| scholarly article | Q13442814 |
| P2093 | author name string | C. Brugnara | |
| L. L. Peters | |||
| S. E. Lux | |||
| N. Mohandas | |||
| D. E. Golan | |||
| B. Gwynn | |||
| C. M. Cohen | |||
| C. Korsgren | |||
| M. R. Cho | |||
| H. K. Jindel | |||
| K. M. John | |||
| P2860 | cites work | Molecular identification and expression of erythroid K:Cl cotransporter in human and mouse erythroleukemic cells | Q24319039 |
| Structure, function, and molecular genetics of erythroid membrane skeletal protein 4.1 in normal and abnormal red blood cells | Q24321431 | ||
| Identification of the binding interface involved in linkage of cytoskeletal protein 4.1 to the erythrocyte anion exchanger | Q24555678 | ||
| Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 | Q25938983 | ||
| Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction | Q25938986 | ||
| Membrane cation and anion transport activities in erythrocytes of hereditary spherocytosis: effects of different membrane protein defects | Q73585701 | ||
| The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) gene | Q28185427 | ||
| Associations of human erythrocyte band 4.2. Binding to ankyrin and to the cytoplasmic domain of band 3 | Q28285838 | ||
| Molecular basis of altered red blood cell membrane properties in Southeast Asian ovalocytosis: role of the mutant band 3 protein in band 3 oligomerization and retention by the membrane skeleton | Q28304088 | ||
| HPRT-deficient (Lesch-Nyhan) mouse embryos derived from germline colonization by cultured cells | Q28511588 | ||
| Neonatal lethality and lymphopenia in mice with a homozygous disruption of the c-abl proto-oncogene | Q28512170 | ||
| Increased cation permeability in mutant mouse red blood cells with defective membrane skeletons | Q28593687 | ||
| Novel inheritance of the murine severe combined anemia and thrombocytopenia (Scat) phenotype | Q33493704 | ||
| Protein 4.1R-deficient mice are viable but have erythroid membrane skeleton abnormalities | Q33835575 | ||
| Control of band 3 lateral and rotational mobility by band 4.2 in intact erythrocytes: release of band 3 oligomers from low-affinity binding sites | Q34017479 | ||
| Red blood cell glycophorins. | Q35362789 | ||
| The organization of proteins in the human red blood cell membrane. A review | Q36196034 | ||
| Unequal synthesis and differential degradation of alpha and beta spectrin during murine erythroid differentiation | Q36219274 | ||
| Regulation of cell volume by active cation transport in high and low potassium sheep red cells | Q36373788 | ||
| Mechanochemistry of protein 4.1's spectrin-actin-binding domain: ternary complex interactions, membrane binding, network integration, structural strengthening | Q36382643 | ||
| Osmotic gradient ektacytometry: comprehensive characterization of red cell volume and surface maintenance | Q36632392 | ||
| cDNA sequence, gene sequence, and properties of murine pallidin (band 4.2), the protein implicated in the murine pallid mutation | Q36726751 | ||
| Anion exchanger 1 (band 3) is required to prevent erythrocyte membrane surface loss but not to form the membrane skeleton | Q38352938 | ||
| Quantitative aspects of ouabain binding to human erythrocyte and cardiac membranes | Q39747234 | ||
| Red cell membrane protein band 4.2: phenotypic, genetic and electron microscopic aspects | Q40732645 | ||
| The structure and function of band 3 (AE1): recent developments (review). | Q41716122 | ||
| Band 3 Campinas: a novel splicing mutation in the band 3 gene (AE1) associated with hereditary spherocytosis, hyperactivity of Na+/Li+ countertransport and an abnormal renal bicarbonate handling | Q42445253 | ||
| Identification of a 185-kDa band 3-related polypeptide in oxyntic cells | Q42642124 | ||
| Phorbol 12-myristate 13-acetate-stimulated phosphorylation of erythrocyte membrane skeletal proteins is blocked by calpain inhibitors: possible role of protein kinase M. | Q42832033 | ||
| Complete deficiency of glycophorin A in red blood cells from mice with targeted inactivation of the band 3 (AE1) gene. | Q44551176 | ||
| Selective modulation of band 4.1 binding to erythrocyte membranes by protein kinase C. | Q45691888 | ||
| A volume-sensitive protein kinase regulates the Na-K-2Cl cotransporter in duck red blood cells. | Q46019445 | ||
| Endothelial Na-K-Cl cotransport regulation by tonicity and hormones: phosphorylation of cotransport protein | Q46503826 | ||
| Defective anion transport activity of the abnormal band 3 in hereditary ovalocytic red blood cells | Q47858863 | ||
| Lateral mobility of integral membrane proteins is increased in spherocytic erythrocytes. | Q50718325 | ||
| Charybdotoxin blocks with high affinity the Ca-activated K+ channel of Hb A and Hb S red cells: individual differences in the number of channels. | Q54119598 | ||
| Ouabain binding and potassium transport in young and old populations of human red cells | Q67460706 | ||
| Localization of the protein 4.1-binding site on the cytoplasmic domain of erythrocyte membrane band 3 | Q67896407 | ||
| Platelet storage pool deficiency associated with inherited abnormalities of the inner ear in the mouse pigment mutants muted and mocha | Q68002368 | ||
| A role for band 4.2 in human erythrocyte band 3 mediated anion transport | Q70480522 | ||
| Regulation by cell volume of Na(+)-K(+)-2Cl- cotransport in vascular endothelial cells: role of protein phosphorylation | Q70712668 | ||
| Specific loss of protein kinase activities in senescent erythrocytes | Q71228962 | ||
| Na(+)-K(+)-2Cl- cotransport, Na+/H+ exchange, and cell volume in ferret erythrocytes | Q71836364 | ||
| Modulation of band 3-ankyrin interaction by protein 4.1. Functional implications in regulation of erythrocyte membrane mechanical properties | Q71903321 | ||
| Combined spectrin and ankyrin deficiency is common in autosomal dominant hereditary spherocytosis | Q72553891 | ||
| Modulation of erythrocyte membrane mechanical function by beta-spectrin phosphorylation and dephosphorylation | Q72631480 | ||
| The gene encoding protein 4.2 is distinct from the mouse platelet storage pool deficiency mutation pallid | Q73470692 | ||
| Red cell membranes of ankyrin-deficient nb/nb mice lack band 3 tetramers but contain normal membrane skeletons | Q73542042 | ||
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | spherocytosis | Q11181178 |
| Erythrocyte membrane protein band 4.2 | Q14908159 | ||
| P304 | page(s) | 1527–1537 | |
| P577 | publication date | 1999-06-01 | |
| P1433 | published in | Journal of Clinical Investigation | Q3186904 |
| P1476 | title | Mild spherocytosis and altered red cell ion transport in protein 4. 2-null mice | |
| P478 | volume | 103 |
| Q35945988 | An 11-amino acid beta-hairpin loop in the cytoplasmic domain of band 3 is responsible for ankyrin binding in mouse erythrocytes. |
| Q33517864 | An experimental assessment of in silico haplotype association mapping in laboratory mice |
| Q33706340 | Analysis of novel sph (spherocytosis) alleles in mice reveals allele-specific loss of band 3 and adducin in alpha-spectrin-deficient red cells |
| Q30505416 | Analysis of the mobilities of band 3 populations associated with ankyrin protein and junctional complexes in intact murine erythrocytes |
| Q30484232 | Characterization of glycolytic enzyme interactions with murine erythrocyte membranes in wild-type and membrane protein knockout mice |
| Q33554484 | Chemical crosslinking studies with the mouse Kcc1 K-Cl cotransporter |
| Q44588845 | Comparative proteomics reveals deficiency of NHE-1 (Slc9a1) in RBCs from the beta-adducin knockout mouse model of hemolytic anemia |
| Q30658984 | Comparative proteomics reveals deficiency of SLC9A1 (sodium/hydrogen exchanger NHE1) in β-adducin null red cells |
| Q35995237 | Concomitant inactivation of Rb and E2f8 in hematopoietic stem cells synergizes to induce severe anemia |
| Q46700067 | DNA methylation in promoter regions of red cell membrane protein genes in healthy individuals and patients with hereditary membrane disorders |
| Q47670415 | Deficient HCO3- transport in an AE1 mutant with normal Cl- transport can be rescued by carbonic anhydrase II presented on an adjacent AE1 protomer |
| Q35848022 | Evidence for a protective role of the Gardos channel against hemolysis in murine spherocytosis |
| Q30377355 | Fluorescence assay of the interaction between hemoglobin and the cytoplasmic domain of erythrocyte membrane band 3. |
| Q35099188 | Formation of mammalian erythrocytes: chromatin condensation and enucleation |
| Q42025646 | Genome-wide identification of TAL1's functional targets: insights into its mechanisms of action in primary erythroid cells |
| Q47684174 | Hereditary Red Cell Membrane Disorders in Japan: Their Genotypic and Phenotypic Features in 1014 Cases Studied |
| Q35923578 | Hereditary haemolytic anaemias: unexpected sequelae of mutations in the genes for erythroid membrane skeletal proteins |
| Q36138840 | Identification of a TAL1 Target Gene Reveals a Positive Role for the LIM Domain-Binding Protein Ldb1 in Erythroid Gene Expression and Differentiation |
| Q46378605 | Interactions of recombinant mouse erythrocyte transglutaminase with membrane skeletal proteins |
| Q34560911 | Ion transport proteins anchor and regulate the cytoskeleton |
| Q42506665 | K-Cl cotransport in red blood cells from patients with KCC3 isoform mutants |
| Q41904633 | Mapping of a spectrin-binding domain of human erythrocyte membrane protein 4.2. |
| Q27230075 | Merozoite surface protein 1 recognition of host glycophorin A mediates malaria parasite invasion of red blood cells |
| Q35577800 | Modularity of CHIP/LDB transcription complexes regulates cell differentiation |
| Q37151198 | Novel roles for erythroid Ankyrin-1 revealed through an ENU-induced null mouse mutant |
| Q36947418 | Parathyroid hormone ablation alters erythrocyte parameters that are rescued by calcium-sensing receptor gene deletion. |
| Q33717604 | Protein 4.2 binds to the carboxyl-terminal EF-hands of erythroid alpha-spectrin in a calcium- and calmodulin-dependent manner |
| Q41265637 | Reduced DIDS-sensitive chloride conductance in Ae1-/- mouse erythrocytes. |
| Q36042361 | Regulation of K-Cl cotransport: from function to genes |
| Q34136096 | Spectrin: the ghost in the machine |
| Q55411797 | Squeezing for Life - Properties of Red Blood Cell Deformability. |
| Q36850738 | Strain-specific variations in cation content and transport in mouse erythrocytes |
| Q28585644 | Targeted deletion of alpha-adducin results in absent beta- and gamma-adducin, compensated hemolytic anemia, and lethal hydrocephalus in mice |
| Q28512479 | The carboxyterminal EF domain of erythroid alpha-spectrin is necessary for optimal spectrin-actin binding |
| Q37478093 | The role of hypoxia in 2-butoxyethanol-induced hemangiosarcoma. |
| Q33707936 | Transglutaminase regulation of cell function. |
| Q24534936 | Transglutaminases: nature's biological glues |
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