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1. Full Text Vascular Endothelial Growth Factor Expression of Intercellular Adhesion Molecule 1 (ICAM-1), Vascular Cell Adhesion Molecule 1 (VCAM-1), and E-selectin through Nuclear Factor-κB Activation in Endothelial Cells
by Kim, Injune and Moon, Sang-Ok and Kim, Sung Hoon and Kim, Hyung Jin and Koh, Young Soon and Koh, Gou Young
The Journal of biological chemistry, ISSN 0021-9258, 03/2001, Volume 276, Issue 10, pp. 7614 - 7620
Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Vascular Endothelial Growth Factor A | Vascular Endothelial Growth Factors | Humans | Nitric Oxide Synthase - antagonists & inhibitors | NF-kappa B - metabolism | RNA, Messenger - metabolism | MAP Kinase Kinase 2 | Type C Phospholipases - antagonists & inhibitors | MAP Kinase Kinase 1 | Ribonucleases - metabolism | Flow Cytometry | Time Factors | Intercellular Adhesion Molecule-1 - biosynthesis | E-Selectin - biosynthesis | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Lymphokines - biosynthesis | Umbilical Veins - cytology | Protein Structure, Tertiary | Recombinant Proteins - metabolism | NF-kappa B - antagonists & inhibitors | Signal Transduction | Cells, Cultured | Enzyme Inhibitors - pharmacology | Mitogen-Activated Protein Kinase Kinases - antagonists & inhibitors | Endothelial Growth Factors - biosynthesis | Protein Kinase C - antagonists & inhibitors | Cell Adhesion | Blotting, Western | Phosphotransferases (Alcohol Group Acceptor) - antagonists & inhibitors | Androstadienes - pharmacology | Endothelium, Vascular - metabolism | Models, Biological | Wortmannin | Vascular Cell Adhesion Molecule-1 - biosynthesis | Nitric Oxide Synthase - metabolism | Enzyme Activation | DNA, Complementary - metabolism | Leukocytes - metabolism | Protein-Tyrosine Kinases - antagonists & inhibitors | E-selectin | vascular cell adhesion molecule 1 | intercellular adhesion molecule 1 | vascular endothelial growth factor | Index Medicus
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2. Full Text Dihydromunduletone Is a Small-Molecule Selective Adhesion G Protein-Coupled Receptor Antagonist
by Stoveken, Hannah M and Bahr, Laura L and Anders, M. W and Wojtovich, Andrew P and Smrcka, Alan V and Tall, Gregory G
Molecular pharmacology, ISSN 0026-895X, 09/2016, Volume 90, Issue 3, pp. 214 - 224
Life Sciences & Biomedicine | Pharmacology & Pharmacy | Science & Technology | Small Molecule Libraries - analysis | Small Molecule Libraries - pharmacology | Reproducibility of Results | Receptors, G-Protein-Coupled - metabolism | Humans | Cell Adhesion - drug effects | Peptides - pharmacology | Benzopyrans - chemistry | Small Molecule Libraries - chemistry | Animals | High-Throughput Screening Assays | Retinoids - analysis | Retinoids - chemistry | HEK293 Cells | Receptors, G-Protein-Coupled - antagonists & inhibitors | Flavonoids - pharmacology | Benzopyrans - analysis | Benzopyrans - pharmacology | Peptides - agonists | Retinoids - pharmacology | Index Medicus
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3. Full Text Epithelial cell adhesion molecule overexpression regulates epithelial-mesenchymal transition, stemness and metastasis of nasopharyngeal carcinoma cells via the PTEN/AKT/mTOR pathway
by Wang, Meng-He and Sun, Rui and Zhou, Xiao-Min and Zhang, Mei-Yin and Lu, Jia-Bin and Yang, Yang and Zeng, Li-Si and Yang, Xian-Zi and Shi, Lu and Xiao, Ruo-Wen and Wang, Hui-Yun and Mai, Shi-Juan
Cell death & disease, ISSN 2041-4889, 01/2018, Volume 9, Issue 1, pp. 2 - 2
Life Sciences & Biomedicine | Science & Technology | Cell Biology | Nasopharyngeal Neoplasms - metabolism | Nasopharyngeal Neoplasms - mortality | Cadherins - metabolism | TOR Serine-Threonine Kinases - metabolism | Epithelial Cell Adhesion Molecule - metabolism | Humans | Middle Aged | Male | Phosphoproteins - metabolism | Nasopharyngeal Neoplasms - pathology | TOR Serine-Threonine Kinases - antagonists & inhibitors | PTEN Phosphohydrolase - antagonists & inhibitors | RNA Interference | Epithelial Cell Adhesion Molecule - genetics | Epithelial-Mesenchymal Transition | Adult | Female | Epithelial Cell Adhesion Molecule - antagonists & inhibitors | Proto-Oncogene Proteins c-akt - metabolism | Nasopharyngeal Carcinoma - mortality | PTEN Phosphohydrolase - genetics | Kaplan-Meier Estimate | Proportional Hazards Models | PTEN Phosphohydrolase - metabolism | Nasopharyngeal Carcinoma - metabolism | Sirolimus - pharmacology | Cell Movement - drug effects | Animals | Signal Transduction - drug effects | Mice, Nude | Nasopharyngeal Carcinoma - pathology | Cell Line, Tumor | Mice | Adaptor Proteins, Signal Transducing - metabolism | Proto-Oncogene Proteins c-akt - antagonists & inhibitors | RNA, Small Interfering - metabolism | TOR protein | Cell proliferation | Immunohistochemistry | Phosphorylation | Mesenchyme | Epithelial cells | Mucosa | AKT protein | siRNA | Rapamycin | Metastasis | Cell adhesion molecules | Cell adhesion & migration | Metastases | Nasopharyngeal carcinoma | Survival analysis | Stem cells | Protein expression | PTEN protein | Index Medicus
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4. Full Text Heparan Sulfate Organizes Neuronal Synapses through Neurexin Partnerships
by Zhang, Peng and Lu, Hong and Peixoto, Rui T and Pines, Mary K and Ge, Yuan and Oku, Shinichiro and Siddiqui, Tabrez J and Xie, Yicheng and Wu, Wenlan and Archer-Hartmann, Stephanie and Yoshida, Keitaro and Tanaka, Kenji F and Aricescu, A. Radu and Azadi, Parastoo and Gordon, Michael D and Sabatini, Bernardo L and Wong, Rachel O.L and Craig, Ann Marie
Cell (Cambridge), ISSN 0092-8674, 09/2018, Volume 174, Issue 6, pp. 1450 - 1464.e23
LRRTM | heparan sulphate | synaptic transmission | thorny excrescence | mossy fiber | synaptogenesis | synaptic adhesion protein | proteoglycan | neurexin | neuroligin | Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Humans | Neurons - cytology | Drosophila Proteins - metabolism | Heparitin Sulfate - metabolism | Glycopeptides - analysis | Synapses - metabolism | RNA Interference | Female | Cell Adhesion Molecules, Neuronal - metabolism | Neurons - metabolism | Drosophila Proteins - antagonists & inhibitors | Amino Acid Sequence | Cell Adhesion Molecules, Neuronal - antagonists & inhibitors | Drosophila | Mice, Inbred C57BL | Rats | Neural Cell Adhesion Molecules - genetics | Cell Adhesion Molecules, Neuronal - genetics | Sequence Alignment | Animals | Heparitin Sulfate - chemistry | Neural Cell Adhesion Molecules - metabolism | Protein Binding | Neural Cell Adhesion Molecules - antagonists & inhibitors | Mice | Drosophila Proteins - genetics | RNA, Small Interfering - metabolism | Autism | Yuan (China) | Partnership | Neurons | Zoology | Schizophrenia | Binding proteins | Sulfates | Neurophysiology | Protein binding | Index Medicus
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5. Full Text Cell adhesion molecules and ischemic stroke
by Yilmaz, Gokhan and Granger, D. Neil
Neurological research (New York), ISSN 0161-6412, 10/2008, Volume 30, Issue 8, pp. 783 - 793
STROKE | CEREBRAL ISCHEMIA | ADHESION | LEUKOCYTES | PLATELETS | INFLAMMATION | Cerebral ischemia | Stroke | Inflammation | Leukocytes | Platelets | Adhesion | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Cell Adhesion Molecules - physiology | Humans | Cell Adhesion Molecules - antagonists & inhibitors | Brain Ischemia - metabolism | Brain Ischemia - physiopathology | Stroke - drug therapy | Cell Adhesion Molecules - metabolism | Stroke - physiopathology | Stroke - metabolism | Animals | Signal Transduction - drug effects | Models, Biological | Brain Ischemia - drug therapy | Inflammation Mediators - metabolism | Reperfusion Injury - physiopathology | Anti-Inflammatory Agents - therapeutic use | Signal Transduction - physiology | Inflammation Mediators - antagonists & inhibitors | Inflammation Mediators - physiology | Reperfusion Injury - metabolism | Index Medicus | leukocytes | inflammation | stroke | cerebral ischemia | platelets
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6. Full Text Structures of the CXCR4 Chemokine GPCR with Small-Molecule and Cyclic Peptide Antagonists
by Beili Wu and Ellen Y. T. Chien and Clifford D. Mol and Gustavo Fenalti and Wei Liu and Vsevolod Katritch and Ruben Abagyan and Alexei Brooun and Peter Wells and F. Christopher Bi and Damon J. Hamel and Peter Kuhn and Tracy M. Handel and Vadim Cherezov and Raymond C. Stevens
Science (American Association for the Advancement of Science), ISSN 0036-8075, 11/2010, Volume 330, Issue 6007, pp. 1066 - 1071
Molecules | Receptors | RESEARCH ARTICLE | Cyclic peptides | Disulfides | Ligands | Dimers | Chemokines | Chemokine receptors | HIV 1 | Crystal structure | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Cell Line | Chemokine CXCL12 | Receptors, CXCR4 - antagonists & inhibitors | Humans | Protein Multimerization | Models, Molecular | Recombinant Proteins - chemistry | Crystallography, X-Ray | Thiourea - chemistry | HIV Envelope Protein gp120 - metabolism | Receptors, CXCR4 - metabolism | Spodoptera | Membrane Proteins | Animals | Protein Binding | Protein Conformation | Receptors, CXCR4 - chemistry | Thiourea - analogs & derivatives | Physiological aspects | G proteins | Properties | Structure | Crystals | Peptides | Neurons | Cell adhesion & migration | Regulators | Surveillance | Migration | Index Medicus
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7. Full Text Celastrol suppresses expression of adhesion molecules and chemokines by inhibiting JNK-STAT1/NF-κB activation in poly(I: C)-stimulated astrocytes
by An, Soo Yeon and Youn, Gi Soo and Kim, Hyejin and Choi, Soo Young and Park, Jinseu
BMB reports, ISSN 1976-6696, 2017, Volume 50, Issue 1, pp. 25 - 30
STAT1/NF-κB | Inflammation | Astrocyte | Poly(I:C) | Celastrol | Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Astrocytes - drug effects | Cell Line | Chemokines - biosynthesis | NF-kappa B - antagonists & inhibitors | Poly I-C - pharmacology | Triterpenes - pharmacology | Humans | NF-kappa B - metabolism | STAT1 Transcription Factor - antagonists & inhibitors | STAT1 Transcription Factor - metabolism | MAP Kinase Kinase 4 - metabolism | MAP Kinase Signaling System - drug effects | Intercellular Adhesion Molecule-1 - biosynthesis | MAP Kinase Kinase 4 - antagonists & inhibitors | Vascular Cell Adhesion Molecule-1 - biosynthesis | Chemokines - metabolism | Poly I-C - antagonists & inhibitors | Astrocytes - metabolism | NF-κB | STAT1
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8. Full Text The neural cell adhesion molecules L1 and CHL1 are cleaved by BACE1 protease in vivo
by Zhou, Lujia and Barão, Soraia and Laga, Mathias and Bockstael, Katrijn and Borgers, Marianne and Gijsen, Harry and Annaert, Wim and Moechars, Diederik and Mercken, Marc and Gevaer, Kris and De Strooper, Bart
The Journal of biological chemistry, ISSN 0021-9258, 07/2012, Volume 287, Issue 31, pp. 25927 - 25940
Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Cell Adhesion Molecules - chemistry | Cell Adhesion Molecules - genetics | Neural Cell Adhesion Molecule L1 - genetics | Brain - enzymology | Molecular Sequence Data | Brain - metabolism | Protease Inhibitors - pharmacology | Synapses - metabolism | Proteolysis | Neurons - metabolism | Neural Cell Adhesion Molecule L1 - metabolism | Amino Acid Sequence | Synapses - drug effects | Chlorocebus aethiops | Mutagenesis, Site-Directed | Aspartic Acid Endopeptidases - antagonists & inhibitors | Mice, Inbred C57BL | Cells, Cultured | Synapses - enzymology | Cell Adhesion Molecules - metabolism | Amino Acid Motifs | Mice, Knockout | Brain - drug effects | Amyloid Precursor Protein Secretases - metabolism | Peptide Fragments - chemistry | Animals | Aspartic Acid Endopeptidases - metabolism | Neurons - enzymology | Mice | Amyloid Precursor Protein Secretases - antagonists & inhibitors | Primary Cell Culture | Neural Cell Adhesion Molecule L1 - chemistry | COS Cells | Proteome - metabolism | Amino Acid Substitution | Index Medicus | BACE1 | Neural Adhesion | Alzheimers Disease | Neurons | Protease | CHL1 | Neurobiology | Proteomics | Axon | Axon Guidance
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