Sustainability (Switzerland), ISSN 2071-1050, 06/2018, Volume 10, Issue 6, p. 1979
The demand for urban construction has placed growing pressure on biodiversity conservation. In China, landscape fragmentation caused by rapid urbanization has...
Green space | Morphological spatial pattern analysis | Least-cost path | Focal species | Landscape connectivity | HABITAT PATCHES | GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY | landscape connectivity | green space | least-cost path | focal species | FRAGMENTATION | IDENTIFICATION | SPATIAL-PATTERN | NETWORK ANALYSIS | ENVIRONMENTAL SCIENCES | METHODOLOGY | AREA | morphological spatial pattern analysis | SEGMENTATION | ECOLOGY | SCALE | ENVIRONMENTAL STUDIES | Landscape | Wildlife conservation | Computer simulation | Habitats | Spatial discrimination | Spatial analysis | Biodiversity | Optimization | Case studies | Ecological effects | Urbanization | Corridors | Connectivity | Ecological monitoring | Modelling | Cost analysis | Species | Pattern analysis
Green space | Morphological spatial pattern analysis | Least-cost path | Focal species | Landscape connectivity | HABITAT PATCHES | GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY | landscape connectivity | green space | least-cost path | focal species | FRAGMENTATION | IDENTIFICATION | SPATIAL-PATTERN | NETWORK ANALYSIS | ENVIRONMENTAL SCIENCES | METHODOLOGY | AREA | morphological spatial pattern analysis | SEGMENTATION | ECOLOGY | SCALE | ENVIRONMENTAL STUDIES | Landscape | Wildlife conservation | Computer simulation | Habitats | Spatial discrimination | Spatial analysis | Biodiversity | Optimization | Case studies | Ecological effects | Urbanization | Corridors | Connectivity | Ecological monitoring | Modelling | Cost analysis | Species | Pattern analysis
Journal Article
Nature Medicine, ISSN 1078-8956, 04/2015, Volume 21, Issue 4, pp. 401 - 408
Detection of cyclic-di-adenosine monophosphate (c-di-AMP), a bacterial second messenger, by the host cytoplasmic surveillance pathway (CSP) is known to elicit...
MYCOBACTERIUM-TUBERCULOSIS | MEDICINE, RESEARCH & EXPERIMENTAL | IMMUNE-RESPONSE | I INTERFERON RESPONSE | MACROPHAGES | BIOCHEMISTRY & MOLECULAR BIOLOGY | AUTOPHAGY | GMP | C-DI-AMP | CELL BIOLOGY | HOST-CELL | DNA | INFECTION | Cytokines - metabolism | Signal Transduction | Mice, Inbred C57BL | Virulence | Interferon-gamma - metabolism | Dinucleoside Phosphates - metabolism | Autophagy | Genetic Complementation Test | Macrophages - metabolism | Animals | Interferon-beta - metabolism | Mycobacterium tuberculosis | Tuberculosis - prevention & control | Bacterial Proteins - metabolism | Cytosol - metabolism | Female | Mice | Mice, Inbred BALB C | Nucleotidyltransferases - metabolism | Phosphorus-Oxygen Lyases - metabolism | Tuberculosis - metabolism | Medicine, Experimental | Medical research | Care and treatment | Tuberculosis | Research | Immunotherapy | Signal transduction | Gene expression | Molecular biology | Immune system
MYCOBACTERIUM-TUBERCULOSIS | MEDICINE, RESEARCH & EXPERIMENTAL | IMMUNE-RESPONSE | I INTERFERON RESPONSE | MACROPHAGES | BIOCHEMISTRY & MOLECULAR BIOLOGY | AUTOPHAGY | GMP | C-DI-AMP | CELL BIOLOGY | HOST-CELL | DNA | INFECTION | Cytokines - metabolism | Signal Transduction | Mice, Inbred C57BL | Virulence | Interferon-gamma - metabolism | Dinucleoside Phosphates - metabolism | Autophagy | Genetic Complementation Test | Macrophages - metabolism | Animals | Interferon-beta - metabolism | Mycobacterium tuberculosis | Tuberculosis - prevention & control | Bacterial Proteins - metabolism | Cytosol - metabolism | Female | Mice | Mice, Inbred BALB C | Nucleotidyltransferases - metabolism | Phosphorus-Oxygen Lyases - metabolism | Tuberculosis - metabolism | Medicine, Experimental | Medical research | Care and treatment | Tuberculosis | Research | Immunotherapy | Signal transduction | Gene expression | Molecular biology | Immune system
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 05/2018, Volume 378, Issue 21, pp. 1976 - 1986
In a pilot study, two doses of neoadjuvant nivolumab administered to patients with resectable lung cancer resulted in a major pathological response in 45% and...
MISMATCH-REPAIR DEFICIENCY | TRIAL | MEDICINE, GENERAL & INTERNAL | MULTICENTER | PEMBROLIZUMAB | RESPONSE CRITERIA | SOLID TUMORS | IMMUNE CHECKPOINT BLOCKADE | IMMUNOTHERAPY | OPEN-LABEL | CHEMOTHERAPY | Lung Neoplasms - drug therapy | Adenocarcinoma - pathology | Carcinoma, Squamous Cell - pathology | Humans | Middle Aged | Antibodies, Monoclonal - adverse effects | Antibodies, Monoclonal - therapeutic use | Lung Neoplasms - pathology | Male | Antineoplastic Agents - therapeutic use | Antineoplastic Agents - adverse effects | Aged, 80 and over | Female | Neoadjuvant Therapy | Carcinoma, Non-Small-Cell Lung - pathology | Lung Neoplasms - genetics | Carcinoma, Non-Small-Cell Lung - surgery | Carcinoma, Non-Small-Cell Lung - genetics | Pilot Projects | B7-H1 Antigen - antagonists & inhibitors | Biopsy | Nivolumab | Lung Neoplasms - surgery | Aged | Carcinoma, Non-Small-Cell Lung - drug therapy | Mutation | Drug therapy | Lung cancer | Peptides | PD-1 protein | Body weight | Lymphocytes T | Cancer therapies | Lymphocytes | Immunotherapy | Surgery | Peripheral blood | Drug dosages | Antigens | Lymphatic system | Cell survival | Cloning | Feasibility studies | Non-small cell lung carcinoma | T cell receptors | Gene expression | Patients | Side effects | Chemotherapy | PD-L1 protein | Tumors | Apoptosis
MISMATCH-REPAIR DEFICIENCY | TRIAL | MEDICINE, GENERAL & INTERNAL | MULTICENTER | PEMBROLIZUMAB | RESPONSE CRITERIA | SOLID TUMORS | IMMUNE CHECKPOINT BLOCKADE | IMMUNOTHERAPY | OPEN-LABEL | CHEMOTHERAPY | Lung Neoplasms - drug therapy | Adenocarcinoma - pathology | Carcinoma, Squamous Cell - pathology | Humans | Middle Aged | Antibodies, Monoclonal - adverse effects | Antibodies, Monoclonal - therapeutic use | Lung Neoplasms - pathology | Male | Antineoplastic Agents - therapeutic use | Antineoplastic Agents - adverse effects | Aged, 80 and over | Female | Neoadjuvant Therapy | Carcinoma, Non-Small-Cell Lung - pathology | Lung Neoplasms - genetics | Carcinoma, Non-Small-Cell Lung - surgery | Carcinoma, Non-Small-Cell Lung - genetics | Pilot Projects | B7-H1 Antigen - antagonists & inhibitors | Biopsy | Nivolumab | Lung Neoplasms - surgery | Aged | Carcinoma, Non-Small-Cell Lung - drug therapy | Mutation | Drug therapy | Lung cancer | Peptides | PD-1 protein | Body weight | Lymphocytes T | Cancer therapies | Lymphocytes | Immunotherapy | Surgery | Peripheral blood | Drug dosages | Antigens | Lymphatic system | Cell survival | Cloning | Feasibility studies | Non-small cell lung carcinoma | T cell receptors | Gene expression | Patients | Side effects | Chemotherapy | PD-L1 protein | Tumors | Apoptosis
Journal Article
Rapid Communications in Mass Spectrometry, ISSN 0951-4198, 08/2017, Volume 31, Issue 16, pp. 1353 - 1362
Rationale Fast digestion methods can dramatically accelerate enzyme digestion and increase the throughput of proteomic analysis. However, the peptide...
PROTEOLYTIC DIGESTION | CHEMISTRY, ANALYTICAL | SPECTROSCOPY | TRYPSIN DIGESTION | BIOCHEMICAL RESEARCH METHODS | ACID-HYDROLYSIS | MS/MS | EFFICIENCY | MASS-SPECTROMETRY | PROTEIN IDENTIFICATION | REVEALS | Enzymes | Peptides | Proteolysis | Analysis | Proteins | Trypsin | Reproducibility | Proteomics | Cleavage | Abundance | Digestion | Methods | Quantitative analysis
PROTEOLYTIC DIGESTION | CHEMISTRY, ANALYTICAL | SPECTROSCOPY | TRYPSIN DIGESTION | BIOCHEMICAL RESEARCH METHODS | ACID-HYDROLYSIS | MS/MS | EFFICIENCY | MASS-SPECTROMETRY | PROTEIN IDENTIFICATION | REVEALS | Enzymes | Peptides | Proteolysis | Analysis | Proteins | Trypsin | Reproducibility | Proteomics | Cleavage | Abundance | Digestion | Methods | Quantitative analysis
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2014, Volume 9, Issue 5, p. e97048
Mycobacterium tuberculosis is an important human pathogen, and yet diagnosis remains challenging. Little research has focused on the impact of M. tuberculosis...
IMMUNE-SYSTEM | DISEASES | INTESTINAL MICROBIOTA | MULTIDISCIPLINARY SCIENCES | Microbiota | Animals | Sequence Analysis, RNA | Mycobacterium tuberculosis - physiology | Aerosols | Gastrointestinal Tract - microbiology | RNA, Ribosomal, 16S - genetics | Female | Mice | Biodiversity | Tuberculosis | Microbiota (Symbiotic organisms) | RNA | Analysis | Gastrointestinal system | Health aspects | Biological diversity | rRNA 16S | Digestive system | Infections | Gastrointestinal tract | Genomes | Patients | Asthma | Medicine | Ecological effects | Microorganisms | Immunology | Antibiotics | Lungs | Phylogenetics | Bacteria | Ecological monitoring | Feces | Digestive tract | Immune system
IMMUNE-SYSTEM | DISEASES | INTESTINAL MICROBIOTA | MULTIDISCIPLINARY SCIENCES | Microbiota | Animals | Sequence Analysis, RNA | Mycobacterium tuberculosis - physiology | Aerosols | Gastrointestinal Tract - microbiology | RNA, Ribosomal, 16S - genetics | Female | Mice | Biodiversity | Tuberculosis | Microbiota (Symbiotic organisms) | RNA | Analysis | Gastrointestinal system | Health aspects | Biological diversity | rRNA 16S | Digestive system | Infections | Gastrointestinal tract | Genomes | Patients | Asthma | Medicine | Ecological effects | Microorganisms | Immunology | Antibiotics | Lungs | Phylogenetics | Bacteria | Ecological monitoring | Feces | Digestive tract | Immune system
Journal Article
Nature Communications, ISSN 2041-1723, 12/2013, Volume 4, Issue 1, pp. 2907 - 2907
Responsible for nearly two million deaths each year, the infectious disease tuberculosis remains a serious global health challenge. The emergence of...
SYSTEM | DESIGN | MECHANISM | MEMBRANE | MMPL3 | MULTIDISCIPLINARY SCIENCES | SQ109 | DERIVATIVES | DISCOVERY | Antitubercular Agents - chemistry | Antitubercular Agents - pharmacology | Bacterial Proteins - genetics | Cercopithecus aethiops | Molecular Targeted Therapy | Mycobacterium tuberculosis - drug effects | Dose-Response Relationship, Drug | Animals | Antitubercular Agents - pharmacokinetics | Tuberculosis, Multidrug-Resistant - microbiology | Vero Cells - drug effects | Drug Design | Female | Mice | Mice, Inbred BALB C | Polymorphism, Single Nucleotide | Mutation | Drug Resistance, Multiple, Bacterial - genetics | Vero Cells - microbiology | Drug Resistance, Multiple, Bacterial - drug effects | Indoles - chemistry | Anion Transport Proteins - genetics
SYSTEM | DESIGN | MECHANISM | MEMBRANE | MMPL3 | MULTIDISCIPLINARY SCIENCES | SQ109 | DERIVATIVES | DISCOVERY | Antitubercular Agents - chemistry | Antitubercular Agents - pharmacology | Bacterial Proteins - genetics | Cercopithecus aethiops | Molecular Targeted Therapy | Mycobacterium tuberculosis - drug effects | Dose-Response Relationship, Drug | Animals | Antitubercular Agents - pharmacokinetics | Tuberculosis, Multidrug-Resistant - microbiology | Vero Cells - drug effects | Drug Design | Female | Mice | Mice, Inbred BALB C | Polymorphism, Single Nucleotide | Mutation | Drug Resistance, Multiple, Bacterial - genetics | Vero Cells - microbiology | Drug Resistance, Multiple, Bacterial - drug effects | Indoles - chemistry | Anion Transport Proteins - genetics
Journal Article
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Full Text
Inhibition of innate immune cytosolic surveillance by an M. tuberculosis phosphodiesterase
NATURE CHEMICAL BIOLOGY, ISSN 1552-4450, 02/2017, Volume 13, Issue 2, pp. 210 - 217
Mycobacterium tuberculosis infection leads to cytosolic release of the bacterial cyclic dinucleotide (CDN) c-di-AMP and a host-generated CDN, cGAMP, both of...
MYCOBACTERIUM-TUBERCULOSIS | SYNTHASE | 2ND-MESSENGER | DNA SENSOR | IFN-BETA | CYCLIC GMP-AMP | PROTEIN | PATHWAY | BIOCHEMISTRY & MOLECULAR BIOLOGY | CGAS | C-DI-AMP | Cytosol - microbiology | 2',3'-Cyclic-Nucleotide Phosphodiesterases - metabolism | Immunity, Innate | Cytosol - immunology | Mycobacterium tuberculosis - enzymology | Signal transduction | Enzymes | Bacteria | Tuberculosis
MYCOBACTERIUM-TUBERCULOSIS | SYNTHASE | 2ND-MESSENGER | DNA SENSOR | IFN-BETA | CYCLIC GMP-AMP | PROTEIN | PATHWAY | BIOCHEMISTRY & MOLECULAR BIOLOGY | CGAS | C-DI-AMP | Cytosol - microbiology | 2',3'-Cyclic-Nucleotide Phosphodiesterases - metabolism | Immunity, Innate | Cytosol - immunology | Mycobacterium tuberculosis - enzymology | Signal transduction | Enzymes | Bacteria | Tuberculosis
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 1 - 1
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Journal Article
Analytical and Bioanalytical Chemistry, ISSN 1618-2642, 4/2019, Volume 411, Issue 11, pp. 2273 - 2282
Coronary artery disease (CAD) is a manifestation of systemic atherosclerotic disease. It is assessed by intervention or traditional scoring risk factors....
Biochemistry, general | Urine | Chemistry | Analytical Chemistry | Food Science | Monitoring/Environmental Analysis | Atherosclerosis | Proteomics | iTRAQ | Characterization and Evaluation of Materials | MRM | Laboratory Medicine | DIGESTION | CHEMISTRY, ANALYTICAL | BIOCHEMICAL RESEARCH METHODS | APOLIPOPROTEIN D | IDENTIFICATION | DISCOVERY | Reactive oxygen species | Liver X receptors | Liver | Coronary artery | Data processing | Cardiovascular disease | Functional analysis | Risk analysis | Retinoid X receptors | Coronary artery disease | Risk factors | Proteins | Apolipoprotein E | Nitric oxide | Arteriosclerosis | Diagnostic software | Diagnostic systems | Cardiovascular diseases | Heart diseases
Biochemistry, general | Urine | Chemistry | Analytical Chemistry | Food Science | Monitoring/Environmental Analysis | Atherosclerosis | Proteomics | iTRAQ | Characterization and Evaluation of Materials | MRM | Laboratory Medicine | DIGESTION | CHEMISTRY, ANALYTICAL | BIOCHEMICAL RESEARCH METHODS | APOLIPOPROTEIN D | IDENTIFICATION | DISCOVERY | Reactive oxygen species | Liver X receptors | Liver | Coronary artery | Data processing | Cardiovascular disease | Functional analysis | Risk analysis | Retinoid X receptors | Coronary artery disease | Risk factors | Proteins | Apolipoprotein E | Nitric oxide | Arteriosclerosis | Diagnostic software | Diagnostic systems | Cardiovascular diseases | Heart diseases
Journal Article
BMC Genomics, ISSN 1471-2164, 02/2019, Volume 20, Issue 1, pp. 134 - 134
Background: The amount of RNA per cell, namely the transcriptome size, may vary under many biological conditions including tumor. If the transcriptome size of...
Relative expression ordering | Differentially expressed gene | Absolute mRNA abundances | Cellular mRNA concentration | COPY NUMBER ALTERATIONS | DIFFERENTIAL EXPRESSION | SIGNATURES | DRIVERS | ENABLES | CANCER | FALSE DISCOVERY RATE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | NORMALIZATION | MICROARRAYS | Research | Genetic transcription | Gene expression | Carcinogenesis | Cancer cells | Computer simulation | Identification methods | Tumor cells | Genes | Genomics | Lung cancer | DNA damage | Data processing | Identification | Genomes | Metabolism | Experiments | Carcinogens | Algorithms | Pathways | Ribonucleic acids | DNA methylation | Cell size | Bioinformatics | Deoxyribonucleic acid--DNA | Cancer | Tumors
Relative expression ordering | Differentially expressed gene | Absolute mRNA abundances | Cellular mRNA concentration | COPY NUMBER ALTERATIONS | DIFFERENTIAL EXPRESSION | SIGNATURES | DRIVERS | ENABLES | CANCER | FALSE DISCOVERY RATE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | NORMALIZATION | MICROARRAYS | Research | Genetic transcription | Gene expression | Carcinogenesis | Cancer cells | Computer simulation | Identification methods | Tumor cells | Genes | Genomics | Lung cancer | DNA damage | Data processing | Identification | Genomes | Metabolism | Experiments | Carcinogens | Algorithms | Pathways | Ribonucleic acids | DNA methylation | Cell size | Bioinformatics | Deoxyribonucleic acid--DNA | Cancer | Tumors
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Cancer Science, ISSN 1347-9032, 11/2019
Journal Article
Journal of Chromatography B, ISSN 1570-0232, 06/2019, Volume 1118-1119, pp. 55 - 62
In this study, a coordination imprinted polymer (CIP) solid-phase extraction (SPE) method was developed to determine the residues of flumequine (FLU) in fish...
Flumequine | Graphene oxide | Coordination imprinted polymer | High-performance liquid chromatography | Zinc compounds | Adsorption | Graphene | Analysis | Influenza | Graphite | Detectors | Polymer industry | Polymers | High performance liquid chromatography
Flumequine | Graphene oxide | Coordination imprinted polymer | High-performance liquid chromatography | Zinc compounds | Adsorption | Graphene | Analysis | Influenza | Graphite | Detectors | Polymer industry | Polymers | High performance liquid chromatography
Journal Article
BMC Genomics, ISSN 1471-2164, 01/2018, Volume 19, Issue 1, pp. 99 - 11
Background: Due to experimental batch effects, the application of a quantitative transcriptional signature for disease diagnoses commonly requires inter-sample...
Classifiers | Platform | Relative expression orderings | Batch effects | Diagnostic signature | EXPRESSION ANALYSIS | REJECTION SURVEILLANCE | ULCERATIVE-COLITIS | COLONOSCOPIC SURVEILLANCE | CELL LUNG-CANCER | BREAST-CANCER | PROGNOSTIC SIGNATURE | INFLAMMATORY-BOWEL-DISEASE | FINE-NEEDLE-ASPIRATION | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | TREATMENT DECISIONS | GENETICS & HEREDITY | Colorectal cancer | Physiological aspects | Genetic aspects | Diagnosis | Research | Genetic transcription | Cancer | Case studies | Gastrointestinal diseases | Genes | Quality control | Genetic research
Classifiers | Platform | Relative expression orderings | Batch effects | Diagnostic signature | EXPRESSION ANALYSIS | REJECTION SURVEILLANCE | ULCERATIVE-COLITIS | COLONOSCOPIC SURVEILLANCE | CELL LUNG-CANCER | BREAST-CANCER | PROGNOSTIC SIGNATURE | INFLAMMATORY-BOWEL-DISEASE | FINE-NEEDLE-ASPIRATION | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | TREATMENT DECISIONS | GENETICS & HEREDITY | Colorectal cancer | Physiological aspects | Genetic aspects | Diagnosis | Research | Genetic transcription | Cancer | Case studies | Gastrointestinal diseases | Genes | Quality control | Genetic research
Journal Article
BMC Cancer, ISSN 1471-2407, 12/2019, Volume 19, Issue 1
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 2605 - 9
Pregnancy is associated with the onset of many adaptation processes that are likely to change over the course of gestation. Understanding normal metabolites'...
MATERNAL BMI | WOMEN | PROFILES | ASSOCIATIONS | TYROSINE | INSULIN-RESISTANCE | GLUCOSE | MULTIDISCIPLINARY SCIENCES | LONGITUDINAL METABOLOMICS | Tyrosine | Urine | Metabolomics | Diabetes mellitus | Fetuses | Pregnancy complications | Liquid chromatography | Gestation | Metabolites | Biomarkers | Nutrients | Diabetes | Variation | Health risk assessment | Miscarriage | Gravity
MATERNAL BMI | WOMEN | PROFILES | ASSOCIATIONS | TYROSINE | INSULIN-RESISTANCE | GLUCOSE | MULTIDISCIPLINARY SCIENCES | LONGITUDINAL METABOLOMICS | Tyrosine | Urine | Metabolomics | Diabetes mellitus | Fetuses | Pregnancy complications | Liquid chromatography | Gestation | Metabolites | Biomarkers | Nutrients | Diabetes | Variation | Health risk assessment | Miscarriage | Gravity
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