Protein humans abnormalities drug induced. Medical search. Frequent questions

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Anatomy45

Brain Muscle, Skeletal Liver Cells, Cultured Cerebral Cortex Kidney Heart Skin Lung Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 11 Nerve Fibers, Myelinated Chromosomes, Human, Pair 7 Fetus Myocardium Cell Line Neurons Corpus Callosum Bone and Bones Temporal Lobe Cerebellum Heart Ventricles Frontal Lobe Spermatozoa Forearm Feces Embryo, Mammalian Bone Marrow Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 18 Skull Neural Pathways Face Chromosomes, Human, Pair 14 Chromosomes, Human, X Hippocampus Chromosomes, Human, Pair 8 Chromosomes, Human, 6-12 and X Retina Chromosomes, Human, Pair 12 Chromosomes, Human, Pair 5 Lymphocytes Chromosomes, Human Sympathetic Nervous System Prefrontal Cortex

Organisms15

Mice, Inbred C57BL Mice, Knockout Mice, Transgenic Dogs Mice, Mutant Strains Pan troglodytes Hominidae Rats, Sprague-Dawley Macaca mulatta Animals, Newborn Macaca fascicularis Swine Mice, Inbred Strains Gorilla gorilla Mice, Inbred BALB C

Diseases59

Abnormalities, Multiple Chromosome Aberrations Congenital Abnormalities Chromosome Disorders Eye Abnormalities Disease Models, Animal Craniofacial Abnormalities Cardiovascular Abnormalities Syndrome Skin Abnormalities Urogenital Abnormalities Trisomy Musculoskeletal Abnormalities Tooth Abnormalities Translocation, Genetic Aneuploidy Abnormalities, Drug-Induced Sex Chromosome Aberrations Brain Diseases Fetal Diseases Heart Defects, Congenital Chromosome Deletion Nervous System Malformations Intellectual Disability Zoonoses Down Syndrome Agenesis of Corpus Callosum Atrophy Limb Deformities, Congenital Dog Diseases Infertility, Male Acute Disease Digestive System Abnormalities Body Weight Ocular Motility Disorders Disease Progression Nervous System Diseases Heart Diseases Blood Coagulation Disorders Myelodysplastic Syndromes Abnormal Karyotype Obesity Chronic Disease Cardiomyopathies Arrhythmias, Cardiac Hypertension Epilepsy Metabolic Diseases Retinal Diseases Insulin Resistance Monosomy Microcephaly Fetal Death Sturge-Weber Syndrome Genetic Predisposition to Disease Maxillofacial Abnormalities Seizures Respiratory System Abnormalities Jaw Abnormalities

Chemicals and Drugs17

RNA, Messenger Biological Markers Blood Glucose Insulin Transcription Factors DNA Primers Membrane Proteins Nerve Tissue Proteins DNA-Binding Proteins Triglycerides DNA Proteins Oxygen Carrier Proteins Lipids Glucose Immunoglobulin G

Analytical, Diagnostic and Therapeutic Techniques and Equipment62

Magnetic Resonance Imaging Karyotyping Disease Models, Animal In Situ Hybridization, Fluorescence Reference Values Electrocardiography Case-Control Studies Pedigree Analysis of Variance Retrospective Studies Sensitivity and Specificity Prospective Studies Polymerase Chain Reaction Tomography, X-Ray Computed Electroencephalography Cytogenetic Analysis Risk Factors Immunohistochemistry Follow-Up Studies Ultrasonography, Prenatal Echocardiography Blood Pressure Brain Mapping Chromosome Banding Biopsy Prenatal Diagnosis Prognosis Predictive Value of Tests Models, Biological Heart Rate Chromosome Mapping Sequence Analysis, DNA Prevalence Body Weight Reverse Transcriptase Polymerase Chain Reaction Cohort Studies DNA Mutational Analysis Diffusion Magnetic Resonance Imaging Treatment Outcome Severity of Illness Index Neurologic Examination Models, Animal Gene Targeting Organ Size Microscopy, Electron Tomography, Emission-Computed, Single-Photon Electromyography Obesity Administration, Oral Cross-Over Studies Electroretinography Diffusion Tensor Imaging Reproducibility of Results Blood Flow Velocity Double-Blind Method Gene Expression Profiling Blotting, Western In Situ Hybridization Statistics, Nonparametric Flow Cytometry Radiography, Thoracic Imaging, Three-Dimensional

Psychiatry and Psychology12

Schizophrenia Intellectual Disability Behavior, Animal Functional Laterality Neuropsychological Tests Reaction Time Dominance, Cerebral Psychomotor Performance Developmental Disabilities Motor Activity Cognition Disorders Autistic Disorder

Phenomena and Processes74

Chromosome Aberrations Phenotype Mutation Time Factors Pregnancy Trisomy Species Specificity Base Sequence Translocation, Genetic Aneuploidy Sensitivity and Specificity Sex Chromosome Aberrations Homozygote Heterozygote Aging Genotype Amino Acid Sequence Chromosome Deletion Blood Pressure Gene Deletion Dose-Response Relationship, Drug Chromosomes, Human, Pair 13 Heart Rate Signal Transduction Gene Expression Phylogeny Chromosomes, Human, Pair 11 Mosaicism Alleles Gestational Age Gene Expression Regulation, Developmental Body Weight Gene Expression Regulation Functional Laterality Chromosomes, Human, Pair 7 Genetic Variation Regional Blood Flow Organ Size Abnormal Karyotype Hemodynamics Obesity Reaction Time Anisotropy Chromosomes, Human, Pair 17 Genes, Recessive Chromosomes, Human, Pair 18 Dominance, Cerebral Blood Flow Velocity Energy Metabolism Cell Differentiation Chromosomes, Human, Pair 14 Exons Mutation, Missense Insulin Resistance Chromosomes, Human, X Monosomy Psychomotor Performance Homeostasis Tissue Distribution Motor Activity Polymorphism, Genetic Exercise Chromosomes, Human, Pair 8 Chromosomes, Human, 6-12 and X Genetic Predisposition to Disease Chromosomes, Human, Pair 12 Chromosomes, Human, Pair 5 Gene Dosage Biological Evolution Chromosomes, Human Myocardial Contraction Embryonic and Fetal Development Evolution, Molecular Neural Conduction

Disciplines and Occupations2

Immunohistochemistry Cytogenetics

Anthropology, Education, Sociology and Social Phenomena1

Information Science7

Molecular Sequence Data Base Sequence Image Processing, Computer-Assisted Amino Acid Sequence Prevalence Phylogeny Imaging, Three-Dimensional

Named Groups1

Infant, Newborn

Health Care17

Case-Control Studies Analysis of Variance Retrospective Studies Sensitivity and Specificity Prospective Studies Risk Factors Follow-Up Studies Predictive Value of Tests Age Factors Prevalence Cohort Studies Treatment Outcome Severity of Illness Index Cross-Over Studies Reproducibility of Results Double-Blind Method Statistics, Nonparametric

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Information Science Named Groups Health Care

Abnormalities, Multiple Chromosome Aberrations Congenital Abnormalities Magnetic Resonance Imaging Chromosome Disorders Eye Abnormalities Karyotyping Brain Phenotype Mutation Disease Models, Animal Time Factors Pregnancy Craniofacial Abnormalities Cardiovascular Abnormalities Syndrome Molecular Sequence Data Skin Abnormalities Urogenital Abnormalities Trisomy In Situ Hybridization, Fluorescence Musculoskeletal Abnormalities Mice, Inbred C57BL Mice, Knockout Infant, Newborn Tooth Abnormalities Reference Values Species Specificity Electrocardiography Mice, Transgenic Base Sequence Case-Control Studies Translocation, Genetic Aneuploidy Pedigree Analysis of Variance Image Processing, Computer-Assisted Retrospective Studies Dogs Abnormalities, Drug-Induced Sensitivity and Specificity Sex Chromosome Aberrations Mice, Mutant Strains Prospective Studies Brain Diseases Polymerase Chain Reaction Homozygote Pan troglodytes Schizophrenia Tomography, X-Ray Computed Fetal Diseases Heterozygote Electroencephalography Aging Cytogenetic Analysis Risk Factors Genotype Amino Acid Sequence Heart Defects, Congenital Chromosome Deletion Muscle, Skeletal RNA, Messenger Immunohistochemistry Follow-Up Studies Ultrasonography, Prenatal Liver Echocardiography Cells, Cultured Nervous System Malformations Blood Pressure Brain Mapping Chromosome Banding Cytogenetics Cerebral Cortex Kidney Biopsy Hominidae Prenatal Diagnosis Gene Deletion Intellectual Disability Prognosis Heart Skin Biological Markers Predictive Value of Tests Dose-Response Relationship, Drug Models, Biological Lung Chromosomes, Human, Pair 13 Zoonoses Age Factors Behavior, Animal Down Syndrome Agenesis of Corpus Callosum Heart Rate Atrophy Chromosome Mapping Limb Deformities, Congenital Signal Transduction Gene Expression

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