NOBOX is a key FOXL2 partner involved in ovarian folliculogenesis.

@article{Bouilly2014NOBOXIA,
  title={NOBOX is a key FOXL2 partner involved in ovarian folliculogenesis.},
  author={Justine Bouilly and Reiner A. Veitia and Nadine Binart},
  journal={Journal of molecular cell biology},
  year={2014},
  volume={6 2},
  pages={
          175-7
        }
}
Dear Editor, Early ovarian expression of Newborn oogenesis homeobox (NOBOX), a transcription factor belonging to the homeoprotein class, is decisive for the progression of primordial follicles to the primary follicular stage as demonstrated by the sterility of Nobox 2 female mice (Rajkovic et al., 2004). Consequently, the loss of the Nobox gene causes primary ovarian insufficiency (POI) (Rajkovic et al., 2004) and we have shown that 6.2% of POI cases harbor mutations in the NOBOX gene (Qin et… CONTINUE READING

Citations

Publications citing this paper.
SHOWING 1-9 OF 9 CITATIONS

Familial Multiplicity of Estrogen Insensitivity Associated With a Loss-of-Function ESR1 Mutation

VIEW 1 EXCERPT
CITES METHODS

New NOBOX mutations identified in a large cohort of women with primary ovarian insufficiency decrease KIT-L expression.

VIEW 2 EXCERPTS
CITES BACKGROUND

References

Publications referenced by this paper.
SHOWING 1-10 OF 10 REFERENCES

NOBOX homeobox mutation causes premature ovarian failure.

VIEW 2 EXCERPTS
HIGHLY INFLUENTIAL