Disease: Glucosephosphate isomerase deficiency
- A crucial role for macrophages in the pathology of K/B x N serum-induced arthritis
- A hybrid two-component system protein of a prominent human gut symbiont couples glycan sensing in vivo to carbohydrate metabolism
- A novel binding of GTP stabilizes the structure and modulates the activities of human phosphoglucose isomerase/autocrine motility factor
- A Novel Mutation of Glucose Phosphate Isomerase (GPI) Causing Severe Neonatal Anemia Due to GPI Deficiency
- Ablation of mouse phosphomannose isomerase (Mpi) causes mannose 6-phosphate accumulation, toxicity, and embryonic lethality
- Adenosine 2a Receptor Signal Blockade of Murine Autoimmune Arthritis via Inhibition of Pathogenic Germinal Center-Follicular Helper T Cells
- Ameliorated course of glucose-6-phosphate isomerase (G6PI)-induced arthritis in IFN-gamma receptor knockout mice exposes an arthritis-promoting role of IFN-gamma
- Ameliorated course of glucose-6-phosphate isomerase (G6PI)-induced arthritis in IFN-γ receptor knockout mice exposes an arthritis-promoting role of IFN-γ
- Amoxicillin-induced hemolytic anemia in a child with glucose 6-phosphate isomerase deficiency
- An optimised system for refolding of human glucose 6-phosphate dehydrogenase
- Attenuation of Hemolysis Due to Glucose-6-Phosphate Isomerase Deficiency With Ketogenic Diet - A Case Report
- Autoantibody-mediated arthritis in the absence of C3 and activating Fcγ receptors: C5 is activated by the coagulation cascade
- Case report: Glucose 6-phosphate-isomerase deficiency combine with avascular necrosis of bilateral femoral head
- Characterization of the KRN cell transfer model of rheumatoid arthritis (KRN-CTM), a chronic yet synchronized version of the K/BxN mouse
- Clinical and Molecular Spectrum of Glucose-6-Phosphate Isomerase Deficiency. Report of 12 New Cases
- Clinical, laboratory, and mutational profile of children with glucose phosphate isomerase deficiency: a single centre report
- Confounding factors in the diagnosis and clinical course of rare congenital hemolytic anemias
- Congenital Hemolytic Anemia Because of Glucose Phosphate Isomerase Deficiency: Identification of 2 Novel Missense Mutations in the GPI Gene
- Cutting Edge: Processing of Oxidized Peptides in Macrophages Regulates T Cell Activation and Development of Autoimmune Arthritis
- Defects in leaf carbohydrate metabolism compromise acclimation to high light and lead to a high chlorophyll fluorescence phenotype in Arabidopsis thaliana
- Deglycation activity of the Escherichia coli glycolytic enzyme phosphoglucose isomerase
- Deletion of Syk in neutrophils prevents immune complex arthritis
- Distinct roles of the preparatory and payoff phases of glycolysis in hematopoietic stem cells
- Down-regulation of phosphoglucose isomerase/autocrine motility factor results in mesenchymal-to-epithelial transition of human lung fibrosarcoma cells
- Effects of inherited mutations on catalytic activity and structural stability of human glucose-6-phosphate isomerase expressed in Escherichia coli
- Endothelial prostacyclin protects the kidney from ischemia-reperfusion injury
- Engineering E. coli for simultaneous glucose-xylose utilization during methyl ketone production
- Escherichia coli phosphoglucose isomerase can be substituted by members of the PGI family, the PGI/PMI family, and the cPGI family
- Expression of heterologous non-oxidative pentose phosphate pathway from Bacillus methanolicus and phosphoglucose isomerase deletion improves methanol assimilation and metabolite production by a synthetic Escherichia coli methylotroph
- Gasdermin D deficiency attenuates arthritis induced by traumatic injury but not autoantibody-assembled immune complexes
- GATA4 is a key regulator of steroidogenesis and glycolysis in mouse Leydig cells
- Genetic Analysis of Two Novel GPI Variants Disrupting H Bonds and Localization Characteristics of 55 Gene Variants Associated with Glucose-6-phosphate Isomerase Deficiency
- Glucocorticoid therapy of antigen-induced arthritis depends on the dimerized glucocorticoid receptor in T cells
- Glucose 6 Phosphate Isomerase Deficiency, a Rare Hemolytic Anemia Misdiagnosed as Hereditary Spherocytosis
- Glucose phosphate isomerase (GPI) Tadikonda: Characterization of a novel Pro340Ser mutation
- Glucose phosphate isomerase deficiency demasked by whole-genome sequencing: a case report
- Glucose phosphate isomerase deficiency: enzymatic and familial characterization of Arg346His mutation
- Glucose Phosphate Isomerase Deficiency: High Prevalence of p.Arg347His Mutation in Indian Population Associated with Severe Hereditary Non-Spherocytic Hemolytic Anemia Coupled with Neurological Dysfunction
- Glucose-6-phosphate isomerase deficiency hemolysis
- Glucose-6-phosphate isomerase deficiency results in mTOR activation, failed translocation of lipin 1alpha to the nucleus and hypersensitivity to glucose: Implications for the inherited glycolytic disease
- Glucose-6-phosphate isomerase deficiency results in mTOR activation, failed translocation of lipin 1α to the nucleus and hypersensitivity to glucose: Implications for the inherited glycolytic disease
- Hematopoiesis following disruption of the Pitx2 homeodomain gene
- Hereditary non-spherocytic hemolytic anemia and severe glucose phosphate isomerase deficiency in an Indian patient homozygous for the L487F mutation in the human GPI gene
- Hereditary nonspherocytic hemolytic anemia caused by glucose-6-phosphate isomerase (GPI) deficiency in a Chinese patient: a case report
- Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study
- Host-derived CD4+ T cells attenuate stem cell-mediated transfer of autoimmune arthritis in lethally irradiated C57BL/6.g7 mice
- HuR is a post-transcriptional regulator of core metabolic enzymes in pancreatic cancer
- Identification of haemolytic anaemia caused by glucose phosphate isomerase deficiency in a thalassaemia-endemic region: Correction of misdiagnosis and consideration of the cause of misdiagnosis
- IL-33 exacerbates autoantibody-induced arthritis
- Importance of NADPH supply for improved L-valine formation in Corynebacterium glutamicum
- Inactivation of sll1556 in Synechocystis strain PCC 6803 impairs isoprenoid biosynthesis from pentose phosphate cycle substrates in vitro
- Increased red cell turnover in a line of CD22-deficient mice is caused by Gpi1c: a model for hereditary haemolytic anaemia
- Induction of a B-cell-dependent chronic arthritis with glucose-6-phosphate isomerase
- Inhibition of IRE1 modifies hypoxic regulation of G6PD, GPI, TKT, TALDO1, PGLS and RPIA genes expression in U87 glioma cells
- Integrating transcriptomics and proteomics to show that tanshinone IIA suppresses cell growth by blocking glucose metabolism in gastric cancer cells
- Interleukin-4 can be a key positive regulator of inflammatory arthritis
- Isolation of novel animal cell lines defective in glycerolipid biosynthesis reveals mutations in glucose-6-phosphate isomerase
- iTRAQ protein profile analysis of Citrus sinensis roots in response to long-term boron-deficiency
- K/BxN Serum-Transfer Arthritis as a Model for Human Inflammatory Arthritis
- KRN/I-Ag7 mouse arthritis is independent of complement C3
- Macrophage scavenger receptor 1 (Msr1, SR-A) influences B cell autoimmunity by regulating soluble autoantigen concentration
- Meta-analysis of transcriptomic profiles in <em>Dunaliella tertiolecta</em> reveals molecular pathway responses to different abiotic stresses
- Meta-analysis of transcriptomic profiles in Dunaliella tertiolecta reveals molecular pathway responses to different abiotic stresses
- Metabolic pathway analysis of enzyme-deficient human red blood cells
- Mice Deficient in CIZ/NMP4 Develop an Attenuated Form of K/BxN-Serum Induced Arthritis
- Molecular diagnosis of unexplained haemolytic anaemia using targeted next-generation sequencing panel revealed (p.Ala337Thr) novel mutation in GPI gene in two Indian patients
- Neonatal Fc receptor blockade by Fc engineering ameliorates arthritis in a murine model
- Next-generation sequencing unravels homozygous mutation in glucose-6-phosphate isomerase, GPIc.1040G>A (p.Arg347His) causing hemolysis in an Indian infant
- Next-generation sequencing unravels homozygous mutation in glucose-6-phosphate isomerase, GPIc.1040G>A (p.Arg347His) causing hemolysis in an Indian infant
- Next-Generation Sequencing-Based Diagnosis of Unexplained Inherited Hemolytic Anemias Reveals Wide Genetic and Phenotypic Heterogeneity
- Niche-Selective Inhibition of Pathogenic Th17 Cells by Targeting Metabolic Redundancy
- Nitrate assimilation compensates for cell wall biosynthesis in the absence of Aspergillus fumigatus phosphoglucose isomerase
- Peptidylarginine deiminase type 4 deficiency reduced arthritis severity in a glucose-6-phosphate isomerase-induced arthritis model
- Phosphotransferase system-mediated glucose uptake is repressed in phosphoglucoisomerase-deficient Corynebacterium glutamicum strains
- Plastidial Phosphoglucose Isomerase Is an Important Determinant of Seed Yield through Its Involvement in Gibberellin-Mediated Reproductive Development and Storage Reserve Biosynthesis in Arabidopsis
- Plastidic phosphoglucose isomerase is an important determinant of starch accumulation in mesophyll cells, growth, photosynthetic capacity, and biosynthesis of plastidic cytokinins in Arabidopsis
- Production of D-glucaric acid with phosphoglucose isomerase-deficient Saccharomyces cerevisiae
- Red blood cell disorders in Rwandese neonates: screening for sickle cell disease and glucose-6-phosphate dehydrogenase deficiency
- Red cell glucose phosphate isomerase (GPI): a molecular study of three novel mutations associated with hereditary nonspherocytic hemolytic anemia
- Red cell glycolytic enzyme disorders caused by mutations: an update
- Redirecting carbon flux through pgi-deficient and heterologous transhydrogenase toward efficient succinate production in Corynebacterium glutamicum
- RHBDF1 deficiency suppresses melanoma glycolysis and enhances efficacy of immunotherapy by facilitating glucose-6-phosphate isomerase degradation via TRIM32
- Saccharomyces cerevisiae engineered to produce D-xylonate
- Sclerostin inhibition promotes TNF-dependent inflammatory joint destruction
- Starch Biosynthesis in Guard Cells But Not in Mesophyll Cells Is Involved in CO2-Induced Stomatal Closing
- Study of pathophysiology and molecular characterization of congenital anemia in India using targeted next-generation sequencing approach
- Targeted mast cell silencing protects against joint destruction and angiogenesis in experimental arthritis in mice
- Th17 cells can provide B cell help in autoantibody induced arthritis
- The cellular source and target of IL-21 in K/BxN autoimmune arthritis
- The Mechanism of Starch Over-Accumulation in <em>Chlamydomonas reinhardtii</em> High-Starch Mutants Identified by Comparative Transcriptome Analysis
- The novel compound heterozygous variants identified in a Chinese family with glucose phosphate isomerase deficiency and pathogenicity analysis
- The Role of Follicular Helper T Cell Molecules and Environmental Influences in Autoantibody Production and Progression to Inflammatory Arthritis in Mice
- Tumor aerobic glycolysis confers immune evasion through modulating sensitivity to T cell-mediated bystander killing via TNF-α
- Tumor necrosis factor receptor-associated factor 1 influences KRN/I-Ag7 mouse arthritis autoantibody production
- Two novel mutations (p.(Ser160Pro) and p.(Arg472Cys)) causing glucose-6-phosphate isomerase deficiency are associated with erythroid dysplasia and inappropriately suppressed hepcidin
- Ultra-performance liquid chromatography-tandem mass spectrometry-based multiplex enzyme assay for six enzymes associated with hereditary hemolytic anemia
- Unchanged survival rates of 14-3-3gamma knockout mice after inoculation with pathological prion protein
- Use of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) in the Diagnosis of RBC Membrane Disorders, Enzyme Defects, and Congenital Dyserythropoietic Anemias: A Monocentric Study on 202 Patients
- Using phosphoglucose isomerase-deficient (pgi1delta) Saccharomyces cerevisiae to map the impact of sugar phosphate levels on D-glucose and D-xylose sensing
- Using phosphoglucose isomerase-deficient (pgi1Δ) Saccharomyces cerevisiae to map the impact of sugar phosphate levels on D-glucose and D-xylose sensing