Treatment of progeria and progeroid laminopathies. Medical search. Frequent questions

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Anatomy7

Nuclear Lamina Nuclear Envelope Fibroblasts Cell Nucleus Somatotrophs Cells, Cultured Heterochromatin

Organisms1

Diseases18

Progeria Muscular Dystrophy, Emery-Dreifuss Aging, Premature Lipodystrophy Werner Syndrome Skin Abnormalities Cockayne Syndrome Genetic Diseases, Inborn Syndrome Trichothiodystrophy Syndromes Disease Models, Animal Bone Demineralization, Pathologic Ehlers-Danlos Syndrome Contracture Maxillofacial Abnormalities Abnormalities, Multiple Ataxia Telangiectasia Bone Diseases, Developmental

Chemicals and Drugs14

Lamin Type A Lamins Farnesyltranstransferase Lamin Type B Nuclear Proteins Protein Precursors Membrane Proteins Metalloendopeptidases RecQ Helicases Galactosyltransferases Exodeoxyribonucleases Endonucleases Alkyl and Aryl Transferases Heterochromatin

Analytical, Diagnostic and Therapeutic Techniques and Equipment1

Disease Models, Animal

Phenomena and Processes13

Cell Nucleus Shape Mutation Prenylation Cell Aging Protein Prenylation Aging Longevity Phenotype Protein Modification, Translational Organelle Shape DNA Repair DNA Damage Heterochromatin

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes

Lamin Type A Progeria Nuclear Lamina Muscular Dystrophy, Emery-Dreifuss Aging, Premature Lipodystrophy Lamins Nuclear Envelope Cell Nucleus Shape Werner Syndrome Farnesyltranstransferase Lamin Type B Nuclear Proteins Fibroblasts Protein Precursors Skin Abnormalities Mutation Cockayne Syndrome Cell Nucleus Genetic Diseases, Inborn Membrane Proteins Prenylation Cell Aging Syndrome Metalloendopeptidases Protein Prenylation Trichothiodystrophy Syndromes Aging Disease Models, Animal RecQ Helicases Longevity Bone Demineralization, Pathologic Mice, Knockout Ehlers-Danlos Syndrome Galactosyltransferases Phenotype Protein Modification, Translational Organelle Shape Contracture DNA Repair Exodeoxyribonucleases Maxillofacial Abnormalities Abnormalities, Multiple Endonucleases DNA Damage Somatotrophs Cells, Cultured Ataxia Telangiectasia Bone Diseases, Developmental Alkyl and Aryl Transferases Heterochromatin

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