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The paradox of viable sup45 STOP mutations: a necessary equilibrium between translational readthrough, activity and stability of the protein.
Published in:
Molecular Genetics & Genomics, 2009, v. 282, n. 1, p. 83, doi. 10.1007/s00438-009-0447-5
By:
- Kiktev, Denis;
- Moskalenko, Svetlana;
- Murina, Olga;
- Baudin-Baillieu, Agnès;
- Rousset, Jean-Pierre;
- Zhouravleva, Galina
Publication type:
Article
RNase H2, mutated in Aicardi‐Goutières syndrome, promotes LINE‐1 retrotransposition.
Published in:
EMBO Journal, 2018, v. 37, n. 15, p. 1, doi. 10.15252/embj.201798506
By:
- Benitez‐Guijarro, Maria;
- Lopez‐Ruiz, Cesar;
- Tarnauskaitė, Žygimantė;
- Murina, Olga;
- Mian Mohammad, Mahwish;
- Williams, Thomas C.;
- Fluteau, Adeline;
- Sanchez, Laura;
- Vilar‐Astasio, Raquel;
- Garcia‐Canadas, Marta;
- Cano, David;
- Kempen, Marie‐Jeanne H. C.;
- Sanchez‐Pozo, Antonio;
- Heras, Sara R.;
- Jackson, Andrew P.;
- Reijns, Martin A. M.;
- Garcia‐Perez, Jose L.
Publication type:
Article
Cullin3-KLHL15 ubiquitin ligase mediates CtIP protein turnover to fine-tune DNA-end resection.
Published in:
Nature Communications, 2016, v. 7, n. 8, p. 12628, doi. 10.1038/ncomms12628
By:
- Ferretti, Lorenza P.;
- Himmels, Sarah-Felicitas;
- Trenner, Anika;
- Walker, Christina;
- von Aesch, Christine;
- Eggenschwiler, Aline;
- Murina, Olga;
- Enchev, Radoslav I.;
- Peter, Matthias;
- Freire, Raimundo;
- Porro, Antonio;
- Sartori, Alessandro A.
Publication type:
Article
HELQ promotes RAD51 paralogue-dependent repair to avert germ cell loss and tumorigenesis.
Published in:
Nature, 2013, v. 502, n. 7471, p. 381, doi. 10.1038/nature12565
By:
- Adelman, Carrie A.;
- Lolo, Rafal L.;
- Birkbak, Nicolai J.;
- Murina, Olga;
- Matsuzaki, Kenichiro;
- Horejsi, Zuzana;
- Parmar, Kalindi;
- Borel, Valérie;
- Skehel, J. Mark;
- Stamp, Gordon;
- D'Andrea, Alan;
- Sartori, Alessandro A.;
- Swanton, Charles;
- Boulton, Simon J.
Publication type:
Article
Biallelic variants in DNA2 cause microcephalic primordial dwarfism.
Published in:
Human Mutation, 2019, v. 40, n. 8, p. 1063, doi. 10.1002/humu.23776
By:
- Tarnauskaitė, Žygimantė;
- Bicknell, Louise S.;
- Marsh, Joseph A.;
- Murray, Jennie E.;
- Parry, David A.;
- Logan, Clare V.;
- Bober, Michael B.;
- Silva, Deepthi C.;
- Duker, Angela L.;
- Sillence, David;
- Wise, Carol;
- Jackson, Andrew P.;
- Murina, Olga;
- Reijns, Martin A. M.
Publication type:
Article

Found: 5

The paradox of viable sup45 STOP mutations: a necessary equilibrium between translational readthrough, activity and stability of the protein.

RNase H2, mutated in Aicardi‐Goutières syndrome, promotes LINE‐1 retrotransposition.

Cullin3-KLHL15 ubiquitin ligase mediates CtIP protein turnover to fine-tune DNA-end resection.

HELQ promotes RAD51 paralogue-dependent repair to avert germ cell loss and tumorigenesis.

Biallelic variants in DNA2 cause microcephalic primordial dwarfism.