{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,28]],"date-time":"2026-07-28T05:31:38Z","timestamp":1785216698350,"version":"3.55.0"},"reference-count":99,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[2008,7,1]],"date-time":"2008-07-01T00:00:00Z","timestamp":1214870400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2008,7,1]],"date-time":"2008-07-01T00:00:00Z","timestamp":1214870400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Blood Cells, Molecules, and Diseases"],"published-print":{"date-parts":[[2008,7]]},"DOI":"10.1016\/j.bcmd.2008.01.001","type":"journal-article","created":{"date-parts":[[2008,3,6]],"date-time":"2008-03-06T19:10:56Z","timestamp":1204830656000},"page":"35-43","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":47,"title":["Glycophorin A: Band 3 aid"],"prefix":"10.1016","volume":"41","author":[{"given":"Rosalind C.","family":"Williamson","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ashley M.","family":"Toye","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.bcmd.2008.01.001_bib1","doi-asserted-by":"crossref","first-page":"133","DOI":"10.1097\/00062752-200203000-00009","article-title":"Band 3 anion exchanger and its involvement in erythrocyte and kidney disorders","volume":"9","author":"Tanner","year":"2002","journal-title":"Curr. Opin. Hematol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib2","doi-asserted-by":"crossref","first-page":"155","DOI":"10.3109\/09687689709048178","article-title":"The structure and function of band 3 (AE1): recent developments (review)","volume":"14","author":"Tanner","year":"1997","journal-title":"Mol. Membr. Biol."},{"issue":"Suppl 5","key":"10.1016\/j.bcmd.2008.01.001_bib3","first-page":"S41","article-title":"The AE gene family of Cl\/HCO3- exchangers","volume":"15","author":"Alper","year":"2002","journal-title":"J. Nephrol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib4","doi-asserted-by":"crossref","first-page":"2925","DOI":"10.1182\/blood.V96.9.2925","article-title":"Crystallographic structure and functional interpretation of the cytoplasmic domain of erythrocyte membrane band 3","volume":"96","author":"Zhang","year":"2000","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib5","doi-asserted-by":"crossref","first-page":"4088","DOI":"10.1182\/blood-2004-05-1895","article-title":"Protein-4.2 association with band 3 (AE1, SLCA4) in Xenopus oocytes: effects of three natural protein-4.2 mutations associated with hemolytic anemia","volume":"105","author":"Toye","year":"2005","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib6","doi-asserted-by":"crossref","first-page":"28430","DOI":"10.1074\/jbc.273.43.28430","article-title":"Carbonic anhydrase II binds to the carboxyl terminus of human band 3, the erythrocyte C1-\/HCO3-exchanger","volume":"273","author":"Vince","year":"1998","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.bcmd.2008.01.001_bib7","doi-asserted-by":"crossref","first-page":"13344","DOI":"10.1021\/bi0015111","article-title":"Localization of the Cl-\/HCO3-anion exchanger binding site to the amino-terminal region of carbonic anhydrase II","volume":"39","author":"Vince","year":"2000","journal-title":"Biochemistry"},{"key":"10.1016\/j.bcmd.2008.01.001_bib8","doi-asserted-by":"crossref","first-page":"22163","DOI":"10.1016\/S0021-9258(18)41649-3","article-title":"Glycophorin A facilitates the expression of human band 3-mediated anion transport in Xenopus oocytes","volume":"267","author":"Groves","year":"1992","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.bcmd.2008.01.001_bib9","doi-asserted-by":"crossref","first-page":"4180","DOI":"10.1182\/blood-2002-09-2824","article-title":"A band 3-based macrocomplex of integral and peripheral proteins in the RBC membrane","volume":"101","author":"Bruce","year":"2003","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib10","doi-asserted-by":"crossref","first-page":"2496","DOI":"10.1182\/blood.V97.8.2496","article-title":"Coexpression of band 3 mutants and Rh polypeptides: differential effects of band 3 on the expression of the Rh complex containing D polypeptide and the Rh complex containing CcEe polypeptide","volume":"97","author":"Beckmann","year":"2001","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib11","doi-asserted-by":"crossref","first-page":"85","DOI":"10.1006\/bcmd.2000.0353","article-title":"A membrane metabolon linking carbonic anhydrase with chloride\/bicarbonate anion exchangers","volume":"27","author":"Reithmeier","year":"2001","journal-title":"Blood Cells Mol. Diseases"},{"key":"10.1016\/j.bcmd.2008.01.001_bib12","doi-asserted-by":"crossref","first-page":"2414","DOI":"10.1074\/jbc.M309826200","article-title":"Altered structure and anion transport properties of band 3 (AE1, SLC4A1) in human red cells lacking glycophorin A","volume":"279","author":"Bruce","year":"2004","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.bcmd.2008.01.001_bib13","first-page":"F813","article-title":"Anion exchanger 1 in human kidney and oncocytoma differs from erythroid AE1 in its NH2 terminus","volume":"265","author":"Kollert-Jons","year":"1993","journal-title":"Am. J. Physiol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib14","doi-asserted-by":"crossref","first-page":"32201","DOI":"10.1016\/S0021-9258(18)31621-1","article-title":"The major kidney AE1 isoform does not bind ankyrin (Ank1) in vitro. An essential role for the 79 NH2-terminal amino acid residues of band 3","volume":"269","author":"Ding","year":"1994","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.bcmd.2008.01.001_bib15","doi-asserted-by":"crossref","first-page":"17892","DOI":"10.1074\/jbc.270.30.17892","article-title":"Partial characterization of the cytoplasmic domain of human kidney band 3","volume":"270","author":"Wang","year":"1995","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.bcmd.2008.01.001_bib16","doi-asserted-by":"crossref","first-page":"C347","DOI":"10.1152\/ajpcell.1986.251.3.C347","article-title":"Two types of collecting duct mitochondria-rich (intercalated) cells: lectin and band 3 cytochemistry","volume":"251","author":"Schuster","year":"1986","journal-title":"Am. J. Physiol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib17","doi-asserted-by":"crossref","first-page":"1287","DOI":"10.1126\/science.2933809","article-title":"Colocalization of band 3 with ankyrin and spectrin at the basal membrane of intercalated cells in the rat kidney","volume":"230","author":"Drenckhahn","year":"1985","journal-title":"Science"},{"key":"10.1016\/j.bcmd.2008.01.001_bib18","doi-asserted-by":"crossref","first-page":"5429","DOI":"10.1073\/pnas.86.14.5429","article-title":"Subtypes of intercalated cells in rat kidney collecting duct defined by antibodies against erythroid band 3 and renal vacuolar H+-ATPase","volume":"86","author":"Alper","year":"1989","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"key":"10.1016\/j.bcmd.2008.01.001_bib19","first-page":"47","article-title":"Defective kidney anion-exchanger 1 (AE1, Band 3) trafficking in dominant distal renal tubular acidosis (dRTA)","author":"Toye","year":"2005","journal-title":"Biochem. Soc. Symp."},{"key":"10.1016\/j.bcmd.2008.01.001_bib20","doi-asserted-by":"crossref","first-page":"23","DOI":"10.1016\/j.tracli.2006.02.019","article-title":"Functional interaction between Rh proteins and the spectrin-based skeleton in erythroid and epithelial cells","volume":"13","author":"Nicolas","year":"2006","journal-title":"Transfus. Clin. Biol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib21","doi-asserted-by":"crossref","first-page":"118","DOI":"10.1053\/j.seminhematol.2004.01.002","article-title":"Hereditary spherocytosis\u2014defects in proteins that connect the membrane skeleton to the lipid bilayer","volume":"41","author":"Eber","year":"2004","journal-title":"Semin. Hematol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib22","doi-asserted-by":"crossref","first-page":"214","DOI":"10.1038\/ng0696-214","article-title":"Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis","volume":"13","author":"Eber","year":"1996","journal-title":"Nat. Genet."},{"key":"10.1016\/j.bcmd.2008.01.001_bib23","doi-asserted-by":"crossref","first-page":"2155","DOI":"10.1182\/blood.V81.8.2155.2155","article-title":"Human erythrocyte protein 4.2 deficiency associated with hemolytic anemia and a homozygous 40glutamic acid\u2013>lysine substitution in the cytoplasmic domain of band 3 (band 3Montefiore)","volume":"81","author":"Rybicki","year":"1993","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib24","doi-asserted-by":"crossref","first-page":"4366","DOI":"10.1182\/blood.V88.11.4366.4366","article-title":"Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency","volume":"88","author":"Jarolim","year":"1996","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib25","doi-asserted-by":"crossref","first-page":"522","DOI":"10.1046\/j.1365-2141.1997.4263231.x","article-title":"Total absence of protein 4.2 and partial deficiency of band 3 in hereditary spherocytosis","volume":"99","author":"Kanzaki","year":"1997","journal-title":"Br. J. Haematol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib26","doi-asserted-by":"crossref","first-page":"932","DOI":"10.1046\/j.1365-2141.1998.00868.x","article-title":"Homozygous missense mutation (band 3 Fukuoka: G130R): a mild form of hereditary spherocytosis with near-normal band 3 content and minimal changes of membrane ultrastructure despite moderate protein 4.2 deficiency","volume":"102","author":"Inoue","year":"1998","journal-title":"Br. J. Haematol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib27","doi-asserted-by":"crossref","first-page":"523","DOI":"10.1182\/blood.V80.2.523.523","article-title":"Band 3 Tuscaloosa: Pro327\u2013Arg327 substitution in the cytoplasmic domain of erythrocyte band 3 protein associated with spherocytic hemolytic anemia and partial deficiency of protein 4.2","volume":"80","author":"Jarolim","year":"1992","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib28","doi-asserted-by":"crossref","first-page":"11022","DOI":"10.1073\/pnas.88.24.11022","article-title":"Deletion in erythrocyte band 3 gene in malaria-resistant Southeast Asian ovalocytosis","volume":"88","author":"Jarolim","year":"1991","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"key":"10.1016\/j.bcmd.2008.01.001_bib29","doi-asserted-by":"crossref","first-page":"949","DOI":"10.1139\/o06-200","article-title":"Unraveling trafficking of the kidney anion exchanger 1 in polarized MDCK epithelial cells","volume":"84","author":"Cordat","year":"2006","journal-title":"Biochem. Cell. Biol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib30","doi-asserted-by":"crossref","first-page":"414","DOI":"10.1182\/blood.V90.1.414.414_414_420","article-title":"Modulation of clinical expression and band 3 deficiency in hereditary spherocytosis","volume":"90","author":"Alloisio","year":"1997","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib31","doi-asserted-by":"crossref","first-page":"305","DOI":"10.1080\/096876899294526","article-title":"The red blood cell band 3 variant (band 3Biceetrel:R490C) associated with dominant hereditary spherocytosis causes defective membrane targeting of the molecule and a dominant negative effect","volume":"16","author":"Dhermy","year":"1999","journal-title":"Mol. Membr. Biol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib32","doi-asserted-by":"crossref","first-page":"32","DOI":"10.1046\/j.1365-2141.1997.1893005.x","article-title":"Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects","volume":"98","author":"Dhermy","year":"1997","journal-title":"Br. J. Haematol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib33","doi-asserted-by":"crossref","first-page":"F810","DOI":"10.1152\/ajprenal.00216.2001","article-title":"Impaired trafficking of distal renal tubular acidosis mutants of the human kidney anion exchanger kAE1","volume":"282","author":"Quilty","year":"2002","journal-title":"Am. J. Physiol., Renal. Physiol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib34","doi-asserted-by":"crossref","first-page":"1693","DOI":"10.1172\/JCI119694","article-title":"Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene","volume":"100","author":"Bruce","year":"1997","journal-title":"J. Clin. Invest."},{"key":"10.1016\/j.bcmd.2008.01.001_bib35","doi-asserted-by":"crossref","first-page":"895","DOI":"10.1042\/bj20020574","article-title":"Impaired trafficking of human kidney anion exchanger (kAE1) caused by hetero-oligomer formation with a truncated mutant associated with distal renal tubular acidosis","volume":"368","author":"Quilty","year":"2002","journal-title":"Biochem. J."},{"key":"10.1016\/j.bcmd.2008.01.001_bib36","doi-asserted-by":"crossref","first-page":"1399","DOI":"10.1242\/jcs.00974","article-title":"Regions of human kidney anion exchanger 1 (kAE1) required for basolateral targeting of kAE1 in polarised kidney cells: mis-targeting explains dominant renal tubular acidosis (dRTA)","volume":"117","author":"Toye","year":"2004","journal-title":"J. Cell Sci."},{"key":"10.1016\/j.bcmd.2008.01.001_bib37","doi-asserted-by":"crossref","first-page":"64","DOI":"10.1053\/j.ajkd.2004.03.033","article-title":"Novel compound heterozygous SLC4A1 mutations in Thai patients with autosomal recessive distal renal tubular acidosis","volume":"44","author":"Sritippayawan","year":"2004","journal-title":"Am. J. Kidney Dis."},{"key":"10.1016\/j.bcmd.2008.01.001_bib38","doi-asserted-by":"crossref","first-page":"13833","DOI":"10.1074\/jbc.M400188200","article-title":"A novel missense mutation in AE1 causing autosomal dominant distal renal tubular acidosis retains normal transport function but is mistargeted in polarized epithelial cells","volume":"279","author":"Rungroj","year":"2004","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.bcmd.2008.01.001_bib39","doi-asserted-by":"crossref","first-page":"807","DOI":"10.1093\/ndt\/gfl662","article-title":"Immunohistochemical comparison of a case of inherited distal renal tubular acidosis (with a unique AE1 mutation) with an acquired case secondary to autoimmune disease","volume":"22","author":"Walsh","year":"2007","journal-title":"Nephrol. Dial. Transplant."},{"key":"10.1016\/j.bcmd.2008.01.001_bib40","doi-asserted-by":"crossref","first-page":"396","DOI":"10.1111\/j.1600-0609.2004.00405.x","article-title":"Band 3Tambau: a de novo mutation in the AE1 gene associated with hereditary spherocytosis. Implications for anion exchange and insertion into the red blood cell membrane","volume":"74","author":"Lima","year":"2005","journal-title":"Eur. J. Haematol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib41","doi-asserted-by":"crossref","unstructured":"A.M. Toye, R.C. Williamson, M. Khanfar, B. Bader-Meunier, T. Cynober, M. Thibault, G. Tchernia, M. Dechaux, J. Delaunay, and L.J. Bruce, Band 3 Courcouronnes (Ser667Phe): a trafficking mutant differentially rescued by wild type band 3 and glycophorin A. Blood First Edition Paper, prepublished online January 3, 2008, doi:10.1182\/blood-2007-07-099473.","DOI":"10.1182\/blood-2007-07-099473"},{"key":"10.1016\/j.bcmd.2008.01.001_bib42","doi-asserted-by":"crossref","first-page":"1258","DOI":"10.1038\/ng1656","article-title":"Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride\u2013bicarbonate exchanger, AE1","volume":"37","author":"Bruce","year":"2005","journal-title":"Nat. Genet."},{"key":"10.1016\/j.bcmd.2008.01.001_bib43","doi-asserted-by":"crossref","first-page":"2173","DOI":"10.1172\/JCI4836","article-title":"Novel AE1 mutations in recessive distal renal tubular acidosis. Loss-of-function is rescued by glycophorin A","volume":"102","author":"Tanphaichitr","year":"1998","journal-title":"J. Clin. Invest."},{"key":"10.1016\/j.bcmd.2008.01.001_bib44","first-page":"6b","article-title":"Molecular and genetic characteristics in Japanese patients with hereditary spherocytosis: frequent band 3 mutations and rarer ankyrin mutations","volume":"90","author":"Kanzaki","year":"1997","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib45","doi-asserted-by":"crossref","first-page":"634","DOI":"10.1182\/blood.V85.3.634.bloodjournal853634","article-title":"Mutations of conserved arginines in the membrane domain of erythroid band 3 lead to a decrease in membrane-associated band 3 and to the phenotype of hereditary spherocytosis","volume":"85","author":"Jarolim","year":"1995","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib46","doi-asserted-by":"crossref","first-page":"804","DOI":"10.1111\/j.1365-2141.1995.tb05393.x","article-title":"Band 3 Chur: a variant associated with band 3-deficient hereditary spherocytosis and substitution in a highly conserved position of transmembrane segment 11","volume":"91","author":"Maillet","year":"1995","journal-title":"Br. J. Haematol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib47","doi-asserted-by":"crossref","first-page":"117","DOI":"10.1111\/j.1600-0854.2005.00366.x","article-title":"Dominant and recessive distal renal tubular acidosis mutations of kidney anion exchanger 1 induce distinct trafficking defects in MDCK cells","volume":"7","author":"Cordat","year":"2006","journal-title":"Traffic"},{"key":"10.1016\/j.bcmd.2008.01.001_bib48","doi-asserted-by":"crossref","first-page":"644","DOI":"10.1007\/s00467-003-1112-6","article-title":"A de novo R589C mutation of anion exchanger 1 causing distal renal tubular acidosis","volume":"18","author":"Sritippayawan","year":"2003","journal-title":"Pediatr. Nephrol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib49","doi-asserted-by":"crossref","first-page":"70","DOI":"10.1046\/j.1365-2141.1997.8732504.x","article-title":"Novel band 3 variants (bands 3 Foggia, Napoli I and Napoli II) associated with hereditary spherocytosis and band 3 deficiency: status of the D38A polymorphism within the EPB3 locus","volume":"96","author":"Miraglia del Giudice","year":"1997","journal-title":"Br. J. Haematol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib50","doi-asserted-by":"crossref","first-page":"200","DOI":"10.1159\/000040904","article-title":"Band 3 Tokyo: Thr837\u2013>Ala837 substitution in erythrocyte band 3 protein associated with spherocytic hemolysis","volume":"100","author":"Iwase","year":"1998","journal-title":"Acta Haematol."},{"issue":"Pt 1","key":"10.1016\/j.bcmd.2008.01.001_bib51","doi-asserted-by":"crossref","first-page":"41","DOI":"10.1042\/bj3500041","article-title":"Band 3 mutations, renal tubular acidosis and South-East Asian ovalocytosis in Malaysia and Papua New Guinea: loss of up to 95% band 3 transport in red cells","volume":"350","author":"Bruce","year":"2000","journal-title":"Biochem. J."},{"key":"10.1016\/j.bcmd.2008.01.001_bib52","doi-asserted-by":"crossref","first-page":"1361","DOI":"10.1542\/peds.112.6.1361","article-title":"A novel mutation in the anion exchanger 1 gene is associated with familial distal renal tubular acidosis and nephrocalcinosis","volume":"112","author":"Cheidde","year":"2003","journal-title":"Pediatrics"},{"key":"10.1016\/j.bcmd.2008.01.001_bib53","doi-asserted-by":"crossref","first-page":"6337","DOI":"10.1073\/pnas.95.11.6337","article-title":"Mutations in the chloride\u2013bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis","volume":"95","author":"Karet","year":"1998","journal-title":"Proc. Natl. Acad. Sci. U. S. A."},{"key":"10.1016\/j.bcmd.2008.01.001_bib54","doi-asserted-by":"crossref","first-page":"703","DOI":"10.1042\/bj2560703","article-title":"The complete amino acid sequence of the human erythrocyte membrane anion-transport protein deduced from the cDNA sequence","volume":"256","author":"Tanner","year":"1988","journal-title":"Biochem. J."},{"key":"10.1016\/j.bcmd.2008.01.001_bib55","doi-asserted-by":"crossref","first-page":"987","DOI":"10.1034\/j.1600-0854.2000.011208.x","article-title":"Trafficking and folding defects in hereditary spherocytosis mutants of the human red cell anion exchanger","volume":"1","author":"Quilty","year":"2000","journal-title":"Traffic"},{"key":"10.1016\/j.bcmd.2008.01.001_bib56","doi-asserted-by":"crossref","first-page":"C788","DOI":"10.1152\/ajpcell.00094.2006","article-title":"The human NBCe1-A mutant R881C, associated with proximal renal tubular acidosis, retains function but is mistargeted in polarized renal epithelia","volume":"291","author":"Toye","year":"2006","journal-title":"Am. J. Physiol., Cell Physiol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib57","doi-asserted-by":"crossref","first-page":"3602","DOI":"10.1242\/jcs.03101","article-title":"Ubiquitylation-independent ER-associated degradation of an AE1 mutant associated with dominant hereditary spherocytosis in cattle","volume":"119","author":"Ito","year":"2006","journal-title":"J. Cell Sci."},{"key":"10.1016\/j.bcmd.2008.01.001_bib58","first-page":"1602","article-title":"Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3","volume":"96","author":"Ribeiro","year":"2000","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib59","doi-asserted-by":"crossref","first-page":"4359","DOI":"10.1182\/blood-2005-07-2806","article-title":"The N-terminal 11 amino acids of human erythrocyte band 3 are critical for aldolase binding and protein phosphorylation: implications for band 3 function","volume":"106","author":"Perrotta","year":"2005","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib60","doi-asserted-by":"crossref","first-page":"836","DOI":"10.1038\/355836a0","article-title":"Defective anion transport activity of the abnormal band 3 in hereditary ovalocytic red blood cells","volume":"355","author":"Schofield","year":"1992","journal-title":"Nature"},{"key":"10.1016\/j.bcmd.2008.01.001_bib61","doi-asserted-by":"crossref","first-page":"637","DOI":"10.1053\/beha.1999.0046","article-title":"Erythroid band 3 variants and disease","volume":"12","author":"Bruce","year":"1999","journal-title":"Bailliere's Best Pract. Res. Clin. Haematol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib62","doi-asserted-by":"crossref","first-page":"3311","DOI":"10.1021\/bi011678+","article-title":"Molecular basis and functional consequences of the dominant effects of the mutant band 3 on the structure of normal band 3 in Southeast Asian ovalocytosis","volume":"41","author":"Kuma","year":"2002","journal-title":"Biochemistry"},{"key":"10.1016\/j.bcmd.2008.01.001_bib63","doi-asserted-by":"crossref","first-page":"331","DOI":"10.1016\/j.bcmd.2006.01.008","article-title":"Mutations in band 3 and cation leaky red cells","volume":"36","author":"Bruce","year":"2006","journal-title":"Blood Cells Mol. Diseases"},{"key":"10.1016\/j.bcmd.2008.01.001_bib64","doi-asserted-by":"crossref","first-page":"258","DOI":"10.1016\/S0005-2736(98)00231-4","article-title":"South-east Asian ovalocytic (SAO) erythrocytes have a cold sensitive cation leak: implications for in vitro studies on stored SAO red cells","volume":"1416","author":"Bruce","year":"1999","journal-title":"Biochim. Biophys. Acta"},{"key":"10.1016\/j.bcmd.2008.01.001_bib65","doi-asserted-by":"crossref","first-page":"186","DOI":"10.1016\/0014-5793(93)80270-5","article-title":"The expression of the abnormal human red cell anion transporter from South-East Asian ovalocytes (band 3 SAO) in Xenopus oocytes","volume":"330","author":"Groves","year":"1993","journal-title":"FEBS Lett."},{"key":"10.1016\/j.bcmd.2008.01.001_bib66","doi-asserted-by":"crossref","first-page":"425","DOI":"10.1042\/BJ20051076","article-title":"Trafficking defects of the Southeast Asian ovalocytosis deletion mutant of anion exchanger 1 membrane proteins","volume":"392","author":"Cheung","year":"2005","journal-title":"Biochem. J."},{"key":"10.1016\/j.bcmd.2008.01.001_bib67","doi-asserted-by":"crossref","unstructured":"S. Kittanakom, E. Cordat, R. Reithmeier, Dominant-negative effect of Southeast Asian ovalocytosis anion exchanger 1 in compound heterozygous distal renal tubular acidosis, Biochem. J. in press, doi:10.1042\/BJ20070615.","DOI":"10.1042\/BJ20070615"},{"key":"10.1016\/j.bcmd.2008.01.001_bib68","doi-asserted-by":"crossref","first-page":"1674","DOI":"10.1046\/j.1523-1755.1999.00756.x","article-title":"Autosomal recessive distal renal tubular acidosis associated with Southeast Asian ovalocytosis","volume":"56","author":"Vasuvattakul","year":"1999","journal-title":"Kidney Int."},{"key":"10.1016\/j.bcmd.2008.01.001_bib69","doi-asserted-by":"crossref","first-page":"10","DOI":"10.1046\/j.1523-1755.2002.00417.x","article-title":"Band 3 mutations, distal renal tubular acidosis, and Southeast Asian ovalocytosis","volume":"62","author":"Wrong","year":"2002","journal-title":"Kidney Int."},{"key":"10.1016\/j.bcmd.2008.01.001_bib70","doi-asserted-by":"crossref","first-page":"1151","DOI":"10.1016\/j.biocel.2005.01.002","article-title":"Renal tubular acidosis: developments in our understanding of the molecular basis","volume":"37","author":"Laing","year":"2005","journal-title":"Int. J. Biochem. Cell Biol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib71","doi-asserted-by":"crossref","first-page":"6380","DOI":"10.1074\/jbc.273.11.6380","article-title":"Autosomal dominant distal renal tubular acidosis is associated in three families with heterozygosity for the R589H mutation in the AE1 (band 3) Cl-\/HCO3-exchanger","volume":"273","author":"Jarolim","year":"1998","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.bcmd.2008.01.001_bib72","doi-asserted-by":"crossref","first-page":"21","DOI":"10.1053\/ajkd.2002.33909","article-title":"Autosomal recessive distal renal tubular acidosis caused by G701D mutation of anion exchanger 1 gene","volume":"40","author":"Yenchitsomanus","year":"2002","journal-title":"Am. J. Kidney Dis."},{"key":"10.1016\/j.bcmd.2008.01.001_bib73","doi-asserted-by":"crossref","first-page":"105","DOI":"10.1007\/s00467-002-1018-8","article-title":"Confirmation of the ATP6B1 gene as responsible for distal renal tubular acidosis","volume":"18","author":"Ruf","year":"2003","journal-title":"Pediatr. Nephrol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib74","doi-asserted-by":"crossref","first-page":"71","DOI":"10.1038\/79208","article-title":"Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing","volume":"26","author":"Smith","year":"2000","journal-title":"Nat. Genet."},{"key":"10.1016\/j.bcmd.2008.01.001_bib75","doi-asserted-by":"crossref","first-page":"84","DOI":"10.1038\/5022","article-title":"Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness","volume":"21","author":"Karet","year":"1999","journal-title":"Nat. Genet."},{"key":"10.1016\/j.bcmd.2008.01.001_bib76","doi-asserted-by":"crossref","first-page":"342","DOI":"10.1182\/blood.V99.1.342","article-title":"Band 3 Walton, a C-terminal deletion associated with distal renal tubular acidosis, is expressed in the red cell membrane but retained internally in kidney cells","volume":"99","author":"Toye","year":"2002","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib77","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1038\/ng1082","article-title":"Non-polarized targeting of AE1 causes autosomal dominant distal renal tubular acidosis","volume":"33","author":"Devonald","year":"2003","journal-title":"Nat. Genet."},{"key":"10.1016\/j.bcmd.2008.01.001_bib78","doi-asserted-by":"crossref","first-page":"F1354","DOI":"10.1152\/ajprenal.00015.2006","article-title":"Expression and interaction of two compound heterozygous distal renal tubular acidosis mutants of kidney anion exchanger 1 in epithelial cells","volume":"291","author":"Cordat","year":"2006","journal-title":"Am. J. Physiol. Renal. Physiol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib79","doi-asserted-by":"crossref","first-page":"40960","DOI":"10.1074\/jbc.M405356200","article-title":"Trafficking defects of a novel autosomal recessive distal renal tubular acidosis mutant (S773P) of the human kidney anion exchanger (kAE1)","volume":"279","author":"Kittanakom","year":"2004","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.bcmd.2008.01.001_bib80","doi-asserted-by":"crossref","first-page":"1887","DOI":"10.1021\/bi00550a024","article-title":"Band 3-glycophorin A association in erythrocyte membrane demonstrated by combining protein diffusion measurements with antibody-induced cross-linking","volume":"19","author":"Nigg","year":"1980","journal-title":"Biochemistry"},{"key":"10.1016\/j.bcmd.2008.01.001_bib81","doi-asserted-by":"crossref","first-page":"1881","DOI":"10.1016\/S0006-3495(95)80365-6","article-title":"Loss of rotational mobility of band 3 proteins in human erythrocyte membranes induced by antibodies to glycophorin A","volume":"68","author":"Che","year":"1995","journal-title":"Biophys. J."},{"key":"10.1016\/j.bcmd.2008.01.001_bib82","doi-asserted-by":"crossref","first-page":"1726","DOI":"10.1016\/S0006-3495(94)80965-8","article-title":"Cooperative action between band 3 and glycophorin A in human erythrocytes: immobilization of band 3 induced by antibodies to glycophorin A","volume":"66","author":"Knowles","year":"1994","journal-title":"Biophys. J."},{"key":"10.1016\/j.bcmd.2008.01.001_bib83","doi-asserted-by":"crossref","first-page":"842","DOI":"10.1182\/blood.V76.4.842.842","article-title":"Relationship of the human erythrocyte Wrb antigen to an interaction between glycophorin A and band 3","volume":"76","author":"Telen","year":"1990","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib84","doi-asserted-by":"crossref","first-page":"2146","DOI":"10.1182\/blood.V91.6.2146","article-title":"Complete deficiency of glycophorin A in red blood cells from mice with targeted inactivation of the band 3 (AE1) gene","volume":"91","author":"Hassoun","year":"1998","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib85","doi-asserted-by":"crossref","first-page":"187","DOI":"10.1080\/09687680210141043","article-title":"An N-terminal GFP tag does not alter the functional expression to the plasma membrane of red cell and kidney anion exchanger (AE1) in mammalian cells","volume":"19","author":"Beckmann","year":"2002","journal-title":"Mol. Membr. Biol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib86","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1007\/BF00234488","article-title":"The effects of glycophorin A on the expression of the human red cell anion transporter (band 3) in Xenopus oocytes","volume":"140","author":"Groves","year":"1994","journal-title":"J. Membr. Biol."},{"issue":"Pt 1","key":"10.1016\/j.bcmd.2008.01.001_bib87","doi-asserted-by":"crossref","first-page":"53","DOI":"10.1042\/bj3500053","article-title":"Red-cell glycophorin A\u2013band 3 interactions associated with the movement of band 3 to the cell surface","volume":"350","author":"Young","year":"2000","journal-title":"Biochem. J."},{"key":"10.1016\/j.bcmd.2008.01.001_bib88","doi-asserted-by":"crossref","first-page":"916","DOI":"10.1182\/blood.V84.3.916.916","article-title":"Altered band 3 structure and function in glycophorin A- and B-deficient (MkMk) red blood cells","volume":"84","author":"Bruce","year":"1994","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib89","doi-asserted-by":"crossref","first-page":"31","DOI":"10.3109\/09687689409161027","article-title":"Role of N-glycosylation in the expression of human band 3-mediated anion transport","volume":"11","author":"Groves","year":"1994","journal-title":"Mol. Membr. Biol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib90","doi-asserted-by":"crossref","first-page":"9097","DOI":"10.1074\/jbc.270.16.9097","article-title":"Co-expressed complementary fragments of the human red cell anion exchanger (band 3, AE1) generate stilbene disulfonate-sensitive anion transport","volume":"270","author":"Groves","year":"1995","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.bcmd.2008.01.001_bib91","doi-asserted-by":"crossref","first-page":"541","DOI":"10.1182\/blood.V85.2.541.541","article-title":"Changes in the blood group Wright antigens are associated with a mutation at amino acid 658 in human erythrocyte band 3: a site of interaction between band 3 and glycophorin A under certain conditions","volume":"85","author":"Bruce","year":"1995","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib92","doi-asserted-by":"crossref","first-page":"365","DOI":"10.1111\/j.1744-313X.1984.tb00822.x","article-title":"The Wrb antigen in Sta-positive and Dantu-positive human erythrocytes","volume":"11","author":"Ridgwell","year":"1984","journal-title":"J. Immunogenet."},{"key":"10.1016\/j.bcmd.2008.01.001_bib93","doi-asserted-by":"crossref","first-page":"32954","DOI":"10.1074\/jbc.M302527200","article-title":"Distinct regions of human glycophorin A enhance human red cell anion exchanger (band 3; AE1) transport function and surface trafficking","volume":"278","author":"Young","year":"2003","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.bcmd.2008.01.001_bib94","doi-asserted-by":"crossref","first-page":"4428","DOI":"10.1182\/blood.V92.11.4428","article-title":"Functional cell surface expression of band 3, the human red blood cell anion exchange protein (AE1), in K562 erythroleukemia cells: band 3 enhances the cell surface reactivity of Rh antigens","volume":"92","author":"Beckmann","year":"1998","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib95","doi-asserted-by":"crossref","first-page":"1878","DOI":"10.1182\/blood-2002-03-0706","article-title":"Absence of CD47 in protein 4.2-deficient hereditary spherocytosis in man: an interaction between the Rh complex and the band 3 complex","volume":"100","author":"Bruce","year":"2002","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib96","doi-asserted-by":"crossref","first-page":"338","DOI":"10.1182\/blood-2002-04-1285","article-title":"Evidence that the red cell skeleton protein 4.2 interacts with the Rh membrane complex member CD47","volume":"101","author":"Mouro-Chanteloup","year":"2003","journal-title":"Blood"},{"key":"10.1016\/j.bcmd.2008.01.001_bib97","doi-asserted-by":"crossref","first-page":"485","DOI":"10.1083\/jcb.123.2.485","article-title":"Molecular cloning of integrin-associated protein: an immunoglobulin family member with multiple membrane-spanning domains implicated in alpha v beta 3-dependent ligand binding","volume":"123","author":"Lindberg","year":"1993","journal-title":"J. Cell Biol."},{"key":"10.1016\/j.bcmd.2008.01.001_bib98","doi-asserted-by":"crossref","first-page":"2051","DOI":"10.1126\/science.288.5473.2051","article-title":"Role of CD47 as a marker of self on red blood cells","volume":"288","author":"Oldenborg","year":"2000","journal-title":"Science"},{"issue":"Pt 2","key":"10.1016\/j.bcmd.2008.01.001_bib99","doi-asserted-by":"crossref","first-page":"269","DOI":"10.1042\/bj3390269","article-title":"Transmembrane folding of the human erythrocyte anion exchanger (AE1, Band 3) determined by scanning and insertional N-glycosylation mutagenesis","volume":"339","author":"Popov","year":"1999","journal-title":"Biochem. J."}],"container-title":["Blood Cells, Molecules, and Diseases"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1079979608000028?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1079979608000028?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,21]],"date-time":"2025-10-21T12:24:41Z","timestamp":1761049481000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1079979608000028"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2008,7]]},"references-count":99,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2008,7]]}},"alternative-id":["S1079979608000028"],"URL":"https:\/\/doi.org\/10.1016\/j.bcmd.2008.01.001","relation":{},"ISSN":["1079-9796"],"issn-type":[{"value":"1079-9796","type":"print"}],"subject":[],"published":{"date-parts":[[2008,7]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Glycophorin A: Band 3 aid","name":"articletitle","label":"Article Title"},{"value":"Blood Cells, Molecules, and Diseases","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.bcmd.2008.01.001","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2008 Elsevier Inc. All rights reserved.","name":"copyright","label":"Copyright"}]}}