Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome
2003 · Nature · 2,159 citations
https://doi.org/10.1038/nature01629
M
Maria Eriksson
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Maria Eriksson is an academic researcher from Karolinska University Hospital. The author has contributed to research in topics: Nuclear Structure and Function & RNA Research and Splicing & DNA Repair Mechanisms. The author has an h-index of 34, co-authored 114 publications.
ORCID: 0000-0003-3233-2862Papers by this author
worksEndothelial progerin expression causes cardiovascular pathology through an impaired mechanoresponse
2018 · Journal of Clinical Investigation · 114 citations
https://doi.org/10.1172/jci121297
Expression of the Hutchinson-Gilford Progeria Mutation during Osteoblast Development Results in Loss of Osteocytes, Irregular Mineralization, and Poor Biomechanical Properties
2012 · Journal of Biological Chemistry · 55 citations
https://doi.org/10.1074/jbc.m112.366450
Intra-islet lesions and lobular variations in β-cell mass expansion in ob/ob mice revealed by 3D imaging of intact pancreas
2016 · Scientific Reports · 28 citations
https://doi.org/10.1038/srep34885
Transient expression of an adenine base editor corrects the Hutchinson-Gilford progeria syndrome mutation and improves the skin phenotype in mice
2022 · Nature Communications · 24 citations
https://doi.org/10.1038/s41467-022-30800-y
Kinetics of functional beta cell mass decay in a diphtheria toxin receptor mouse model of diabetes
2017 · Scientific Reports · 9 citations
https://doi.org/10.1038/s41598-017-12124-w
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