(Q24296610)

protein dimerization activity

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Joseph Casey

6

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author name string

Gonzalo L Vilas

1

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Sampath K Loganathan

2

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Anita Quon

3

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Periasamy Sundaresan

4

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Eranga N Vithana

Mutational spectrum of SLC4A11 in autosomal recessive CHED in Saudi Arabia

5

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language of work or name

English

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publication date

February 2012

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published in

Human Mutation

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volume

33

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issue

2

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page(s)

419-28

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cites work

1 reference

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Molecular physiology and genetics of Na+-independent SLC4 anion exchangers

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Trafficking defects of the Southeast Asian ovalocytosis deletion mutant of anion exchanger 1 membrane proteins

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Dominant and recessive distal renal tubular acidosis mutations of kidney anion exchanger 1 induce distinct trafficking defects in MDCK cells

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Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome)

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Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy

21 January 2018

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Identification of mutations in the SLC4A11 gene in patients with recessive congenital hereditary endothelial dystrophy

21 January 2018

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Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11

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Genetics of corneal endothelial dystrophies

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Oligomeric structure and minimal functional unit of the electrogenic sodium bicarbonate cotransporter NBCe1-A.

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Analysis of the native quaternary structure of vanilloid receptor 1.

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Trafficking defects of a novel autosomal recessive distal renal tubular acidosis mutant (S773P) of the human kidney anion exchanger (kAE1).

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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

21 January 2018

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Peripheral protein quality control removes unfolded CFTR from the plasma membrane

21 January 2018

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NaBC1 is a ubiquitous electrogenic Na+ -coupled borate transporter essential for cellular boron homeostasis and cell growth and proliferation

21 January 2018

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21 January 2018

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Impaired trafficking of human kidney anion exchanger (kAE1) caused by hetero-oligomer formation with a truncated mutant associated with distal renal tubular acidosis

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Missense mutations in the sodium borate cotransporter SLC4A11 cause late-onset Fuchs corneal dystrophy

21 January 2018

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Signal integration in the endoplasmic reticulum unfolded protein response

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The mammalian unfolded protein response

21 January 2018

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A biochemical framework for SLC4A11, the plasma membrane protein defective in corneal dystrophies

21 January 2018

1 reference

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Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21655

SLC4A11 mutations in Fuchs endothelial corneal dystrophy.

21 January 2018

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Novel topology in C-terminal region of the human plasma membrane anion exchanger, AE1.

21 January 2018

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AE2 anion exchanger polypeptide is a homooligomer in pig gastric membranes: a chemical cross-linking study

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Characterization of an established line of canine kidney cells (MDCK).

21 January 2018

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7 January 2021

Cholate-solubilized erythrocyte glucose transporters exist as a mixture of homodimers and homotetramers

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Differential targeting of facilitative glucose transporters in polarized epithelial cells

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7 January 2021

Novel method for evaluation of the oligomeric structure of membrane proteins

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https://api.crossref.org/works/10.1002%2FHUMU.21655

7 January 2021