Ota H, Sato H, Mizumoto S, Wakai K, Yoneda K, Yamamoto K
Sci Rep. 2023; 13(1):11618.
PMID: 37463954
PMC: 10354070.
DOI: 10.1038/s41598-023-38746-x.
Sreekumar S, Wattjes J, Niehues A, Mengoni T, Mendes A, Morris E
Nat Commun. 2022; 13(1):7125.
PMID: 36418307
PMC: 9684148.
DOI: 10.1038/s41467-022-34483-3.
Wu J, Chopra P, Boons G, Zaia J
Glycobiology. 2021; 32(3):208-217.
PMID: 33822051
PMC: 8966481.
DOI: 10.1093/glycob/cwab023.
Chopra P, Joshi A, Wu J, Lu W, Yadavalli T, Wolfert M
Proc Natl Acad Sci U S A. 2021; 118(3).
PMID: 33441484
PMC: 7826381.
DOI: 10.1073/pnas.2012935118.
Alabbas A, Desai U
Glycobiology. 2020; 30(10):768-773.
PMID: 32193533
PMC: 7526740.
DOI: 10.1093/glycob/cwaa027.
Heparanase as an Additional Tool for Detecting Structural Peculiarities of Heparin Oligosaccharides.
Alekseeva A, Urso E, Mazzini G, Naggi A
Molecules. 2019; 24(23).
PMID: 31810297
PMC: 6930493.
DOI: 10.3390/molecules24234403.
Synthesis of 3--Sulfated Disaccharide and Tetrasaccharide Standards for Compositional Analysis of Heparan Sulfate.
Dhurandhare V, Pagadala V, Ferreira A, De Muynck L, Liu J
Biochemistry. 2019; 59(34):3186-3192.
PMID: 31608625
PMC: 7269455.
DOI: 10.1021/acs.biochem.9b00838.
Sources, Extraction and Biomedical Properties of Polysaccharides.
Ullah S, Khalil A, Shaukat F, Song Y
Foods. 2019; 8(8).
PMID: 31374889
PMC: 6723881.
DOI: 10.3390/foods8080304.
Specificity and action pattern of heparanase Bp, a β-glucuronidase from Burkholderia pseudomallei.
Yu Y, Williams A, Zhang X, Fu L, Xia K, Xu Y
Glycobiology. 2019; 29(8):572-581.
PMID: 31143933
PMC: 6639543.
DOI: 10.1093/glycob/cwz039.
Recombinant Heparin-New Opportunities.
Glass C
Front Med (Lausanne). 2018; 5:341.
PMID: 30564580
PMC: 6288228.
DOI: 10.3389/fmed.2018.00341.
Bioactive polysaccharides from natural resources including Chinese medicinal herbs on tissue repair.
Li Q, Niu Y, Xing P, Wang C
Chin Med. 2018; 13:7.
PMID: 29445417
PMC: 5802060.
DOI: 10.1186/s13020-018-0166-0.
Structural Analysis of Heparin-Derived 3-O-Sulfated Tetrasaccharides: Antithrombin Binding Site Variants.
Chen Y, Lin L, Agyekum I, Zhang X, St Ange K, Yu Y
J Pharm Sci. 2016; 106(4):973-981.
PMID: 28007564
PMC: 5553205.
DOI: 10.1016/j.xphs.2016.11.023.
GlycCompSoft: Software for Automated Comparison of Low Molecular Weight Heparins Using Top-Down LC/MS Data.
Wang X, Liu X, Li L, Zhang F, Hu M, Ren F
PLoS One. 2016; 11(12):e0167727.
PMID: 27942011
PMC: 5152843.
DOI: 10.1371/journal.pone.0167727.
Analysis of heparin oligosaccharides by capillary electrophoresis-negative-ion electrospray ionization mass spectrometry.
Lin L, Liu X, Zhang F, Chi L, Jonathan Amster I, Leach 3rd F
Anal Bioanal Chem. 2016; 409(2):411-420.
PMID: 27325464
PMC: 5173454.
DOI: 10.1007/s00216-016-9662-1.
Bioengineered heparins and heparan sulfates.
Fu L, Suflita M, Linhardt R
Adv Drug Deliv Rev. 2015; 97:237-49.
PMID: 26555370
PMC: 4753095.
DOI: 10.1016/j.addr.2015.11.002.
A purification process for heparin and precursor polysaccharides using the pH responsive behavior of chitosan.
Bhaskar U, Hickey A, Li G, Mundra R, Zhang F, Fu L
Biotechnol Prog. 2015; 31(5):1348-59.
PMID: 26147064
PMC: 4652654.
DOI: 10.1002/btpr.2144.
Bottom-up low molecular weight heparin analysis using liquid chromatography-Fourier transform mass spectrometry for extensive characterization.
Li G, Steppich J, Wang Z, Sun Y, Xue C, Linhardt R
Anal Chem. 2014; 86(13):6626-32.
PMID: 24905078
PMC: 4082394.
DOI: 10.1021/ac501301v.
Analysis of 3-O-sulfo group-containing heparin tetrasaccharides in heparin by liquid chromatography-mass spectrometry.
Li G, Yang B, Li L, Zhang F, Xue C, Linhardt R
Anal Biochem. 2014; 455:3-9.
PMID: 24680753
PMC: 4030551.
DOI: 10.1016/j.ab.2014.02.033.
Structure and activity of a new low-molecular-weight heparin produced by enzymatic ultrafiltration.
Fu L, Zhang F, Li G, Onishi A, Bhaskar U, Sun P
J Pharm Sci. 2014; 103(5):1375-83.
PMID: 24634007
PMC: 3998821.
DOI: 10.1002/jps.23939.
Method to detect contaminants in heparin using radical depolymerization and liquid chromatography-mass spectrometry.
Li G, Cai C, Li L, Fu L, Chang Y, Zhang F
Anal Chem. 2013; 86(1):326-30.
PMID: 24364596
PMC: 3927312.
DOI: 10.1021/ac403625a.