Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders
Top Cited Papers
- 1 July 2013
- journal article
- review article
- Published by Elsevier BV in Blood Reviews
- Vol. 27 (4), 167-178
- https://doi.org/10.1016/j.blre.2013.04.003
Abstract
No abstract availableThis publication has 123 references indexed in Scilit:
- Refinement of the hereditary xerocytosis locus on chromosome 16q in a large Canadian kindredBlood Cells, Molecules, and Diseases, 2011
- ATP-dependent Mechanism Protects Spectrin against Glycation in Human Erythrocytes*Published by Elsevier BV ,2010
- Piezo1 and Piezo2 Are Essential Components of Distinct Mechanically Activated Cation ChannelsScience, 2010
- Red cell membrane: past, present, and futureBlood, 2008
- Structural and functional effects of hereditary hemolytic anemia-associated point mutations in the alpha spectrin tetramer siteBlood, 2008
- Protein 4.1R-dependent multiprotein complex: New insights into the structural organization of the red blood cell membraneProceedings of the National Academy of Sciences of the United States of America, 2008
- Pathogenic proline mutation in the linker between spectrin repeats: disease caused by spectrin unfoldingBlood, 2006
- Tropomyosin modulates erythrocyte membrane stabilityBlood, 2006
- Phospholipid binding by proteins of the spectrin family: a comparative studyBiochemical and Biophysical Research Communications, 2005
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970