Mar 30, 2025 · SLC1A3 (Solute Carrier Family 1 Member 3) is a Protein Coding gene. Diseases associated with SLC1A3 include Episodic Ataxia, Type 6 and Alternating Hemiplegia Of …

Mar 8, 2025 · Title: Ataxia-linked SLC1A3 mutations alter EAAT1 chloride channel activity and glial regulation of CNS function. Microscopic Characterization of the Chloride Permeation …

The SLC1A3 gene provides instructions for making a protein called excitatory amino acid transporter 1 (EAAT1). The EAAT1 protein is primarily found in nervous system cells called …

However, many clinical trials indicated severe ASNase toxicity in patients with solid tumors, with resistant mechanisms not well understood. Here, we took a functional genetic approach and …

Apr 2, 2018 · EAAT1 (SLC1A3) is a member of a family of high-affinity sodium-dependent transporter molecules that regulate neurotransmitter concentrations at the excitatory …

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.

Nov 19, 2024 · Elevated levels of SLC1A3 promote HCC cell motility and invasion and can affect the prognosis of HCC by modifying immune responses and epithelial-mesenchymal transition. …

Mar 30, 2025 · SLC1A1 (Solute Carrier Family 1 Member 1) is a Protein Coding gene. Diseases associated with SLC1A1 include Dicarboxylic Aminoaciduria and Schizophrenia 18. Among its …

Feb 8, 2025 · These data reveal that stem/progenitor cell activation is synchronized over distinct niches during growth and identify SLC1A3 as a general marker and effector of activated …

Feb 15, 2022 · EA6 patients have mutations in SLC1A3, the gene which encodes the human excitatory amino acid transporter 1 (hEAAT1). The etiology of EA6 likely traces to Bergmann …