SLC4A1 gene

Known as: SW, FR, Froese blood group 
This gene plays a role in carbon dioxide transport from tissues to lungs.
National Institutes of Health

Papers overview

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2013
2013
AE1 mediates electroneutral 1:1 exchange of bicarbonate for chloride across the plasma membrane of erythrocytes and type A cells… (More)
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2013
2013
The anion exchanger 1 (AE1), a member of bicarbonate transporter family SLC4, mediates an electroneutral chloride/bicarbonate… (More)
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2009
2009
Southeast Asian ovalocytosis (SAO) is an erythrocyte abnormality that protects affected individuals from cerebral malaria. This… (More)
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2007
2007
Mutations in the human gene that encodes the AE1 Cl(-)/HCO(3)(-) exchanger (SLC4A1) cause autosomal recessive and dominant forms… (More)
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2004
2004
BACKGROUND Mutations in the SLC4A1 gene have been found to cause either autosomal dominant (AD) or autosomal recessive (AR… (More)
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2002
2002
Autosomal dominant distal renal tubular acidosis (dRTA) has been associated with several mutations in the anion exchanger AE1… (More)
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Highly Cited
2002
Highly Cited
2002
Cytosolic carbonic anhydrase II (CAII) and the cytoplasmic C-terminal tails of chloride/bicarbonate anion exchange (AE) proteins… (More)
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2000
2000
Hereditary spherocytosis (HS) is a common inherited hemolytic anemia caused by mutations in erythrocyte proteins including the… (More)
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1999
1999
alphaIIbb3 integrin is a heterodimeric receptor facilitating platelet aggregation. Both genes are on chromosome 17q21.32… (More)
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1993
1993
We report the genetic identification, molecular cloning, and characterization of a dominant mutant at the amylose extender1 locus… (More)
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