2005, ISBN 0870137522, xiv, 377
Water quality concerns are not new to the Great Lakes. They emerged early in the 20th century, in 1909, and matured in 1972 and 1978. They remain a prominent...
Water | Pollution | Water quality management | Law and legislation | Qualité | Water quality | Gestion | Eau | Droit
Water | Pollution | Water quality management | Law and legislation | Qualité | Water quality | Gestion | Eau | Droit
Book
2016, Critical constructions : studies on education and society, ISBN 168123324X, xxxii, 319 pages
Book
1997, 26
Book
Nature, ISSN 0028-0836, 2012, Volume 491, Issue 7422, pp. 119 - 124
Crohn's disease and ulcerative colitis, the two common forms of inflammatory bowel disease (IBD), affect over 2.5 million people of European ancestry, with...
HYPER-IGE SYNDROME | RISK LOCI | NETWORK | NUMBER | METAANALYSIS | TUBERCULOSIS | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY | MUTATIONS | EXPRESSION | Crohn Disease - genetics | Humans | Inflammatory Bowel Diseases - immunology | Colitis, Ulcerative - genetics | Mycobacterium tuberculosis - immunology | Inflammatory Bowel Diseases - physiopathology | Colitis, Ulcerative - immunology | Host-Pathogen Interactions - immunology | Mycobacterium tuberculosis - pathogenicity | Haplotypes - genetics | Mycobacterium - pathogenicity | Mycobacterium Infections - genetics | Inflammatory Bowel Diseases - genetics | Crohn Disease - microbiology | Mycobacterium Infections - microbiology | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Reproducibility of Results | Mycobacterium - immunology | Crohn Disease - immunology | Genome, Human - genetics | Phenotype | Colitis, Ulcerative - microbiology | Host-Pathogen Interactions - genetics | Polymorphism, Single Nucleotide - genetics | Inflammatory Bowel Diseases - microbiology | Crohn Disease - physiopathology | Colitis, Ulcerative - physiopathology | Inflammatory bowel disease | Candidates | Tuberculosis | Architecture | Genetics | Genomes | Diabetes | Gene expression | Health risk assessment | Immune system | Rheumatology and Autoimmunity | Basic Medicine | Medical Genetics | Medicinsk genetik | Clinical Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Reumatologi och inflammation | Medicinska och farmaceutiska grundvetenskaper | Klinisk medicin
HYPER-IGE SYNDROME | RISK LOCI | NETWORK | NUMBER | METAANALYSIS | TUBERCULOSIS | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY | MUTATIONS | EXPRESSION | Crohn Disease - genetics | Humans | Inflammatory Bowel Diseases - immunology | Colitis, Ulcerative - genetics | Mycobacterium tuberculosis - immunology | Inflammatory Bowel Diseases - physiopathology | Colitis, Ulcerative - immunology | Host-Pathogen Interactions - immunology | Mycobacterium tuberculosis - pathogenicity | Haplotypes - genetics | Mycobacterium - pathogenicity | Mycobacterium Infections - genetics | Inflammatory Bowel Diseases - genetics | Crohn Disease - microbiology | Mycobacterium Infections - microbiology | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Reproducibility of Results | Mycobacterium - immunology | Crohn Disease - immunology | Genome, Human - genetics | Phenotype | Colitis, Ulcerative - microbiology | Host-Pathogen Interactions - genetics | Polymorphism, Single Nucleotide - genetics | Inflammatory Bowel Diseases - microbiology | Crohn Disease - physiopathology | Colitis, Ulcerative - physiopathology | Inflammatory bowel disease | Candidates | Tuberculosis | Architecture | Genetics | Genomes | Diabetes | Gene expression | Health risk assessment | Immune system | Rheumatology and Autoimmunity | Basic Medicine | Medical Genetics | Medicinsk genetik | Clinical Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Reumatologi och inflammation | Medicinska och farmaceutiska grundvetenskaper | Klinisk medicin
Journal Article
Public Administration, ISSN 0033-3298, 06/2009, Volume 87, Issue 2, pp. 430 - 431
Journal Article
Nature Genetics, ISSN 1061-4036, 06/2009, Volume 41, Issue 6, pp. 666 - 676
Elevated blood pressure is a common, heritable cause of cardiovascular disease worldwide. To date, identification of common genetic variants influencing blood...
LOW-RENIN HYPERTENSION | COMMON VARIANTS | POPULATION | PUBLIC-HEALTH | METHYLENETETRAHYDROFOLATE REDUCTASE GENE | RISK | POLYMORPHISM | MUTATIONS | CELL-DIFFERENTIATION | UMCG Approved | BARTTERS-SYNDROME | GENETICS & HEREDITY | Cardiovascular Diseases - physiopathology | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Blood Pressure - genetics | Europe | Humans | Diastole - genetics | Chromosome Mapping | Systole - genetics | DNA-Binding Proteins - genetics | Fibroblast Growth Factor 5 - genetics | Open Reading Frames - genetics | Cardiovascular Diseases - genetics | India | Genetic Variation | Proteins - genetics | Methylenetetrahydrofolate Reductase (NADPH2) - genetics | Cytochrome P-450 CYP1A2 - genetics | Phospholipase C delta - genetics | Steroid 17-alpha-Hydroxylase - genetics | Polymorphism, Single Nucleotide | Hypertension | Physiological aspects | Genetic aspects | Blood pressure | Research | Single nucleotide polymorphisms | Cardiovascular diseases | Risk factors | Studies | Data analysis | Genomics | Cardiovascular disease | Gene loci | Statistics | Meta-analysis | Medical and Health Sciences | MEDICINE | Medicin och hälsovetenskap | MEDICIN
LOW-RENIN HYPERTENSION | COMMON VARIANTS | POPULATION | PUBLIC-HEALTH | METHYLENETETRAHYDROFOLATE REDUCTASE GENE | RISK | POLYMORPHISM | MUTATIONS | CELL-DIFFERENTIATION | UMCG Approved | BARTTERS-SYNDROME | GENETICS & HEREDITY | Cardiovascular Diseases - physiopathology | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Blood Pressure - genetics | Europe | Humans | Diastole - genetics | Chromosome Mapping | Systole - genetics | DNA-Binding Proteins - genetics | Fibroblast Growth Factor 5 - genetics | Open Reading Frames - genetics | Cardiovascular Diseases - genetics | India | Genetic Variation | Proteins - genetics | Methylenetetrahydrofolate Reductase (NADPH2) - genetics | Cytochrome P-450 CYP1A2 - genetics | Phospholipase C delta - genetics | Steroid 17-alpha-Hydroxylase - genetics | Polymorphism, Single Nucleotide | Hypertension | Physiological aspects | Genetic aspects | Blood pressure | Research | Single nucleotide polymorphisms | Cardiovascular diseases | Risk factors | Studies | Data analysis | Genomics | Cardiovascular disease | Gene loci | Statistics | Meta-analysis | Medical and Health Sciences | MEDICINE | Medicin och hälsovetenskap | MEDICIN
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Chest, ISSN 0012-3692, 09/2015, Volume 148, Issue 3, pp. 746 - 751
BACKGROUND: Indwelling pleural catheters (IPCs) are an effective option in the management of malignant pleural effusion. Up to 14% of patients with IPCs...
COMPLICATED PARAPNEUMONIC EFFUSIONS | CONTROLLED-TRIAL | STREPTOKINASE | MANAGEMENT | EFFICACY | PLEURODESIS | ALTEPLASE | RESPIRATORY SYSTEM | INSTILLATION | INFECTION | UROKINASE | CRITICAL CARE MEDICINE | Urokinase-Type Plasminogen Activator - therapeutic use | Humans | Middle Aged | Male | Treatment Outcome | Tissue Plasminogen Activator - therapeutic use | Streptokinase - therapeutic use | Pleural Effusion, Malignant - therapy | Fibrinolytic Agents - therapeutic use | Catheters, Indwelling - adverse effects | Thrombolytic Therapy - methods | Female | Aged | Retrospective Studies | Symptomatology | Usage | Analysis | Fibrinolysis | Hemorrhage | Catheters | Risk factors
COMPLICATED PARAPNEUMONIC EFFUSIONS | CONTROLLED-TRIAL | STREPTOKINASE | MANAGEMENT | EFFICACY | PLEURODESIS | ALTEPLASE | RESPIRATORY SYSTEM | INSTILLATION | INFECTION | UROKINASE | CRITICAL CARE MEDICINE | Urokinase-Type Plasminogen Activator - therapeutic use | Humans | Middle Aged | Male | Treatment Outcome | Tissue Plasminogen Activator - therapeutic use | Streptokinase - therapeutic use | Pleural Effusion, Malignant - therapy | Fibrinolytic Agents - therapeutic use | Catheters, Indwelling - adverse effects | Thrombolytic Therapy - methods | Female | Aged | Retrospective Studies | Symptomatology | Usage | Analysis | Fibrinolysis | Hemorrhage | Catheters | Risk factors
Journal Article
9.
Full Text
A powerful approach to the study of moderate effect modification in observational studies
Biometrics, ISSN 0006-341X, 12/2018, Volume 74, Issue 4, pp. 1161 - 1170
Summary Effect modification means the magnitude or stability of a treatment effect varies as a function of an observed covariate. Generally, larger and more...
Causal inference | Observational study | Sensitivity analysis | Design sensitivity | Effect modification | Testing twice | Epidemiology | Causal effects | CONFIDENCE-INTERVALS | STATISTICS & PROBABILITY | SENSITIVITY-ANALYSIS | BIOLOGY | MATHEMATICAL & COMPUTATIONAL BIOLOGY | Analysis | Exercise
Causal inference | Observational study | Sensitivity analysis | Design sensitivity | Effect modification | Testing twice | Epidemiology | Causal effects | CONFIDENCE-INTERVALS | STATISTICS & PROBABILITY | SENSITIVITY-ANALYSIS | BIOLOGY | MATHEMATICAL & COMPUTATIONAL BIOLOGY | Analysis | Exercise
Journal Article
10.
Full Text
The Major Genetic Determinants of HIV-1 Control Affect HLA Class I Peptide Presentation
Science, ISSN 0036-8075, 12/2010, Volume 330, Issue 6010, pp. 1551 - 1557
Infectious and inflammatory diseases have repeatedly shown strong genetic associations within the major histocompatibility complex (MHC); however, the basis...
HLA antigens | Haplotypes | HIV | REPORTS | Alleles | HLA B antigens | Amino acids | AIDS | HLA C antigens | Research universities | Medical schools | ALLELES | THERAPY | MULTIDISCIPLINARY SCIENCES | SURFACE EXPRESSION | MHC | INFECTION | ABSENCE | RESTRICTION | ASSOCIATION | DISEASE PROGRESSION | Humans | Amino Acids - physiology | HLA-C Antigens - chemistry | HIV Long-Term Survivors | Viral Load | HLA-A Antigens - metabolism | HIV Infections - immunology | Antigen Presentation | HLA-C Antigens - immunology | HLA-B Antigens - genetics | HLA-B Antigens - chemistry | HLA-C Antigens - metabolism | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Hispanic Americans - genetics | HIV Infections - genetics | HIV Infections - virology | HLA-B Antigens - immunology | African Americans - genetics | Models, Molecular | Logistic Models | Immunity, Innate | Disease Progression | HLA-B Antigens - metabolism | HIV-1 - immunology | HLA-A Antigens - immunology | HIV Antigens - immunology | HLA-A Antigens - genetics | Protein Conformation | Genes, MHC Class I | Polymorphism, Single Nucleotide | HLA-A Antigens - chemistry | HLA-C Antigens - genetics | CD8-Positive T-Lymphocytes - immunology | HIV Infections - ethnology | Cohort Studies
HLA antigens | Haplotypes | HIV | REPORTS | Alleles | HLA B antigens | Amino acids | AIDS | HLA C antigens | Research universities | Medical schools | ALLELES | THERAPY | MULTIDISCIPLINARY SCIENCES | SURFACE EXPRESSION | MHC | INFECTION | ABSENCE | RESTRICTION | ASSOCIATION | DISEASE PROGRESSION | Humans | Amino Acids - physiology | HLA-C Antigens - chemistry | HIV Long-Term Survivors | Viral Load | HLA-A Antigens - metabolism | HIV Infections - immunology | Antigen Presentation | HLA-C Antigens - immunology | HLA-B Antigens - genetics | HLA-B Antigens - chemistry | HLA-C Antigens - metabolism | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Hispanic Americans - genetics | HIV Infections - genetics | HIV Infections - virology | HLA-B Antigens - immunology | African Americans - genetics | Models, Molecular | Logistic Models | Immunity, Innate | Disease Progression | HLA-B Antigens - metabolism | HIV-1 - immunology | HLA-A Antigens - immunology | HIV Antigens - immunology | HLA-A Antigens - genetics | Protein Conformation | Genes, MHC Class I | Polymorphism, Single Nucleotide | HLA-A Antigens - chemistry | HLA-C Antigens - genetics | CD8-Positive T-Lymphocytes - immunology | HIV Infections - ethnology | Cohort Studies
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