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Publications by Rüdiger Wentzell

Neonatal Progeria: Increased Ratio of Progerin to Lamin a Leads to Progeria of the Newborn

European Journal of Human Genetics

English

Related publications

Progeria in Twins

Journal of Medical Genetics

English

Targeted Transgenic Expression of the Mutation Causing Hutchinson-Gilford Progeria Syndrome Leads to Proliferative and Degenerative Epidermal Disease

Journal of Cell Science

English

A G613A Missense in the Hutchinson’s Progeria Lamin a/C Gene Causes a Lone, Autosomal Dominant Atrioventricular Block

Immunity and Ageing

English

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

English

Progerin Impairs Chromosome Maintenance by Depleting CENP-F From Metaphase Kinetochores in Hutchinson-Gilford Progeria Fibroblasts

English

Nucleocytoplasmic Communication in Progeria

English

A Syndrome Resembling Progeria: A Review of Two Cases

Archives of Disease in Childhood

English

Discordant Gene Expression Signatures and Related Phenotypic Differences in Lamin A- And a/C-Related Hutchinson-Gilford Progeria Syndrome (HGPS)

Multidisciplinary

English

Progeria of the Heart in Type 1 Diabetic Children?

Journal of Cardiovascular Ultrasound

English