Caenorhabditis elegans triple null mutant lacking UDP-N-acetyl-D-glucosamine:alpha-3-D-mannoside beta1,2-N-acetylglucosaminyltransferase I.

scientific article published on September 2004

Caenorhabditis elegans triple null mutant lacking UDP-N-acetyl-D-glucosamine:alpha-3-D-mannoside beta1,2-N-acetylglucosaminyltransferase I. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1042/BJ20040793
P932PMC publication ID1133976
P698PubMed publication ID15228383

P2093author name stringHarry Schachter
Vernon N Reinhold
Andrew M Spence
Shaoxian Zhu
Andrew Hanneman
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Expression of recombinant rabbit UDP-GlcNAc: alpha 3-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I catalytic domain in Sf9 insect cellsQ42068430
Synthesis of paucimannose N-glycans by Caenorhabditis elegans requires prior actions of UDP-N-acetyl-D-glucosamine:alpha-3-D-mannoside beta1,2-N-acetylglucosaminyltransferase I, alpha3,6-mannosidase II and a specific membrane-bound beta-N-acetylglucQ42088439
Tunicamycin and corynetoxin poisoning in sheepQ43740031
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Modeling human congenital disorder of glycosylation type IIa in the mouse: conservation of asparagine-linked glycan-dependent functions in mammalian physiology and insights into disease pathogenesisQ43862863
Structural analysis of N-linked glycans in Caenorhabditis elegansQ44011492
Toxic effects of a single parenteral dose of tunicamycin in late stage pregnancy in ratsQ44076173
Isolation of null alleles of the Caenorhabditis elegans gly-12, gly-13 and gly-14 genes, all of which encode UDP-GlcNAc: alpha-3-D-mannoside beta1,2-N-acetylglucosaminyltransferase I activityQ44456228
Acute hepatotoxicity with resultant pulmonary and cerebral embolism in guinea pigs given tunicamycinQ46538296
Functional purification and characterization of a GDP-fucose: beta-N-acetylglucosamine (Fuc to Asn linked GlcNAc) alpha 1,3-fucosyltransferase from mung beansQ50755711
Deficient uridine diphosphate-N-acetylglucosamine:glycoprotein N-acetylglucosaminyltransferase activity in a clone of Chinese hamster ovary cells with altered surface glycoproteinsQ67286504
The control of glycoprotein synthesis: N-acetylglucosamine linkage to a mannose residue as a signal for the attachment of L-fucose to the asparagine-linked N-acetylglucosamine residue of glycopeptide from alpha1-acid glycoproteinQ67851174
Carbohydrate-deficient glycoprotein syndrome type II. An autosomal recessive N-acetylglucosaminyltransferase II deficiency different from typical hereditary erythroblastic multinuclearity, with a positive acidified-serum lysis test (HEMPAS)Q71865336
Three genes of the MAP kinase cascade, mek-2, mpk-1/sur-1 and let-60 ras, are required for meiotic cell cycle progression in Caenorhabditis elegansQ72051509
DNA sequencing with chain-terminating inhibitorsQ22066207
The genetics of Caenorhabditis elegansQ24533408
Mutations in the MGAT2 gene controlling complex N-glycan synthesis cause carbohydrate-deficient glycoprotein syndrome type II, an autosomal recessive disease with defective brain developmentQ24675799
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingQ25938984
The nematode Caenorhabditis elegans synthesizes unusual O-linked glycans: identification of glucose-substituted mucin-type O-glycans and short chondroitin-like oligosaccharidesQ28367224
Mice lacking N-acetylglucosaminyltransferase I activity die at mid-gestation, revealing an essential role for complex or hybrid N-linked carbohydratesQ28588255
Mice with a homozygous deletion of the Mgat2 gene encoding UDP-N-acetylglucosamine:alpha-6-D-mannoside beta1,2-N-acetylglucosaminyltransferase II: a model for congenital disorder of glycosylation type IIaQ28589941
Purification, cDNA cloning, and expression of GDP-L-Fuc:Asn-linked GlcNAc alpha1,3-fucosyltransferase from mung beans.Q30741800
The fine structure of Caenorhabditis elegans N-glycansQ30859339
Affinity capturing and gene assignment of soluble glycoproteins produced by the nematode Caenorhabditis elegansQ31093061
Carbohydrate deficient glycoprotein syndrome type II: a deficiency in Golgi localised N-acetyl-glucosaminyltransferase II.Q33624870
Carbohydrate-mediated recognition systems in innate immunityQ33864381
Genetic model organisms in the study of N-glycansQ34351309
Glycosylation in the control of selectin counter-receptor structure and functionQ34862092
Chinese hamster ovary cells selected for resistance to the cytotoxicity of phytohemagglutinin are deficient in a UDP-N-acetylglucosamine--glycoprotein N-acetylglucosaminyltransferase activityQ35087395
Functional post-translational proteomics approach to study the role of N-glycans in the development of Caenorhabditis elegansQ35091646
The glycomes of Caenorhabditis elegans and other model organisms.Q35091671
Hallmarks of Caenorhabditis elegans N-glycosylation: complexity and controversyQ35135539
Alpha-mannosidase-II deficiency results in dyserythropoiesis and unveils an alternate pathway in oligosaccharide biosynthesis.Q36872019
P433issuePt 3
P407language of work or nameEnglishQ1860
P921main subjectCaenorhabditis elegansQ91703
P304page(s)995-1001
P577publication date2004-09-01
P1433published inBiochemical JournalQ864221
P1476titleCaenorhabditis elegans triple null mutant lacking UDP-N-acetyl-D-glucosamine:alpha-3-D-mannoside beta1,2-N-acetylglucosaminyltransferase I.
P478volume382

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