A general strategy for the chemoenzymatic synthesis of asymmetrically branched N-glycans
about
Electrochemistry of nonconjugated proteins and glycoproteins. Toward sensors for biomedicine and glycomicsHemagglutinin Receptor Specificity and Structural Analyses of Respiratory Droplet-Transmissible H5N1 VirusesThe neoglycolipid (NGL)-based oligosaccharide microarray system poised to decipher the meta-glycomeMutation of the Second Sialic Acid-Binding Site, Resulting in Reduced Neuraminidase Activity, Preceded the Emergence of H7N9 Influenza A Virus.Combining 3D structure with glycan array data provides insight into the origin of glycan specificityA multifunctional anomeric linker for the chemoenzymatic synthesis of complex oligosaccharides.Macrocyclic bis-thioureas catalyze stereospecific glycosylation reactions.PNA-encoded synthesis (PES) of a 10 000-member hetero-glycoconjugate library and microarray analysis of diverse lectins.Construction of a high-mannose-type glycan library by a renewed top-down chemo-enzymatic approach.Efficient Chemoenzymatic Synthesis of an N-glycan Isomer Library.The detection and discovery of glycan motifs in biological samples using lectins and antibodies: new methods and opportunities.Approaches toward High-Mannose-Type Glycan Libraries.Identification of the binding roles of terminal and internal glycan epitopes using enzymatically synthesized N-glycans containing tandem epitopes.Construction and characterisation of a heparan sulphate heptasaccharide microarray.Synthesis of lacto-N-tetraose.A latent reactive handle for functionalising heparin-like and LMWH deca- and dodecasaccharides.Chemical Methods for Encoding and Decoding of Posttranslational ModificationsModular synthesis of N-glycans and arrays for the hetero-ligand binding analysis of HIV antibodiesChemical and chemoenzymatic synthesis of glycoproteins for deciphering functions.Characterizing Protein Glycosylation through On-Chip Glycan Modification and ProbingThe challenge and promise of glycomics.Adaptive immune activation: glycosylation does matter.Synthesis of fluorous photolabile aldehyde and carbamate and alkyl carbamate protecting groups for carbohydrate-associated amines.Fluorous-assisted chemoenzymatic synthesis of heparan sulfate oligosaccharides.Chemistry of natural glycan microarrays.Synthesis of asymmetrical multiantennary human milk oligosaccharides.Label-Free Detection of Glycan-Protein Interactions for Array Development by Surface-Enhanced Raman Spectroscopy (SERS).Targeted methods for quantitative analysis of protein glycosylation.Sialylation of lactosyl lipids in membrane microdomains by T. cruzi trans-sialidase.N-(2-Acetamido-2-de-oxy-β-d-gluco-pyranos-yl)-N-(3-azido-prop-yl)-O-methyl-hydroxyl-amineSugared biomaterial binding lectins: achievements and perspectives.Can glycoprofiling be helpful in detecting prostate cancer?Identification of carbohydrate anomers using ion mobility-mass spectrometry.Total syntheses of five uvacalols: structural validation of uvacalol A, uvacalol B and uvacalol C and disproval of the structures of uvacalol E and uvacalol G.Programmed chemo-enzymatic synthesis of the oligosaccharide component of a carbohydrate-based antibacterial vaccine candidate.An ultrasensitive impedimetric glycan biosensor with controlled glycan density for detection of lectins and influenza hemagglutininsBiochemistry: Constructing complicated carbohydrates.Chemistry. A path to complex carbohydrates.Stereocontrolled 1,2-cis glycosylation as the driving force of progress in synthetic carbohydrate chemistry.A minimalist approach to stereoselective glycosylation with unprotected donors.
P2860
Q26822552-81659152-272C-4BAB-946C-E6AE8D4DB7FBQ27680490-265E6165-8691-4C1C-AFBF-01B8521ED41AQ28655480-CA480854-74AC-4FFA-9839-A8695DF9C78DQ30398660-348130B0-D8E0-42D4-B088-4538F47FC9C0Q31048953-75B40D4A-8C41-495A-8D27-424899AA5956Q33924672-A50C547B-56C5-49FF-BBFB-765CFD8D5BB1Q34549089-B7945CF3-0630-4BF3-838F-51B271413042Q35232193-E9B267CD-0F3F-4B3E-A5D0-F75043B81535Q35542490-590B6B3F-85BC-4AEA-88C4-72FD1FD16C11Q35791275-DAF58640-6F7A-42C0-B160-16E227E87F4CQ35794259-87968658-16F9-41C1-9756-B18188A37308Q35817722-8DEE6E34-8348-46BA-99E6-D2CD4149853DQ36165697-632F43EC-B184-4630-AA45-5B5ED2DD89E0Q36255119-89E58A41-E8BC-4FFC-B13B-983B1F58FF26Q36284753-D3F34D00-55E7-4964-B5D4-8D6D3562B401Q36354764-B8CFB68A-1E50-4BC1-B140-ACFC65B226C2Q36654176-E6B97433-4335-40EC-9F38-C40DB82B0195Q36725490-1B0BB808-6636-47B0-9CA9-A6DBA9353002Q37581781-AD2B0CD0-1A47-4591-86FF-CF815353671DQ37623120-5DEEB9EB-C3B8-4B0F-9478-F3AC02CAAF2CQ37638949-B5D08D78-8775-4909-86F2-65D88EAB0F84Q37663706-D95F19AB-FE5D-4303-89CC-B3D2DDA3BE27Q37714098-9B809518-BB06-4451-80B2-E1983A0134A1Q37721690-B0488029-A125-43DB-B3C4-E18671223BF9Q38184301-FC252F0D-C6C4-46F0-B17D-DA4E03F02373Q38287911-BA1F79EA-6C1F-4A3D-BFE5-65B9EA61AB98Q38292044-4A38E9F4-2EB2-4BE6-82CE-50C0D305AE5CQ38293204-3784F994-43B3-4D5B-AB13-D2CAEF4FF065Q38303580-1284C17D-5F30-48C9-9AA8-99210FF70A4FQ38786666-74F14E2B-CBC9-4DBD-B104-71E5EFBB33F8Q38807532-F79D6DEB-35B4-4C72-90D4-BFC90BB29243Q38852467-902FCE69-E24B-4F87-81BC-A37D1D208D9EQ40489012-69F52C1C-544F-40EB-896C-1A4BDFBB8E4CQ41472936-49E6E883-E624-4077-B128-E433CFEB4568Q41609325-33A5A0CA-B8D3-4E72-943C-E6745A5C840FQ42151473-5563344D-DFD2-4118-8243-B8C2A4900FCBQ42259612-FC32A055-425E-4FA2-859F-234EA4FA067EQ42281299-E9E4C0C3-CACE-4194-81AA-D0451BC8C38EQ42495215-E4AB220D-5C06-4867-A9B7-5FDC113A3D0FQ42611963-CF7FE82F-3BA4-4010-91CF-CE35CDC62313
P2860
A general strategy for the chemoenzymatic synthesis of asymmetrically branched N-glycans
description
2013 nî lūn-bûn
@nan
2013 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
A general strategy for the chemoenzymatic synthesis of asymmetrically branched N-glycans
@ast
A general strategy for the chemoenzymatic synthesis of asymmetrically branched N-glycans
@en
A general strategy for the chemoenzymatic synthesis of asymmetrically branched N-glycans
@nl
type
label
A general strategy for the chemoenzymatic synthesis of asymmetrically branched N-glycans
@ast
A general strategy for the chemoenzymatic synthesis of asymmetrically branched N-glycans
@en
A general strategy for the chemoenzymatic synthesis of asymmetrically branched N-glycans
@nl
prefLabel
A general strategy for the chemoenzymatic synthesis of asymmetrically branched N-glycans
@ast
A general strategy for the chemoenzymatic synthesis of asymmetrically branched N-glycans
@en
A general strategy for the chemoenzymatic synthesis of asymmetrically branched N-glycans
@nl
P2093
P2860
P356
P1433
P1476
A general strategy for the chemoenzymatic synthesis of asymmetrically branched N-glycans
@en
P2093
James C Paulson
John Glushka
Robert P de Vries
Ryan McBride
Shailesh G Ambre
Zoeisha S Chinoy
P2860
P304
P356
10.1126/SCIENCE.1236231
P407
P577
2013-07-01T00:00:00Z