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Publications by Björn Rozell
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
Differential Expression of A-Type and B-Type Lamins During Hair Cycling
PLoS ONE
Multidisciplinary
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
