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Clonal Hematopoiesis in CN: Insights from Somatic Mutation Analysis Klimiankou, Maksim; Kandabarau, Sergey; Zeidler, Cornelia; Pogozhykh, Denys; Kadah, Sevda; Behrens, Yvonne Lisa; Dale, David C.; Makaryan, Vahagn; Kelley, Merideth; Bolyard, Audrey Anna; Mezger, Markus; Gruenes, Claudia; Lang, Peter; Lengerke, Claudia; Welte, Karl; Skokowa, Julia 分享 收藏
Modulating G-CSFR Signaling Using De Novo Designed Cytokines 使用从头设计的细胞因子调节G-CSFR信号通路 Ullrich, Timo; Alvarez, Birte Hernandez; Pollmann, Christoph; Ritter, Malte Ulrich; Haaf, Jeremy; Aghaallaei, Narges; Piehler, Jacob; Tesakov, Ivan; El-Riz, Maya; Maksymenko, Kateryna; Hatskovska, Valeriia; Kandabarau, Sergey; Klimiankou, Maksim; Lengerke, Claudia; Welte, Karl; Lupas, Andrei; Skokowa, Julia; ElGamacy, Mohammad 分享 收藏
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CRISPR-Cas9n-mediated ELANE promoter editing for gene therapy of severe congenital neutropenia Nasri, Masoud; Ritter, Malte U.; Mir, Perihan; Dannenmann, Benjamin; Kaufmann, Masako M.; Arreba-Tutusaus, Patricia; Xu, Yun; Borbaran-Bravo, Natalia; Klimiankou, Maksim; Lengerke, Claudia; Zeidler, Cornelia; Cathomen, Toni; Welte, Karl; Skokowa, Julia 分享 收藏
NAMPT/SIRT2-mediated inhibition of the p53-p21 signaling pathway is indispensable for maintenance and hematopoietic differentiation of human iPS cells (vol 12, 112, 2021) Xu, Yun; Nasri, Masoud; Dannenmann, Benjamin; Mir, Perihan; Zahabi, Azadeh; Welte, Karl; Morishima, Tatsuya; Skokowa, Julia 分享 收藏
Differential transcriptional control of hematopoiesis in congenital and cyclic neutropenia patients harboring ELANE mutations Zeidler, Alexander; Borbaran-Bravo, Natalia; Dannenmann, Benjamin; Ritter, Malte; Nasri, Masoud; Klimiankou, Maksim; Kandabarau, Sergey; Zahabi, Azadeh; Koenig, Josef; Zeidler, Cornelia; Skokowa, Julia; Welte, Karl 分享 收藏
iPSC modeling of stage-specific leukemogenesis reveals BAALC as a key oncogene in severe congenital neutropenia (vol 28, pg 906, 2021) Dannenmann, Benjamin; Klimiankou, Maksim; Oswald, Benedikt; Solovyeva, Anna; Mardan, Jehan; Nasri, Masoud; Ritter, Malte; Zahabi, Azadeh; Arreba-Tutusaus, Patricia; Mir, Perihan; Stein, Frederic; Kandabarau, Siarhei; Lachmann, Nico; Moritz, Thomas; Morishima, Tatsuya; Konantz, Martina; Lengerke, Claudia; Ripperger, Tim; Steinemann, Doris; Erlacher, Miriam; Niemeyer, Charlotte M.; Zeidler, Cornelia; Welte, Karl; Skokowa, Julia 分享 收藏
The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children: A Consensus Between the European Hematology Association and the EuNet-INNOCHRON COST Action Fioredda, Francesca; Skokowa, Julia; Tamary, Hannah; Spanoudakis, Michail; Farruggia, Piero; Almeida, Antonio; Guardo, Daniela; Hoglund, Petter; Newburger, Peter E.; Palmblad, Jan; Touw, Ivo P.; Zeidler, Cornelia; Warren, Alan J.; Dale, David C.; Welte, Karl; Dufour, Carlo; Papadaki, Helen A. 分享 收藏
A topological refactoring design strategy yields highly stable granulopoietic proteins Skokowa, Julia; Hernandez Alvarez, Birte; Coles, Murray; Ritter, Malte; Nasri, Masoud; Haaf, Jeremy; Aghaallaei, Narges; Xu, Yun; Mir, Perihan; Krahl, Ann-Christin; Rogers, Katherine W.; Maksymenko, Kateryna; Bajoghli, Baubak; Welte, Karl; Lupas, Andrei N.; Muller, Patrick; ElGamacy, Mohammad 分享 收藏
Rolf Neth (October 6, 1926-March 17, 2020) (vol 34, pg 1717, 2020) Hehlmann, Rudiger; Gallo, Robert; Hoelzer, Dieter; Welte, Karl; Gale, Robert Peter; Zander, Axel 分享 收藏
A unique role of p53 haploinsufficiency or loss in the development of acute myeloid leukemia with FLT3-ITD mutation p53单倍体不足或缺失在FLT3-ITD突变的急性髓系白血病发展中的独特作用 Yang, Min; Pan, Zengkai; Huang, Kezhi; Busche, Guntram; Liu, Hongyun; Gohring, Gudrun; Rumpel, Regina; Dittrich-Breiholz, Oliver; Talbot, Steven; Scherr, Michaela; Chaturvedi, Anuhar; Eder, Matthias; Skokowa, Julia; Zhou, Jianfeng; Welte, Karl; von Neuhoff, Nils; Liu, Ligen; Ganser, Arnold; Li, Zhixiong 分享 收藏
iPSC modeling of stage-specific leukemogenesis reveals BAALC as a key oncogene in severe congenital neutropenia Dannenmann, Benjamin; Klimiankou, Maksim; Oswald, Benedikt; Solovyeva, Anna; Mardan, Jehan; Nasri, Masoud; Ritter, Malte; Zahabi, Azadeh; Arreba-Tutusaus, Patricia; Mir, Perihan; Stein, Frederic; Kandabarau, Siarhei; Lachmann, Nico; Moritz, Thomas; Morishima, Tatsuya; Konantz, Martina; Lengerke, Claudia; Ripperger, Tim; Steinemann, Doris; Erlacher, Miriam; Niemeyer, Charlotte M.; Zeidler, Cornelia; Welte, Karl; Skokowa, Julia 分享 收藏
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Generation and characterization of a novel hematopoietic progenitor cell line with DC differentiation potential (vol 20, pg 870, 2006) Rathinam, C.; Sauer, M.; Ghosh, A.; Rudolph, C.; Hegazy, A.; Schlegelberger, B.; Welte, K.; Klein, C. 分享 收藏
Cooperating, congenital neutropenia associated Csf3r and Runx1 mutations activate pro-inflammatory signaling and inhibit myeloid differentiation of mouse HSPCs Ritter, Malte; Klimiankou, Maksim; Klimenkova, Olga; Schambach, Axel; Hoffmann, Dirk; Schmidt, Amy; Kanz, Lothar; Link, Daniel C.; Welte, Karl; Skokowa, Julia 分享 收藏
Congenital and Acquired Chronic Neutropenias: Challenges, Perspectives and Implementation of the EuNet-INNOCHRON Action Papadaki, Helen A.; Mavroudi, Irene; Almeida, Antonio; Bux, Juergen; Cichy, Joanna; Dale, David C.; Donadieu, Jean; Hoglund, Petter; Karanfilski, Oliver; Mecucci, Cristina; Palmblad, Jan; Skokowa, Julia; Stamatopoulos, Kostas; Touw, Ivo; Warren, Alan J.; Welte, Karl; Zeidler, Cornelia; Dufour, Carlo 分享 收藏
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