Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Esther J Cooke"'
Autor:
Esther J. Cooke, Bilgimol C. Joseph, Chanond A. Nasamran, Kathleen M. Fisch, Annette von Drygalski
Publikováno v:
Journal of Thrombosis and Haemostasis.
Autor:
Srila Gopal, Morten A. Karsdal, Tine Wyseure, Chanond A Nasamran, Esther J Cooke, Kathleen M. Fisch, Tina Manon-Jensen, Jenny Y Zhou, Annette von Drygalski, Laurent O. Mosnier
Publikováno v:
J Thromb Haemost
Background Vascular remodeling associated with hemophilic arthropathy (HA) may contribute to bleed propagation, but the mechanisms remain poorly understood. Objectives To explore molecular mechanisms of HA and the effects of hemostasis correction on
Autor:
Niels Behrendt, Laurent O. Mosnier, Esther J Cooke, Annette von Drygalski, Paul Declerck, Tine Wyseure, Joost C. M. Meijers
Publikováno v:
Wyseure, T, Cooke, E J, Declerck, P J, Behrendt, N, Meijers, J C M, Von Drygalski, A & Mosnier, L O 2018, ' Defective TAFI activation in hemophilia a mice is a major contributor to joint bleeding ', Blood, vol. 132, no. 15, pp. 1593-1603 . https://doi.org/10.1182/blood-2018-01-828434
Blood, 132(15), 1593-1603. American Society of Hematology
Blood, 132(15), 1593-1603. American Society of Hematology
Joint bleeds are common in congenital hemophilia but rare in acquired hemophilia A (aHA) for reasons unknown. To identify key mechanisms responsible for joint-specific bleeding in congenital hemophilia, bleeding phenotypes after joint injury and tail
Autor:
Samantha Ruiz, Esther J Cooke, Annette von Drygalski, Jenny Y Zhou, Bilgimol Chumappumkal Joseph, Sonha Nguyen
Publikováno v:
Blood. 138:3175-3175
Introduction Local and systemic molecular responses to hemarthroses in hemophilia are not well understood. Emerging clinical evidence suggests that treatment with FVIII-Fc Fusion protein (FcFVIII), using the Fc-portion of immunoglobulin for half-life
Autor:
John Morser, Merissa Olmer, Bettina Wanko, Yosuke Morodomi, Martin Lotz, Jenny Y Zhou, Ruchi Agashe, Tingyi Yang, Annette von Drygalski, Laurent O. Mosnier, Tine Wyseure, Niels Behrendt, Esther J Cooke
Publikováno v:
Wyseure, T, Yang, T, Zhou, J Y, Cooke, E J, Wanko, B, Olmer, M, Agashe, R, Morodomi, Y, Behrendt, N, Lotz, M, Morser, J, von Drygalski, A & Mosnier, L O 2019, ' TAFI deficiency causes maladaptive vascular remodeling after hemophilic joint bleeding ', JCI Insight, vol. 4, no. 19, e128379, pp. 1-19 . https://doi.org/10.1172/jci.insight.128379
Excessive vascular remodeling is characteristic of hemophilic arthropathy (HA) and may contribute to joint bleeding and the progression of HA. Mechanisms for pathological vascular remodeling after hemophilic joint bleeding are unknown. In hemophilia,
Autor:
S. Holle, Richard F. W. Barnes, Randy E. Moore, A Ceponis, A. von Drygalski, Colleen M. Moran, Tudor H. Hughes, Esther J Cooke, E. J. Martin
Publikováno v:
Haemophilia. 23:135-143
Introduction and Objectives Intra-articular corticosteroid injections are standard of care for managing joint pain secondary to osteoarthritis or rheumatoid arthritis but are rarely used in haemophilic arthropathy. We have introduced and evaluated th
Publikováno v:
Blood. 136:20-20
Introduction Hemophilic joint bleeding leads to toxic synovial iron accumulation, contributing to synovitis. Mechanisms of blood and iron clearance from the joint remain largely unknown. This study aimed to explore synovial lymphatic vessel remodelin
Autor:
Shweta Joshi, Vikas Bhat, Annette von Drygalski, Esther J Cooke, Laurent O. Mosnier, Jenny Y Zhou, Donald L. Durden, Tine Wyseure
Publikováno v:
Thrombosis and haemostasis. 118(6)
Vascular remodelling is a prominent feature of haemophilic arthropathy (HA) that may underlie re-bleeding, yet the nature of vascular changes and underlying mechanisms remain largely unknown. Here, we aimed to characterize synovial vascular remodelli
Publikováno v:
Blood. 134:157-157
Introduction Hemarthrosis in hemophilia causes toxic iron accumulation in the joint, which contributes to synovitis. This study aimed to explore mechanisms and timing of iron clearance from the joint space in mouse models of induced hemarthrosis. Met
Autor:
Alice E, Navein, Esther J, Cooke, Jennifer R, Davies, Terence G, Smith, Lois H M, Wells, Atsushi, Ohazama, Christopher, Healy, Paul T, Sharpe, Sam L, Evans, Bronwen A J, Evans, Marcela, Votruba, Timothy, Wells
Publikováno v:
Human Molecular Genetics
Mitochondrial dysfunction connects metabolic disturbance with numerous pathologies, but the significance of mitochondrial activity in bone remains unclear. We have, therefore, characterized the skeletal phenotype in the Opa3L122P mouse model for Cost