Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Aron Flagg"'
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 6, Iss 2, Pp 81-83 (2021)
Establishing the diagnosis of classical Hodgkin lymphoma (cHL) in a timely fashion can be a challenge, as there are no pathognomonic signs or symptoms. The percutaneous needle biopsy (CNB) of the tumor gained increased popularity due to its minimal i
Externí odkaz:
https://doaj.org/article/ab5a223fa0d9480a963869c05e9e6f5e
Autor:
Andrew R. Patterson, Mehari Endale, Kristin Lampe, Halil I. Aksoylar, Aron Flagg, Jim R. Woodgett, David Hildeman, Michael B. Jordan, Harinder Singh, Zeynep Kucuk, Jack Bleesing, Kasper Hoebe
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-15 (2018)
Loss of function GIMAP5 mutation is associated with lymphopenia, but how it mediates T cell homeostasis is unclear. Here the authors study Gimap5−/− mice and a patient with GIMAP5 deficiency to show how this GTPAse negatively regulates GSK3β act
Externí odkaz:
https://doaj.org/article/09487aa202ff4465abb8756803164dd9
Autor:
Upendra Mahat, Bhavuk Garg, Chao-Yie Yang, Hrishikesh Mehta, Rabi Hanna, Heesun J. Rogers, Aron Flagg, Andrei I. Ivanov, Seth J. Corey
Publikováno v:
Blood Advances. 6:2581-2594
Neutrophils migrate into inflamed tissue, engage in phagocytosis, and clear pathogens or apoptotic cells. These processes require well-coordinated events involving the actin cytoskeleton. We describe a child with severe neutropenia and episodes of so
Publikováno v:
Transplantation and Cellular Therapy. 29:S297-S298
Publikováno v:
Transplantation and Cellular Therapy. 29:S285-S286
Publikováno v:
Transplantation and Cellular Therapy. 29:S286-S287
Publikováno v:
Blood. 140:10460-10461
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 6, Iss 2, Pp 81-83 (2021)
Establishing the diagnosis of classical Hodgkin lymphoma (cHL) in a timely fashion can be a challenge, as there are no pathognomonic signs or symptoms. The percutaneous needle biopsy (CNB) of the tumor gained increased popularity due to its minimal i
Publikováno v:
Pediatr Hematol Oncol
Approximately 30–40% of relapses in pediatric acute lymphoblastic leukemia (ALL) are extra-medullary. KMT2A gene rearrangements are common in patients with infantile ALL. Chloromas are rare tumors composed of collections of acute leukemic cells tha
Publikováno v:
Cleveland Clinic Journal of Medicine. 87:153-164
Megaloblastic anemia causes macrocytic anemia from ineffective red blood cell production and intramedullary hemolysis. The most common causes are folate (vitamin B9) deficiency and cobalamin (vitamin B12) deficiency. Megaloblastic anemia can be diagn