Search Results - "Berg, Inge"

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    Flipping the medical classroom: Effect on workload, interactivity, motivation and retention of knowledge by Bouwmeester, Rianne A.M., de Kleijn, Renske A.M., van den Berg, Inge E.T., ten Cate, Olle Th.J., van Rijen, Harold V.M., Westerveld, Hendrika E.

    Published in Computers and education (01-10-2019)
    “…Engagement with homework assignments is important to be able to actively process content during in-class activities in flipped classroom education. Active…”
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    Journal Article
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    Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11 by van Mil, Saskia W C, van der Woerd, Wendy L, van der Brugge, Gerda, Sturm, Ekkehard, Jansen, Peter L M, Bull, Laura N, van den Berg, Inge E T, Berger, Ruud, Houwen, Roderick H J, Klomp, Leo W J

    Published in Gastroenterology (New York, N.Y. 1943) (01-08-2004)
    “…Progressive familial intrahepatic cholestasis (PFIC) and benign recurrent intrahepatic cholestasis (BRIC) are hereditary liver disorders; PFIC is characterized…”
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    A panel of DNA methylation markers for the classification of consensus molecular subtypes 2 and 3 in patients with colorectal cancer by Berg, Inge, Smid, Marcel, Coebergh van den Braak, Robert R. J., Wiel, Mark A., Deurzen, Carolien H. M., Weerd, Vanja, Martens, John W. M., IJzermans, Jan N. M., Wilting, Saskia M.

    Published in Molecular oncology (01-12-2021)
    “…Consensus molecular subtypes (CMSs) can guide precision treatment of colorectal cancer (CRC). We aim to identify methylation markers to distinguish between…”
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    Hyperinsulinism of infancy associated with a novel splice site mutation in the SCHAD gene by Hussain, Khalid, Clayton, Peter T., Krywawych, Steve, Chatziandreou, Ilenia, Mills, Phillipa, Ginbey, D.W., Geboers, Ans J.J.M., Berger, Ruud, van den Berg, Inge E.T., Eaton, Simon

    Published in The Journal of pediatrics (01-05-2005)
    “…Fatty acids play an important role in regulating insulin secretion, but the mechanisms are unclear. We report a case of a novel splice site mutation in the…”
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    The N-terminus of the human copper transporter 1 (hCTR1) is localized extracellularly, and interacts with itself by Klomp, Adriana E M, Juijn, Jenneke A, van der Gun, Linda T M, van den Berg, Inge E T, Berger, Ruud, Klomp, Leo W J

    Published in Biochemical journal (15-03-2003)
    “…We have used indirect immunofluorescense studies and glycosylation-site insertion and deletion mapping to characterize the topology of human copper transporter…”
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    Chronic liver disease in murine hereditary tyrosinemia type 1 induces resistance to cell death by Vogel, Arndt, van den Berg, Inge E.T., Al‐Dhalimy, Muhsen, Groopman, John, Ou, Ching‐Nan, Ryabinina, Olga, Iordanov, Mihail S., Finegold, Milton, Grompe, Markus

    Published in Hepatology (Baltimore, Md.) (01-02-2004)
    “…The murine model of hereditary tyrosinemia type 1 (HT1) was used to analyze the relationship between chronic liver disease and programmed cell death in vivo…”
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    Actual survival after resection of primary colorectal cancer: results from a prospective multicenter study by van den Berg, Inge, Coebergh van den Braak, Robert R J, van Vugt, Jeroen L A, Ijzermans, Jan N M, Buettner, Stefan

    Published in World journal of surgical oncology (05-04-2021)
    “…Colorectal cancer is the third most common type of cancer in the world. We characterize a cohort of patients who survived up to 5 years without recurrence and…”
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    Fic1 is expressed at apical membranes of different epithelial cells in the digestive tract and is induced in the small intestine during postnatal development of mice by VAN MIL, Saskia W. C, VAN OORT, Masja M, VAN DEN BERG, Inge E. T, BERGER, Ruud, HOUWEN, Roderick H. J, KLOMP, Leo W. J

    Published in Pediatric research (01-12-2004)
    “…Mutations in ATP8B1 are associated with FIC1 disease, an autosomal recessive disorder in which intrahepatic cholestasis is the predominant manifestation…”
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    Kidneys of mice with hereditary tyrosinemia type I are extremely sensitive to cytotoxicity by JACOBS, Saskia M. M, VAN BEURDEN, Denis H. A, KLOMP, Leo W. J, BERGER, Ruud, VAN DEN BERG, Inge E. T

    Published in Pediatric research (01-03-2006)
    “…Children with hereditary tyrosinemia type 1 (HT1) suffer from liver failure, renal tubular dysfunction, and rickets. The disease is caused by deficiency of…”
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    Renal proximal tubular cells acquire resistance to cell death stimuli in mice with hereditary tyrosinemia type 1 by Luijerink, Marjanka C., Van Beurden, Ellen A.C.M., Malingré, Helga E.M., Jacobs, Saskia M.M., Grompe, Markus, Klomp, Leo W.J., Berger, Ruud, van den bERG, Inge E.T.

    Published in Kidney international (01-09-2004)
    “…Renal proximal tubular cells acquire resistance to cell death stimuli in mice with hereditary tyrosinemia type 1. Hereditary tyrosinemia type 1 (HT1), which is…”
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    Structural organization of the human short-chain L-3-hydroxyacyl-CoA dehydrogenase gene by Vredendaal, P J, van den Berg, I E, Stroobants, A K, van der A, D L, Malingré, H E, Berger, R

    Published in Mammalian genome (01-09-1998)
    “…The third step in the mitochondrial beta-oxidation spiral of short-chain fatty acids is catalyzed by short-chain L-3-hydroxyacyl-CoA dehydrogenase (HADHSC; EC…”
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    Circular RNA in Chemonaive Lymph Node Negative Colon Cancer Patients by van den Berg, Inge, Smid, Marcel, Coebergh van den Braak, Robert R J, van Deurzen, Carolien H M, de Weerd, Vanja, Foekens, John A, IJzermans, Jan N M, Martens, John W M, Wilting, Saskia M

    Published in Cancers (15-04-2021)
    “…Circular RNAs (circRNAs) appear important in tumor progression of colon cancer (CC). We identified an extensive catalog of circRNAs in 181 chemonaive stage…”
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