Mutations lamin type a. Medical search. Frequent questions

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Anatomy11

Nuclear Lamina Nuclear Envelope Cell Nucleus Cell Line HeLa Cells COS Cells Fibroblasts Cells, Cultured Nuclear Matrix Chromatin Oocytes

Organisms9

Escherichia coli Saccharomyces cerevisiae Drosophila melanogaster Cercopithecus aethiops Cricetinae Mice, Mutant Strains Drosophila Mice, Transgenic Xenopus

Diseases13

Progeria Muscular Dystrophy, Emery-Dreifuss Lipodystrophy Lipodystrophy, Familial Partial Syndrome Genetic Predisposition to Disease Aging, Premature Abnormalities, Multiple Genetic Diseases, X-Linked Retinitis Pigmentosa Cardiomyopathy, Dilated Muscular Dystrophies Porphyrias, Hepatic

Chemicals and Drugs40

Lamin Type A Lamin Type B Lamins Nuclear Proteins Thymopoietins Codon, Nonsense Membrane Proteins DNA Primers DNA-Binding Proteins Mutant Proteins Codon DNA Transcription Factors Bacterial Proteins Recombinant Proteins RNA, Messenger Carrier Proteins DNA, Mitochondrial Proto-Oncogene Proteins B-raf Recombinant Fusion Proteins DNA, Neoplasm Protein Precursors Drosophila Proteins Caspase 6 Intermediate Filament Proteins Proteins Proto-Oncogene Proteins Eye Proteins DNA, Complementary Mutagens Saccharomyces cerevisiae Proteins Ethylnitrosourea RNA Splice Sites Tumor Suppressor Protein p53 Chromatin BRCA2 Protein Repressor Proteins Fungal Proteins ras Proteins Escherichia coli Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment24

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

Phenomena and Processes80

Point Mutation Mutation, Missense Mutation Frameshift Mutation Germ-Line Mutation Mutation Rate Base Sequence Exons Heterozygote Amino Acid Substitution Amino Acid Sequence Alleles Polymorphism, Single-Stranded Conformational Mutagenesis Genotype Homozygote Codon, Nonsense Protein Structure, Tertiary Genes, Recessive Sequence Deletion Genes, Dominant Phenotype Protein Binding Suppression, Genetic Sequence Homology, Amino Acid Binding Sites Codon Gene Deletion Transfection Founder Effect Genes, p53 Genetic Predisposition to Disease Plasmids Genetic Linkage Genes, Lethal Transcription, Genetic Consanguinity Polymorphism, Genetic Introns Promoter Regions, Genetic Exome Genes, BRCA1 Mutagenesis, Insertional Protein Conformation Signal Transduction Phosphorylation Gene Frequency Structure-Activity Relationship Genetic Variation Protein Prenylation Microsatellite Repeats Genes, Bacterial Kinetics Mitosis Conserved Sequence Gene Expression Regulation Recombination, Genetic Drug Resistance, Viral Genes Genes, Suppressor Protein Transport Gene Expression Protein Structure, Secondary Cell Nucleus Shape INDEL Mutation Polymorphism, Restriction Fragment Length Penetrance Temperature Genes, BRCA2 RNA Splicing RNA Splice Sites Selection, Genetic Genes, Fungal Evolution, Molecular DNA Repair Protein Processing, Post-Translational Chromatin Polymorphism, Single Nucleotide Amino Acid Motifs DNA Replication

Disciplines and Occupations1

Immunohistochemistry

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Named Groups1

Health Care4

Genetic Testing Family Health Age of Onset Temperature

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 Lamin Type B Lamins Point Mutation Mutation, Missense Mutation Frameshift Mutation Nuclear Lamina Germ-Line Mutation Nuclear Envelope Progeria Pedigree Nuclear Proteins Mutation Rate Base Sequence Exons Molecular Sequence Data Heterozygote Muscular Dystrophy, Emery-Dreifuss Amino Acid Substitution Thymopoietins Amino Acid Sequence DNA Mutational Analysis Polymerase Chain Reaction Alleles Polymorphism, Single-Stranded Conformational Mutagenesis, Site-Directed Mutagenesis Genotype Homozygote Cell Nucleus Sequence Analysis, DNA Codon, Nonsense Protein Structure, Tertiary Genes, Recessive Cell Line Sequence Deletion Genes, Dominant Phenotype Membrane Proteins DNA Primers Genetic Testing Protein Binding Escherichia coli DNA-Binding Proteins Lipodystrophy Models, Molecular Suppression, Genetic Sequence Homology, Amino Acid Binding Sites Chromosome Mapping Mutant Proteins Codon Gene Deletion Lipodystrophy, Familial Partial Cloning, Molecular DNA Syndrome Transfection Transcription Factors Genetic Complementation Test Founder Effect Sequence Alignment Genes, p53 Genetic Predisposition to Disease Saccharomyces cerevisiae Plasmids HeLa Cells Genetic Linkage Models, Genetic Genes, Lethal Transcription, Genetic Consanguinity Aging, Premature Bacterial Proteins COS Cells Recombinant Proteins Fibroblasts RNA, Messenger Polymorphism, Genetic Introns Carrier Proteins Promoter Regions, Genetic Heterozygote Detection Drosophila melanogaster Exome DNA, Mitochondrial Proto-Oncogene Proteins B-raf Genes, BRCA1 Mutagenesis, Insertional Cells, Cultured Family Health Recombinant Fusion Proteins Nuclear Matrix Protein Conformation Signal Transduction Phosphorylation Gene Frequency DNA, Neoplasm Protein Precursors

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