Disease: Fructose-1-6-bisphosphatase deficiency
- 1,25-Dihydroxyvitamin D regulates macrophage activation through FBP1/PKR and ameliorates arthritis in TNF-transgenic mice
- 1alpha,25(OH)(2)D(3) ameliorates insulin resistance by alleviating gammadelta T cell inflammation via enhancing fructose-1,6-bisphosphatase 1 expression
- 1α,25(OH)<sub>2</sub>D<sub>3</sub> ameliorates insulin resistance by alleviating γδ T cell inflammation via enhancing fructose-1,6-bisphosphatase 1 expression
- A Chinese Adult Patient with Fructose 1,6-bisphosphatase Deficiency
- A Heterocyst-Specific Antisense RNA Contributes to Metabolic Reprogramming in Nostoc sp. PCC 7120
- A Japanese boy with fructose-1,6-bisphosphatase deficiency who had a novel <em>FBP1</em> mutation (p.Phe90Val)
- A Japanese boy with fructose-1,6-bisphosphatase deficiency who had a novel FBP1 mutation (p.Phe90Val)
- A nitrogen stress-inducible small RNA regulates CO2 fixation in Nostoc
- A novel variant in the FBP1 gene causes fructose-1,6-bisphosphatase deficiency through increased ubiquitination
- A novel variant of fructose-1,6-bisphosphatase gene identified in an adult with newly diagnosed hepatitis C
- A potential role for muscle in glucose homeostasis: in vivo kinetic studies in glycogen storage disease type 1a and fructose-1,6-bisphosphatase deficiency
- A summary of molecular genetic findings in fructose-1,6-bisphosphatase deficiency with a focus on a common long-range deletion and the role of MLPA analysis
- A Toxoplasma gondii Gluconeogenic Enzyme Contributes to Robust Central Carbon Metabolism and Is Essential for Replication and Virulence
- An extremely rare case of hypoglycemia with a novel mutation and review of the literature: fructose-1,6 bisphosphatase deficiency in an adult man
- An interesting newborn case of fructose 1-6 diphosphatase deficiency triggered after thyme juice ingestion
- Boron deficiency decreases growth and photosynthesis, and increases starch and hexoses in leaves of citrus seedlings
- Chloroplastic thioredoxin m functions as a major regulator of Calvin cycle enzymes during photosynthesis in vivo
- ChREBP deficiency leads to diarrhea-predominant irritable bowel syndrome
- Clinical and molecular characterization of Indian patients with fructose-1, 6-bisphosphatase deficiency: Identification of a frequent variant (E281K)
- Clinical and Molecular Characterization of Patients with Fructose 1,6-Bisphosphatase Deficiency
- cpFBPaseII, a novel redox-independent chloroplastic isoform of fructose-1,6-bisphosphatase
- Documentation of a novel FBP1 gene mutation in the Arabian ethnicity: a case report
- Dynamic light caused less photosynthetic suppression, rather than more, under nitrogen deficit conditions than under sufficient nitrogen supply conditions in soybean
- Effect of phosphoglycerate mutase and fructose 1,6-bisphosphatase deficiency on symbiotic Burkholderia phymatum
- Ethanolic extract of Commiphora mukul gum resin attenuates streptozotocin-induced alterations in carbohydrate and lipid metabolism in rats
- Etiology and outcome of inborn errors of metabolism
- Exogenous brassinosteroids alleviate calcium deficiency-induced tip-burn by maintaining cell wall structural stability and higher photosynthesis in mini Chinese Cabbage
- Exon 2 deletion represents a common mutation in Turkish patients with fructose-1,6-bisphosphatase deficiency
- Expression of a phosphate-starvation inducible fructose-1,6-bisphosphatase gene in common bean nodules correlates with phosphorus use efficiency
- Foetal life protein restriction in male mink (Neovison vison) kits lowers post-weaning protein oxidation and the relative abundance of hepatic fructose-1,6-bisphosphatase mRNA
- Fructose 1,6 bisphosphatase deficiency: outcomes of patients in a single center in Turkey and identification of novel splice site and indel mutations in <em>FBP1</em>
- Fructose 1,6 bisphosphatase deficiency: outcomes of patients in a single center in Turkey and identification of novel splice site and indel mutations in FBP1
- Fructose 1,6-<em>bis</em>phosphatase: getting the message across
- Fructose 1,6-bisphosphatase deficiency as a cause of childhood interstitial lung disease
- Fructose 1,6-bisphosphatase deficiency as a cause of recessive serious hypoglycaemia
- Fructose 1,6-bisphosphatase deficiency: clinical, biochemical and genetic features in French patients
- Fructose 1,6-bisphosphatase deficiency: enzyme and mutation analysis performed on calcitriol-stimulated monocytes with a note on long-term prognosis
- Fructose 1,6-bisphosphatase: getting the message across
- Fructose-1,6-bisphosphatase 1 dephosphorylates and inhibits TERT for tumor suppression
- Fructose-1,6-bisphosphatase 1 suppresses PPARalpha-mediated gene transcription and non-small-cell lung cancer progression
- Fructose-1,6-bisphosphatase 1 suppresses PPARα-mediated gene transcription and non-small-cell lung cancer progression
- Fructose-1,6-bisphosphatase deficiency
- Fructose-1,6-bisphosphatase deficiency as a cause of recurrent hypoglycemia and metabolic acidosis: Clinical and molecular findings in Malaysian patients
- Fructose-1,6-bisphosphatase deficiency caused by a novel homozygous Alu element insertion in the FBP1 gene and delayed diagnosis
- Fructose-1,6-bisphosphatase deficiency causes fatty liver disease and requires long-term hepatic follow-up
- Fructose-1,6-bisphosphatase deficiency presented with complex febrile convulsion
- Fructose-1,6-bisphosphatase deficiency with confirmed molecular diagnosis. An important cause of hypoglycemia in children
- Fructose-1,6-bisphosphatase deficiency: a case of a successful pregnancy by closely monitoring metabolic control
- Fructose-1,6-bisphosphatase deficiency: A pediatric case report
- Fructose-1,6-bisphosphatase is a nonenzymatic safety valve that curtails AKT activation to prevent insulin hyperresponsiveness
- Fructose-1,6-diphosphatase deficiency: a treatable neurometabolic disorder
- Genetic analysis of a child with fructose-1, 6 bisphosphatase deficiency
- Genetic analysis of fructose-1,6-bisphosphatase (FBPase) deficiency in nine consanguineous Pakistani families
- Genetic analysis of patients with fructose-1,6-bisphosphatase deficiency
- Genetic Analysis of Tyrosinemia Type 1 and Fructose-1, 6 Bisphosphatase Deficiency Affected in Pakistani Cohorts
- Genetic diagnosis of fructose-1, 6-bisphosphatase deficiency: a case report
- GID E3 ligase supramolecular chelate assembly configures multipronged ubiquitin targeting of an oligomeric metabolic enzyme
- Gluconeogenesis defect presenting with resistant hyperglycemia and acidosis mimicking diabetic ketoacidosis
- Growth and photosynthetic down-regulation in Coffea arabica in response to restricted root volume
- Hepatic but not Intestinal FBP1 Is Required for Fructose Metabolism and Tolerance
- Identification of genotype-biochemical phenotype correlations associated with fructose 1,6-bisphosphatase deficiency
- Immunodeficiency with susceptibility to lymphoma with complex genotype affecting energy metabolism (<em>FBP1, ACAD9)</em> and vesicle trafficking <em>(RAB27A)</em>
- Impact of hematopoietic cyclooxygenase-1 deficiency on obesity-linked adipose tissue inflammation and metabolic disorders in mice
- Inborn errors of carbohydrate metabolism
- Inborn Errors of Fructose Metabolism. What Can We Learn from Them?
- International practices in the dietary management of fructose 1-6 biphosphatase deficiency
- LIX1-like protein promotes liver cancer progression <em>via</em> miR-21-3p-mediated inhibition of fructose-1,6-bisphosphatase
- LIX1-like protein promotes liver cancer progression via miR-21-3p-mediated inhibition of fructose-1,6-bisphosphatase
- Loss of fructose-1,6-bisphosphatase induces glycolysis and promotes apoptosis resistance of cancer stem-like cells: an important role in hexavalent chromium-induced carcinogenesis
- Melatonin improved glucose homeostasis is associated with the reprogrammed gut microbiota and reduced fecal levels of short-chain fatty acids in db/db mice
- Morphophysiological and transcriptome analysis reveal that reprogramming of metabolism, phytohormones and root development pathways governs the potassium (K(+)) deficiency response in two contrasting chickpea cultivars
- Morphophysiological and transcriptome analysis reveal that reprogramming of metabolism, phytohormones and root development pathways governs the potassium (K<sup>+</sup>) deficiency response in two contrasting chickpea cultivars
- Mutations in two zinc-cluster proteins activate alternative respiratory and gluconeogenic pathways and restore senescence in long-lived respiratory mutants of Podospora anserina
- NADPH Thioredoxin Reductase C and Thioredoxins Act Concertedly in Seedling Development
- Novel compound heterozygous mutations in the fructose-1,6-bisphosphatase gene cause hypoglycemia and lactic acidosis
- Novel compound heterozygous mutations of the FBP1 gene in a patient with hypoglycemia and lactic acidosis: A case report
- Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency
- Novel fructose bisphosphatase 1 gene mutation presenting as recurrent episodes of vomiting in an Indian child
- Novel fructose-1,6-bisphosphatase gene mutation in two siblings
- Novel Mutation with Fructose-1,6-Bisphosphatase Deficiency
- Overexpression of a brassinosteroid biosynthetic gene Dwarf enhances photosynthetic capacity through activation of Calvin cycle enzymes in tomato
- Overexpression of transcription factor ZmPTF1 improves low phosphate tolerance of maize by regulating carbon metabolism and root growth
- Pitfall in the Diagnosis of Fructose-1,6-Bisphosphatase Deficiency: Difficulty in Detecting Glycerol-3-Phosphate with Solvent Extraction in Urinary GC/MS Analysis
- Recurrent infantile hypoglycemia due to combined fructose-1,6-diphosphatase deficiency and growth hormone deficiency
- Secondary disorders of glycosylation in inborn errors of fructose metabolism
- Seedling growth and photosynthetic response of <em>Pterocarpus indicus</em> L. to shading stress
- Severe lactic acidosis requiring continuos haemodiafiltration in a young patient with unrecognized metabolic abnormality. Case report
- SirT1 knockdown in liver decreases basal hepatic glucose production and increases hepatic insulin responsiveness in diabetic rats
- Status epilepticus due to fructose-1,6-bisphosphatase deficiency caused by <em>FBP1</em> gene mutation
- Status epilepticus due to fructose-1,6-bisphosphatase deficiency caused by FBP1 gene mutation
- Succinate Dehydrogenase-Deficient Renal Cancer Featuring Fructose-1,6-Biphosphatase Loss, Pyruvate Kinase M2 Overexpression, and SWI/SNF Chromatin Remodeling Complex Aberrations: A Rare Case Report
- The combination of NAD+-dependent deacetylase gene deletion and the interruption of gluconeogenesis causes increased glucose metabolism in budding yeast
- The fructose-1,6-bisphosphatase deficiency and the p.(Lys204ArgfsTer72) variant
- The key gluconeogenic enzyme fructose-1,6-bisphosphatase is secreted during prolonged glucose starvation and is internalized following glucose re-feeding via the non-classical secretory and internalizing pathways in Saccharomyces cerevisiae
- Thioredoxin Selectivity for Thiol-based Redox Regulation of Target Proteins in Chloroplasts
- Three successful pregnancies through dietary management of fructose-1,6-bisphosphatase deficiency
- Transcriptomic and proteomic approach to identify differentially expressed genes and proteins in Arabidopsis thaliana mutants lacking chloroplastic 1 and cytosolic FBPases reveals several levels of metabolic regulation
- Transient pseudo-hypertriglyceridemia: a useful biochemical marker of fructose-1,6-bisphosphatase deficiency
- ULK1/2 Constitute a Bifurcate Node Controlling Glucose Metabolic Fluxes in Addition to Autophagy
- Urinary organic metabolite screening of children with influenza-associated encephalopathy for inborn errors of metabolism using GC/MS