Modelling IRF8 Deficient Human Hematopoiesis and Dendritic Cell Development with Engineered iPS Cells
Sontag, Stephanie, Förster, Malrun, Qin, Jie, Wanek, Paul, Mitzka, Saskia, Schüler, Herdit M., Koschmieder, Steffen, Rose‐John, Stefan, Seré, Kristin, Zenke, Martin
Published in Stem cells (Dayton, Ohio) (01.04.2017)
Published in Stem cells (Dayton, Ohio) (01.04.2017)
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The role of Nav1.7 in human nociceptors: insights from human induced pluripotent stem cell-derived sensory neurons of erythromelalgia patients
Meents, Jannis E, Bressan, Elisangela, Sontag, Stephanie, Foerster, Alec, Hautvast, Petra, Rösseler, Corinna, Hampl, Martin, Schüler, Herdit, Goetzke, Roman, Le, Thi Kim Chi, Kleggetveit, Inge Petter, Le Cann, Kim, Kerth, Clara, Rush, Anthony M, Rogers, Marc, Kohl, Zacharias, Schmelz, Martin, Wagner, Wolfgang, Jørum, Ellen, Namer, Barbara, Winner, Beate, Zenke, Martin, Lampert, Angelika
Published in Pain (Amsterdam) (01.06.2019)
Published in Pain (Amsterdam) (01.06.2019)
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CRISPR/Cas9-engineered human ES cells harboring heterozygous and homozygous c-KIT knockout
de Toledo, Marcelo A.S., Fu, Xuhuang, Kluge, Frederick, Götz, Katrin, Schmitz, Susanne, Wanek, Paul, Schüler, Herdit M., Pannen, Kristina, Chatain, Nicolas, Koschmieder, Steffen, Brümmendorf, Tim H., Zenke, Martin
Published in Stem cell research (01.04.2022)
Published in Stem cell research (01.04.2022)
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Nintedanib targets KIT D816V neoplastic cells derived from induced pluripotent stem cells of systemic mastocytosis
Toledo, Marcelo A.S., Gatz, Malrun, Sontag, Stephanie, Gleixner, Karoline V., Eisenwort, Gregor, Feldberg, Kristina, Hamouda, Ahmed E.I., Kluge, Frederick, Guareschi, Riccardo, Rossetti, Giulia, Sechi, Antonio S., Dufva, Olli M.J., Mustjoki, Satu M., Maurer, Angela, Schüler, Herdit M., Goetzke, Roman, Braunschweig, Till, Kaiser, Anne, Panse, Jens, Jawhar, Mohamad, Reiter, Andreas, Hilberg, Frank, Ettmayer, Peter, Wagner, Wolfgang, Koschmieder, Steffen, Brümmendorf, Tim H., Valent, Peter, Chatain, Nicolas, Zenke, Martin
Published in Blood (15.04.2021)
Published in Blood (15.04.2021)
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To clone or not to clone? Induced pluripotent stem cells can be generated in bulk culture
Willmann, Charlotte A, Hemeda, Hatim, Pieper, Lisa A, Lenz, Michael, Qin, Jie, Joussen, Sylvia, Sontag, Stephanie, Wanek, Paul, Denecke, Bernd, Schüler, Herdit M, Zenke, Martin, Wagner, Wolfgang
Published in PloS one (29.05.2013)
Published in PloS one (29.05.2013)
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Towards personalized medicine with iPS cell technology: a case report of advanced systemic mastocytosis with associated eosinophilia
Atakhanov, Salim, Christen, Deborah, Rolles, Benjamin, Schüler, Herdit M., Panse, Jens, Chatain, Nicolas, Koschmieder, Steffen, Brümmendorf, Tim H., Toledo, Marcelo A. S., Zenke, Martin
Published in Annals of hematology (01.11.2022)
Published in Annals of hematology (01.11.2022)
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CRISPR/Cas9 mediated CXCL4 knockout in human iPS cells of polycythemia vera patient with JAK2 V617F mutation
Boehnke, Janik, Atakhanov, Salim, Toledo, Marcelo A.S., Schüler, Herdit M., Sontag, Stephanie, Chatain, Nicolas, Koschmieder, Steffen, Brümmendorf, Tim H., Kramann, Rafael, Zenke, Martin
Published in Stem cell research (01.08.2021)
Published in Stem cell research (01.08.2021)
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Transformation of primary murine peritoneal mast cells by constitutive KIT activation is accompanied by loss of Cdkn2a/Arf expression
Capellmann, Sandro, Sonntag, Roland, Schüler, Herdit, Meurer, Steffen K, Gan, Lin, Kauffmann, Marlies, Horn, Katharina, Königs-Werner, Hiltrud, Weiskirchen, Ralf, Liedtke, Christian, Huber, Michael
Published in Frontiers in immunology (30.03.2023)
Published in Frontiers in immunology (30.03.2023)
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Proinflammatory phenotype of iPS cell-derived JAK2 V617F megakaryocytes induces fibrosis in 3D in vitro bone marrow niche
Flosdorf, Niclas, Böhnke, Janik, de Toledo, Marcelo A.S., Lutterbach, Niklas, Lerma, Vanesa Gómez, Graßhoff, Martin, Olschok, Kathrin, Gupta, Siddharth, Tharmapalan, Vithurithra, Schmitz, Susanne, Götz, Katrin, Schüler, Herdit M., Maurer, Angela, Sontag, Stephanie, Küstermann, Caroline, Seré, Kristin, Wagner, Wolfgang, Costa, Ivan G., Brümmendorf, Tim H., Koschmieder, Steffen, Chatain, Nicolas, Castilho, Miguel, Schneider, Rebekka K., Zenke, Martin
Published in Stem cell reports (13.02.2024)
Published in Stem cell reports (13.02.2024)
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Genetic and Molecular Characterization of the Immortalized Murine Hepatic Stellate Cell Line GRX
Schröder, Sarah K, Schüler, Herdit M, Petersen, Kamilla V, Tesauro, Cinzia, Knudsen, Birgitta R, Pedersen, Finn S, Krus, Frederike, Buhl, Eva M, Roeb, Elke, Roderfeld, Martin, Borojevic, Radovan, Almeida, Jamie L, Weiskirchen, Ralf
Published in Cells (Basel, Switzerland) (30.04.2022)
Published in Cells (Basel, Switzerland) (30.04.2022)
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CALR frameshift mutations in MPN patient-derived iPSCs accelerate maturation of megakaryocytes
Olschok, Kathrin, Han, Lijuan, de Toledo, Marcelo A.S., Böhnke, Janik, Graßhoff, Martin, Costa, Ivan G., Theocharides, Alexandre, Maurer, Angela, Schüler, Herdit M., Buhl, Eva Miriam, Pannen, Kristina, Baumeister, Julian, Kalmer, Milena, Gupta, Siddharth, Boor, Peter, Gezer, Deniz, Brümmendorf, Tim H., Zenke, Martin, Chatain, Nicolas, Koschmieder, Steffen
Published in Stem cell reports (09.11.2021)
Published in Stem cell reports (09.11.2021)
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Genetic counseling in Robertsonian translocations der(13;14): Frequencies of reproductive outcomes and infertility in 101 pedigrees
Engels, Hartmut, Eggermann, Thomas, Caliebe, Almut, Jelska, Anna, Schubert, Regine, Schüler, Herdit M., Panasiuk, Barbara, Zaremba, Jacek, Latos-Bieleńska, Anna, Jakubowski, Lucjusz, Zerres, Klaus P., Schwanitz, Gesa, Midro, Alina T.
Published in American journal of medical genetics. Part A (15.10.2008)
Published in American journal of medical genetics. Part A (15.10.2008)
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A phenotype map for 14q32.3 terminal deletions
Engels, Hartmut, Schüler, Herdit M., Zink, Alexander M., Wohlleber, Eva, Brockschmidt, Antje, Hoischen, Alexander, Drechsler, Matthias, Lee, Jennifer A., Ludwig, Kerstin U., Kubisch, Christian, Schwanitz, Gesa, Weber, Ruthild G., Leube, Barbara, Hennekam, Raoul C. M., Rudnik-Schöneborn, Sabine, Kreiß-Nachtsheim, Martina, Reutter, Heiko
Published in American journal of medical genetics. Part A (01.04.2012)
Published in American journal of medical genetics. Part A (01.04.2012)
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Patient with three euchromatic supernumerary marker chromosomes derived from chromosomes 1, 12, and 18: Characterization and evaluation of the aberrations
Schwanitz, Gesa, Hagh, Javad Karim Zad, Rad, Isa Abdi, Omrani, Mir Davood, Gamerdinger, Ulrike, Schubert, Regine, Elbracht, Miriam, Eggermann, Thomas, Eggermann, Katja, Spengler, Sabrina, Schüler, Herdit, Gogiel, Magdalena
Published in American journal of medical genetics. Part A (01.03.2014)
Published in American journal of medical genetics. Part A (01.03.2014)
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Rare proximal interstitial deletion of chromosome 4q, del(4)(q13.2q21.22): New case and comparison with the literature
Eggermann, Katja, Bergmann, Carsten, Heil, Inge, Eggermann, Thomas, Zerres, Klaus, Schüler, Herdit M.
Published in American journal of medical genetics. Part A (15.04.2005)
Published in American journal of medical genetics. Part A (15.04.2005)
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Replicative senescence of mesenchymal stem cells causes DNA-methylation changes which correlate with repressive histone marks
Schellenberg, Anne, Lin, Qiong, Schüler, Herdit, Koch, Carmen M, Joussen, Sylvia, Denecke, Bernd, Walenda, Gudrun, Pallua, Norbert, Suschek, Christoph V, Zenke, Martin, Wagner, Wolfga
Published in Aging (Albany, NY.) (01.09.2011)
Published in Aging (Albany, NY.) (01.09.2011)
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Inherited cases of CNOT3‐associated intellectual developmental disorder with speech delay, autism, and dysmorphic facies
Meyer, Robert, Begemann, Matthias, Demuth, Stephanie, Kraft, Florian, Dey, Daniela, Schüler, Herdit, Busse, Sabine, Häusler, Martin, Zerres, Klaus, Kurth, Ingo, Eggermann, Thomas, Elbracht, Miriam
Published in Clinical genetics (01.10.2020)
Published in Clinical genetics (01.10.2020)
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A Newly Established Murine Cell Line as a Model for Hepatocellular Cancer in Non-Alcoholic Steatohepatitis
Kroh, Andreas, Walter, Jeanette, Schüler, Herdit, Nolting, Jochen, Eickhoff, Roman, Heise, Daniel, Neumann, Ulf Peter, Cramer, Thorsten, Ulmer, Tom Florian, Fragoulis, Athanassios
Published in International journal of molecular sciences (12.11.2019)
Published in International journal of molecular sciences (12.11.2019)
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Proximal 11p deletion syndrome (P11pDS): additional evaluation of the clinical and molecular aspects
WUYTS, Wim, WAEBER, Gerard, MEINECKE, Peter, SCHÜLER, Herdit, GOECKE, Timm O, VAN HUL, Wim, BARTSCH, Oliver
Published in European journal of human genetics : EJHG (01.05.2004)
Published in European journal of human genetics : EJHG (01.05.2004)
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A new case of proximal monosomy 1p36, extending the phenotype
Rudnik-Schöneborn, Sabine, Zerres, Klaus, Häusler, Martin, Lott, Alexandra, Krings, Timo, Schüler, Herdit M.
Published in American journal of medical genetics. Part A (01.08.2008)
Published in American journal of medical genetics. Part A (01.08.2008)
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