| scholarly article | Q13442814 |
| P356 | DOI | 10.1182/BLOOD.V99.1.342 |
| P698 | PubMed publication ID | 11756190 |
| P50 | author | Lesley J Bruce | Q40761032 |
| Ashley M Toye | Q61118603 | ||
| P2093 | author name string | Robert J Unwin | |
| Michael J A Tanner | |||
| Oliver Wrong | |||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | renal tubular acidosis | Q1516211 |
| distal renal tubular acidosis | Q2896802 | ||
| P304 | page(s) | 342-347 | |
| P577 | publication date | 2002-01-01 | |
| P1433 | published in | Blood | Q885070 |
| P1476 | 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 | |
| P478 | volume | 99 |
| Q36947880 | A new class of endoplasmic reticulum export signal PhiXPhiXPhi for transmembrane proteins and its selective interaction with Sec24C |
| Q42853667 | A novel SLC4A1 variant in an autosomal dominant distal renal tubular acidosis family with a severe phenotype |
| Q24305531 | A novel missense mutation in AE1 causing autosomal dominant distal renal tubular acidosis retains normal transport function but is mistargeted in polarized epithelial cells |
| Q24338331 | A substrate access tunnel in the cytosolic domain is not an essential feature of the solute carrier 4 (SLC4) family of bicarbonate transporters |
| Q37860148 | Anion exchanger 1 in red blood cells and kidney: Band 3's in a pod. |
| Q34455334 | Anion exchanger 1 interacts with nephrin in podocytes |
| Q46624401 | As2O3 enhances the anion transport activity of band 3 and the action is related with the C-terminal 16 residues of the protein |
| Q47120898 | Asymmetry of inverted-topology repeats in the AE1 anion exchanger suggests an elevator-like mechanism. |
| Q37019944 | Band 3 Courcouronnes (Ser667Phe): a trafficking mutant differentially rescued by wild-type band 3 and glycophorin A. |
| Q39760186 | Band 3 Edmonton I, a novel mutant of the anion exchanger 1 causing spherocytosis and distal renal tubular acidosis. |
| Q44545325 | Carboxyl-terminal truncations of human anion exchanger impair its trafficking to the plasma membrane |
| Q39680622 | Cell surface rescue of kidney anion exchanger 1 mutants by disruption of chaperone interactions |
| 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 |
| Q31157467 | Direct interaction and cooperative role of tumor suppressor p16 with band 3 (AE1). |
| Q40142123 | Effect of block deletions in the C-terminus on the functional expression of human anion exchanger 1 (AE1). |
| Q28573248 | Glyceraldehyde 3-phosphate dehydrogenase is required for band 3 (anion exchanger 1) membrane residency in the mammalian kidney |
| Q35923578 | Hereditary haemolytic anaemias: unexpected sequelae of mutations in the genes for erythroid membrane skeletal proteins |
| Q39656914 | Human kidney anion exchanger 1 interacts with adaptor-related protein complex 1 μ1A (AP-1 mu1A) |
| Q40531923 | Identification of a carboxyl-terminal motif essential for the targeting of Na+-HCO-3 cotransporter NBC1 to the basolateral membrane |
| Q40704496 | Impaired trafficking of human kidney anion exchanger (kAE1) caused by hetero-oligomer formation with a truncated mutant associated with distal renal tubular acidosis |
| Q36844436 | Inherited renal acidoses. |
| Q37860156 | Mis-trafficking of bicarbonate transporters: implications to human diseases |
| Q40457704 | Missense mutations in Na+:HCO3- cotransporter NBC1 show abnormal trafficking in polarized kidney cells: a basis of proximal renal tubular acidosis. |
| Q37241873 | Molecular mechanisms of autosomal dominant and recessive distal renal tubular acidosis caused by SLC4A1 (AE1) mutations |
| Q36050939 | Mutation conferring apical-targeting motif on AE1 exchanger causes autosomal dominant distal RTA. |
| Q24293024 | Non-polarized targeting of AE1 causes autosomal dominant distal renal tubular acidosis |
| Q34658988 | Nonsense-mediated decay in genetic disease: friend or foe? |
| Q36498954 | Nonsense-mediated mRNA decay modulates clinical outcome of genetic disease |
| Q34160435 | Novel topology in C-terminal region of the human plasma membrane anion exchanger, AE1. |
| Q37412431 | Regulated acid-base transport in the collecting duct |
| Q36436532 | Regulation of AE2-mediated Cl- transport by intracellular or by extracellular pH requires highly conserved amino acid residues of the AE2 NH2-terminal cytoplasmic domain |
| Q37216871 | RhCG is the major putative ammonia transporter expressed in the human kidney, and RhBG is not expressed at detectable levels. |
| Q53059447 | Role of adaptor proteins and clathrin in the trafficking of human kidney anion exchanger 1 (kAE1) to the cell surface. |
| Q38785677 | The carboxyl-terminally truncated kidney anion exchanger 1 R901X dRTA mutant is unstable at the plasma membrane |
| Q41836732 | The crystal structure of the regulatory domain of the human sodium-driven chloride/bicarbonate exchanger. |
| Q30440948 | The divergence, actions, roles, and relatives of sodium-coupled bicarbonate transporters |
| Q40278577 | The human NBCe1-A mutant R881C, associated with proximal renal tubular acidosis, retains function but is mistargeted in polarized renal epithelia |
| Q38338952 | Trafficking defects of a novel autosomal recessive distal renal tubular acidosis mutant (S773P) of the human kidney anion exchanger (kAE1). |
| Q36704530 | Unraveling trafficking of the kidney anion exchanger 1 in polarized MDCK epithelial cells |
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