Regulation of pendrin by pH: dependence on glycosylation

A Azroyan, K Laghmani, G Crambert… - Biochemical …, 2011 - portlandpress.com
Mutations in the anion exchanger pendrin are responsible for Pendred syndrome, an
autosomal recessive disease characterized by deafness and goitre. Pendrin is highly …
被引用次数：47 相关文章
[PDF] researchgate.net

[PDF][PDF] REGULATION OF PENDRIN BY pH: DEPENDENCE ON GLYCOSYLATION

A Azroyan, K Laghmani, G Crambert, D Mordasini… - 2010 - researchgate.net
Mutations of the anion exchanger pendrin are responsible for Pendred syndrome, an
autosomal recessive disease characterized by deafness and goiter. Pendrin is highly …

Regulation of pendrin by pH: dependence on glycosylation.

A Azroyan, K Laghmani, G Crambert… - The Biochemical …, 2011 - europepmc.org
Mutations in the anion exchanger pendrin are responsible for Pendred syndrome, an
autosomal recessive disease characterized by deafness and goitre. Pendrin is highly …

[引用][C] Regulation of pendren by pH: dependence on glycosylation

A AZROYAN - Biochem J, 2011 - cir.nii.ac.jp

Regulation of pendrin by pH: dependence on glycosylation

A Azroyan, K Laghmani, G Crambert… - The Biochemical …, 2011 - pubmed.ncbi.nlm.nih.gov
Mutations in the anion exchanger pendrin are responsible for Pendred syndrome, an
autosomal recessive disease characterized by deafness and goitre. Pendrin is highly …

Regulation of pendrin by pH: dependence on glycosylation

A Azroyan, K Laghmani, G Crambert… - Biochemical …, 2011 - hal.sorbonne-universite.fr
Mutations of the anion exchanger pendrin are responsible for Pendred syndrome, an
autosomal recessive disease characterized by deafness and goiter. Pendrin is highly …

Regulation of pendrin by pH: dependence on glycosylation

A Azroyan, K Laghmani, G Crambert, D Mordasini… - Biochemical …, 2011 - hal.science
Mutations of the anion exchanger pendrin are responsible for Pendred syndrome, an
autosomal recessive disease characterized by deafness and goiter. Pendrin is highly …
[PDF] academia.edu

[PDF][PDF] REGULATION OF PENDRIN BY pH: DEPENDENCE ON GLYCOSYLATION

A Azroyan, K Laghmani, G Crambert, D Mordasini… - 2010 - academia.edu
Mutations of the anion exchanger pendrin are responsible for Pendred syndrome, an
autosomal recessive disease characterized by deafness and goiter. Pendrin is highly …
[PDF] academia.edu

[PDF][PDF] Regulation of pendrin by pH: dependence on glycosylation

A Azroyan, K Laghmani, G Crambert, D Mordasini… - 2010 - academia.edu
Mutations of the anion exchanger pendrin are responsible for Pendred syndrome, an
autosomal recessive disease characterized by deafness and goiter. Pendrin is highly …

Regulation of pendrin by pH: dependence on glycosylation

A Azroyan, K Laghmani, G Crambert… - Biochemical …, 2011 - hal.sorbonne-universite.fr
Mutations of the anion exchanger pendrin are responsible for Pendred syndrome, an
autosomal recessive disease characterized by deafness and goiter. Pendrin is highly …