Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Walter H.A. Kahr"'
Autor:
Chris Ward, Nicola Curry, Magdy El-Ekiaby, Kerstin Jurk, Henri H. Versteeg, Charithani Keragala, Tal Burstyn-Cohen, Silvio Antoniak, Yuko Suzuki, Ross I. Baker, Olivier Christophe, Shoshana Revel-Vilk, Alice Hart, Carsten Deppermann, Huyen Tran, Nicola Pozzi, Walter H.A. Kahr, Steven P. Grover, Philip Wenzel, Ashley C. Brown, Cécile Oury, Susan M. Shea, James Fredenburgh, Freda H. Passam, James Winearls, Hunter B. Moore, Soumitra Tole, Eileen Merriman, Geoffrey D. Barnes, Z. Leonardo Liu, Michelle Sholzberg, José Rivera, Ana Marín-Quilez
Publikováno v:
Research and Practice in Thrombosis and Haemostasis, Vol 8, Iss 5, Pp 102498- (2024)
Externí odkaz:
https://doaj.org/article/423f0865a53343d687904a487723fe50
Autor:
Magdalena Riedl, Damien G. Noone, Meraj A. Khan, Fred G. Pluthero, Walter H.A. Kahr, Nades Palaniyar, Christoph Licht
Publikováno v:
Kidney International Reports, Vol 2, Iss 1, Pp 66-75 (2017)
Atypical hemolytic uremic syndrome is a thrombotic microangiopathy, which is linked to hereditary or autoimmune defects in complement activators or regulators present in blood and on vascular endothelial cells. Acute thrombotic microangiopathy episod
Externí odkaz:
https://doaj.org/article/aef5b57bca55432e98cb01f520e8c78e
Autor:
Denisa Urban, Fred G. Pluthero, Hilary Christensen, Shoma Baidya, Margaret L. Rand, Animitra Das, Prakeshkumar S. Shah, David Chitayat, Victor S. Blanchette, Walter H.A. Kahr
Publikováno v:
Haematologica, Vol 102, Iss 2 (2017)
Externí odkaz:
https://doaj.org/article/6fc4307c758d41d6a5e5489204d8d23d
Autor:
Joshua eYuen, Fred G. Pluthero, David N. Douda, Magdalena eRiedl, Ahmed eCherry, Marina eUlanova, Walter H.A. Kahr, Nades ePalaniyar, Christoph eLicht
Publikováno v:
Frontiers in Immunology, Vol 7 (2016)
Neutrophils deposit antimicrobial proteins such as myeloperoxidase and proteases on chromatin, which they release as neutrophil extracellular traps (NETs). Neutrophils also carry key components of the complement alternative pathway (AP) such as prope
Externí odkaz:
https://doaj.org/article/7bea660d8dc941dcb3885490050d0e3e
Autor:
Richard J.Y. Liu, Yusef Al-Molieh, Shao Z. Chen, Marko Drobac, Denisa Urban, Chang H. Chen, Helen H.Y. Yao, Ryan S.Q. Geng, Ling Li, Fred G. Pluthero, Samir Benlekbir, John L. Rubinstein, Walter H.A. Kahr
Publikováno v:
Journal of Biological Chemistry. 299:104718
Autor:
Daniel Diatlov, Arlette Bohorquez, Melanie Jackson, Melina Cheong, Walter H.A. Kahr, Kevin H.M. Kuo, Melanie Kirby-Allen, Christoph Licht
Publikováno v:
Blood. 140:2517-2518
Autor:
Arlette Bohorquez, NIyousha Rostam, Carolina Ortiz-Sandoval, Claire Howard, Walter H.A. Kahr, Christopher J. Campbell, Christoph Licht
Publikováno v:
Blood. 140:2665-2666
Autor:
Monica Penon‐Portmann, Sarah K. Westbury, Ling Li, Fred G. Pluthero, Richard J.Y. Liu, Helen H.Y. Yao, Ryan S.Q. Geng, Neil Warner, Aleixo M. Muise, Stephanie Lotz‐Esquivel, Marianela Howell‐Ramirez, Pablo Saborío‐Chacon, Sara Fernández‐Rojas, Manuel Saborio‐Rocafort, Mildred Jiménez‐Hernández, Carolina Wang‐Zuniga, Walter Cartín‐Sánchez, Joseph T. Shieh, Ramses Badilla‐Porras, Walter H.A. Kahr
Publikováno v:
Penon-Portmann, M, Westbury, S K, Li, L, Pluthero, F G, Liu, R J Y L, Yao, H H Y, Kahr, W H A & et, A 2022, ' Platelet VPS16B is dependent on VPS33B expression, as determined in two siblings with arthrogryposis, renal dysfunction, and cholestasis syndrome ', Journal of Thrombosis and Haemostasis, vol. 20, no. 7, pp. 1712-1719 . https://doi.org/10.1111/jth.15711
BackgroundPlatelet α-granule biogenesis in precursor megakaryocytes is critically dependent on VPS33B and VPS16B, as demonstrated by the platelet α-granule deficiency seen in the rare multisystem disorder arthrogryposis, renal dysfunction and chole
Autor:
Natalie Mathews, Fred G. Pluthero, Margaret L. Rand, Ann Marie Stain, Manuel Carcao, Victor S. Blanchette, Walter H.A. Kahr
Publikováno v:
Research and practice in thrombosis and haemostasis. 6(6)
Severe hemophilia A (SHA) patients vary in severity of bleeding, arthropathy, and requirements for replacement factor VIII (FVIII). Baseline hemostatic activity assays using calibrated automated thrombography (CAT) and thromboelastography (TEG) may o