Endocrinology, ISSN 0013-7227, 2018, Volume 159, Issue 12, pp. 3925 - 3936
Medication for nonalcoholic fatty liver disease (NAFLD) is an unmet need. Glucocorticoid (GC) stress hormones drive fat metabolism in the liver, but both full...
DENSITY | PLATFORM | PROJECT | CHOLESTEROL | METABOLISM | EFFICACY | PATHWAY | ENDOCRINOLOGY & METABOLISM | WEIGHT-GAIN | HEPATIC STEATOSIS | EXPRESSION | Fat metabolism | Glucocorticoids | Liver | Genes | Menopause | Lipids | Stimulation | Genomes | Lipoprotein lipase | Hormones | Lipase | Accumulation | Mimicry | High fat diet | Fatty liver | Modulation | Efflux | Nutrient deficiency | Liver diseases | Gene expression | Fatty acids | Cholesterol | Lipoproteins (very low density) | Gas chromatography | Diet | Low fat diet | Metabolic disorders
DENSITY | PLATFORM | PROJECT | CHOLESTEROL | METABOLISM | EFFICACY | PATHWAY | ENDOCRINOLOGY & METABOLISM | WEIGHT-GAIN | HEPATIC STEATOSIS | EXPRESSION | Fat metabolism | Glucocorticoids | Liver | Genes | Menopause | Lipids | Stimulation | Genomes | Lipoprotein lipase | Hormones | Lipase | Accumulation | Mimicry | High fat diet | Fatty liver | Modulation | Efflux | Nutrient deficiency | Liver diseases | Gene expression | Fatty acids | Cholesterol | Lipoproteins (very low density) | Gas chromatography | Diet | Low fat diet | Metabolic disorders
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Large-scale plasma metabolome analysis reveals alterations in HDL metabolism in migraine
Neurology, ISSN 0028-3878, 01/2019, Volume 92, Issue 16, pp. E1899 - E1911
markdownabstractObjective To identify a plasma metabolomic biomarker signature for migraine. Methods Plasma samples from 8 Dutch cohorts (n = 10,153: 2,800...
BIOMARKERS | RISK-FACTORS | CARDIOVASCULAR-DISEASE | GLOBAL TEST | LIPOPROTEINS | ASSOCIATION | EPIDEMIOLOGY | CLINICAL NEUROLOGY | 101 | 223
BIOMARKERS | RISK-FACTORS | CARDIOVASCULAR-DISEASE | GLOBAL TEST | LIPOPROTEINS | ASSOCIATION | EPIDEMIOLOGY | CLINICAL NEUROLOGY | 101 | 223
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 2019, Volume 294, Issue 1, pp. 1 - 9
RNA-binding proteins (RBPs) play important roles in the control of gene expression and the coordination of different layers of post-transcriptional regulation....
computational biology | next generation sequencing | BIOCHEMISTRY & MOLECULAR BIOLOGY | translation control | RNA-protein interaction | HIDDEN MARKOV-MODELS | BINDING PROTEIN | PREDICTION | CLIP | RNA-binding protein | RNA-seq | SEQUENCE | SITES | SELECTION | statistics
computational biology | next generation sequencing | BIOCHEMISTRY & MOLECULAR BIOLOGY | translation control | RNA-protein interaction | HIDDEN MARKOV-MODELS | BINDING PROTEIN | PREDICTION | CLIP | RNA-binding protein | RNA-seq | SEQUENCE | SITES | SELECTION | statistics
Journal Article
Blood, ISSN 0006-4971, 11/2018, Volume 132, Issue Supplement 1, pp. 2762 - 2762
Abstract Introduction Acute myeloid leukemia (AML) is characterized by uncontrolled proliferation of malignant myeloid progenitor cells in the bone marrow that...
Journal Article
Biomedicine & Pharmacotherapy, ISSN 0753-3322, 12/2018, Volume 108, pp. 1123 - 1134
Mutations in the or genes are the cause of autosomal dominant polycystic kidney disease (ADPKD). The encoded proteins localize within the cell membrane and...
Shear stress | Renal epithelial cell | Mechanotransduction | RNA-seq | Next generation sequencing | Polycystic kidney disease | MEDICINE, RESEARCH & EXPERIMENTAL | RENAL EPITHELIAL-CELLS | ACCELERATES CYSTOGENESIS | INJURY | ENDOCYTOSIS | WNT SIGNALING PATHWAYS | THERAPY | MODELS | GENE | CALCIUM | PHARMACOLOGY & PHARMACY | PRIMARY CILIA | Polycystic Kidney Diseases - genetics | Kidney Tubules, Proximal - pathology | Epithelial Cells - metabolism | Organ Size | Stress, Mechanical | TRPP Cation Channels - deficiency | Male | Gene Expression Profiling | Signal Transduction - genetics | Cilia - metabolism | Animals | Polycystic Kidney Diseases - pathology | Gene Deletion | Transcription, Genetic | Mice | TRPP Cation Channels - metabolism
Shear stress | Renal epithelial cell | Mechanotransduction | RNA-seq | Next generation sequencing | Polycystic kidney disease | MEDICINE, RESEARCH & EXPERIMENTAL | RENAL EPITHELIAL-CELLS | ACCELERATES CYSTOGENESIS | INJURY | ENDOCYTOSIS | WNT SIGNALING PATHWAYS | THERAPY | MODELS | GENE | CALCIUM | PHARMACOLOGY & PHARMACY | PRIMARY CILIA | Polycystic Kidney Diseases - genetics | Kidney Tubules, Proximal - pathology | Epithelial Cells - metabolism | Organ Size | Stress, Mechanical | TRPP Cation Channels - deficiency | Male | Gene Expression Profiling | Signal Transduction - genetics | Cilia - metabolism | Animals | Polycystic Kidney Diseases - pathology | Gene Deletion | Transcription, Genetic | Mice | TRPP Cation Channels - metabolism
Journal Article
Biomedicine & Pharmacotherapy, ISSN 0753-3322, 12/2018, Volume 108, p. 1123
Mutations in the PKD1 or PKD2 genes are the cause of autosomal dominant polycystic kidney disease (ADPKD). The encoded proteins localize within the cell...
RNA sequencing | Anopheles | RNA | Genes | Genetic research | Bone morphogenetic proteins | Comparative analysis | Transforming growth factors | Gene expression | Polycystic kidney disease
RNA sequencing | Anopheles | RNA | Genes | Genetic research | Bone morphogenetic proteins | Comparative analysis | Transforming growth factors | Gene expression | Polycystic kidney disease
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Alternative mRNA transcription, processing, and translation: insights from RNA sequencing
Trends in Genetics, ISSN 0168-9525, 2015, Volume 31, Issue 3, pp. 128 - 139
Highlights • RNA sequencing uncovers mechanisms regulating gene expression. • Use of alternative TSSs, PASs, and exons is the rule. • Alternative translation...
Medical Education | RNA sequencing | translation | alternative splicing | transcriptome | gene expression | alternative polyadenylation | Alternative polyadenylation | Alternative splicing | Translation | Gene expression | Transcriptome | HUMAN TISSUES | MAMMALIAN-CELLS | BREAST-CANCER | 3' UNTRANSLATED REGIONS | OPEN READING FRAMES | IN-VIVO | GENETICS & HEREDITY | SECONDARY STRUCTURE | POLYMERASE-II | ANALYSIS GENE-EXPRESSION | GENOME-WIDE IDENTIFICATION | Protein Biosynthesis | Sequence Analysis, RNA | Alternative Splicing | Humans | RNA, Messenger - genetics | Polyadenylation | Transcription, Genetic | Gene Expression Profiling | High-Throughput Nucleotide Sequencing - methods | Promoter Regions, Genetic - genetics | Genetic translation | Messenger RNA | Genetic transcription
Medical Education | RNA sequencing | translation | alternative splicing | transcriptome | gene expression | alternative polyadenylation | Alternative polyadenylation | Alternative splicing | Translation | Gene expression | Transcriptome | HUMAN TISSUES | MAMMALIAN-CELLS | BREAST-CANCER | 3' UNTRANSLATED REGIONS | OPEN READING FRAMES | IN-VIVO | GENETICS & HEREDITY | SECONDARY STRUCTURE | POLYMERASE-II | ANALYSIS GENE-EXPRESSION | GENOME-WIDE IDENTIFICATION | Protein Biosynthesis | Sequence Analysis, RNA | Alternative Splicing | Humans | RNA, Messenger - genetics | Polyadenylation | Transcription, Genetic | Gene Expression Profiling | High-Throughput Nucleotide Sequencing - methods | Promoter Regions, Genetic - genetics | Genetic translation | Messenger RNA | Genetic transcription
Journal Article
Blood, ISSN 0006-4971, 12/2016, Volume 128, Issue 22, pp. 1701 - 1701
Abstract Background Acute myeloid leukemia (AML) is caused by cooperating oncogenic driver mutations that induce uncontrolled proliferation in combination with...
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 2012, Volume 40, Issue 18, pp. 9272 - 9285
Cells release RNA-carrying vesicles and membrane-free RNA/protein complexes into the extracellular milieu. Horizontal vesicle-mediated transfer of such shuttle...
International (English) | PROTEIN | PARTICLE | MEMBRANE-VESICLES | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSCRIPTION | COMPLEXES | EXOSOMES | MICROVESICLES | MICRORNAS | IDENTIFICATION | LYMPHOCYTES | Coculture Techniques | Dendritic Cells - immunology | Cells, Cultured | RNA, Small Untranslated - physiology | RNA, Transfer - analysis | Sequence Analysis, RNA | MicroRNAs - analysis | RNA, Small Untranslated - analysis | T-Lymphocytes - chemistry | RNA, Small Untranslated - chemistry | Repetitive Sequences, Nucleic Acid | T-Lymphocytes - immunology | Transport Vesicles - chemistry | High-Throughput Nucleotide Sequencing | RNA, Transfer - chemistry | MicroRNAs - chemistry | Dendritic Cells - chemistry | Biotypes | Vesicles | non-coding RNA | tRNA | Data processing | Evolution | miRNA | RNA
International (English) | PROTEIN | PARTICLE | MEMBRANE-VESICLES | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSCRIPTION | COMPLEXES | EXOSOMES | MICROVESICLES | MICRORNAS | IDENTIFICATION | LYMPHOCYTES | Coculture Techniques | Dendritic Cells - immunology | Cells, Cultured | RNA, Small Untranslated - physiology | RNA, Transfer - analysis | Sequence Analysis, RNA | MicroRNAs - analysis | RNA, Small Untranslated - analysis | T-Lymphocytes - chemistry | RNA, Small Untranslated - chemistry | Repetitive Sequences, Nucleic Acid | T-Lymphocytes - immunology | Transport Vesicles - chemistry | High-Throughput Nucleotide Sequencing | RNA, Transfer - chemistry | MicroRNAs - chemistry | Dendritic Cells - chemistry | Biotypes | Vesicles | non-coding RNA | tRNA | Data processing | Evolution | miRNA | RNA
Journal Article
Blood, ISSN 0006-4971, 12/2014, Volume 124, Issue 21, pp. 2658 - 2658
Abstract The erythroid progenitor compartment possesses a large expansion capacity, both in vivo and in vitro, which enables a rapid restoration of peripheral...
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Systematic identification of trans eQTLs as putative drivers of known disease associations
Nature Genetics, ISSN 1061-4036, 10/2013, Volume 45, Issue 10, pp. 1238 - 1243
Identifying the downstream effects of disease-associated SNPs is challenging. To help overcome this problem, we performed expression quantitative trait locus...
POPULATION | INTERFERON | MYOCARDIAL-INFARCTION | VARIANTS | GENE-EXPRESSION | SUSCEPTIBILITY LOCI | LUPUS-ERYTHEMATOSUS | RISK | GENOME-WIDE ASSOCIATION | BLOOD | CELLS | C1Q | POLYMORPHISMS | GENETICS & HEREDITY | CIS | Diabetes Mellitus, Type 1 - genetics | Genetic Predisposition to Disease | Polymorphism, Single Nucleotide | Quantitative Trait Loci | Humans | Lupus Erythematosus, Systemic - genetics | Quantitative trait loci | Genetic aspects | Systemic lupus erythematosus | Single nucleotide polymorphisms | Research | Identification and classification | Studies | Genomes | Disease | Gene expression | Binding sites | Meta-analysis
POPULATION | INTERFERON | MYOCARDIAL-INFARCTION | VARIANTS | GENE-EXPRESSION | SUSCEPTIBILITY LOCI | LUPUS-ERYTHEMATOSUS | RISK | GENOME-WIDE ASSOCIATION | BLOOD | CELLS | C1Q | POLYMORPHISMS | GENETICS & HEREDITY | CIS | Diabetes Mellitus, Type 1 - genetics | Genetic Predisposition to Disease | Polymorphism, Single Nucleotide | Quantitative Trait Loci | Humans | Lupus Erythematosus, Systemic - genetics | Quantitative trait loci | Genetic aspects | Systemic lupus erythematosus | Single nucleotide polymorphisms | Research | Identification and classification | Studies | Genomes | Disease | Gene expression | Binding sites | Meta-analysis
Journal Article
F1000Research, ISSN 2046-1402, 2017, Volume 6, p. 1888
Background: Huntington's Disease (HD) is an incurable disease of the adult brain. Massive changes in gene expression are a prominent feature. Epigenetic...
Journal Article