VERDUYN-LUNEL, F. M, HERMSEN, J. T, MELCHERS, W. J. G, TE MORSCHE, R. H. M, DRENTH, J. P. H

“…Chronic hepatitis C virus (HCV) is transmitted by blood-blood contact and this leads to high HCV prevalence in risk populations such as haemophilia patients…”
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Genetic heterogeneity and exclusion of a modifying locus at 2q in a family with autosomal dominant primary erythermalgia by Burns, T.M., Te Morsche, R.H.M., Jansen, J.B.M.J., H. Drenth, J.P.

“…Summary Background  Primary erythermalgia is a rare disorder characterized by recurrent attacks of red, warm and painful hands and/or feet. In a previous study…”
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Hepatic cyst penetration of cefazolin in patients receiving aspiration sclerotherapy by Lantinga, M A, Wijnands, T F M, Te Morsche, R H M, de Sévaux, R G L, Kuipers, S, Allegaert, K, Burger, D, Drenth, J P H

“…Hepatic cyst infection is a potentially severe complication in cystic disease. Treatment demands effective antibiotic concentrations within the infected cyst…”
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Detoxification enzyme polymorphisms are not involved in duodenal adenomatosis in familial adenomatous polyposis by Berkhout, M., Roelofs, H. M. J., te Morsche, R. H. M., Dekker, E., van Krieken, J. H. J. M., Nagengast, F. M., Peters, W. H. M.

“…Background: Patients with familial adenomatous polyposis (FAP) are at high risk of developing duodenal adenomas and carcinomas. Besides germline mutations in…”
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Genetic polymorphism in UDP-glucuronosyltransferase 2B7 and colorectal cancer risk by van der Logt, E M J, te Morsche, R H M, Groenendaal, N, Roelofs, H M J, de Metz, M, van der Stappen, J W, Nagengast, F M, Peters, W H M

“…Colorectal cancer (CRC) is one of the most common malignancies in the Western world. CRC is strongly associated with lifestyle factors. Susceptibility to CRC…”
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Nav1.7-related small fiber neuropathy: Impaired slow-inactivation and DRG neuron hyperexcitability by HAN, C, HOEIJMAKERS, J. G. J, FABER, C. G, MERKIES, I. S. J, WAXMAN, S. G, AHN, H.-S, ZHAO, P, SHAH, P, LAURIA, G, GERRITS, M. M, TE MORSCHE, R. H. M, DIB-HAJJ, S. D, DRENTH, J. P. H

“…Although small fiber neuropathy (SFN) often occurs without apparent cause, the molecular etiology of idiopathic SFN (I-SFN) has remained enigmatic. Sodium…”
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Secondary and tertiary structure modeling reveals effects of novel mutations in polycystic liver disease genes PRKCSH and SEC63 by Waanders, E, Venselaar, H, Te Morsche, RHM, De Koning, DB, Kamath, PS, Torres, VE, Somlo, S, Drenth, JPH

“…Waanders E, Venselaar H, te Morsche RHM, de Koning DB, Kamath PS, Torres VE, Somlo S, Drenth JPH. Secondary and tertiary structure modeling reveals effects of…”
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Genetic polymorphisms in UDP-glucuronosyltransferases and glutathione S-transferases and colorectal cancer risk by van der Logt, E.M.J., Bergevoet, S.M., Roelofs, H.M.J., van Hooijdonk, Z., te Morsche, R.H.M., Wobbes, T., de Kok, J.B., Nagengast, F.M., Peters, W.H.M.

“…Colorectal cancer (CRC) is one of the most common malignancies in the Western world showing an increasing incidence, and has been associated with genetic and…”
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Polymorphisms of UDP-glucuronosyltransferase 1A7 are not involved in pancreatic diseases by Verlaan, M, Drenth, J P H, Truninger, K, Koudova, M, Schulz, H-U, Bargetzi, M, Künzli, B, Friess, H, Cerny, M, Kage, A, Landt, O, te Morsche, R H M, Rosendahl, J, Luck, W, Nickel, R, Halangk, J, Becker, M, Macek, M, Jansen, J B M J, Witt, H

“…Background: Xenobiotic mediated cellular injury is thought to play a major role in the pathogenesis of pancreatic diseases. Genetic variations that reduce the…”
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No genetic association between EPHX1 and Crohn’s disease by Peters, W H M, van der Logt, E M J, te Morsche, R H M, Roelofs, H M J, de Jong, D J, Naber, T H J

“…The Tyr allele frequencies of 0.70 and 0.68 obtained for cases and controls, respectively, were very similar to the corresponding values of 0.71 and 0.70, as…”
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Haptoglobin and its association with the HELLP syndrome by Raijmakers, M T M, Roes, E M, te Morsche, R H M, Steegers, E A P, Peters, W H M

“…Systemic maternal oxidative stress may result in the clinical manifestations seen in women with pre-eclampsia, including dysfunction of the vascular…”
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From gene to disease; primary erythermalgia--a neuropathic disease as a consequence of mutations in a sodium pump gene by Drenth, J P H, te Morsche, R H M, Michiels, J J

“…Primary erythermalgia is a rare autosomal dominant inherited disorder characterized by recurrent attacks of red, warm and painful burning extremities. The gene…”
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From gene to disease; hepatocystin and autosomal dominant polycystic liver disease by Jansen, J B M J, Morsche, R H M Te, Drenth, J P H

“…Polycystic liver disease (PCLD, MIM 174050) is a dominantly inherited condition characterised by the presence in the liver of multiple cysts of biliary…”
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