CDG

(redirected from Congenital disorder of glycosylation)
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AcronymDefinition
CDGCaisse de Dépôt et de Gestion (French; Moroccan federal depository)
CDGCentre de Gestion
CDGCommunity Development Group (various locations)
CDGCDMA Development Group
CDGC++ Documentation Generator
CDGCompact Disc Plus Graphics
CDGCommanding
CDGCenter for Digital Government (Folsom, CA)
CDGCentre for Democratic Governance (various locations)
CDGComdotgame
CDGCzech Digital Group
CDGCongenital Disorder of Glycosylation
CDGCarbohydrate-Deficient Glycoprotein
CDGChris Duarte Group (band)
CDGCave Diving Group (UK)
CDGComme Des Garcon
CDGCompagnie des Garages (French car company)
CDGParis, France - Charles De Gaulle (Airport Code)
CDGCareer Development Grant (various organizations)
CDGConsumer Digital Imaging Group (Eastman Kodak Company)
CDGChristian-Doppler-Forschungsgesellschaft (German: Christian Doppler Research Association )
CDGCapacitance Diaphragm Gauge
CDGControl Dependence Graph
CDGCompetitive Development Group
CDGCompact Disk + Graphics
CDGConcept Development Group
CDGCentre des Droits des Gens (French: Centre for People’s Rights; Morocco)
CDGCompletely Decomposed Granite
CDGCasting Directors' Guild (cinema)
CDGControlled Demolition Group (contractor; UK)
CDGComponent-Dependency Graph
CDGCoverage Directed Generation
CDGConstitutional Delay of Growth
CDGContext-Dependent Grammar
CDGCarl Duisberg Gesellschaft eV
CDGCustomer Development Group
CDGCoder-Decoder Group
CDGCultural Development Group
CDGChambres de Guérison (French: Healing Rooms)
CDGChemical Defense Group
CDGClassical Differential Geometry
CDGCountry Development Group
CDGClimate Dynamics Group
CDGCornerstone Development Group, LLC (Hampton, VA)
CDGCentre Downwash Generating (aerodynamics, fluid dynamics, automotive)
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References in periodicals archive ?
Genetic complementation reveals a novel human congenital disorder of glycosylation of type II due to inactivation of the Golgi CMP-sialic acid transporter.
Congenital disorder of glycosylation id presenting with hyperinsulinemic hypoglycemia and islet cell hyperplasia.
Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter.
Congenital disorder of glycosylation Ia with deficient phosphomannomutase activity but normal plasma glycoprotein pattern.
Deficiency of GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase causes congenital disorder of glycosylation type Ik.
Genetic and metabolic analysis of the first adult with congenital disorder of glycosylation type Ib: long-term outcome and effects of mannose supplementation.
Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type le.
[3] Nonstandard abbreviations: PI, protease inhibitor; CDG-Ia, congenital disorder of glycosylation type Ia; 2D-PAGE, two-dimensional polyacrylamide gel electrophoresis; and MALD1-TOF-MS, matrix-assisted laser desorptionionization time-of-flight mass spectrometry.
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