Polyposis coli an autosomal dominant. Medical search. Frequent questions

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Anatomy29

Chromosomes, Human, Pair 5 Colon Microtubules Intestinal Mucosa Cell Line Rectum Chromosomes, Human, Pair 2 Cell Nucleus Colonic Pouches Chromosomes, Human, Pair 1 Intestines Tumor Cells, Cultured Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 16 Epithelial Cells HCT116 Cells Cell Line, Tumor Cytoplasm COS Cells Cell Surface Extensions Cell Membrane Chromosomes, Human, Pair 4 Cells, Cultured Chromosomes, Human, Pair 10 Chromosomes, Human, Pair 12 Chromosomes, Human, Pair 17 Kidney HT29 Cells Chromosomes, Human, Pair 6

Organisms8

Escherichia coli Escherichia coli O157 Escherichia coli K12 Mice, Inbred C57BL Mice, Mutant Strains Mice, Transgenic Campylobacter coli Mice, Knockout

Diseases71

Adenomatous Polyposis Coli Intestinal Polyposis Intestinal Polyps Polycystic Kidney, Autosomal Dominant Gardner Syndrome Polyps Escherichia coli Infections Intestinal Neoplasms Adenoma Fibromatosis, Aggressive Colorectal Neoplasms Colonic Neoplasms Retinitis Pigmentosa Colonic Polyps Duodenal Neoplasms Fibromatosis, Abdominal Optic Atrophy, Autosomal Dominant Peutz-Jeghers Syndrome Osteoma Syndrome Polycystic Kidney Diseases Cataract CADASIL Neoplastic Syndromes, Hereditary Hamartoma Syndrome, Multiple Neoplasms, Multiple Primary Spinocerebellar Degenerations Genetic Predisposition to Disease Dementia, Multi-Infarct Cerebellar Ataxia Sinusitis Fibroma Spastic Paraplegia, Hereditary Disease Models, Animal Hand Deformities, Congenital Epidermal Cyst Chromosome Disorders Rhinitis Cysts Abnormalities, Multiple Foot Deformities, Congenital Nails, Malformed Telangiectasia, Hereditary Hemorrhagic Cell Transformation, Neoplastic Adenocarcinoma Hearing Loss, Sensorineural Chromosome Deletion Spinocerebellar Ataxias Ectodermal Dysplasia Gastrointestinal Neoplasms Tuberous Sclerosis Keratoderma, Palmoplantar Precancerous Conditions Eye Diseases, Hereditary Disease Progression Charcot-Marie-Tooth Disease Syndactyly Carcinoma Epilepsy, Frontal Lobe Hamartoma Neurofibromatosis 1 Rectal Neoplasms Genetic Diseases, Inborn Skin Diseases, Genetic Deafness Mandibulofacial Dysostosis Asthma, Aspirin-Induced Exostoses, Multiple Hereditary Bone Diseases, Developmental Tooth Abnormalities Hereditary Sensory and Motor Neuropathy

Chemicals and Drugs61

Adenomatous Polyposis Coli Protein beta Catenin Cytoskeletal Proteins Escherichia coli Proteins Axin Protein Trans-Activators TRPP Cation Channels Wnt Proteins TCF Transcription Factors Armadillo Domain Proteins Glycogen Synthase Kinase 3 Transcription Factor 7-Like 2 Protein Axin Signaling Complex Lymphoid Enhancer-Binding Factor 1 Sulindac Glycogen Synthase Kinases Apc1 Subunit, Anaphase-Promoting Complex-Cyclosome Genetic Markers DNA Primers Cadherins Bacterial Proteins Transcription Factors Membrane Proteins DNA-Binding Proteins DNA, Bacterial Repressor Proteins Zebrafish Proteins Codon Eye Proteins Proteins Codon, Nonsense RNA, Messenger Recombinant Proteins Recombinant Fusion Proteins Proto-Oncogene Proteins Microtubule-Associated Proteins Adhesins, Escherichia coli Adaptor Proteins, Signal Transducing gamma-Crystallins Carrier Proteins DNA DNA, Neoplasm beta-Crystallin A Chain Wnt1 Protein Tumor Suppressor Proteins Rhodopsin Neoplasm Proteins DNA Glycosylases Nuclear Proteins Xenopus Proteins Bone Morphogenetic Protein Receptors, Type I Drosophila Proteins alpha Catenin Protein-Serine-Threonine Kinases Peripherins Smad4 Protein Desmoplakins DNA, Complementary Anti-Inflammatory Agents, Non-Steroidal Cyclooxygenase 2 beta-Crystallin B Chain

Analytical, Diagnostic and Therapeutic Techniques and Equipment23

Pedigree DNA Mutational Analysis Chromosome Mapping Polymerase Chain Reaction Colectomy Proctocolectomy, Restorative Cloning, Molecular Genetic Testing Sequence Analysis, DNA Disease Models, Animal Colonic Pouches Transfection Immunohistochemistry Amino Acid Substitution Blotting, Western Models, Biological Reverse Transcriptase Polymerase Chain Reaction Electroretinography Duodenoscopy Microscopy, Fluorescence Models, Genetic Sequence Alignment Models, Molecular

Psychiatry and Psychology1

Dementia, Multi-Infarct

Phenomena and Processes75

Genes, APC Genes, Dominant Mutation Genetic Linkage Phenotype Chromosomes, Human, Pair 5 Base Sequence Germ-Line Mutation Lod Score Mutation, Missense Amino Acid Sequence Frameshift Mutation Heterozygote Genotype Polymorphism, Single-Stranded Conformational Exons Signal Transduction Alleles Loss of Heterozygosity Point Mutation Microsatellite Repeats Haplotypes Protein Binding Wnt Signaling Pathway Genetic Markers Sequence Deletion Genetic Heterogeneity Genes, Bacterial Protein Structure, Tertiary Penetrance Gene Deletion Genetic Predisposition to Disease Genes, Recessive Plasmids Promoter Regions, Genetic Sequence Homology, Amino Acid Codon Chromosomes, Human, Pair 2 Codon, Nonsense Binding Sites Transcription, Genetic Polymorphism, Genetic Transfection Chromosomes, Human, Pair 1 Amino Acid Substitution Chromosomes, Human, Pair 19 Chromosomes, Human, Pair 16 Gene Expression Genes, MCC Gene Expression Regulation, Neoplastic Chromosome Deletion Time Factors Genes, Tumor Suppressor Gene Expression Regulation Phosphorylation Gene Expression Regulation, Bacterial Kinetics Cell Division Protein Transport Down-Regulation Chromosomes, Human, Pair 4 Mutagenesis DNA Methylation Homozygote Chromosomes, Human, Pair 10 Apoptosis Chromosomes, Human, Pair 12 Chromosomes, Human, Pair 17 Operon Cell Proliferation Polymorphism, Restriction Fragment Length Gene Silencing Genes, ras Chromosomes, Human, Pair 6 Genes

Disciplines and Occupations1

Immunohistochemistry

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care3

Family Health Age of Onset Genetic Testing

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

Adenomatous Polyposis Coli Adenomatous Polyposis Coli Protein Genes, APC Intestinal Polyposis Genes, Dominant Intestinal Polyps Polycystic Kidney, Autosomal Dominant beta Catenin Pedigree Mutation Cytoskeletal Proteins Gardner Syndrome Escherichia coli Proteins Axin Protein Polyps Escherichia coli DNA Mutational Analysis Genetic Linkage Escherichia coli Infections Intestinal Neoplasms Adenoma Fibromatosis, Aggressive Phenotype Molecular Sequence Data Chromosomes, Human, Pair 5 Colorectal Neoplasms Base Sequence Trans-Activators Germ-Line Mutation Lod Score Colonic Neoplasms TRPP Cation Channels Wnt Proteins Retinitis Pigmentosa Mutation, Missense Colonic Polyps Duodenal Neoplasms Chromosome Mapping Fibromatosis, Abdominal Amino Acid Sequence Optic Atrophy, Autosomal Dominant Frameshift Mutation Peutz-Jeghers Syndrome TCF Transcription Factors Polymerase Chain Reaction Osteoma Escherichia coli O157 Heterozygote Armadillo Domain Proteins Glycogen Synthase Kinase 3 Genotype Transcription Factor 7-Like 2 Protein Syndrome Polymorphism, Single-Stranded Conformational Exons Signal Transduction Axin Signaling Complex Lymphoid Enhancer-Binding Factor 1 Colectomy Alleles Sulindac Glycogen Synthase Kinases Polycystic Kidney Diseases Loss of Heterozygosity Point Mutation Microsatellite Repeats Cataract CADASIL Colon Haplotypes Protein Binding Wnt Signaling Pathway Neoplastic Syndromes, Hereditary Apc1 Subunit, Anaphase-Promoting Complex-Cyclosome Genetic Markers Proctocolectomy, Restorative DNA Primers Sequence Deletion Genetic Heterogeneity Microtubules Genes, Bacterial Cadherins Intestinal Mucosa Family Health Bacterial Proteins Cloning, Molecular Protein Structure, Tertiary Hamartoma Syndrome, Multiple Neoplasms, Multiple Primary Age of Onset Cell Line Genetic Testing Penetrance Transcription Factors Spinocerebellar Degenerations Escherichia coli K12 Gene Deletion Genetic Predisposition to Disease Genes, Recessive Plasmids

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