PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 20947823-7 2011 Circulating haptoglobin and glutathione/total glutathione were significantly higher in the sm22alpha-GLUT1 mice postinjury compared with controls (n=4, P<0.05), suggesting increased flux through the pentose phosphate pathway. Pentosephosphates 202-219 solute carrier family 2 (facilitated glucose transporter), member 1 Mus musculus 101-106 24726364-4 2014 Overexpression of the glucose transporter GLUT1 in myeloid cells caused increased glycolysis and flux through the pentose phosphate pathway but did not induce cytokines. Pentosephosphates 114-131 solute carrier family 2 (facilitated glucose transporter), member 1 Mus musculus 42-47 26573871-4 2016 The underlying mechanisms were defined that the anticancer effects of apigenin were reversed by ectopic GLUT1 overexpression and galactose supplementation, through activation of pentose phosphate pathway-mediated NADPH generation. Pentosephosphates 178-195 solute carrier family 2 (facilitated glucose transporter), member 1 Mus musculus 104-109 35499042-11 2022 Specifically, elevated O-GlcNAcylation increased glucose uptake via glucose transporter 1 (GLUT1) leading to glucose metabolic flow into the pentose phosphate pathways and HBP, which regulate the metabolic reprogramming of endometrial cells. Pentosephosphates 141-158 solute carrier family 2 (facilitated glucose transporter), member 1 Mus musculus 68-89 35499042-11 2022 Specifically, elevated O-GlcNAcylation increased glucose uptake via glucose transporter 1 (GLUT1) leading to glucose metabolic flow into the pentose phosphate pathways and HBP, which regulate the metabolic reprogramming of endometrial cells. Pentosephosphates 141-158 solute carrier family 2 (facilitated glucose transporter), member 1 Mus musculus 91-96 30659108-11 2019 Together, our findings suggest that although lack of GLUT1 blunted glycolysis and the pentose phosphate pathway, MPhi were metabolically flexible enough that inflammatory cytokine release was not dramatically regulated, yet phagocytic defects hindered MPhi function in chronic diseases. Pentosephosphates 86-103 solute carrier family 2 (facilitated glucose transporter), member 1 Mus musculus 53-58