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Blood
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July 24, 2020
Red cell membrane disorders: structure meets function
Mary Risinger, Theodosia A Kalfa
Hematology/Oncology Clinics of North America
|
April 30, 2019
Rare Hereditary Hemolytic Anemias: Diagnostic Approach and Considerations in Management
Mary Risinger, Myesa Emberesh, Theodosia A Kalfa
Current Opinion in Hematology
|
July 8, 2025
Advances on the genetic basis of red cell membrane disorders
Mary Risinger, Wenying Zhang, Theodosia A Kalfa
Blood Cells, Molecules & Diseases
|
May 18, 2011
Volume regulation and KCl cotransport in reticulocyte populations of sickle and normal red blood cells
Maa-Ohui Quarmyne, Mary Risinger, Andrew Linkugel, et al.
Blood
|
October 7, 2006
Urea stimulation of KCl cotransport induces abnormal volume reduction in sickle reticulocytes
Clinton H Joiner, R Kirk Rettig, Maorong Jiang, et al.
Blood
|
January 16, 2020
RGL2 Deficiency Impairs Human Erythropoiesis By Altering Terminal Erythroid Differentiation and Apoptosis
Harry Lesmana, Georgios E Christakopoulos, Mary Risinger, et al.
American Journal of Hematology
|
March 7, 2026
Cryohydrocytosis: When Cold Breaks the Membrane
Athina Ntoumaziou, Mary Risinger, Yasmin Elgammal, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
May 20, 2022
Rapid degradation of protein tyrosine phosphatase 1B in sickle cells: Possible contribution to sickle cell membrane weakening
Panae Noomuna, John M Hausman, Ruhani Sansoya, et al.
Pediatric Blood & Cancer
|
November 6, 2018
Hereditary elliptocytosis-associated alpha-spectrin mutation p.L155dup as a modifier of sickle cell disease severity
Mary Risinger, Georgios E Christakopoulos, Corinna L Schultz, et al.
American Journal of Hematology
|
March 28, 2023
Hemolytic anemia and macrothrombocytopenia: A lipid problem?
Mary Risinger, Phyllis S Kim, Roberto X Rodriguez, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 18) with videos related to
Sort By:
Page
of 2
Blood
|
July 24, 2020
Red cell membrane disorders: structure meets function
Mary Risinger, Theodosia A Kalfa
Hematology/Oncology Clinics of North America
|
April 30, 2019
Rare Hereditary Hemolytic Anemias: Diagnostic Approach and Considerations in Management
Mary Risinger, Myesa Emberesh, Theodosia A Kalfa
Current Opinion in Hematology
|
July 8, 2025
Advances on the genetic basis of red cell membrane disorders
Mary Risinger, Wenying Zhang, Theodosia A Kalfa
Blood Cells, Molecules & Diseases
|
May 18, 2011
Volume regulation and KCl cotransport in reticulocyte populations of sickle and normal red blood cells
Maa-Ohui Quarmyne, Mary Risinger, Andrew Linkugel, et al.
Blood
|
October 7, 2006
Urea stimulation of KCl cotransport induces abnormal volume reduction in sickle reticulocytes
Clinton H Joiner, R Kirk Rettig, Maorong Jiang, et al.
Blood
|
January 16, 2020
RGL2 Deficiency Impairs Human Erythropoiesis By Altering Terminal Erythroid Differentiation and Apoptosis
Harry Lesmana, Georgios E Christakopoulos, Mary Risinger, et al.
American Journal of Hematology
|
March 7, 2026
Cryohydrocytosis: When Cold Breaks the Membrane
Athina Ntoumaziou, Mary Risinger, Yasmin Elgammal, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
May 20, 2022
Rapid degradation of protein tyrosine phosphatase 1B in sickle cells: Possible contribution to sickle cell membrane weakening
Panae Noomuna, John M Hausman, Ruhani Sansoya, et al.
Pediatric Blood & Cancer
|
November 6, 2018
Hereditary elliptocytosis-associated alpha-spectrin mutation p.L155dup as a modifier of sickle cell disease severity
Mary Risinger, Georgios E Christakopoulos, Corinna L Schultz, et al.
American Journal of Hematology
|
March 28, 2023
Hemolytic anemia and macrothrombocytopenia: A lipid problem?
Mary Risinger, Phyllis S Kim, Roberto X Rodriguez, et al.
Page
of 2