Genes for late onset alzheimer disease. Medical search. Frequent questions

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Anatomy29

Brain Neurofibrillary Tangles Neurofibrils Hippocampus Neurons Substantia Innominata Cerebral Cortex Lewy Bodies Temporal Lobe Neuropil Threads Chromosomes, Human, Pair 21 Sural Nerve Nerve Fibers, Myelinated CA2 Region, Hippocampal Cells, Cultured Frontal Lobe Entorhinal Cortex Microglia Astrocytes PC12 Cells Cerebral Ventricles Parahippocampal Gyrus Cell Line Axons Blood-Brain Barrier Cerebellum Neurites Extrapyramidal Tracts HEK293 Cells

Organisms4

Mice, Transgenic Mice, Inbred C57BL Mice, Knockout Lemur

Diseases47

Alzheimer Disease Plaque, Amyloid Atrophy Dementia Dementia, Vascular Genetic Predisposition to Disease Lewy Body Disease Disease Progression Nerve Degeneration Disease Models, Animal Memory Disorders Cerebral Amyloid Angiopathy Cerebellar Ataxia Prodromal Symptoms Parkinson Disease Tauopathies Neurodegenerative Diseases Huntington Disease Down Syndrome Frontotemporal Dementia Amnesia Ornithine Carbamoyltransferase Deficiency Disease Psychomotor Agitation Osteochondrosis Kluver-Bucy Syndrome Frontotemporal Lobar Degeneration Amyloidosis Brain Diseases Postmortem Changes Cerebrospinal Fluid Otorrhea Spinocerebellar Degenerations Gliosis Aphasia, Primary Progressive Charcot-Marie-Tooth Disease Leukodystrophy, Metachromatic Glucose Metabolism Disorders Friedreich Ataxia Sepsis Hypokinesia Cerebrovascular Disorders Infant, Premature, Diseases Hydrocephalus, Normal Pressure Neuromuscular Diseases Encephalitis Dysarthria Nervous System Diseases Gangliosidoses

Chemicals and Drugs58

Amyloid beta-Peptides tau Proteins Amyloid beta-Protein Precursor Apolipoprotein E4 Amyloid Precursor Protein Secretases Presenilin-1 Apolipoproteins E Amyloid Presenilin-2 Peptide Fragments Memantine Presenilins Aspartic Acid Endopeptidases Aniline Compounds Cholinesterase Inhibitors Amyloidogenic Proteins Biological Markers Nerve Tissue Proteins Protease Nexins Phenylcarbamates Nootropic Agents Indans Clioquinol Thiazoles Apolipoprotein E3 Insulysin Tacrine Monomeric Clathrin Assembly Proteins Membrane Proteins Apolipoprotein E2 Galantamine Myelin P0 Protein Benzothiazoles Neurocalcin LDL-Receptor Related Proteins Glycogen Synthase Kinase 3 Cyclin-Dependent Kinase 5 Clusterin Microtubule-Associated Proteins PrPC Proteins Aluminum Caspase 6 Alzheimer Vaccines Prions Neurofilament Proteins Fluorodeoxyglucose F18 RNA, Messenger Congo Red Endopeptidases Peptides Neuroprotective Agents alpha-Synuclein Protein Isoforms Protein Precursors DNA Neprilysin Ethylene Glycols Acetylcholinesterase

Analytical, Diagnostic and Therapeutic Techniques and Equipment42

Magnetic Resonance Imaging Pedigree Longitudinal Studies Disease Models, Animal Risk Factors Case-Control Studies Autopsy Cohort Studies Genetic Testing Prodromal Symptoms Positron-Emission Tomography Severity of Illness Index Heterozygote Detection Follow-Up Studies Retrospective Studies DNA Mutational Analysis Reference Values Immunohistochemistry Prospective Studies Predictive Value of Tests Models, Biological Analysis of Variance Neurologic Examination Incidence Reproducibility of Results Chromosome Mapping Treatment Outcome Cross-Sectional Studies Enzyme-Linked Immunosorbent Assay Blotting, Western Sensitivity and Specificity Genome-Wide Association Study Early Diagnosis Microscopy, Electron Chi-Square Distribution Polymerase Chain Reaction Prevalence Brain Mapping Logistic Models Immunotherapy, Active Prognosis Electroencephalography

Psychiatry and Psychology22

Alzheimer Disease Dementia Cognition Disorders Neuropsychological Tests Dementia, Vascular Mild Cognitive Impairment Mental Status Schedule Cognition Lewy Body Disease Memory Disorders Huntington Disease Frontotemporal Dementia Amnesia Psychomotor Agitation Memory Kluver-Bucy Syndrome Frontotemporal Lobar Degeneration Psychiatric Status Rating Scales Maze Learning Aphasia, Primary Progressive Cognitive Reserve Brief Psychiatric Rating Scale

Phenomena and Processes39

Aging Genetic Predisposition to Disease Genotype Mutation Time Factors Alleles Brain Chemistry Phenotype Heterozygote Gene Frequency Polymorphism, Single Nucleotide Genetic Linkage Homozygote Chromosomes, Human, Pair 21 Phosphorylation Amino Acid Sequence Lod Score Polymorphism, Genetic Mutation, Missense Haplotypes Genes, Dominant Oxidative Stress Protein Binding Base Sequence Protein Multimerization Protein Structure, Tertiary Exons Solubility Sensitivity and Specificity Proteolysis Genetic Variation Linkage Disequilibrium Protein Processing, Post-Translational Cerebrovascular Circulation Chi-Square Distribution Gene Expression Regulation Point Mutation Genes, Recessive Gene Expression

Disciplines and Occupations1

Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena2

National Institute on Aging (U.S.)Autopsy

Information Science6

Molecular Sequence Data Amino Acid Sequence Incidence Image Processing, Computer-Assisted Base Sequence Prevalence

Named Groups3

Infant, Newborn Caregivers Osteopathic Physicians

Health Care29

Age of Onset National Institute on Aging (U.S.)Longitudinal Studies Age Factors Risk Factors Case-Control Studies Cohort Studies Genetic Testing Severity of Illness Index Family Health Follow-Up Studies Retrospective Studies Prospective Studies Predictive Value of Tests Analysis of Variance Caregivers Incidence Sex Factors Intensive Care Units, Neonatal Reproducibility of Results Treatment Outcome Cross-Sectional Studies Sensitivity and Specificity Genome-Wide Association Study Comorbidity Chi-Square Distribution Prevalence Osteopathic Physicians Logistic Models

Geographicals3

Dominican Republic Caribbean Region United States

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

Alzheimer Disease Amyloid beta-Peptides Age of Onset tau Proteins Amyloid beta-Protein Precursor Brain Neurofibrillary Tangles Apolipoprotein E4 Plaque, Amyloid Atrophy Dementia Cognition Disorders Amyloid Precursor Protein Secretases Presenilin-1 Neuropsychological Tests Apolipoproteins E Amyloid Dementia, Vascular Neurofibrils Mild Cognitive Impairment Magnetic Resonance Imaging Aging National Institute on Aging (U.S.)Presenilin-2 Hippocampus Peptide Fragments Genetic Predisposition to Disease Mental Status Schedule Mice, Transgenic Genotype Neurons Cognition Lewy Body Disease Pedigree Memantine Presenilins Mutation Disease Progression Aspartic Acid Endopeptidases Longitudinal Studies Aniline Compounds Nerve Degeneration Time Factors Cholinesterase Inhibitors Age Factors Disease Models, Animal Alleles Memory Disorders Substantia Innominata Cerebral Cortex Risk Factors Case-Control Studies Cerebral Amyloid Angiopathy Autopsy Cohort Studies Amyloidogenic Proteins Cerebellar Ataxia Biological Markers Brain Chemistry Nerve Tissue Proteins Genetic Testing Prodromal Symptoms Positron-Emission Tomography Severity of Illness Index Protease Nexins Phenylcarbamates Parkinson Disease Tauopathies Neurodegenerative Diseases Huntington Disease Phenotype Heterozygote Nootropic Agents Indans Down Syndrome Gene Frequency Lewy Bodies Clioquinol Thiazoles Frontotemporal Dementia Amnesia Molecular Sequence Data Temporal Lobe Ornithine Carbamoyltransferase Deficiency Disease Polymorphism, Single Nucleotide Heterozygote Detection Family Health Psychomotor Agitation Follow-Up Studies Neuropil Threads Retrospective Studies Osteochondrosis Apolipoprotein E3 Insulysin Memory Genetic Linkage Tacrine DNA Mutational Analysis Homozygote Reference Values

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