Page 1 | Search Results | Blood | American Society of Hematology

1-5 of 5

Sort by

Sort Order Select

Journal Articles

Gene disruption of dematin causes precipitous loss of erythrocyte membrane stability and severe hemolytic anemia

Yunzhe Lu, Toshihiko Hanada, Yuko Fujiwara, Jennifer O. Nwankwo, Adam J. Wieschhaus, John Hartwig, Sha Huang, Jongyoon Han, Athar H. Chishti

Blood (2016) 128 (1): 93–103.

https://doi.org/10.1182/blood-2016-01-692251

Published: 2016

Includes: Supplemental data

Journal Articles

B cell–intrinsic deficiency of the Wiskott-Aldrich syndrome protein (WASp) causes severe abnormalities of the peripheral B-cell compartment in mice

Blood (2012) 119 (12): 2819–2828.

https://doi.org/10.1182/blood-2011-09-379412

Published: 2012

Includes: Supplemental data

Journal Articles

Tropomodulin 1-null mice have a mild spherocytic elliptocytosis with appearance of Tropomodulin 3 in red blood cells and disruption of the membrane skeleton

Jeannette D. Moyer, Roberta B. Nowak, Nancy E. Kim, Sandra K. Larkin, Luanne L. Peters, John Hartwig, Frans A. Kuypers, Velia M. Fowler

Blood (2010) 116 (14): 2590–2599.

https://doi.org/10.1182/blood-2010-02-268458

Published: 2010

Includes: Supplemental data

Journal Articles

Cloning of the human platelet F11 receptor: a cell adhesion molecule member of the immunoglobulin superfamily involved in platelet aggregation: Presented in part at the XVIIth Congress of the International Society on Thrombosis and Haemostasis, Washington, DC, August 14-21, 1999.

Malgorzata B. Sobocka, Tomasz Sobocki, Probal Banerjee, Cipora Weiss, Julie I. Rushbrook, Allen J. Norin, John Hartwig, Moro O. Salifu, Mariana S. Markell, Anna Babinska, Yigal H. Ehrlich, Elizabeth Kornecki

Blood (2000) 95 (8): 2600–2609.

https://doi.org/10.1182/blood.V95.8.2600

Published: 2000

Journal Articles

Lymphocyte-Specific Protein 1 Expression in Eukaryotic Cells Reproduces the Morphologic and Motile Abnormality of NAD 47/89 Neutrophils

Thomas H. Howard, John Hartwig, Casey Cunningham

Blood (1998) 91 (12): 4786–4795.

https://doi.org/10.1182/blood.V91.12.4786

Published: 1998

NARROW

Gene disruption of dematin causes precipitous loss of erythrocyte membrane stability and severe hemolytic anemia

B cell–intrinsic deficiency of the Wiskott-Aldrich syndrome protein (WASp) causes severe abnormalities of the peripheral B-cell compartment in mice

Tropomodulin 1-null mice have a mild spherocytic elliptocytosis with appearance of Tropomodulin 3 in red blood cells and disruption of the membrane skeleton

Cloning of the human platelet F11 receptor: a cell adhesion molecule member of the immunoglobulin superfamily involved in platelet aggregation: Presented in part at the XVIIth Congress of the International Society on Thrombosis and Haemostasis, Washington, DC, August 14-21, 1999.

Lymphocyte-Specific Protein 1 Expression in Eukaryotic Cells Reproduces the Morphologic and Motile Abnormality of NAD 47/89 Neutrophils

Email alerts

ASH Publications

American Society of Hematology

Gene disruption of dematin causes precipitous loss of erythrocyte membrane stability and severe hemolytic anemia

B cell–intrinsic deficiency of the Wiskott-Aldrich syndrome protein (WASp) causes severe abnormalities of the peripheral B-cell compartment in mice

Tropomodulin 1-null mice have a mild spherocytic elliptocytosis with appearance of Tropomodulin 3 in red blood cells and disruption of the membrane skeleton

Cloning of the human platelet F11 receptor: a cell adhesion molecule member of the immunoglobulin superfamily involved in platelet aggregation: Presented in part at the XVIIth Congress of the International Society on Thrombosis and Haemostasis, Washington, DC, August 14-21, 1999.

Lymphocyte-Specific Protein 1 Expression in Eukaryotic Cells Reproduces the Morphologic and Motile Abnormality of NAD 47/89 Neutrophils

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only