Camille Desgrouas

4PUBLICATIONS
10CO-AUTHORS
Cell and nuclear divisionMechanobiologyPredictive and prognostic markersDevelopmental genetics (incl. sex determination)
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Publications (4)

|Feb 26, 2025
Homozygous loss of function variant in LMNB2 gene causes major brain malformation and perinatal death.

Camille Desgrouas, Igor Deryabin, Clémence Duvillier

|Feb 24, 2025
Rare ZMPSTE24 variants increase risk of hypertriglyceridemia and metabolic syndrome.

Lauriane Le Collen, Camille Desgrouas, Céline Lukas Croisier

|Jan 12, 2024
Perilipin 1: a systematic review on its functions on lipid metabolism and atherosclerosis in mice and humans.

Camille Desgrouas, Tabea Thalheim, Mathieu Cerino

|Jan 11, 2022
A Rare Mutation in LMNB2 Associated with Lipodystrophy Drives Premature Cell Senescence.

Alice-Anaïs Varlet, Camille Desgrouas, Cécile Jebane

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