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Publications by Christoph Noppen
Discordant Gene Expression Signatures and Related Phenotypic Differences in Lamin A- And a/C-Related Hutchinson-Gilford Progeria Syndrome (HGPS)
PLoS ONE
Multidisciplinary
Immunogenicity of Nonreplicating Recombinant Vaccinia Expressing HLA-A201 Targeted or Complete MART-1/Melan-A Antigen
Cancer Gene Therapy
Cancer Research
Molecular Medicine
Molecular Biology
Related publications
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
Hutchinson-Gilford Progeria Syndrome: A Premature Aging Disease Caused by LMNA Gene Mutations
Ageing Research Reviews
Biochemistry
Aging
Neurology
Molecular Biology
Biotechnology
Hutchinson-Gilford Progeria Syndrome With Bilateral Blephroptosis and Cataracts
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
Medicine
Radiological Diagnosis of a Rare Premature Aging Genetic Disorder: Progeria (Hutchinson-Gilford Syndrome)
Case Reports in Radiology
Hutchinson-Gilford Syndrome
Ranolazine Treatment for Refractory Angina in a Patient With Hutchinson-Gilford Progeria Syndrome and End Stage Aortic Stenosis
Cardiogenetics
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 as an Inspiration for F. Scott Fitzgeraldʼs Fictional Character ʻBenjamin Buttonʼ
