Disease: Phosphoglucomutase deficiency type 3
- A novel congenital disorder of glycosylation type without central nervous system involvement caused by mutations in the phosphoglucomutase 1 gene
- A Nuclear Mutation in Nicotiana sylvestris Causing a Thiamine-Reversible Defect in Synthesis of Chloroplast Pigments
- A Quantification of the Significance of Assimilatory Starch for Growth of Arabidopsis thaliana L. Heynh
- A Starchless Mutant of Nicotiana sylvestris Containing a Modified Plastid Phosphoglucomutase
- An engineered lipid remodeling system using a galactolipid synthase promoter during phosphate starvation enhances oil accumulation in plants
- Aspen growth is not limited by starch reserves
- Autolytic enzyme-deficient mutants of Bacillus subtilis 168
- Bacteriophage resistance in Bacillus subtilis 168, W23, and interstrain transformants
- Biochemical analysis using biopsied muscle in 72 patients with metabolic myopathies
- Biochemical characterization of avirulent exoC mutants of Agrobacterium tumefaciens
- Capsule Production and Glucose Metabolism Dictate Fitness during <em>Serratia marcescens</em> Bacteremia
- Carbohydrate-deficient glycoprotein syndrome type 1a: a variant phenotype with borderline cognitive dysfunction, cerebellar hypoplasia, and coagulation disturbances
- CT295 Is <em>Chlamydia trachomatis'</em> Phosphoglucomutase and a Type 3 Secretion Substrate
- CT295 Is Chlamydia trachomatis' Phosphoglucomutase and a Type 3 Secretion Substrate
- Defects in leaf carbohydrate metabolism compromise acclimation to high light and lead to a high chlorophyll fluorescence phenotype in Arabidopsis thaliana
- Eleven percent intact PGM3 in a severely immunodeficient patient with a novel splice-site mutation, a case report
- Genetic analysis of phosphomannomutase/phosphoglucomutase from Vibrio furnissii and characterization of its role in virulence
- Human neoplastic and normal cells in tissue culture. I. Cell lines derived from malignant melanomas and normal melanocytes
- Impaired glycogen breakdown and synthesis in phosphoglucomutase 1 deficiency
- Mammalian phosphomannomutase PMM1 is the brain IMP-sensitive glucose-1,6-bisphosphatase
- Metabolic disorders in patients with primary carbohydrate deficient glycoprotein syndrome
- Multi-Omics Profiling in PGM3 and STAT3 Deficiencies: A Tale of Two Patients
- Overexpression of Mycobacterium tuberculosis manB, a phosphomannomutase that increases phosphatidylinositol mannoside biosynthesis in Mycobacterium smegmatis and mycobacterial association with human macrophages
- Phosphomannomutase deficiency is a cause of carbohydrate-deficient glycoprotein syndrome type I
- Possible involvement of bacterial autolytic enzymes in flagellar morphogenesis
- Purification of a beta-Amylase that Accumulates in Arabidopsis thaliana Mutants Defective in Starch Metabolism
- Reduced gravitropic sensitivity in roots of a starch-deficient mutant of Nicotiana sylvestris
- Reduced gravitropic sensitivity in roots of a starch-deficient mutant ofNicotiana sylvestris
- Root graviresponsiveness and cellular differentiation in wild-type and a starchless mutant of Arabidopsis thaliana
- Teichoic acids and lipids associated with the membrane of a Bacillus licheniformis mutant and the membrane lipids of the parental strain