L. Jullien

[RTEL1 (regulator of telomere elongation helicase 1), a DNA helicase essential for genome stability].

P. Revy, A. Londoño-Vallejo, J. de Villartay, 2013, Medecine sciences : M/S.

Human RTEL1 deficiency causes Hoyeraal-Hreidarsson syndrome with short telomeres and genome instability.

A. Fischer, J. Soulier, C. Picard, 2013, Human molecular genetics.

Mutations of the RTEL1 Helicase in a Hoyeraal‐Hreidarsson Syndrome Patient Highlight the Importance of the ARCH Domain

J. Soulier, P. Revy, T. Leblanc, 2016, Human mutation.

Extended clinical and genetic spectrum associated with biallelic RTEL1 mutations.

A. Fischer, J. Soulier, P. Revy, 2016, Blood advances.

Gain of oncogenic function of p53 mutants regulates E-cadherin expression uncoupled from cell invasion in colon cancer cells

P. Roux, L. Roger, V. Gire, 2010, Journal of Cell Science.

Eroded human telomeres are more prone to remain uncapped and to trigger a G2 checkpoint response

Pierre Roux, P. Roux, V. Gire, 2012, Nucleic acids research.