JAMA Dermatology, ISSN 2168-6068, 04/2014, Volume 150, Issue 4, pp. 406 - 406
Journal Article
JAMA Dermatology, ISSN 2168-6068, 2014, Volume 150, Issue 4, p. 406
Journal Article
Science and Public Policy, ISSN 0302-3427, 04/2016, Volume 43, Issue 2, pp. 289 - 290
Journal Article
4.
Full Text
Abstracts of the HIV Research for Prevention Meeting, HIVR4P, 21-25 October, 2018, Madrid
AIDS Research and Human Retroviruses, ISSN 0889-2229, 10/2018, Volume 34, Issue S1, pp. 1 - 407
Journal Article
2010, Volume 8, 2
Reference
2004, STUDIES IN CELTIC HISTORY; 22., ISBN 9781843830900
Book
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 2098 - 16
textabstractGeneral cognitive function is a prominent and relatively stable human trait that is associated with many important life outcomes. We combine...
COMMON VARIANTS | METAANALYSIS | REACTION-TIME | PROCESSING SPEED | MULTIDISCIPLINARY SCIENCES | INTELLIGENCE DIFFERENCES | SCHIZOPHRENIA | DCDC2 | DISCOVERY | GENOME-WIDE ASSOCIATION | REVEALS | Multifactorial Inheritance - genetics | Genetic Predisposition to Disease | Humans | Middle Aged | Genetic Loci - genetics | Neurodegenerative Diseases - genetics | Neurodevelopmental Disorders - genetics | Reaction Time - genetics | Young Adult | Mental Disorders - genetics | Adolescent | Aged, 80 and over | Cognition - physiology | Polymorphism, Single Nucleotide - genetics | Adult | Aged | Hypertension | Brain | Cognitive ability | Genomes | Gene expression | Neurodevelopmental disorders | Loci | Consortia | Illnesses | Mathematical analysis | Reaction time | Heritability | Gene loci | Polygenic inheritance | brain cortex | Medical and Health Sciences | Medicin och hälsovetenskap | major clinical study | osteoarthritis | Article | heart infarction | Klinisk medicin | lung cancer | identification method | longevity | grip strength | angina pectoris | genetic correlation | human | major depression | Neurologi | cognition | data set | aged | brain | gene locus | Clinical Medicine | Neurology | genome | vision | genetic analysis | controlled study | response time | adolescent | nervous system disorder | adult | hypertension | gene expression
COMMON VARIANTS | METAANALYSIS | REACTION-TIME | PROCESSING SPEED | MULTIDISCIPLINARY SCIENCES | INTELLIGENCE DIFFERENCES | SCHIZOPHRENIA | DCDC2 | DISCOVERY | GENOME-WIDE ASSOCIATION | REVEALS | Multifactorial Inheritance - genetics | Genetic Predisposition to Disease | Humans | Middle Aged | Genetic Loci - genetics | Neurodegenerative Diseases - genetics | Neurodevelopmental Disorders - genetics | Reaction Time - genetics | Young Adult | Mental Disorders - genetics | Adolescent | Aged, 80 and over | Cognition - physiology | Polymorphism, Single Nucleotide - genetics | Adult | Aged | Hypertension | Brain | Cognitive ability | Genomes | Gene expression | Neurodevelopmental disorders | Loci | Consortia | Illnesses | Mathematical analysis | Reaction time | Heritability | Gene loci | Polygenic inheritance | brain cortex | Medical and Health Sciences | Medicin och hälsovetenskap | major clinical study | osteoarthritis | Article | heart infarction | Klinisk medicin | lung cancer | identification method | longevity | grip strength | angina pectoris | genetic correlation | human | major depression | Neurologi | cognition | data set | aged | brain | gene locus | Clinical Medicine | Neurology | genome | vision | genetic analysis | controlled study | response time | adolescent | nervous system disorder | adult | hypertension | gene expression
Journal Article
BMC Pediatrics, ISSN 1471-2431, 01/2013, Volume 13, Issue 1, pp. 13 - 13
Background: There is little reliable information on the prevalence of fetal alcohol spectrum disorders (FASD) in Australia and no coordinated national approach...
DIAGNOSIS | HEALTH-PROFESSIONALS KNOWLEDGE | GUIDELINES | PRACTICE FOLLOWING PROVISION | PEDIATRICIANS KNOWLEDGE | PEDIATRICS | EXPOSURE | ATTITUDES | CONSUMPTION | EDUCATIONAL RESOURCES | TOOL | Pregnancy | Attitude of Health Personnel | Delphi Technique | Fetal Alcohol Spectrum Disorders - diagnosis | Humans | Mass Screening - organization & administration | Female | Male | Surveys and Questionnaires | Australia | Mass Screening - methods | Fetal alcohol syndrome | Medical research | Public health | Alcohol use | Children & youth
DIAGNOSIS | HEALTH-PROFESSIONALS KNOWLEDGE | GUIDELINES | PRACTICE FOLLOWING PROVISION | PEDIATRICIANS KNOWLEDGE | PEDIATRICS | EXPOSURE | ATTITUDES | CONSUMPTION | EDUCATIONAL RESOURCES | TOOL | Pregnancy | Attitude of Health Personnel | Delphi Technique | Fetal Alcohol Spectrum Disorders - diagnosis | Humans | Mass Screening - organization & administration | Female | Male | Surveys and Questionnaires | Australia | Mass Screening - methods | Fetal alcohol syndrome | Medical research | Public health | Alcohol use | Children & youth
Journal Article
BioScience, ISSN 0006-3568, 10/2018, Volume 68, Issue 10, pp. 805 - 812
Abstract According to a recent survey, ecologists and evolutionary biologists feel that theoretical and empirical research should coexist in a tight feedback...
Sexual selection | Science of science | Theory | Citation network | Speciation | EVOLUTION | sexual selection | BIOLOGY | citation network | SELECTION | theory | science of science | speciation | Network analysis (Planning) | Usage | Research | Evolutionary biology | Analysis | Sexual selection in animals | Life Sciences | Populations and Evolution | Mathematics | Biodiversity | Professional Biologist
Sexual selection | Science of science | Theory | Citation network | Speciation | EVOLUTION | sexual selection | BIOLOGY | citation network | SELECTION | theory | science of science | speciation | Network analysis (Planning) | Usage | Research | Evolutionary biology | Analysis | Sexual selection in animals | Life Sciences | Populations and Evolution | Mathematics | Biodiversity | Professional Biologist
Journal Article
2008, Annual review of nursing research, ISBN 0826101267, Volume 26, xiv, 311
Book
11/2012
Poly(methacrylic acid -co- methyl methacrylate) beads were previously shown to have a therapeutic effect on wound closure through the promotion of...
Host response | Angiogenesis | Wound healing | 0541 | Biomaterial
Host response | Angiogenesis | Wound healing | 0541 | Biomaterial
Dissertation
2006, ISBN 1851829474, 352
Book
Journal of Leukocyte Biology, ISSN 0741-5400, 05/2015, Volume 97, Issue 5, pp. 821 - 824
Discussion on Syk tyrosine kinase functioning as a positive and negative regulator of NLRP3 inflammasome activation.
IL‐1β tyrosine kinase | IL-1β tyrosine kinase
IL‐1β tyrosine kinase | IL-1β tyrosine kinase
Journal Article
2002, ISBN 0933856733, 384
Book
American Journal of Ophthalmology, ISSN 0002-9394, 2015, Volume 160, Issue 6, pp. 1133 - 1141.e9
Purpose To identify factors associated with best-corrected visual acuity (BCVA) presentation and 2-year outcome in 479 intermediate, posterior, and panuveitic...
Ophthalmology | Glucocorticoids - administration & dosage | Follow-Up Studies | Tomography, Optical Coherence | Humans | Middle Aged | Drug Implants | Male | Treatment Outcome | Visual Acuity | Time Factors | Panuveitis - diagnosis | Female | Aged | Panuveitis - drug therapy | Clinical trials | Fishes | Diabetic retinopathy | Health sciences | Reading | Hospitals | Review boards | Colleges & universities | Tomography
Ophthalmology | Glucocorticoids - administration & dosage | Follow-Up Studies | Tomography, Optical Coherence | Humans | Middle Aged | Drug Implants | Male | Treatment Outcome | Visual Acuity | Time Factors | Panuveitis - diagnosis | Female | Aged | Panuveitis - drug therapy | Clinical trials | Fishes | Diabetic retinopathy | Health sciences | Reading | Hospitals | Review boards | Colleges & universities | Tomography
Journal Article
Nature, ISSN 0028-0836, 02/2017, Volume 542, Issue 7642, pp. 433 - 438
The genomes of individuals with severe, undiagnosed developmental disorders are enriched in damaging de novo mutations (DNMs) in developmentally important...
INTELLECTUAL DISABILITY | METAANALYSIS | VARIANTS | GENETICS | HEART-DEFECTS | MULTIDISCIPLINARY SCIENCES | GENES | SEQUENCE | FRAMEWORK | DISCOVERY | GENOME | Prevalence | Humans | Middle Aged | Parents | Male | Mi-2 Nucleosome Remodeling and Deacetylase Complex - genetics | Developmental Disabilities - genetics | Casein Kinase II - genetics | Autoantigens - genetics | Young Adult | ras GTPase-Activating Proteins - genetics | Adult | Female | Child | CDC2 Protein Kinase - genetics | Histone-Lysine N-Methyltransferase - genetics | Repressor Proteins - genetics | Sex Characteristics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Mutation - genetics | Nerve Tissue Proteins - genetics | Sequence Analysis, DNA | Homeodomain Proteins - genetics | DEAD-box RNA Helicases - genetics | Exome - genetics | Phenotype | Myeloid-Lymphoid Leukemia Protein - genetics | Adolescent | Heredity - genetics | Protein Phosphatase 2C - genetics | Cohort Studies | Child development deviations | Genetic aspects | Genetic disorders | Developmental disabilities | Distribution | Genes | Families & family life | Births | Genomes | Mutation | Causality | Estimates | Age | TRIO | MYT1L | EHMT1 | HNRNPU | SUV420H1 | COL4A3BP | SYNGAP1 | PPP2R1A | POGZ | EP300 | KCNH1 | SCN1A | MEF2C | CDKL5 | CSNK2A1 | DYRK1A | CASK | ALG13 | FOXP1 | KAT6B | TBL1XR1 | KAT6A | SCN8A | KCNQ2 | EEF1A2 | KCNQ3 | ADNP | PhenIcons | SET | KMT2A | ANKRD11 | STXBP1 | FOXG1 | ZC4H2 | ITPR1 | De novo mutation | Seizures | ZBTB18 | CREBBP | SMAD4 | PDHA1 | IQSEC2 | AUTS2 | BCL11A | BRAF | SMARCA2 | GRIN2B | MED13L | GNAO1 | CNOT3 | TCF4 | SCN2A | CDK13 | GABRB3 | SETD5 | KDM5B | Developmental Disease | DDX3X | CHD8 | PTEN | CHD4 | TCF20 | CTCF | CHD2 | WDR45 | SLC6A1 | MECP2 | CHAMP1 | KIF1A | Average Faces | MSL3 | PPP2R5D | SMC1A | ARID1B | DNM1 | CNKSR2 | PACS1 | WAC | ZMYND11 | AHDC1 | NFIX | SATB2 | HDAC8 | PPM1D | GNAI1 | PURA | PUF60 | NSD1 | Intellectual Disability | SLC35A2 | DYNC1H1 | NAA10 | USP9X | PTPN11 | GATAD2B | ASXL1 | KANSL1 | ASXL3 | CTNNB1 | QRICH1
INTELLECTUAL DISABILITY | METAANALYSIS | VARIANTS | GENETICS | HEART-DEFECTS | MULTIDISCIPLINARY SCIENCES | GENES | SEQUENCE | FRAMEWORK | DISCOVERY | GENOME | Prevalence | Humans | Middle Aged | Parents | Male | Mi-2 Nucleosome Remodeling and Deacetylase Complex - genetics | Developmental Disabilities - genetics | Casein Kinase II - genetics | Autoantigens - genetics | Young Adult | ras GTPase-Activating Proteins - genetics | Adult | Female | Child | CDC2 Protein Kinase - genetics | Histone-Lysine N-Methyltransferase - genetics | Repressor Proteins - genetics | Sex Characteristics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Mutation - genetics | Nerve Tissue Proteins - genetics | Sequence Analysis, DNA | Homeodomain Proteins - genetics | DEAD-box RNA Helicases - genetics | Exome - genetics | Phenotype | Myeloid-Lymphoid Leukemia Protein - genetics | Adolescent | Heredity - genetics | Protein Phosphatase 2C - genetics | Cohort Studies | Child development deviations | Genetic aspects | Genetic disorders | Developmental disabilities | Distribution | Genes | Families & family life | Births | Genomes | Mutation | Causality | Estimates | Age | TRIO | MYT1L | EHMT1 | HNRNPU | SUV420H1 | COL4A3BP | SYNGAP1 | PPP2R1A | POGZ | EP300 | KCNH1 | SCN1A | MEF2C | CDKL5 | CSNK2A1 | DYRK1A | CASK | ALG13 | FOXP1 | KAT6B | TBL1XR1 | KAT6A | SCN8A | KCNQ2 | EEF1A2 | KCNQ3 | ADNP | PhenIcons | SET | KMT2A | ANKRD11 | STXBP1 | FOXG1 | ZC4H2 | ITPR1 | De novo mutation | Seizures | ZBTB18 | CREBBP | SMAD4 | PDHA1 | IQSEC2 | AUTS2 | BCL11A | BRAF | SMARCA2 | GRIN2B | MED13L | GNAO1 | CNOT3 | TCF4 | SCN2A | CDK13 | GABRB3 | SETD5 | KDM5B | Developmental Disease | DDX3X | CHD8 | PTEN | CHD4 | TCF20 | CTCF | CHD2 | WDR45 | SLC6A1 | MECP2 | CHAMP1 | KIF1A | Average Faces | MSL3 | PPP2R5D | SMC1A | ARID1B | DNM1 | CNKSR2 | PACS1 | WAC | ZMYND11 | AHDC1 | NFIX | SATB2 | HDAC8 | PPM1D | GNAI1 | PURA | PUF60 | NSD1 | Intellectual Disability | SLC35A2 | DYNC1H1 | NAA10 | USP9X | PTPN11 | GATAD2B | ASXL1 | KANSL1 | ASXL3 | CTNNB1 | QRICH1
Journal Article