Journal of Virology, ISSN 0022-538X, 03/2008, Volume 82, Issue 5, pp. 2241 - 2249
Erratum ( vol. 82 , p. 6783 ) Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious...
PROGRAMMED CELL-DEATH | POLIOVIRUS INFECTION | HUMAN-DISEASE | VIROLOGY | HUMAN HEPATOMA-CELLS | SIGNALING PATHWAY | ENDOPLASMIC-RETICULUM | IMMORTALIZED HUMAN HEPATOCYTES | REPLICATION COMPLEX | CORE PROTEIN | CONJUGATION SYSTEM | Enzyme-Linked Immunosorbent Assay | Humans | Genotype | DNA Primers | Microscopy, Electron | Autophagy | Blotting, Western | Hepatitis Viruses - genetics | Base Sequence | Hepatitis Viruses - growth & development | Polymerase Chain Reaction | Cell Line, Tumor | Serial Passage | Pathogenesis and Immunity
PROGRAMMED CELL-DEATH | POLIOVIRUS INFECTION | HUMAN-DISEASE | VIROLOGY | HUMAN HEPATOMA-CELLS | SIGNALING PATHWAY | ENDOPLASMIC-RETICULUM | IMMORTALIZED HUMAN HEPATOCYTES | REPLICATION COMPLEX | CORE PROTEIN | CONJUGATION SYSTEM | Enzyme-Linked Immunosorbent Assay | Humans | Genotype | DNA Primers | Microscopy, Electron | Autophagy | Blotting, Western | Hepatitis Viruses - genetics | Base Sequence | Hepatitis Viruses - growth & development | Polymerase Chain Reaction | Cell Line, Tumor | Serial Passage | Pathogenesis and Immunity
Journal Article
Molecular Pharmacology, ISSN 0026-895X, 02/2008, Volume 73, Issue 2, pp. 399 - 409
We previously demonstrated that curcumin, a polyphenolic antioxidant purified from turmeric, up-regulated peroxisome proliferator-activated receptor (PPAR)-γ...
FAT-STORING CELLS | EXTRACELLULAR-MATRIX GENES | CELLULAR ACTIVATION | TUMOR-NECROSIS-FACTOR | HEPATIC STELLATE CELLS | LIPID-PEROXIDATION | INTERFERON-GAMMA | EPIDERMAL-GROWTH-FACTOR | PHARMACOLOGY & PHARMACY | CARBON-TETRACHLORIDE | FACTOR-ALPHA | Inflammation - pathology | Liver - pathology | Liver Cirrhosis - prevention & control | Curcumin - therapeutic use | Liver - metabolism | Oxidative Stress - physiology | Curcumin - pharmacology | Rats | Male | Antioxidants - pharmacology | Carbon Tetrachloride Poisoning - prevention & control | Rats, Sprague-Dawley | Liver Cirrhosis - chemically induced | Antioxidants - therapeutic use | Inflammation - metabolism | Animals | Carbon Tetrachloride Poisoning - metabolism | Liver - drug effects | Liver Cirrhosis - metabolism | Liver Cirrhosis - pathology | Inflammation - prevention & control | Oxidative Stress - drug effects
FAT-STORING CELLS | EXTRACELLULAR-MATRIX GENES | CELLULAR ACTIVATION | TUMOR-NECROSIS-FACTOR | HEPATIC STELLATE CELLS | LIPID-PEROXIDATION | INTERFERON-GAMMA | EPIDERMAL-GROWTH-FACTOR | PHARMACOLOGY & PHARMACY | CARBON-TETRACHLORIDE | FACTOR-ALPHA | Inflammation - pathology | Liver - pathology | Liver Cirrhosis - prevention & control | Curcumin - therapeutic use | Liver - metabolism | Oxidative Stress - physiology | Curcumin - pharmacology | Rats | Male | Antioxidants - pharmacology | Carbon Tetrachloride Poisoning - prevention & control | Rats, Sprague-Dawley | Liver Cirrhosis - chemically induced | Antioxidants - therapeutic use | Inflammation - metabolism | Animals | Carbon Tetrachloride Poisoning - metabolism | Liver - drug effects | Liver Cirrhosis - metabolism | Liver Cirrhosis - pathology | Inflammation - prevention & control | Oxidative Stress - drug effects
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2014, Volume 9, Issue 1, p. e86656
Intestinal epithelial cells (IECs) overlying the villi play a prominent role in absorption of digested nutrients and establish a barrier that separates the...
NANOPARTICLES | TRANSPORT | BACTERIA | DENDRITIC CELLS | PERMEABILITY | MACROMOLECULES | ENTEROCYTES | MULTIDISCIPLINARY SCIENCES | ENDOCYTOSIS | MUCUS | PATCH | Ovalbumin | Enterocytes - metabolism | Mice, Inbred C57BL | Antigens - metabolism | Blotting, Western | Lipopolysaccharides | Particle Size | Microscopy, Confocal | Absorption | Animals | Dextrans | Intestine, Small - cytology | Mice | Intestine, Small - metabolism | Microscopy, Fluorescence | Dextran | Albumin | Antigens | Dendritic cells | Epithelial cells | Mucosa | Vaccines | Immunity | Experiments | Small intestine | Chlorpromazine | Molecular weight | Nanoparticles | Proteins | Connective tissues | Biomedical materials | Microorganisms | Endocytosis | Rodents | Bacteria | Nutrients | Physiology | Peyer's patches | CD11c antigen | Immunoglobulins | Passageways | Particulates | Lamina propria | Gene expression | Epithelium | Immunological tolerance | Enterocytes | Microscopy | Diet | Pharmacy | In vivo methods and tests | Molecular biology
NANOPARTICLES | TRANSPORT | BACTERIA | DENDRITIC CELLS | PERMEABILITY | MACROMOLECULES | ENTEROCYTES | MULTIDISCIPLINARY SCIENCES | ENDOCYTOSIS | MUCUS | PATCH | Ovalbumin | Enterocytes - metabolism | Mice, Inbred C57BL | Antigens - metabolism | Blotting, Western | Lipopolysaccharides | Particle Size | Microscopy, Confocal | Absorption | Animals | Dextrans | Intestine, Small - cytology | Mice | Intestine, Small - metabolism | Microscopy, Fluorescence | Dextran | Albumin | Antigens | Dendritic cells | Epithelial cells | Mucosa | Vaccines | Immunity | Experiments | Small intestine | Chlorpromazine | Molecular weight | Nanoparticles | Proteins | Connective tissues | Biomedical materials | Microorganisms | Endocytosis | Rodents | Bacteria | Nutrients | Physiology | Peyer's patches | CD11c antigen | Immunoglobulins | Passageways | Particulates | Lamina propria | Gene expression | Epithelium | Immunological tolerance | Enterocytes | Microscopy | Diet | Pharmacy | In vivo methods and tests | Molecular biology
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2012, Volume 7, Issue 6, p. e39565
HIV-1 circulates both as free virus and within immune cells, with the level of free virus being predictive of clinical course. Both forms of HIV-1 cross the...
HIV-1 GP120 | ADSORPTIVE ENDOCYTOSIS | ENVELOPE GLYCOPROTEIN GP120 | MULTIDISCIPLINARY SCIENCES | ENDOTHELIAL-CELLS | MOUSE | SURFACE-PROTEINS | MEDIATED TRANSPORT | RAT-BRAIN | MANNOSE 6-PHOSPHATE RECEPTOR | LYSOSOMAL-ENZYME | HIV-1 - metabolism | Transcytosis - physiology | Calcium - metabolism | Endothelial Cells - metabolism | Brain - virology | Male | Wheat Germ Agglutinins - metabolism | Receptor, IGF Type 2 - metabolism | Blood-Brain Barrier - metabolism | Brain - metabolism | Animals | Biological Transport | Signal Transduction - physiology | Blood-Brain Barrier - virology | Mice | Endothelial Cells - virology | Cyclic AMP - metabolism | Brain | Brain research | Analysis | Cyclic adenylic acid | HIV (Viruses) | Sulfates | Sugars | Monosaccharides | Endothelium | Phosphates | Health sciences | Neurosciences | Membranes | Phosphorylation | Calcium | Viruses | Mannose | Insulin-like growth factors | Adipocytes | Mannan | Protamine sulfate | Blood-brain barrier | Archives & records | Human immunodeficiency virus--HIV | Physiology | Immune system | Heparan sulfate | Enzymes | Stroke | Endothelial cells | CD4 antigen | Virology | Medicine | Pathology | Perfusion | Protamine | Insulin resistance | Sulfate | Transport | Galactosylceramide | Geriatrics | HIV | Human immunodeficiency virus
HIV-1 GP120 | ADSORPTIVE ENDOCYTOSIS | ENVELOPE GLYCOPROTEIN GP120 | MULTIDISCIPLINARY SCIENCES | ENDOTHELIAL-CELLS | MOUSE | SURFACE-PROTEINS | MEDIATED TRANSPORT | RAT-BRAIN | MANNOSE 6-PHOSPHATE RECEPTOR | LYSOSOMAL-ENZYME | HIV-1 - metabolism | Transcytosis - physiology | Calcium - metabolism | Endothelial Cells - metabolism | Brain - virology | Male | Wheat Germ Agglutinins - metabolism | Receptor, IGF Type 2 - metabolism | Blood-Brain Barrier - metabolism | Brain - metabolism | Animals | Biological Transport | Signal Transduction - physiology | Blood-Brain Barrier - virology | Mice | Endothelial Cells - virology | Cyclic AMP - metabolism | Brain | Brain research | Analysis | Cyclic adenylic acid | HIV (Viruses) | Sulfates | Sugars | Monosaccharides | Endothelium | Phosphates | Health sciences | Neurosciences | Membranes | Phosphorylation | Calcium | Viruses | Mannose | Insulin-like growth factors | Adipocytes | Mannan | Protamine sulfate | Blood-brain barrier | Archives & records | Human immunodeficiency virus--HIV | Physiology | Immune system | Heparan sulfate | Enzymes | Stroke | Endothelial cells | CD4 antigen | Virology | Medicine | Pathology | Perfusion | Protamine | Insulin resistance | Sulfate | Transport | Galactosylceramide | Geriatrics | HIV | Human immunodeficiency virus
Journal Article
American Journal of Physiology - Renal Physiology, ISSN 0363-6127, 2013, Volume 304, Issue 8, pp. 1066 - 1075
El-Achkar TM, McCracken R, Liu Y, Heitmeier MR, Bourgeois S, Ryerse J, Wu XR. Tamm-Horsfall protein translocates to the basolateral domain of thick ascending...
Kidney injury | Tubular cross talk | Uromodulin | LOCALIZATION | PHYSIOLOGY | RAT-KIDNEY | RENAL ISCHEMIA | REPERFUSION | tubular cross talk | NEPHROPATHY | GENE-EXPRESSION | UROLOGY & NEPHROLOGY | uromodulin | MICE | GLYCOPROTEIN | MUTATIONS | kidney injury | Prognosis | Reperfusion Injury - pathology | Acute Kidney Injury - pathology | Loop of Henle - metabolism | Loop of Henle - ultrastructure | Renal Circulation - physiology | Uromodulin - metabolism | Nephritis - pathology | Biomarkers - blood | Mice, 129 Strain | Microscopy, Immunoelectron | Uromodulin - blood | Mice, Knockout | Animals | Loop of Henle - cytology | Uromodulin - urine | Recovery of Function - physiology | Cell Polarity - physiology | Nephritis - metabolism | Signal Transduction - physiology | Mice | Acute Kidney Injury - metabolism | Reperfusion Injury - metabolism | Disease Models, Animal | Proteins | Translocation (Genetics) | Ischemia | Physiological aspects | Genetic aspects | Research | Health aspects | Acute renal failure | Call for Papers
Kidney injury | Tubular cross talk | Uromodulin | LOCALIZATION | PHYSIOLOGY | RAT-KIDNEY | RENAL ISCHEMIA | REPERFUSION | tubular cross talk | NEPHROPATHY | GENE-EXPRESSION | UROLOGY & NEPHROLOGY | uromodulin | MICE | GLYCOPROTEIN | MUTATIONS | kidney injury | Prognosis | Reperfusion Injury - pathology | Acute Kidney Injury - pathology | Loop of Henle - metabolism | Loop of Henle - ultrastructure | Renal Circulation - physiology | Uromodulin - metabolism | Nephritis - pathology | Biomarkers - blood | Mice, 129 Strain | Microscopy, Immunoelectron | Uromodulin - blood | Mice, Knockout | Animals | Loop of Henle - cytology | Uromodulin - urine | Recovery of Function - physiology | Cell Polarity - physiology | Nephritis - metabolism | Signal Transduction - physiology | Mice | Acute Kidney Injury - metabolism | Reperfusion Injury - metabolism | Disease Models, Animal | Proteins | Translocation (Genetics) | Ischemia | Physiological aspects | Genetic aspects | Research | Health aspects | Acute renal failure | Call for Papers
Journal Article
Journal of Virology, ISSN 0022-538X, 05/2006, Volume 80, Issue 9, pp. 4633 - 4639
Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley...
GENOTYPES | HEPATOCELLULAR-CARCINOMA | IN-VITRO | REPLICATION | THERAPY | VIROLOGY | HUMAN HEPATOMA-CELLS | CORE PROTEIN | CULTURE | EXPRESSION | GENOME | Gold | Hepacivirus - isolation & purification | Microscopy, Electron, Transmission | Genome, Viral - genetics | Humans | Virion - metabolism | Microscopy, Immunoelectron | Hepatocytes - cytology | RNA, Viral - genetics | Virus Replication | Culture Media | Gene Expression Regulation, Viral | Cell Death | Hepatocytes - virology | Hepacivirus - physiology | Clone Cells | Genome and Regulation of Viral Gene Expression
GENOTYPES | HEPATOCELLULAR-CARCINOMA | IN-VITRO | REPLICATION | THERAPY | VIROLOGY | HUMAN HEPATOMA-CELLS | CORE PROTEIN | CULTURE | EXPRESSION | GENOME | Gold | Hepacivirus - isolation & purification | Microscopy, Electron, Transmission | Genome, Viral - genetics | Humans | Virion - metabolism | Microscopy, Immunoelectron | Hepatocytes - cytology | RNA, Viral - genetics | Virus Replication | Culture Media | Gene Expression Regulation, Viral | Cell Death | Hepatocytes - virology | Hepacivirus - physiology | Clone Cells | Genome and Regulation of Viral Gene Expression
Journal Article
Pain, ISSN 0304-3959, 11/2013, Volume 154, Issue 11, pp. 2432 - 2440
Peroxynitrite contributes to chemotherapy-induced neuropathic pain via post-translational nitration and inactivation of mitochondrial superoxide dismutase...
Peroxynitrite | Oxaliplatin | Bortezomib | Mitochondrial dysfunction | Peripheral nerve sensory axons | Chemotherapy-induced painful peripheral neuropathy | Paclitaxel | ATP depletion | Superoxide dismutase | Neuropathic pain | NITRIC-OXIDE SYNTHASE | RADICAL PRODUCTION | RAT SCIATIC-NERVE | CELL-LINES | CANCER | NEUROSCIENCES | CLINICAL NEUROLOGY | PERMEABILITY TRANSITION | PROTEIN-TYROSINE NITRATION | DISEASE | ANESTHESIOLOGY | Neoplasm Transplantation | Paclitaxel - pharmacology | Neuralgia - metabolism | Male | Axons - physiology | Hyperalgesia - psychology | Mitochondria - ultrastructure | Organoplatinum Compounds - pharmacology | Peripheral Nerves - physiology | Sensory Receptor Cells - physiology | Antineoplastic Agents - adverse effects | Adenosine Triphosphate - metabolism | Neuralgia - chemically induced | Antineoplastic Agents - pharmacology | Energy Metabolism - physiology | Superoxide Dismutase - metabolism | Physical Stimulation | Rats | Mitochondria - drug effects | Peroxynitrous Acid - physiology | Rats, Sprague-Dawley | Protein Processing, Post-Translational - physiology | Animals | Hyperalgesia - drug therapy | Antineoplastic Agents, Phytogenic - pharmacology | Pyrazines - pharmacology | Boronic Acids - pharmacology | Nitration | Chemotherapy | Superoxide | Cancer | Chemotherapy-induced painful peripheral | neuropathy
Peroxynitrite | Oxaliplatin | Bortezomib | Mitochondrial dysfunction | Peripheral nerve sensory axons | Chemotherapy-induced painful peripheral neuropathy | Paclitaxel | ATP depletion | Superoxide dismutase | Neuropathic pain | NITRIC-OXIDE SYNTHASE | RADICAL PRODUCTION | RAT SCIATIC-NERVE | CELL-LINES | CANCER | NEUROSCIENCES | CLINICAL NEUROLOGY | PERMEABILITY TRANSITION | PROTEIN-TYROSINE NITRATION | DISEASE | ANESTHESIOLOGY | Neoplasm Transplantation | Paclitaxel - pharmacology | Neuralgia - metabolism | Male | Axons - physiology | Hyperalgesia - psychology | Mitochondria - ultrastructure | Organoplatinum Compounds - pharmacology | Peripheral Nerves - physiology | Sensory Receptor Cells - physiology | Antineoplastic Agents - adverse effects | Adenosine Triphosphate - metabolism | Neuralgia - chemically induced | Antineoplastic Agents - pharmacology | Energy Metabolism - physiology | Superoxide Dismutase - metabolism | Physical Stimulation | Rats | Mitochondria - drug effects | Peroxynitrous Acid - physiology | Rats, Sprague-Dawley | Protein Processing, Post-Translational - physiology | Animals | Hyperalgesia - drug therapy | Antineoplastic Agents, Phytogenic - pharmacology | Pyrazines - pharmacology | Boronic Acids - pharmacology | Nitration | Chemotherapy | Superoxide | Cancer | Chemotherapy-induced painful peripheral | neuropathy
Journal Article
Molecular Cancer Research, ISSN 1541-7786, 08/2009, Volume 7, Issue 8, pp. 1268 - 1284
Proteasome inhibitors induce rapid death of cancer cells. We show that in epithelial cancer cells, such death is associated with dramatic and simultaneous...
BAX/BAK | Mitochondria | BH3-only proteins | CANCER-CELLS | CYTOCHROME-C | P53-DEPENDENT APOPTOSIS | ONCOLOGY | BAX | MITOCHONDRIAL-FRAGMENTATION | BCL-2 PROTEINS | RETICULUM | NF-KAPPA-B | MULTIPLE-MYELOMA CELLS | P53 | CELL BIOLOGY | Permeability - drug effects | Apoptosis - drug effects | HCT116 Cells | Humans | Tumor Suppressor Protein p53 - metabolism | bcl-2-Associated X Protein - metabolism | Mitochondria - metabolism | Mitochondria - drug effects | bcl-2 Homologous Antagonist-Killer Protein - metabolism | Mitochondria - ultrastructure | Mitochondrial Membranes - drug effects | Up-Regulation - drug effects | Leupeptins - pharmacology | Proto-Oncogene Proteins c-bcl-2 - metabolism | Animals | Myeloid Cell Leukemia Sequence 1 Protein | Mitochondrial Membranes - ultrastructure | Protein Biosynthesis - drug effects | Mice | Proteasome Inhibitors | RNA, Small Interfering - metabolism
BAX/BAK | Mitochondria | BH3-only proteins | CANCER-CELLS | CYTOCHROME-C | P53-DEPENDENT APOPTOSIS | ONCOLOGY | BAX | MITOCHONDRIAL-FRAGMENTATION | BCL-2 PROTEINS | RETICULUM | NF-KAPPA-B | MULTIPLE-MYELOMA CELLS | P53 | CELL BIOLOGY | Permeability - drug effects | Apoptosis - drug effects | HCT116 Cells | Humans | Tumor Suppressor Protein p53 - metabolism | bcl-2-Associated X Protein - metabolism | Mitochondria - metabolism | Mitochondria - drug effects | bcl-2 Homologous Antagonist-Killer Protein - metabolism | Mitochondria - ultrastructure | Mitochondrial Membranes - drug effects | Up-Regulation - drug effects | Leupeptins - pharmacology | Proto-Oncogene Proteins c-bcl-2 - metabolism | Animals | Myeloid Cell Leukemia Sequence 1 Protein | Mitochondrial Membranes - ultrastructure | Protein Biosynthesis - drug effects | Mice | Proteasome Inhibitors | RNA, Small Interfering - metabolism
Journal Article
9.
Full Text
Pathogenesis of Morquio A syndrome: An autopsied case reveals systemic storage disorder
Molecular Genetics and Metabolism, ISSN 1096-7192, 07/2013, Volume 109, Issue 3, pp. 301 - 311
Mucopolysaccharidosis IVA (MPS IVA; Morquio A syndrome) is a lysosomal storage disorder caused by deficiency of N-acetylgalactosamine-6-sulfate sulfatase,...
Mucopolysaccharidosis IVA | Chondroitin-6-sulfate | Cervical fusion | Pathogenesis | Keratan sulfate | MPS IVA | MEDICINE, RESEARCH & EXPERIMENTAL | MODEL | DEFICIENCY | CARTILAGE | DISEASE | ENDOCRINOLOGY & METABOLISM | GENETICS & HEREDITY | Young Adult | Magnetic Resonance Imaging | Phenotype | Autopsy | Humans | Male | Tomography, X-Ray Computed | Mucopolysaccharidosis IV - diagnosis | Mucopolysaccharidosis IV - etiology | Acute respiratory distress syndrome | Heart | Glycosaminoglycans | Sulfates | Analysis | Bone dysplasia
Mucopolysaccharidosis IVA | Chondroitin-6-sulfate | Cervical fusion | Pathogenesis | Keratan sulfate | MPS IVA | MEDICINE, RESEARCH & EXPERIMENTAL | MODEL | DEFICIENCY | CARTILAGE | DISEASE | ENDOCRINOLOGY & METABOLISM | GENETICS & HEREDITY | Young Adult | Magnetic Resonance Imaging | Phenotype | Autopsy | Humans | Male | Tomography, X-Ray Computed | Mucopolysaccharidosis IV - diagnosis | Mucopolysaccharidosis IV - etiology | Acute respiratory distress syndrome | Heart | Glycosaminoglycans | Sulfates | Analysis | Bone dysplasia
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 05/2012, Volume 32, Issue 18, pp. 6149 - 6160
Chemotherapy-induced peripheral neuropathy (CIPN) accompanied by chronic neuropathic pain is a major dose-limiting side effect of a large number of antitumoral...
BREAST-CANCER | MECHANICAL ALLODYNIA | REACTIVE OXYGEN | INDUCED HYPERALGESIA | NITRIC-OXIDE SYNTHASE | DECOMPOSITION CATALYSTS | PERIPHERAL NEUROPATHY | SUPEROXIDE-DISMUTASE | TYROSINE NITRATION | UP-REGULATION | NEUROSCIENCES | Spinal Cord - drug effects | Spinal Cord - metabolism | Cytokines - metabolism | Neuralgia - metabolism | Paclitaxel - adverse effects | Rats | Male | Antineoplastic Agents - therapeutic use | Paclitaxel - therapeutic use | Rats, Sprague-Dawley | Animals | Neuralgia - prevention & control | Antineoplastic Agents - adverse effects | Peroxynitrous Acid - metabolism | Neuralgia - chemically induced | Peroxynitrous Acid - antagonists & inhibitors | Drug Delivery Systems - methods
BREAST-CANCER | MECHANICAL ALLODYNIA | REACTIVE OXYGEN | INDUCED HYPERALGESIA | NITRIC-OXIDE SYNTHASE | DECOMPOSITION CATALYSTS | PERIPHERAL NEUROPATHY | SUPEROXIDE-DISMUTASE | TYROSINE NITRATION | UP-REGULATION | NEUROSCIENCES | Spinal Cord - drug effects | Spinal Cord - metabolism | Cytokines - metabolism | Neuralgia - metabolism | Paclitaxel - adverse effects | Rats | Male | Antineoplastic Agents - therapeutic use | Paclitaxel - therapeutic use | Rats, Sprague-Dawley | Animals | Neuralgia - prevention & control | Antineoplastic Agents - adverse effects | Peroxynitrous Acid - metabolism | Neuralgia - chemically induced | Peroxynitrous Acid - antagonists & inhibitors | Drug Delivery Systems - methods
Journal Article
Molecular and Cellular Biology, ISSN 0270-7306, 01/2008, Volume 28, Issue 1, pp. 269 - 281
Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley...
HISTONE METHYLTRANSFERASES | INTERACTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | ZINC-FINGER PROTEIN | TRANSCRIPTIONAL REPRESSION | ADENOVIRUS E1A | GENE-EXPRESSION | C-TERMINAL DOMAIN | SUMO MODIFICATION | ASSOCIATION | SUMOYLATION | CELL BIOLOGY | Cell Line | Humans | Alcohol Oxidoreductases - metabolism | DNA-Binding Proteins - genetics | Mutation - genetics | DNA-Binding Proteins - deficiency | Mice, Knockout | Alcohol Oxidoreductases - genetics | DNA-Binding Proteins - metabolism | p300-CBP Transcription Factors - metabolism | Animals | Cell Nucleus - metabolism | p300-CBP Transcription Factors - genetics | Kruppel-Like Transcription Factors - metabolism | Protein Binding | Trans-Activators - metabolism | Mice | SUMO-1 Protein - metabolism | Transcription, Genetic - genetics | Alcohol Oxidoreductases - deficiency
HISTONE METHYLTRANSFERASES | INTERACTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | ZINC-FINGER PROTEIN | TRANSCRIPTIONAL REPRESSION | ADENOVIRUS E1A | GENE-EXPRESSION | C-TERMINAL DOMAIN | SUMO MODIFICATION | ASSOCIATION | SUMOYLATION | CELL BIOLOGY | Cell Line | Humans | Alcohol Oxidoreductases - metabolism | DNA-Binding Proteins - genetics | Mutation - genetics | DNA-Binding Proteins - deficiency | Mice, Knockout | Alcohol Oxidoreductases - genetics | DNA-Binding Proteins - metabolism | p300-CBP Transcription Factors - metabolism | Animals | Cell Nucleus - metabolism | p300-CBP Transcription Factors - genetics | Kruppel-Like Transcription Factors - metabolism | Protein Binding | Trans-Activators - metabolism | Mice | SUMO-1 Protein - metabolism | Transcription, Genetic - genetics | Alcohol Oxidoreductases - deficiency
Journal Article
Eukaryotic Cell, ISSN 1535-9778, 10/2008, Volume 7, Issue 10, pp. 1685 - 1698
Classifications Services EC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit...
PROTEIN-KINASE-C | CHITIN SYNTHASE | GENE | PATHWAY | CHITOSAN | NITRIC-OXIDE | CALCINEURIN | MICROBIOLOGY | WALL INTEGRITY | HOMOLOGOUS RECOMBINATION | SACCHAROMYCES-CEREVISIAE | Protein Kinase C - genetics | Sequence Deletion | Virulence Factors - genetics | Oxidative Stress | Signal Transduction | Cryptococcus neoformans - genetics | Cell Wall - genetics | Fungal Proteins - genetics | Melanins - metabolism | Cryptococcus neoformans - metabolism | Cryptococcus neoformans - pathogenicity | Nitroso Compounds - metabolism | Protein Kinase C - metabolism | Cell Wall - metabolism | Chitin - metabolism | Mitogen-Activated Protein Kinases - genetics | Virulence Factors - metabolism | Fungal Proteins - metabolism | Mitogen-Activated Protein Kinases - metabolism
PROTEIN-KINASE-C | CHITIN SYNTHASE | GENE | PATHWAY | CHITOSAN | NITRIC-OXIDE | CALCINEURIN | MICROBIOLOGY | WALL INTEGRITY | HOMOLOGOUS RECOMBINATION | SACCHAROMYCES-CEREVISIAE | Protein Kinase C - genetics | Sequence Deletion | Virulence Factors - genetics | Oxidative Stress | Signal Transduction | Cryptococcus neoformans - genetics | Cell Wall - genetics | Fungal Proteins - genetics | Melanins - metabolism | Cryptococcus neoformans - metabolism | Cryptococcus neoformans - pathogenicity | Nitroso Compounds - metabolism | Protein Kinase C - metabolism | Cell Wall - metabolism | Chitin - metabolism | Mitogen-Activated Protein Kinases - genetics | Virulence Factors - metabolism | Fungal Proteins - metabolism | Mitogen-Activated Protein Kinases - metabolism
Journal Article
Journal of Virology, ISSN 0022-538X, 04/1996, Volume 70, Issue 4, pp. 2296 - 2306
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MOUSE CELLS | TUMOR-NECROSIS-FACTOR | MW PROTEIN | VIROLOGY | MESSENGER-RNA | FACTOR CYTOLYSIS | PREVENTS CYTOLYSIS | DELETION MUTANTS | E3 TRANSCRIPTION UNIT | REGION E3 | E1A PROTEINS | Amino Acid Sequence | Adenovirus E3 Proteins - genetics | Cell Survival | Humans | KB Cells | Adenoviruses, Human - physiology | Cytopathogenic Effect, Viral | Molecular Sequence Data | Viral Plaque Assay | Adenoviruses, Human - pathogenicity | Adenovirus E3 Proteins - physiology | Virus Replication | Mutation
MOUSE CELLS | TUMOR-NECROSIS-FACTOR | MW PROTEIN | VIROLOGY | MESSENGER-RNA | FACTOR CYTOLYSIS | PREVENTS CYTOLYSIS | DELETION MUTANTS | E3 TRANSCRIPTION UNIT | REGION E3 | E1A PROTEINS | Amino Acid Sequence | Adenovirus E3 Proteins - genetics | Cell Survival | Humans | KB Cells | Adenoviruses, Human - physiology | Cytopathogenic Effect, Viral | Molecular Sequence Data | Viral Plaque Assay | Adenoviruses, Human - pathogenicity | Adenovirus E3 Proteins - physiology | Virus Replication | Mutation
Journal Article
Journal of Cerebral Blood Flow & Metabolism, ISSN 0271-678X, 02/2009, Volume 29, Issue 2, pp. 411 - 422
By isolating for the first time ever a peptide transporter from the blood—brain barrier (BBB) and developing an antisense that selectively targets the...
Antisense | Stroke | Blood-brain barrier | PACAP | Alzheimer's disease | Peptide | blood-brain barrier | CYCLASE-ACTIVATING POLYPEPTIDE | peptide | PACAP RECEPTOR | SAMP8 MICE | BARRIER | AMYLOID PRECURSOR PROTEIN | stroke | NEUROSCIENCES | BETA | ENDOCRINOLOGY & METABOLISM | DEFICITS | HEMATOLOGY | EXPRESSION | antisense | APOLIPOPROTEIN-A-I | BLOOD | Genetic Therapy | Alzheimer Disease - therapy | Membrane Transport Proteins - isolation & purification | Adenosine Triphosphatases - metabolism | Brain - enzymology | Male | Alzheimer Disease - enzymology | Stroke - genetics | Alzheimer Disease - pathology | Stroke - enzymology | Stroke - pathology | Animals | Oligonucleotides, Antisense - genetics | Membrane Transport Proteins - genetics | Pituitary Adenylate Cyclase-Activating Polypeptide - metabolism | Protein Binding | Membrane Transport Proteins - metabolism | Mice | Alzheimer Disease - genetics | Endothelial Cells - enzymology | Stroke - therapy | Disease Models, Animal
Antisense | Stroke | Blood-brain barrier | PACAP | Alzheimer's disease | Peptide | blood-brain barrier | CYCLASE-ACTIVATING POLYPEPTIDE | peptide | PACAP RECEPTOR | SAMP8 MICE | BARRIER | AMYLOID PRECURSOR PROTEIN | stroke | NEUROSCIENCES | BETA | ENDOCRINOLOGY & METABOLISM | DEFICITS | HEMATOLOGY | EXPRESSION | antisense | APOLIPOPROTEIN-A-I | BLOOD | Genetic Therapy | Alzheimer Disease - therapy | Membrane Transport Proteins - isolation & purification | Adenosine Triphosphatases - metabolism | Brain - enzymology | Male | Alzheimer Disease - enzymology | Stroke - genetics | Alzheimer Disease - pathology | Stroke - enzymology | Stroke - pathology | Animals | Oligonucleotides, Antisense - genetics | Membrane Transport Proteins - genetics | Pituitary Adenylate Cyclase-Activating Polypeptide - metabolism | Protein Binding | Membrane Transport Proteins - metabolism | Mice | Alzheimer Disease - genetics | Endothelial Cells - enzymology | Stroke - therapy | Disease Models, Animal
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 11/2010, Volume 30, Issue 46, pp. 15400 - 15408
The clinical efficacy of opiates for pain control is severely limited by analgesic tolerance and hyperalgesia. Herein we show that chronic morphine upregulates...
CENTRAL SENSITIZATION | SPHINGOSINE KINASE 1 | INDUCED HYPERALGESIA | MORPHINE ANTINOCICEPTIVE TOLERANCE | NITRIC-OXIDE | PAIN HYPERSENSITIVITY | GLUTAMINE-SYNTHETASE | THERAPEUTIC TARGETS | INFLAMMATORY PAIN | RAT SENSORY NEURONS | NEUROSCIENCES | Sphingosine - physiology | Neuroglia - physiology | Analgesics, Opioid - pharmacology | Rats | Analgesics, Opioid - therapeutic use | Male | Pain Measurement - drug effects | Sphingolipids - physiology | Rats, Sprague-Dawley | Hyperalgesia - physiopathology | Neuroglia - drug effects | Pain Measurement - methods | Sphingosine - analogs & derivatives | Animals | Hyperalgesia - drug therapy | Lysophospholipids - physiology
CENTRAL SENSITIZATION | SPHINGOSINE KINASE 1 | INDUCED HYPERALGESIA | MORPHINE ANTINOCICEPTIVE TOLERANCE | NITRIC-OXIDE | PAIN HYPERSENSITIVITY | GLUTAMINE-SYNTHETASE | THERAPEUTIC TARGETS | INFLAMMATORY PAIN | RAT SENSORY NEURONS | NEUROSCIENCES | Sphingosine - physiology | Neuroglia - physiology | Analgesics, Opioid - pharmacology | Rats | Analgesics, Opioid - therapeutic use | Male | Pain Measurement - drug effects | Sphingolipids - physiology | Rats, Sprague-Dawley | Hyperalgesia - physiopathology | Neuroglia - drug effects | Pain Measurement - methods | Sphingosine - analogs & derivatives | Animals | Hyperalgesia - drug therapy | Lysophospholipids - physiology
Journal Article
Virology, ISSN 0042-6822, 2009, Volume 392, Issue 1, pp. 62 - 72
Abstract Head and neck squamous cell carcinomas (HNSCC) are one of the leading causes of cancer deaths world wide. Up-regulation of the epidermal growth factor...
Infectious Disease | BCL-2 | Adenovirus | BCL-xL | MCL-1 | HNSCC | E1B-19K | EGFR | Cisplatin | Apoptosis | CARCINOMA-CELLS | INDUCED APOPTOSIS | E1A-MEDIATED SUPPRESSION | DELETION | GROWTH-FACTOR RECEPTOR | VIROLOGY | GENE | DEATH EFFECTOR | INFECTED-CELLS | ONCOLYTIC ADENOVIRUS | REPLICATING ADENOVIRUS | Receptor, Epidermal Growth Factor - genetics | Carcinoma, Squamous Cell - genetics | Carcinoma, Squamous Cell - metabolism | Humans | bcl-X Protein - genetics | Drug Resistance, Neoplasm | Head and Neck Neoplasms - metabolism | Proto-Oncogene Proteins c-bcl-2 - metabolism | Receptor, Epidermal Growth Factor - metabolism | Base Sequence | Cell Survival | Down-Regulation | Head and Neck Neoplasms - therapy | Adenoviruses, Human - physiology | Carcinoma, Squamous Cell - therapy | Oncolytic Virotherapy | Myeloid Cell Leukemia Sequence 1 Protein | Cell Line, Tumor | Head and Neck Neoplasms - genetics | Adenoviruses, Human - genetics | Mutation | DNA, Viral - genetics | Genetic Vectors | bcl-X Protein - metabolism | Proto-Oncogene Proteins c-bcl-2 - genetics | Chemotherapy | Squamous cell carcinoma | Epidermal growth factor | Cell death | Health aspects | Cancer | BCL-2, BCL-xL | E1B-19K, EGFR | adenovirus | apoptosis | cisplatin
Infectious Disease | BCL-2 | Adenovirus | BCL-xL | MCL-1 | HNSCC | E1B-19K | EGFR | Cisplatin | Apoptosis | CARCINOMA-CELLS | INDUCED APOPTOSIS | E1A-MEDIATED SUPPRESSION | DELETION | GROWTH-FACTOR RECEPTOR | VIROLOGY | GENE | DEATH EFFECTOR | INFECTED-CELLS | ONCOLYTIC ADENOVIRUS | REPLICATING ADENOVIRUS | Receptor, Epidermal Growth Factor - genetics | Carcinoma, Squamous Cell - genetics | Carcinoma, Squamous Cell - metabolism | Humans | bcl-X Protein - genetics | Drug Resistance, Neoplasm | Head and Neck Neoplasms - metabolism | Proto-Oncogene Proteins c-bcl-2 - metabolism | Receptor, Epidermal Growth Factor - metabolism | Base Sequence | Cell Survival | Down-Regulation | Head and Neck Neoplasms - therapy | Adenoviruses, Human - physiology | Carcinoma, Squamous Cell - therapy | Oncolytic Virotherapy | Myeloid Cell Leukemia Sequence 1 Protein | Cell Line, Tumor | Head and Neck Neoplasms - genetics | Adenoviruses, Human - genetics | Mutation | DNA, Viral - genetics | Genetic Vectors | bcl-X Protein - metabolism | Proto-Oncogene Proteins c-bcl-2 - genetics | Chemotherapy | Squamous cell carcinoma | Epidermal growth factor | Cell death | Health aspects | Cancer | BCL-2, BCL-xL | E1B-19K, EGFR | adenovirus | apoptosis | cisplatin
Journal Article