Progeria gene. Medical search. Frequent questions

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Anatomy10

Nuclear Lamina Fibroblasts Nuclear Envelope Somatotrophs Cell Nucleus Heterochromatin Cells, Cultured Skin Bone and Bones Cell Line

Organisms2

Mice, Transgenic Mice, Knockout

Diseases12

Aging, Premature Werner Syndrome Bone Demineralization, Pathologic Skin Abnormalities Contracture Lipodystrophy Maxillofacial Abnormalities Cockayne Syndrome Bone Diseases, Developmental Syndrome Progeria Disease Models, Animal

Chemicals and Drugs11

Lamin Type A Farnesyltranstransferase Protein Precursors Nuclear Proteins Lamins Lamin Type B Metalloendopeptidases Alkyl and Aryl Transferases Heterochromatin Membrane Proteins Enzyme Inhibitors

Analytical, Diagnostic and Therapeutic Techniques and Equipment1

Disease Models, Animal

Phenomena and Processes16

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

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

Lamin Type A Aging, Premature Farnesyltranstransferase Cell Nucleus Shape Nuclear Lamina Werner Syndrome Prenylation Protein Precursors Protein Prenylation Bone Demineralization, Pathologic Fibroblasts Nuclear Envelope Nuclear Proteins Skin Abnormalities Lamins Protein Modification, Translational Lamin Type B Organelle Shape Contracture Lipodystrophy Maxillofacial Abnormalities Metalloendopeptidases Cell Aging Somatotrophs Cockayne Syndrome Cell Nucleus Aging Bone Diseases, Developmental Phenotype Mutation Syndrome Alkyl and Aryl Transferases Progeria Heterochromatin Longevity Cells, Cultured Membrane Proteins Skin Disease Models, Animal Enzyme Inhibitors DNA Repair Heterozygote Mitosis DNA Damage Bone and Bones Mice, Transgenic Cell Line Mice, Knockout Protein Binding

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