Red cell life span heterogeneity in hematologically normal people is sufficient to alter HbA1c von Cohen, Robert M., Franco, Robert S., Khera, Paramjit K., Smith, Eric P., Lindsell, Christopher J., Ciraolo, Peter J., Palascak, Mary B., Joiner, Clinton H.

Volltext

Erythrocyte NADPH oxidase activity modulated by Rac GTPases, PKC, and plasma cytokines contributes to oxidative stress in sickle cell disease von George, Alex, Pushkaran, Suvarnamala, Konstantinidis, Diamantis G., Koochaki, Sebastian, Malik, Punam, Mohandas, Narla, Zheng, Yi, Joiner, Clinton H., Kalfa, Theodosia A.

Volltext

Contribution of alternative complement pathway to delayed hemolytic transfusion reaction in sickle cell disease von Chonat, Satheesh, Quarmyne, Maa-Ohui, Bennett, Caroline M, Dean, Christina L, Joiner, Clinton H, Fasano, Ross M, Stowell, Sean R

Volltext

Eculizumab for complement mediated thrombotic microangiopathy in sickle cell disease von Chonat, Satheesh, Graciaa, Sara, Shin, H. Stella, Newton, Joanna G., Quarmyne, Maa-Ohui, Boudreaux, Jeanne, Tang, Amy, Zerra, Patricia E., Rollins, Margo R., Josephson, Cassandra D., Brown, Clark, Joiner, Clinton H., Fasano, Ross M., Stowell, Sean R.

Volltext

Quantifying the Cerebral Hemometabolic Response to Blood Transfusion in Pediatric Sickle Cell Disease With Diffuse Optical Spectroscopies von Lee, Seung Yup, Brothers, Rowan O., Turrentine, Katherine B., Quadri, Ayesha, Sathialingam, Eashani, Cowdrick, Kyle R., Gillespie, Scott, Bai, Shasha, Goldman-Yassen, Adam E., Joiner, Clinton H., Brown, R. Clark, Buckley, Erin M.

Volltext

Evidence for Interindividual Heterogeneity in the Glucose Gradient Across the Human Red Blood Cell Membrane and Its Relationship to Hemoglobin Glycation von KHERA, Paramjit K, JOINER, Clinton H, CARRUTHERS, Anthony, LINDSELL, Christopher J, SMITH, Eric P, FRANCE, Robert S, HOLMES, Yancey R, COHEN, Robert M

Volltext

Pharmacological inhibition of calpain‐1 prevents red cell dehydration and reduces Gardos channel activity in a mouse model of sickle cell disease von De Franceschi, Lucia, Franco, Robert S., Bertoldi, Mariarita, Brugnara, Carlo, Matté, Alessandro, Siciliano, Angela, Wieschhaus, Adam J., Chishti, Athar H., Joiner, Clinton H.

Volltext

Rac GTPases regulate the morphology and deformability of the erythrocyte cytoskeleton von Kalfa, Theodosia A., Pushkaran, Suvarnamala, Mohandas, Narla, Hartwig, John H., Fowler, Velia M., Johnson, James F., Joiner, Clinton H., Williams, David A., Zheng, Yi

Volltext

K-Cl Cotransporter Gene Expression during Human and Murine Erythroid Differentiation von Pan, Dao, Kalfa, Theodosia A., Wang, Daren, Risinger, Mary, Crable, Scott, Ottlinger, Anna, Chandra, Sharat, Mount, David B., Hübner, Christian A., Franco, Robert S., Joiner, Clinton H.

Volltext

The inflammatory profiles of pulmonary alveolar macrophages and alveolar type 2 cells in SCD von Gbotosho, Oluwabukola T, Li, Wei, Joiner, Clinton H, Brown, Lou Ann S, Hyacinth, Hyacinth I

Volltext

Extracellular fluid tonicity impacts sickle red blood cell deformability and adhesion von Carden, Marcus A., Fay, Meredith E., Lu, Xinran, Mannino, Robert G., Sakurai, Yumiko, Ciciliano, Jordan C., Hansen, Caroline E., Chonat, Satheesh, Joiner, Clinton H., Wood, David K., Lam, Wilbur A.

Volltext

Sites of Regulated Phosphorylation that Control K-Cl Cotransporter Activity von Rinehart, Jesse, Maksimova, Yelena D., Tanis, Jessica E., Stone, Kathryn L., Hodson, Caleb A., Zhang, Junhui, Risinger, Mary, Pan, Weijun, Wu, Dianqing, Colangelo, Christopher M., Forbush, Biff, Joiner, Clinton H., Gulcicek, Erol E., Gallagher, Patrick G., Lifton, Richard P.

Volltext

Changes in urine albumin to creatinine ratio with the initiation of hydroxyurea therapy among children and adolescents with sickle cell disease von Tehseen, Sarah, Joiner, Clinton H., Lane, Peter A., Yee, Marianne E.

Volltext

Survival of transfused red blood cells from a donor with alpha‐thalassemia trait in a recipient with sickle cell disease von Yee, Marianne E. M., Covington, Mischa L., Zerra, Patricia E., McCoy, James W., Easley, Kirk A., Joiner, Clinton H., Bryksin, Janetta, Francis, Richard O., Lough, Christopher M., Patel, Niren, Kutlar, Abdullah, Josephson, Cassandra D., Roback, John D., Stowell, Sean R., Fasano, Ross M.

Volltext

Post‐transfusion biotin‐labeled red blood cell survival studies in pediatric sickle cell disease with antibodies of uncertain significance von Yee, Marianne E. M., Zerra, Patricia E., McCoy, James W., Covington, Mischa L., Stowell, Sean R., Joiner, Clinton H., Lough, Christopher M., Delvadia, Bhaveshkumar B., Josephson, Cassandra D., Roback, John D., Fasano, Ross M.

Volltext

Sickle Mice Are Sensitive to Hypoxia/Ischemia-Induced Stroke but Respond to Tissue-Type Plasminogen Activator Treatment von Sun, Yu-Yo, Lee, Jolly, Huang, Henry, Wagner, Mary B, Joiner, Clinton H, Archer, David R, Kuan, Chia-Yi

Volltext

Microvasculature-on-a-chip for the long-term study of endothelial barrier dysfunction and microvascular obstruction in disease von Qiu, Yongzhi, Ahn, Byungwook, Sakurai, Yumiko, Hansen, Caroline E., Tran, Reginald, Mimche, Patrice N., Mannino, Robert G., Ciciliano, Jordan C., Lamb, Tracey J., Joiner, Clinton H., Ofori-Acquah, Solomon F., Lam, Wilbur A.

Volltext

Estimation of glomerular filtration rate using serum cystatin C and creatinine in adults with sickle cell anemia von Yee, Marianne E M, Lane, Peter A, Archer, David R, Joiner, Clinton H, Eckman, James R, Guasch, Antonio

Volltext

Losartan therapy decreases albuminuria with stable glomerular filtration and permselectivity in sickle cell anemia von Yee, Marianne E., Lane, Peter A., Archer, David R., Joiner, Clinton H., Eckman, James R., Guasch, Antonio

Volltext

Normal saline is associated with increased sickle red cell stiffness and prolonged transit times in a microfluidic model of the capillary system von Carden, Marcus A., Fay, Meredith, Sakurai, Yumiko, McFarland, Brynn, Blanche, Sydney, DiPrete, Caleb, Joiner, Clinton H., Sulchek, Todd, Lam, Wilbur A.

Volltext