Solute Carrier Family 38 Member 1 (SLC38A1) ELISA Kits

Pig (Porcine) Solute Carrier Family 38 Member 1 (SLC38A1) interaction partners

1. SNAT1 mediated L-citrulline transport modulates eNOS (show NOS3 ELISA Kits) coupling and thus regulates nitric oxide production in hypoxic pulmonary arterial endothelial cells from newborn piglets.

2. Prolonged hypoxia increased SNAT1 expression in pulmonary artery endothelial cells, enhancing the ability to transport l-citrulline.

Human Solute Carrier Family 38 Member 1 (SLC38A1) interaction partners

1. High SNAT1 expression is associated with increased cell migration in breast neoplasms.

2. this study indicates that inhibition of miRNA-593-3p by insulin (show INS ELISA Kits) promotes glucose metabolism through the regulation of Slc38a1 and CLIP3 expression, and provides a new insight into the role and mechanism of insulin (show INS ELISA Kits)-induced glycolysis.

3. Results found that SLC38A1 was up-regulated in colorectal cancer cells (CRC (show CALR ELISA Kits)) and significantly associated with tumor invasion and advanced disease stage. Its overexpression enhanced growth and migration of HCT116 cells providing evidence that activation of SLC38A1 may play a critical role in CRC (show CALR ELISA Kits) development and progression.

4. In the absence of SLC1A5 (show SLC1A5 ELISA Kits) there is a crucial role of SNAT1 in supplying glutamine (show GFPT1 ELISA Kits) for glutaminolysis with SNAT2 acting as a "backup" for glutamine (show GFPT1 ELISA Kits) transport.

5. The SLC38A1 protein was very low or undetectable in healthy gastric mucosa but strong staining of SLC38A1 protein was found in the cytoplasm in more than half of gastric cancer samples. SLC38A1 knockdown decreased tumor cell proliferation and migration.

6. SLC38A1 and SLC38A2 transcript levels are altered in placental malaria with intervillositis.

7. The cross-talk between Akt (show AKT1 ELISA Kits) signaling and SNAT1 might play a critical role in the development and progression of breast cancer

8. Increased expression of ATA1 is frequent in human hilar cholangiocarcinoma and significantly correlated with the progression of cholangiocarcinoma, suggesting the importance of ATA1 in cancer development and progression.

9. The results of this study provided that RAB2A and SLC38A1, were associated with the density of calbindin (show CALB1 ELISA Kits)-positive neurons and the number of perineuronal oligodendrocytes in psychiatric disorders.

10. results suggest that slc38a1 may play a role in the mechanisms underlying the determination of cellular viability in astrocytes through modulation of intracellular ROS (show ROS1 ELISA Kits) generation

Mouse (Murine) Solute Carrier Family 38 Member 1 (SLC38A1) interaction partners

1. Hence, pro-degenerative MAPK signaling functions upstream of SARM1 by limiting the levels of the essential axonal survival factor NMNAT2 to promote injury-dependent SARM1 activation.

2. Changes in transporter expression likely reflect different amino acid requirements during development. Findings include the differential expression of SNAT1 in the inner and outer cells of the compacted morula and nuclear localisation of SNAT2 in the trophectoderm and placental lineages.

3. Overexpression of X-box binding protein-1 (show XBP1 ELISA Kits) led to a marked increase in luciferase activity in P19 cells transfected with the Slc38a1 reporter plasmid. These results suggest that theanine accelerates cellular proliferation and subsequent neuronal specification through a mechanism relevant to upregulation of Slc38a1 gene in undifferentiated neural progenitor cells

4. We found that MeCP2 acts as a microglia-specific transcriptional repressor of

5. GlnT would promote both proliferation and neuronal differentiation through a mechanism relevant to the upregulation of particular proneural genes in undifferentiated P19 cells.

6. Inner hair cells express glutamine transporter SLC38A1.

7. In this study, the in vivo endothelial membrane localization of the sodium-dependent glutamine (show GFPT1 ELISA Kits) transporters Snat3 (Slc38a3) and Snat1 (Slc38a1) was investigated in the mouse brain microvasculature.