Author

A. M. Villeneuve

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Cell Biology· 2

Signature Assays, Organisms & Methods

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Organism:C. elegans· 2 Research Focus:cell signaling & trafficking· 2 Approach:experimental assay· 2 Research Focus:chromatin & epigenetic regulation· 1 Assay:fluorescence / live-cell microscopy· 1 Approach:genetic perturbation / CRISPR· 1 Assay:proteomics· 1

Frequent Co-Authors

A. Woglar· 2 shared A. Boettiger· 1 shared B. Roelens· 1 shared C. C. Akerib· 1 shared C. C. Salazar· 1 shared J. Haversat· 1 shared K. Klatt· 1 shared K. Yamaya· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersCell Biology

A. Woglar

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2 papers

Recent·Most cited

Robust designation of meiotic crossover sites by CDK-2 through phosphorylation of the MutSγ complex

J. Haversat, A. Woglar, K. Klatt, C. C. Akerib, V. Roberts, C. C. Salazar, S.-Y. Chen, S. Arur, A. M. Villeneuve, Y. Kim

The paper shows CDK-2 phosphorylates MSH-5 to promote crossover formation during meiosis by enhancing recruitment of crossover-promoting complexes.

bioRxiv · Aug 31, 2021Cell Biology

Quantitative Cytogenetics Reveals Molecular Stoichiometry and Longitudinal Organization of Meiotic Chromosome Axes and Loops

A. Woglar, K. Yamaya, B. Roelens, A. Boettiger, S. Kohler, A. M. Villeneuve

This study uses quantitative cytogenetic methods in C. elegans to reveal the molecular stoichiometry and organization of meiotic chromosome axes and loops involving HORMA-domain proteins and cohesin complexes.

bioRxiv · May 2, 2020Cell Biology