Science, ISSN 0036-8075, 5/2008, Volume 320, Issue 5876, pp. 661 - 664
Mutations in mitochondrial DNA (mtDNA) occur at high frequency in human tumors, but whether these mutations alter tumor cell behavior has been unclear. We used...
Tumor cell line | Myeloid cells | Reactive oxygen species | NIH 3T3 cells | Cell lines | HeLa cells | Reports | Mitochondrial DNA | Metastasis | Genetic mutation | Tumors | LUNG-CARCINOMA CELLS | APOPTOSIS | MTDNA | MULTIDISCIPLINARY SCIENCES | MOUSE | PREVENTION | PARAGANGLIOMA | TUMORIGENICITY | BINDING | CANCER | GENOME | Free Radical Scavengers - pharmacology | Reactive Oxygen Species - metabolism | Humans | Hybrid Cells | DNA, Mitochondrial | NADH Dehydrogenase - genetics | NADH Dehydrogenase - metabolism | Electron Transport Complex I - metabolism | Neoplasm Metastasis - genetics | Animals | Electron Transport Complex I - genetics | DNA, Neoplasm | Acetylcysteine - pharmacology | Cell Line, Tumor | Antineoplastic Agents - pharmacology | Mice | HeLa Cells | Mutation | Oxygen | Gene mutations | Influence | Genetic aspects | Research | Properties | Oncology | Cells
Tumor cell line | Myeloid cells | Reactive oxygen species | NIH 3T3 cells | Cell lines | HeLa cells | Reports | Mitochondrial DNA | Metastasis | Genetic mutation | Tumors | LUNG-CARCINOMA CELLS | APOPTOSIS | MTDNA | MULTIDISCIPLINARY SCIENCES | MOUSE | PREVENTION | PARAGANGLIOMA | TUMORIGENICITY | BINDING | CANCER | GENOME | Free Radical Scavengers - pharmacology | Reactive Oxygen Species - metabolism | Humans | Hybrid Cells | DNA, Mitochondrial | NADH Dehydrogenase - genetics | NADH Dehydrogenase - metabolism | Electron Transport Complex I - metabolism | Neoplasm Metastasis - genetics | Animals | Electron Transport Complex I - genetics | DNA, Neoplasm | Acetylcysteine - pharmacology | Cell Line, Tumor | Antineoplastic Agents - pharmacology | Mice | HeLa Cells | Mutation | Oxygen | Gene mutations | Influence | Genetic aspects | Research | Properties | Oncology | Cells
Journal Article
Scientific Reports, ISSN 2045-2322, 05/2015, Volume 5, Issue 1, p. 10434
Age-associated accumulation of somatic mutations in mitochondrial DNA (mtDNA) has been proposed to be responsible for the age-associated mitochondrial...
PLURIPOTENT STEM-CELLS | AGING PHENOTYPES | COMPLEMENTATION | MULTIDISCIPLINARY SCIENCES | MICE | DYSFUNCTION | FUNCTIONAL INTEGRITY | DNA MUTATIONS | Acyltransferases - antagonists & inhibitors | Reactive Oxygen Species - metabolism | Oligonucleotide Array Sequence Analysis | Epigenesis, Genetic | Humans | Infant | DNA, Mitochondrial - analysis | Acyltransferases - metabolism | Acyltransferases - genetics | Cellular Reprogramming | Lipase - antagonists & inhibitors | RNA Interference | Aged, 80 and over | Aging | Cell Differentiation | Induced Pluripotent Stem Cells - cytology | Child | Real-Time Polymerase Chain Reaction | Fibroblasts - metabolism | Induced Pluripotent Stem Cells - metabolism | Cell Line | Glycine Hydroxymethyltransferase - genetics | Oxygen Consumption | Glycine - biosynthesis | Gene Dosage | Mitochondria - metabolism | Lipase - metabolism | Glycine Hydroxymethyltransferase - metabolism | Sequence Analysis, DNA | Phenotype | Fibroblasts - cytology | Lipase - genetics | RNA, Small Interfering - metabolism | Genomes | Mitochondrial DNA | Glycine | Defects | DNA microarrays | Stem cells | Fibroblasts | Epigenetics | Mutation | Electron transport | Respiration | Age | Pluripotency | Inhibitory postsynaptic potentials | Geriatrics
PLURIPOTENT STEM-CELLS | AGING PHENOTYPES | COMPLEMENTATION | MULTIDISCIPLINARY SCIENCES | MICE | DYSFUNCTION | FUNCTIONAL INTEGRITY | DNA MUTATIONS | Acyltransferases - antagonists & inhibitors | Reactive Oxygen Species - metabolism | Oligonucleotide Array Sequence Analysis | Epigenesis, Genetic | Humans | Infant | DNA, Mitochondrial - analysis | Acyltransferases - metabolism | Acyltransferases - genetics | Cellular Reprogramming | Lipase - antagonists & inhibitors | RNA Interference | Aged, 80 and over | Aging | Cell Differentiation | Induced Pluripotent Stem Cells - cytology | Child | Real-Time Polymerase Chain Reaction | Fibroblasts - metabolism | Induced Pluripotent Stem Cells - metabolism | Cell Line | Glycine Hydroxymethyltransferase - genetics | Oxygen Consumption | Glycine - biosynthesis | Gene Dosage | Mitochondria - metabolism | Lipase - metabolism | Glycine Hydroxymethyltransferase - metabolism | Sequence Analysis, DNA | Phenotype | Fibroblasts - cytology | Lipase - genetics | RNA, Small Interfering - metabolism | Genomes | Mitochondrial DNA | Glycine | Defects | DNA microarrays | Stem cells | Fibroblasts | Epigenetics | Mutation | Electron transport | Respiration | Age | Pluripotency | Inhibitory postsynaptic potentials | Geriatrics
Journal Article
Human Pathology, ISSN 0046-8177, 2012, Volume 43, Issue 3, pp. 356 - 363
Summary The diagnosis of alveolar soft part sarcoma is commonly based on characteristic histology and distinctive periodic acid–Schiff–positive crystals;...
Pathology | Immunohistochemistry | ASPSCR1-TFE3 fusion transcript | Differential diagnosis | Alveolar soft part sarcoma | RT-PCR | GENE FUSIONS | IMMUNOREACTIVITY | NEOPLASMS | PATHOLOGY | Diagnosis, Differential | Oncogene Proteins, Fusion - metabolism | Humans | Middle Aged | Gene Fusion | Male | Paraffin Embedding | Sarcoma, Alveolar Soft Part - genetics | Young Adult | Cell Nucleus - metabolism | Oncogene Proteins, Fusion - genetics | Adolescent | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - genetics | Basigin - metabolism | Adult | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - metabolism | Female | Sarcoma, Alveolar Soft Part - metabolism | Sarcoma, Alveolar Soft Part - diagnosis | Polymerase chain reaction | Sarcoma | Comparative analysis | Methods | Cancer | Proteins | Tumors
Pathology | Immunohistochemistry | ASPSCR1-TFE3 fusion transcript | Differential diagnosis | Alveolar soft part sarcoma | RT-PCR | GENE FUSIONS | IMMUNOREACTIVITY | NEOPLASMS | PATHOLOGY | Diagnosis, Differential | Oncogene Proteins, Fusion - metabolism | Humans | Middle Aged | Gene Fusion | Male | Paraffin Embedding | Sarcoma, Alveolar Soft Part - genetics | Young Adult | Cell Nucleus - metabolism | Oncogene Proteins, Fusion - genetics | Adolescent | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - genetics | Basigin - metabolism | Adult | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - metabolism | Female | Sarcoma, Alveolar Soft Part - metabolism | Sarcoma, Alveolar Soft Part - diagnosis | Polymerase chain reaction | Sarcoma | Comparative analysis | Methods | Cancer | Proteins | Tumors
Journal Article
Psychiatry and Clinical Neurosciences, ISSN 1323-1316, 08/2014, Volume 68, Issue 8, pp. 631 - 639
Aim Postnatal depression has demonstrated long‐term consequences on child cognitive and emotional development; however, the link between maternal and child...
bonding disorder | Mother‐to‐Infant Bonding Scale | Edinburgh Postnatal Depression Scale | post‐partum period | maternal mood | Mother-to-Infant Bonding Scale | post-partum period | CHILDBEARING | PSYCHIATRY | POSTNATAL DEPRESSION | DISORDERS | COGNITIVE-DEVELOPMENT | JAPANESE WOMEN | NEUROSCIENCES | CLINICAL NEUROLOGY | IMPACT | MOOD | INVENTORY | CHILDBIRTH | BONDING SCALE | Pregnancy | Pregnancy Complications - psychology | Young Adult | Mother-Child Relations - psychology | Object Attachment | Depression, Postpartum - psychology | Prospective Studies | Humans | Self Report | Depression - psychology | Adult | Female | Postpartum depression | Child development | Pregnant women | Analysis | Postpartum period
bonding disorder | Mother‐to‐Infant Bonding Scale | Edinburgh Postnatal Depression Scale | post‐partum period | maternal mood | Mother-to-Infant Bonding Scale | post-partum period | CHILDBEARING | PSYCHIATRY | POSTNATAL DEPRESSION | DISORDERS | COGNITIVE-DEVELOPMENT | JAPANESE WOMEN | NEUROSCIENCES | CLINICAL NEUROLOGY | IMPACT | MOOD | INVENTORY | CHILDBIRTH | BONDING SCALE | Pregnancy | Pregnancy Complications - psychology | Young Adult | Mother-Child Relations - psychology | Object Attachment | Depression, Postpartum - psychology | Prospective Studies | Humans | Self Report | Depression - psychology | Adult | Female | Postpartum depression | Child development | Pregnant women | Analysis | Postpartum period
Journal Article
JOURNAL OF NUCLEAR MEDICINE, ISSN 0161-5505, 11/2012, Volume 53, Issue 11, pp. 1716 - 1722
The aim of this study was to investigate the effects of the point-spread function (PSF) and time-of-flight (TOF) on improving F-18-FDG PET/CT images in...
TOMOGRAPHY | noise-equivalent counts | DOPED LUTETIUM OXYORTHOSILICATE | point-spread function | NOISE | image quality | LUNG-CANCER | IMPACT | POSITRON-EMISSION | SCAN DURATION | time-of-flight | PET/CT | F-18-FDG | PATIENT WEIGHT | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | EQUIVALENT | Time Factors | Humans | Middle Aged | Multimodal Imaging - methods | Tomography, X-Ray Computed | Colorectal Neoplasms - diagnostic imaging | Positron-Emission Tomography | Image Processing, Computer-Assisted - methods | Phantoms, Imaging | Quality Control | Studies | Algorithms | Fluorides | Noise | Scanners
TOMOGRAPHY | noise-equivalent counts | DOPED LUTETIUM OXYORTHOSILICATE | point-spread function | NOISE | image quality | LUNG-CANCER | IMPACT | POSITRON-EMISSION | SCAN DURATION | time-of-flight | PET/CT | F-18-FDG | PATIENT WEIGHT | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | EQUIVALENT | Time Factors | Humans | Middle Aged | Multimodal Imaging - methods | Tomography, X-Ray Computed | Colorectal Neoplasms - diagnostic imaging | Positron-Emission Tomography | Image Processing, Computer-Assisted - methods | Phantoms, Imaging | Quality Control | Studies | Algorithms | Fluorides | Noise | Scanners
Journal Article
Journal of Epidemiology, ISSN 0917-5040, 09/2017, Volume 27, Issue 9, pp. 447 - 450
Leber hereditary optic neuropathy (LHON) is a maternally inherited optic neuropathy that leads to central loss of vision, predominantly in young males. Most...
Annual incidence | Leber hereditary optic neuropathy | Penetrance | Mitochondrial DNA | Gender proportion | POPULATION | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | CLINICAL-FEATURES | MUTATIONS | MITOCHONDRIAL-DNA | Japan - epidemiology | DNA, Mitochondrial - genetics | Health Surveys | Humans | Optic Atrophy, Hereditary, Leber - epidemiology | Adult | Female | Male | Optic Atrophy, Hereditary, Leber - genetics | Mutation | Incidence | Confidence intervals | Optic neuropathy | Mathematical analysis | Neuropathy | Males | Females | Epidemiology | Eyes & eyesight | Deoxyribonucleic acid--DNA
Annual incidence | Leber hereditary optic neuropathy | Penetrance | Mitochondrial DNA | Gender proportion | POPULATION | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | CLINICAL-FEATURES | MUTATIONS | MITOCHONDRIAL-DNA | Japan - epidemiology | DNA, Mitochondrial - genetics | Health Surveys | Humans | Optic Atrophy, Hereditary, Leber - epidemiology | Adult | Female | Male | Optic Atrophy, Hereditary, Leber - genetics | Mutation | Incidence | Confidence intervals | Optic neuropathy | Mathematical analysis | Neuropathy | Males | Females | Epidemiology | Eyes & eyesight | Deoxyribonucleic acid--DNA
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 08/2010, Volume 120, Issue 8, pp. 2867 - 2875
Ticks are ectoparasitic arthropods that can transmit a variety of microorganisms to humans and animals during blood feeding, causing serious infectious...
MEDICINE, RESEARCH & EXPERIMENTAL | MOUSE BASOPHIL | MAST CELL-DEFICIENT | CHRONIC ALLERGIC INFLAMMATION | IN-VIVO | TRYPTASE MMCP-6 | HAEMAPHYSALIS-LONGICORNIS TICKS | GUINEA-PIGS | PATHOGEN TRANSMISSION | HOST-RESISTANCE | DERMACENTOR-VARIABILIS | Receptors, IgE - physiology | Animals | Mice, Inbred C57BL | Basophils - physiology | Mast Cells - physiology | Mice | Immunoglobulin E - blood | Tick Infestations - immunology | Tryptases - physiology | Prevention | Lyme disease | Proteases | Basophils | Cellular immunity | Research | Properties | Risk factors
MEDICINE, RESEARCH & EXPERIMENTAL | MOUSE BASOPHIL | MAST CELL-DEFICIENT | CHRONIC ALLERGIC INFLAMMATION | IN-VIVO | TRYPTASE MMCP-6 | HAEMAPHYSALIS-LONGICORNIS TICKS | GUINEA-PIGS | PATHOGEN TRANSMISSION | HOST-RESISTANCE | DERMACENTOR-VARIABILIS | Receptors, IgE - physiology | Animals | Mice, Inbred C57BL | Basophils - physiology | Mast Cells - physiology | Mice | Immunoglobulin E - blood | Tick Infestations - immunology | Tryptases - physiology | Prevention | Lyme disease | Proteases | Basophils | Cellular immunity | Research | Properties | Risk factors
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 09/2017, Volume 114, Issue 37, pp. E7697 - E7706
Cancer cells alter their metabolism for the production of precursors of macromolecules. However, the control mechanisms underlying this reprogramming are...
Metabolomics | Metabolism | MYC | Colorectal cancer | Omics | CELLS | colorectal cancer | MITOCHONDRIAL BIOGENESIS | PHOSPHORYLATION | MULTIDISCIPLINARY SCIENCES | TUMORS | omics | REPRESSION | GENE | metabolomics | MUTATION | metabolism | CARCINOMA | EXPRESSION | Adenoma - genetics | Colorectal Neoplasms - genetics | Humans | Carcinogenesis - genetics | Cell Proliferation - physiology | Transcriptome | Male | Genes, myc | Pyrimidines - biosynthesis | Carcinogenesis - metabolism | Metabolomics - methods | Proto-Oncogene Proteins c-myc - metabolism | Adenoma - metabolism | Animals | Female | Mice | Proto-Oncogene Proteins c-myc - genetics | Colorectal Neoplasms - metabolism | Disease Models, Animal | Physiological aspects | Health aspects | Methods | Cancer cells | Biological Sciences | PNAS Plus
Metabolomics | Metabolism | MYC | Colorectal cancer | Omics | CELLS | colorectal cancer | MITOCHONDRIAL BIOGENESIS | PHOSPHORYLATION | MULTIDISCIPLINARY SCIENCES | TUMORS | omics | REPRESSION | GENE | metabolomics | MUTATION | metabolism | CARCINOMA | EXPRESSION | Adenoma - genetics | Colorectal Neoplasms - genetics | Humans | Carcinogenesis - genetics | Cell Proliferation - physiology | Transcriptome | Male | Genes, myc | Pyrimidines - biosynthesis | Carcinogenesis - metabolism | Metabolomics - methods | Proto-Oncogene Proteins c-myc - metabolism | Adenoma - metabolism | Animals | Female | Mice | Proto-Oncogene Proteins c-myc - genetics | Colorectal Neoplasms - metabolism | Disease Models, Animal | Physiological aspects | Health aspects | Methods | Cancer cells | Biological Sciences | PNAS Plus
Journal Article
9.
Full Text
Emergence of nontrivial magnetic excitations in a spin-liquid state of kagomé volborthite
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 8/2016, Volume 113, Issue 31, pp. 8653 - 8657
When quantum fluctuations destroy underlying long-range ordered states, novel quantum states emerge. Spin-liquid (SL) states of frustrated quantum...
FIELDS | thermal transport | CAF2 | MULTIDISCIPLINARY SCIENCES | THERMAL HALL CONDUCTIVITY | PHONON-SCATTERING | spin liquid | QUANTUM MAGNET | frustrated magnetism | LATTICE | TB3GA5O12 | Physics - Strongly Correlated Electrons | Physical Sciences
FIELDS | thermal transport | CAF2 | MULTIDISCIPLINARY SCIENCES | THERMAL HALL CONDUCTIVITY | PHONON-SCATTERING | spin liquid | QUANTUM MAGNET | frustrated magnetism | LATTICE | TB3GA5O12 | Physics - Strongly Correlated Electrons | Physical Sciences
Journal Article
ISPRS International Journal of Geo-Information, ISSN 2220-9964, 10/2016, Volume 5, Issue 10, p. 182
Road anomalies, such as cracks, pits and puddles, have generally been identified by citizen reports made by e-mail or telephone; however, it is difficult for...
road anomaly | smartphone | opportunistic sensing | avoidance | behavior recognition
road anomaly | smartphone | opportunistic sensing | avoidance | behavior recognition
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 02/2019, Volume 39, Issue 9, pp. 1588 - 1604
Neurons have high plasticity in developmental and juvenile stages that decreases in adulthood. Mitochondrial dynamics are highly important in neurons to...
MFN2 | Progressive neurodegeneration | Hyperactivity | Mitochondrial dynamics | Cognitive impairment | MITOCHONDRIAL FUSION | hyperactivity | PHENOTYPES | NEUROSCIENCES | MOUSE MODELS | mitochondrial dynamics | DRP1 | PATHOGENESIS | DISEASES | DNA | cognitive impairment | MICE | MUTATIONS | progressive neurodegeneration | Lethal effects | Cell survival | Neurodegenerative diseases | Neurons | Abnormalities | Mimicry | Neurological diseases | Learning | Mitochondria | Neurodegeneration | Dependence | Plasticity (developmental) | Brain damage | Brain injury
MFN2 | Progressive neurodegeneration | Hyperactivity | Mitochondrial dynamics | Cognitive impairment | MITOCHONDRIAL FUSION | hyperactivity | PHENOTYPES | NEUROSCIENCES | MOUSE MODELS | mitochondrial dynamics | DRP1 | PATHOGENESIS | DISEASES | DNA | cognitive impairment | MICE | MUTATIONS | progressive neurodegeneration | Lethal effects | Cell survival | Neurodegenerative diseases | Neurons | Abnormalities | Mimicry | Neurological diseases | Learning | Mitochondria | Neurodegeneration | Dependence | Plasticity (developmental) | Brain damage | Brain injury
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2019, Volume 14, Issue 3, p. e0213283
Accumulation of mutations in mitochondrial DNA (mtDNA) is thought to be responsible for mitochondrial, and other, diseases and biological phenomena, such as...
APOPTOSIS | HSP60 | DISEASES | CLONAL EXPANSION | MULTIDISCIPLINARY SCIENCES | MICE | GENERATION | EXPLAINS | DYSFUNCTION | DRIFT | MTDNA MUTATIONS | Mitochondrial diseases | Genetic aspects | Mitochondrial DNA | Research | Gene mutations | Cell lines | Animal models | Complex formation | Cybrids | Disease | DNA polymerase | Homology | Mutation rates | Tissues | Defects | Proteins | Polyethylene glycol | Aging | Deoxyribonucleic acid--DNA | Polypeptides | Neurodegenerative diseases | Abnormalities | Diabetes mellitus | Organs | Diseases | Neurological diseases | Environmental science | Mutagenesis | Quality control | Mutation | Respiration | Platelets | Cancer | Deoxyribonucleic acid | DNA
APOPTOSIS | HSP60 | DISEASES | CLONAL EXPANSION | MULTIDISCIPLINARY SCIENCES | MICE | GENERATION | EXPLAINS | DYSFUNCTION | DRIFT | MTDNA MUTATIONS | Mitochondrial diseases | Genetic aspects | Mitochondrial DNA | Research | Gene mutations | Cell lines | Animal models | Complex formation | Cybrids | Disease | DNA polymerase | Homology | Mutation rates | Tissues | Defects | Proteins | Polyethylene glycol | Aging | Deoxyribonucleic acid--DNA | Polypeptides | Neurodegenerative diseases | Abnormalities | Diabetes mellitus | Organs | Diseases | Neurological diseases | Environmental science | Mutagenesis | Quality control | Mutation | Respiration | Platelets | Cancer | Deoxyribonucleic acid | DNA
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 425 - 8
Accumulation of somatic mutations in mitochondrial DNA (mtDNA) has been proposed to be responsible for human aging and age-associated mitochondrial respiration...
Translation | tRNA fMet | Serine | Gene regulation | Lethality | Mitochondrial DNA | Embryos | Defects | Hypotheses | Fibroblasts | Aging | Epigenetics | Glycine C-acetyltransferase | Acetyltransferase | Mutation | Electron transport | Respiration | Age | Geriatrics
Translation | tRNA fMet | Serine | Gene regulation | Lethality | Mitochondrial DNA | Embryos | Defects | Hypotheses | Fibroblasts | Aging | Epigenetics | Glycine C-acetyltransferase | Acetyltransferase | Mutation | Electron transport | Respiration | Age | Geriatrics
Journal Article
Neuroscience Research, ISSN 0168-0102, 12/2015, Volume 101, pp. 15 - 23
Environmental factors during perinatal period have various effects on behavior. The present study examined the effects of prenatal stress and neonatal handling...
Neonatal handling | Anxiety | Serotonin receptor | Spatial learning | Prenatal stress | BRAIN-REGIONS | 5-HT1A RECEPTORS | BEHAVIOR | RECEPTOR EXPRESSION | GESTATIONAL STRESS | POSTNATAL STIMULATION | NEUROSCIENCES | HIPPOCAMPUS | MATERNAL STRESS | RAT-BRAIN | GRANULE CELLS | Animals, Newborn | Frontal Lobe - metabolism | Prenatal Exposure Delayed Effects - psychology | Mice, Inbred C57BL | Receptor, Serotonin, 5-HT2C - metabolism | Anxiety - physiopathology | Male | Prenatal Exposure Delayed Effects - physiopathology | RNA, Messenger - metabolism | Prenatal Exposure Delayed Effects - metabolism | Receptors, Serotonin - metabolism | Spatial Learning - physiology | Pregnancy | Hippocampus - metabolism | Animals | Stress, Psychological - metabolism | Maternal Behavior | Female | Mice | Handling (Psychology) | Receptor, Serotonin, 5-HT2A - metabolism | Anxiety - metabolism | Receptor, Serotonin, 5-HT1A - metabolism | Stress, Psychological - physiopathology | Infants (Newborn) | Serotonin | Pregnant women
Neonatal handling | Anxiety | Serotonin receptor | Spatial learning | Prenatal stress | BRAIN-REGIONS | 5-HT1A RECEPTORS | BEHAVIOR | RECEPTOR EXPRESSION | GESTATIONAL STRESS | POSTNATAL STIMULATION | NEUROSCIENCES | HIPPOCAMPUS | MATERNAL STRESS | RAT-BRAIN | GRANULE CELLS | Animals, Newborn | Frontal Lobe - metabolism | Prenatal Exposure Delayed Effects - psychology | Mice, Inbred C57BL | Receptor, Serotonin, 5-HT2C - metabolism | Anxiety - physiopathology | Male | Prenatal Exposure Delayed Effects - physiopathology | RNA, Messenger - metabolism | Prenatal Exposure Delayed Effects - metabolism | Receptors, Serotonin - metabolism | Spatial Learning - physiology | Pregnancy | Hippocampus - metabolism | Animals | Stress, Psychological - metabolism | Maternal Behavior | Female | Mice | Handling (Psychology) | Receptor, Serotonin, 5-HT2A - metabolism | Anxiety - metabolism | Receptor, Serotonin, 5-HT1A - metabolism | Stress, Psychological - physiopathology | Infants (Newborn) | Serotonin | Pregnant women
Journal Article
SCIENTIFIC REPORTS, ISSN 2045-2322, 11/2019, Volume 9, Issue 1, pp. 1 - 11
In a previous study, we proposed that age-related mitochondrial respiration defects observed in elderly subjects are partially due to age-associated...
MITOCHONDRIAL-DNA MUTATIONS | NUCLEAR | METABOANALYST | DISEASES | NEURAL-TUBE DEFECTS | MULTIDISCIPLINARY SCIENCES | MICE | PHENOTYPES | DYSFUNCTION | DEFICIENCY | DELETION | Taurine | Liver diseases | Growth rate | Anemia | Serine | Cell division | Lethality | Embryo fibroblasts | Nucleotides | Embryos | Defects | Mitochondria | Erythroblasts | Rodents | Metabolic pathways | Electron transport | Respiration | Age | Geriatrics
MITOCHONDRIAL-DNA MUTATIONS | NUCLEAR | METABOANALYST | DISEASES | NEURAL-TUBE DEFECTS | MULTIDISCIPLINARY SCIENCES | MICE | PHENOTYPES | DYSFUNCTION | DEFICIENCY | DELETION | Taurine | Liver diseases | Growth rate | Anemia | Serine | Cell division | Lethality | Embryo fibroblasts | Nucleotides | Embryos | Defects | Mitochondria | Erythroblasts | Rodents | Metabolic pathways | Electron transport | Respiration | Age | Geriatrics
Journal Article