QuickView for SLC9A1;jsessionid=FA04C7ADFD465BECBF577F9773E6058A (gene)

1. Deletion of Slc9a1 in Cx3cr1+ cells stimulated microglial subcluster CREB1 signaling and microglia-o…
2. Slc9a1 plays a vital role in chitosan oligosaccharide transport across the intestinal mucosa of mice…
3. Role of Genetic Mutations of the Na+/H+ Exchanger Isoform 1, in Human Disease and Protein Targeting …
4. Overexpression of NHE1 suppresses ABCA1 protein expression via increasing calpain activity in RAW264…
5. Mutation of SLC9A1, encoding the major Na⁺/H⁺ exchanger, causes ataxia-deafness Lichtenstein-Knorr s…

There were no clinical trials for SLC9A1;jsessionid=FA04C7ADFD465BECBF577F9773E6058A