QuickView for SLC12A1;jsessionid=61F77E210169985AA1F6FF5998A4B322 (gene)

1. Dysregulation of the WNK4-SPAK/OSR1 pathway has a minor effect on baseline NKCC2 phosphorylation.
2. Association of SLC12A1 and GLUR4 Ion Transporters with Neoadjuvant Chemoresistance in Luminal Locall…
3. Novel SLC12A1 mutations cause Bartter syndrome in two patients with different prognoses.
4. Functional characterization of SLC12A1 gene variants in 3 patients with Bartter syndrome type Ⅰ].
5. Tubular-specific CDK12 knockout causes a defect in urine concentration due to premature cleavage of …

There were no clinical trials for SLC12A1;jsessionid=61F77E210169985AA1F6FF5998A4B322