Mutation that causes progeria. Medical search. Frequent questions

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Anatomy16

Nuclear Lamina Fibroblasts Nuclear Envelope Cell Nucleus Somatotrophs Cell Line Cells, Cultured Skin Heterochromatin Bone and Bones COS Cells X Chromosome HeLa Cells HEK293 Cells Cell Line, Tumor CHO Cells

Organisms11

Escherichia coli Mice, Transgenic Mice, Knockout Saccharomyces cerevisiae Mice, Mutant Strains Drosophila melanogaster Cercopithecus aethiops Cricetinae Drosophila HIV-1 Mice, Inbred C57BL

Diseases28

Aging, Premature Werner Syndrome Bone Demineralization, Pathologic Skin Abnormalities Contracture Lipodystrophy Maxillofacial Abnormalities Syndrome Bone Diseases, Developmental Cockayne Syndrome Disease Models, Animal Progeria Genetic Predisposition to Disease Genetic Diseases, X-Linked Retinitis Pigmentosa Abnormalities, Multiple Eye Abnormalities Chromosome Deletion Osteochondrodysplasias Deafness Genetic Diseases, Inborn Mitochondrial Diseases Colorectal Neoplasms Hearing Loss, Sensorineural Breast Neoplasms Cell Transformation, Neoplastic Lung Neoplasms Ovarian Neoplasms

Chemicals and Drugs69

Lamin Type A Farnesyltranstransferase Protein Precursors Nuclear Proteins Lamins Lamin Type B Metalloendopeptidases Membrane Proteins Codon, Nonsense Alkyl and Aryl Transferases Heterochromatin DNA Primers Enzyme Inhibitors Codon DNA-Binding Proteins Transcription Factors DNA Mutant Proteins Bacterial Proteins DNA, Mitochondrial Proto-Oncogene Proteins B-raf Carrier Proteins DNA, Neoplasm RNA, Messenger Recombinant Proteins Eye Proteins Mutagens Proto-Oncogene Proteins Saccharomyces cerevisiae Proteins Proteins Ethylnitrosourea RNA Splice Sites Recombinant Fusion Proteins Tumor Suppressor Protein p53 BRCA2 Protein Repressor Proteins Fungal Proteins ras Proteins Escherichia coli Proteins DNA, Complementary Drosophila Proteins DNA, Bacterial DNA Transposable Elements Genetic Markers Trans-Activators Codon, Terminator Ethyl Methanesulfonate Arginine Adenosine Triphosphatases Homeodomain Proteins Protein-Serine-Threonine Kinases Alanine Tumor Suppressor Proteins Neoplasm Proteins Glycine BRCA1 Protein Nerve Tissue Proteins Adaptor Proteins, Signal Transducing Serine HIV Reverse Transcriptase Membrane Transport Proteins Cytoskeletal Proteins Cysteine DNA Gyrase Cystic Fibrosis Transmembrane Conductance Regulator MutS Homolog 2 Protein Cell Cycle Proteins DNA, Viral Sodium Channels

Analytical, Diagnostic and Therapeutic Techniques and Equipment25

Pedigree Amino Acid Substitution Polymerase Chain Reaction DNA Mutational Analysis Mutagenesis, Site-Directed Sequence Analysis, DNA Disease Models, Animal Genetic Testing Models, Molecular Chromosome Mapping Genetic Complementation Test Cloning, Molecular Sequence Alignment Models, Genetic Transfection Heterozygote Detection Mutagenesis, Insertional Crosses, Genetic Restriction Mapping Reverse Transcriptase Polymerase Chain Reaction Genetic Association Studies Blotting, Western Models, Biological Immunohistochemistry Blotting, Southern

Psychiatry and Psychology1

Phenomena and Processes111

Point Mutation Mutation, Missense Mutation Cell Nucleus Shape Prenylation Protein Prenylation Frameshift Mutation Germ-Line Mutation Heterozygote Protein Modification, Translational Organelle Shape Phenotype Mutation Rate Exons Base Sequence Cell Aging Amino Acid Substitution Aging Alleles Polymorphism, Single-Stranded Conformational Amino Acid Sequence Codon, Nonsense Genotype Homozygote Mutagenesis DNA Repair Protein Binding Genes, Recessive Sequence Deletion Genes, Dominant Longevity Protein Structure, Tertiary Heterochromatin Suppression, Genetic Codon Binding Sites Sequence Homology, Amino Acid Gene Deletion Founder Effect Genes, p53 Mitosis Genetic Linkage Genetic Predisposition to Disease Consanguinity Plasmids Transfection Genes, Lethal Exome Polymorphism, Genetic Genes, BRCA1 Mutagenesis, Insertional Transcription, Genetic Gene Frequency Promoter Regions, Genetic Genetic Variation Introns Genes, Bacterial Protein Conformation Recombination, Genetic DNA Damage Microsatellite Repeats Structure-Activity Relationship Drug Resistance, Viral Genes Signal Transduction Genes, Suppressor Kinetics Conserved Sequence INDEL Mutation Polymorphism, Restriction Fragment Length Penetrance Temperature Genes, BRCA2 RNA Splicing RNA Splice Sites Selection, Genetic Genes, Fungal Evolution, Molecular Protein Structure, Secondary Polymorphism, Single Nucleotide Gene Expression Gene Expression Regulation Genetic Heterogeneity DNA Transposable Elements Genetic Markers Drug Resistance, Microbial Amino Acid Motifs Phosphorylation Loss of Heterozygosity X Chromosome Codon, Terminator Mosaicism Gene Expression Regulation, Bacterial Chromosome Deletion Virus Replication Protein Transport Drug Resistance Genes, APC Nucleic Acid Conformation Phylogeny Operon Ultraviolet Rays Genes, Regulator Time Factors Dimerization Alternative Splicing Protein Folding Sequence Homology, Nucleic Acid Base Pair Mismatch Gene Dosage Drug Resistance, Bacterial

Disciplines and Occupations1

Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena1

Information Science4

Base Sequence Molecular Sequence Data Amino Acid Sequence Phylogeny

Named Groups2

Jews Asian Continental Ancestry Group

Health Care5

Genetic Testing Family Health Age of Onset Temperature Ultraviolet Rays

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

Lamin Type A Aging, Premature Point Mutation Mutation, Missense Farnesyltranstransferase Mutation Cell Nucleus Shape Nuclear Lamina Werner Syndrome Prenylation Protein Precursors Protein Prenylation Frameshift Mutation Nuclear Proteins Fibroblasts Bone Demineralization, Pathologic Germ-Line Mutation Skin Abnormalities Nuclear Envelope Heterozygote Lamins Pedigree Protein Modification, Translational Lamin Type B Organelle Shape Contracture Phenotype Lipodystrophy Maxillofacial Abnormalities Syndrome Mutation Rate Metalloendopeptidases Exons Cell Nucleus Base Sequence Cell Aging Amino Acid Substitution Membrane Proteins Bone Diseases, Developmental Somatotrophs Aging Polymerase Chain Reaction DNA Mutational Analysis Cockayne Syndrome Molecular Sequence Data Alleles Polymorphism, Single-Stranded Conformational Cell Line Mutagenesis, Site-Directed Cells, Cultured Amino Acid Sequence Codon, Nonsense Genotype Homozygote Mutagenesis Alkyl and Aryl Transferases Sequence Analysis, DNA DNA Repair Disease Models, Animal Protein Binding Genes, Recessive Progeria Skin Sequence Deletion Genes, Dominant Longevity Genetic Testing Protein Structure, Tertiary Heterochromatin DNA Primers Escherichia coli Suppression, Genetic Enzyme Inhibitors Models, Molecular Chromosome Mapping Mice, Transgenic Codon Binding Sites Sequence Homology, Amino Acid DNA-Binding Proteins Genetic Complementation Test Gene Deletion Founder Effect Transcription Factors Genes, p53 Cloning, Molecular Mice, Knockout Mitosis Sequence Alignment DNA Mutant Proteins Genetic Linkage Genetic Predisposition to Disease Saccharomyces cerevisiae Consanguinity Bacterial Proteins Plasmids Models, Genetic Transfection Genes, Lethal

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