The chloride channel (CLC) protein family comprises ion channels and proton-coupled anion transporters with fundamental physiological roles in humans. Several properties of CLC proteins defy the rigid dichotomy between ion channels and transporters as these opposite thermodynamic mechanisms of transport are implemented in a very similar structural architecture. All the CLC transporters are expressed in intracellular organelles where they are somehow important for the ionic homeostasis of these compartments. However, their specific physiological role is still unclear. This chapter focuses on the biophysical properties and physiological role of the endosomal Cl−/H+ antiporter ClC-5 mutated in Dent’s disease
Dent's disease, which is a renal tubular disorder characterized by low molecular weight proteinuria,...
The ClC-5 chloride channel resides mainly in vesicles of the endocytotic pathway and contributes to ...
Dent's disease is an hereditary renal tubular disorder characterized by low-molecular-weight (LMW) p...
CLC-5 plays a critical role in the process of endocytosis in the proximal tubule of the kidney and m...
CLC-5 plays a critical role in the process of endocytosis in the proximal tubule of the kidney and m...
Eukaryotic members of the CLC gene family function as plasma membrane chloride channels, or may prov...
CLC genes are expressed in species from bacteria to human and encode Cl(-)-channels or Cl(-)/H(+)-ex...
KEY POINTS The reabsorptive activity of renal proximal tubule cells is mediated by receptor-mediate...
CLC anion transporters are found in all phyla and form a gene family of eight members in mammals. Tw...
ClC-5 is a chloride (Cl-) channel expressed in renal tubules and is critical for normal tubular func...
International audienceChloride channels are expressed in almost all cell membranes and are potential...
After providing a personal description of the convoluted path leading 25 years ago to the molecular ...
Loss-of-function mutations of the ClC-5 chloride channel lead to Dent's disease, a syndrome characte...
Ion channels have historically been viewed as distinct from secondary active transporters. However, ...
Proteins of the CLC gene family assemble to homo- or sometimes heterodimers and either function as C...
Dent's disease, which is a renal tubular disorder characterized by low molecular weight proteinuria,...
The ClC-5 chloride channel resides mainly in vesicles of the endocytotic pathway and contributes to ...
Dent's disease is an hereditary renal tubular disorder characterized by low-molecular-weight (LMW) p...
CLC-5 plays a critical role in the process of endocytosis in the proximal tubule of the kidney and m...
CLC-5 plays a critical role in the process of endocytosis in the proximal tubule of the kidney and m...
Eukaryotic members of the CLC gene family function as plasma membrane chloride channels, or may prov...
CLC genes are expressed in species from bacteria to human and encode Cl(-)-channels or Cl(-)/H(+)-ex...
KEY POINTS The reabsorptive activity of renal proximal tubule cells is mediated by receptor-mediate...
CLC anion transporters are found in all phyla and form a gene family of eight members in mammals. Tw...
ClC-5 is a chloride (Cl-) channel expressed in renal tubules and is critical for normal tubular func...
International audienceChloride channels are expressed in almost all cell membranes and are potential...
After providing a personal description of the convoluted path leading 25 years ago to the molecular ...
Loss-of-function mutations of the ClC-5 chloride channel lead to Dent's disease, a syndrome characte...
Ion channels have historically been viewed as distinct from secondary active transporters. However, ...
Proteins of the CLC gene family assemble to homo- or sometimes heterodimers and either function as C...
Dent's disease, which is a renal tubular disorder characterized by low molecular weight proteinuria,...
The ClC-5 chloride channel resides mainly in vesicles of the endocytotic pathway and contributes to ...
Dent's disease is an hereditary renal tubular disorder characterized by low-molecular-weight (LMW) p...