Journal of Biological Chemistry, ISSN 0021-9258, 03/2012, Volume 287, Issue 12, pp. 9322 - 9326
As key enzymes in the regulation of biological phosphorylations, protein-tyrosine phosphatases are central to the control of cellular signaling and metabolism....
INHIBITION | REDOX REGULATION | FLUCTUATIONS | BIOCHEMISTRY & MOLECULAR BIOLOGY | ZN(II) | PURIFICATION | CATALYTIC DOMAIN | TARGETS | COORDINATION | CELL | ZN2 | Protein Structure, Tertiary | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - genetics | Signal Transduction | Enzyme Inhibitors - chemistry | Humans | Enzyme Inhibitors - pharmacology | Kinetics | Zinc - pharmacology | Zinc - chemistry | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - chemistry | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - metabolism | Enzymes | Enzyme Inhibitors | Endothelial Cell Physiology | Enzyme Regulation | Zinc Enzymes | Reports | Enzyme Kinetics | Transition Metal Signaling | Metalloenzymes | Protein-tyrosine phosphatases | Zinc
INHIBITION | REDOX REGULATION | FLUCTUATIONS | BIOCHEMISTRY & MOLECULAR BIOLOGY | ZN(II) | PURIFICATION | CATALYTIC DOMAIN | TARGETS | COORDINATION | CELL | ZN2 | Protein Structure, Tertiary | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - genetics | Signal Transduction | Enzyme Inhibitors - chemistry | Humans | Enzyme Inhibitors - pharmacology | Kinetics | Zinc - pharmacology | Zinc - chemistry | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - chemistry | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - metabolism | Enzymes | Enzyme Inhibitors | Endothelial Cell Physiology | Enzyme Regulation | Zinc Enzymes | Reports | Enzyme Kinetics | Transition Metal Signaling | Metalloenzymes | Protein-tyrosine phosphatases | Zinc
Journal Article
European Journal of Medicinal Chemistry, ISSN 0223-5234, 01/2018, Volume 144, pp. 318 - 329
A new series of blood-brain barrier permeable molecules designed to mimic the activity of Pleiotrophin in the CNS has been designed and synthesized. These...
Molecular dynamics | Drug addiction | CNS disorders | Synthesis | PTPRZ1 | Humans | Anti-Inflammatory Agents, Non-Steroidal - chemistry | Structure-Activity Relationship | Enzyme Inhibitors - chemical synthesis | Central Nervous System Diseases - metabolism | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Cytokines - chemistry | Dose-Response Relationship, Drug | Carrier Proteins - pharmacology | Cytokines - chemical synthesis | Enzyme Inhibitors - chemistry | Carrier Proteins - chemistry | Molecular Structure | Anti-Inflammatory Agents, Non-Steroidal - chemical synthesis | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - antagonists & inhibitors | Cell Line | Cell Survival - drug effects | Carrier Proteins - chemical synthesis | Enzyme Inhibitors - pharmacology | Models, Molecular | Rats | Blood-Brain Barrier - drug effects | Blood-Brain Barrier - metabolism | Animals | Central Nervous System Diseases - drug therapy | Mice | Cytokines - pharmacology | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - metabolism | Molecular Dynamics
Molecular dynamics | Drug addiction | CNS disorders | Synthesis | PTPRZ1 | Humans | Anti-Inflammatory Agents, Non-Steroidal - chemistry | Structure-Activity Relationship | Enzyme Inhibitors - chemical synthesis | Central Nervous System Diseases - metabolism | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Cytokines - chemistry | Dose-Response Relationship, Drug | Carrier Proteins - pharmacology | Cytokines - chemical synthesis | Enzyme Inhibitors - chemistry | Carrier Proteins - chemistry | Molecular Structure | Anti-Inflammatory Agents, Non-Steroidal - chemical synthesis | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - antagonists & inhibitors | Cell Line | Cell Survival - drug effects | Carrier Proteins - chemical synthesis | Enzyme Inhibitors - pharmacology | Models, Molecular | Rats | Blood-Brain Barrier - drug effects | Blood-Brain Barrier - metabolism | Animals | Central Nervous System Diseases - drug therapy | Mice | Cytokines - pharmacology | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - metabolism | Molecular Dynamics
Journal Article
Molecular and Cellular Biology, ISSN 0270-7306, 10/2012, Volume 32, Issue 20, pp. 4116 - 4130
Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley...
Receptor, IGF Type 1 - metabolism | Insulin-Like Growth Factor I - pharmacology | Humans | PTEN Phosphohydrolase - metabolism | Serine - metabolism | Insulin-Like Growth Factor Binding Protein 2 - metabolism | Insulin-Like Growth Factor Binding Protein 2 - genetics | Cell Movement - drug effects | Animals | Signal Transduction - drug effects | Cell Proliferation - drug effects | Mice | Insulin-Like Growth Factor I - metabolism | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - metabolism | Muscle, Smooth, Vascular - drug effects
Receptor, IGF Type 1 - metabolism | Insulin-Like Growth Factor I - pharmacology | Humans | PTEN Phosphohydrolase - metabolism | Serine - metabolism | Insulin-Like Growth Factor Binding Protein 2 - metabolism | Insulin-Like Growth Factor Binding Protein 2 - genetics | Cell Movement - drug effects | Animals | Signal Transduction - drug effects | Cell Proliferation - drug effects | Mice | Insulin-Like Growth Factor I - metabolism | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - metabolism | Muscle, Smooth, Vascular - drug effects
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 11/2012, Volume 287, Issue 48, pp. 40339 - 40349
The role of pleiotrophin and its receptors RPTPβ/ζ and Syndecan-3 during tumor metastasis remains unknown. RPTPβ/ζ knockdown initiates EMT, promotes...
Prostatic Neoplasms - metabolism | Prostatic Neoplasms - pathology | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - genetics | Syndecan-3 - metabolism | Up-Regulation | Phosphorylation | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - deficiency | Signal Transduction | Humans | Syndecan-3 - genetics | Male | Mice, Knockout | Neoplasm Metastasis | Animals | Prostatic Neoplasms - genetics | Mice, Nude | Cell Line, Tumor | Prostatic Neoplasms - enzymology | Mice | Cell Movement | Growth Factors | Pleiotrophin | Tumor Metastases | Prostate Cancer | Cell Surface Receptor | RPTP | EMT | Cell Biology | Syndecan-3
Prostatic Neoplasms - metabolism | Prostatic Neoplasms - pathology | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - genetics | Syndecan-3 - metabolism | Up-Regulation | Phosphorylation | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - deficiency | Signal Transduction | Humans | Syndecan-3 - genetics | Male | Mice, Knockout | Neoplasm Metastasis | Animals | Prostatic Neoplasms - genetics | Mice, Nude | Cell Line, Tumor | Prostatic Neoplasms - enzymology | Mice | Cell Movement | Growth Factors | Pleiotrophin | Tumor Metastases | Prostate Cancer | Cell Surface Receptor | RPTP | EMT | Cell Biology | Syndecan-3
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 10/2012, Volume 32, Issue 43, pp. 15066 - 15075
Oligodendrocyte progenitor cells (OPCs) persist in human white matter, yet the mechanisms by which they are maintained in an undifferentiated state are...
RNA, Small Interfering - genetics | Cytarabine - pharmacology | Humans | Glycogen Synthase Kinase 3 beta | TCF Transcription Factors - metabolism | Oligodendroglia - drug effects | Carrier Proteins - pharmacology | Fetus | Immunosuppressive Agents - pharmacology | Brain - cytology | Receptor, Platelet-Derived Growth Factor alpha - metabolism | Cells, Cultured | Enzyme Inhibitors - pharmacology | Gene Expression Regulation, Developmental - drug effects | Glycogen Synthase Kinase 3 - metabolism | beta Catenin - metabolism | Tyrosine - metabolism | Deoxyuridine - analogs & derivatives | Analysis of Variance | Signal Transduction - drug effects | Cell Differentiation - drug effects | Deoxyuridine - metabolism | Intercellular Signaling Peptides and Proteins - pharmacology | Stem Cells - drug effects | Cell Proliferation - drug effects | Cytokines - pharmacology | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - metabolism | RNA, Small Interfering - metabolism
RNA, Small Interfering - genetics | Cytarabine - pharmacology | Humans | Glycogen Synthase Kinase 3 beta | TCF Transcription Factors - metabolism | Oligodendroglia - drug effects | Carrier Proteins - pharmacology | Fetus | Immunosuppressive Agents - pharmacology | Brain - cytology | Receptor, Platelet-Derived Growth Factor alpha - metabolism | Cells, Cultured | Enzyme Inhibitors - pharmacology | Gene Expression Regulation, Developmental - drug effects | Glycogen Synthase Kinase 3 - metabolism | beta Catenin - metabolism | Tyrosine - metabolism | Deoxyuridine - analogs & derivatives | Analysis of Variance | Signal Transduction - drug effects | Cell Differentiation - drug effects | Deoxyuridine - metabolism | Intercellular Signaling Peptides and Proteins - pharmacology | Stem Cells - drug effects | Cell Proliferation - drug effects | Cytokines - pharmacology | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - metabolism | RNA, Small Interfering - metabolism
Journal Article
Molecular Neurobiology, ISSN 0893-7648, 1/2017, Volume 54, Issue 1, pp. 495 - 510
Pleiotrophin (PTN) and midkine (MK) are secreted growth factors and cytokines, proposed to be significant neuromodulators with multiple neuronal functions. PTN...
Neurology | Neurosciences | Biomedicine | Opiate dependence | Glial fibrillary acidic protein | Neurobiology | Pleiotrophin | Reward pathway | Midkine | Cell Biology | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - biosynthesis | Ventral Tegmental Area - drug effects | Drug Administration Schedule | Rats, Wistar | Carrier Proteins - biosynthesis | Rats | Male | Animals | Substance Withdrawal Syndrome - metabolism | Ventral Tegmental Area - metabolism | Morphine - administration & dosage | Cytokines - biosynthesis | Morphine - adverse effects
Neurology | Neurosciences | Biomedicine | Opiate dependence | Glial fibrillary acidic protein | Neurobiology | Pleiotrophin | Reward pathway | Midkine | Cell Biology | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - biosynthesis | Ventral Tegmental Area - drug effects | Drug Administration Schedule | Rats, Wistar | Carrier Proteins - biosynthesis | Rats | Male | Animals | Substance Withdrawal Syndrome - metabolism | Ventral Tegmental Area - metabolism | Morphine - administration & dosage | Cytokines - biosynthesis | Morphine - adverse effects
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 2005, Volume 335, Issue 1, pp. 232 - 239
Pleiotrophin (PTN the protein, the gene) signals through a unique mechanism; it inactivates the tyrosine phosphatase activity of its receptor, the...
Receptor protein tyrosine phosphatase β/ζ | β-Adducin | Pleiotrophin
Receptor protein tyrosine phosphatase β/ζ | β-Adducin | Pleiotrophin
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 2005, Volume 332, Issue 3, pp. 664 - 669
Pleiotrophin (PTN the protein, the gene) signals downstream targets through inactivation of its receptor, the transmembrane receptor protein tyrosine...
Fyn | Cytoskeletal stability | Receptor protein tyrosine phosphataseβ/ζ | Pleiotrophin
Fyn | Cytoskeletal stability | Receptor protein tyrosine phosphataseβ/ζ | Pleiotrophin
Journal Article
International Journal of Neuropsychopharmacology, ISSN 1461-1457, 1/2016, Volume 19, Issue 1, pp. 1 - 13
Background: Most classes of addictive substances alter the function and structural plasticity of the brain reward circuitry. Midkine (MK) and pleiotrophin...
Morphine | Astrocyte | Withdrawal | Midkine | Glial fibrillary acidic protein | Pleiotrophin | Astrocytes - drug effects | Cytokines - metabolism | Morphine - pharmacology | Rats, Wistar | Analgesics, Opioid - pharmacology | Rats | Glial Fibrillary Acidic Protein - metabolism | Animals | Carrier Proteins - metabolism | Analysis of Variance | Signal Transduction - drug effects | Time Factors | Naloxone - pharmacology | Narcotic Antagonists - pharmacology | Neurons - metabolism | Neurons - drug effects | Nucleus Accumbens - drug effects | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - metabolism | Astrocytes - metabolism
Morphine | Astrocyte | Withdrawal | Midkine | Glial fibrillary acidic protein | Pleiotrophin | Astrocytes - drug effects | Cytokines - metabolism | Morphine - pharmacology | Rats, Wistar | Analgesics, Opioid - pharmacology | Rats | Glial Fibrillary Acidic Protein - metabolism | Animals | Carrier Proteins - metabolism | Analysis of Variance | Signal Transduction - drug effects | Time Factors | Naloxone - pharmacology | Narcotic Antagonists - pharmacology | Neurons - metabolism | Neurons - drug effects | Nucleus Accumbens - drug effects | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - metabolism | Astrocytes - metabolism
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 3/2000, Volume 97, Issue 6, pp. 2603 - 2608
Pleiotrophin (PTN) is a platelet-derived growth factor-inducible, 18-kDa heparin-binding cytokine that signals diverse phenotypes in normal and deregulated...
Molecules | Biological Sciences | Phosphorylation | Receptors | Cell growth | Phosphatases | Antibodies | Ligands | Cell membranes | Catalytic activity | Tumors
Molecules | Biological Sciences | Phosphorylation | Receptors | Cell growth | Phosphatases | Antibodies | Ligands | Cell membranes | Catalytic activity | Tumors
Journal Article
Current Medicinal Chemistry, ISSN 0929-8673, 2009, Volume 16, Issue 25, pp. 3322 - 3329
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 05/2011, Volume 286, Issue 18, pp. 15980 - 15988
Protein tyrosine phosphorylation is a ubiquitous, fundamental biochemical mechanism that regulates essential eukaryotic cellular functions. The level of...
SIGNAL-TRANSDUCTION | EPITHELIAL-CELLS | FACTOR SCATTER FACTOR | BIOCHEMISTRY & MOLECULAR BIOLOGY | C-MET | MAP KINASES | TPR-MET | HUMAN ENDOTHELIAL-CELLS | HUMAN KERATINOCYTES | FACTOR/SCATTER FACTOR | SMALL-MOLECULE INHIBITOR | Phosphorylation - physiology | Proto-Oncogene Proteins c-met - metabolism | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - genetics | Vascular Endothelial Growth Factor A - biosynthesis | Cell Proliferation | Humans | Gene Expression Regulation - physiology | MAP Kinase Kinase 1 - metabolism | MAP Kinase Kinase 2 - metabolism | Vascular Endothelial Growth Factor A - genetics | Cell Movement - physiology | Proto-Oncogene Proteins c-met - genetics | MAP Kinase Kinase 1 - genetics | Receptors, Growth Factor - genetics | HEK293 Cells | Mutation | Keratinocytes - enzymology | MAP Kinase Kinase 2 - genetics | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - metabolism | Receptors, Growth Factor - metabolism | MAP Kinases (MAPKs) | Signal Transduction | Growth Factors | Phosphotyrosine Receptor | Cell Motility | Phosphotyrosine | Tyrosine Protein Kinase (Tyrosine Kinase) | Phosphotyrosine Signaling | Tyrosine Protein Phosphatase (Tyrosine Phosphatase)
SIGNAL-TRANSDUCTION | EPITHELIAL-CELLS | FACTOR SCATTER FACTOR | BIOCHEMISTRY & MOLECULAR BIOLOGY | C-MET | MAP KINASES | TPR-MET | HUMAN ENDOTHELIAL-CELLS | HUMAN KERATINOCYTES | FACTOR/SCATTER FACTOR | SMALL-MOLECULE INHIBITOR | Phosphorylation - physiology | Proto-Oncogene Proteins c-met - metabolism | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - genetics | Vascular Endothelial Growth Factor A - biosynthesis | Cell Proliferation | Humans | Gene Expression Regulation - physiology | MAP Kinase Kinase 1 - metabolism | MAP Kinase Kinase 2 - metabolism | Vascular Endothelial Growth Factor A - genetics | Cell Movement - physiology | Proto-Oncogene Proteins c-met - genetics | MAP Kinase Kinase 1 - genetics | Receptors, Growth Factor - genetics | HEK293 Cells | Mutation | Keratinocytes - enzymology | MAP Kinase Kinase 2 - genetics | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - metabolism | Receptors, Growth Factor - metabolism | MAP Kinases (MAPKs) | Signal Transduction | Growth Factors | Phosphotyrosine Receptor | Cell Motility | Phosphotyrosine | Tyrosine Protein Kinase (Tyrosine Kinase) | Phosphotyrosine Signaling | Tyrosine Protein Phosphatase (Tyrosine Phosphatase)
Journal Article
Nature Neuroscience, ISSN 1097-6256, 05/2000, Volume 3, Issue 5, pp. 437 - 444
Voltage-gated sodium channels in brain neurons were found to associate with receptor protein tyrosine phosphatase beta (RPTP beta) and its catalytically...
CHONDROITIN SULFATE | NERVOUS-SYSTEM | RPTP-BETA | SRC | EXTRACELLULAR-MATRIX | KINASE-C | RAT-BRAIN | HIPPOCAMPAL-NEURONS | NEUROSCIENCES | TENASCIN-R | SUBUNIT | Phosphorylation | Chondroitin Sulfate Proteoglycans - chemistry | Humans | Neurons - cytology | Protein Tyrosine Phosphatases - metabolism | Receptor-Like Protein Tyrosine Phosphatases, Class 5 | Electric Conductivity | Sodium - metabolism | Carbonic Anhydrases - chemistry | Recombinant Fusion Proteins - metabolism | Phosphotyrosine - metabolism | Protein Tyrosine Phosphatases - antagonists & inhibitors | Nerve Tissue Proteins - chemistry | Protein Tyrosine Phosphatases - chemistry | Protein Isoforms - metabolism | Transfection | Protein Isoforms - chemistry | Sodium Channels - metabolism | Cell Membrane - metabolism | Neurons - metabolism | Binding Sites | Cell Line | Nerve Tissue Proteins - antagonists & inhibitors | Brain - cytology | Catalytic Domain | Chondroitin Sulfate Proteoglycans - metabolism | Rats | Recombinant Fusion Proteins - chemistry | Precipitin Tests | Nerve Tissue Proteins - metabolism | Animals | Sodium Channels - chemistry | Protein Binding | Recombinant Fusion Proteins - genetics | Sodium Channels - genetics | Ion Channel Gating
CHONDROITIN SULFATE | NERVOUS-SYSTEM | RPTP-BETA | SRC | EXTRACELLULAR-MATRIX | KINASE-C | RAT-BRAIN | HIPPOCAMPAL-NEURONS | NEUROSCIENCES | TENASCIN-R | SUBUNIT | Phosphorylation | Chondroitin Sulfate Proteoglycans - chemistry | Humans | Neurons - cytology | Protein Tyrosine Phosphatases - metabolism | Receptor-Like Protein Tyrosine Phosphatases, Class 5 | Electric Conductivity | Sodium - metabolism | Carbonic Anhydrases - chemistry | Recombinant Fusion Proteins - metabolism | Phosphotyrosine - metabolism | Protein Tyrosine Phosphatases - antagonists & inhibitors | Nerve Tissue Proteins - chemistry | Protein Tyrosine Phosphatases - chemistry | Protein Isoforms - metabolism | Transfection | Protein Isoforms - chemistry | Sodium Channels - metabolism | Cell Membrane - metabolism | Neurons - metabolism | Binding Sites | Cell Line | Nerve Tissue Proteins - antagonists & inhibitors | Brain - cytology | Catalytic Domain | Chondroitin Sulfate Proteoglycans - metabolism | Rats | Recombinant Fusion Proteins - chemistry | Precipitin Tests | Nerve Tissue Proteins - metabolism | Animals | Sodium Channels - chemistry | Protein Binding | Recombinant Fusion Proteins - genetics | Sodium Channels - genetics | Ion Channel Gating
Journal Article
Neoplasia, ISSN 1476-5586, 2012, Volume 14, Issue 11, pp. 1015 - 1022
Abstract Head and neck squamous cell carcinoma (HNSCC) is the sixth most common cancer and has a high rate of mortality. Emerging evidence indicates that...
Oncology | IN-VITRO | INVASIVE GROWTH | ONCOLOGY | HEPATOCYTE GROWTH-FACTOR | C-MET | KINASE | SCATTER-FACTOR | EXPRESSION | CANCER | MOTILITY | FAMILY | Proto-Oncogene Proteins c-met - metabolism | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - genetics | Phosphorylation | Cell Proliferation | Carcinoma, Squamous Cell - genetics | Carcinoma, Squamous Cell - metabolism | Humans | Hepatocyte Growth Factor - pharmacology | Cell Movement - genetics | Down-Regulation - genetics | Head and Neck Neoplasms - metabolism | Proto-Oncogene Proteins c-met - genetics | Squamous Cell Carcinoma of Head and Neck | MAP Kinase Signaling System - drug effects | Cell Line, Tumor | Head and Neck Neoplasms - genetics | Neoplasm Invasiveness - genetics | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - metabolism
Oncology | IN-VITRO | INVASIVE GROWTH | ONCOLOGY | HEPATOCYTE GROWTH-FACTOR | C-MET | KINASE | SCATTER-FACTOR | EXPRESSION | CANCER | MOTILITY | FAMILY | Proto-Oncogene Proteins c-met - metabolism | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - genetics | Phosphorylation | Cell Proliferation | Carcinoma, Squamous Cell - genetics | Carcinoma, Squamous Cell - metabolism | Humans | Hepatocyte Growth Factor - pharmacology | Cell Movement - genetics | Down-Regulation - genetics | Head and Neck Neoplasms - metabolism | Proto-Oncogene Proteins c-met - genetics | Squamous Cell Carcinoma of Head and Neck | MAP Kinase Signaling System - drug effects | Cell Line, Tumor | Head and Neck Neoplasms - genetics | Neoplasm Invasiveness - genetics | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - metabolism
Journal Article
Cancer Research, ISSN 0008-5472, 02/2006, Volume 66, Issue 4, pp. 2271 - 2278
The receptor protein tyrosine phosphatase beta (RPTP beta) is a functional biomarker for several solid tumor types. RPTP beta expression is largely restricted...
RPTP-BETA | DOMAIN | PLEIOTROPHIN | ONCOLOGY | PHOSPHORYLATION | PTP-ZETA | CELL-ADHESION | MICE | PROTEOGLYCAN | TENASCIN | EXPRESSION | Antibody Specificity | Glioblastoma - enzymology | Immunization | Immunotoxins - immunology | Protein Tyrosine Phosphatases - biosynthesis | Enzyme-Linked Immunosorbent Assay | Nerve Tissue Proteins - immunology | Antibodies, Monoclonal - pharmacology | Humans | Receptor-Like Protein Tyrosine Phosphatases, Class 5 | Immunotoxins - pharmacology | Protein Tyrosine Phosphatases - immunology | Glioblastoma - therapy | Xenograft Model Antitumor Assays | Animals | Flow Cytometry | Mice, Nude | Nerve Tissue Proteins - biosynthesis | Cell Line, Tumor | Female | Mice | Mice, Inbred BALB C | Antibodies, Monoclonal - immunology
RPTP-BETA | DOMAIN | PLEIOTROPHIN | ONCOLOGY | PHOSPHORYLATION | PTP-ZETA | CELL-ADHESION | MICE | PROTEOGLYCAN | TENASCIN | EXPRESSION | Antibody Specificity | Glioblastoma - enzymology | Immunization | Immunotoxins - immunology | Protein Tyrosine Phosphatases - biosynthesis | Enzyme-Linked Immunosorbent Assay | Nerve Tissue Proteins - immunology | Antibodies, Monoclonal - pharmacology | Humans | Receptor-Like Protein Tyrosine Phosphatases, Class 5 | Immunotoxins - pharmacology | Protein Tyrosine Phosphatases - immunology | Glioblastoma - therapy | Xenograft Model Antitumor Assays | Animals | Flow Cytometry | Mice, Nude | Nerve Tissue Proteins - biosynthesis | Cell Line, Tumor | Female | Mice | Mice, Inbred BALB C | Antibodies, Monoclonal - immunology
Journal Article
Hippocampus, ISSN 1050-9631, 01/2011, Volume 21, Issue 1, pp. 81 - 92
This study documents the spatial and temporal expression of three structurally related chondroitin sulfated proteoglycans (CSPGs) during synaptic regeneration...
entorhinal lesion | dentate gyrus | synaptic plasticity | gene expression | proteoglycan | Proteoglycan | Dentate gyrus | Gene expression | Entorhinal lesion | Synaptic plasticity | TEMPORAL-LOBE EPILEPSY | CHONDROITIN SULFATE PROTEOGLYCANS | HIGH-AFFINITY BINDING | ENTORHINAL CORTEX LESION | NEUROSCIENCES | TRAUMATIC BRAIN-INJURY | NEURITE OUTGROWTH | RAT FASCIA-DENTATA | SPINAL-CORD-INJURY | CENTRAL-NERVOUS-SYSTEM | CELL-ADHESION MOLECULES | Immunohistochemistry | Microscopy, Electron, Transmission | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - biosynthesis | Rats | Male | Brain Injuries - metabolism | Reverse Transcriptase Polymerase Chain Reaction | Rats, Sprague-Dawley | Blotting, Western | Hippocampus - metabolism | Microscopy, Confocal | Animals | Neuronal Plasticity - physiology | Synapses - metabolism | Protein Isoforms - biosynthesis | Neurogenesis - physiology | Entorhinal Cortex - injuries
entorhinal lesion | dentate gyrus | synaptic plasticity | gene expression | proteoglycan | Proteoglycan | Dentate gyrus | Gene expression | Entorhinal lesion | Synaptic plasticity | TEMPORAL-LOBE EPILEPSY | CHONDROITIN SULFATE PROTEOGLYCANS | HIGH-AFFINITY BINDING | ENTORHINAL CORTEX LESION | NEUROSCIENCES | TRAUMATIC BRAIN-INJURY | NEURITE OUTGROWTH | RAT FASCIA-DENTATA | SPINAL-CORD-INJURY | CENTRAL-NERVOUS-SYSTEM | CELL-ADHESION MOLECULES | Immunohistochemistry | Microscopy, Electron, Transmission | Receptor-Like Protein Tyrosine Phosphatases, Class 5 - biosynthesis | Rats | Male | Brain Injuries - metabolism | Reverse Transcriptase Polymerase Chain Reaction | Rats, Sprague-Dawley | Blotting, Western | Hippocampus - metabolism | Microscopy, Confocal | Animals | Neuronal Plasticity - physiology | Synapses - metabolism | Protein Isoforms - biosynthesis | Neurogenesis - physiology | Entorhinal Cortex - injuries
Journal Article
Infection and Immunity, ISSN 0019-9567, 12/2006, Volume 74, Issue 12, pp. 6571 - 6580
Classifications Services IAI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit...
INFECTIOUS DISEASES | RPTP-BETA | VACUOLATING CYTOTOXIN | MEMBRANE CHANNEL FORMATION | CELLULAR VACUOLATION | IMMUNOLOGY | CYTOCHROME-C RELEASE | ANION-SELECTIVE CHANNELS | TOXIN VACA | PLASMA-MEMBRANE | BINDING | GPI-ANCHORED PROTEINS | Phosphatidylinositol Diacylglycerol-Lyase - pharmacology | Membrane Microdomains - metabolism | Humans | Cells, Cultured | Nerve Tissue Proteins - analysis | Nitrobenzoates - pharmacology | Membrane Microdomains - chemistry | Protein Tyrosine Phosphatases - metabolism | Receptor-Like Protein Tyrosine Phosphatases, Class 5 | Protein Transport - drug effects | Bacterial Proteins - analysis | Phosphoinositide Phospholipase C | beta-Cyclodextrins - pharmacology | Activating Transcription Factor 2 - metabolism | Nerve Tissue Proteins - metabolism | p38 Mitogen-Activated Protein Kinases - drug effects | Protein Tyrosine Phosphatases - analysis | Activating Transcription Factor 2 - agonists | Vacuoles - chemistry | Vacuoles - metabolism | Bacterial Proteins - metabolism | p38 Mitogen-Activated Protein Kinases - metabolism | Cellular Microbiology | Pathogen-Host Cell Molecular Interactions
INFECTIOUS DISEASES | RPTP-BETA | VACUOLATING CYTOTOXIN | MEMBRANE CHANNEL FORMATION | CELLULAR VACUOLATION | IMMUNOLOGY | CYTOCHROME-C RELEASE | ANION-SELECTIVE CHANNELS | TOXIN VACA | PLASMA-MEMBRANE | BINDING | GPI-ANCHORED PROTEINS | Phosphatidylinositol Diacylglycerol-Lyase - pharmacology | Membrane Microdomains - metabolism | Humans | Cells, Cultured | Nerve Tissue Proteins - analysis | Nitrobenzoates - pharmacology | Membrane Microdomains - chemistry | Protein Tyrosine Phosphatases - metabolism | Receptor-Like Protein Tyrosine Phosphatases, Class 5 | Protein Transport - drug effects | Bacterial Proteins - analysis | Phosphoinositide Phospholipase C | beta-Cyclodextrins - pharmacology | Activating Transcription Factor 2 - metabolism | Nerve Tissue Proteins - metabolism | p38 Mitogen-Activated Protein Kinases - drug effects | Protein Tyrosine Phosphatases - analysis | Activating Transcription Factor 2 - agonists | Vacuoles - chemistry | Vacuoles - metabolism | Bacterial Proteins - metabolism | p38 Mitogen-Activated Protein Kinases - metabolism | Cellular Microbiology | Pathogen-Host Cell Molecular Interactions
Journal Article