Chemical approaches to define the structure-activity relationship of heparin-like glycosaminoglycans.
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Diverse Roles of Heparan Sulfate and Heparin in Wound RepairProfiling heparin-chemokine interactions using synthetic toolsModular synthesis of heparan sulfate oligosaccharides for structure-activity relationship studies.Enzymatic synthesis of heparin related polysaccharides on sensor chips: rapid screening of heparin-protein interactions.CCR2 chemokines bind selectively to acetylated heparan sulfate octasaccharides.Combinatorial enzymatic synthesis of heparan sulfate.Using an enzymatic combinatorial approach to identify anticoagulant heparan sulfate structures.New glucuronic acid donors for the modular synthesis of heparan sulfate oligosaccharidesTowards the assembly of heparin and heparan sulfate oligosaccharide libraries: efficient synthesis of uronic acid and disaccharide building blocks.Preactivation-based, one-pot combinatorial synthesis of heparin-like hexasaccharides for the analysis of heparin-protein interactions.Effect of heparin oligomer chain length on the activation of valvular interstitial cells.Glycocalyx remodeling with proteoglycan mimetics promotes neural specification in embryonic stem cellsSulodexide: a renewed interest in this glycosaminoglycan.Synthesis of a targeted library of heparan sulfate hexa- to dodecasaccharides as inhibitors of β-secretase: potential therapeutics for Alzheimer's disease.Characterization of annexin A1 glycan binding reveals binding to highly sulfated glycans with preference for highly sulfated heparan sulfate and heparin.Modular synthesis of heparin-related tetra-, hexa- and octasaccharides with differential o-6 protections: programming for regiodefined 6-o-modifications.Complete mass spectral characterization of a synthetic ultralow-molecular-weight heparin using collision-induced dissociation.Metabolic engineering of Chinese hamster ovary cells: towards a bioengineered heparinSynthetic heparan sulfate dodecasaccharides reveal single sulfation site interconverts CXCL8 and CXCL12 chemokine biology.Fluorous supported modular synthesis of heparan sulfate oligosaccharides.Strategies in synthesis of heparin/heparan sulfate oligosaccharides: 2000-present.The chemical neurobiology of carbohydratesCarbohydrate post-glycosylational modifications.Opportunities and challenges in synthetic oligosaccharide and glycoconjugate research.Heparan sulfate proteoglycans: structure, protein interactions and cell signaling.Toward automated oligosaccharide synthesis.Glycosaminoglycans in biomedicine.Heparin/heparan sulphate interactions with complement--a possible target for reduction of renal function loss?Synthetic oligosaccharides as active pharmaceutical ingredients: lessons learned from the full synthesis of one heparin derivative on a large scale.Synthesis of amine-functionalized heparin oligosaccharides for the investigation of carbohydrate-protein interactions in microtiter plates.Synthesis of heparin oligosaccharides and their interaction with eosinophil-derived neurotoxin.A Dilemma in the Glycosaminoglycan-Based Therapy: Synthetic or Naturally Unique Molecules?Targeting heparin and heparan sulfate protein interactions.Identification of core active disaccharides in heparin for HGF-inducing activity.Anomeric reactivity-based one-pot synthesis of heparin-like oligosaccharides.Tailored design and synthesis of heparan sulfate oligosaccharide analogues using sequential one-pot multienzyme systemsHeparan sulfate separation, sequencing, and isomeric differentiation: ion mobility spectrometry reveals specific iduronic and glucuronic acid-containing hexasaccharides.Synthetic Oligosaccharide Libraries and Microarray Technology: A Powerful Combination for the Success of Current Glycosaminoglycan Interactomics.Using structurally defined oligosaccharides to understand the interactions between proteins and heparan sulfate.Benzylidene Acetal Protecting Group as Carboxylic Acid Surrogate: Synthesis of Functionalized Uronic Acids and Sugar Amino Acids.
P2860
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P2860
Chemical approaches to define the structure-activity relationship of heparin-like glycosaminoglycans.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Chemical approaches to define ...... parin-like glycosaminoglycans.
@ast
Chemical approaches to define ...... parin-like glycosaminoglycans.
@en
type
label
Chemical approaches to define ...... parin-like glycosaminoglycans.
@ast
Chemical approaches to define ...... parin-like glycosaminoglycans.
@en
prefLabel
Chemical approaches to define ...... parin-like glycosaminoglycans.
@ast
Chemical approaches to define ...... parin-like glycosaminoglycans.
@en
P1476
Chemical approaches to define ...... parin-like glycosaminoglycans.
@en
P2093
Christian Noti
Peter H Seeberger
P304
P356
10.1016/J.CHEMBIOL.2005.05.013
P577
2005-07-01T00:00:00Z