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Autor:
Ava Keyvani Chahi, Muluken S. Belew, Joshua Xu, He Tian Tony Chen, Stefan Rentas, Veronique Voisin, Gabriela Krivdova, Eric Lechman, Sajid A. Marhon, Daniel D. De Carvalho, John E. Dick, Gary D. Bader, Kristin J. Hope
Publikováno v:
Blood. 140:992-1008
Hematopoietic stem cell (HSC) dormancy is understood as supportive of HSC function and its long-term integrity. Although regulation of stress responses incurred as a result of HSC activation is recognized as important in maintaining stem cell functio
Autor:
Leif S. Ludwig, Caleb A. Lareau, Erik L. Bao, Nan Liu, Taiju Utsugisawa, Alex M. Tseng, Samuel A. Myers, Jeffrey M. Verboon, Jacob C. Ulirsch, Wendy Luo, Christoph Muus, Claudia Fiorini, Meagan E. Olive, Christopher M. Vockley, Mathias Munschauer, Abigail Hunter, Hiromi Ogura, Toshiyuki Yamamoto, Hiroko Inada, Shinichiro Nakagawa, Shuichi Ohzono, Vidya Subramanian, Roberto Chiarle, Bertil Glader, Steven A. Carr, Martin J. Aryee, Anshul Kundaje, Stuart H. Orkin, Aviv Regev, Timothy L. McCavit, Hitoshi Kanno, Vijay G. Sankaran
Publikováno v:
Blood
Master regulators, such as the hematopoietic transcription factor (TF) GATA1, play an essential role in orchestrating lineage commitment and differentiation. However, the precise mechanisms by which such TFs regulate transcription through interaction
Autor:
Robert K. Bradley, Patrick Nugent, Khrystyna North, Jasmine Naru, Eunhee Kim, Janine O. Ilagan, Joseph Pangallo, Sergei Doulatov, Martina Sarchi, Derek L. Stirewalt, Arvind R. Subramaniam, Rochelle Bergantinos, Massiel Chavez Stolla, Omar Abdel-Wahab, Janis L. Abkowitz, Courtnee Clough
Publikováno v:
Blood. 139:2038-2049
SF3B1 splicing factor mutations are near-universally found in myelodysplastic syndromes (MDS) with ring sideroblasts (RS), a clonal hematopoietic disorder characterized by abnormal erythroid cells with iron-loaded mitochondria. Despite this remarkabl
Autor:
Markus G. Manz, Dirk Loeffler, Arne Wehling, Florin Schneiter, Tobias Kull, Claudia Lengerke, Timm Schroeder, Weijia Wang
Publikováno v:
Blood, 139 (13)
Blood
Blood
Understanding human hematopoietic stem cell fate control is important for its improved therapeutic manipulation. Asymmetric cell division, the asymmetric inheritance of factors during division instructing future daughter cell fates, was recently desc
Autor:
François Morlé, Stéphane Giraudier, Eric Soler, Naomi Taylor, Charlotte Andrieu-Soler, Olivier Hermine, Patrick Mayeux, Célia Floquet, Rose Ann Padua, Frédérique Verdier, Sarah Ducamp, Michaela Fontenay, Mohammad Salma, Elisabeth M. Cramer-Borde, Ismael Boussaid, Anna Raimbault, Isabelle Hatin, Diane d'Allard, Amandine Houvert, Narla Mohandas, Boris Guyot, Emilie-Fleur Gautier, Sandrina Kinet, Marjorie Leduc, Pierre-Emmanuel Gleizes, Jean-Jacques Diaz, Salomé Le Goff, François Guillonneau, Nathalie Montel-Lehry
Publikováno v:
Blood
Blood, American Society of Hematology, 2021, 137 (1), pp.89-102. ⟨10.1182/blood.2019003439⟩
Blood, 2020, ⟨10.1182/blood.2019003439⟩
Blood, American Society of Hematology, 2020, ⟨10.1182/blood.2019003439⟩
Blood, American Society of Hematology, 2020, 137 (1), pp.89-102. ⟨10.1182/blood.2019003439⟩
Blood, 2021, 137 (1), pp.89-102. ⟨10.1182/blood.2019003439⟩
Blood, American Society of Hematology, 2021, 137 (1), pp.89-102. ⟨10.1182/blood.2019003439⟩
Blood, 2020, ⟨10.1182/blood.2019003439⟩
Blood, American Society of Hematology, 2020, ⟨10.1182/blood.2019003439⟩
Blood, American Society of Hematology, 2020, 137 (1), pp.89-102. ⟨10.1182/blood.2019003439⟩
Blood, 2021, 137 (1), pp.89-102. ⟨10.1182/blood.2019003439⟩
The role of ribosome biogenesis in erythroid development is supported by the recognition of erythroid defects in ribosomopathies in both Diamond-Blackfan anemia and 5q− syndrome. Whether ribosome biogenesis exerts a regulatory function on normal er
Autor:
David Yudovich, Agatheeswaran Subramaniam, Roman A. Zubarev, Roman Galeev, Jonas Larsson, Alexandra Bäckström, Massimiliano Gaetani, Mayur Vilas Jain, Jun Chen, Kristijonas Žemaitis, Mehrnaz Safaee Talkhoncheh, Shubhranshu Debnath
Publikováno v:
Blood
Culture conditions in which hematopoietic stem cells (HSCs) can be expanded for clinical benefit are highly sought after. Here, we report that inhibition of the epigenetic regulator lysine-specific histone demethylase 1A (LSD1) induces a rapid expans
Autor:
Siyang Hao, Baiye Ruan, Jie Xiang, K. Sandeep Prabhu, Yuanting Chen, Fenghua Qian, Robert F. Paulson, Bastihalli T. Diwakar
Publikováno v:
Blood
Anemic stress induces stress erythropoiesis, which rapidly generates new erythrocytes to restore tissue oxygenation. Stress erythropoiesis is best understood in mice where it is extramedullary and occurs primarily in the spleen. However, both human a
Autor:
Aparna Gopal, Megan Fuller, Yu Deng, Mark Boldin, Jennifer M Grants, Aly Karsan, Joanna Wegrzyn, David J.H.F. Knapp, Connie J. Eaves, T. Roderick Docking, Tony Hui, Jenny Li, Marion Shadbolt, Kieran O'Neill, Jeremy Parker, Martin Hirst
Publikováno v:
Blood
Aging is associated with significant changes in the hematopoietic system, including increased inflammation, impaired hematopoietic stem cell (HSC) function, and increased incidence of myeloid malignancy. Inflammation of aging (“inflammaging”) has
Autor:
Rhys S. Allan, Naiara G. Bediaga, Gaetano Naselli, Timothy M. Johanson, Leonard C. Harrison, Nadia Iannarella, Christine R. Keenan
Publikováno v:
Blood. 135:2049-2058
Loss of heterochromatin has been proposed as a universal mechanism of aging across different species and cell types. However, a comprehensive analysis of hematopoietic changes caused by heterochromatin loss is lacking. Moreover, there is conflict in
Autor:
Georg W. Herget, Bodo Grimbacher, Marta Rizzi, Arianna Troilo, Klaus Warnatz, Justyna Rawluk, Jens Thiel, Claudia Wehr, Michele Proietti, Natalie Frede, Miriam Erlacher, Raquel Lorenzetti, Nadezhda Camacho-Ordonez, Reinhard E. Voll, Julian Staniek, M.-T. Schleyer, Nils Venhoff, Lukas Konstantinidis, Ulrich Salzer, Iga Janowska
Publikováno v:
Blood
Common variable immunodeficiency (CVID) is a disease characterized by increased susceptibility to infections, hypogammaglobulinemia, and immune dysregulation. Although CVID is thought to be a disorder of the peripheral B-cell compartment, in 25% of p