检索结果 - Ehsan Bahrami
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Estimated Glucose Disposal Rate: A Potential Determinant for Microvascular and Macrovascular Complications in Type 2 Diabetes 由 Ehsan Bahrami Hezaveh, Rana Hashemi, Mohammadamin Noorafrooz, Fatemeh Mohammadi, Amirhossein Yadegar, Sahar Karimpour Reyhan, Manouchehr Nakhjavani, Alireza Esteghamati, Soghra Rabizadeh
出版 2025Artigo -
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Diverse potential of secretome from natural killer cells and monocyte-derived macrophages in activating stellate cells 由 Julia Sauer, Agnes A. Steixner-Kumar, Svenja Gabler, Maciej Motyka, Jörg F. Rippmann, Stefan Brosa, Dennis Boettner, Tanja Schönberger, Charlotte Lempp, Vanessa Frodermann, Eric J. Simon, Oliver Krenkel, Ehsan Bahrami
出版 2024Artigo -
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Myb-like, SWIRM, and MPN domains 1 (MYSM1) deficiency: Genotoxic stress-associated bone marrow failure and developmental aberrations 由 Ehsan Bahrami, Maximilian Witzel, Tomáš Raček, Jacek Puchałka, Sebastian Hollizeck, Naschla Greif-Kohistani, Daniel Kotlarz, Hans‐Peter Horny, Regina Feederle, Heinrich Schmidt, Roya Sherkat, Doris Steinemann, Gudrun Göhring, Brigitte Schlegelbeger, Michael H. Albert, Waleed Al–Herz, Christoph Klein
出版 2017Artigo -
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Chromatin-remodeling factor SMARCD2 regulates transcriptional networks controlling differentiation of neutrophil granulocytes 由 Maximilian Witzel, Daniel Petersheim, Yanxin Fan, Ehsan Bahrami, Tomáš Raček, Meino Rohlfs, Jacek Puchałka, Christian Mertes, Julien Gagneur, Christoph Ziegenhain, Wolfgang Enard, Asbjørg Stray‐Pedersen, Peter D. Arkwright, Miguel R. Abboud, Vahid Pazhakh, Graham J. Lieschke, Peter Krawitz, Maik Dahlhoff, Marlon R. Schneider, Eckhard Wolf, Hans-Peter Horny, Heinrich Schmidt, Alejandro A. Schäffer, Christoph Klein
出版 2017Artigo -
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Human RIPK1 deficiency causes combined immunodeficiency and inflammatory bowel diseases 由 Yue Li, Marita Führer, Ehsan Bahrami, Piotr Socha, Maja Klaudel‐Dreszler, A. Bouzidi, Yanshan Liu, Anna S. Lehle, Thomas Magg, Sebastian Hollizeck, Meino Rohlfs, Raffaele Conca, Michael Field, Neil Warner, Mordechai Slae, Eyal Shteyer, Dan Turner, Rachida Boukari, Reda Belbouab, Christoph Walz, Moritz M. Gaidt, Veit Hornung, Bernd Baumann, Ulrich Pannicke, Eman Al Idrissi, Hamza AlGhamdi, Fernando E. Sepulveda, Marine Gil, Geneviève de Saint Basile, Manfred Hönig, Sibylle Koletzko, Aleixo M. Muise, Scott B. Snapper, Klaus Schwarz, Christoph Klein, Daniel Kotlarz
出版 2018Artigo -
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Mutations in Tetratricopeptide Repeat Domain 7A Result in a Severe Form of Very Early Onset Inflammatory Bowel Disease 由 Yaron Avitzur, Conghui Guo, Lucas A. Mastropaolo, Ehsan Bahrami, Hannah Chen, Zhen Zhao, Abdul Elkadri, Sandeep Dhillon, Ryan Murchie, Ramzi Fattouh, Hien Q. Huynh, Jennifer L. Walker, Paul W. Wales, Ernest Cutz, Yoichi Kakuta, Joel T. Dudley, Jochen Kammermeier, Fiona Powrie, Neil Shah, Christoph Walz, Michaela Nathrath, Daniel Kotlarz, Jacek Puchaka, Jonathan R. Krieger, Tomáš Raček, Thomas Kirchner, Thomas D. Walters, John H. Brumell, Anne M. Griffiths, Nima Rezaei, Parisa Rashtian, Mohammad Najafi, Maryam Monajemzadeh, Stephen Pelsue, Dermot McGovern, Holm H. Uhlig, Eric E. Schadt, Christoph Klein, Scott B. Snapper, Aleixo M. Muise
出版 2014Artigo
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Biology
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Stem cell
Transcription factor
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Bone marrow failure
CEBPA
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Cellular differentiation
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Chromatin
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Compound heterozygosity
Congenital Neutropenia
Coronary artery disease