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index medicus (72) 72
humans (63) 63
animals (46) 46
anion exchange protein 1, erythrocyte - genetics (41) 41
anion exchange protein 1, erythrocyte - metabolism (37) 37
distal renal tubular acidosis (31) 31
renal tubular-acidosis (31) 31
biochemistry & molecular biology (30) 30
autosomal-dominant (28) 28
mutation (27) 27
anion exchanger 1 (25) 25
acidosis, renal tubular - genetics (23) 23
cell biology (21) 21
cell line (21) 21
physiology (21) 21
urology & nephrology (21) 21
band-3 (20) 20
cells (18) 18
ae1 (17) 17
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kidney - metabolism (16) 16
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anion-exchanger kae1 (15) 15
male (15) 15
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hereditary spherocytosis (14) 14
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trafficking (14) 14
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membrane proteins (13) 13
southeast-asian ovalocytosis (13) 13
anion exchanger (12) 12
cl-/hco3-exchanger (12) 12
kidney (12) 12
amino acid sequence (11) 11
anion exchange protein 1, erythrocyte - chemistry (11) 11
epithelial-cells (11) 11
gene expression (11) 11
glycophorin-a (11) 11
h+-atpase (11) 11
kidneys (11) 11
plasma-membrane (11) 11
acidosis (10) 10
cell membrane - metabolism (10) 10
gene (10) 10
hek293 cells (10) 10
intercalated cells (10) 10
membrane (10) 10
protein binding (10) 10
bicarbonates - metabolism (9) 9
cytoplasmic domain (9) 9
kidney anion exchanger 1 (9) 9
pedigree (9) 9
protein transport (9) 9
biophysics (8) 8
carbonic-anhydrase-ii (8) 8
collecting duct (8) 8
hydrogen-ion concentration (8) 8
mutations (8) 8
physiological aspects (8) 8
proteins (8) 8
southeast asian ovalocytosis (8) 8
trafficking defects (8) 8
anion transport proteins - metabolism (7) 7
asian ovalocytosis (7) 7
binding-site (7) 7
intracellular ph (7) 7
kidney anion-exchanger-1 (7) 7
molecular sequence data (7) 7
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slc4a1 (7) 7
vacuolar h+-atpase (7) 7
amino acid substitution (6) 6
antiporters - metabolism (6) 6
band-3 protein (6) 6
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analysis (5) 5
anion transport proteins - genetics (5) 5
antiporters - genetics (5) 5
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Molecular Membrane Biology, ISSN 0968-7688, 02/2017, Volume 34, Issue 1-2, pp. 50 - 64
Mutations in the gene encoding the kidney anion exchanger 1 (kAE1) can lead to distal renal tubular acidosis (dRTA). dRTA mutations reported within the... 
membrane protein | endocytosis | recycling | epithelium | adaptor proteins | trafficking | distal renal tubular acidosis | Kidney | MDCK CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CARBONIC-ANHYDRASE II | TUBULAR-ACIDOSIS | PLASMA-MEMBRANE | HUMAN KIDNEY | CELL BIOLOGY | BINDING-SITE | ANION-EXCHANGER 1 | AUTOSOMAL-DOMINANT | ERYTHROID AE1 | SORTING SIGNALS
Journal Article
Clinical Kidney Journal, ISSN 2048-8505, 02/2017, Volume 10, Issue 1, pp. 135 - 140
Distal renal tubular acidosis caused by missense mutations in kidney isoform of anion exchanger 1 (kAE1/SLC4A1), the basolateral membrane Cl-/HCO3- exchanger... 
KAE1 | Genetics | Distal renal tubular acidosis | Slc4a1 | Kidney isoform of anion exchanger 1 | CL-/HCO3-EXCHANGER | BAND-3 | kidney isoform of anion exchanger 1 | slc4a1 | ANION-EXCHANGER AE2 | TRAFFICKING | distal renal tubular acidosis | genetics | kAE1 | GENE | MUTATION | UROLOGY & NEPHROLOGY | AUTOSOMAL-DOMINANT | H+-ATPASE | POLARIZED EPITHELIAL-CELLS | SUBUNIT | Genetic Diseases
Journal Article
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 2006, Volume 350, Issue 3, pp. 723 - 730
Journal Article
Nephron, ISSN 1660-8151, 03/2019, Volume 141, Issue 3, pp. 207 - 212
Hereditary forms of distal renal tubular acidosis (dRTA) are rare and mainly caused by mutations in ATP6V1B1, ATP6V0A4 and SLC4A1. About 20 mutations in SLC4A1... 
Experimental Nephrology and Genetics: Case Study of Genetic Interest | Hypokalemia | Case report | Distal renal tubular acidosis | Inherited | Anion exchanger 1 | MUTANT | KAE1 | BAND-3 | TRAFFICKING DEFECTS | SLC4A1 | AE1 | TRANSPORT | GENE | ANION-EXCHANGER-1 | UROLOGY & NEPHROLOGY | SPHEROCYTOSIS
Journal Article
Human Mutation, ISSN 1059-7794, 02/2012, Volume 33, Issue 2, pp. 419 - 428
Journal Article
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, ISSN 0006-291X, 10/2010, Volume 401, Issue 1, pp. 85 - 91
Kidney anion exchanger 1 (kAE1) mediates chloride (Cl-) and bicarbonate (HCO3-) exchange at the basolateral membrane of kidney alpha-intercalated cells.... 
KAE1 | CELLS | Band 3 | Distal renal tubular acidosis | Protein-protein interaction | MEMBRANE | BIOCHEMISTRY & MOLECULAR BIOLOGY | Kidney anion exchanger 1 | AE1 | BIOPHYSICS | GENE | IMPAIRED TRAFFICKING | AUTOSOMAL-DOMINANT | RENAL TUBULAR-ACIDOSIS | MUTATIONS | DRTA | Adaptor-related protein complex 1 mu1A | Protein trafficking
Journal Article
Biochemical Journal, ISSN 0264-6021, 12/2005, Volume 392, Issue 3, pp. 425 - 434
Human AE1 (anion exchanger 1) is a membrane glycoprotein found in erythrocytes and as a truncated form (kAE1) in the BLM (basolateral membrane) of... 
Anion exchanger 1 (AE1) | Membrane protein | Southeast Asian ovalocytosis (SAO) | Distal renal tubular acidosis (dRTA) | Kidney | CARBONIC-ANHYDRASE | distal renal tubular acidosis (dRTA) | BIOCHEMISTRY & MOLECULAR BIOLOGY | HEREDITARY SPHEROCYTOSIS | kidney | GLYCOPHORIN-A | ERYTHROCYTE BAND-3 | anion exchanger 1 (AE1) | IMPAIRED TRAFFICKING | membrane protein | XENOPUS-OOCYTES | ANION-EXCHANGER KAE1 | RED-BLOOD-CELLS | RENAL TUBULAR-ACIDOSIS | BAND-3 PROTEIN | Cell Line | Mutagenesis, Site-Directed | Humans | Elliptocytosis, Hereditary - genetics | Gene Expression Regulation | Anion Exchange Protein 1, Erythrocyte - chemistry | Mutation - genetics | Protein Transport | Asia, Southeastern | Animals | Elliptocytosis, Hereditary - metabolism | Anion Exchange Protein 1, Erythrocyte - metabolism | Gene Deletion | Dogs | Protein Structure, Quaternary | Anion Exchange Protein 1, Erythrocyte - genetics | Dimerization | Index Medicus | MDCK, Madin–Darby canine kidney | kAE1, anion exchanger 1 (kidney isoform) | CFTR, cystic fibrosis transmembrane conductance regulator | HEK-293, human embryonic kidney | EndoH, endoglycosidase H | VSVG, vesicular stomatitis virus glycoprotein | GPA, glycophorin A | DMEM, Dulbecco's modified Eagle's medium | TM, transmembrane segment | GAPDH, glyceraldehyde-3-phosphate dehydrogenase | dRTA, distal renal tubular acidosis | C12E8, octa(ethylene glycol) dodecyl ether | HS, hereditary spherocytosis | HA, haemagglutinin | AE1, anion exchanger 1 (erythroid isoform) | PNGase F, peptide N-glycosidase F | BLM, basolateral membrane | CNX, calnexin | NHS-SS-biotin, sulpho-succinimidyl 2-(biotin-amido)ethyl-1,3-dithiopropionate | ER, endoplasmic reticulum | SAO, Southeast Asian ovalocytosis
Journal Article
Journal Article