Analysis of
aquaporin expression in liver with a focus on hepatocytes.
The four genes network (figure 2C) was composed of the genes that codify for the glial fibrillary acid protein (GFAP),
aquaporin 1 (AQP1), the acidic form of the complement factor 4 (c4a), and the apelin receptor (APLNR).
When autoantibody binds against the
Aquaporin 4 channel there occurs hyper permeability at the blood brain barrier, perivascular inflammation, astrocyte damage and inflammation which form the main components of pathogenesis in NMO.
Genetic forms of nephrogenic diabetes insipidus (NDI): Vasopressin receptor defect (X-linked) and
aquaporin defect (autosomal recessive and dominant).
Aquaporin 5 (AQP 5), HMGB1, and p-NF-[kappa]B expression in AT I cells
Aquaporin water channels--from atomic structure to clinical medicine.
To validate the expression profiling by Illumina sequencing, the expression levels of twenty DEGs (11 upregulated and 9 downregulated) involved with beta-glucosidase, pectate lyase,
aquaporin, vacuolar processing, heat shock protein, chaperone, and glutamate-cysteine ligase were selected for qRT-PCR analysis (Table S1).
Schrier, "Effect of primary polydipsia on
aquaporin and sodium transporter abundance," American Journal of Physiology-Renal Physiology, vol.
It could be due to release of antidiuretic hormone or by a direct effect of amiodarone on vasopressin (V2) or
aquaporin receptors in kidneys [13].
Other studies [13, 53, 54] have also shown a significant homology between plants and bacterial
aquaporin with human AQP4 that is expressed in the astrocytic foot processes.
The disease is mediated by autoantibodies against
aquaporin 4 (AQP4) [2].