Erwan Watrin
Rennes, 35000, France
Last Updated: 09/26/2026
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Found 24 publications
TDG orchestrates ATF4-dependent gene transcription during retinoic acid-induced cell fate acquisition.
Journal: Nucleic acids research
Published: March 17, 2025
The cohesin ATPase cycle is mediated by specific conformational dynamics and interface plasticity of SMC1A and SMC3 ATPase domains.
Journal: Cell reports
Published: December 15, 2023
Proteomic study identifies Aurora-A-mediated regulation of alternative splicing through multiple splicing factors.
Journal: The Journal of biological chemistry
Published: September 28, 2023
The histone methyltransferase NSD3 contributes to sister chromatid cohesion and to cohesin loading at mitotic exit.
Journal: Journal of cell science
Published: January 25, 2023
Overarching control of autophagy and DNA damage response by CHD6 revealed by modeling a rare human pathology.
Journal: Nature communications
Published: February 11, 2021
Targeting the histone demethylase LSD1 prevents cardiomyopathy in a mouse model of laminopathy.
Journal: The Journal of clinical investigation
Published: January 15, 2020
Synonymous variants in holoprosencephaly alter codon usage and impact the Sonic Hedgehog protein.
Journal: Brain : a journal of neurology
Published: October 25, 2019
Alteration of SC35 localization by transfection reagents.
Journal: Biochimica et biophysica acta. Molecular cell research
Published: September 06, 2019
Targeted panel sequencing establishes the implication of planar cell polarity pathway and involves new candidate genes in neural tube defect disorders.
Journal: Human genetics
Published: September 17, 2018
Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly.
Journal: Brain : a journal of neurology
Published: June 12, 2018
Recent advances in understanding inheritance of holoprosencephaly.
Journal: American journal of medical genetics. Part C, Seminars in medical genetics
Published: April 06, 2018
Last Updated: 09/26/2026