Day: October 18, 2021

Zika Virus Requires the Expression of Claudin-7 for Optimal Replication in Human Endothelial Cells
Mutant KCNJ3 and KCNJ5 Potassium Channels as Novel Molecular Targets in Bradyarrhythmias and Atrial Fibrillation.
PCTP contributes to human platelet activation by enhancing dense granule secretion
PTPN5 promotes follicle-stimulating hormone secretion through regulating intracellular calcium homeostasis

PTPN5 promotes follicle-stimulating hormone secretion through regulating intracellular calcium homeostasisPTPN5 promotes follicle-stimulating hormone secretion through regulating intracellular calcium homeostasis

Protein tyrosine phosphatase non-receptor kind 5 (PTPN5), additionally known as striatal-enriched protein tyrosine phosphatase (STEP), is very expressed in neurons of the basal ganglia, hippocampus, cortex, and associated constructions, additionally

Coloboma may be a shared feature in a spectrum of disorders caused by mutations in the WDR37-PACS1-PACS2 axis
The antibiotic robenidine exhibits guanabenz-like cytoprotective properties by a mechanism independent of protein phosphatase PP1:PPP1R15A.

The antibiotic robenidine exhibits guanabenz-like cytoprotective properties by a mechanism independent of protein phosphatase PP1:PPP1R15A.The antibiotic robenidine exhibits guanabenz-like cytoprotective properties by a mechanism independent of protein phosphatase PP1:PPP1R15A.

The aminoguanidine compound robenidine is extensively used as an antibiotic for the management of coccidiosis, a protozoal an infection in poultry and rabbits. Apparently, robenidine is structurally much like guanabenz

Identification of Androgen Receptor Metabolic Correlome Reveals the Repression of Ceramide Kinase by Androgens
Generation of an induced pluripotent stem cell line from a Bartter syndrome patient with the homozygote mutation p.A244D (c.731C>A) in SLC12A1 gene

Generation of an induced pluripotent stem cell line from a Bartter syndrome patient with the homozygote mutation p.A244D (c.731C>A) in SLC12A1 geneGeneration of an induced pluripotent stem cell line from a Bartter syndrome patient with the homozygote mutation p.A244D (c.731C>A) in SLC12A1 gene

Bartter Syndrome (BS) is a gaggle of uncommon inherited autosome-recessive illness, which might be attributable to the gene mutations of sodium-potassium-chloride cotransporter gene (SLC12A1). Right here, the urine cells (UCs)

P23 Acts as Functional RBP in the Macrophage Inflammation Response