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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
9
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pubmed:dateCreated |
1997-11-6
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pubmed:abstractText |
Band 3 (anion exchanger 1, AE1) is one of the most abundant proteins of the erythrocyte membrane. We have previously characterized twenty AE1 gene defects underlying spherocytic haemolytic anaemia with band 3 deficiency. Since AE1 is also expressed in the intercalated cells of renal cortical collecting ducts where it is thought to participate in urine acidification, we asked whether the spherocytogenic AE1 mutations also affect the regulation of urine acidity.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0931-0509
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
12
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1869-73
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9306337-Acidosis,
pubmed-meshheading:9306337-Adolescent,
pubmed-meshheading:9306337-Adult,
pubmed-meshheading:9306337-Aged,
pubmed-meshheading:9306337-Anion Exchange Protein 1, Erythrocyte,
pubmed-meshheading:9306337-Bicarbonates,
pubmed-meshheading:9306337-Erythrocytes,
pubmed-meshheading:9306337-Female,
pubmed-meshheading:9306337-Humans,
pubmed-meshheading:9306337-Hydrogen-Ion Concentration,
pubmed-meshheading:9306337-Kidney Diseases,
pubmed-meshheading:9306337-Kidney Tubules, Distal,
pubmed-meshheading:9306337-Male,
pubmed-meshheading:9306337-Middle Aged,
pubmed-meshheading:9306337-Mutation,
pubmed-meshheading:9306337-Spherocytosis, Hereditary,
pubmed-meshheading:9306337-Sulfates,
pubmed-meshheading:9306337-Urine
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pubmed:year |
1997
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pubmed:articleTitle |
Incomplete distal renal tubular acidosis coinherited with a mutation in the band 3 (AE1) gene.
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pubmed:affiliation |
1st Medical Department, 1st Medical Faculty, Charles University, Praha, Czech Republic.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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