Journal of Neuroscience, ISSN 0270-6474, 03/2004, Volume 24, Issue 13, pp. 3370 - 3378
The mechanisms of action of human synthetic and naturally secreted cell-derived amyloid beta-peptide (Abeta)(1-42) on the induction of long-term potentiation...
Metabotropic glutamate receptors | Cdk5 | JNK | LTP | Amyloid β-protein | Alzheimer's disease | p38 MAPK | Hippocampus | NEURONAL APOPTOSIS | hippocampus | ALZHEIMERS-DISEASE | MAP KINASE | metabotropic glutamate receptors | amyloid beta-protein | SYNAPTIC PLASTICITY | FREQUENCY STIMULATION | AREA CA1 | NEUROSCIENCES | IN-VITRO | PATHWAY | MICE | PRECURSOR PROTEIN | Receptors, Metabotropic Glutamate - drug effects | Cyclin-Dependent Kinases - metabolism | Amyloid beta-Peptides - pharmacology | Humans | Amyloid beta-Peptides - secretion | Peptide Fragments - pharmacology | Receptors, Metabotropic Glutamate - metabolism | Hippocampus - drug effects | Ovary - cytology | Excitatory Postsynaptic Potentials - drug effects | Cyclin-Dependent Kinases - drug effects | Dose-Response Relationship, Drug | Excitatory Postsynaptic Potentials - physiology | Long-Term Potentiation - drug effects | Amyloid beta-Peptides - genetics | JNK Mitogen-Activated Protein Kinases | Long-Term Potentiation - physiology | Receptor, Metabotropic Glutamate 5 | Female | Electric Stimulation - methods | Peptide Fragments - genetics | p38 Mitogen-Activated Protein Kinases | CHO Cells | Ovary - metabolism | Cricetinae | Enzyme Inhibitors - pharmacology | Peptide Fragments - secretion | Rats | Excitatory Amino Acid Antagonists - pharmacology | Cyclin-Dependent Kinase 5 | Animals | Ovary - secretion | Hippocampus - physiology | In Vitro Techniques | Mitogen-Activated Protein Kinases - drug effects | Mitogen-Activated Protein Kinases - metabolism | Plasticity | Development | amyloid β-protein | Repair
Metabotropic glutamate receptors | Cdk5 | JNK | LTP | Amyloid β-protein | Alzheimer's disease | p38 MAPK | Hippocampus | NEURONAL APOPTOSIS | hippocampus | ALZHEIMERS-DISEASE | MAP KINASE | metabotropic glutamate receptors | amyloid beta-protein | SYNAPTIC PLASTICITY | FREQUENCY STIMULATION | AREA CA1 | NEUROSCIENCES | IN-VITRO | PATHWAY | MICE | PRECURSOR PROTEIN | Receptors, Metabotropic Glutamate - drug effects | Cyclin-Dependent Kinases - metabolism | Amyloid beta-Peptides - pharmacology | Humans | Amyloid beta-Peptides - secretion | Peptide Fragments - pharmacology | Receptors, Metabotropic Glutamate - metabolism | Hippocampus - drug effects | Ovary - cytology | Excitatory Postsynaptic Potentials - drug effects | Cyclin-Dependent Kinases - drug effects | Dose-Response Relationship, Drug | Excitatory Postsynaptic Potentials - physiology | Long-Term Potentiation - drug effects | Amyloid beta-Peptides - genetics | JNK Mitogen-Activated Protein Kinases | Long-Term Potentiation - physiology | Receptor, Metabotropic Glutamate 5 | Female | Electric Stimulation - methods | Peptide Fragments - genetics | p38 Mitogen-Activated Protein Kinases | CHO Cells | Ovary - metabolism | Cricetinae | Enzyme Inhibitors - pharmacology | Peptide Fragments - secretion | Rats | Excitatory Amino Acid Antagonists - pharmacology | Cyclin-Dependent Kinase 5 | Animals | Ovary - secretion | Hippocampus - physiology | In Vitro Techniques | Mitogen-Activated Protein Kinases - drug effects | Mitogen-Activated Protein Kinases - metabolism | Plasticity | Development | amyloid β-protein | Repair
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 09/2006, Volume 281, Issue 35, pp. 25457 - 25465
Hyperphosphorylation of the microtubule-associated protein tau is a characteristic feature of neurodegenerative tauopathies including Alzheimer disease....
NEUROFIBRILLARY TANGLES | PHOSPHORYLATES TAU | MICROTUBULE-BINDING | ALZHEIMERS-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | GLYCOGEN-SYNTHASE KINASE-3 | PAIRED HELICAL FILAMENTS | AMYLOID PRECURSOR PROTEIN | P25 EXPRESSION | ACTIVATOR P25 | TRANSGENIC MICE | Glycogen Synthase Kinase 3 - physiology | Phosphorylation | Mice, Inbred C57BL | Gene Expression Regulation | Mice, Transgenic | Epitopes | Phosphoproteins - metabolism | tau Proteins - chemistry | Proline - chemistry | Hippocampus - metabolism | Animals | tau Proteins - physiology | Cyclin-Dependent Kinase 5 - physiology | Heterozygote | Mice
NEUROFIBRILLARY TANGLES | PHOSPHORYLATES TAU | MICROTUBULE-BINDING | ALZHEIMERS-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | GLYCOGEN-SYNTHASE KINASE-3 | PAIRED HELICAL FILAMENTS | AMYLOID PRECURSOR PROTEIN | P25 EXPRESSION | ACTIVATOR P25 | TRANSGENIC MICE | Glycogen Synthase Kinase 3 - physiology | Phosphorylation | Mice, Inbred C57BL | Gene Expression Regulation | Mice, Transgenic | Epitopes | Phosphoproteins - metabolism | tau Proteins - chemistry | Proline - chemistry | Hippocampus - metabolism | Animals | tau Proteins - physiology | Cyclin-Dependent Kinase 5 - physiology | Heterozygote | Mice
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 5893 - 14
Pleiotrophin (PTN) stimulates endothelial cell migration through binding to receptor protein tyrosine phosphatase beta/zeta (RPTP beta/zeta) and...
VITRO | AFFIN REGULATORY PEPTIDE | PROTEIN | NEURITE OUTGROWTH | CDK5 | SIGNALING PATHWAY | ANGIOGENESIS IN-VIVO | MULTIDISCIPLINARY SCIENCES | TYROSINE-PHOSPHATASE BETA/ZETA | GENE-EXPRESSION | BRAIN | Tyrosine | Immunoprecipitation | Threonine | Cyclin-dependent kinases | Pleiotrophin | Extracellular signal-regulated kinase | Mass spectroscopy | Src protein | Kinases | Carbazole | Cyclin-dependent kinase 5 | Endothelial cells | Cell adhesion & migration | 1-Phosphatidylinositol 3-kinase | Cyclin-dependent kinase | Angiogenesis | Next-generation sequencing | Protein-serine/threonine kinase | Cell migration | Protein-tyrosine-phosphatase | Biological Sciences | Biochemistry and Molecular Biology | Naturvetenskap | Natural Sciences | Biokemi och molekylärbiologi | Biologiska vetenskaper
VITRO | AFFIN REGULATORY PEPTIDE | PROTEIN | NEURITE OUTGROWTH | CDK5 | SIGNALING PATHWAY | ANGIOGENESIS IN-VIVO | MULTIDISCIPLINARY SCIENCES | TYROSINE-PHOSPHATASE BETA/ZETA | GENE-EXPRESSION | BRAIN | Tyrosine | Immunoprecipitation | Threonine | Cyclin-dependent kinases | Pleiotrophin | Extracellular signal-regulated kinase | Mass spectroscopy | Src protein | Kinases | Carbazole | Cyclin-dependent kinase 5 | Endothelial cells | Cell adhesion & migration | 1-Phosphatidylinositol 3-kinase | Cyclin-dependent kinase | Angiogenesis | Next-generation sequencing | Protein-serine/threonine kinase | Cell migration | Protein-tyrosine-phosphatase | Biological Sciences | Biochemistry and Molecular Biology | Naturvetenskap | Natural Sciences | Biokemi och molekylärbiologi | Biologiska vetenskaper
Journal Article
Brain Research Bulletin, ISSN 0361-9230, 06/2017, Volume 132, pp. 28 - 38
Alzheimer's disease (AD) is one of the most frequently encountered diseases in adults with progressive loss of memory and behavioral changes. Inspite of there...
Deregulation | Neurofibrillary tangles | Cdk5 | Alzheimer's disease | Amyloid precursor protein | OXIDATIVE STRESS | AXONAL-TRANSPORT | CDK5 ACTIVITY | NEUROSCIENCES | NEURODEGENERATIVE DISEASES | CASCADE RELEVANCE | MITOCHONDRIAL FISSION | S-NITROSYLATION | A-BETA-PRODUCTION | Alzheimer Disease - drug therapy | Animals | Alzheimer Disease - enzymology | Humans | Cyclin-Dependent Kinase 5 - metabolism | Proline | Drug discovery | Amyloid beta-protein | Target marketing
Deregulation | Neurofibrillary tangles | Cdk5 | Alzheimer's disease | Amyloid precursor protein | OXIDATIVE STRESS | AXONAL-TRANSPORT | CDK5 ACTIVITY | NEUROSCIENCES | NEURODEGENERATIVE DISEASES | CASCADE RELEVANCE | MITOCHONDRIAL FISSION | S-NITROSYLATION | A-BETA-PRODUCTION | Alzheimer Disease - drug therapy | Animals | Alzheimer Disease - enzymology | Humans | Cyclin-Dependent Kinase 5 - metabolism | Proline | Drug discovery | Amyloid beta-protein | Target marketing
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 11/2010, Volume 285, Issue 46, pp. 35932 - 35943
Angiogenesis contributes to various pathological conditions. Due to the resistance against existing antiangiogenic therapy, an urgent need exists to understand...
NEURONAL MIGRATION | ROSCOVITINE | METASTASIS | CDK5 | PHOSPHORYLATION | ACTIN POLYMERIZATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | FOCAL ADHESION KINASE | RHO-GTPASES | CANCER | RAC1 ACTIVITY | Neovascularization, Physiologic - drug effects | Humans | Cell Movement - physiology | Cyclin-Dependent Kinase 5 - genetics | Cyclin-Dependent Kinase Inhibitor p27 - metabolism | Microtubules - metabolism | RNA Interference | Chorioallantoic Membrane - drug effects | Female | Phosphorylation - drug effects | Vascular Endothelial Growth Factor A - pharmacology | Endothelial Cells - physiology | Chorioallantoic Membrane - blood supply | Purines - pharmacology | Mice, Inbred C57BL | Umbilical Cord - enzymology | Cells, Cultured | Cell Adhesion | Chick Embryo | Serine - metabolism | Blotting, Western | Cyclin-Dependent Kinase 5 - metabolism | Cell Movement - drug effects | Microscopy, Confocal | Neovascularization, Physiologic - physiology | Cyclin-Dependent Kinase 5 - antagonists & inhibitors | Animals | Signal Transduction - drug effects | Endothelial Cells - cytology | Mice | Protein Kinase Inhibitors - pharmacology | Endothelial Cells - enzymology | CDK (Cyclin-dependent Kinase) | Protein Kinases | Signal Transduction | Tumor Therapy | Cell Motility | Rho | Cytoskeleton | Confocal Microscopy | Chemotaxis | Cell Biology | Endothelium
NEURONAL MIGRATION | ROSCOVITINE | METASTASIS | CDK5 | PHOSPHORYLATION | ACTIN POLYMERIZATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | FOCAL ADHESION KINASE | RHO-GTPASES | CANCER | RAC1 ACTIVITY | Neovascularization, Physiologic - drug effects | Humans | Cell Movement - physiology | Cyclin-Dependent Kinase 5 - genetics | Cyclin-Dependent Kinase Inhibitor p27 - metabolism | Microtubules - metabolism | RNA Interference | Chorioallantoic Membrane - drug effects | Female | Phosphorylation - drug effects | Vascular Endothelial Growth Factor A - pharmacology | Endothelial Cells - physiology | Chorioallantoic Membrane - blood supply | Purines - pharmacology | Mice, Inbred C57BL | Umbilical Cord - enzymology | Cells, Cultured | Cell Adhesion | Chick Embryo | Serine - metabolism | Blotting, Western | Cyclin-Dependent Kinase 5 - metabolism | Cell Movement - drug effects | Microscopy, Confocal | Neovascularization, Physiologic - physiology | Cyclin-Dependent Kinase 5 - antagonists & inhibitors | Animals | Signal Transduction - drug effects | Endothelial Cells - cytology | Mice | Protein Kinase Inhibitors - pharmacology | Endothelial Cells - enzymology | CDK (Cyclin-dependent Kinase) | Protein Kinases | Signal Transduction | Tumor Therapy | Cell Motility | Rho | Cytoskeleton | Confocal Microscopy | Chemotaxis | Cell Biology | Endothelium
Journal Article
Journal of Chemical Information and Modeling, ISSN 1549-9596, 02/2014, Volume 54, Issue 2, pp. 470 - 480
In this study, we applied steered molecular dynamics (SMD) simulations to investigate the unbinding mechanism of nine inhibitors of the enzyme cyclin-dependent...
CHEMISTRY, MEDICINAL | MECHANISM | BINDING AFFINITIES | DOCKING | DRUG DESIGN | COMPUTER SCIENCE, INFORMATION SYSTEMS | ATOMISTIC SIMULATIONS | FREE-ENERGIES | TAU-PHOSPHORYLATION | CHEMISTRY, MULTIDISCIPLINARY | AQUAGLYCEROPORIN GLPF | COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS | FORCE-FIELD | INHIBITORS | Cyclin-Dependent Kinase 5 - chemistry | Cyclin-Dependent Kinase 5 - antagonists & inhibitors | Inhibitory Concentration 50 | Protein Binding | Ligands | Protein Conformation | Protein Kinase Inhibitors - pharmacology | Molecular Dynamics Simulation | Cyclin-Dependent Kinase 5 - metabolism | Protein Kinase Inhibitors - metabolism
CHEMISTRY, MEDICINAL | MECHANISM | BINDING AFFINITIES | DOCKING | DRUG DESIGN | COMPUTER SCIENCE, INFORMATION SYSTEMS | ATOMISTIC SIMULATIONS | FREE-ENERGIES | TAU-PHOSPHORYLATION | CHEMISTRY, MULTIDISCIPLINARY | AQUAGLYCEROPORIN GLPF | COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS | FORCE-FIELD | INHIBITORS | Cyclin-Dependent Kinase 5 - chemistry | Cyclin-Dependent Kinase 5 - antagonists & inhibitors | Inhibitory Concentration 50 | Protein Binding | Ligands | Protein Conformation | Protein Kinase Inhibitors - pharmacology | Molecular Dynamics Simulation | Cyclin-Dependent Kinase 5 - metabolism | Protein Kinase Inhibitors - metabolism
Journal Article
Nature Neuroscience, ISSN 1097-6256, 07/2007, Volume 10, Issue 7, pp. 880 - 886
Learning is accompanied by modulation of postsynaptic signal transduction pathways in neurons. Although the neuronal protein kinase cyclin-dependent kinase 5...
MEMORY | CALPAIN | NR2B SUBUNIT | LONG-TERM-POTENTIATION | NEURONS | RECEPTOR | MICE | CDK5 ACTIVITY | RAT-BRAIN | EXPRESSION | NEUROSCIENCES | Synapses - drug effects | Receptors, N-Methyl-D-Aspartate - drug effects | Immunoprecipitation | Learning - drug effects | Synapses - physiology | Neuronal Plasticity - drug effects | Male | Hippocampus - drug effects | Reverse Transcriptase Polymerase Chain Reaction | Excitatory Postsynaptic Potentials - drug effects | Receptors, N-Methyl-D-Aspartate - physiology | Blotting, Western | Brain Chemistry - physiology | Mice, Knockout | Learning - physiology | Animals | Neuronal Plasticity - physiology | Cyclin-Dependent Kinase 5 - physiology | Mice | Hippocampus - physiology | Brain Chemistry - genetics | Neuroplasticity | Control | Physiological aspects | Cyclic adenylic acid | Research | Protein kinases | Motor learning | Neurotransmitter receptors | Biochemistry, Molecular Biology | Receptors, N-Methyl-D-Aspartate | Cyclin-Dependent Kinase 5 | Learning | Life Sciences | Neuronal Plasticity | Excitatory Postsynaptic Potentials | Brain Chemistry | Molecular biology | Synapses | Hippocampus
MEMORY | CALPAIN | NR2B SUBUNIT | LONG-TERM-POTENTIATION | NEURONS | RECEPTOR | MICE | CDK5 ACTIVITY | RAT-BRAIN | EXPRESSION | NEUROSCIENCES | Synapses - drug effects | Receptors, N-Methyl-D-Aspartate - drug effects | Immunoprecipitation | Learning - drug effects | Synapses - physiology | Neuronal Plasticity - drug effects | Male | Hippocampus - drug effects | Reverse Transcriptase Polymerase Chain Reaction | Excitatory Postsynaptic Potentials - drug effects | Receptors, N-Methyl-D-Aspartate - physiology | Blotting, Western | Brain Chemistry - physiology | Mice, Knockout | Learning - physiology | Animals | Neuronal Plasticity - physiology | Cyclin-Dependent Kinase 5 - physiology | Mice | Hippocampus - physiology | Brain Chemistry - genetics | Neuroplasticity | Control | Physiological aspects | Cyclic adenylic acid | Research | Protein kinases | Motor learning | Neurotransmitter receptors | Biochemistry, Molecular Biology | Receptors, N-Methyl-D-Aspartate | Cyclin-Dependent Kinase 5 | Learning | Life Sciences | Neuronal Plasticity | Excitatory Postsynaptic Potentials | Brain Chemistry | Molecular biology | Synapses | Hippocampus
Journal Article
Journal of Neuroscience Research, ISSN 0360-4012, 08/2015, Volume 93, Issue 8, pp. 1258 - 1266
Inappropriate activation of cyclin‐dependent kinase 5 (CDK5) resulting from proteolytic release of the activator fragment p25 from the membrane contributes to...
β‐amyloid plaques | PP2A | GSK3β Ser9 | Alzheimer's disease | CDK5 RNAi | β-amyloid plaques | TAU-PROTEIN | ABNORMAL HYPERPHOSPHORYLATION | PHOSPHORYLATION | ALZHEIMERS-DISEASE | NEUROSCIENCES | GSK3 beta Ser9 | beta-amyloid plaques | PROTEIN PHOSPHATASES | CDK5 | A-BETA | NEUROFIBRILLARY DEGENERATION | MICE | Gene Targeting - methods | Phosphoric Monoester Hydrolases - genetics | Glycogen Synthase Kinase 3 - antagonists & inhibitors | Glycogen Synthase Kinase 3 beta | Mice, Transgenic | Glycogen Synthase Kinase 3 - metabolism | Cyclin-Dependent Kinase 5 - metabolism | Cyclin-Dependent Kinase 5 - genetics | Amyloid beta-Peptides - antagonists & inhibitors | Cyclin-Dependent Kinase 5 - antagonists & inhibitors | Animals | Glycogen Synthase Kinase 3 - genetics | Amyloid beta-Peptides - genetics | Protein Aggregation, Pathological - prevention & control | Amyloid beta-Peptides - metabolism | Mice | Phosphoric Monoester Hydrolases - metabolism | Protein Aggregation, Pathological - genetics | Protein Aggregation, Pathological - metabolism | Phosphoric Monoester Hydrolases - antagonists & inhibitors
β‐amyloid plaques | PP2A | GSK3β Ser9 | Alzheimer's disease | CDK5 RNAi | β-amyloid plaques | TAU-PROTEIN | ABNORMAL HYPERPHOSPHORYLATION | PHOSPHORYLATION | ALZHEIMERS-DISEASE | NEUROSCIENCES | GSK3 beta Ser9 | beta-amyloid plaques | PROTEIN PHOSPHATASES | CDK5 | A-BETA | NEUROFIBRILLARY DEGENERATION | MICE | Gene Targeting - methods | Phosphoric Monoester Hydrolases - genetics | Glycogen Synthase Kinase 3 - antagonists & inhibitors | Glycogen Synthase Kinase 3 beta | Mice, Transgenic | Glycogen Synthase Kinase 3 - metabolism | Cyclin-Dependent Kinase 5 - metabolism | Cyclin-Dependent Kinase 5 - genetics | Amyloid beta-Peptides - antagonists & inhibitors | Cyclin-Dependent Kinase 5 - antagonists & inhibitors | Animals | Glycogen Synthase Kinase 3 - genetics | Amyloid beta-Peptides - genetics | Protein Aggregation, Pathological - prevention & control | Amyloid beta-Peptides - metabolism | Mice | Phosphoric Monoester Hydrolases - metabolism | Protein Aggregation, Pathological - genetics | Protein Aggregation, Pathological - metabolism | Phosphoric Monoester Hydrolases - antagonists & inhibitors
Journal Article
Journal of Hepatology, ISSN 0168-8278, 2015, Volume 63, Issue 1, pp. 102 - 113
Background & Aims For a long time cyclin dependent kinase 5 (Cdk5) was thought to be exclusively important in neuronal cells. However, increasing evidence...
Gastroenterology and Hepatology | Roscovitine | HCC | Cdk5 | Chemosensitization | DNA damage | Sn38 | CELLS | MULTICENTER | DNA-DAMAGE | FLUOROURACIL | METASTATIC COLORECTAL-CANCER | NUCLEAR-LOCALIZATION | COMBINATION CHEMOTHERAPY | IRINOTECAN | INHIBITOR | GASTROENTEROLOGY & HEPATOLOGY | Camptothecin - therapeutic use | Liver Neoplasms - genetics | Cyclin-Dependent Kinase 5 - drug effects | Humans | Gene Expression Regulation, Neoplastic | Liver Neoplasms - drug therapy | Treatment Outcome | Antineoplastic Agents - therapeutic use | Mice, SCID | Cyclin-Dependent Kinase 5 - genetics | Animals | Carcinoma, Hepatocellular - drug therapy | Carcinoma, Hepatocellular - genetics | Liver Neoplasms - metabolism | RNA, Neoplasm - genetics | Female | Mice | Purines - therapeutic use | Cyclin-Dependent Kinase 5 - biosynthesis | Cyclin-Dependent Kinases - antagonists & inhibitors | Camptothecin - analogs & derivatives | Carcinoma, Hepatocellular - metabolism | Development and progression | Health aspects | Hepatoma
Gastroenterology and Hepatology | Roscovitine | HCC | Cdk5 | Chemosensitization | DNA damage | Sn38 | CELLS | MULTICENTER | DNA-DAMAGE | FLUOROURACIL | METASTATIC COLORECTAL-CANCER | NUCLEAR-LOCALIZATION | COMBINATION CHEMOTHERAPY | IRINOTECAN | INHIBITOR | GASTROENTEROLOGY & HEPATOLOGY | Camptothecin - therapeutic use | Liver Neoplasms - genetics | Cyclin-Dependent Kinase 5 - drug effects | Humans | Gene Expression Regulation, Neoplastic | Liver Neoplasms - drug therapy | Treatment Outcome | Antineoplastic Agents - therapeutic use | Mice, SCID | Cyclin-Dependent Kinase 5 - genetics | Animals | Carcinoma, Hepatocellular - drug therapy | Carcinoma, Hepatocellular - genetics | Liver Neoplasms - metabolism | RNA, Neoplasm - genetics | Female | Mice | Purines - therapeutic use | Cyclin-Dependent Kinase 5 - biosynthesis | Cyclin-Dependent Kinases - antagonists & inhibitors | Camptothecin - analogs & derivatives | Carcinoma, Hepatocellular - metabolism | Development and progression | Health aspects | Hepatoma
Journal Article
Journal of Medicinal Chemistry, ISSN 0022-2623, 02/2014, Volume 57, Issue 3, pp. 578 - 599
The success of imatinib, a BCR-ABL inhibitor for the treatment of chronic myelogenous leukemia, has created a great impetus for the development of additional...
G ARREST | TUMOR INVASION | IN-VITRO | DESIGN | CHEMISTRY, MEDICINAL | BIOLOGICAL EVALUATION | CELL-CYCLE | PHARMACOLOGICAL INHIBITION | PD 0332991 | PHASE-I | CANCER | Neoplasm Transplantation | Apoptosis - drug effects | Pyridines - chemistry | Pyrimidines - chemical synthesis | Antineoplastic Agents - chemical synthesis | Humans | Structure-Activity Relationship | Pyrimidines - chemistry | Repressor Proteins - antagonists & inhibitors | Heterografts | Female | Antineoplastic Agents - pharmacology | Cyclin-Dependent Kinase 4 - antagonists & inhibitors | Pyridines - chemical synthesis | Pyrimidines - pharmacology | Antineoplastic Agents - chemistry | Animals | Protein Kinases | Mice, Nude | Cell Line, Tumor | Mice | Molecular Docking Simulation | Pyridines - pharmacology | Cell Cycle - drug effects | Drug Screening Assays, Antitumor | Index Medicus
G ARREST | TUMOR INVASION | IN-VITRO | DESIGN | CHEMISTRY, MEDICINAL | BIOLOGICAL EVALUATION | CELL-CYCLE | PHARMACOLOGICAL INHIBITION | PD 0332991 | PHASE-I | CANCER | Neoplasm Transplantation | Apoptosis - drug effects | Pyridines - chemistry | Pyrimidines - chemical synthesis | Antineoplastic Agents - chemical synthesis | Humans | Structure-Activity Relationship | Pyrimidines - chemistry | Repressor Proteins - antagonists & inhibitors | Heterografts | Female | Antineoplastic Agents - pharmacology | Cyclin-Dependent Kinase 4 - antagonists & inhibitors | Pyridines - chemical synthesis | Pyrimidines - pharmacology | Antineoplastic Agents - chemistry | Animals | Protein Kinases | Mice, Nude | Cell Line, Tumor | Mice | Molecular Docking Simulation | Pyridines - pharmacology | Cell Cycle - drug effects | Drug Screening Assays, Antitumor | Index Medicus
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 10/2012, Volume 32, Issue 42, pp. 14709 - 14721
The number of functional transient receptor potential vanilloid 1 (TRPV1) channels at the surface, especially at the peripheral terminals of primary sensory...
CAPSAICIN RECEPTOR | TRANSPORT | ACTIVATED ION-CHANNEL | PROTEIN | ROOT GANGLION NEURONS | PHOSPHORYLATION | HYPERALGESIA | PRIMARY SENSORY NEURONS | FHA DOMAIN | NEUROSCIENCES | CELL-LINE | Animals, Newborn | Protein Structure, Tertiary | Pain Threshold - physiology | Cricetinae | Phosphorylation | Cricetulus | Hot Temperature - adverse effects | Membrane Glycoproteins - metabolism | Cells, Cultured | Rats | Male | Protein Transport - physiology | Threonine - metabolism | Rats, Sprague-Dawley | TRPV Cation Channels - metabolism | Animals | TRPV Cation Channels - antagonists & inhibitors | Cell Line, Tumor | Cyclin-Dependent Kinase 5 - physiology | Kinesin - physiology | Nociceptors - metabolism | CHO Cells | Protein Binding - physiology
CAPSAICIN RECEPTOR | TRANSPORT | ACTIVATED ION-CHANNEL | PROTEIN | ROOT GANGLION NEURONS | PHOSPHORYLATION | HYPERALGESIA | PRIMARY SENSORY NEURONS | FHA DOMAIN | NEUROSCIENCES | CELL-LINE | Animals, Newborn | Protein Structure, Tertiary | Pain Threshold - physiology | Cricetinae | Phosphorylation | Cricetulus | Hot Temperature - adverse effects | Membrane Glycoproteins - metabolism | Cells, Cultured | Rats | Male | Protein Transport - physiology | Threonine - metabolism | Rats, Sprague-Dawley | TRPV Cation Channels - metabolism | Animals | TRPV Cation Channels - antagonists & inhibitors | Cell Line, Tumor | Cyclin-Dependent Kinase 5 - physiology | Kinesin - physiology | Nociceptors - metabolism | CHO Cells | Protein Binding - physiology
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 13676 - 19
Cyclin-dependent kinase 5 (CDK5) plays a pivotal role in neural development and neurodegeneration. CDK5 activity can be regulated by posttranslational...
S-NITROSYLATION | NERVOUS-SYSTEM | RETINOIC ACID | CDK5 | NEUROTROPHIC FACTOR | BDNF TRANSCRIPTION | MULTIDISCIPLINARY SCIENCES | DEACETYLASE SIRT1 | TRANSCRIPTION FACTOR | NEURODEGENERATIVE DISEASES | CEREBRAL-CORTEX | Phosphorylation | Transcription | Axonogenesis | Gene regulation | Cyclin-dependent kinases | Fetuses | Kinases | SIRT1 protein | Embryos | Cyclin-dependent kinase 5 | Cyclin-dependent kinase | Brain-derived neurotrophic factor | Deacetylation | Neurodegeneration | Lysine | Acetylation | Hippocampus
S-NITROSYLATION | NERVOUS-SYSTEM | RETINOIC ACID | CDK5 | NEUROTROPHIC FACTOR | BDNF TRANSCRIPTION | MULTIDISCIPLINARY SCIENCES | DEACETYLASE SIRT1 | TRANSCRIPTION FACTOR | NEURODEGENERATIVE DISEASES | CEREBRAL-CORTEX | Phosphorylation | Transcription | Axonogenesis | Gene regulation | Cyclin-dependent kinases | Fetuses | Kinases | SIRT1 protein | Embryos | Cyclin-dependent kinase 5 | Cyclin-dependent kinase | Brain-derived neurotrophic factor | Deacetylation | Neurodegeneration | Lysine | Acetylation | Hippocampus
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 08/2011, Volume 31, Issue 33, pp. 12029 - 12035
Cyclin-dependent kinase 5 (Cdk5) and its activator p35 have been implicated in drug addiction, neurodegenerative diseases such as Alzheimer's, learning and...
GLUTAMATE RECEPTORS | NMDA RECEPTORS | CDK5 | MAGUK SCAFFOLDING PROTEINS | SURFACE EXPRESSION | TRAFFICKING | DEGRADATION | MICE | ENDOCYTOSIS | SYNAPTIC PLASTICITY | NEUROSCIENCES | Disks Large Homolog 4 Protein | Male | Mice, Knockout | Protein Interaction Mapping | Hippocampus - metabolism | Animals | Neurons - enzymology | Guanylate Kinases - metabolism | Cyclin-Dependent Kinase 5 - physiology | Female | Hippocampus - enzymology | Membrane Proteins - metabolism | Mice | Neurons - metabolism | Ubiquitination - physiology | Organ Culture Techniques
GLUTAMATE RECEPTORS | NMDA RECEPTORS | CDK5 | MAGUK SCAFFOLDING PROTEINS | SURFACE EXPRESSION | TRAFFICKING | DEGRADATION | MICE | ENDOCYTOSIS | SYNAPTIC PLASTICITY | NEUROSCIENCES | Disks Large Homolog 4 Protein | Male | Mice, Knockout | Protein Interaction Mapping | Hippocampus - metabolism | Animals | Neurons - enzymology | Guanylate Kinases - metabolism | Cyclin-Dependent Kinase 5 - physiology | Female | Hippocampus - enzymology | Membrane Proteins - metabolism | Mice | Neurons - metabolism | Ubiquitination - physiology | Organ Culture Techniques
Journal Article
European Journal of Medicinal Chemistry, ISSN 0223-5234, 08/2015, Volume 101, pp. 274 - 287
An efficient synthetic strategy was developed to modulate the structure of the tetrahydropyridine isoindolone (Valmerin) skeleton. A library of more than 30...
Pyridoisoindolone | Valmerin | In vitro assays | CDK5 | GSK3 | Kinase research | In vitro assays | THERAPEUTICS | CHEMISTRY, MEDICINAL | ANTICANCER AGENTS | PYRIDINE | DYRK1A | CDK INHIBITORS | NEUROINFLAMMATION | BIOLOGICAL EVALUATION | CYTOTOXIC AGENTS | CDK5/P25 | DERIVATIVES | Isoindoles - chemistry | Protein Kinase Inhibitors - chemical synthesis | Piperidines - chemistry | Glycogen Synthase Kinase 3 - antagonists & inhibitors | Humans | Models, Molecular | Isoindoles - chemical synthesis | Structure-Activity Relationship | Glycogen Synthase Kinase 3 - metabolism | Piperidines - chemical synthesis | Cyclin-Dependent Kinase 5 - metabolism | Dose-Response Relationship, Drug | Cyclin-Dependent Kinase 5 - antagonists & inhibitors | Protein Kinase Inhibitors - chemistry | Piperidines - pharmacology | Cell Line, Tumor | Cell Proliferation - drug effects | Molecular Structure | Protein Kinase Inhibitors - pharmacology | Isoindoles - pharmacology | Glycogen | Synthesis | Analysis | Medicinal Chemistry | Life Sciences | Chemical Sciences | Cancer
Pyridoisoindolone | Valmerin | In vitro assays | CDK5 | GSK3 | Kinase research | In vitro assays | THERAPEUTICS | CHEMISTRY, MEDICINAL | ANTICANCER AGENTS | PYRIDINE | DYRK1A | CDK INHIBITORS | NEUROINFLAMMATION | BIOLOGICAL EVALUATION | CYTOTOXIC AGENTS | CDK5/P25 | DERIVATIVES | Isoindoles - chemistry | Protein Kinase Inhibitors - chemical synthesis | Piperidines - chemistry | Glycogen Synthase Kinase 3 - antagonists & inhibitors | Humans | Models, Molecular | Isoindoles - chemical synthesis | Structure-Activity Relationship | Glycogen Synthase Kinase 3 - metabolism | Piperidines - chemical synthesis | Cyclin-Dependent Kinase 5 - metabolism | Dose-Response Relationship, Drug | Cyclin-Dependent Kinase 5 - antagonists & inhibitors | Protein Kinase Inhibitors - chemistry | Piperidines - pharmacology | Cell Line, Tumor | Cell Proliferation - drug effects | Molecular Structure | Protein Kinase Inhibitors - pharmacology | Isoindoles - pharmacology | Glycogen | Synthesis | Analysis | Medicinal Chemistry | Life Sciences | Chemical Sciences | Cancer
Journal Article
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Full Text
Regulation of androgen receptor and prostate cancer growth by cyclin-dependent kinase 5
Journal of Biological Chemistry, ISSN 0021-9258, 09/2011, Volume 286, Issue 38, pp. 33141 - 33149
Prostate cancer is the most frequently diagnosed male malignancy. The normal prostate development and prostate cancer progression are mediated by androgen...
CELLS | TRANSCRIPTIONAL ACTIVITY | ACTIVATION | PROTEIN | CDK5 | INDUCED APOPTOSIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | SUBCELLULAR-LOCALIZATION | NEURODEGENERATION | PHOSPHORYLATION SITES | SIGNAL TRANSDUCER | Prostatic Neoplasms - metabolism | Prostatic Neoplasms - pathology | Phosphorylation | Transcriptional Activation - genetics | Cell Proliferation | Humans | Receptors, Androgen - metabolism | Male | Phosphoserine - metabolism | Cyclin-Dependent Kinase 5 - metabolism | Animals | Receptors, Androgen - genetics | Models, Biological | Cell Line, Tumor | Mice | Protein Processing, Post-Translational | Protein Stability | Protein Translocation | Androgen Receptor | p35 | Signal Transduction | Cdk5 | Prostate Cancer | Protein Phosphorylation | Serine Threonine Protein Kinase | Protein Degradation | Protein-Protein Interactions
CELLS | TRANSCRIPTIONAL ACTIVITY | ACTIVATION | PROTEIN | CDK5 | INDUCED APOPTOSIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | SUBCELLULAR-LOCALIZATION | NEURODEGENERATION | PHOSPHORYLATION SITES | SIGNAL TRANSDUCER | Prostatic Neoplasms - metabolism | Prostatic Neoplasms - pathology | Phosphorylation | Transcriptional Activation - genetics | Cell Proliferation | Humans | Receptors, Androgen - metabolism | Male | Phosphoserine - metabolism | Cyclin-Dependent Kinase 5 - metabolism | Animals | Receptors, Androgen - genetics | Models, Biological | Cell Line, Tumor | Mice | Protein Processing, Post-Translational | Protein Stability | Protein Translocation | Androgen Receptor | p35 | Signal Transduction | Cdk5 | Prostate Cancer | Protein Phosphorylation | Serine Threonine Protein Kinase | Protein Degradation | Protein-Protein Interactions
Journal Article