Wayne A Cabral

7PUBLICATIONS
18CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Infant and child healthMedical molecular engineering of nucleic acids and proteinsHydrometallurgyRespiratory diseases
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Publications (7)

|Sep 03, 2026
In Vivo Base Editing Partially Rescues Bone Dysplasia in a Mouse Model of Hutchinson-Gilford Progeria Syndrome.

|Oct 18, 2024
Angiopoietin-2 reverses endothelial cell dysfunction in progeria vasculature.

Sahar Vakili, Elizabeth K Izydore, Leonhard Losert

|Jun 26, 2023
Bone dysplasia in Hutchinson-Gilford progeria syndrome is associated with dysregulated differentiation and function of bone cell populations.

Wayne A Cabral, Chris Stephan, Masahiko Terajima

|Mar 12, 2021
A targeted antisense therapeutic approach for Hutchinson-Gilford progeria syndrome.

Michael R Erdos, Wayne A Cabral, Urraca L Tavarez

|Jan 07, 2021
In vivo base editing rescues Hutchinson-Gilford progeria syndrome in mice.

Luke W Koblan, Michael R Erdos, Christopher Wilson

|May 15, 2020
Evaluation of musculoskeletal phenotype of the G608G progeria mouse model with lonafarnib, pravastatin, and zoledronic acid as treatment groups.

Maria B Cubria, Sebastian Suarez, Aidin Masoudi

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Frequent Collaborators

4 joint publications

Urraca L Tavarez

3 joint publications

Francis S Collins

3 joint publications

Michael R Erdos

3 joint publications

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