BMC Public Health, ISSN 1471-2458, 2011, Volume 11, Issue 1, pp. 7 - 7
Background: International data on child maltreatment are largely derived from child protection agencies, and predominantly report only substantiated cases of...
VIOLENCE | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | Child Abuse - statistics & numerical data | International Classification of Diseases | Child Abuse, Sexual - statistics & numerical data | Humans | Child, Preschool | Hospitalization - statistics & numerical data | Child Abuse - classification | Male | Data Collection - methods | Australia - epidemiology | Child Welfare | Adolescent | Female | Child | Population Surveillance - methods | Child sexual abuse | Demographic aspects | Laws, regulations and rules | Medical records | Public health administration | Research | Management
VIOLENCE | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | Child Abuse - statistics & numerical data | International Classification of Diseases | Child Abuse, Sexual - statistics & numerical data | Humans | Child, Preschool | Hospitalization - statistics & numerical data | Child Abuse - classification | Male | Data Collection - methods | Australia - epidemiology | Child Welfare | Adolescent | Female | Child | Population Surveillance - methods | Child sexual abuse | Demographic aspects | Laws, regulations and rules | Medical records | Public health administration | Research | Management
Journal Article
BMC Public Health, ISSN 1471-2458, 2012, Volume 12, Issue 1, pp. 563 - 563
Background: While child maltreatment is recognised as a global problem, solid epidemiological data on the prevalence of child maltreatment and risk factors...
Injury surveillance | Morbidity data | Clinical documentation | Child maltreatment | Data linkage | CHILD-ABUSE | PRESCHOOL-CHILDREN | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | EMERGENCY-DEPARTMENT | ACCIDENT | FRACTURES | Humans | Risk Factors | Medical Records | Wounds and Injuries - etiology | Child, Preschool | Documentation - statistics & numerical data | Infant | Male | Hospitalization | Child Abuse | Wounds and Injuries - therapy | Adolescent | Female | Retrospective Studies | Child | Queensland | Medical research | Child abuse | Hospital care | Medicine, Experimental | Medical records | Alcohol and youth | Evidence (Law) | Children | Epidemiology | Risk factors | Injuries | Studies | Child abuse & neglect | Hospitals
Injury surveillance | Morbidity data | Clinical documentation | Child maltreatment | Data linkage | CHILD-ABUSE | PRESCHOOL-CHILDREN | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | EMERGENCY-DEPARTMENT | ACCIDENT | FRACTURES | Humans | Risk Factors | Medical Records | Wounds and Injuries - etiology | Child, Preschool | Documentation - statistics & numerical data | Infant | Male | Hospitalization | Child Abuse | Wounds and Injuries - therapy | Adolescent | Female | Retrospective Studies | Child | Queensland | Medical research | Child abuse | Hospital care | Medicine, Experimental | Medical records | Alcohol and youth | Evidence (Law) | Children | Epidemiology | Risk factors | Injuries | Studies | Child abuse & neglect | Hospitals
Journal Article
Aging Cell, ISSN 1474-9718, 12/2015, Volume 14, Issue 6, pp. 1085 - 1093
Summary Sarcopenia, the age‐induced loss of skeletal muscle mass and function, results from the contributions of both fiber atrophy and loss of myofibers. We...
cell death | necrosis | mitochondria | apoptosis | aging | skeletal muscle | ETS abnormalities | sarcopenia | Sarcopenia | Mitochondria | Cell death | Aging | Skeletal muscle | Apoptosis | Necrosis | SYSTEM | RHESUS-MONKEYS | ATROPHY | DNA-DELETION MUTATIONS | CELL-DEATH | CELL BIOLOGY | GERIATRICS & GERONTOLOGY | MASS | Biomarkers - metabolism | Mitochondria - enzymology | Rats, Inbred F344 | Rats | Male | Necrosis - pathology | Quadriceps Muscle - physiopathology | Animals | DNA, Mitochondrial - genetics | Aging - physiology | Sarcopenia - pathology | Muscle Fibers, Skeletal - pathology | Apoptosis - physiology | Electron Transport - physiology | Sequence Deletion - genetics | Muscles | Enzymes | Mitochondrial DNA | Musculoskeletal system | Gangrene | Mutation | Age | Original
cell death | necrosis | mitochondria | apoptosis | aging | skeletal muscle | ETS abnormalities | sarcopenia | Sarcopenia | Mitochondria | Cell death | Aging | Skeletal muscle | Apoptosis | Necrosis | SYSTEM | RHESUS-MONKEYS | ATROPHY | DNA-DELETION MUTATIONS | CELL-DEATH | CELL BIOLOGY | GERIATRICS & GERONTOLOGY | MASS | Biomarkers - metabolism | Mitochondria - enzymology | Rats, Inbred F344 | Rats | Male | Necrosis - pathology | Quadriceps Muscle - physiopathology | Animals | DNA, Mitochondrial - genetics | Aging - physiology | Sarcopenia - pathology | Muscle Fibers, Skeletal - pathology | Apoptosis - physiology | Electron Transport - physiology | Sequence Deletion - genetics | Muscles | Enzymes | Mitochondrial DNA | Musculoskeletal system | Gangrene | Mutation | Age | Original
Journal Article
BMC Public Health, ISSN 1471-2458, 2011, Volume 11, Issue 1, pp. 8 - 8
Background: Internationally, research on child maltreatment-related injuries has been hampered by a lack of available routinely collected health data to...
ABUSE | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | International Classification of Diseases | Reproducibility of Results | Data Collection - standards | Humans | Child, Preschool | Child Abuse - classification | Infant | Male | Hospitals | Adolescent | Sex Distribution | Female | Retrospective Studies | Child | Population Surveillance | Child Abuse - diagnosis | Queensland | Medical records | Child abuse | Research | Information management | Reporting | Quality management | Child abuse & neglect | Codes | Data collection | Injuries | Children & youth
ABUSE | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | International Classification of Diseases | Reproducibility of Results | Data Collection - standards | Humans | Child, Preschool | Child Abuse - classification | Infant | Male | Hospitals | Adolescent | Sex Distribution | Female | Retrospective Studies | Child | Population Surveillance | Child Abuse - diagnosis | Queensland | Medical records | Child abuse | Research | Information management | Reporting | Quality management | Child abuse & neglect | Codes | Data collection | Injuries | Children & youth
Journal Article
Nature, ISSN 0028-0836, 02/2010, Volume 463, Issue 7282, pp. 763 - 768
Three subfamilies of grasses, the Ehrhartoideae, Panicoideae and Pooideae, provide the bulk of human nutrition and are poised to become major sources of...
TRITICEAE | EVOLUTION | INTRASPECIES DIVERSITY | MULTIDISCIPLINARY SCIENCES | DYNAMICS | DIVERGENCE | AGROBACTERIUM-MEDIATED TRANSFORMATION | WHEAT | IDENTIFICATION | MAP | RICE | Synteny - genetics | Genome, Plant - genetics | Genomics | Molecular Sequence Data | Poaceae - genetics | RNA, Plant - analysis | RNA, Plant - genetics | Sequence Analysis, DNA | Poaceae - classification | Gene Fusion - genetics | Oryza - genetics | Genes, Plant - genetics | DNA Transposable Elements - genetics | Crops, Agricultural - genetics | Sorghum - genetics | Transcription, Genetic - genetics | Chromosomes, Plant - genetics | Evolution, Molecular | Analysis | Wetland flora | Genomes | Genetic aspects | Research | Grasses | Chromosomes | Genetics | Artificial chromosomes | Data bases | Rice | Life Sciences | Cellular Biology
TRITICEAE | EVOLUTION | INTRASPECIES DIVERSITY | MULTIDISCIPLINARY SCIENCES | DYNAMICS | DIVERGENCE | AGROBACTERIUM-MEDIATED TRANSFORMATION | WHEAT | IDENTIFICATION | MAP | RICE | Synteny - genetics | Genome, Plant - genetics | Genomics | Molecular Sequence Data | Poaceae - genetics | RNA, Plant - analysis | RNA, Plant - genetics | Sequence Analysis, DNA | Poaceae - classification | Gene Fusion - genetics | Oryza - genetics | Genes, Plant - genetics | DNA Transposable Elements - genetics | Crops, Agricultural - genetics | Sorghum - genetics | Transcription, Genetic - genetics | Chromosomes, Plant - genetics | Evolution, Molecular | Analysis | Wetland flora | Genomes | Genetic aspects | Research | Grasses | Chromosomes | Genetics | Artificial chromosomes | Data bases | Rice | Life Sciences | Cellular Biology
Journal Article
PLoS pathogens, ISSN 1553-7366, 11/2018, Volume 14, Issue 11, p. e1007414
Chronic wasting disease (CWD), an environmentally transmissible, fatal prion disease is endemic in North America, present in South Korea and has recently been...
TRANSMISSION | PROTEIN | VIROLOGY | MINERALS | RECPRP | ORGANIC-MATTER | MICROBIOLOGY | CHRONIC WASTING DISEASE | FATE | PARASITOLOGY | Humus | Research | Organic matter | Chronic wasting disease | Incubation | Elk | Acidic soils | Soil degradation | Transmissible spongiform encephalopathy | Organic soils | Molecular weight | Soil conservation | Proteins | Soils | Environmental science | Acids | Infectivity | Prions | Soil organic matter | Humic acids | Prion protein | Organic compounds
TRANSMISSION | PROTEIN | VIROLOGY | MINERALS | RECPRP | ORGANIC-MATTER | MICROBIOLOGY | CHRONIC WASTING DISEASE | FATE | PARASITOLOGY | Humus | Research | Organic matter | Chronic wasting disease | Incubation | Elk | Acidic soils | Soil degradation | Transmissible spongiform encephalopathy | Organic soils | Molecular weight | Soil conservation | Proteins | Soils | Environmental science | Acids | Infectivity | Prions | Soil organic matter | Humic acids | Prion protein | Organic compounds
Journal Article
Aging Cell, ISSN 1474-9718, 12/2016, Volume 15, Issue 6, pp. 1132 - 1139
Summary With age, somatically derived mitochondrial DNA (mtDNA) deletion mutations arise in many tissues and species. In skeletal muscle, deletion mutations...
mitochondrial DNA deletion mutation | aging | muscle | sarcopenia | APOPTOSIS | ATROPHY | CELL BIOLOGY | GERIATRICS & GERONTOLOGY | BIOGENESIS | GENE-EXPRESSION | AMP KINASE | MICE | HUMAN SKELETAL-MUSCLES | HEALTHY-MEN | BETA-GUANIDINOPROPIONIC ACID | Muscles | Genetic aspects | Mitochondrial DNA | Mutation | Age | Deoxyribonucleic acid--DNA | Original
mitochondrial DNA deletion mutation | aging | muscle | sarcopenia | APOPTOSIS | ATROPHY | CELL BIOLOGY | GERIATRICS & GERONTOLOGY | BIOGENESIS | GENE-EXPRESSION | AMP KINASE | MICE | HUMAN SKELETAL-MUSCLES | HEALTHY-MEN | BETA-GUANIDINOPROPIONIC ACID | Muscles | Genetic aspects | Mitochondrial DNA | Mutation | Age | Deoxyribonucleic acid--DNA | Original
Journal Article
Child Abuse & Neglect, ISSN 0145-2134, 2009, Volume 33, Issue 11, pp. 791 - 808
Abstract Objective The objectives of this article are to explore the extent to which the International Statistical Classification of Diseases and Related...
Pediatrics | Psychiatry | Child maltreatment | ICD | Health data | UNITED-STATES | PSYCHOLOGY, SOCIAL | PHYSICAL ABUSE | HEAD-INJURY | PUBLIC-HEALTH SURVEILLANCE | SHAKEN-BABY-SYNDROME | HOSPITALIZED CHILDREN | PEDIATRIC INJURIES | TRAUMATIC BRAIN-INJURIES | INFANTS | SOCIAL WORK | FAMILY STUDIES | YOUNG-CHILDREN | Social Science Research | Research Utilization | Databases | Classification | Literature Reviews | Data Analysis | At Risk Persons | Identification | Research | Child Abuse | Child Abuse - statistics & numerical data | International Classification of Diseases | Cross-Sectional Studies | Humans | Wounds and Injuries - prevention & control | Child, Preschool | Child Abuse - classification | Child Abuse - prevention & control | Infant | Incidence | Wounds and Injuries - classification | Mandatory Reporting | Health Care Costs - statistics & numerical data | Adolescent | Wounds and Injuries - diagnosis | Wounds and Injuries - economics | Child Advocacy - legislation & jurisprudence | Child | Child Abuse - diagnosis | Evaluation | Child abuse | Data collections | Medical research | Child abuse & neglect | Statistics | Meta-analysis
Pediatrics | Psychiatry | Child maltreatment | ICD | Health data | UNITED-STATES | PSYCHOLOGY, SOCIAL | PHYSICAL ABUSE | HEAD-INJURY | PUBLIC-HEALTH SURVEILLANCE | SHAKEN-BABY-SYNDROME | HOSPITALIZED CHILDREN | PEDIATRIC INJURIES | TRAUMATIC BRAIN-INJURIES | INFANTS | SOCIAL WORK | FAMILY STUDIES | YOUNG-CHILDREN | Social Science Research | Research Utilization | Databases | Classification | Literature Reviews | Data Analysis | At Risk Persons | Identification | Research | Child Abuse | Child Abuse - statistics & numerical data | International Classification of Diseases | Cross-Sectional Studies | Humans | Wounds and Injuries - prevention & control | Child, Preschool | Child Abuse - classification | Child Abuse - prevention & control | Infant | Incidence | Wounds and Injuries - classification | Mandatory Reporting | Health Care Costs - statistics & numerical data | Adolescent | Wounds and Injuries - diagnosis | Wounds and Injuries - economics | Child Advocacy - legislation & jurisprudence | Child | Child Abuse - diagnosis | Evaluation | Child abuse | Data collections | Medical research | Child abuse & neglect | Statistics | Meta-analysis
Journal Article
Emerging Infectious Diseases, ISSN 1080-6040, 09/2017, Volume 23, Issue 9, pp. 1598 - 1600
Human and mouse prion proteins share a structural motif that regulates resistance to common chronic wasting disease (CWD) prion strains. Successful...
ENCEPHALOPATHY | INFECTIOUS DISEASES | TRANSMISSION | IMMUNOLOGY | HAMSTERS | ADAPTATION | Prions - metabolism | Protein Conformation, alpha-Helical | Cricetinae | Species Specificity | Humans | Host Specificity | Wasting Disease, Chronic - pathology | Prions - chemistry | Deer | Wasting Disease, Chronic - transmission | Animals | Protein Conformation, beta-Strand | Mice | Protein Stability | prions and related diseases | chronic wasting disease | zoonoses | pathogen-host interactions | mice | Research Letter | host range | pathogenicity | Canada | cervids | prion diseases | Chronic Wasting Disease Prion Strain Emergence and Host Range Expansion | prions
ENCEPHALOPATHY | INFECTIOUS DISEASES | TRANSMISSION | IMMUNOLOGY | HAMSTERS | ADAPTATION | Prions - metabolism | Protein Conformation, alpha-Helical | Cricetinae | Species Specificity | Humans | Host Specificity | Wasting Disease, Chronic - pathology | Prions - chemistry | Deer | Wasting Disease, Chronic - transmission | Animals | Protein Conformation, beta-Strand | Mice | Protein Stability | prions and related diseases | chronic wasting disease | zoonoses | pathogen-host interactions | mice | Research Letter | host range | pathogenicity | Canada | cervids | prion diseases | Chronic Wasting Disease Prion Strain Emergence and Host Range Expansion | prions
Journal Article
Molecular Neurobiology, ISSN 0893-7648, 3/2018, Volume 55, Issue 3, pp. 2384 - 2396
Prion diseases are fatal transmissible neurodegenerative disorders affecting humans and various mammals. In spite of intensive efforts, there is no effective...
Neurology | Therapeutic RNAi | Neurosciences | Prion disease | Biomedicine | Neurobiology | Immune stimulator | Differentiated C2C12 cells | Neuronal and glial cells | Cell Biology | RNA INTERFERENCE | PROLONGS SURVIVAL | DOWN-REGULATION | NEUROSCIENCES | INFECTED MICE | SCRAPIE | IN-VITRO | HEPATITIS-C VIRUS | DISEASE | MOLECULAR-MECHANISMS | INNATE IMMUNITY | Cell Survival - drug effects | Lipopolysaccharides - toxicity | Humans | Cells, Cultured | MicroRNAs - metabolism | Prion Proteins - metabolism | Animals | HEK293 Cells | Cell Line, Tumor | Mice | MicroRNAs - genetics | Prion Proteins - genetics | Prion Proteins - antagonists & inhibitors | Cell Survival - physiology | Nervous system diseases | MicroRNA | Prions | Communicable diseases | Cells | Cell culture | Immunostimulation | Myotubes | Propagation | Neurodegenerative diseases | RNA-mediated interference | Medical treatment | MiRNA | Cultures | Poly (I:C) | Glial cells | Neuronal-glial interactions | Proteins | MicroRNAs | Isoforms | Replication | Prion protein
Neurology | Therapeutic RNAi | Neurosciences | Prion disease | Biomedicine | Neurobiology | Immune stimulator | Differentiated C2C12 cells | Neuronal and glial cells | Cell Biology | RNA INTERFERENCE | PROLONGS SURVIVAL | DOWN-REGULATION | NEUROSCIENCES | INFECTED MICE | SCRAPIE | IN-VITRO | HEPATITIS-C VIRUS | DISEASE | MOLECULAR-MECHANISMS | INNATE IMMUNITY | Cell Survival - drug effects | Lipopolysaccharides - toxicity | Humans | Cells, Cultured | MicroRNAs - metabolism | Prion Proteins - metabolism | Animals | HEK293 Cells | Cell Line, Tumor | Mice | MicroRNAs - genetics | Prion Proteins - genetics | Prion Proteins - antagonists & inhibitors | Cell Survival - physiology | Nervous system diseases | MicroRNA | Prions | Communicable diseases | Cells | Cell culture | Immunostimulation | Myotubes | Propagation | Neurodegenerative diseases | RNA-mediated interference | Medical treatment | MiRNA | Cultures | Poly (I:C) | Glial cells | Neuronal-glial interactions | Proteins | MicroRNAs | Isoforms | Replication | Prion protein
Journal Article
Science, ISSN 0036-8075, 5/2010, Volume 328, Issue 5982, pp. 1154 - 1158
Prions are infectious proteins composed of the abnormal disease-causing isoform PrP Sc , which induces conformational conversion of the host-encoded normal...
Nervous system diseases | Disease transmission | Neuropathology | Transgenic animals | Synaptic transmission | Prions | REPORTS | Prion diseases | Mice | Elks | Deer | SCRAPIE | DEER | TRANSMISSION | ELK | MULTIDISCIPLINARY SCIENCES | ADAPTATION | CREUTZFELDT-JAKOB-DISEASE | VARIANT CJD | CHRONIC WASTING DISEASE | TRANSGENIC MICE | PRP | Amino Acid Sequence | Disease Susceptibility | Species Specificity | PrPSc Proteins - analysis | Selection, Genetic | Mice, Transgenic | Wasting Disease, Chronic - pathology | PrPC Proteins - chemistry | PrPSc Proteins - chemistry | Protein Folding | PrPSc Proteins - genetics | Wasting Disease, Chronic - transmission | Animals | Brain - pathology | Protein Conformation | Brain Chemistry | Mutation | PrPSc Proteins - pathogenicity | PrPC Proteins - genetics | Serial Passage | Proteins | Gene mutations | Physiological aspects | Genetic aspects | Research | Conformation | Elk | Rodents | Animal diseases
Nervous system diseases | Disease transmission | Neuropathology | Transgenic animals | Synaptic transmission | Prions | REPORTS | Prion diseases | Mice | Elks | Deer | SCRAPIE | DEER | TRANSMISSION | ELK | MULTIDISCIPLINARY SCIENCES | ADAPTATION | CREUTZFELDT-JAKOB-DISEASE | VARIANT CJD | CHRONIC WASTING DISEASE | TRANSGENIC MICE | PRP | Amino Acid Sequence | Disease Susceptibility | Species Specificity | PrPSc Proteins - analysis | Selection, Genetic | Mice, Transgenic | Wasting Disease, Chronic - pathology | PrPC Proteins - chemistry | PrPSc Proteins - chemistry | Protein Folding | PrPSc Proteins - genetics | Wasting Disease, Chronic - transmission | Animals | Brain - pathology | Protein Conformation | Brain Chemistry | Mutation | PrPSc Proteins - pathogenicity | PrPC Proteins - genetics | Serial Passage | Proteins | Gene mutations | Physiological aspects | Genetic aspects | Research | Conformation | Elk | Rodents | Animal diseases
Journal Article