Impaired trafficking of human kidney anion exchanger (kAE1) caused by hetero-oligomer formation with a truncated mutant associated with distal renal tubular acidosis.
about
Oligomerization of SLC4A11 protein and the severity of FECD and CHED2 corneal dystrophies caused by SLC4A11 mutationsA novel missense mutation in AE1 causing autosomal dominant distal renal tubular acidosis retains normal transport function but is mistargeted in polarized epithelial cellsKidney stone disease.Defective membrane expression of the Na(+)-HCO(3)(-) cotransporter NBCe1 is associated with familial migraineNBCe1A dimer assemble visualized by bimolecular fluorescence complementationIncomplete distal renal tubular acidosis from a heterozygous mutation of the V-ATPase B1 subunit.Unraveling trafficking of the kidney anion exchanger 1 in polarized MDCK epithelial cells.Inherited renal acidoses.A new class of endoplasmic reticulum export signal PhiXPhiXPhi for transmembrane proteins and its selective interaction with Sec24CMolecular mechanisms of autosomal dominant and recessive distal renal tubular acidosis caused by SLC4A1 (AE1) mutations.PDLIM5 links kidney anion exchanger 1 (kAE1) to ILK and is required for membrane targeting of kAE1.Mis-trafficking of bicarbonate transporters: implications to human diseases.Trafficking defects of a novel autosomal recessive distal renal tubular acidosis mutant (S773P) of the human kidney anion exchanger (kAE1).The carboxyl-terminally truncated kidney anion exchanger 1 R901X dRTA mutant is unstable at the plasma membrane.Degradation mechanism of a Golgi-retained distal renal tubular acidosis mutant of the kidney anion exchanger 1 in renal cells.Misfolded endoplasmic reticulum retained subunits cause degradation of wild-type subunits of arylsulfatase A heteromers.Cell surface rescue of kidney anion exchanger 1 mutants by disruption of chaperone interactions.Band 3 Edmonton I, a novel mutant of the anion exchanger 1 causing spherocytosis and distal renal tubular acidosis.Effect of block deletions in the C-terminus on the functional expression of human anion exchanger 1 (AE1).Expression and interaction of two compound heterozygous distal renal tubular acidosis mutants of kidney anion exchanger 1 in epithelial cells.Trafficking defects of the Southeast Asian ovalocytosis deletion mutant of anion exchanger 1 membrane proteins.Palmitoylation is not required for trafficking of human anion exchanger 1 to the cell surface.Renal peroxiredoxin 6 interacts with anion exchanger 1 and plays a novel role in pH homeostasis.Carboxyl-terminal truncations of human anion exchanger impair its trafficking to the plasma membrane.Identification of dominant negative effect of L522P mutation in the electrogenic Na⁺-HCO₃⁻ cotransporter NBCe1.Deficient HCO3- transport in an AE1 mutant with normal Cl- transport can be rescued by carbonic anhydrase II presented on an adjacent AE1 protomer.Role of adaptor proteins and clathrin in the trafficking of human kidney anion exchanger 1 (kAE1) to the cell surface.
P2860
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P2860
Impaired trafficking of human kidney anion exchanger (kAE1) caused by hetero-oligomer formation with a truncated mutant associated with distal renal tubular acidosis.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
2002年论文
@zh
2002年论文
@zh-cn
name
Impaired trafficking of human ...... distal renal tubular acidosis.
@en
type
label
Impaired trafficking of human ...... distal renal tubular acidosis.
@en
prefLabel
Impaired trafficking of human ...... distal renal tubular acidosis.
@en
P2093
P2860
P356
P1433
P1476
Impaired trafficking of human ...... distal renal tubular acidosis.
@en
P2093
Emmanuelle Cordat
Janne A Quilty
Reinhart A F Reithmeier
P2860
P304
P356
10.1042/BJ20020574
P407
P577
2002-12-01T00:00:00Z