ERCC6L2 syndrome: attack of the TP53 clones von Wlodarski, Marcin W.

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The rise of Apollo, protector of telomeres von Wlodarski, Marcin W.

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GENOME SEQUENCING APPROACHES FOR DIAGNOSIS AND DISCOVERY OF BMF/MDS SPECIFIC GENETIC ALTERATIONS von Wlodarski, Marcin

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The arrival of personalized genomics in bone marrow failure von Wlodarski, Marcin W

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GATA2 deficiency and related myeloid neoplasms von Wlodarski, Marcin W, Collin, Matthew, Horwitz, Marshall S

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Germline predisposition in myeloid neoplasms: Unique genetic and clinical features of GATA2 deficiency and SAMD9/SAMD9L syndromes von Sahoo, Sushree S., Kozyra, Emilia J., Wlodarski, Marcin W.

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Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents von Wlodarski, Marcin W., Hirabayashi, Shinsuke, Pastor, Victor, Starý, Jan, Hasle, Henrik, Masetti, Riccardo, Dworzak, Michael, Schmugge, Markus, van den Heuvel-Eibrink, Marry, Ussowicz, Marek, De Moerloose, Barbara, Catala, Albert, Smith, Owen P., Sedlacek, Petr, Lankester, Arjan C., Zecca, Marco, Bordon, Victoria, Matthes-Martin, Susanne, Abrahamsson, Jonas, Kühl, Jörn Sven, Sykora, Karl-Walter, Albert, Michael H., Przychodzien, Bartlomiej, Maciejewski, Jaroslaw P., Schwarz, Stephan, Göhring, Gudrun, Schlegelberger, Brigitte, Cseh, Annámaria, Noellke, Peter, Yoshimi, Ayami, Locatelli, Franco, Baumann, Irith, Strahm, Brigitte, Niemeyer, Charlotte M.

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Inducible Pluripotent Stem Cell Models to Study Bone Marrow Failure and MDS Predisposition Syndromes von Sahoo, Sushree S., Khiami, Majd, Wlodarski, Marcin W.

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DNA Repair Syndromes and Cancer: Insights Into Genetics and Phenotype Patterns von Sharma, Richa, Lewis, Sara, Wlodarski, Marcin W

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Clonal hematopoiesis in children with predisposing conditions von Attardi, Enrico, Corey, Seth J., Wlodarski, Marcin W.

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Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans von Buonocore, Federica, Kühnen, Peter, Suntharalingham, Jenifer P, Del Valle, Ignacio, Digweed, Martin, Stachelscheid, Harald, Khajavi, Noushafarin, Didi, Mohammed, Brady, Angela F, Blankenstein, Oliver, Procter, Annie M, Dimitri, Paul, Wales, Jerry K H, Ghirri, Paolo, Knöbl, Dieter, Strahm, Brigitte, Erlacher, Miriam, Wlodarski, Marcin W, Chen, Wei, Kokai, George K, Anderson, Glenn, Morrogh, Deborah, Moulding, Dale A, McKee, Shane A, Niemeyer, Charlotte M, Grüters, Annette, Achermann, John C

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Reduced toxicity conditioning for hematopoietic stem cell transplantation in children with Diamond-Blackfan anemia von Qudeimat, Amr, Suryaprakash, Shruthi, Madden, Renee, Srinivasan, Ashok, Wlodarski, Marcin W, Bhoopalan, Senthil Velan

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Gain-of-function mutations in RPA1 cause a syndrome with short telomeres and somatic genetic rescue von Sharma, Richa, Sahoo, Sushree S., Honda, Masayoshi, Granger, Sophie L., Goodings, Charnise, Sanchez, Louis, Künstner, Axel, Busch, Hauke, Beier, Fabian, Pruett-Miller, Shondra M., Valentine, Marcus B., Fernandez, Alfonso G., Chang, Ti-Cheng, Géli, Vincent, Churikov, Dmitri, Hirschi, Sandrine, Pastor, Victor B., Boerries, Melanie, Lauten, Melchior, Kelaidi, Charikleia, Cooper, Megan A., Nicholas, Sarah, Rosenfeld, Jill A., Polychronopoulou, Sophia, Kannengiesser, Caroline, Saintomé, Carole, Niemeyer, Charlotte M., Revy, Patrick, Wold, Marc S., Spies, Maria, Erlacher, Miriam, Coulon, Stéphane, Wlodarski, Marcin W.

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Human hnRNPA1 reorganizes telomere-bound replication protein A von Granger, Sophie L, Sharma, Richa, Kaushik, Vikas, Razzaghi, Mortezaali, Honda, Masayoshi, Gaur, Paras, Bhat, Divya S, Labenz, Sabryn M, Heinen, Jenna E, Williams, Blaine A, Tabei, S M Ali, Wlodarski, Marcin W, Antony, Edwin, Spies, Maria

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The ghost of parvovirus past: Idiopathic pure red cell aplasia responding to IVIG following resolved perinatal parvovirus B19 infection von Gray, Nathan, Sims, Kacie, Lewis, Sara, Lei, Shaohua, Bhatt, Nidhi, Gheorghe, Gabriela, Takemoto, Clifford, Wlodarski, Marcin W.

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Frequency and prognostic impact of mutations in SRSF2, U2AF1, and ZRSR2 in patients with myelodysplastic syndromes von Thol, Felicitas, Kade, Sofia, Schlarmann, Carola, Löffeld, Patrick, Morgan, Michael, Krauter, Jürgen, Wlodarski, Marcin W., Kölking, Britta, Wichmann, Martin, Görlich, Kerstin, Göhring, Gudrun, Bug, Gesine, Ottmann, Oliver, Niemeyer, Charlotte M., Hofmann, Wolf-Karsten, Schlegelberger, Brigitte, Ganser, Arnold, Heuser, Michael

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Heterogeneity of GATA2-related myeloid neoplasms von Hirabayashi, Shinsuke, Wlodarski, Marcin W., Kozyra, Emilia, Niemeyer, Charlotte M.

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Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7 von Pastor, Victor B, Sahoo, Sushree S, Boklan, Jessica, Schwabe, Georg C, Saribeyoglu, Ebru, Strahm, Brigitte, Lebrecht, Dirk, Voss, Matthias, Bryceson, Yenan T, Erlacher, Miriam, Ehninger, Gerhard, Niewisch, Marena, Schlegelberger, Brigitte, Baumann, Irith, Achermann, John C, Shimamura, Akiko, Hochrein, Jochen, Tedgård, Ulf, Nilsson, Lars, Hasle, Henrik, Boerries, Melanie, Busch, Hauke, Niemeyer, Charlotte M, Wlodarski, Marcin W

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Massively parallel base editing to map variant effects in human hematopoiesis von Martin-Rufino, Jorge D., Castano, Nicole, Pang, Michael, Grody, Emanuelle I., Joubran, Samantha, Caulier, Alexis, Wahlster, Lara, Li, Tongqing, Qiu, Xiaojie, Riera-Escandell, Anna Maria, Newby, Gregory A., Al’Khafaji, Aziz, Chaudhary, Santosh, Black, Susan, Weng, Chen, Munson, Glen, Liu, David R., Wlodarski, Marcin W., Sims, Kacie, Oakley, Jamie H., Fasano, Ross M., Xavier, Ramnik J., Lander, Eric S., Klein, Daryl E., Sankaran, Vijay G.

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Hematopoietic cell transplantation and gene therapy for Diamond-Blackfan anemia: state of the art and science von Bhoopalan, Senthil Velan, Suryaprakash, Shruthi, Sharma, Akshay, Wlodarski, Marcin W.

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