SAE technical paper series, Volume 2008-36-0398.
The main objective of this paper is to make a prospective analysis about the tendencies of the world wide strategies of commercial vehicles development, in...
Trucks | Globalization
Trucks | Globalization
eJournal
Book
Clinical Chemistry, ISSN 0009-9147, 11/2010, Volume 56, Issue 11, pp. 1767 - 1771
BACKGROUND: Several placental microRNAs (miRNAs) have been identified as pregnancy-associated molecules with the potential for use in estimating the condition...
MEDICAL LABORATORY TECHNOLOGY | MESSENGER-RNA | CLUSTER | PROGRESS | PRENATAL-DIAGNOSIS | NUCLEIC-ACIDS | Placenta - metabolism | Chromosomes, Human, Pair 19 - genetics | Oligonucleotide Array Sequence Analysis | Humans | Female | MicroRNAs - blood | Biomarkers - blood | Pregnancy - blood | Reverse Transcriptase Polymerase Chain Reaction | Chromosomes, Human, Pair 14 - genetics | Pregnancy | Womens health | Chromosomes | Fetuses
MEDICAL LABORATORY TECHNOLOGY | MESSENGER-RNA | CLUSTER | PROGRESS | PRENATAL-DIAGNOSIS | NUCLEIC-ACIDS | Placenta - metabolism | Chromosomes, Human, Pair 19 - genetics | Oligonucleotide Array Sequence Analysis | Humans | Female | MicroRNAs - blood | Biomarkers - blood | Pregnancy - blood | Reverse Transcriptase Polymerase Chain Reaction | Chromosomes, Human, Pair 14 - genetics | Pregnancy | Womens health | Chromosomes | Fetuses
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 9/2011, Volume 108, Issue 36, pp. 14914 - 14919
Nakajo-Nishimura syndrome (NNS) is a disorder that segregates in an autosomal recessive fashion. Symptoms include periodic fever, skin rash, partial...
Cytokines | Fibroblasts | Inflammation | Skin | Graduate schools | Cellular immunity | Autoimmune diseases | Genetic mutation | Wasting syndrome | Muscular atrophy | ACTIVATION | HYPER-GAMMA-GLOBULINEMIA | INFLAMMATORY DISEASES | INHIBITOR BORTEZOMIB | KINASE PHOSPHATASES | MULTIDISCIPLINARY SCIENCES | MAMMALIAN 20S PROTEASOME | MUSCULAR-ATROPHY | INTERLEUKIN-6 | STRESS | NF-KAPPA-B | Inflammation - pathology | Autoimmune Diseases - enzymology | Cytokines - metabolism | Humans | Muscular Atrophy - pathology | Male | Muscular Atrophy - genetics | Mutation, Missense | Muscular Atrophy - enzymology | Syndrome | Autoimmune Diseases - genetics | Proteasome Endopeptidase Complex - genetics | Inflammation - metabolism | Inflammation - genetics | Female | Proteasome Endopeptidase Complex - metabolism | Autoimmune Diseases - pathology | Cytokines - genetics | Ubiquitination - genetics | Amino Acid Substitution | Gene mutations | Physiological aspects | Genetic aspects | Research | Ubiquitin-proteasome system | Health aspects | Biological Sciences
Cytokines | Fibroblasts | Inflammation | Skin | Graduate schools | Cellular immunity | Autoimmune diseases | Genetic mutation | Wasting syndrome | Muscular atrophy | ACTIVATION | HYPER-GAMMA-GLOBULINEMIA | INFLAMMATORY DISEASES | INHIBITOR BORTEZOMIB | KINASE PHOSPHATASES | MULTIDISCIPLINARY SCIENCES | MAMMALIAN 20S PROTEASOME | MUSCULAR-ATROPHY | INTERLEUKIN-6 | STRESS | NF-KAPPA-B | Inflammation - pathology | Autoimmune Diseases - enzymology | Cytokines - metabolism | Humans | Muscular Atrophy - pathology | Male | Muscular Atrophy - genetics | Mutation, Missense | Muscular Atrophy - enzymology | Syndrome | Autoimmune Diseases - genetics | Proteasome Endopeptidase Complex - genetics | Inflammation - metabolism | Inflammation - genetics | Female | Proteasome Endopeptidase Complex - metabolism | Autoimmune Diseases - pathology | Cytokines - genetics | Ubiquitination - genetics | Amino Acid Substitution | Gene mutations | Physiological aspects | Genetic aspects | Research | Ubiquitin-proteasome system | Health aspects | Biological Sciences
Journal Article
Prenatal Diagnosis, ISSN 0197-3851, 03/2013, Volume 33, Issue 3, pp. 214 - 222
ABSTRACT Objective The aim of this study was to characterize placenta‐specific microRNAs in fetal growth restriction (FGR) pregnancy. Method Placenta‐specific...
MATERNAL PLASMA | CIRCULATION | GENETICS & HEREDITY | RNAS | PREECLAMPSIA | IDENTIFICATION | EXPRESSION | OBSTETRICS & GYNECOLOGY | Fetal Growth Retardation - blood | Humans | Gene Expression Regulation, Developmental - genetics | Fetal Growth Retardation - genetics | Male | MicroRNAs - metabolism | Fetal Growth Retardation - metabolism | Gene Expression Profiling | Reverse Transcriptase Polymerase Chain Reaction | Gestational Age | Case-Control Studies | Placenta - metabolism | Pregnancy | Young Adult | Chromosomes, Human, Pair 19 - genetics | Adult | Female | MicroRNAs - blood | MicroRNAs - genetics | Chromosomes, Human, Pair 19 - metabolism | MicroRNA | Pregnant women | Growth | Analysis | Fetus | Chemical properties
MATERNAL PLASMA | CIRCULATION | GENETICS & HEREDITY | RNAS | PREECLAMPSIA | IDENTIFICATION | EXPRESSION | OBSTETRICS & GYNECOLOGY | Fetal Growth Retardation - blood | Humans | Gene Expression Regulation, Developmental - genetics | Fetal Growth Retardation - genetics | Male | MicroRNAs - metabolism | Fetal Growth Retardation - metabolism | Gene Expression Profiling | Reverse Transcriptase Polymerase Chain Reaction | Gestational Age | Case-Control Studies | Placenta - metabolism | Pregnancy | Young Adult | Chromosomes, Human, Pair 19 - genetics | Adult | Female | MicroRNAs - blood | MicroRNAs - genetics | Chromosomes, Human, Pair 19 - metabolism | MicroRNA | Pregnant women | Growth | Analysis | Fetus | Chemical properties
Journal Article
1968, 225
Book
1912, 2, 4, 16, 6, ii p., [85] leaves of plates
Book
Clinical Chemistry, ISSN 0009-9147, 09/2013, Volume 59, Issue 9, pp. 1410 - 1412
Placentaspecific C19MC is imprinted in the placenta, with expression from the paternally inherited chromosome (5 ). [...]the increased expression of genes...
RNA-SEQ | PLACENTA | MEDICAL LABORATORY TECHNOLOGY | Pregnancy | Uterus - pathology | MicroRNAs - analysis | Humans | Female | MicroRNAs - blood | Uterine Neoplasms - diagnosis | Hydatidiform Mole - blood | Hydatidiform Mole - diagnosis | Uterine Neoplasms - blood | Plasma | Chromosomes | MicroRNAs
RNA-SEQ | PLACENTA | MEDICAL LABORATORY TECHNOLOGY | Pregnancy | Uterus - pathology | MicroRNAs - analysis | Humans | Female | MicroRNAs - blood | Uterine Neoplasms - diagnosis | Hydatidiform Mole - blood | Hydatidiform Mole - diagnosis | Uterine Neoplasms - blood | Plasma | Chromosomes | MicroRNAs
Journal Article
9.
Full Text
Localization of the primary taste cortex by contrasting passive and attentive conditions
Experimental Brain Research, ISSN 0014-4819, 6/2013, Volume 227, Issue 2, pp. 185 - 197
The primary taste cortex is located in the insula. However, exactly where in the insula the human primary taste cortex is located remains a controversial...
Neurology | Neurosciences | Biomedicine | Top-down influence | Taste coding | Primary taste cortex | Functional MRI | HUMAN BRAIN | CORTICAL REPRESENTATION | SELECTIVE ATTENTION | HUMANS | AVERSIVE TASTE | NEUROSCIENCES | PREFRONTAL CORTEX | PERCEPTION | GUSTATORY CORTEX | UMAMI TASTE | FMRI | Sodium Chloride - pharmacology | Humans | Linear Models | Male | Taste - physiology | Oxygen - blood | Visual Cortex - physiology | Somatosensory Cortex - physiology | Young Adult | Attention - physiology | Magnetic Resonance Imaging | Image Processing, Computer-Assisted | Discrimination (Psychology) | Brain Mapping | Somatosensory Cortex - blood supply | Adult | Female | Sodium Glutamate - pharmacology | Causality | Nonlinear Dynamics | Photic Stimulation | Motion Perception - physiology | Neuroimaging | Olfactory cortex | Usage | Physiological aspects | Taste | Research | Methods
Neurology | Neurosciences | Biomedicine | Top-down influence | Taste coding | Primary taste cortex | Functional MRI | HUMAN BRAIN | CORTICAL REPRESENTATION | SELECTIVE ATTENTION | HUMANS | AVERSIVE TASTE | NEUROSCIENCES | PREFRONTAL CORTEX | PERCEPTION | GUSTATORY CORTEX | UMAMI TASTE | FMRI | Sodium Chloride - pharmacology | Humans | Linear Models | Male | Taste - physiology | Oxygen - blood | Visual Cortex - physiology | Somatosensory Cortex - physiology | Young Adult | Attention - physiology | Magnetic Resonance Imaging | Image Processing, Computer-Assisted | Discrimination (Psychology) | Brain Mapping | Somatosensory Cortex - blood supply | Adult | Female | Sodium Glutamate - pharmacology | Causality | Nonlinear Dynamics | Photic Stimulation | Motion Perception - physiology | Neuroimaging | Olfactory cortex | Usage | Physiological aspects | Taste | Research | Methods
Journal Article
Academic Radiology, ISSN 1076-6332, 2015, Volume 22, Issue 2, pp. 210 - 216
Rationale and Objectives To elucidate the characteristics of four types of tumors, including squamous cell carcinoma (SCC), malignant lymphoma (ML), malignant...
Radiology | ADC | head and neck tumor | DCE-MRI | pharmacokinetic analyses | TK model | TIC | Pharmacokinetic analyses | Head and neck tumor | DIAGNOSTIC-VALUE | HEAD | PERMEABILITY | MALIGNANT-LYMPHOMA | KINETIC-PARAMETERS | CANCER | SALIVARY-GLAND TUMORS | TRACER | BENIGN | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | Diagnosis, Differential | Reproducibility of Results | Carcinoma, Squamous Cell - pathology | Humans | Image Interpretation, Computer-Assisted - methods | Middle Aged | Contrast Media - pharmacokinetics | Male | Jaw Neoplasms - pathology | Young Adult | Algorithms | Models, Biological | Computer Simulation | Sensitivity and Specificity | Aged, 80 and over | Adult | Female | Gadolinium DTPA - pharmacokinetics | Lymphoma - pathology | Aged | Image Enhancement - methods | Diffusion Magnetic Resonance Imaging - methods | Salivary Gland Neoplasms - pathology | Facial Neoplasms - pathology | Care and treatment | Squamous cell carcinoma | Lymphomas | Magnetic resonance imaging
Radiology | ADC | head and neck tumor | DCE-MRI | pharmacokinetic analyses | TK model | TIC | Pharmacokinetic analyses | Head and neck tumor | DIAGNOSTIC-VALUE | HEAD | PERMEABILITY | MALIGNANT-LYMPHOMA | KINETIC-PARAMETERS | CANCER | SALIVARY-GLAND TUMORS | TRACER | BENIGN | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | Diagnosis, Differential | Reproducibility of Results | Carcinoma, Squamous Cell - pathology | Humans | Image Interpretation, Computer-Assisted - methods | Middle Aged | Contrast Media - pharmacokinetics | Male | Jaw Neoplasms - pathology | Young Adult | Algorithms | Models, Biological | Computer Simulation | Sensitivity and Specificity | Aged, 80 and over | Adult | Female | Gadolinium DTPA - pharmacokinetics | Lymphoma - pathology | Aged | Image Enhancement - methods | Diffusion Magnetic Resonance Imaging - methods | Salivary Gland Neoplasms - pathology | Facial Neoplasms - pathology | Care and treatment | Squamous cell carcinoma | Lymphomas | Magnetic resonance imaging
Journal Article
Scientific Reports, ISSN 2045-2322, 03/2016, Volume 6, Issue 1, p. 22985
Droplet digital PCR (ddPCR), a method for measuring target nucleic acid sequence quantity, is useful for determining somatic mutation rates using TaqMan...
PORT-WINE STAIN | PNAS | QUANTIFICATION | DNA | MULTIDISCIPLINARY SCIENCES | STEM-CELL DIFFERENTIATION | GTP-Binding Protein alpha Subunits, Gq-G11 - genetics | Gene Frequency | Humans | Sensitivity and Specificity | Mutant Proteins - genetics | Sturge-Weber Syndrome - diagnosis | Polymerase Chain Reaction - methods | Polymerase chain reaction | DNA probes | Gene frequency | Mutation rates | Leukocytes | Mutation | Peptide nucleic acids | Saliva | Deoxyribonucleic acid--DNA | Blood | Endothelial cells
PORT-WINE STAIN | PNAS | QUANTIFICATION | DNA | MULTIDISCIPLINARY SCIENCES | STEM-CELL DIFFERENTIATION | GTP-Binding Protein alpha Subunits, Gq-G11 - genetics | Gene Frequency | Humans | Sensitivity and Specificity | Mutant Proteins - genetics | Sturge-Weber Syndrome - diagnosis | Polymerase Chain Reaction - methods | Polymerase chain reaction | DNA probes | Gene frequency | Mutation rates | Leukocytes | Mutation | Peptide nucleic acids | Saliva | Deoxyribonucleic acid--DNA | Blood | Endothelial cells
Journal Article
Monthly Notices of the Royal Astronomical Society, ISSN 0035-8711, 01/2018, Volume 473, Issue 2, pp. 1570 - 1575
The dispersion measure (DM) of high-redshift (z greater than or similar to 6) transient objects such as fast radio bursts can be a powerful tool to probe the...
First stars | Reionization | Dark ages | reionization | dark ages | first stars | ENVIRONMENT | MINKOWSKI FUNCTIONALS | LYMAN-CONTINUUM | FAST RADIO-BURST | COSMIC REIONIZATION | FLUCTUATIONS | ASTRONOMY & ASTROPHYSICS | GROWTH | EPOCH | SIMULATIONS | HOST GALAXY | Size distribution | Red shift | Bubbles | Radio bursts | Ionization | Intergalactic media | Potential probes | Probability distribution | Dispersion | Variance | Physics - Cosmology and Nongalactic Astrophysics
First stars | Reionization | Dark ages | reionization | dark ages | first stars | ENVIRONMENT | MINKOWSKI FUNCTIONALS | LYMAN-CONTINUUM | FAST RADIO-BURST | COSMIC REIONIZATION | FLUCTUATIONS | ASTRONOMY & ASTROPHYSICS | GROWTH | EPOCH | SIMULATIONS | HOST GALAXY | Size distribution | Red shift | Bubbles | Radio bursts | Ionization | Intergalactic media | Potential probes | Probability distribution | Dispersion | Variance | Physics - Cosmology and Nongalactic Astrophysics
Journal Article
Nature Genetics, ISSN 1061-4036, 2017, Volume 49, Issue 2, pp. 238 - 248
Arhinia, or absence of the nose, is a rare malformation of unknown etiology that is often accompanied by ocular and reproductive defects. Sequencing of 40...
CHROMOSOME | DOMAIN | METHYLATION | GENETICS & HEREDITY | HYPOPLASIA | FSHD1 | X INACTIVATION | GNRH | INHERITANCE | EXPRESSION | PREDICTION | Genetic Predisposition to Disease - genetics | Nose - abnormalities | Choanal Atresia - genetics | Microphthalmos - genetics | Humans | Child, Preschool | Infant | Male | Muscular Dystrophies - genetics | Mutation - genetics | Chromosomal Proteins, Non-Histone - genetics | Phenotype | Adolescent | Female | Child | Microphthalmos | Gene mutations | Genetic aspects | Gene expression | Health aspects | Risk factors | Studies | Proteins | Consortia | Medical research | Genes | Zebrafish | Genomes | Mutation | Informatics | Muscular dystrophy | Defects
CHROMOSOME | DOMAIN | METHYLATION | GENETICS & HEREDITY | HYPOPLASIA | FSHD1 | X INACTIVATION | GNRH | INHERITANCE | EXPRESSION | PREDICTION | Genetic Predisposition to Disease - genetics | Nose - abnormalities | Choanal Atresia - genetics | Microphthalmos - genetics | Humans | Child, Preschool | Infant | Male | Muscular Dystrophies - genetics | Mutation - genetics | Chromosomal Proteins, Non-Histone - genetics | Phenotype | Adolescent | Female | Child | Microphthalmos | Gene mutations | Genetic aspects | Gene expression | Health aspects | Risk factors | Studies | Proteins | Consortia | Medical research | Genes | Zebrafish | Genomes | Mutation | Informatics | Muscular dystrophy | Defects
Journal Article
Journal of Obstetrics and Gynaecology Research, ISSN 1341-8076, 05/2018, Volume 44, Issue 5, pp. 840 - 851
Aim The aim of this study was to establish the reference values for circulating pregnancy‐associated placental microRNAs in maternal plasma and clarify their...
obstetric management | biological marker | maternal plasma | pregnancy‐associated placental microRNA | reference value | pregnancy-associated placental microRNA | QUANTIFICATION | PLACENTA-SPECIFIC MICRORNAS | CELL-FREE | RNAS | PREECLAMPSIA | IDENTIFICATION | OBSTETRICS & GYNECOLOGY | BIOMARKERS | WOMEN | MIRNAS | FETAL | Hypertension | Pregnancy | MicroRNA | Genetic transcription | Pregnant women | Polymerase chain reaction | Chromosome 19 | Transformation | Placenta | MicroRNAs | MiRNA | Gestation
obstetric management | biological marker | maternal plasma | pregnancy‐associated placental microRNA | reference value | pregnancy-associated placental microRNA | QUANTIFICATION | PLACENTA-SPECIFIC MICRORNAS | CELL-FREE | RNAS | PREECLAMPSIA | IDENTIFICATION | OBSTETRICS & GYNECOLOGY | BIOMARKERS | WOMEN | MIRNAS | FETAL | Hypertension | Pregnancy | MicroRNA | Genetic transcription | Pregnant women | Polymerase chain reaction | Chromosome 19 | Transformation | Placenta | MicroRNAs | MiRNA | Gestation
Journal Article
Nature Genetics, ISSN 1061-4036, 09/2010, Volume 42, Issue 9, pp. 790 - 793
We demonstrate the successful application of exome sequencing to discover a gene for an autosomal dominant disorder, Kabuki syndrome (OMIM%147920). We...
MENTAL-RETARDATION | ABNORMALITIES | GROWTH | GENES | ALR | GENETICS & HEREDITY | CONSTRAINT | CAPTURE | EARS | Mutation - physiology | Genetic Predisposition to Disease | Validation Studies as Topic | Gene Frequency | Humans | Polymorphism, Single Nucleotide | DNA-Binding Proteins - genetics | Neoplasm Proteins - genetics | Sequence Analysis, DNA - methods | Abnormalities, Multiple - genetics | Syndrome | Genetic Linkage | Usage | Methyltransferases | Physiological aspects | Kabuki syndrome | Genetic aspects | Research | Nucleotide sequencing | Risk factors
MENTAL-RETARDATION | ABNORMALITIES | GROWTH | GENES | ALR | GENETICS & HEREDITY | CONSTRAINT | CAPTURE | EARS | Mutation - physiology | Genetic Predisposition to Disease | Validation Studies as Topic | Gene Frequency | Humans | Polymorphism, Single Nucleotide | DNA-Binding Proteins - genetics | Neoplasm Proteins - genetics | Sequence Analysis, DNA - methods | Abnormalities, Multiple - genetics | Syndrome | Genetic Linkage | Usage | Methyltransferases | Physiological aspects | Kabuki syndrome | Genetic aspects | Research | Nucleotide sequencing | Risk factors
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 09/2013, Volume 161, Issue 9, pp. 2234 - 2243
Kabuki syndrome is a congenital anomaly syndrome characterized by developmental delay, intellectual disability, specific facial features including long...
genotype–phenotype correlation | MLL2 | mutation | Kabuki syndrome | KDM6A | Genotype-phenotype correlation | Mutation | METHYLATION | genotype-phenotype correlation | ALR | POLYCOMB | GENE | GENETICS & HEREDITY | UTX | SPECTRUM | EXPRESSION | EARS | Face - abnormalities | Humans | Child, Preschool | Infant | Male | Histone Demethylases - genetics | Exome | Young Adult | Facies | Adult | Female | Neoplasm Proteins - genetics | Nuclear Proteins - genetics | Child | Abnormalities, Multiple - genetics | Infant, Newborn | Genetic Association Studies | Mutation Rate | DNA-Binding Proteins - genetics | Hematologic Diseases - diagnosis | Phenotype | Abnormalities, Multiple - diagnosis | Adolescent | Hematologic Diseases - genetics | High-Throughput Nucleotide Sequencing | Vestibular Diseases - diagnosis | Vestibular Diseases - genetics | Amino Acid Substitution | X Chromosome Inactivation | Growth rate | Congenital defects | Body height
genotype–phenotype correlation | MLL2 | mutation | Kabuki syndrome | KDM6A | Genotype-phenotype correlation | Mutation | METHYLATION | genotype-phenotype correlation | ALR | POLYCOMB | GENE | GENETICS & HEREDITY | UTX | SPECTRUM | EXPRESSION | EARS | Face - abnormalities | Humans | Child, Preschool | Infant | Male | Histone Demethylases - genetics | Exome | Young Adult | Facies | Adult | Female | Neoplasm Proteins - genetics | Nuclear Proteins - genetics | Child | Abnormalities, Multiple - genetics | Infant, Newborn | Genetic Association Studies | Mutation Rate | DNA-Binding Proteins - genetics | Hematologic Diseases - diagnosis | Phenotype | Abnormalities, Multiple - diagnosis | Adolescent | Hematologic Diseases - genetics | High-Throughput Nucleotide Sequencing | Vestibular Diseases - diagnosis | Vestibular Diseases - genetics | Amino Acid Substitution | X Chromosome Inactivation | Growth rate | Congenital defects | Body height
Journal Article