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1. Full Text TM6SF2 rs58542926 influences hepatic fibrosis progression in patients with non-alcoholic fatty liver disease
by Liu, Yang-Lin and Reeves, Helen L and Burt, Alastair D and Tiniakos, Dina and McPherson, Stuart and Leathart, Julian B. S and Allison, Michael E. D and Alexander, Graeme J and Piguet, Anne-Christine and Anty, Rodolphe and Donaldson, Peter and Aithal, Guruprasad P and Francque, Sven and Van Gaal, Luc and Clement, Karine and Ratziu, Vlad and Dufour, Jean-Francois and Day, Christopher P and Daly, Ann K and Anstee, Quentin M
Nature Communications, ISSN 2041-1723, 06/2014, Volume 5, Issue 1, pp. 4309 - 4309
Non-alcoholic fatty liver disease (NAFLD) is an increasingly common condition, strongly associated with the metabolic syndrome, that can lead to progressive... 
CONFERS SUSCEPTIBILITY | GENETIC-VARIATION | NAFLD | CHOLESTEROL | STEATOSIS | MULTIDISCIPLINARY SCIENCES | LOCI | LINKAGE | VARIANT | SEVERITY | GENOME-WIDE ASSOCIATION | Index Medicus
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2. Full Text Chondroitin sulfate proteoglycans potently inhibit invasion and serve as a central organizer of the brain tumor microenvironment
by Silver, Daniel J and Siebzehnrubl, Florian A and Schildts, Michela J and Yachnis, Anthony T and Smith, George M and Smith, Amy A and Scheffler, Bjorn and Reynolds, Brent A and Silver, Jerry and Steindler, Dennis A
Journal of Neuroscience, ISSN 0270-6474, 2013, Volume 33, Issue 39, pp. 15603 - 15617
Glioblastoma (GBM) remains the most pervasive and lethal of all brain malignancies. One factor that contributes to this poor prognosis is the highly invasive... 
IN-VITRO | NEURITE OUTGROWTH | GLIOMA | REGENERATION | GROWTH | SPINAL-CORD | REACTIVE ASTROCYTES | SUBVENTRICULAR ZONE | MICROGLIAL CELLS | EXPRESSION | NEUROSCIENCES | Microglia - metabolism | Chondroitin Sulfate Proteoglycans - genetics | Humans | Middle Aged | Astrocytes - pathology | Brain Neoplasms - pathology | Tumor Microenvironment | Male | Brain Neoplasms - metabolism | Glioma - metabolism | Glioma - pathology | Microglia - pathology | Adult | Female | Child | Neoplasm Invasiveness | Cells, Cultured | Chondroitin Sulfate Proteoglycans - metabolism | Glycosylation | Xenograft Model Antitumor Assays | Animals | Receptor-Like Protein Tyrosine Phosphatases, Class 2 - metabolism | Cell Line, Tumor | Mice | Astrocytes - metabolism | Cell Movement | Index Medicus
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3. Full Text Semaphorin 5A Is a Bifunctional Axon Guidance Cue Regulated by Heparan and Chondroitin Sulfate Proteoglycans
by Kantor, David B and Chivatakarn, Onanong and Peer, Katherine L and Oster, Stephen F and Inatani, Masaru and Hansen, Michael J and Flanagan, John G and Yamaguchi, Yu and Sretavan, David W and Giger, Roman J and Kolodkin, Alex L
Neuron, ISSN 0896-6273, 2004, Volume 44, Issue 6, pp. 961 - 975
The response of neuronal growth cones to axon guidance cues depends on the developmental context in which these cues are encountered. We show here that the... 
SYSTEM | GROWTH CONES | NEURITE OUTGROWTH | DEVELOPING MOUSE | NETRIN-1 | RECEPTOR | N-SYNDECAN | RAT-BRAIN | EXPRESSION | BINDING | NEUROSCIENCES | Cell Line | Nerve Tissue Proteins - physiology | Chondroitin Sulfate Proteoglycans - genetics | Membrane Proteins - genetics | Mesencephalon - metabolism | Humans | Axons - metabolism | Rats | Nerve Tissue Proteins - genetics | Rats, Sprague-Dawley | Dose-Response Relationship, Drug | Pregnancy | Chondroitin Sulfate Proteoglycans - physiology | Membrane Proteins - biosynthesis | Animals | Mesencephalon - embryology | Heparan Sulfate Proteoglycans - genetics | Membrane Proteins - physiology | Semaphorins | Nerve Tissue Proteins - biosynthesis | Female | Mice | Organ Culture Techniques | Heparan Sulfate Proteoglycans - physiology | Proteins | Heparan sulfate | Chondroitin sulfate | Rodents | Cell adhesion & migration | Index Medicus
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4. Full Text Cohesin is positioned in mammalian genomes by transcription, CTCF and Wapl
by Busslinger, Georg A and Stocsits, Roman R and Van Der Lelij, Petra and Axelsson, Elin and Tedeschi, Antonio and Galjart, Niels and Peters, Jan-Michael
Nature, ISSN 0028-0836, 04/2017, Volume 544, Issue 7651, pp. 503 - 507
Mammalian genomes are spatially organized by CCCTC-binding factor (CTCF) and cohesin into chromatin loops(1,2) and topologically associated domains(3-6), which... 
CHIP-SEQ | SISTER CHROMATIDS | COMPLEX | RNA-SEQ | DNA | MULTIDISCIPLINARY SCIENCES | GENE-EXPRESSION | GENERATION | DOMAINS | DIFFERENTIAL EXPRESSION ANALYSIS | CHROMATIN ARCHITECTURE | Chromatin - metabolism | Chondroitin Sulfate Proteoglycans - genetics | Chromosomes, Mammalian - genetics | Genome - genetics | Male | Repressor Proteins - deficiency | Cell Cycle Proteins - genetics | Female | Binding Sites | Repressor Proteins - metabolism | Fibroblasts - metabolism | Chromosomal Proteins, Non-Histone - metabolism | Cell Cycle Proteins - metabolism | Cells, Cultured | Repressor Proteins - genetics | Cell Cycle Proteins - deficiency | DNA - metabolism | Chondroitin Sulfate Proteoglycans - deficiency | Chromosomal Proteins, Non-Histone - deficiency | Chromosomal Proteins, Non-Histone - genetics | Protein Transport | DNA - genetics | Proteins - genetics | Animals | Proteins - metabolism | CCCTC-Binding Factor | Transcription Initiation Site | Fibroblasts - cytology | Mice | Transcription, Genetic - genetics | Chromosomes, Mammalian - metabolism | Chromatin - genetics | Genomes | Gene expression | Localization | Experiments | Deoxyribonucleic acid--DNA | Index Medicus | cohesin island | Nipbl | Cohesin movement | transcription | CTCF | genome architecture | Wapl
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5. Full Text Eco1-Dependent Cohesin Acetylation during Establishment of Sister Chromatid Cohesion
by Tom Rolef Ben-Shahar and Sebastian Heeger and Chris Lehane and Philip East and Helen Flynn and Mark Skehel and Frank Uhlmann
Science, ISSN 0036-8075, 7/2008, Volume 321, Issue 5888, pp. 563 - 566
Replicated chromosomes are held together by the chromosomal cohesin complex from the time of their synthesis in S phase onward. This requires the replication... 
Diploidy | DNA replication | Interphase | Chromatids | Cell cycle | Reports | Complementation | Acetylation | Genetic mutation | Chromosomes | Saccharomycetales | ATP HYDROLYSIS | FISSION YEAST | PROTEIN | STABILITY | MULTIDISCIPLINARY SCIENCES | RESOLUTION | S-PHASE | CHROMOSOMES | SACCHAROMYCES-CEREVISIAE | ASSOCIATION | DNA-REPLICATION | Acetyltransferases - metabolism | Chromatids - physiology | Chondroitin Sulfate Proteoglycans - genetics | Chondroitin Sulfate Proteoglycans - chemistry | Saccharomyces cerevisiae - genetics | Acetyltransferases - genetics | Protein Subunits - metabolism | Cell Cycle Proteins - chemistry | S Phase | Cell Cycle Proteins - genetics | Nuclear Proteins - genetics | Chromosomes, Fungal - physiology | Protein Subunits - genetics | Saccharomyces cerevisiae - physiology | Chromosomal Proteins, Non-Histone - metabolism | Cell Cycle Proteins - metabolism | Chondroitin Sulfate Proteoglycans - metabolism | DNA Replication | Nuclear Proteins - metabolism | Saccharomyces cerevisiae Proteins - genetics | Nuclear Proteins - chemistry | Acetyltransferases - chemistry | Chromosomal Proteins, Non-Histone - genetics | DNA Repair | Alleles | DNA, Fungal - metabolism | Saccharomyces cerevisiae Proteins - metabolism | Protein Subunits - chemistry | Mutation | Chromosomal Proteins, Non-Histone - chemistry | Saccharomyces cerevisiae - growth & development | Saccharomyces cerevisiae Proteins - chemistry | Suppression, Genetic | Allelomorphism | Yeast fungi | Genetic aspects | Biochemical genetics | Research | Observations | Identification and classification | Genetics | Biochemistry | Biomedical research | Chemical synthesis | Index Medicus
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6. Full Text Characterization of a DNA exit gate in the human cohesin ring
by Huis In't Veld, Pim J and Herzog, Franz and Ladurner, Rene and Davidson, Iain F and Piric, Sabina and Kreidl, Emanuel and Bhaskara, Venugopal and Aebersold, Ruedi and Peters, Jan-Michael
Science, ISSN 0036-8075, 11/2014, Volume 346, Issue 6212, pp. 968 - 972
Chromosome segregation depends on sister chromatid cohesion mediated by cohesin. The cohesin subunits Smc1, Smc3, and Scc1 form tripartite rings that are... 
ATP HYDROLYSIS | COMPLEX | REPLICATION | CHROMATIN | ACETYLATION | MULTIDISCIPLINARY SCIENCES | SCC2 | CHROMOSOMES | BINDING | ASSOCIATION | WAPL | Chromatin - metabolism | Chondroitin Sulfate Proteoglycans - genetics | Chondroitin Sulfate Proteoglycans - chemistry | Humans | Protein Multimerization | Molecular Sequence Data | Phosphoproteins - metabolism | Phosphoproteins - chemistry | Cell Cycle Proteins - chemistry | Mass Spectrometry | Cell Cycle Proteins - genetics | Nuclear Proteins - genetics | Protein Structure, Tertiary | Proto-Oncogene Proteins - metabolism | Amino Acid Sequence | Chromosome Segregation | Chromosomal Proteins, Non-Histone - metabolism | Cell Cycle Proteins - metabolism | Chondroitin Sulfate Proteoglycans - metabolism | DNA Replication | Nuclear Proteins - metabolism | Proto-Oncogene Proteins - genetics | DNA - metabolism | Phosphoproteins - genetics | Microscopy, Electron | Nuclear Proteins - chemistry | Chromosomal Proteins, Non-Histone - genetics | Carrier Proteins - genetics | Animals | Carrier Proteins - metabolism | Separase - metabolism | Chromosomal Proteins, Non-Histone - chemistry | Genetic research | Research | Nucleotide sequencing | DNA sequencing | Mutation | Chromosomes | Deoxyribonucleic acid--DNA | Cell adhesion & migration | Index Medicus | Mutations | Cohesion | Deoxyribonucleic acid | Strands | Cleavage | Gates | Rings (mathematics)
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7. Full Text Functional Axonal Regeneration through Astrocytic Scar Genetically Modified to Digest Chondroitin Sulfate Proteoglycans
by Cafferty, William B. J and Yang, Shih-Hung and Duffy, Philip J and Li, Shuxin and Strittmatter, Stephen M
Journal of Neuroscience, ISSN 0270-6474, 02/2007, Volume 27, Issue 9, pp. 2176 - 2185
Axotomized neurons within the damaged CNS are thought to be prevented from functional regeneration by inhibitory molecules such as chondroitin sulfate... 
Proteoglycan | Dorsal rhizotomy | Chondroitin sulfate | Spinal cord injury | Axon regeneration | Traumatic injury | spinal cord injury | SENSORY AXONS | NEURITE GROWTH-INHIBITORS | ROOT ENTRY ZONE | chondroitin sulfate | axon regeneration | NOGO-66 RECEPTOR | traumatic injury | DEFICIENT MICE | NEUROSCIENCES | MYELIN-ASSOCIATED GLYCOPROTEIN | proteoglycan | IN-VIVO | SPINAL-CORD-INJURY | CENTRAL-NERVOUS-SYSTEM | dorsal rhizotomy | Nerve Regeneration - genetics | Up-Regulation | Sensation - physiology | Chondroitin Sulfate Proteoglycans - genetics | Chondroitin Sulfate Proteoglycans - metabolism | Male | Mice, Transgenic | Axons - physiology | Astrocytes - enzymology | Chondroitin ABC Lyase - metabolism | Animals | Thoracic Vertebrae | Cicatrix - physiopathology | Skin - innervation | Female | Mice | Rhizotomy | Spinal Cord Injuries - physiopathology | Pain Measurement | Forelimb | Index Medicus
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8. Full Text A Molecular Determinant for the Establishment of Sister Chromatid Cohesion
by Elçin Ünal and Jill M. Heidinger-Pauli and Woong Kim and Vincent Guacci and Itay Onn and Steven P. Gygi and Douglas E. Koshland
Science, ISSN 0036-8075, 7/2008, Volume 321, Issue 5888, pp. 566 - 569
Chromosome segregation, transcriptional regulation, and repair of DNA double-strand breaks require the cohesin protein complex. Cohesin holds the replicated... 
Yeasts | Chromatin | Interphase | Chromatids | DNA | Cell cycle | Reports | Acetylation | Chromosomes | Genetic mutation | Saccharomycetales | REPAIR | MULTIDISCIPLINARY SCIENCES | RESOLUTION | COMPLEXES | DOUBLE-STRAND BREAKS | CONDENSATION | PROTEINS | SACCHAROMYCES-CEREVISIAE | BINDING | ACETYLTRANSFERASE | DNA-REPLICATION | Chromatin - metabolism | Acetyltransferases - metabolism | Chromatids - physiology | Immunoprecipitation | Chondroitin Sulfate Proteoglycans - genetics | Chondroitin Sulfate Proteoglycans - chemistry | Saccharomyces cerevisiae - genetics | Molecular Sequence Data | Acetyltransferases - genetics | Cell Cycle Proteins - chemistry | Cell Division | S Phase | Cell Cycle Proteins - genetics | G2 Phase | Lysine - metabolism | Nuclear Proteins - genetics | Chromosomes, Fungal - physiology | Protein Structure, Tertiary | Amino Acid Sequence | Saccharomyces cerevisiae - physiology | Chromosomal Proteins, Non-Histone - metabolism | Cell Cycle Proteins - metabolism | Chondroitin Sulfate Proteoglycans - metabolism | Nuclear Proteins - metabolism | Saccharomyces cerevisiae Proteins - genetics | Chromosomal Proteins, Non-Histone - genetics | G1 Phase | Saccharomyces cerevisiae Proteins - metabolism | Mutation | Chromosomal Proteins, Non-Histone - chemistry | Saccharomyces cerevisiae - growth & development | Amino Acid Substitution | Saccharomyces cerevisiae Proteins - chemistry | Yeast fungi | Genetic aspects | Biochemical genetics | Research | Gene expression | Identification and classification | Proteins | Genetics | Molecular biology | DNA repair | Index Medicus
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9. Full Text Genes encoding proteoglycans are associated with the risk of anterior cruciate ligament ruptures
by Mannion, Sasha and Mtintsilana, Asanda and Posthumus, Michael and van der Merwe, Willem and Hobbs, Hayden and Collins, Malcolm and September, Alison V
British Journal of Sports Medicine, ISSN 0306-3674, 12/2014, Volume 48, Issue 22, pp. 1640 - 1646
Background Genetic variants within genes involved in fibrillogenesis have previously been implicated in anterior cruciate ligament (ACL) injury susceptibility.... 
DECORIN | SPORT SCIENCES | INJURIES | LEUCINE-RICH PROTEOGLYCANS | DYSTROPHY | BIGLYCAN | GROWTH | ESTROGEN | EXTRACELLULAR-MATRIX | MOUSE UTERUS | EXPRESSION | Fibromodulin | Haplotypes | Genetic Predisposition to Disease - genetics | Chondroitin Sulfate Proteoglycans - genetics | Fibrillar Collagens - genetics | Biglycan - genetics | Anterior Cruciate Ligament Injuries | Extracellular Matrix Proteins - genetics | Humans | Risk Factors | Genotype | Male | Keratan Sulfate - genetics | Aggrecans - genetics | Case-Control Studies | Rupture - genetics | Polymorphism, Single Nucleotide - genetics | Adult | Female | Lumican | Decorin - genetics | Proteoglycans - genetics | Knee | Proteoglycans | Physiological aspects | Genetic aspects | Anterior cruciate ligament | Injuries | Risk factors | Sports injuries | Biological variation | Ligaments | Genes | Polymorphism | Chromosomes | Index Medicus
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10. Full Text The chondroitin sulfate proteoglycans neurocan, brevican, phosphacan, and versican are differentially regulated following spinal cord injury
by Jones, Leonard L and Margolis, Richard U and Tuszynski, Mark H
Experimental Neurology, ISSN 0014-4886, 2003, Volume 182, Issue 2, pp. 399 - 411
Chondroitin sulfate proteoglycans (CSPGs) are extracellular matrix (ECM) molecules that are widely expressed throughout the developing and adult CNS. In vitro... 
CSPG | Regeneration | Extracellular matrix | Astrocyte | Inhibition | CNS injury | PUTATIVE INHIBITORY MOLECULES | FUNCTIONAL RECOVERY | regeneration | inhibition | NEUROSCIENCES | NEURITE OUTGROWTH | ADULT-RAT | OLIGODENDROCYTE PROGENITORS | REACTIVE ASTROCYTES | CELL-ADHESION MOLECULES | CENTRAL-NERVOUS-SYSTEM | ACTIVATED MACROPHAGES | astrocyte | extracellular matrix | PROTEIN-TYROSINE-PHOSPHATASE | Immunohistochemistry | Chondroitin Sulfate Proteoglycans - genetics | Spinal Cord Injuries - metabolism | Lectins, C-Type | Rats, Inbred F344 | Astrocytes - pathology | Chondroitin Sulfate Proteoglycans - metabolism | Rats | Receptor-Like Protein Tyrosine Phosphatases, Class 5 | Nerve Tissue Proteins - genetics | Disease Progression | Spinal Cord Injuries - pathology | Glial Fibrillary Acidic Protein - biosynthesis | Nerve Tissue Proteins - metabolism | Versicans | Animals | In Situ Hybridization | Time Factors | Brevican | Female | Astrocytes - metabolism | Disease Models, Animal | Index Medicus
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11. Full Text Specific genes involved in synthesis and editing of heparan sulfate proteoglycans show altered expression patterns in breast cancer
by Fernández-Vega, Iván and García, Olivia and Crespo, Ainara and Castañón, Sonia and Menéndez, Primitiva and Astudillo, Aurora and Quirós, Luis M
BMC Cancer, ISSN 1471-2407, 01/2013, Volume 13, Issue 1, pp. 24 - 24
Background: The expression of a specific set of genes controls the different structures of heparan sulfate proteoglycans (HSPGs), which are involved in the... 
Heparan sulfate | Proteoglycan | Glycosaminoglycan | Breast cancer | Invasive ductal carcinoma | POSTTRANSCRIPTIONAL REGULATION | CELLS | METASTASIS | ANGIOGENESIS | SYNDECAN-1 EXPRESSION | ORGANIZATION | DEACETYLASE/N-SULFOTRANSFERASE ISOZYMES | ONCOLOGY | BIOSYNTHESIS | GROWTH | DIFFERENTIAL ROLES | Carcinoma, Ductal, Breast - genetics | Immunohistochemistry | Sulfotransferases - genetics | Chondroitin Sulfates - metabolism | Membrane Proteins - genetics | Humans | Syndecan-1 - genetics | Gene Expression Regulation, Neoplastic | RNA, Messenger - analysis | Gene Expression Profiling - methods | Glypicans - genetics | Gene Expression Regulation, Enzymologic | Breast Neoplasms - enzymology | Breast Neoplasms - genetics | Glucuronidase - genetics | Heparan Sulfate Proteoglycans - genetics | Breast Neoplasms - pathology | Heparan Sulfate Proteoglycans - metabolism | Polymerase Chain Reaction | Biomarkers, Tumor - metabolism | Female | Biomarkers, Tumor - genetics | Carcinoma, Ductal, Breast - metabolism | Carcinoma, Ductal, Breast - secondary | Proteoglycans | Physiological aspects | Development and progression | Genetic aspects | Research | Gene expression | Enzymes | Glycosaminoglycans | RNA | Analysis | Genes | Genetic research | Metastasis | Sulfates | Index Medicus
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12. Full Text Chondroitin sulfates play a major role in breast cancer metastasis: A role for CSPG4 and CHST11 gene expression in forming surface P-selectin ligands in aggressive breast cancer cells
by Cooney, Craig A and Jousheghany, Fariba and Yao-Borengasser, Aiwei and Phanavanh, Bounleut and Gomes, Tina and Kieber-Emmons, Ann M and Siegel, Eric R and Suva, Larry J and Ferrone, Soldano and Kieber-Emmons, Thomas and Monzavi-Karbassi, Behjatolah
Breast Cancer Research, ISSN 1465-5411, 06/2011, Volume 13, Issue 3, pp. R58 - R58
Introduction: We have previously demonstrated that chondroitin sulfate glycosaminoglycans (CS-GAGs) on breast cancer cells function as P-selectin ligands. This... 
SYNDECAN-1 | DERMATAN SULFATE | MELANOMA-ASSOCIATED ANTIGEN | ONCOLOGY | TUMOR-METASTASIS | DISTINCT | MOLECULAR-CLONING | HEPARAN-SULFATE | MONOCLONAL-ANTIBODIES | PROTEOGLYCAN | CARCINOMA IN-SITU | Chondroitin Sulfates - metabolism | Chondroitin Sulfate Proteoglycans - genetics | Chondroitin Sulfate Proteoglycans - chemistry | P-Selectin - metabolism | Humans | Gene Expression Regulation, Neoplastic | Breast Neoplasms - metabolism | Neoplasm Metastasis | RNA Interference | Female | Sulfotransferases - metabolism | Membrane Proteins - metabolism | Sulfotransferases - genetics | Membrane Proteins - genetics | Chondroitin Sulfate Proteoglycans - metabolism | Proteoglycans - analysis | P-Selectin - genetics | Animals | Breast Neoplasms - genetics | Membrane Proteins - chemistry | Breast Neoplasms - pathology | Cell Line, Tumor | Ligands | Mice | Mice, Inbred BALB C | RNA, Small Interfering | Polymerase chain reaction | Usage | Cancer cells | Physiological aspects | Breast cancer | Genetic aspects | Research | Gene expression | Index Medicus
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