scholarly article | Q13442814 |
P50 | author | Hudson H. Freeze | Q38320794 |
P2093 | author name string | David A Scott | |
Marie-Estelle Losfeld | |||
Mie Ichikawa | |||
P2860 | cites work | Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy | Q24564669 |
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Deletion of genes encoding cytochrome oxidases and quinol monooxygenase blocks the aerobic-anaerobic shift in Escherichia coli K-12 MG1655. | Q34177720 | ||
Mannose efflux from the cells: a potential source of mannose in blood | Q34695595 | ||
Phosphomannose isomerase inhibitors improve N-glycosylation in selected phosphomannomutase-deficient fibroblasts | Q35604388 | ||
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Mass isotopomer analysis of metabolically labeled nucleotide sugars and N- and O-glycans for tracing nucleotide sugar metabolisms | Q37160924 | ||
Mannose corrects altered N-glycosylation in carbohydrate-deficient glycoprotein syndrome fibroblasts | Q37353246 | ||
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Failure of short-term mannose therapy of patients with carbohydrate-deficient glycoprotein syndrome type 1A. | Q38333419 | ||
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Human fibroblasts prefer mannose over glucose as a source of mannose for N-glycosylation. Evidence for the functional importance of transported mannose | Q41091656 | ||
Glycogen: a carbohydrate source for GLUT-1 glycosylation during glucose deprivation of 3T3-L1 adipocytes | Q42814443 | ||
Rapid activation of glycogen phosphorylase by the endoplasmic reticulum unfolded protein response | Q44132514 | ||
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Oral mannose therapy persistently corrects the severe clinical symptoms and biochemical abnormalities of phosphomannose isomerase deficiency | Q44218677 | ||
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Compartmentation of lactate originating from glycogen and glucose in cultured astrocytes | Q46845563 | ||
A comparison of three methods of glycogen measurement in tissues | Q48532632 | ||
Functional characterisation of human SGLT-5 as a novel kidney-specific sodium-dependent sugar transporter | Q50337162 | ||
Successful prenatal mannose treatment for congenital disorder of glycosylation-Ia in mice. | Q50776761 | ||
Mannose 6-Phosphate: Anomeric Form Used by Phosphomannose Isomerase and Its l-Epimerization by Phosphoglucose Isomerase | Q55061500 | ||
Mannose supplementation in carbohydrate-deficient glycoprotein syndrome type I and phosphomannomutase deficiency | Q74827807 | ||
P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | mannose | Q10809118 |
P304 | page(s) | 6751-6761 | |
P577 | publication date | 2014-01-09 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | The metabolic origins of mannose in glycoproteins | |
P478 | volume | 289 |
Q38290461 | A mouse model of a human congenital disorder of glycosylation caused by loss of PMM2. |
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Q42272453 | Perhaps a wee bit of sugar would help |
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