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Journal of Molecular Biology, ISSN 0022-2836, 2008, Volume 380, Issue 2, pp. 425 - 436
Journal Article
Amyloid, ISSN 1350-6129, 10/2016, Volume 23, Issue 4, pp. 209 - 213
The Nomenclature Committee of the International Society of Amyloidosis (ISA) met during the XVth Symposium of the Society, 3 July-7 July 2016, Uppsala, Sweden,... 
inclusion body | nomenclature | amyloidosis | Amyloid fibril | amyloid protein | MEDICINE, RESEARCH & EXPERIMENTAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSTHYRETIN AMYLOIDOSIS | MEDICINE, GENERAL & INTERNAL | TRANSMISSION | SEMEN | DISEASE | SENILE SYSTEMIC AMYLOIDOSIS | Staining and Labeling - methods | Prealbumin - genetics | Guidelines as Topic | Apolipoprotein C-III - chemistry | Protein Precursors - chemistry | Humans | Apolipoprotein C-III - metabolism | tau Proteins - metabolism | Amyloidosis - diagnosis | Amyloidogenic Proteins - chemistry | Apolipoprotein C-III - genetics | Apolipoprotein C-II - genetics | tau Proteins - chemistry | Sequence Analysis, Protein | tau Proteins - genetics | Amyloidosis - genetics | Amyloidosis - classification | Prealbumin - chemistry | alpha-Synuclein - genetics | Apolipoprotein C-II - chemistry | Amyloidogenic Proteins - genetics | Biomarkers - metabolism | Gene Expression | Protein Precursors - genetics | Amyloidosis - pathology | Terminology as Topic | Protein Precursors - metabolism | alpha-Synuclein - chemistry | Amyloidogenic Proteins - metabolism | Prealbumin - metabolism | Apolipoprotein C-II - metabolism | Birefringence | Congo Red - chemistry | alpha-Synuclein - metabolism | Coloring Agents - chemistry | Index Medicus | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Cell and Molecular Biology | Cell- och molekylärbiologi
Journal Article
Endocrinology, ISSN 0013-7227, 07/2015, Volume 156, Issue 7, pp. 2632 - 2645
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2012, Volume 7, Issue 11, pp. e49981 - e49981
Journal Article
Toxicology and Applied Pharmacology, ISSN 0041-008X, 2008, Volume 226, Issue 3, pp. 244 - 250
Polybrominated diphenyl ethers (PBDEs) are a class of polyhalogenated aromatic compounds commercially used as fire retardants in consumer products. These... 
Transporters | Thyroid hormone | Cytochrome P450s | Mice | UGT | BDE 47 | POLYCHLORINATED-BIPHENYLS PCBS | thyroid hormone | transporters | cytochrome P450s | NUCLEAR RECEPTORS | MONOCARBOXYLATE TRANSPORTER-8 | mice | SERUM THYROXINE LEVEL | PREGNANE-X-RECEPTOR | UDP-GLUCURONOSYLTRANSFERASE | BROMINATED FLAME RETARDANTS | CONSTITUTIVE ANDROSTANE RECEPTOR | BILIARY-EXCRETION | PHARMACOLOGY & PHARMACY | TOXICOLOGY | MICROSOMAL-ENZYME INDUCERS | Cytochrome P-450 CYP2B1 - genetics | Gene Expression Regulation, Enzymologic - drug effects | Prealbumin - genetics | Aryl Hydrocarbon Hydroxylases - biosynthesis | Protein Kinases - genetics | Liver - enzymology | Aryl Hydrocarbon Hydroxylases - genetics | Thyroxine - blood | RNA, Messenger - metabolism | Dose-Response Relationship, Drug | Cytochrome P450 Family 2 | Glucuronosyltransferase - genetics | Flame Retardants - toxicity | ATP-Binding Cassette Transporters - genetics | Liver - drug effects | Membrane Transport Proteins - genetics | Female | Membrane Transport Proteins - metabolism | Polybrominated Biphenyls - toxicity | Environmental Pollutants - toxicity | Halogenated Diphenyl Ethers | Protein Kinases - biosynthesis | Steroid Hydroxylases - genetics | Thyroid Gland - drug effects | Cytochrome P-450 CYP2B1 - biosynthesis | Mice, Inbred C57BL | Enzyme Induction | ATP-Binding Cassette Transporters - biosynthesis | Endocrine Disruptors - toxicity | Animals | Glucuronosyltransferase - metabolism | Prealbumin - metabolism | ATP Binding Cassette Transporter, Sub-Family B - biosynthesis | Thyroid Gland - metabolism | ATP Binding Cassette Transporter, Sub-Family B - genetics | Steroid Hydroxylases - biosynthesis | RNA | Prealbumin | Triiodothyronine | Index Medicus | KIDNEYS | HOMEOSTASIS | DOSES | PHENYL ETHER | ACUTE EXPOSURE | LIVER | THYROXINE | AROMATICS | MICE | CONSUMER PRODUCTS | RECEPTORS | 60 APPLIED LIFE SCIENCES
Journal Article
Genes, Brain and Behavior, ISSN 1601-1848, 03/2013, Volume 12, Issue 2, pp. 263 - 274
Many studies have utilized the Inbred Long Sleep and Inbred Short Sleep mouse strains to model the genetic influence on initial sensitivity to ethanol. The... 
Inbred Short Sleep | Tophat | Lore | loss‐of‐righting‐reflex | RNA | Inbred Long Sleep | Cufflinks | QTL | Alcohol | eQTL | WGCNA | sequencing | RNA-sequencing | Loss-of-righting-reflex | Lore QTL | STRAINS | ALCOHOL-CONSUMPTION | QTLS | NEUROSCIENCES | loss-of-righting-reflex | QUANTITATIVE TRAIT LOCI | MUTANT MICE | GENETIC DISSECTION | RNA-SEQ | BEHAVIORAL SCIENCES | ETHANOL SENSITIVITY | EXPRESSION | TOOL | Prealbumin - genetics | Transcription, Genetic - drug effects | Enkephalins - metabolism | Dopamine and cAMP-Regulated Phosphoprotein 32 - genetics | Transcriptome | Male | Gene Expression Profiling | Gene Regulatory Networks | Brain - metabolism | Exome | Enkephalins - genetics | Tumor Suppressor Proteins - genetics | Myosins - metabolism | Tumor Suppressor Proteins - metabolism | Protein Precursors - genetics | Sleep - genetics | Mice, Inbred Strains | Myosins - genetics | Sleep - drug effects | Polymorphism, Genetic | Protein Precursors - metabolism | Ethanol - pharmacology | Animals | Sequence Analysis, RNA | Prealbumin - metabolism | High-Throughput Nucleotide Sequencing | Mice | Transcription, Genetic - genetics | Quantitative genetics | Phosphatases | Sleep | Behavior genetics | Genes | Myosin | Muscle proteins | Proteins | Kinases | Index Medicus | Brain | Prodynorphin | Ethanol | Phosphoprotein phosphatase | transthyretin | MAP kinase | Proenkephalin | Ras protein | Potassium channels | Gene expression | Gene polymorphism | DNA microarrays | Neostriatum | Inbreeding | alcohol | RNA-Sequencing
Journal Article
Human Mutation, ISSN 1059-7794, 08/2002, Volume 20, Issue 2, pp. 98 - 109
The inclusion of a mutation in a pathology‐based database such as the Human Gene Mutation Database (HGMD) is a two‐stage process: first, the mutation must... 
molecular epidemiology | AT3 | ARSA | biophysical properties | SERPINC1 | genotype–phenotype | clinical detection | missense mutation | p53 | PROC | TTR | PAH | TP53 | Clinical detection | Genotype-phenotype | Missense mutation | Biophysical properties | Molecular epidemiology | TRANSTHYRETIN | ACTIVE-SITE | CRYSTAL-STRUCTURE | PHENYLKETONURIA | PHENOTYPE | genotype-phenotype | HUMAN PHENYLALANINE-HYDROXYLASE | PREDICTION | GENETICS & HEREDITY | FORCE-FIELD | MUTATIONS | PROTEIN STABILITY CHANGES | Phenylalanine Hydroxylase - genetics | Protein C - chemistry | Prealbumin - genetics | Prealbumin - deficiency | Phenylketonurias - genetics | Protein C - physiology | Amyloid Neuropathies, Familial - metabolism | Humans | Genetic Diseases, Inborn - genetics | Phenylalanine Hydroxylase - deficiency | Databases, Genetic | Antithrombin III Deficiency - genetics | Mutation, Missense - genetics | Antithrombin III - genetics | Arylsulfatases - genetics | Arylsulfatases - physiology | Databases, Protein | Genetic Diseases, Inborn - metabolism | Prealbumin - chemistry | Phenylketonurias - enzymology | Antithrombin III Deficiency - metabolism | Antithrombin III - chemistry | Amyloid Neuropathies, Familial - genetics | Genotype | Phenylalanine Hydroxylase - physiology | Arylsulfatases - chemistry | Protein Structure, Secondary - genetics | Leukodystrophy, Metachromatic - genetics | Phenotype | Protein C Deficiency - metabolism | Genetic Diseases, Inborn - enzymology | Amino Acid Substitution - genetics | Arylsulfatases - deficiency | Leukodystrophy, Metachromatic - enzymology | Antithrombin III - physiology | Models, Genetic | Protein C Deficiency - genetics | Biophysics - methods | Phenylalanine Hydroxylase - chemistry | Prealbumin - physiology | Protein C - genetics | Index Medicus
Journal Article