Nuclear disease genes. Medical search. Frequent questions

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Anatomy26

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 Chromosomes, Human, Pair 12 Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 11 Cilia Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 13 Hybrid Cells Chromosomes, Human Brain Eye Cell Line Retina

Organisms5

Caenorhabditis elegans Drosophila melanogaster Zebrafish Saccharomyces cerevisiae Mice, Knockout

Diseases41

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

Chemicals and Drugs31

Genetic Markers Nerve Tissue Proteins Proteins TRPP Cation Channels Eye Proteins Cation Transport Proteins SMN Complex Proteins Nuclear Proteins DNA, Satellite Presenilin-2 DNA Probes snRNP Core Proteins RNA Splice Sites Carrier Proteins DNA, Complementary Ribonucleoproteins, Small Nuclear DNA Primers DNA Proteome Adenosine Triphosphatases Membrane Proteins Intracellular Signaling Peptides and Proteins Codon, Nonsense Copper Molecular Chaperones Membrane Glycoproteins Presenilin-1 RNA, Messenger RNA-Binding Proteins Nucleotides Amyloid beta-Protein Precursor

Analytical, Diagnostic and Therapeutic Techniques and Equipment41

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 Likelihood Functions Statistical Distributions Cloning, Molecular Polymerase Chain Reaction Models, Statistical Chromosome Banding Oligonucleotide Array Sequence Analysis Genetic Techniques Disease Models, Animal Sample Size Reproducibility of Results Cluster Analysis Matched-Pair Analysis High-Throughput Nucleotide Sequencing Sequence Alignment Case-Control Studies Mutagenesis, Insertional Bayes Theorem ROC Curve Models, Biological Molecular Diagnostic Techniques Blotting, Northern Genetic Therapy In Situ Hybridization Comparative Genomic Hybridization Research Design Probability

Psychiatry and Psychology5

Huntington Disease Intellectual Disability Nuclear Family Family Alzheimer Disease

Phenomena and Processes106

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

Disciplines and Occupations8

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

Anthropology, Education, Sociology and Social Phenomena2

Nuclear Family Family

Information Science20

Databases, Genetic Algorithms Molecular Sequence Data Software Base Sequence Serial Publications Internet Amino Acid Sequence 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 Artificial Intelligence

Named Groups3

Jews Asian Continental Ancestry Group European Continental Ancestry Group

Health Care16

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

Geographicals1

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

Genetic Diseases, Inborn Disease Genetic Linkage Chromosome Mapping Pedigree Genetic Markers Databases, Genetic Hepatolenticular Degeneration Genome, Human Genetic Predisposition to Disease Lod Score Huntington Disease Computational Biology Genes, Recessive Linkage Disequilibrium Phenotype Mutation Haplotypes Genes, Dominant Exome Models, Genetic Protein Interaction Maps Protein Interaction Mapping Gene Regulatory Networks Alleles Genetic Heterogeneity Genetics, Medical Consanguinity Machado-Joseph Disease Genetic Structures DNA Mutational Analysis Chromosomes, Human, Pair 4 Polymorphism, Single Nucleotide Genetic Testing Genome-Wide Association Study Menkes Kinky Hair Syndrome Algorithms Molecular Sequence Data Genotype Genes Genes, Essential Chromosomes, Human, Pair 16 Genetic Association Studies Nerve Tissue Proteins Gene Expression Profiling Software Trinucleotide Repeats Homozygote Penetrance Proteins Base Sequence Polycystic Kidney Diseases Gene Frequency Exons Synostosis Mutation, Missense Neuronal Ceroid-Lipofuscinoses Chromosomes, Human, Pair 5 Heterozygote Genomics Trinucleotide Repeat Expansion Chromosomes, Human, X Founder Effect Sequence Analysis, DNA Retinal Diseases X Chromosome Drug Repositioning Microsatellite Repeats Chromosomes, Human, Pair 1 Multifactorial Inheritance Neuromuscular Diseases Retinitis Pigmentosa Darier Disease TRPP Cation Channels Chromosomes, Human, Pair 3 Serial Publications Eye Proteins Kidney Diseases, Cystic Polymorphism, Genetic Muscular Atrophy, Spinal Heterozygote Detection Mitochondrial Diseases Internet Chromosomes, Human, Pair 20 Eye Diseases, Hereditary Chromosomes, Artificial, Yeast Physical Chromosome Mapping Leber Congenital Amaurosis Genome Intellectual Disability Amino Acid Sequence Osteochondrodysplasias Cation Transport Proteins Genetic Variation Evolution, Molecular Molecular Sequence Annotation Syndrome Chromosomes, Human, Pair 12 SMN Complex Proteins Polymorphism, Restriction Fragment Length

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