RATIONALE: ABCC6 plays a crucial role in ectopic calcification; mutations of the gene cause pseudoxanthoma elasticum and general arterial calcification of infancy. To elucidate the role of ABCC6 in cellular physiology and disease, it is crucial to establish the exact subcellular localization of the native ABCC6 protein. OBJECTIVE: In a recent article in Circulation Research, ABCC6 was reported to localize to the mitochondria-associated membrane and not the plasma membrane. As the suggested mitochondrial localization is inconsistent with published data and the presumed role of ABCC6, we performed experiments to determine the cellular localization of ABCC6 in its physiological environment. METHODS AND RESULTS: We performed immunofluorescent l...
ABC transporters represent a large family of ATP-driven transmembrane transporters involved in uni- ...
ATP‐binding cassette subfamily C member 6 gene/protein (ABCC6) is an ATP‐dependent transmembrane tra...
ABCC6 belongs to the adenosine triphosphate-binding cassette (ABC) gene subfamily C. This protein fa...
RATIONALE:: ABCC6 plays a crucial role in ectopic calcification; mutations of the gene cause pseudox...
BACKGROUND: A recent article in Circulation Research suggests that the protein ABCC6, which when def...
Abnormal mineralization occurs in the context of several common conditions, including advanced age, ...
ABCC6 protein is an ATP-dependent transporter that is mainly found in the basolateral plasma membran...
ABCC6 is a human ATP binding cassette (ABC) transporter of the plasma membrane associated with Pseud...
Because vascular or cardiac mineralization is inversely correlated with morbidity and long-term surv...
Pseudoxanthoma elasticum (PXE) is an inherited metabolic disease with autosomal recessive inheritanc...
Background: Pseudoxanthoma elasticum (PXE) is characterized by progressive ectopic mineralization of...
OBJECTIVE: Mutations in ABCC6 underlie the ectopic mineralization disorder pseudoxanthoma elasticum ...
Inactivating mutations in ABCC6 underlie the rare hereditary mineralization disorder pseudoxanthoma ...
The ATP-binding cassette sub-family C member 6 transporter (ABCC6) is an ATP dependent transporter ...
Pseudoxanthoma elasticum (PXE) is a complex autosomal recessive disease caused by mutations of ABCC6...
ABC transporters represent a large family of ATP-driven transmembrane transporters involved in uni- ...
ATP‐binding cassette subfamily C member 6 gene/protein (ABCC6) is an ATP‐dependent transmembrane tra...
ABCC6 belongs to the adenosine triphosphate-binding cassette (ABC) gene subfamily C. This protein fa...
RATIONALE:: ABCC6 plays a crucial role in ectopic calcification; mutations of the gene cause pseudox...
BACKGROUND: A recent article in Circulation Research suggests that the protein ABCC6, which when def...
Abnormal mineralization occurs in the context of several common conditions, including advanced age, ...
ABCC6 protein is an ATP-dependent transporter that is mainly found in the basolateral plasma membran...
ABCC6 is a human ATP binding cassette (ABC) transporter of the plasma membrane associated with Pseud...
Because vascular or cardiac mineralization is inversely correlated with morbidity and long-term surv...
Pseudoxanthoma elasticum (PXE) is an inherited metabolic disease with autosomal recessive inheritanc...
Background: Pseudoxanthoma elasticum (PXE) is characterized by progressive ectopic mineralization of...
OBJECTIVE: Mutations in ABCC6 underlie the ectopic mineralization disorder pseudoxanthoma elasticum ...
Inactivating mutations in ABCC6 underlie the rare hereditary mineralization disorder pseudoxanthoma ...
The ATP-binding cassette sub-family C member 6 transporter (ABCC6) is an ATP dependent transporter ...
Pseudoxanthoma elasticum (PXE) is a complex autosomal recessive disease caused by mutations of ABCC6...
ABC transporters represent a large family of ATP-driven transmembrane transporters involved in uni- ...
ATP‐binding cassette subfamily C member 6 gene/protein (ABCC6) is an ATP‐dependent transmembrane tra...
ABCC6 belongs to the adenosine triphosphate-binding cassette (ABC) gene subfamily C. This protein fa...