N. Avazeri

The phosphoinositide-phospholipase C (PI-PLC) pathway in the mouse oocyte.

C. Poirot, B. Lefèvre, A. Pesty, 2007, Critical reviews in eukaryotic gene expression.

Meiosis resumption, calcium-sensitive period, and PLC-beta1 relocation into the nucleus in the mouse oocyte.

B. Lefèvre, A. Pesty, A. Courtot, 2003, Cellular signalling.

The germinal vesicle of the mouse oocyte contains elements of the phosphoinositide cycle: what is their role at meiosis resumption?

B. Lefèvre, A. Pesty, N. Avazeri, 1998, Reproduction, nutrition, development.

Nuclear calcium release by InsP3-receptor channels plays a role in meiosis reinitiation in the mouse oocyte.

B. Lefèvre, A. Pesty, N. Avazeri, 1998, Cell calcium.

Regulation of spontaneous meiosis resumption in mouse oocytes by various conventional PKC isozymes depends on cellular compartmentalization

B. Lefèvre, A. Courtot, N. Avazeri, 2004, Journal of Cell Science.

Cytoplasmic and nuclear phospholipase C-beta 1 relocation: role in resumption of meiosis in the mouse oocyte.

C. Duquenne, B. Lefèvre, A. Pesty, 2000, Molecular biology of the cell.

The PKC pathway and in particular its β1 isoform is clearly involved in meiotic arrest maintenance but poorly in FSH‐induced meiosis resumption of the mouse cumulus cell enclosed oocyte

A. Denys, N. Avazeri, B. Lefévre, 2007, Molecular reproduction and development.

Lead cations affect the control of both meiosis arrest and meiosis resumption of the mouse oocyte in vitro at least via the PKC pathway.

A. Denys, N. Avazeri, B. Lefévre, 2006, Biochimie.