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Glycosaminoglycans

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Cover of 'Glycosaminoglycans'

Table of Contents

  1. Altmetric Badge
    Book Overview
  2. Altmetric Badge
    Chapter 1 Automated Synthesis of Chondroitin Sulfate Oligosaccharides
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    Chapter 2 Enzymatic synthesis of heparan sulfate and heparin.
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    Chapter 3 Production of Size-Defined Heparosan, Heparan Sulfate, and Heparin Oligosaccharides by Enzymatic Depolymerization
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    Chapter 4 Chemical modification of heparin and heparosan.
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    Chapter 5 Synthesis of Sulfur Isotope-Labeled Sulfate Donor, 3′-Phosphoadenosine-5′-Phosphosulfate, for Studying Glycosaminoglycan Functions
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    Chapter 6 Preparation of Isotope-Enriched Heparan Sulfate Precursors for Structural Biology Studies
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    Chapter 7 Glycosaminoglycans
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    Chapter 8 Synthesis of Selective Inhibitors of Heparan Sulfate and Chondroitin Sulfate Proteoglycan Biosynthesis
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    Chapter 9 Ascidian (Chordata-Tunicata) Glycosaminoglycans: Extraction, Purification, Biochemical, and Spectroscopic Analysis
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    Chapter 10 Human Blood Glycosaminoglycans: Isolation and Analysis
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    Chapter 11 Chromatographic Molecular Weight Measurements for Heparin, Its Fragments and Fractions, and Other Glycosaminoglycans
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    Chapter 12 Mass Spectrometric Methods for the Analysis of Heparin and Heparan Sulfate
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    Chapter 13 Validated Capillary Electrophoretic Assays for Disaccharide Composition Analysis of Galactosaminoglycans in Biologic Samples and Drugs/Nutraceuticals
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    Chapter 14 Fast Screening of Glycosaminoglycan Disaccharides by Fluorophore-Assisted Carbohydrate Electrophoresis (FACE): Applications to Biologic Samples and Pharmaceutical Formulations
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    Chapter 15 Capillary Electrophoretic Analysis of Isolated Sulfated Polysaccharides to Characterize Pharmaceutical Products
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    Chapter 16 Methods for Measuring Exchangeable Protons in Glycosaminoglycans
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    Chapter 17 Heparan Sulfate Structure: Methods to Study N -Sulfation and NDST Action
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    Chapter 18 Analysis of Hyaluronan Synthase Activity
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    Chapter 19 A rapid, nonradioactive assay for measuring heparan sulfate C-5 epimerase activity using hydrogen/deuterium exchange-mass spectrometry.
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    Chapter 20 Aggrecan: Approaches to Study Biophysical and Biomechanical Properties
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    Chapter 21 Use of flow cytometry for characterization and fractionation of cell populations based on their expression of heparan sulfate epitopes.
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    Chapter 22 A transgenic approach to live imaging of heparan sulfate modification patterns.
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    Chapter 23 Informatics Tools to Advance the Biology of Glycosaminoglycans and Proteoglycans
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    Chapter 24 Designing “High-Affinity, High-Specificity” Glycosaminoglycan Sequences Through Computerized Modeling
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    Chapter 25 Using Isothermal Titration Calorimetry to Determine Thermodynamic Parameters of Protein–Glycosaminoglycan Interactions
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    Chapter 26 Characterizing protein-glycosaminoglycan interactions using solution NMR spectroscopy.
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    Chapter 27 Glycosaminoglycans
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    Chapter 28 Studying Glycosaminoglycan–Protein Interactions Using Capillary Electrophoresis
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    Chapter 29 Histochemical Analysis of Heparan Sulfate 3- O -Sulfotransferase Expression in Mouse Brain
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    Chapter 30 Keratan Sulfate: Biosynthesis, Structures, and Biological Functions
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    Chapter 31 The sulfs: expression, purification, and substrate specificity.
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    Chapter 32 The Detection of Glycosaminoglycans in Pancreatic Islets and Lymphoid Tissues
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    Chapter 33 Nonradioactive Glycosyltransferase and Sulfotransferase Assay to Study Glycosaminoglycan Biosynthesis
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    Chapter 34 Mapping Proteoglycan Functions with Glycosidases
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    Chapter 35 Cell substrate patterning with glycosaminoglycans to study their biological roles in the central nervous system.
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    Chapter 36 Analyzing the role of heparan sulfate proteoglycans in axon guidance in vivo in zebrafish.
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    Chapter 37 Murine Models in the Evaluation of Heparan Sulfate-Based Anticoagulants
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    Chapter 38 Genetic approaches in the study of heparan sulfate functions in Drosophila.
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    Chapter 39 Measuring Sulfatase Expression and Invasion in Glioblastoma
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    Chapter 40 Synthesis and biomedical applications of xylosides.
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    Chapter 41 A Strategic Approach to Identification of Selective Inhibitors of Cancer Stem Cells
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    Chapter 42 Analysis of the Heavy-Chain Modification and TSG-6 Activity in Pathological Hyaluronan Matrices
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    Chapter 43 Heparan Sulfate Modulates Slit3-Induced Endothelial Cell Migration
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    Chapter 44 Glycosaminoglycans
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    Chapter 45 Role of glycosaminoglycans in infectious disease.
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    Chapter 46 Isolation and purification of versican and analysis of versican proteolysis.
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    Chapter 47 Analysis of Human Hyaluronan Synthase Gene Transcriptional Regulation and Downstream Hyaluronan Cell Surface Receptor Mobility in Myofibroblast Differentiation
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    Chapter 48 Erratum: Using Isothermal Titration Calorimetry to Determine Thermodynamic Parameters of Protein–Glycosaminoglycan Interactions
Attention for Chapter 35: Cell substrate patterning with glycosaminoglycans to study their biological roles in the central nervous system.
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Chapter title
Cell substrate patterning with glycosaminoglycans to study their biological roles in the central nervous system.
Chapter number 35
Book title
Glycosaminoglycans
Published in
Methods in molecular biology, January 2015
DOI 10.1007/978-1-4939-1714-3_35
Pubmed ID
Book ISBNs
978-1-4939-1713-6, 978-1-4939-1714-3
Authors

Tony W Hsiao, Vimal P Swarup, Colin D Eichinger, Vladimir Hlady, Tony W. Hsiao, Vimal P. Swarup, Colin D. Eichinger, Hsiao, Tony W., Swarup, Vimal P., Eichinger, Colin D., Hlady, Vladimir

Abstract

Microcontact printing (μCP) based techniques have been developed for creating cell culture substrates with discrete placement of CNS-expressed molecules. These substrates can be used to study various components of the complex molecular environment in the central nervous system (CNS) and related cellular responses. Macromolecules such as glycosaminoglycans (GAGs), proteoglycans (PGs), or proteins are amenable to printing. Detailed protocols for both adsorption based as well as covalent reaction printing of cell culture substrates are provided. By utilizing a modified light microscope, precise placement of two or more types of macromolecules by sequential μCP can be used to create desired spatial arrangements containing multicomponent PG, GAG, and protein surface patterns for studying CNS cell behavior. Examples of GAG stripe assays for neuronal pathfinding and directed outgrowth, and dot gradients of PG + laminin for astrocyte migration studies are provided.

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Mendeley readers

The data shown below were compiled from readership statistics for 1 Mendeley reader of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 1 100%

Demographic breakdown

Readers by professional status Count As %
Professor > Associate Professor 1 100%
Readers by discipline Count As %
Agricultural and Biological Sciences 1 100%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 2. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 18 June 2015.
All research outputs
#14,787,304
of 22,766,595 outputs
Outputs from Methods in molecular biology
#4,676
of 13,090 outputs
Outputs of similar age
#197,789
of 352,895 outputs
Outputs of similar age from Methods in molecular biology
#295
of 996 outputs
Altmetric has tracked 22,766,595 research outputs across all sources so far. This one is in the 32nd percentile – i.e., 32% of other outputs scored the same or lower than it.
So far Altmetric has tracked 13,090 research outputs from this source. They receive a mean Attention Score of 3.3. This one has gotten more attention than average, scoring higher than 59% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 352,895 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 41st percentile – i.e., 41% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 996 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 66% of its contemporaries.