Search Results - "Muckenthaler, M"

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    HFE and ALK3 act in the same signaling pathway by Traeger, L., Schnittker, J., Dogan, D.Y., Oguama, D., Kuhlmann, T., Muckenthaler, M.U., Krijt, J., Urzica, E.I., Steinbicker, A.U.

    Published in Free radical biology & medicine (20-11-2020)
    “…Hepcidin deficiency leads to iron overload by increased dietary iron uptake and iron release from storage cells. The most frequent mutation in Hfe leads to…”
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    Journal Article
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    The favorable effect of activating NOTCH1 receptor mutations on long-term outcome in T-ALL patients treated on the ALL–BFM 2000 protocol can be separated from FBXW7 loss of function by Kox, C, Zimmermann, M, Stanulla, M, Leible, S, Schrappe, M, Ludwig, W-D, Koehler, R, Tolle, G, Bandapalli, O R, Breit, S, Muckenthaler, M U, Kulozik, A E

    Published in Leukemia (01-12-2010)
    “…Precursor T-cell acute lymphoblastic leukemia (T-ALL) remains an important challenge in pediatric oncology. Because of the particularly poor prognosis of…”
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    Maternal iron status in early pregnancy and DNA methylation in offspring: an epigenome-wide meta-analysis by Taeubert, M J, de Prado-Bert, P, Geurtsen, M L, Mancano, G, Vermeulen, M J, Reiss, I K M, Caramaschi, D, Sunyer, J, Sharp, G C, Julvez, J, Muckenthaler, M U, Felix, J F

    Published in Clinical epigenetics (03-05-2022)
    “…Unbalanced iron homeostasis in pregnancy is associated with an increased risk of adverse birth and childhood health outcomes. DNA methylation has been…”
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    Identification of a genetically defined ultra-high-risk group in relapsed pediatric T-lymphoblastic leukemia by Richter-Pechańska, P, Kunz, J B, Hof, J, Zimmermann, M, Rausch, T, Bandapalli, O R, Orlova, E, Scapinello, G, Sagi, J C, Stanulla, M, Schrappe, M, Cario, G, Kirschner-Schwabe, R, Eckert, C, Benes, V, Korbel, J O, Muckenthaler, M U, Kulozik, A E

    Published in Blood cancer journal (New York) (03-02-2017)
    “…In the search for genes that define critical steps of relapse in pediatric T-cell acute lymphoblastic leukemia (T-ALL) and can serve as prognostic markers, we…”
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    A new paradigm to understand and treat diabetic neuropathy by Hidmark, A, Fleming, T, Vittas, S, Mendler, M, Deshpande, D, Groener, J B, Müller, B P, Reeh, P W, Sauer, S K, Pham, M, Muckenthaler, M U, Bendszus, M, Nawroth, P P

    “…The clinical symptoms of diabetic neuropathy (DN) manifest in a time dependent manner as a positive symptoms (i. e. pain, hypersensitivity, tingling, cramps,…”
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    Heme controls ferroportin1 (FPN1) transcription involving Bach1, Nrf2 and a MARE/ARE sequence motif at position −7007 of the FPN1 promoter by MARRO, Samuele, CHIABRANDO, Deborah, MESSANA, Erika, STOLTE, Jens, TURCO, Emilia, TOLOSANO, Emanuela, MUCKENTHALER, Martina U

    Published in Haematologica (Roma) (01-08-2010)
    “…Macrophages of the reticuloendothelial system play a key role in recycling iron from hemoglobin of senescent or damaged erythrocytes. Heme oxygenase 1 degrades…”
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    Hereditary hyperferritinemia cataract syndrome--the first family in Germany by Millonig, G, Holzer, M P, Tolle, G, Auffarth, G U, Muckenthaler, M U, Seitz, H K, Mueller, S

    Published in Zeitschrift fur Gastroenterologie (01-12-2009)
    “…We report on a 23-year-old woman who presented with elevated serum ferritin values at our department. She had undergone cataract surgery at the age of 14 and…”
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    HFE Downregulates Iron Uptake From Transferrin and Induces Iron-Regulatory Protein Activity in Stably Transfected Cells by Riedel, H.D., Muckenthaler, M.U., Gehrke, S.G., Mohr, I., Brennan, K., Herrmann, T., Fitscher, B.A., Hentze, M.W., Stremmel, W.

    Published in Blood (01-12-1999)
    “…Hereditary hemochromatosis (HH) is a common autosomal-recessive disorder of iron metabolism. More than 80% of HH patients are homozygous for a point mutation…”
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    Comparison of fluorescent tag DNA labeling methods used for expression analysis by DNA microarrays by Richter, A, Schwager, C, Hentze, S, Ansorge, W, Hentze, M W, Muckenthaler, M

    Published in BioTechniques (01-09-2002)
    “…Gene expression profiling by DNA microarrays has found wide application in many fields of biomedical research. The protocols for this technique are not yet…”
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    Iron refractory iron deficiency anemia by De Falco, Luigia, Sanchez, Mayka, Silvestri, Laura, Kannengiesser, Caroline, Muckenthaler, Martina U, Iolascon, Achille, Gouya, Laurent, Camaschella, Clara, Beaumont, Carole

    Published in Haematologica (Roma) (01-06-2013)
    “…Iron refractory iron deficiency anemia is a hereditary recessive anemia due to a defect in the TMPRSS6 gene encoding Matriptase-2. This protein is a…”
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    The murine growth differentiation factor 15 is not essential for systemic iron homeostasis in phlebotomized mice by Casanovas, Guillem, Vujić Spasic, Maja, Casu, Carla, Rivella, Stefano, Strelau, Jens, Unsicker, Klaus, Muckenthaler, Martina U

    Published in Haematologica (Roma) (01-03-2013)
    “…In conditions of increased erythropoiesis, expression of hepcidin, the master regulator of systemic iron homeostasis, is decreased to allow for the release of…”
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