Tangier disease gene as abca1. Medical search. Frequent questions

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Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 5 Chromosomes, Human, X X Chromosome Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 20 Chromosomes, Artificial, Yeast Foam Cells Chromosomes, Human, Pair 2 Cell Line Chromosomes, Human, Pair 12 Macrophages BALB 3T3 Cells Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 6 Cells, Cultured Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 11 Cilia Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 22 Brain Chromosomes, Human, Pair 13 Retina Hybrid Cells Chromosomes, Human

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Mice, Knockout Mice, Inbred C57BL Caenorhabditis elegans Mice, Transgenic

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Genetic Diseases, Inborn Disease Tangier Disease Genetic Predisposition to Disease Hepatolenticular Degeneration Huntington Disease Machado-Joseph Disease Menkes Kinky Hair Syndrome Retinal Diseases Ichthyosis, Lamellar Retinitis Pigmentosa Polycystic Kidney Diseases Synostosis Neuronal Ceroid-Lipofuscinoses Eye Diseases, Hereditary Macular Degeneration Neuromuscular Diseases Darier Disease Kidney Diseases, Cystic Muscular Atrophy, Spinal Mitochondrial Diseases Leber Congenital Amaurosis Intellectual Disability Osteochondrodysplasias Syndrome Polycystic Kidney, Autosomal Dominant Rare Diseases Disease Models, Animal Polycystic Kidney, Autosomal Recessive Alzheimer Disease Retinal Degeneration Spinocerebellar Degenerations Atherosclerosis Abnormalities, Multiple Retinal Dystrophies Muscular Dystrophies Lymphoproliferative Disorders Parkinson Disease Hearing Loss, Sensorineural

Chemicals and Drugs44

ATP Binding Cassette Transporter 1 ATP-Binding Cassette Transporters Genetic Markers Apolipoprotein A-I Cholesterol Orphan Nuclear Receptors Nerve Tissue Proteins Lipoproteins, HDL Proteins Hydrocarbons, Fluorinated Eye Proteins TRPP Cation Channels Cation Transport Proteins RNA, Messenger SMN Complex Proteins Nuclear Proteins Carrier Proteins Scavenger Receptors, Class B DNA, Complementary DNA, Satellite Presenilin-2 DNA Probes Phospholipids DNA Primers snRNP Core Proteins RNA Splice Sites Membrane Proteins Receptors, Cytoplasmic and Nuclear DNA Hydroxycholesterols Cholesterol, HDL Adenosine Triphosphatases Lipoproteins Ribonucleoproteins, Small Nuclear Lipofuscin Proteome DNA-Binding Proteins Apolipoproteins E Intracellular Signaling Peptides and Proteins Presenilin-1 Membrane Glycoproteins Codon, Nonsense Probucol Lipids

Analytical, Diagnostic and Therapeutic Techniques and Equipment34

Chromosome Mapping Pedigree Models, Genetic Protein Interaction Mapping DNA Mutational Analysis Genetic Testing Genome-Wide Association Study Genetic Association Studies Gene Expression Profiling Sequence Analysis, DNA Drug Repositioning Heterozygote Detection Physical Chromosome Mapping Molecular Sequence Annotation Polymerase Chain Reaction Oligonucleotide Array Sequence Analysis Cloning, Molecular Likelihood Functions Statistical Distributions Disease Models, Animal Models, Statistical Chromosome Banding Models, Biological Genetic Techniques Case-Control Studies Reproducibility of Results Transfection Sample Size Cluster Analysis Sequence Alignment Matched-Pair Analysis High-Throughput Nucleotide Sequencing Blotting, Northern Reverse Transcriptase Polymerase Chain Reaction

Psychiatry and Psychology5

Huntington Disease Intellectual Disability Alzheimer Disease Nuclear Family Family

Phenomena and Processes103

Genetic Linkage Genetic Markers Genetic Predisposition to Disease Mutation Genome, Human Genes, Recessive Lod Score Phenotype Linkage Disequilibrium Haplotypes Genes, Dominant Exome Alleles Protein Interaction Maps Gene Regulatory Networks Consanguinity Genetic Heterogeneity Polymorphism, Single Nucleotide Genotype Genetic Structures Chromosomes, Human, Pair 4 Algorithms Chromosomes, Human, Pair 16 Homozygote Mutation, Missense Genes Base Sequence Genes, Essential Heterozygote Exons Gene Frequency Trinucleotide Repeats Penetrance Founder Effect Chromosomes, Human, Pair 5 Trinucleotide Repeat Expansion Chromosomes, Human, X Microsatellite Repeats Amino Acid Sequence Lipid Metabolism Polymorphism, Genetic X Chromosome Gene Expression Regulation Chromosomes, Human, Pair 1 Multifactorial Inheritance Genetic Variation Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 20 Chromosomes, Artificial, Yeast Genome Evolution, Molecular Chromosomes, Human, Pair 2 Polymorphism, Restriction Fragment Length Biological Transport Gene Deletion Chromosomes, Human, Pair 12 Conserved Sequence Frameshift Mutation Genes, Duplicate Chromosomes, Human, Pair 17 Statistical Distributions Chromosomes, Human, Pair 6 Polymorphism, Single-Stranded Conformational Sequence Homology, Amino Acid Repetitive Sequences, Amino Acid DNA, Satellite Sequence Tagged Sites Gene Expression Point Mutation Expressed Sequence Tags Genes, Neoplasm RNA Splice Sites Genes, Lethal Quantitative Trait Loci Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 11 Sequence Deletion Recombination, Genetic Gene Library Protein Binding Chromosomes, Human, Pair 19 Sequence Homology, Nucleic Acid Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 22 Inheritance Patterns Transfection Organ Specificity DNA Copy Number Variations Repetitive Sequences, Nucleic Acid Alternative Splicing Protein Structure, Tertiary Genes, Helminth Signal Transduction Introns Chromosomes, Human, Pair 13 Crossing Over, Genetic Codon, Nonsense RNA Interference Gene Dosage Genes, Insect Selection, Genetic Protein Transport Chromosomes, Human

Disciplines and Occupations7

Computational Biology Genetics, Medical Genomics Genetics, Population Molecular Biology Systems Biology Systems Integration

Anthropology, Education, Sociology and Social Phenomena2

Nuclear Family Family

Information Science19

Databases, Genetic Molecular Sequence Data Algorithms Base Sequence Software Amino Acid Sequence Serial Publications Internet Molecular Sequence Annotation Computer Simulation PubMed Data Mining Databases, Factual Databases, Nucleic Acid Support Vector Machines User-Computer Interface Information Storage and Retrieval Systems Integration Database Management Systems

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Health Care13

Genetic Testing Genome-Wide Association Study Age of Onset Family Health Likelihood Functions Statistical Distributions Models, Statistical Case-Control Studies Reproducibility of Results Sample Size Cluster Analysis Matched-Pair Analysis Database Management Systems

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

ATP Binding Cassette Transporter 1 Genetic Diseases, Inborn Disease ATP-Binding Cassette Transporters Genetic Linkage Chromosome Mapping Pedigree Genetic Markers Tangier Disease Databases, Genetic Genetic Predisposition to Disease Hepatolenticular Degeneration Mutation Genome, Human Genes, Recessive Lod Score Huntington Disease Apolipoprotein A-I Phenotype Computational Biology Linkage Disequilibrium Haplotypes Genes, Dominant Exome Models, Genetic Alleles Protein Interaction Maps Cholesterol Protein Interaction Mapping Gene Regulatory Networks Orphan Nuclear Receptors DNA Mutational Analysis Consanguinity Genetic Heterogeneity Polymorphism, Single Nucleotide Genetics, Medical Molecular Sequence Data Machado-Joseph Disease Genetic Testing Genotype Genetic Structures Chromosomes, Human, Pair 4 Genome-Wide Association Study Menkes Kinky Hair Syndrome Algorithms Genetic Association Studies Chromosomes, Human, Pair 16 Homozygote Mutation, Missense Genes Base Sequence Genes, Essential Heterozygote Gene Expression Profiling Exons Nerve Tissue Proteins Lipoproteins, HDL Gene Frequency Retinal Diseases Software Trinucleotide Repeats Ichthyosis, Lamellar Retinitis Pigmentosa Proteins Penetrance Founder Effect Polycystic Kidney Diseases Synostosis Sequence Analysis, DNA Neuronal Ceroid-Lipofuscinoses Chromosomes, Human, Pair 5 Genomics Trinucleotide Repeat Expansion Chromosomes, Human, X Microsatellite Repeats Hydrocarbons, Fluorinated Amino Acid Sequence Eye Diseases, Hereditary Lipid Metabolism Macular Degeneration Eye Proteins Polymorphism, Genetic X Chromosome Drug Repositioning Gene Expression Regulation Chromosomes, Human, Pair 1 Multifactorial Inheritance Neuromuscular Diseases Darier Disease Genetic Variation TRPP Cation Channels Chromosomes, Human, Pair 3 Serial Publications Kidney Diseases, Cystic Muscular Atrophy, Spinal Heterozygote Detection Mitochondrial Diseases Internet Chromosomes, Human, Pair 20 Chromosomes, Artificial, Yeast

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