Chemical approaches to deciphering the glycosaminoglycan code.
about
Chondroitin-4-sulfation negatively regulates axonal guidance and growthSulfated oligosaccharides (heparin and fucoidan) binding and dimerization of stromal cell-derived factor-1 (SDF-1/CXCL 12) are coupled as evidenced by affinity CE-MS analysis.Regulation of intracellular signaling by extracellular glycan remodeling.Novel glycosaminoglycan biosynthetic inhibitors affect tumor-associated angiogenesis.Evaluation of alkyne-modified isoprenoids as chemical reporters of protein prenylation.Transcript analysis of stem cellsElucidating glycosaminoglycan-protein-protein interactions using carbohydrate microarray and computational approaches.Improvement of the digestibility of sulfated hyaluronans by bovine testicular hyaluronidase: a UV spectroscopic and mass spectrometric studyHighly efficient syntheses of hyaluronic acid oligosaccharides.High-performance liquid chromatography-mass spectrometry for mapping and sequencing glycosaminoglycan-derived oligosaccharides.A facile method for oxidation of primary alcohols to carboxylic acids and its application in glycosaminoglycan syntheses.ELECTRON DETACHMENT DISSOCIATION OF SYNTHETIC HEPARAN SULFATE GLYCOSAMINOGLYCAN TETRASACCHARIDES VARYING IN DEGREE OF SULFATION AND HEXURONIC ACID STEREOCHEMISTRY.Harnessing glycomics technologies: integrating structure with function for glycan characterization.Installation of electron-donating protective groups, a strategy for glycosylating unreactive thioglycosyl acceptors using the preactivation-based glycosylation method.The chemical neurobiology of carbohydratesRecent advances in chemical proteomics: exploring the post-translational proteome.Regenerative potential of glycosaminoglycans for skin and bone.Sugar glues for broken neuronsGlycodendrimers as Chondroitin Sulfate Mimetics: Synthesis and Binding to Growth Factor Midkine.Improvement on binding of chondroitin sulfate derivatives to midkine by increasing hydrophobicity.Glycomics of proteoglycan biosynthesis in murine embryonic stem cell differentiation.Synthesis of chondroitin/dermatan sulfate-like oligosaccharides and evaluation of their protein affinity by fluorescence polarization.Synthesis of amine-functionalized heparin oligosaccharides for the investigation of carbohydrate-protein interactions in microtiter plates.Mucin-like Region of Herpes Simplex Virus Type 1 Attachment Protein Glycoprotein C (gC) Modulates the Virus-Glycosaminoglycan InteractionBinding Kinetics and Lateral Mobility of HSV-1 on End-Grafted Sulfated Glycosaminoglycans.Conformational Populations of β-(1→4) O-Glycosidic Linkages Using Redundant NMR J-Couplings and Circular Statistics.Neuroactive chondroitin sulfate glycomimeticsSugar-dependent modulation of neuronal development, regeneration, and plasticity by chondroitin sulfate proteoglycans.ESI-MS differential fragmentation of positional isomers of sulfated oligosaccharides derived from carrageenans and agarans.End-functionalized glycopolymers as mimetics of chondroitin sulfate proteoglycansAutomated solid-phase synthesis of chondroitin sulfate glycosaminoglycans.Production of carbohydrate building blocks from red seaweed polysaccharides. Efficient conversion of galactans into C-glycosyl aldehydes.Discovery of a Small-Molecule Modulator of Glycosaminoglycan Sulfation.Total synthesis of sialic acid by a sequential rhodium-catalyzed aziridination and Barbier allylation of D-glycal.Analysis of glycosaminoglycan-derived, precolumn, 2-aminoacridone-labeled disaccharides with LC-fluorescence and LC-MS detection.
P2860
Q30483928-7AF57FC9-FCDF-4B98-82CC-9BE968968E31Q33370024-BB9DE6C8-665D-4D29-AEF6-D100D0F3D385Q33675552-592F4CA9-A3C0-48C1-8B38-331F9E63F11EQ34540672-A92FFDCA-30DE-4A35-B2CD-0B06B497B9E9Q34679579-6521E5FD-266C-4B91-B71C-B21181E3AD7BQ35014413-6C2ABDC8-0CBB-4F95-9B69-0429D240A218Q35049136-0F288350-7F08-45AB-BA6D-E18A94112873Q35196193-57C0A5E1-603B-4022-8ECB-0C5FC778F058Q35677246-CC557C35-5B5C-44EF-AFB6-B605F049754BQ35984139-81F1BB64-2FC9-4415-BC39-F801E9FB325CQ36002444-01CB4A52-450D-4ABC-BC6C-7BCC56FC5010Q36453197-C2BC8ED9-8946-443F-BA5F-C26DB2ECBDBCQ37095486-BD3FD24C-9395-438E-9FBA-E36FB28EE461Q37141532-6B14C808-7A08-4467-831E-2C40BF21CAE3Q37152815-402316F2-5442-45A3-B46B-00ABB07CFBC9Q37537095-5E3E3135-3F6A-40CC-B461-2972CD69B404Q37970313-6B627027-F262-4F97-88E8-093537983984Q38256971-CF637BBC-35D3-4DE7-B055-C0D8F7AF5A1EQ38287940-30964EBB-8B12-4ED7-B9C4-9B116D4F123AQ38293154-141E06E1-416B-414C-BE39-749C5331A7D5Q38297633-4CAD9ED7-AFFA-473A-92D4-FBE3D93E5F86Q38316258-9993532B-EE4E-446E-94C8-FA77EB0EFAA4Q38328126-67C4AD26-50DC-4C70-BEA2-6F58FA4C38D5Q38854789-0DD32A25-E3B8-44A9-BE7A-289F459CE74AQ40126963-006E0FF0-D719-4704-9B73-6A6F0AC79058Q41360188-E132C361-4E78-437E-827E-21D281323A82Q41825737-5D9C838A-3C44-4050-9418-B727E976A383Q42133466-87FDEF05-FEBA-4FDA-BA5E-0BCA693644DBQ42169559-E8012544-F51D-4F66-A6D2-9BF501C8F880Q42579389-C58CF1ED-34ED-48E8-B4F9-CECCC21FB88BQ43420107-9936D1F5-0CBA-4003-9442-BA189A37D3AEQ46155468-D1E11F19-DE55-4E47-9D7E-E4ADE1E6F4C0Q46646980-8306937E-842E-4A68-87A2-72752A445FFBQ51515981-54D592B1-F4A9-4D79-A325-F119A42F6F74Q53625004-7C337444-12FB-4AD9-857C-3D4B80EB4BA7
P2860
Chemical approaches to deciphering the glycosaminoglycan code.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh
2005年學術文章
@zh-hant
name
Chemical approaches to deciphering the glycosaminoglycan code.
@ast
Chemical approaches to deciphering the glycosaminoglycan code.
@en
type
label
Chemical approaches to deciphering the glycosaminoglycan code.
@ast
Chemical approaches to deciphering the glycosaminoglycan code.
@en
prefLabel
Chemical approaches to deciphering the glycosaminoglycan code.
@ast
Chemical approaches to deciphering the glycosaminoglycan code.
@en
P1476
Chemical approaches to deciphering the glycosaminoglycan code.
@en
P2093
Cristal I Gama
Linda C Hsieh-Wilson
P304
P356
10.1016/J.CBPA.2005.10.003
P577
2005-10-18T00:00:00Z