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Works by Brekelmans, Carlijn

Results: 3

1

Neurofibromatosis type 1‐related pseudarthrosis: Beyond the pseudarthrosis site.

Published in:

Human Mutation, 2019, v. 40, n. 10, p. 1760, doi. 10.1002/humu.23783

By:

Brekelmans, Carlijn;
Hollants, Silke;
Groote, Caroline;
Sohier, Natalie;
Maréchal, Marina;
Geris, Liesbet;
Luyten, Frank P.;
Ginckels, Lieve;
Sciot, Raf;
Ravel, Thomy;
Smet, Luc;
Lammens, Johan;
Legius, Eric;
Brems, Hilde

Publication type:

Article

2

Constitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variants.

Published in:

NPJ Precision Oncology, 2024, v. 8, n. 1, p. 1, doi. 10.1038/s41698-024-00603-z

By:

Gallon, Richard;
Brekelmans, Carlijn;
Martin, Marie;
Bours, Vincent;
Schamschula, Esther;
Amberger, Albert;
Muleris, Martine;
Colas, Chrystelle;
Dekervel, Jeroen;
De Hertogh, Gert;
Coupier, Jérôme;
Colleye, Orphal;
Sepulchre, Edith;
Burn, John;
Brems, Hilde;
Legius, Eric;
Wimmer, Katharina

Publication type:

Article

3

The histone methyltransferase G9a regulates tolerance to oxidative stress–induced energy consumption.

Published in:

PLoS Biology, 2019, v. 17, n. 3, p. 1, doi. 10.1371/journal.pbio.2006146

By:

Riahi, Human;
Brekelmans, Carlijn;
Foriel, Sarah;
Merkling, Sarah H.;
Lyons, Taylor A.;
Itskov, Pavel M.;
Kleefstra, Tjitske;
Ribeiro, Carlos;
van Rij, Ronald P.;
Kramer, Jamie M.;
Schenck, Annette

Publication type:

Article