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Summary Expression Phenotypes Gene Literature (17) GO Terms (1) Nucleotides (170) Proteins (50) Interactants (187) Wiki
XB-GENEPAGE-1003256

Papers associated with slc38a3



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Developmental regulation of cellular metabolism is required for intestinal elongation and rotation., Grzymkowski JK, Chiu YC, Jima DD, Wyatt BH, Jayachandran S, Stutts WL, Nascone-Yoder NM., Development. February 15, 2024; 151 (4):                                       


HNF1B Alters an Evolutionarily Conserved Nephrogenic Program of Target Genes., Grand K, Stoltz M, Rizzo L, Röck R, Kaminski MM, Salinas G, Getwan M, Naert T, Pichler R, Lienkamp SS., J Am Soc Nephrol. March 1, 2023; 34 (3): 412-432.                          


Perturbation of astroglial Slc38 glutamine transporters by NH4 + contributes to neurophysiologic manifestations in acute liver failure., Hamdani EH, Popek M, Frontczak-Baniewicz M, Utheim TP, Albrecht J, Zielińska M, Chaudhry FA., FASEB J. July 1, 2021; 35 (7): e21588.      


Specific transport of 3-fluoro-l-α-methyl-tyrosine by LAT1 explains its specificity to malignant tumors in imaging., Wei L, Tominaga H, Ohgaki R, Wiriyasermkul P, Hagiwara K, Okuda S, Kaira K, Oriuchi N, Nagamori S, Kanai Y., Cancer Sci. March 1, 2016; 107 (3): 347-52.        


Transport of L-glutamine, L-alanine, L-arginine and L-histidine by the neuron-specific Slc38a8 (SNAT8) in CNS., Hägglund MGA, Hellsten SV, Bagchi S, Philippot G, Löfqvist E, Nilsson VCO, Almkvist I, Karlsson E, Sreedharan S, Tafreshiha A, Fredriksson R., J Mol Biol. March 27, 2015; 427 (6 Pt B): 1495-1512.


E2a is necessary for Smad2/3-dependent transcription and the direct repression of lefty during gastrulation., Wills AE, Baker JC., Dev Cell. February 9, 2015; 32 (3): 345-57.                  


Protein kinase C-mediated phosphorylation of a single serine residue on the rat glial glutamine transporter SN1 governs its membrane trafficking., Nissen-Meyer LS, Popescu MC, Hamdani el H, Chaudhry FA., J Neurosci. April 27, 2011; 31 (17): 6565-75.


Substrate-dependent interference of carbonic anhydrases with the glutamine transporter SNAT3-induced conductance., Weise A, Schneider HP, McKenna R, Deitmer JW., Cell Physiol Biochem. January 1, 2011; 27 (1): 79-90.


Rapid downregulation of the rat glutamine transporter SNAT3 by a caveolin-dependent trafficking mechanism in Xenopus laevis oocytes., Balkrishna S, Bröer A, Kingsland A, Bröer S., Am J Physiol Cell Physiol. November 1, 2010; 299 (5): C1047-57.


Mutation of asparagine 76 in the center of glutamine transporter SNAT3 modulates substrate-induced conductances and Na+ binding., Bröer S, Schneider HP, Bröer A, Deitmer JW., J Biol Chem. September 18, 2009; 284 (38): 25823-31.


The sodium-bicarbonate cotransporter NBCe1 supports glutamine efflux via SNAT3 (SLC38A3) co-expressed in Xenopus oocytes., Wendel C, Becker HM, Deitmer JW., Pflugers Arch. February 1, 2008; 455 (5): 885-93.


Enzymatic suppression of the membrane conductance associated with the glutamine transporter SNAT3 expressed in Xenopus oocytes by carbonic anhydrase II., Weise A, Becker HM, Deitmer JW., J Gen Physiol. August 1, 2007; 130 (2): 203-15.              


Heterologous expression of the glutamine transporter SNAT3 in Xenopus oocytes is associated with four modes of uncoupled transport., Schneider HP, Bröer S, Bröer A, Deitmer JW., J Biol Chem. February 9, 2007; 282 (6): 3788-98.


Mouse oocytes regulate metabolic cooperativity between granulosa cells and oocytes: amino acid transport., Eppig JJ, Pendola FL, Wigglesworth K, Pendola JK., Biol Reprod. August 1, 2005; 73 (2): 351-7.


Evolutionarily conserved non-AUG translation initiation in NAT1/p97/DAP5 (EIF4G2)., Takahashi K, Maruyama M, Tokuzawa Y, Murakami M, Oda Y, Yoshikane N, Makabe KW, Ichisaka T, Yamanaka S., Genomics. March 1, 2005; 85 (3): 360-71.


Astroglial glutamine transport by system N is upregulated by glutamate., Bröer A, Deitmer JW, Bröer S., Glia. December 1, 2004; 48 (4): 298-310.


Bidirectional substrate fluxes through the system N (SNAT5) glutamine transporter may determine net glutamine flux in rat liver., Baird FE, Beattie KJ, Hyde AR, Ganapathy V, Rennie MJ, Taylor PM., J Physiol. September 1, 2004; 559 (Pt 2): 367-81.

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