Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Moira M. Lancelot"'
Autor:
Jiusheng Deng, Moira M. Lancelot, Ryan Jajosky, Marianne M Yee, Natia Saakadze, Sean R Stowell, John D. Roback
Publikováno v:
Blood. 140:5708-5708
Autor:
David R. Light, Sharada A. Sarnaik, Moira M. Lancelot, Nancy Moore, Dipti Gupta, Patrick C. Hines, William E. Hobbs, Jennell White, Sriram Krishnamoorthy
Publikováno v:
British Journal of Haematology. 174:970-982
Summary Very Late Antigen-4 (VLA-4, α4β1-integrin, ITGA4) orchestrates cell-cell and cell-endothelium adhesion. Given the proposed role of VLA-4 in sickle cell disease (SCD) pathophysiology, we evaluated the ability of the VLA-4 blocking antibody n
Publikováno v:
Clinical Hemorheology and Microcirculation
Sickle cell disease (SCD) is characterized by microvascular occlusion mediated by adhesive interactions of sickle erythrocytes (SSRBCs) to the endothelium. Most in vitro flow adhesion assays measure SSRBC adhesion during continuous flow, although in
Publikováno v:
British Journal of Haematology. 178:479-481
Keywords: erythrocytes; adhesion; VLA-4; sickle cell disease; low molecular weight heparin
Autor:
Efstathios Beltaos, Sruthi Polavarapu, Aditya Joshi, Nandita Bhattacharjee, Babatunde Sobowale, Moira M. Lancelot
Publikováno v:
Clinical Medicine & Research. 13:36-40
We describe a premature neonate with an extensive plexiform neurofibroma. Prenatal ultrasound at 32 weeks of gestation was normal. Postnatal examination was significant for a palpable left neck mass. Magnetic resonance imaging (MRI) of the head demon
Autor:
Sriram Krishnamoorthy, William E. Hobbs, David R. Light, Patrick C. Hines, Moira M. Lancelot, Arjan van der Flier, Haiyan Jiang, Dipti Gupta, Jennell White, Robert T. Peters
Publikováno v:
Blood. 124:221-221
Sickle cell disease (SCD) is caused by a point mutation in the beta-chain of hemoglobin, which triggers a complex pathophysiology resulting in recurrent, painful vaso-occlusive events (VOCs) and chronic hemolytic anemia. Among other abnormalities, si
Publikováno v:
Blood. 120:3238-3238
Abstract 3238 Introduction: Sickle cell disease (SCD) is characterized by microvascular occlusion mediated in part by adhesion of sickle erythrocytes (SS RBCs) to the vasculature. Advanced flow adhesion (FA) technology facilitates SS RBC adhesion stu
Publikováno v:
Blood. 120:2113-2113
Abstract 2113 Background and Significance Vaso-occlusion in sickle cell disease (SCD) that leads to painful events and complications is caused in part by adhesion of sickled erythrocytes (SSRBCs) to components of the vascular wall and to circulating
Autor:
Sharada A. Sarnaik, Moira M. Lancelot
Publikováno v:
Blood. 118:2143-2143
Abstract 2143 Background: About 11% of patients with sickle cell disease (SCD) will develop and ischemic stroke by 20 years. Patients with SCD and Moyamoya Syndrome (MMS) are at an especially high risk for developing stroke. Encephaloduroarteriosynag
Autor:
Lancelot M; Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA, United States., Fibben K; Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA, United States., Sullivan J; The Atlanta Center for Microsystems-Engineered Point-of-Care Technologies, Atlanta, GA, United States.; Department of Pediatrics, Emory University School of Medicine and Children's Healthcare of Atlanta, Atlanta, GA, United States., O'Sick W; Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA, United States., McLendon K; Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA, United States., Wu H; Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA, United States., Rao A; The Atlanta Center for Microsystems-Engineered Point-of-Care Technologies, Atlanta, GA, United States.; Department of Pediatrics, Emory University School of Medicine and Children's Healthcare of Atlanta, Atlanta, GA, United States., Bassit LC; The Atlanta Center for Microsystems-Engineered Point-of-Care Technologies, Atlanta, GA, United States.; Department of Pediatrics, Emory University School of Medicine and Children's Healthcare of Atlanta, Atlanta, GA, United States.; Laboratory of Biochemical Pharmacology, Emory University, Atlanta, GA, United States., Greenleaf M; The Atlanta Center for Microsystems-Engineered Point-of-Care Technologies, Atlanta, GA, United States., Miller P; Rapid Acceleration of Diagnostics (RADx), Maryland, MD, United States., Krull W; Rapid Acceleration of Diagnostics (RADx), Maryland, MD, United States., Tyburski E; The Atlanta Center for Microsystems-Engineered Point-of-Care Technologies, Atlanta, GA, United States., Roback JD; Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA, United States., Lam WA; Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA, United States.; The Atlanta Center for Microsystems-Engineered Point-of-Care Technologies, Atlanta, GA, United States.; Department of Pediatrics, Emory University School of Medicine and Children's Healthcare of Atlanta, Atlanta, GA, United States.; Aflac Cancer & Blood Disorders Center at Children's Healthcare of Atlanta, Atlanta, GA, United States., Damhorst GL; The Atlanta Center for Microsystems-Engineered Point-of-Care Technologies, Atlanta, GA, United States.; Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, GA, United States.
Publikováno v:
Frontiers in microbiology [Front Microbiol] 2023 Aug 07; Vol. 14, pp. 1219214. Date of Electronic Publication: 2023 Aug 07 (Print Publication: 2023).