Annachiara De Sandre-Giovannoli

7PUBLICATIONS
27CO-AUTHORS
Medical molecular engineering of nucleic acids and proteinsMechanobiologyMedical parasitologyCell physiologyMolecular evolution
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Publications (7)

|Feb 25, 2022
MG132 Induces Progerin Clearance and Improves Disease Phenotypes in HGPS-like Patients' Cells.

Karim Harhouri, Pierre Cau, Frank Casey

|Oct 20, 2020
Author Correction: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology.

Sahar Elouej, Karim Harhouri, Morgane Le Mao

|Sep 12, 2020
Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology.

Sahar Elouej, Karim Harhouri, Morgane Le Mao

|Aug 19, 2020
Vulnerability of progeroid smooth muscle cells to biomechanical forces is mediated by MMP13.

Patricia R Pitrez, Luís Estronca, Luís Miguel Monteiro

|Dec 13, 2019
Outcomes of 4 years of molecular genetic diagnosis on a panel of genes involved in premature aging syndromes, including laminopathies and related disorders.

Maude Grelet, Véronique Blanck, Sabine Sigaudy

|Apr 27, 2018
MicroRNAs in hereditary and sporadic premature aging syndromes and other laminopathies.

Diane Frankel, Valérie Delecourt, Karim Harhouri

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Frequent Collaborators

6 joint publications

Karim Harhouri

2 joint publications

Diane Frankel

2 joint publications

Patrice Roll

2 joint publications

Nicolas Lévy