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Plos One|April 28, 2012
The proline rich homeodomain protein PRH/Hhex forms stable oligomers that are highly resistant to denaturationAnshuman Shukla, Nicholas M Burton, Padma-Sheela Jayaraman, et al.
Frontiers in Physiology|March 31, 2022
Reticulocyte Maturation and Variant Red Blood CellsChristian J Stevens-Hernandez, Joanna F Flatt, Sabine Kupzig, et al.
Nephron. Physiology|January 14, 2010
Distal renal tubular acidosis in Filipino children, caused by mutations of the anion-exchanger SLC4A1 (AE1, Band 3) geneFrancisco E Anacleto, Lesley J Bruce, Peter Clayton, et al.
Kidney International|June 26, 2002
Band 3 mutations, distal renal tubular acidosis, and Southeast Asian ovalocytosisOliver Wrong, Lesley J Bruce, Robert J Unwin, et al.
Blood|May 20, 2008
Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotypeBelinda K Singleton, Nicholas M Burton, Carole Green, et al.
Transfusion|November 12, 2023
Vesiculation in irradiated and cation-leaky-stored red blood cellsChristian J Stevens-Hernandez, Gyongyver Gyorffy, Athinoula Meli, et al.
Vox Sanguinis|August 19, 2025
Improving the stability of cultured red blood cells during storageChristian J Stevens-Hernandez, Sabine Kupzig, Paraskevi Diamanti, et al.
British Journal of Haematology|January 25, 2011
South-east Asian ovalocytosis and the cryohydrocytosis form of hereditary stomatocytosis show virtually indistinguishable cation permeability defectsHélène Guizouarn, Franck Borgese, Nicole Gabillat, et al.
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