Search Results - "Te Morsche, R.H.M"

P1264 CLINICAL HETEROGENEITY IN POLYCYSTIC LIVER DISEASE FAMILIES by Cnossen, W.R, Salomon, J, te Morsche, R.H.M, Drenth, J.P.H

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1394 COPY NUMBER ASSAY IN POLYCYSTIC LIVER DISEASE BY MULTIPLEX LIGATION-DEPENDENT PROBE AMPLIFICATION by Maurits, J.S.F, Cnossen, W.R, Waanders, E, te Morsche, R.H.M, Drenth, J.P.H

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346 SOMATIC INACTIVATION IN POLYCYSTIC LIVER SEC63 GERMLINE CARRIERS OCCURS THROUGH LOSS OF HETEROZYGOSITY by Janssen, M.J, Salomon, J, te Morsche, R.H.M, Drenth, J.P.H

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696 LOSS OF HETEROZYGOSITY IN LIVER CYSTS OF AUTOSOMAL DOMINANT POLYCYSTIC LIVER DISEASE (PCLD) DEPENDS ON GERMLINE MUTATION OF THE PATIENT by Janssen, M.J, Woudenberg, J, te Morsche, R.H.M, Drenth, J.P.H

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1387 IDENTIFICATION OF A NOVEL GENE ASSOCIATED WITH POLYCYSTIC LIVER AND KIDNEY DISEASES by Cnossen, W.R, te Morsche, R.H.M, Hoischen, A, Gilissen, C, Chrispijn, M, Venselaar, H, Mehdi, S, Bergmann, C, Veltman, J.A, Drenth, J.P.H

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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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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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46 IN AUTOSOMAL DOMINANT POLYCYSTIC LIVER DISEASE (PCLD) CYSTS DEVELOP THROUGH A CELLULAR RECESSIVE MECHANISM INVOLVING LOSS OF HETEROZYGOSITY AND SOMATIC MUTATIONS by Janssen, M.J, Waanders, E, Dijkman, H.B.P.M, te Morsche, R.H.M, Woudenberg, J, Drenth, J.P.H

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884 POLYCYSTIC LIVER DISEASE: A CLINICAL ANALYSIS OF 116 PATIENTS by de Koning, D.B, van Keimpema, L, te Morsche, R.H.M, van den Berg, A.P, Jansen, P.L, de Man, R.A, Nevens, F, van Hoek, B, Drenth, J.P.H

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438 SECONDARY AND TERTIARY STRUCTURE MODELING REVEALS EFFECTS OF NOVEL MUTATIONS IN POLYCYSTIC LIVER DISEASE GENES PRKCSH AND SEC63 by Waanders, E, De Koning, D.B, Te Morsche, R.H.M, Venselaar, H, Kamath, P.S, Torres, V.E, Somlo, S, Drenth, J.P.H

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SAT-050 - Compound library screening for the identification of a new treatment for polycystic liver disease by van de Laarschot, L., van der Ende, K., Te Morsche, R.H.M., Drenth, J.P.H.

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Compound library screening for the identification of a new treatment for polycystic liver disease by van de Laarschot, L., van der Ende, K., Te Morsche, R.H.M., Drenth, J.P.H.

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Droplet Digital Polymerase Chain Reaction Enables Rapid Detection And Characterisation Of Bacteraemia In Chronic Parenteral Nutrition Patients by Gillis, V., Dalloyaux, D., Te Morsche, R.H.M., van Ingen, J., Sir, O., Bleeker-Rovers, C.P., Wertheim, H.F., Wouters, Y., Wanten, G.J.

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Na v 1.7-related small fiber neuropathy: Impaired slow-inactivation and DRG neuron hyperexcitability by Han, C., Hoeijmakers, J.G.J., 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., Faber, C.G., Merkies, I.S.J., Waxman, S.G.

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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 by Estacion, Mark, Dib-Hajj, Sulayman D., Benke, Paul J., te Morsche, R.H.M., Eastman, Emmanuella M., Macala, Lawrence J., Drenth, Joost P.H., Waxman, Stephen G.

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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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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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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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