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Publications by Antti Koskela
Expression of the Hutchinson-Gilford Progeria Mutation During Osteoblast Development Results in Loss of Osteocytes, Irregular Mineralization, and Poor Biomechanical Properties
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Related publications
Targeted Transgenic Expression of the Mutation Causing Hutchinson-Gilford Progeria Syndrome Leads to Proliferative and Degenerative Epidermal Disease
Journal of Cell Science
Cell Biology
Vascular Smooth Muscle Cell Loss Underpins the Accelerated Atherosclerosis in Hutchinson-Gilford Progeria Syndrome
Nucleus
Medicine
Cell Biology
Hutchinson-Gilford Progeria Syndrome With Bilateral Blephroptosis and Cataracts
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
Medicine
Hutchinson-Gilford Progeria Syndrome: A Premature Aging Disease Caused by LMNA Gene Mutations
Ageing Research Reviews
Biochemistry
Aging
Neurology
Molecular Biology
Biotechnology
Radiological Diagnosis of a Rare Premature Aging Genetic Disorder: Progeria (Hutchinson-Gilford Syndrome)
Case Reports in Radiology
Hutchinson-Gilford Syndrome
Discordant Gene Expression Signatures and Related Phenotypic Differences in Lamin A- And a/C-Related Hutchinson-Gilford Progeria Syndrome (HGPS)
PLoS ONE
Multidisciplinary
Accumulation of Mutant Lamin a Causes Progressive Changes in Nuclear Architecture in Hutchinson-Gilford Progeria Syndrome
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
The Defective Nuclear Lamina in Hutchinson-Gilford Progeria Syndrome Disrupts the Nucleocytoplasmic Ran Gradient and Inhibits Nuclear Localization of Ubc9
Molecular and Cellular Biology
Cell Biology
Molecular Biology
