Role x inactivation in all cells. Medical search. Frequent questions

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Anatomy29

X Chromosome Chromosomes, Human, X Hybrid Cells Ring Chromosomes Sex Chromosomes Embryo, Mammalian Stem Cells Cell Line Chromosomes, Mammalian Y Chromosome Chromosomes, Artificial, Yeast Blastocyst Cells, Cultured Fibroblasts Chromatin Placenta Trophoblasts Chromosomes, Artificial, Bacterial Embryonic Stem Cells Chromosomes, Human, Pair 7 Lymphocytes Clone Cells Oocytes Neurons Liver Cell Line, Tumor Myocardium Cell Membrane Tumor Cells, Cultured

Organisms12

Equidae Mice, Transgenic Mice, Inbred C57BL Escherichia coli Xenopus laevis Mice, Knockout Xenopus Rabbits Cattle Decapodiformes Rats, Sprague-Dawley Cricetinae

Diseases10

Sex Chromosome Aberrations Incontinentia Pigmenti Turner Syndrome Ring Chromosomes Orofaciodigital Syndromes Rett Syndrome Intellectual Disability Pelizaeus-Merzbacher Disease Genetic Diseases, X-Linked Translocation, Genetic

Chemicals and Drugs80

RNA, Long Noncoding RNA, Untranslated Histones Arylsulfatases Receptors, Androgen Polycomb-Group Proteins Steryl-Sulfatase Transcription Factors DAX-1 Orphan Nuclear Receptor Methyl-CpG-Binding Protein 2 Genetic Markers Repressor Proteins Polycomb Repressive Complex 2 Oxidoreductases, N-Demethylating DNA Probes Lysine Sodium Channels Chromatin Glucosephosphate Dehydrogenase DNA Polycomb Repressive Complex 1 Hypoxanthine Phosphoribosyltransferase DNA-Binding Proteins DNA Primers Proteins RNA Kv1.4 Potassium Channel RNA, Messenger Potassium Channels Calcium Muscimol Potassium Channels, Voltage-Gated Green Fluorescent Proteins Barium Factor X Calcium Channels Bacterial Proteins Enzyme Reactivators Recombinant Proteins Shaker Superfamily of Potassium Channels Enzyme Inhibitors Sodium Channel Blockers Potassium Sodium Shal Potassium Channels Chloramines Disinfectants Cysteine Dithiothreitol Potassium Channel Blockers Diethyl Pyrocarbonate Calcium Channels, L-Type Chlorine Ion Channels Adenosine Triphosphate Tumor Suppressor Protein p53 Hydrogen Peroxide GABA Agonists Tetrodotoxin Cyclin-Dependent Kinase Inhibitor p16 Phenylglyoxal Carrier Proteins NAV1.4 Voltage-Gated Sodium Channel Tetraethylammonium Protein-Serine-Threonine Kinases Tumor Suppressor Proteins Sulfhydryl Compounds Ethylmaleimide Calcium Channel Blockers Cell Cycle Proteins Pyridoxal Phosphate Affinity Labels Retinoblastoma Protein Sulfhydryl Reagents Nuclear Proteins Ether-A-Go-Go Potassium Channels 4-Aminopyridine Dithionitrobenzoic Acid Egtazic Acid Membrane Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment26

In Situ Hybridization, Fluorescence Chromosome Mapping Pedigree Virus Inactivation Karyotyping Polymerase Chain Reaction Heterozygote Detection Models, Genetic Chromosome Banding Blotting, Southern Crosses, Genetic Patch-Clamp Techniques Restriction Mapping Reverse Transcriptase Polymerase Chain Reaction Gene Expression Profiling Models, Biological Mutagenesis, Site-Directed Transfection Enzyme Stability Cloning, Molecular Mutagenesis, Insertional Electrophoresis, Polyacrylamide Gel Blotting, Western Models, Molecular Amino Acid Substitution Chromatography, High Pressure Liquid

Psychiatry and Psychology3

Intellectual Disability Nuclear Family Mothers

Phenomena and Processes94

Dosage Compensation, Genetic X Chromosome Inactivation X Chromosome Genes, X-Linked Chromosomes, Human, X Sex Chromosome Aberrations Genomic Imprinting Mosaicism Gene Silencing Ring Chromosomes Heterozygote Alleles Genetic Linkage Virus Inactivation DNA Methylation Sex Chromosomes Methylation Mutation Long Interspersed Nucleotide Elements Kinetics Phenotype Transgenes Gene Deletion Chromosomes, Mammalian Y Chromosome Chromosomes, Artificial, Yeast Genetic Markers Base Sequence Translocation, Genetic Epigenesis, Genetic CpG Islands Transcription, Genetic Embryonic and Fetal Development Ion Channel Gating Gene Expression Regulation, Developmental Chromatin Sequence Deletion Acetylation Gene Expression Regulation Cell Differentiation Membrane Potentials Trinucleotide Repeats Chromosomes, Artificial, Bacterial Amino Acid Sequence Gene Expression Chromosomes, Human, Pair 7 DNA Replication Microsatellite Repeats Promoter Regions, Genetic Exons Hot Temperature Repetitive Sequences, Nucleic Acid Genes Time Factors Species Specificity Binding Sites Evolution, Molecular Hydrogen-Ion Concentration Pregnancy Polymorphism, Restriction Fragment Length Enzyme Activation Temperature Protein Binding Genotype Signal Transduction Electric Conductivity Regulatory Sequences, Nucleic Acid Phosphorylation Oxidation-Reduction Action Potentials Dose-Response Relationship, Drug Transfection Structure-Activity Relationship Microbial Viability Substrate Specificity Protein Structure, Tertiary Protein Conformation Ultraviolet Rays Enzyme Stability Mutagenesis, Insertional Point Mutation Sequence Homology, Amino Acid Genes, Tumor Suppressor Apoptosis Hydrostatic Pressure Gene Expression Regulation, Bacterial Catalysis Plasmids Molecular Weight Amino Acid Substitution Gene Expression Regulation, Neoplastic Mutagenesis Hydrolysis Loss of Heterozygosity

Disciplines and Occupations1

Electrophysiology

Anthropology, Education, Sociology and Social Phenomena2

Nuclear Family Mothers

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups3

Twins, Monozygotic Triplets Mothers

Health Care4

Hot Temperature Disinfection Temperature Ultraviolet Rays

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

Dosage Compensation, Genetic X Chromosome Inactivation X Chromosome RNA, Long Noncoding RNA, Untranslated Genes, X-Linked Chromosomes, Human, X Sex Chromosome Aberrations Genomic Imprinting Incontinentia Pigmenti In Situ Hybridization, Fluorescence Turner Syndrome Mosaicism Hybrid Cells Gene Silencing Ring Chromosomes Heterozygote Equidae Alleles Twins, Monozygotic Chromosome Mapping Genetic Linkage Orofaciodigital Syndromes Pedigree Rett Syndrome Virus Inactivation Histones DNA Methylation Sex Chromosomes Methylation Karyotyping Molecular Sequence Data Mutation Arylsulfatases Receptors, Androgen Polycomb-Group Proteins Steryl-Sulfatase Intellectual Disability Long Interspersed Nucleotide Elements Embryo, Mammalian Transcription Factors Stem Cells Kinetics Phenotype Triplets Pelizaeus-Merzbacher Disease Cell Line Transgenes Gene Deletion DAX-1 Orphan Nuclear Receptor Genetic Diseases, X-Linked Methyl-CpG-Binding Protein 2 Chromosomes, Mammalian Y Chromosome Chromosomes, Artificial, Yeast Genetic Markers Blastocyst Repressor Proteins Polymerase Chain Reaction Base Sequence Heterozygote Detection Translocation, Genetic Epigenesis, Genetic Polycomb Repressive Complex 2 Oxidoreductases, N-Demethylating CpG Islands Transcription, Genetic Cells, Cultured DNA Probes Embryonic and Fetal Development Lysine Sodium Channels Ion Channel Gating Fibroblasts Gene Expression Regulation, Developmental Chromatin Sequence Deletion Placenta Glucosephosphate Dehydrogenase DNA Acetylation Polycomb Repressive Complex 1 Gene Expression Regulation Mice, Transgenic Models, Genetic Cell Differentiation Trophoblasts Membrane Potentials Trinucleotide Repeats Chromosome Banding Blotting, Southern Chromosomes, Artificial, Bacterial Hypoxanthine Phosphoribosyltransferase Embryonic Stem Cells Mice, Inbred C57BL DNA-Binding Proteins Nuclear Family Crosses, Genetic Amino Acid Sequence Gene Expression

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