Publications by authors named "Beau Mitchell"

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Genetic disarray follows mutant KLF1-E325K expression in a congenital dyserythropoietic anemia patient.
Lilian Varricchio, Antanas Planutis, Deepa Manwani, Julie Jaffray, W Beau Mitchell

Haematologica· December 2019

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Storage characteristics of multiple-donor pooled red blood cells compared to single-donor red blood cell units.
Aabhas Mathur, Raquibul Chowdhury, Christopher D Hillyer, W Beau Mitchell, Beth H Shaz

Transfusion· December 2016

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Altered heme-mediated modulation of dendritic cell function in sickle cell alloimmunization.
Emmanuelle Godefroy, Yunfeng Liu, Patricia Shi, W Beau Mitchell, Devin Cohen

Haematologica· September 2016

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A novel inflammatory role for platelets in sickle cell disease.
Jennifer Davila, Deepa Manwani, Ljiljana Vasovic, Mauro Avanzi, Joan Uehlinger, W Beau Mitchell

Platelets· June 2016

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A novel bioreactor and culture method drives high yields of platelets from stem cells.
Mauro P Avanzi, Oluwasijibomi E Oluwadara, Melissa M Cushing, Maxwell L Mitchell, Stephen Fischer, W Beau Mitchell

Transfusion· January 2016

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Effects of eltrombopag on platelet count and platelet activation in Wiskott-Aldrich syndrome/X-linked thrombocytopenia.
Anja J Gerrits, Emily A Leven, Andrew L Frelinger, Sophie L Brigstocke, Michelle A Berny-Lang, W Beau Mitchell

Blood· September 2015

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Erythroid transcription factor EKLF/KLF1 mutation causing congenital dyserythropoietic anemia type IV in a patient of Taiwanese origin: review of all reported cases and development of a clinical diagnostic paradigm.
Julie A Jaffray, W Beau Mitchell, Merlin Nithya Gnanapragasam, Surya V Seshan, Xinhuo Guo

Blood Cells Mol Dis· August 2013

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How low can you go?
W Beau Mitchell, James B Bussel

Blood· June 2013

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Optimizing megakaryocyte polyploidization by targeting multiple pathways of cytokinesis.
Mauro P Avanzi, Amanda Chen, Wu He, W Beau Mitchell

Transfusion· November 2012

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Managing incidentally diagnosed isolated factor VII deficiency perioperatively: a brief expert consensus report.
Sujit Sheth, Gerald Soff, Beau Mitchell, David Green, Shipra Kaicker

Expert Rev Hematol· February 2012

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Mapping early conformational changes in alphaIIb and beta3 during biogenesis reveals a potential mechanism for alphaIIbbeta3 adopting its bent conformation.
W Beau Mitchell, Jihong Li, Marta Murcia, Nathalie Valentin, Peter J Newman

Blood· May 2007

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alphaIIbbeta3 biogenesis is controlled by engagement of alphaIIb in the calnexin cycle via the N15-linked glycan.
W Beau Mitchell, JiHong Li, Deborah L French, Barry S Coller

Blood· April 2006

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Molecular diversity of Glanzmann thrombasthenia in southern India: new insights into mRNA splicing and structure-function correlations of alphaIIbbeta3 integrin (ITGA2B, ITGB3).
Hava Peretz, Nurit Rosenberg, Meytal Landau, Saly Usher, Everette J R Nelson, Beau W Mitchell

Hum Mutat· April 2006

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Integrin beta3 regions controlling binding of murine mAb 7E3: implications for the mechanism of integrin alphaIIbbeta3 activation.
Andrea Artoni, JiHong Li, Beau Mitchell, Jian Ruan, Junichi Takagi

Proc Natl Acad Sci U S A· September 2004

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Evidence for megakaryocyte engraftment following reduced-intensity conditioning.
Deborah L French, Steven Fruchtman, W Beau Mitchell, Barry S Coller, Hava Peretz

Exp Hematol· September 2004

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Two novel mutations in the alpha IIb calcium-binding domains identify hydrophobic regions essential for alpha IIbbeta 3 biogenesis.
W Beau Mitchell, Ji Hong Li, Fiza Singh, Alan D Michelson, James Bussel

Blood· March 2003

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Two new beta3 integrin mutations in Indian patients with Glanzmann thrombasthenia: localization of mutations affecting cysteine residues in integrin beta3.
Sona Nair, Jihong Li, W Beau Mitchell, Dipika Mohanty, Barry S Coller

Thromb Haemost· September 2002

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