About: Evidence for a (1 leads to 4)-linked 4-O-( -L-idopyranosyluronic acid 2-sulfate)-(2-deoxy-2-sulfoamino-D-glucopyranosyl 6-sulfate) sequence in heparin. Long-range H-H coupling in 4-deoxy-hex-4-enopyranosides

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About: Evidence for a (1 leads to 4)-linked 4-O-( -L-idopyranosyluronic acid 2-sulfate)-(2-deoxy-2-sulfoamino-D-glucopyranosyl 6-sulfate) sequence in heparin. Long-range H-H coupling in 4-deoxy-hex-4-enopyranosides Goto Sponge NotDistinct Permalink

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scientific article published on 01 June 1971

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 1971 (uk) im Juni 1971 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xunu de 1971 (ast) scientific article published on 01 June 1971 (en)
publication date	wds:Q70681538-7330B31D-0093-4CC5-A691-669BB5B7BF85
publication date	1971-06-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q70681538-2919EA47-2D54-43E5-9991-85A63F8AFC6D wds:Q70681538-52DB2E93-EA5A-46F6-A2C6-3394DB255F62 wds:Q70681538-7E94B3BD-FD38-46FF-B05F-B23231EE3C7E wds:Q70681538-ED01E7B4-27DC-44CF-B877-8EC702442A21 wds:Q70681538-EE48514A-6ADF-4969-BDD6-18E7C10D7276 wds:Q70681538-F7747D71-1A56-4D59-94CB-5718A63E7538
cites work	Novel heparin degradation products. Isolation and characterization of novel disaccharides and oligosaccharides produced from heparin by bacterial degradation Enzymic degradation of heparin. A glucosaminidase and a glycuronidase from Flavobacterium heparinum Enzymic degradation of heparin A sulphamidase and a sulphoesterase from Flavobacterium heparinum A uronic acid isomerase in Flavobacterium heparinum. Configuration of the glycosidic linkage of 2-amino-2-deoxy-D-glucopyranose to D-glucuronic acid in heparin The degradation of oligogalacturonides by the polygalacturonase of Bacillus polymyxa
author name string	wds:Q70681538-B4B4B02D-CE51-420F-92A2-05BD98735FD8 wds:Q70681538-D0A507B7-BB1E-44FB-85BC-DA52B1AC7A12 wds:Q70681538-D29720CB-67D1-4B39-873F-F53C832A88BC
author name string	C P Dietrich A S Perlin D M Mackie
rdfs:label	Evidence for a (1 leads to 4)-linked 4-O-( -L-idopyranosyluronic acid 2-sulfate)-(2-deoxy-2-sulfoamino-D-glucopyranosyl 6-sulfate) sequence in heparin. Long-range H-H coupling in 4-deoxy-hex-4-enopyranosides (en) Evidence for a (1 leads to 4)-linked 4-O-( -L-idopyranosyluronic acid 2-sulfate)-(2-deoxy-2-sulfoamino-D-glucopyranosyl 6-sulfate) sequence in heparin. Long-range H-H coupling in 4-deoxy-hex-4-enopyranosides (nl)
skos:prefLabel	Evidence for a (1 leads to 4)-linked 4-O-( -L-idopyranosyluronic acid 2-sulfate)-(2-deoxy-2-sulfoamino-D-glucopyranosyl 6-sulfate) sequence in heparin. Long-range H-H coupling in 4-deoxy-hex-4-enopyranosides (en) Evidence for a (1 leads to 4)-linked 4-O-( -L-idopyranosyluronic acid 2-sulfate)-(2-deoxy-2-sulfoamino-D-glucopyranosyl 6-sulfate) sequence in heparin. Long-range H-H coupling in 4-deoxy-hex-4-enopyranosides (nl)
name	Evidence for a (1 leads to 4)-linked 4-O-( -L-idopyranosyluronic acid 2-sulfate)-(2-deoxy-2-sulfoamino-D-glucopyranosyl 6-sulfate) sequence in heparin. Long-range H-H coupling in 4-deoxy-hex-4-enopyranosides (en) Evidence for a (1 leads to 4)-linked 4-O-( -L-idopyranosyluronic acid 2-sulfate)-(2-deoxy-2-sulfoamino-D-glucopyranosyl 6-sulfate) sequence in heparin. Long-range H-H coupling in 4-deoxy-hex-4-enopyranosides (nl)
title	wds:Q70681538-F9294DE6-6711-4B06-9DF0-EBFBCDAD747A
title	Evidence for a (1 leads to 4)-linked 4-O-( -L-idopyranosyluronic acid 2-sulfate)-(2-deoxy-2-sulfoamino-D-glucopyranosyl 6-sulfate) sequence in heparin. Long-range H-H coupling in 4-deoxy-hex-4-enopyranosides (en)
page(s)	wds:Q70681538-DC88F5B5-679B-4290-AED2-B6932F926A97
page(s)	185-194
instance of	wds:Q70681538-590313B7-4963-4C6D-A160-0278AF2409F9
instance of	scholarly article
PubMed ID	wds:Q70681538-4C8E9BCA-26F3-43F9-A003-21B7146F7E93
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/5151386
PubMed ID	5151386
published in	wds:Q70681538-AFC5F53B-73E8-4D24-B4F3-0C90E4BB60A2
published in	Carbohydrate Research
issue	wds:Q70681538-ABE328C2-4301-4295-A0FA-51C407FCA131
volume	wds:Q70681538-B716F7C7-B2EB-428B-85E0-3ED32832AE59
issue	2
volume	18
DOI	wds:Q70681538-7DB4B77E-DC8E-4C3C-9E35-218F4CFF63FC
DOI	http://dx.doi.org/10.1016/S0008-6215(00)80341-9
DOI	10.1016/S0008-6215(00)80341-9
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q70681538
is cites work of	Structure and biological activity of heparin. Heparan sulfate and heparin interactions with proteins NMR solution conformation of heparin-derived hexasaccharide Structure of heparin-derived tetrasaccharides Applications of magnetic resonance to basic biology and clinical research Depolymerization and De–N–Acetylation of Glycosaminoglycuronans by the Action of Alkali in the Presence of Sodium Borohydride Heparin binding to platelet factor-4. An NMR and site-directed mutagenesis study: arginine residues are crucial for binding Molecular structure of the carbohydrate-protein linkage region fragments from connective-tissue proteoglycans Heparinase II from Flavobacterium heparinum. HPLC analysis of the saccharides generated from chemically modified heparins A major common trisulfated hexasaccharide core sequence, hexuronic acid(2-sulfate)-glucosamine(N-sulfate)-iduronic acid-N-acetylglucosamine-glucuronic acid-glucosamine(N-sulfate), isolated from the low sulfated irregular region of porcine intestinal Conversion of N-sulfated glucosamine to N-sulfated mannosamine in an unsaturated heparin disaccharide by non-enzymatic, base-catalyzed C-2 epimerization during enzymatic oligosaccharide preparation Host-Pathogen Interactions : XXIX. Oligogalacturonides Released from Sodium Polypectate by Endopolygalacturonic Acid Lyase Are Elicitors of Phytoalexins in Soybean. Specificity of flavobacterial glycuronidases acting on disaccharides derived from glycosaminoglycans A 13C-N.M.R. spectral study of chondroitin sulfates A, B, and C: evidence of heterogeneity Solution structures of chemoenzymatically synthesized heparin and its precursors. NMR solution conformation of heparin-derived tetrasaccharide A method for the determination of uronic acid sequence in alginates Determination of Heparin and Related Sulfated Mucopolysaccharides Letter: Standardisation of heparin for clinical use Electrofocusing of heparin: Fractionation of heparin into 21 components distinguishable from other acidic mucopolysaccharides Isolation and partial characterization of three induced enzymes from flavobacterium heparinum involved in the degradation of heparin and heparitin sulfates 13C-NMR relation study of heparin-disaccharide interactions with tripeptides GRG and GKG. Structural characteristics of heparan sulfates with varying sulfate contents Relation of Chemical Structure of Heparin to Its Anticoagulant Activity Bacteriophage-induced acidic heteropolysaccharide lyases that convert the acidic heteropolysaccharides of Rhizobium trifolii into oligosaccharide units. Comparative assessment of the effects of gender-specific heparan sulfates on mesenchymal stem cells A new approach for heparin standardization: combination of scanning UV spectroscopy, nuclear magnetic resonance and principal component analysis. The Distribution of Sulfated Uronic Acid and Hexosamine Residues in Heparin and Heparan Sulfate Extension of sugar chains by enolate addition to methyl 2,3-di-O-acetyl-4-deoxy-β-l-threo-hex-4-enodialdo-1,5-pyranoside New Applications of Heparin and Other Glycosaminoglycans. Structure of heparin. Characterization of the products formed from heparin by the action of a heparinase and a heparitinase from Flavobacterium heparinum Some Recent Developments in the Pharmacology of Heparin Acids and other products of oxidation of sugars Coagulation factor IX mediates serotype-specific binding of species A adenoviruses to host cells Letter: Radioimmunoassay for carcino-embryonic antigen Structure and biological activity of heparin and other glycosaminoglycans The Uronidic Linkages in Heparitin Sulfate Synthesis and biological evaluation of a radiolabeled analog of methyl 2-acetamido-2,4-dideoxy-beta-D-xylo-hexopyranoside directed towards influencing cellular glycosaminoglycan biosynthesis Synthesis of Heparin Saccharides III. Synthesis of Derivatives of D‐Glucosamine as Starting Materials for Disaccharides The Chemistry of Heparin Low-Molecular-Weight Derivative of Heparin that is Orally Active in Mice Regioselectivity in the sulfation of dermatan sulfate and methyl 4,6-O-benzylidene-α-d-idopyranoside Heparin and a cyclic octaphenol-octasulfonic acid (GL-522-Y-1) bind with high affinity to a 47-kda protein from vascular endothelial cell surface and stimulate the synthesis and structural changes of heparan sulfate proteoglycan Identification of heparin in publications Crude Heparin Preparations Unveil the Presence of Structurally Diverse Oversulfated Contaminants
is cites work of	wds:Q37811638-3CD70304-4736-4D40-B1C2-70F82A89A1FF wds:Q35536842-7A2F96DC-8857-4592-A228-205FDD62224B wds:Q38331863-1A532E5F-E9ED-42EF-B7D3-C93D6D5C5662 wds:Q54396509-555508AB-2D18-4CA0-AF0A-4A0F132F216C

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