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The membrane-associated protein encoded by ABCA3 is a member of the superfamily of ATP-binding cassette (ABC) transporters. Additionally we are shipping ABCA3 Kits (4) and and many more products for this protein.
Showing 10 out of 14 products:
transporter oligomerization is crucial for ABCA3 function.
The TGGAG haplotype may be a risk factor for Respiratory Distress Syndrome in preterm infants in this Chinese population. The haplotype TGGAG was significantly more frequent in RDS (show PRPH2 Antibodies) infants than in non-RDS (show PRPH2 Antibodies) infants.
Rare mutations in surfactant-associated genes contribute to neonatal respiratory distress syndrome. We resequenced all exons of the ATP-binding cassette member A3 (ABCA3) and we found three ABCA3 mutations in the Han [minor allele frequency (MAF (show MAF Antibodies))=0.003] and 7 in the Zhuang (MAF (show MAF Antibodies)=0.011) cohorts. The contribution of these rare ABCA3 mutations to disease burden in the south China population is still unknown.
The clinical features of ABCA3 mutations, including onset, severity or clinical course are very heterogeneous. In the two siblings we had a lightly discordant course that could be explained by exposure to different environmental stresses or variable penetrance.
These results provide evidence of ABCA3 as an MLF efflux transporter in human macrophages and support its role in the direct antileishmanial effect of this alkylphosphocholine drug.
Studies indicate that ATP-binding cassette (ABC (show ABCB6 Antibodies)), subfamily A (show CYP Antibodies), member 3 (ABCA3) is developmentally regulated.
Data discussed the structural features of ABCA3 and how the use of bioinformatics tools could help researchers to obtain a reliable structural model to locate relevant mutations and make genotype/phenotype correlations of affected patients. [review]
SLCO1B3 699GG and 344TT genotypes are associated with non-response to IM, while ABCA3 4548-91 CC/CA genotypes are related to poor CMR in CML patients treated with standard-dose imatinib.
Accumulation of free cholesterol as a result of a loss of ABCA3 export function represents a novel pathomechanism in ABCA3-induced Diffuse parenchymal lung disease.
Report of ABCA3 mutations in a family with one child exhibiting interstitial lung disease.
Abca3 haploinsufficiency results in an altered biochemical and lung mechanical phenotype, as well as a greater lung injury induced by hyperoxia or mechanical ventilation.
The majority of mice in which Abca3 was deleted in alveolar type II cells died shortly after birth from respiratory distress related to surfactant deficiency.
Identification of LBM180, a lamellar body limiting membrane protein of alveolar type II cells, as the ABC transporter (show TAP2 Antibodies) protein (show LAPTM4A Antibodies) ABCA3
showed for the first time expression and subcellular localization of abcb11 (show ABCB11 Antibodies) and abca3 in mouse kidney
ABCA3 is necessary for lamellar body biogenesis, surfactant protein-B processing, and lung development late in gestation.
The phenotype of respiratory failure immediately after birth corresponds to the clinical course of severe ABCA3 mutations in human newborns.
Abca3 gene expression is mediated by discrete cis (show CISH Antibodies)-acting cassettes that mediate pulmonary cell- and lipid-sensitive pathways regulating surfactant homeostasis.
Iportance of a functional catalytic cycle in lipid transport of ABCA3 suggestsa pathophysiological mechanism of pediatric intterstitial lung disease due to ABCA3 mutation.
The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. The full transporter encoded by this gene may be involved in development of resistance to xenobiotics and engulfment during programmed cell death.
ABC transporter 3
, ABC-C transporter
, ATP-binding cassette sub-family A member 3
, ATP-binding cassette transporter 3
, ATP-binding cassette, sub-family A (ABC1), member 3