Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Amanda M Li"'
Autor:
Marisa Connell, Helen Chen, Jihong Jiang, Chia-Wei Kuan, Abbas Fotovati, Tony LH Chu, Zhengcheng He, Tess C Lengyell, Huaibiao Li, Torsten Kroll, Amanda M Li, Daniel Goldowitz, Lucien Frappart, Aspasia Ploubidou, Millan S Patel, Linda M Pilarski, Elizabeth M Simpson, Philipp F Lange, Douglas W Allan, Christopher A Maxwell
Publikováno v:
eLife, Vol 6 (2017)
Oriented cell division is one mechanism progenitor cells use during development and to maintain tissue homeostasis. Common to most cell types is the asymmetric establishment and regulation of cortical NuMA-dynein complexes that position the mitotic s
Externí odkaz:
https://doaj.org/article/16ea9b4f47284197a021ef8d519f1ea6
Autor:
Jacob, Rozmus, Sima T, Bhatt, Nataliya Prokopenko, Buxbaum, Geoffrey D E, Cuvelier, Amanda M, Li, Carrie L, Kitko, Kirk R, Schultz
Publikováno v:
Frontiers in Pediatrics. 10
Hematopoietic cell transplant is a curative therapy for many pediatric patients with high risk acute lymphoblastic leukemia. Its therapeutic mechanism is primarily based on the generation of an alloreactive graft-versus-leukemia effect that can elimi
Publikováno v:
Bone Marrow Transplantation. 56:2031-2033
Publikováno v:
Bone marrow transplantation. 56(8)
Autor:
Angela Yen, Damiano Rondelli, la Fuente Josu de, Amanda M. Li, Jennifer Domm, Montalembert Mariane de, Tony W. Ho, Donna A. Wall, Brenda K. Eustace, Juergen Foell, Sujit Sheth, Haydar Frangoul, Rupert Handgretinger, Akshay Sharma, Sandeep Soni, Antonis Kattamis, Andrew Kernytsky, Franco Locatelli, Stephan A. Grupp, M. Domenica Cappellini, Julie A. Lekstrom-Himes, Selim Corbacioglu, David Altshuler, Markus Y. Mapara, Yi-Shan Chen, Martin H. Steinberg
Transfusion-dependent β-thalassemia (TDT) and sickle cell disease (SCD) are severe monogenic diseases with severe and potentially life-threatening manifestations. BCL11A is a transcription factor that represses γ-globin expression and fetal hemoglo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::294f2984b8848005c8f160412c9178cd
https://hdl.handle.net/10807/228473
https://hdl.handle.net/10807/228473
Autor:
Mignon L. Loh, Elizabeth A. Raetz, Olga Militano, Amanda M. Li, Meenakshi Devidas, Cindy Wang, Karen R. Rabin, Anne L. Angiolillo, Johann Hitzler, Rachel E. Rau, John Kairalla, Sumit Gupta, Maki Okada
Publikováno v:
Blood. 138:2304-2304
INTRODUCTION Children with Down Syndrome (DS) and B-lymphoblastic leukemia (B-ALL) are at an increased risk of both relapse and treatment-related mortality, compared to those without DS. On COG study AALL1731 for de novo B-ALL, patients with DS and h
Autor:
Christopher Brown, Michael C. Jensen, Colleen Annesley, Ashley Wilson, Corinne Summers, Josh Gustafson, Rebecca Gardner, Julie R. Park, Jodi L. Skiles, Qian Vicky Wu, Michael A. Pulsipher, Stephanie Mgebroff, Catherine Lindgren, Wenjun Huang, Anant Vatsayan, Amanda M. Li
Publikováno v:
Blood. 138:470-470
Introduction: CAR T cells in B-ALL have recently focused on the dual targeting of CD19 and CD22 to enhance long term remissions and prevent antigen negative recurrence that is frequently encountered with single antigen targeting. However, a barrier t
Autor:
Sylvia Stockler-Ipsiroglu, Heather J. Sutherland, Santhosh Thyagu, Dawn Maze, Sandra Sirrs, Amanda M. Li, Richard A. Schreiber, Suzanne Vercauteren, Kirk R. Schultz
Publikováno v:
Pediatric hematology and oncology. 35(1)
Glycogen storage disease (GSD) type 1 is a rare autosomal recessive inherited condition. The 1b subtype comprises the minority of cases, with an estimated prevalence of 1 in 500,000 children. Patients with glycogen storage disease type 1b are often t
Autor:
Abbas Fotovati, Chris L. Fryer, P. Daniel McNeely, Stephen Yip, Lucie Lafay-Cousin, Katrin Scheinemann, Amanda M Li, Anne-Sophie Carret, Beverly Wilson, Cynthia Hawkins, Nada Jabado, Juliette Hukin, Sandra E. Dunn, Uri Tabori, David D. Eisenstat, Christopher Dunham, Donna L. Johnston, Shayna Zelcer, Mariana Rachel Dias da Silva, Glenda Hendson
Publikováno v:
Cancer. 121:1499-1507
BACKGROUND The cure rate for childhood intracranial ependymoma is approximately 70% in the setting of a gross total resection followed by radiation, but management remains challenging in patients with residual disease. Therefore, robust biomarkers ar
Autor:
Linda M. Pilarski, Chia-Wei Kuan, Douglas W. Allan, Abbas Fotovati, Millan S. Patel, Aspasia Ploubidou, Dan Goldowitz, Jihong Jiang, Zhengcheng He, Huaibiao Li, Helen Chen, Amanda M Li, Christopher A. Maxwell, Tony L.H. Chu, Tess C Lengyell, Lucien Frappart, Marisa Connell, Philipp F. Lange, Elizabeth M. Simpson, Torsten Kroll
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4fd0f1bce58db3b2f56796f36e800d2
https://doi.org/10.7554/elife.28672.027
https://doi.org/10.7554/elife.28672.027