Internal Medicine, ISSN 0918-2918, 2018, Volume 57, Issue 6, pp. 909 - 910
Journal Article
ISSN 1359-7345, 7/2012, Volume 48, Issue 63, pp. 7841 - 7843
1,4,5,8-Tetraethynylnaphthalene derivatives 4a-c were synthesized for the first time. X-ray crystallographic structure analysis of 4a revealed three different...
Journal Article
The American Journal of Gastroenterology, ISSN 0002-9270, 12/2007, Volume 102, Issue 12, pp. 2708 - 2715
BACKGROUND: Nonalcoholic fatty liver disease (NAFLD) is closely associated with the metabolic syndrome.AIM: We evaluated the association among the metabolic...
DIAGNOSIS | GENERAL-POPULATION | JAPAN | SONOGRAPHY | PREVALENCE | HISTOLOGY | GASTROENTEROLOGY & HEPATOLOGY | Severity of Illness Index | Japan - epidemiology | Metabolic Syndrome - diagnostic imaging | Cross-Sectional Studies | Area Under Curve | Humans | Middle Aged | Logistic Models | Male | Metabolic Syndrome - complications | Fatty Liver - diagnostic imaging | Intra-Abdominal Fat - diagnostic imaging | Biopsy | Adolescent | Ultrasonography | Adult | Female | Aged | Fatty Liver - epidemiology | Metabolic Syndrome - epidemiology | Fatty Liver - etiology | Obesity | Fatty liver
DIAGNOSIS | GENERAL-POPULATION | JAPAN | SONOGRAPHY | PREVALENCE | HISTOLOGY | GASTROENTEROLOGY & HEPATOLOGY | Severity of Illness Index | Japan - epidemiology | Metabolic Syndrome - diagnostic imaging | Cross-Sectional Studies | Area Under Curve | Humans | Middle Aged | Logistic Models | Male | Metabolic Syndrome - complications | Fatty Liver - diagnostic imaging | Intra-Abdominal Fat - diagnostic imaging | Biopsy | Adolescent | Ultrasonography | Adult | Female | Aged | Fatty Liver - epidemiology | Metabolic Syndrome - epidemiology | Fatty Liver - etiology | Obesity | Fatty liver
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 05/2016, Volume 81, Issue 9, pp. 3735 - 3743
Diindenopyrene 4b and its diastereomer, which are extended homologues of 1,6- and 1,8-pyrenoquinodimethanes fused by indene units, respectively, were...
BIRADICAL CHARACTER | P-QUINODIMETHANES | FUSION MODE | CYCLIZATIONS | PARALLEL TRIPLE BONDS | MOLECULAR-STRUCTURE | KEKULE HYDROCARBON | CHEMISTRY, ORGANIC | CLOSED-SHELL | ALKYNES | SUBSTITUTED QUINODIMETHANS | Chemical reactions | Chemical properties | Ring formation (Chemistry) | Chemical compounds | Analysis
BIRADICAL CHARACTER | P-QUINODIMETHANES | FUSION MODE | CYCLIZATIONS | PARALLEL TRIPLE BONDS | MOLECULAR-STRUCTURE | KEKULE HYDROCARBON | CHEMISTRY, ORGANIC | CLOSED-SHELL | ALKYNES | SUBSTITUTED QUINODIMETHANS | Chemical reactions | Chemical properties | Ring formation (Chemistry) | Chemical compounds | Analysis
Journal Article
Scientific Reports, ISSN 2045-2322, 02/2017, Volume 7, Issue 1, p. 42339
The cancer drug gemcitabine (GEM) is a key drug for treating pancreatic ductal adenocarcinoma (PDAC), but PDAC cells develop chemoresistance after long-term...
ADJUVANT CHEMOTHERAPY | SURVIVAL | MIR-155 | CELLS | INTERFERON-ALPHA | THERAPY | BIOGENESIS | MULTIDISCIPLINARY SCIENCES | UP-REGULATION | CANCER | EXPRESSION | Exosomes - drug effects | Exosomes - metabolism | Adenocarcinoma - ultrastructure | Adenocarcinoma - pathology | Prognosis | Microdissection | Apoptosis - drug effects | Humans | Apoptosis - genetics | Deoxycytidine - pharmacology | Drug Resistance, Neoplasm | MicroRNAs - metabolism | Antineoplastic Agents - therapeutic use | Carcinoma, Pancreatic Ductal - genetics | Pancreatic Neoplasms - drug therapy | Deoxycytidine - therapeutic use | Time Factors | Carcinoma, Pancreatic Ductal - ultrastructure | Adenocarcinoma - genetics | Antineoplastic Agents - pharmacology | Gene Expression Regulation, Neoplastic - drug effects | Pancreatic Neoplasms - pathology | Pancreatic Neoplasms - ultrastructure | Pancreatic Neoplasms - genetics | Up-Regulation - genetics | Adenocarcinoma - drug therapy | Carcinoma, Pancreatic Ductal - pathology | Up-Regulation - drug effects | Xenograft Model Antitumor Assays | Carcinoma, Pancreatic Ductal - drug therapy | Animals | Cell Line, Tumor | Mice | MicroRNAs - genetics | Deoxycytidine - analogs & derivatives | Adenocarcinoma | Intercellular signalling | Gemcitabine | Secretion | Pancreatic cancer | Chemoresistance | MiRNA | Pancreas | Exosomes | Apoptosis
ADJUVANT CHEMOTHERAPY | SURVIVAL | MIR-155 | CELLS | INTERFERON-ALPHA | THERAPY | BIOGENESIS | MULTIDISCIPLINARY SCIENCES | UP-REGULATION | CANCER | EXPRESSION | Exosomes - drug effects | Exosomes - metabolism | Adenocarcinoma - ultrastructure | Adenocarcinoma - pathology | Prognosis | Microdissection | Apoptosis - drug effects | Humans | Apoptosis - genetics | Deoxycytidine - pharmacology | Drug Resistance, Neoplasm | MicroRNAs - metabolism | Antineoplastic Agents - therapeutic use | Carcinoma, Pancreatic Ductal - genetics | Pancreatic Neoplasms - drug therapy | Deoxycytidine - therapeutic use | Time Factors | Carcinoma, Pancreatic Ductal - ultrastructure | Adenocarcinoma - genetics | Antineoplastic Agents - pharmacology | Gene Expression Regulation, Neoplastic - drug effects | Pancreatic Neoplasms - pathology | Pancreatic Neoplasms - ultrastructure | Pancreatic Neoplasms - genetics | Up-Regulation - genetics | Adenocarcinoma - drug therapy | Carcinoma, Pancreatic Ductal - pathology | Up-Regulation - drug effects | Xenograft Model Antitumor Assays | Carcinoma, Pancreatic Ductal - drug therapy | Animals | Cell Line, Tumor | Mice | MicroRNAs - genetics | Deoxycytidine - analogs & derivatives | Adenocarcinoma | Intercellular signalling | Gemcitabine | Secretion | Pancreatic cancer | Chemoresistance | MiRNA | Pancreas | Exosomes | Apoptosis
Journal Article
Nature, ISSN 0028-0836, 07/2016, Volume 535, Issue 7610, pp. 117 - 121
Clusters of galaxies are the most massive gravitationally bound objects in the Universe and are still forming. They are thus important probes(1) of...
NGC 1275 | GALAXY CLUSTERS | TURBULENT VELOCITY | MULTIDISCIPLINARY SCIENCES | LINE | GAS | NGC-1275 | CONSTRAINTS | X-RAY SPECTROSCOPY | XMM-NEWTON | FEEDBACK | Clusters | Observations | Stars | Cosmology | Astrophysics | Velocity | Stars & galaxies | ASTRONOMY AND ASTROPHYSICS | GRQC | ASTRO
NGC 1275 | GALAXY CLUSTERS | TURBULENT VELOCITY | MULTIDISCIPLINARY SCIENCES | LINE | GAS | NGC-1275 | CONSTRAINTS | X-RAY SPECTROSCOPY | XMM-NEWTON | FEEDBACK | Clusters | Observations | Stars | Cosmology | Astrophysics | Velocity | Stars & galaxies | ASTRONOMY AND ASTROPHYSICS | GRQC | ASTRO
Journal Article
7.
Preventive role of tetraspanin CD9 in systemic inflammation of chronic obstructive pulmonary disease
American Journal of Respiratory Cell and Molecular Biology, ISSN 1044-1549, 12/2015, Volume 53, Issue 6, pp. 751 - 760
Chronic obstructive pulmonary disease (COPD) is frequently associated with extrapulmonary complications, including cardiovascular disease, diabetes, and...
Cd9 | Chronic obstructive pulmonary disease | Inflammation | Macrophage | Tetraspanin | METABOLIC SYNDROME | CD81 | BIOCHEMISTRY & MOLECULAR BIOLOGY | MUSCLE-CELL FUSION | macrophage | MACROPHAGE ACTIVATION | SECONDARY PREVENTION | MICE LACKING | CELL BIOLOGY | IN-VITRO | inflammation | tetraspanin | RESPIRATORY SYSTEM | REDUCING LIPIDS | ANTIINFLAMMATORY THERAPIES | CD9 | CHOLESTEROL-BIOSYNTHESIS | chronic obstructive pulmonary disease | Up-Regulation | Animals | Membrane Microdomains - metabolism | Humans | Tetraspanin-29 - physiology | Pulmonary Disease, Chronic Obstructive - immunology | Macrophage Activation | Cardiovascular disease | Insulin resistance | Health risk assessment | Cholesterol
Cd9 | Chronic obstructive pulmonary disease | Inflammation | Macrophage | Tetraspanin | METABOLIC SYNDROME | CD81 | BIOCHEMISTRY & MOLECULAR BIOLOGY | MUSCLE-CELL FUSION | macrophage | MACROPHAGE ACTIVATION | SECONDARY PREVENTION | MICE LACKING | CELL BIOLOGY | IN-VITRO | inflammation | tetraspanin | RESPIRATORY SYSTEM | REDUCING LIPIDS | ANTIINFLAMMATORY THERAPIES | CD9 | CHOLESTEROL-BIOSYNTHESIS | chronic obstructive pulmonary disease | Up-Regulation | Animals | Membrane Microdomains - metabolism | Humans | Tetraspanin-29 - physiology | Pulmonary Disease, Chronic Obstructive - immunology | Macrophage Activation | Cardiovascular disease | Insulin resistance | Health risk assessment | Cholesterol
Journal Article
Cell Reports, ISSN 2211-1247, 11/2015, Volume 13, Issue 6, pp. 1110 - 1117
Regulatory B cells (Breg) have immune suppressive functions in various autoimmune/inflammation models and diseases and are found to be enriched in diverse B...
INFLAMMATORY RESPONSES | AUTOIMMUNITY | IMMUNE-RESPONSES | B10 CELLS | GENE-EXPRESSION | EXOSOMES | TETRASPANIN | MICE | PROTEOMIC ANALYSIS | SUBSET | CELL BIOLOGY | B-Lymphocytes, Regulatory - metabolism | Animals | Interleukin-10 - genetics | Mice, Inbred C57BL | B-Lymphocytes, Regulatory - cytology | Cells, Cultured | Transcriptome | Interleukin-10 - metabolism | Mice | Tetraspanin-29 - metabolism | Tetraspanin-29 - genetics
INFLAMMATORY RESPONSES | AUTOIMMUNITY | IMMUNE-RESPONSES | B10 CELLS | GENE-EXPRESSION | EXOSOMES | TETRASPANIN | MICE | PROTEOMIC ANALYSIS | SUBSET | CELL BIOLOGY | B-Lymphocytes, Regulatory - metabolism | Animals | Interleukin-10 - genetics | Mice, Inbred C57BL | B-Lymphocytes, Regulatory - cytology | Cells, Cultured | Transcriptome | Interleukin-10 - metabolism | Mice | Tetraspanin-29 - metabolism | Tetraspanin-29 - genetics
Journal Article
Chemical Engineering Science, ISSN 0009-2509, 10/2014, Volume 118, pp. 208 - 213
In this study, the preservation ability of natural gas hydrate (NGH) with different particle size from 0.50 mm to 30 mm was investigated. It is known that...
Self-preservation | Particle size | Ice film | Clathrate hydrate | Natural gas hydrate | ENGINEERING, CHEMICAL | METHANE CLATHRATE HYDRATE | CH4 HYDRATE | 1 ATM | ICE | ANOMALOUS PRESERVATION | Methane | Methane hydrate | Gas industry | Powders | Storage | Natural gas
Self-preservation | Particle size | Ice film | Clathrate hydrate | Natural gas hydrate | ENGINEERING, CHEMICAL | METHANE CLATHRATE HYDRATE | CH4 HYDRATE | 1 ATM | ICE | ANOMALOUS PRESERVATION | Methane | Methane hydrate | Gas industry | Powders | Storage | Natural gas
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 2447 - 7
The aim of this study was to investigate the clinical impact of sarcopenia on the efficacy of programmed death (PD)-1 inhibitors. We retrospectively reviewed...
CHECKPOINT INHIBITORS | SOLID TUMORS | MULTIDISCIPLINARY SCIENCES | MASS | CLINICAL-IMPLICATIONS | DOUBLE-BLIND | TOXICITY | BODY-COMPOSITION | NIVOLUMAB | PROGNOSTIC VALUE | OBESITY SKELETAL-MUSCLE | Sarcopenia | Vertebrae | Pembrolizumab | PD-1 protein | Computed tomography | Lung cancer | Medical records | Tomography | Psoas muscle | Non-small cell lung carcinoma | Apoptosis
CHECKPOINT INHIBITORS | SOLID TUMORS | MULTIDISCIPLINARY SCIENCES | MASS | CLINICAL-IMPLICATIONS | DOUBLE-BLIND | TOXICITY | BODY-COMPOSITION | NIVOLUMAB | PROGNOSTIC VALUE | OBESITY SKELETAL-MUSCLE | Sarcopenia | Vertebrae | Pembrolizumab | PD-1 protein | Computed tomography | Lung cancer | Medical records | Tomography | Psoas muscle | Non-small cell lung carcinoma | Apoptosis
Journal Article
Internal Medicine, ISSN 0918-2918, 2018
Journal Article
PLoS genetics, ISSN 1553-7390, 12/2010, Volume 6, Issue 12, pp. e1001229 - 14
PTEN-induced kinase 1 (PINK1), which is required for mitochondrial homeostasis, is a gene product responsible for early-onset Parkinson's disease (PD). Another...
INDUCED CELL-DEATH | LIFE-SPAN | OXIDATIVE STRESS | MUTANTS | SIGNALING PATHWAY | UBIQUITIN-PROTEIN LIGASE | GENETICS & HEREDITY | MITOPHAGY | MUTATIONS | RECESSIVE PARKINSONISM | PARKINSONS-DISEASE | Protein Kinases - metabolism | Mitochondria - enzymology | Protein Kinases - genetics | Down-Regulation | Humans | Gene Silencing | Protein-Serine-Threonine Kinases - genetics | Ubiquitin-Protein Ligases - metabolism | Parkinson Disease - genetics | Drosophila Proteins - metabolism | Drosophila - enzymology | Animals | Mitochondria - genetics | HEK293 Cells | Protein Binding | Parkinson Disease - metabolism | Drosophila Proteins - genetics | Ubiquitin-Protein Ligases - genetics | Phosphoglycerate Kinase - genetics | Protein-Serine-Threonine Kinases - metabolism | Disease Models, Animal | Drosophila - genetics | Phosphoglycerate Kinase - metabolism | Parkinson's disease | Drosophila | Genes | Physiological aspects | Genetic aspects | Research | Risk factors | Proteins | Studies | Genotype & phenotype | Mitochondria | Insects | Parkinsons disease | Homeostasis | Kinases | Binding sites | Metabolic disorders
INDUCED CELL-DEATH | LIFE-SPAN | OXIDATIVE STRESS | MUTANTS | SIGNALING PATHWAY | UBIQUITIN-PROTEIN LIGASE | GENETICS & HEREDITY | MITOPHAGY | MUTATIONS | RECESSIVE PARKINSONISM | PARKINSONS-DISEASE | Protein Kinases - metabolism | Mitochondria - enzymology | Protein Kinases - genetics | Down-Regulation | Humans | Gene Silencing | Protein-Serine-Threonine Kinases - genetics | Ubiquitin-Protein Ligases - metabolism | Parkinson Disease - genetics | Drosophila Proteins - metabolism | Drosophila - enzymology | Animals | Mitochondria - genetics | HEK293 Cells | Protein Binding | Parkinson Disease - metabolism | Drosophila Proteins - genetics | Ubiquitin-Protein Ligases - genetics | Phosphoglycerate Kinase - genetics | Protein-Serine-Threonine Kinases - metabolism | Disease Models, Animal | Drosophila - genetics | Phosphoglycerate Kinase - metabolism | Parkinson's disease | Drosophila | Genes | Physiological aspects | Genetic aspects | Research | Risk factors | Proteins | Studies | Genotype & phenotype | Mitochondria | Insects | Parkinsons disease | Homeostasis | Kinases | Binding sites | Metabolic disorders
Journal Article
Animal Science Journal, ISSN 1344-3941, 02/2018, Volume 89, Issue 2, pp. 273 - 288
Growth hormone secretagogue receptor 1a (GHSR1a), growth hormone (GH), growth hormone receptor (GHR), non‐SMC condensin I complex, subunit G (NCAPG) and...
NCAPG | carcass and fatty acids traits | epistasis | GHSR1a/GH/GHR | Japanese Black cattle | GHRELIN RECEPTOR | AGRICULTURE, DAIRY & ANIMAL SCIENCE | SECRETAGOGUE RECEPTOR | SEX | HETERODIMERIZATION | BEEF-CATTLE | GHR | CASTRATED MALE | GHSR1a | FEMALE CATTLE | CROSS | 4 AGES | ASSOCIATION | Cattle - metabolism | Multifactorial Inheritance - genetics | Meat - analysis | Fatty Acids - analysis | Commerce | Male | 5' Untranslated Regions - genetics | Epistasis, Genetic - genetics | Meat - economics | Receptors, Ghrelin - genetics | Stearoyl-CoA Desaturase - genetics | Cattle - genetics | Receptors, Somatotropin - genetics | Adipose Tissue - metabolism | Growth Hormone - genetics | Animals | Alleles | Cell Cycle Proteins - genetics | Female | Lipid Metabolism - genetics | Somatotropin | Analysis | Genes | Genetic research | Physiological aspects | Beef cattle | Fatty acids | Genetic polymorphisms | Adipose tissues | Adipose tissue | Epistasis | Stearoyl-CoA desaturase | Desaturase | Condensin | Fatty acid composition | 5' Untranslated Regions | Cattle | Growth hormones | Growth hormone | Physical growth | Polymorphism
NCAPG | carcass and fatty acids traits | epistasis | GHSR1a/GH/GHR | Japanese Black cattle | GHRELIN RECEPTOR | AGRICULTURE, DAIRY & ANIMAL SCIENCE | SECRETAGOGUE RECEPTOR | SEX | HETERODIMERIZATION | BEEF-CATTLE | GHR | CASTRATED MALE | GHSR1a | FEMALE CATTLE | CROSS | 4 AGES | ASSOCIATION | Cattle - metabolism | Multifactorial Inheritance - genetics | Meat - analysis | Fatty Acids - analysis | Commerce | Male | 5' Untranslated Regions - genetics | Epistasis, Genetic - genetics | Meat - economics | Receptors, Ghrelin - genetics | Stearoyl-CoA Desaturase - genetics | Cattle - genetics | Receptors, Somatotropin - genetics | Adipose Tissue - metabolism | Growth Hormone - genetics | Animals | Alleles | Cell Cycle Proteins - genetics | Female | Lipid Metabolism - genetics | Somatotropin | Analysis | Genes | Genetic research | Physiological aspects | Beef cattle | Fatty acids | Genetic polymorphisms | Adipose tissues | Adipose tissue | Epistasis | Stearoyl-CoA desaturase | Desaturase | Condensin | Fatty acid composition | 5' Untranslated Regions | Cattle | Growth hormones | Growth hormone | Physical growth | Polymorphism
Journal Article
Patient Preference and Adherence, ISSN 1177-889X, 03/2014, Volume 8, pp. 361 - 370
Idiopathic pulmonary fibrosis (IPF) is a devastating chronic fibrotic lung disease. Although the precise cause of the disease is still unknown, recent studies...
Efficacy | Safety | Pirfenidone | Anti-fibrotic drugs | LUNG FIBROSIS | DIAGNOSIS | SUSCEPTIBILITY | N-ACETYLCYSTEINE | efficacy | FACTOR-ALPHA | AGENT | anti-fibrotic drugs | MEDICINE, GENERAL & INTERNAL | TUMOR-NECROSIS-FACTOR | pirfenidone | END-POINT | safety | VITAL CAPACITY | GENOME-WIDE ASSOCIATION | Drug therapy | Pulmonary fibrosis | Disease | Cytokines | Mortality | Clinical trials | Fibroblasts | Extracellular matrix | Tumor necrosis factor-TNF | Inflammation | Interferon | Growth factors
Efficacy | Safety | Pirfenidone | Anti-fibrotic drugs | LUNG FIBROSIS | DIAGNOSIS | SUSCEPTIBILITY | N-ACETYLCYSTEINE | efficacy | FACTOR-ALPHA | AGENT | anti-fibrotic drugs | MEDICINE, GENERAL & INTERNAL | TUMOR-NECROSIS-FACTOR | pirfenidone | END-POINT | safety | VITAL CAPACITY | GENOME-WIDE ASSOCIATION | Drug therapy | Pulmonary fibrosis | Disease | Cytokines | Mortality | Clinical trials | Fibroblasts | Extracellular matrix | Tumor necrosis factor-TNF | Inflammation | Interferon | Growth factors
Journal Article
Journal of Immunology, ISSN 0022-1767, 06/2018, Volume 200, Issue 11, pp. 3790 - 3800
Amino acid metabolism plays important roles in innate immune cells, including macrophages. Recently, we reported that a lysosomal adaptor protein, Lamtor1,...
DEFENSE | RECRUITMENT | MTORC1 | ACTIVATION | RAG GTPASES | BIOGENESIS | PATHWAY | INFLAMMATION | TFEB | IMMUNOLOGY | MACROPHAGE POLARIZATION | TOR protein | Translocation | Phosphorylation | Transcription factors | Immune response | Amino acids | Chemoreception | Rapamycin | Inflammation | Metabolism | Macrophages | Autophagy | Nuclear transport | Lipopolysaccharides | Proteins | Bleomycin | Acids | Protease inhibitors | Rodents | Mice | Alveoli | Lysosomal protein | Trachea | Immune system
DEFENSE | RECRUITMENT | MTORC1 | ACTIVATION | RAG GTPASES | BIOGENESIS | PATHWAY | INFLAMMATION | TFEB | IMMUNOLOGY | MACROPHAGE POLARIZATION | TOR protein | Translocation | Phosphorylation | Transcription factors | Immune response | Amino acids | Chemoreception | Rapamycin | Inflammation | Metabolism | Macrophages | Autophagy | Nuclear transport | Lipopolysaccharides | Proteins | Bleomycin | Acids | Protease inhibitors | Rodents | Mice | Alveoli | Lysosomal protein | Trachea | Immune system
Journal Article