Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Upendra Mahat"'
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:
Pediatric Hematology and Oncology. 38:658-662
Cytotoxic T-lymphocyte-associated protein 4 (CTLA4) is an immune checkpoint, which downregulates T cell activation and T regulatory cell function. CTLA4 haploinsufficiency (CTLA4 HI) leads to T cel...
Publikováno v:
Pediatric hematology and oncology. 38(7)
Cytotoxic T-lymphocyte-associated protein 4 (CTLA4) is an immune checkpoint, which downregulates T cell activation and T regulatory cell function. CTLA4 haploinsufficiency (CTLA4 HI) leads to T cell hyperactivation, immunodeficiency and variable degr
Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) is an immune checkpoint, which downregulates T cell activation and T regulatory cell function. CTLA-4 haploinsufficiency (CTLA4 HI) leads to T cell hyperactivation, immune dysregulation, lymphoprol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c917376e226e6a0def5479a9d603687f
https://doi.org/10.22541/au.160331932.20989541/v1
https://doi.org/10.22541/au.160331932.20989541/v1
Publikováno v:
Pediatric hematology and oncology. 37(2)
Cytotoxic T-lymphocyte-associated protein 4 (CTLA4) haploinsufficiency (HI) is an immune dysregulation disorder characterized by T lymphocyte hyperactivation, and generalized lymphoproliferative and autoimmune disorders. Patients with CTLA4 haploinsu
Autor:
Seth J. Corey, Aron Flagg, Heesun J. Rogers, Upendra Mahat, Andrei I. Ivanov, Hrishikesh M Mehta, Bhavuk Garg, Chao Yie Yang
Publikováno v:
Blood. 138:434-434
Introduction: As critical effectors of innate immune response, neutrophils migrate from the vasculature into inflamed tissue, where they engage in phagocytosis and clearance of pathogens and apoptotic cells. Migration, phagocytosis, and granule relea
Publikováno v:
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation. 26(3)
Prolonged thrombocytopenia after hematopoietic stem cell transplantation (HSCT) is a strong risk factor for transplantation-related morbidity and mortality, and no standard treatment guideline exists. Thrombopoietin receptor agonists (TPO-RAs), eltro
Publikováno v:
Pediatric bloodcancerREFERENCES. 66(11)
Complement activation plays an important role in the pathogenesis of atypical hemolytic uremic syndrome. Eculizumab is a monoclonal antibody that blocks complement activity and has been approved for use in the treatment of atypical hemolytic uremic s
Publikováno v:
Journal of pediatric and adolescent gynecology. 32(4)
Background Beckwith-Wiedemann syndrome (BWS) is the most common pediatric overgrowth syndrome. BWS has a broad phenotypic presentation along with an increased propensity to develop various embryonal tumors. There are very few reported cases of gonada
Publikováno v:
Progress in Pediatric Cardiology. 56:101190
Three stage cardiac reconstruction is a common surgical procedure performed in children with complex cyanotic congenital heart diseases (CCHD) such as hypoplastic left heart syndrome (HLHS) and related single ventricle physiology. The perioperative p