| 701248 |
Orientation of the band 3 polypeptide from human erythrocyte membranes. Identification of NH2-terminal sequence and site of carbohydrate attachment. |
| 1352774 |
Anion-proton cotransport through the human red blood cell band 3 protein. Role of glutamate 681. |
| 1378323 |
Band 3 Tuscaloosa: Pro-327-->Arg substitution in the cytoplasmic domain of erythrocyte band 3 protein associated with spherocytic hemolytic anemia and partial deficiency of protein 4.2. |
| 1527044 |
A structural study of the membrane domain of band 3 by tryptic digestion. Conformational change of band 3 in situ induced by alkali treatment. |
| 1538405 |
Basis of unique red cell membrane properties in hereditary ovalocytosis. |
| 1678289 |
Human erythrocyte band 3 polymorphism (band 3 Memphis): characterization of the structural modification (Lys 56-->Glu) by protein chemistry methods. |
| 1722314 |
Deletion in erythrocyte band 3 gene in malaria-resistant Southeast Asian ovalocytosis. |
| 1885574 |
Palmitoylation of cysteine 69 from the COOH-terminal of band 3 protein in the human erythrocyte membrane. Acylation occurs in the middle of the consensus sequence of F--I-IICLAVL found in band 3 protein and G2 protein of Rift Valley fever virus. |
| 1998697 |
Phosphorylation sites in human erythrocyte band 3 protein. |
| 2594752 |
Cloning and characterization of band 3, the human erythrocyte anion-exchange protein (AE1). |
| 2790053 |
Primary structure of the cytoplasmic domain of human erythrocyte protein band 3. Comparison with its sequence in the mouse. |
| 3223947 |
The complete amino acid sequence of the human erythrocyte membrane anion-transport protein deduced from the cDNA sequence. |
| 3372523 |
Localization of the pyridoxal phosphate binding site at the COOH-terminal region of erythrocyte band 3 protein. |
| 6345535 |
Amino acid sequence of the N alpha-terminal 201 residues of human erythrocyte membrane band 3. |
| 6615451 |
The human erythrocyte anion-transport protein. Partial amino acid sequence, conformation and a possible molecular mechanism for anion exchange. |
| 7506871 |
Anion exchanger 1 in human kidney and oncocytoma differs from erythroid AE1 in its NH2 terminus. |
| 7530501 |
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. |
| 7665627 |
The ANK repeats of erythrocyte ankyrin form two distinct but cooperative binding sites for the erythrocyte anion exchanger. |
| 7812009 |
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. |
| 8045253 |
Three-dimensional map of the dimeric membrane domain of the human erythrocyte anion exchanger, Band 3. |
| 8168533 |
The solution structures of the first and second transmembrane-spanning segments of band 3. |
| 8206915 |
Band 3 Memphis variant II. Altered stilbene disulfonate binding and the Diego (Dia) blood group antigen are associated with the human erythrocyte band 3 mutation Pro-854-->Leu. |
| 8343110 |
Band 3 HT, a human red-cell variant associated with acanthocytosis and increased anion transport, carries the mutation Pro-868-->Leu in the membrane domain of band 3. |
| 8471774 |
Human erythrocyte protein 4.2 deficiency associated with hemolytic anemia and a homozygous 40 glutamic acid-->lysine substitution in the cytoplasmic domain of band 3 (band 3Montefiore). |
| 8508760 |
Two-dimensional structure of the membrane domain of human band 3, the anion transport protein of the erythrocyte membrane. |
| 8527430 |
Solution structure of a band 3 peptide inhibitor bound to aldolase: a proposed mechanism for regulating binding by tyrosine phosphorylation. |
| 8547122 |
Band 3 Chur: a variant associated with band 3-deficient hereditary spherocytosis and substitution in a highly conserved position of transmembrane segment 11. |
| 8640229 |
Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis. |
| 8943874 |
Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency. |
| 9012689 |
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. |
| 9191821 |
Blood group antigens Rb(a), Tr(a), and Wd(a) are located in the third ectoplasmic loop of erythroid band 3. |
| 9207478 |
Modulation of clinical expression and band 3 deficiency in hereditary spherocytosis. |
| 9233560 |
Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects. |
| 9312167 |
Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene. |
| 9454576 |
Insights into tyrosine phosphorylation control of protein-protein association from the NMR structure of a band 3 peptide inhibitor bound to glyceraldehyde-3-phosphate dehydrogenase. |
| 9600966 |
Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis. |
| 9709005 |
NMR solution structure of a cytoplasmic surface loop of the human red cell anion transporter, band 3. |
| 9709782 |
A Gly565-->Ala substitution in human erythroid band 3 accounts for the Wu blood group polymorphism. |
| 9765907 |
Studies on the structure of a transmembrane region and a cytoplasmic loop of the human red cell anion exchanger. |
| 9845551 |
Characterization of seven low incidence blood group antigens carried by erythrocyte band 3 protein. |
| 9854053 |
Novel AE1 mutations in recessive distal renal tubular acidosis: loss-of-function is rescued by glycophorin A. |
| 9973643 |
Band 3 Tokyo: Thr837-->Ala837 substitution in erythrocyte band 3 protein associated with spherocytic hemolysis. |
| 10580570 |
Arginine 490 is a hot spot for mutation in the band 3 gene in hereditary spherocytosis. |
| 10738034 |
Amino acid substitutions in human erythroid protein band 3 account for the low-incidence antigens NFLD and BOW. |
| 10745622 |
Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population. |
| 10861210 |
Processing of N-linked oligosaccharide depends on its location in the anion exchanger, AE1, membrane glycoprotein. |
| 10926824 |
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. |
| 10942405 |
Sequential phosphorylation of protein band 3 by Syk and Lyn tyrosine kinases in intact human erythrocytes: identification of primary and secondary phosphorylation sites. |
| 10942416 |
Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3. |
| 11049968 |
Crystallographic structure and functional interpretation of the cytoplasmic domain of erythrocyte membrane band 3. |
| 11061863 |
An amino acid substitution in the putative second extracellular loop of RBC band 3 accounts for the Froese blood group polymorphism. |
| 11155072 |
Distinctive Swann blood group genotypes: molecular investigations. |
| 11208088 |
Trafficking and folding defects in hereditary spherocytosis mutants of the human red cell anion exchanger. |
| 11380459 |
Band 3 Cape Town (E90K) causes severe hereditary spherocytosis in combination with band 3 Prague III. |
| 14734552 |
A novel missense mutation in AE1 causing autosomal dominant distal renal tubular acidosis retains normal transport function but is mistargeted in polarized epithelial cells. |
| 15211439 |
Novel compound heterozygous SLC4A1 mutations in Thai patients with autosomal recessive distal renal tubular acidosis. |
| 15489334 |
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |
| 15813913 |
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. |
| 16227998 |
Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1. |
| 16252102 |
Recessive distal renal tubular acidosis in Sarawak caused by AE1 mutations. |
| 20151848 |
Impaired trafficking and intracellular retention of mutant kidney anion exchanger 1 proteins (G701D and A858D) associated with distal renal tubular acidosis. |
| 21269460 |
Initial characterization of the human central proteome. |
| 21849667 |
Loss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65S. |
| 23219802 |
Stomatin interacts with GLUT1/SLC2A1, band 3/SLC4A1, and aquaporin-1 in human erythrocyte membrane domains. |
| 24121512 |
A substrate access tunnel in the cytosolic domain is not an essential feature of the solute carrier 4 (SLC4) family of bicarbonate transporters. |
| 24275569 |
An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome. |
| 26049106 |
Transmembrane protein 139 (TMEM139) interacts with human kidney isoform of anion exchanger 1 (kAE1). |
| 26542571 |
Crystal structure of the anion exchanger domain of human erythrocyte band 3. |
