1998, ISBN 1878448862, xvii, 272
Book
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
Nature, ISSN 0028-0836, 2017, Volume 551, Issue 7678, pp. 75 - 79
Gravitational waves were discovered with the detection of binary black-hole mergers(1) and they should also be detectable from lower-mass neutron-star mergers....
ELEMENTS | RATES | DISTANCE | FAINT TYPE | OUTFLOWS | MULTIDISCIPLINARY SCIENCES | LIGHT CURVES | OBSERVATORY SUPERNOVA SEARCH | SPECTRA | GALAXY | Galaxies | Supernovae | Gravitational waves | Radiation | Neutrons | Radioisotopes | Iron | Ejecta | Light | Optical communication | Opacity | Isotopes | Nuclear capture | Gravity | Neutron stars | Light speed | Electromagnetic radiation | Nuclear electric power generation | Universe | Velocity | Physical properties | Wavelengths | Binary stars | Astronomical models | Predictions | Line spectra | Nuclides | Ejection | Physics - High Energy Astrophysical Phenomena | Fysik | Physical Sciences | Astronomi, astrofysik och kosmologi | Naturvetenskap | Natural Sciences | Astronomy, Astrophysics and Cosmology
ELEMENTS | RATES | DISTANCE | FAINT TYPE | OUTFLOWS | MULTIDISCIPLINARY SCIENCES | LIGHT CURVES | OBSERVATORY SUPERNOVA SEARCH | SPECTRA | GALAXY | Galaxies | Supernovae | Gravitational waves | Radiation | Neutrons | Radioisotopes | Iron | Ejecta | Light | Optical communication | Opacity | Isotopes | Nuclear capture | Gravity | Neutron stars | Light speed | Electromagnetic radiation | Nuclear electric power generation | Universe | Velocity | Physical properties | Wavelengths | Binary stars | Astronomical models | Predictions | Line spectra | Nuclides | Ejection | Physics - High Energy Astrophysical Phenomena | Fysik | Physical Sciences | Astronomi, astrofysik och kosmologi | Naturvetenskap | Natural Sciences | Astronomy, Astrophysics and Cosmology
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 7/1996, Volume 134, Issue 2, pp. 295 - 306
Formation of coatomer-coated vesicles from Golgi-enriched membranes requires the activation of a small GTP-binding protein, ADP ribosylation factor (ARF). ARF...
Ethanol | Centrifugation | Cell lines | Coated vesicles | Lipids | Acute kidney failure | Cell membranes | CHO cells | Cytosol | P branes | COATOMER | GTP-BINDING PROTEIN | CISTERNAE | ARF | PURIFICATION | MEMBRANES | REQUIRES | ENDOPLASMIC-RETICULUM | TRANSPORT VESICLES | BETA-COP | CELL BIOLOGY | Cricetinae | Phosphatidylinositol 4,5-Diphosphate | Intracellular Membranes - enzymology | Phosphatidylinositol Phosphates - metabolism | ADP-Ribosylation Factors | Phospholipase D - metabolism | Ethanol - pharmacology | Animals | Bacterial Proteins - metabolism | Golgi Apparatus - metabolism | Phosphatidic Acids - metabolism | Lipid Bilayers - metabolism | Golgi Apparatus - ultrastructure | CHO Cells | GTP-Binding Proteins - metabolism | Ribose | Analysis | Physiological aspects | Adenosine diphosphate | Phospholipases | Research | Golgi apparatus
Ethanol | Centrifugation | Cell lines | Coated vesicles | Lipids | Acute kidney failure | Cell membranes | CHO cells | Cytosol | P branes | COATOMER | GTP-BINDING PROTEIN | CISTERNAE | ARF | PURIFICATION | MEMBRANES | REQUIRES | ENDOPLASMIC-RETICULUM | TRANSPORT VESICLES | BETA-COP | CELL BIOLOGY | Cricetinae | Phosphatidylinositol 4,5-Diphosphate | Intracellular Membranes - enzymology | Phosphatidylinositol Phosphates - metabolism | ADP-Ribosylation Factors | Phospholipase D - metabolism | Ethanol - pharmacology | Animals | Bacterial Proteins - metabolism | Golgi Apparatus - metabolism | Phosphatidic Acids - metabolism | Lipid Bilayers - metabolism | Golgi Apparatus - ultrastructure | CHO Cells | GTP-Binding Proteins - metabolism | Ribose | Analysis | Physiological aspects | Adenosine diphosphate | Phospholipases | Research | Golgi apparatus
Journal Article
Space Science Reviews, ISSN 0038-6308, 12/2015, Volume 195, Issue 1, pp. 3 - 48
The MAVEN spacecraft launched in November 2013, arrived at Mars in September 2014, and completed commissioning and began its one-Earth-year primary science...
MAVEN | Mars | Extraterrestrial Physics, Space Sciences | Astrophysics and Astroparticles | Planetology | Atmosphere | Aerospace Technology and Astronautics | Physics | Solar-wind interactions | VENUS | MARTIAN ATMOSPHERE | PLASMA ACCELERATION | OXYGEN-ION PRECIPITATION | PLANETARY-ATMOSPHERES | ABUNDANCE | CRUSTAL MAGNETIZATION | EXPRESS | ASTRONOMY & ASTROPHYSICS | SOLAR-WIND | MAGNETIC-FIELD | Magnetosphere | Atmosphere, Upper | Mars (Planet) | Evolution | Space exploration | Spacecraft | Mars spacecraft | Escape structures | Mars atmosphere | Upper atmosphere | Sun | Mars missions | Solar and Stellar Astrophysics | Earth and Planetary Astrophysics | Sciences of the Universe | Astrophysics | Fysik | Physical Sciences | Astronomi, astrofysik och kosmologi | Naturvetenskap | Natural Sciences | Astronomy, Astrophysics and Cosmology
MAVEN | Mars | Extraterrestrial Physics, Space Sciences | Astrophysics and Astroparticles | Planetology | Atmosphere | Aerospace Technology and Astronautics | Physics | Solar-wind interactions | VENUS | MARTIAN ATMOSPHERE | PLASMA ACCELERATION | OXYGEN-ION PRECIPITATION | PLANETARY-ATMOSPHERES | ABUNDANCE | CRUSTAL MAGNETIZATION | EXPRESS | ASTRONOMY & ASTROPHYSICS | SOLAR-WIND | MAGNETIC-FIELD | Magnetosphere | Atmosphere, Upper | Mars (Planet) | Evolution | Space exploration | Spacecraft | Mars spacecraft | Escape structures | Mars atmosphere | Upper atmosphere | Sun | Mars missions | Solar and Stellar Astrophysics | Earth and Planetary Astrophysics | Sciences of the Universe | Astrophysics | Fysik | Physical Sciences | Astronomi, astrofysik och kosmologi | Naturvetenskap | Natural Sciences | Astronomy, Astrophysics and Cosmology
Journal Article
Australian Journal of Earth Sciences, ISSN 0812-0099, 2019, Volume 66, Issue 3, pp. 379 - 410
Gold deposits in the Agnew district display markedly different structural styles. The Waroonga and Songvang deposits are hosted in layer-parallel extensional...
Eastern Goldfields | deformation | Scotty Creek Basin | Lawlers | Agnew | gold mineralisation | YILGARN CRATON | KALGOORLIE TERRANE | SHEAR ZONE | SEDIMENTATION | CRUSTAL | GREENSTONE-BELT | GEOSCIENCES, MULTIDISCIPLINARY | EVOLUTION | LEONORA | AGE CONSTRAINTS | PROVINCE
Eastern Goldfields | deformation | Scotty Creek Basin | Lawlers | Agnew | gold mineralisation | YILGARN CRATON | KALGOORLIE TERRANE | SHEAR ZONE | SEDIMENTATION | CRUSTAL | GREENSTONE-BELT | GEOSCIENCES, MULTIDISCIPLINARY | EVOLUTION | LEONORA | AGE CONSTRAINTS | PROVINCE
Journal Article
Nature, ISSN 0028-0836, 03/2015, Volume 519, Issue 7542, pp. 223 - 228
Despite three decades of successful, predominantly phenotype-driven discovery of the genetic causes of monogenic disorders(1), up to half of children with...
INTELLECTUAL DISABILITY | HUMAN-DISEASE | DE-NOVO MUTATIONS | MULTIDISCIPLINARY SCIENCES | FRAMEWORK | MODEL | AUTISM SPECTRUM DISORDERS | COPY-NUMBER VARIATION | CHILDREN | Rare Diseases - genetics | Humans | Parents | Child, Preschool | Infant | Male | Developmental Disabilities - genetics | Dynamin I - genetics | Mutation, Missense - genetics | Polycomb Repressive Complex 1 - genetics | Gene Expression Regulation, Developmental | Transposases - genetics | Female | Nuclear Proteins - genetics | Child | Developmental Disabilities - diagnosis | Infant, Newborn | Guanine Nucleotide Exchange Factors - genetics | Protein Phosphatase 2 - genetics | Protein-Serine-Threonine Kinases - genetics | United Kingdom | Phosphoproteins - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Nerve Tissue Proteins - genetics | Genome, Human - genetics | Homeodomain Proteins - genetics | Zebrafish - genetics | Chromosomal Proteins, Non-Histone - genetics | Carrier Proteins - genetics | DEAD-box RNA Helicases - genetics | Exome - genetics | Animals | Adolescent | Chromosome Aberrations | Genes, Dominant - genetics | Usage | Genomics | Child development deviations | Genetic aspects | Research | Risk factors | Developmental disabilities | Studies | Hypotheses | Genes | Developmental psychology | Families & family life | Genomes | Mutation | Children & youth
INTELLECTUAL DISABILITY | HUMAN-DISEASE | DE-NOVO MUTATIONS | MULTIDISCIPLINARY SCIENCES | FRAMEWORK | MODEL | AUTISM SPECTRUM DISORDERS | COPY-NUMBER VARIATION | CHILDREN | Rare Diseases - genetics | Humans | Parents | Child, Preschool | Infant | Male | Developmental Disabilities - genetics | Dynamin I - genetics | Mutation, Missense - genetics | Polycomb Repressive Complex 1 - genetics | Gene Expression Regulation, Developmental | Transposases - genetics | Female | Nuclear Proteins - genetics | Child | Developmental Disabilities - diagnosis | Infant, Newborn | Guanine Nucleotide Exchange Factors - genetics | Protein Phosphatase 2 - genetics | Protein-Serine-Threonine Kinases - genetics | United Kingdom | Phosphoproteins - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Nerve Tissue Proteins - genetics | Genome, Human - genetics | Homeodomain Proteins - genetics | Zebrafish - genetics | Chromosomal Proteins, Non-Histone - genetics | Carrier Proteins - genetics | DEAD-box RNA Helicases - genetics | Exome - genetics | Animals | Adolescent | Chromosome Aberrations | Genes, Dominant - genetics | Usage | Genomics | Child development deviations | Genetic aspects | Research | Risk factors | Developmental disabilities | Studies | Hypotheses | Genes | Developmental psychology | Families & family life | Genomes | Mutation | Children & youth
Journal Article
PHYSICAL REVIEW LETTERS, ISSN 0031-9007, 05/2006, Volume 96, Issue 19
We report an observation of the decay B-s(0)-> D-s(-)pi(+) in p (p) over bar collisions at root s = 1.96 TeV using 115 pb(-1) of data collected by the CDF II...
PHYSICS, MULTIDISCIPLINARY | PHYSICS | DECAYS | COLLISIONS
PHYSICS, MULTIDISCIPLINARY | PHYSICS | DECAYS | COLLISIONS
Journal Article