Comment to: Single-cell profiling reveals the trajectories of natural killer cell differentiation in bone marrow and a stress signature induced by acute myeloid leukemia

por Melsen, Janine E., Lugthart, Gertjan, van Ostaijen-ten Dam, Monique M., Schilham, Marco W.
Publicado no Cell Mol Immunol (2021)

Normal Numbers of Stem Cell Memory T Cells Despite Strongly Reduced Naive T Cells Support Intact Memory T Cell Compartment in Ataxia Telangiectasia

por Weitering, Thomas J., Melsen, Janine E., van Ostaijen-ten Dam, Monique M., Weemaes, Corry M. R., Schilham, Marco W., van der Burg, Mirjam
Publicado no Front Immunol (2021)

Protocol for Isolation, Stimulation and Functional Profiling of Primary and iPSC-derived Human NK Cells

por Melsen, Janine E., Themeli, Maria, van Ostaijen-Ten Dam, Monique M., van Beelen, Els, Lugthart, Gertjan, Hoeben, Rob C., Schilham, Marco W., Mikkers, Harald M.
Publicado no Bio Protoc (2020)

Human Bone Marrow-Resident Natural Killer Cells Have a Unique Transcriptional Profile and Resemble Resident Memory CD8(+) T Cells

por Melsen, Janine E., Lugthart, Gertjan, Vervat, Carly, Kielbasa, Szymon M., van der Zeeuw, Sander A. J., Buermans, Henk P. J., van Ostaijen-ten Dam, Monique M., Lankester, Arjan C., Schilham, Marco W.
Publicado no Front Immunol (2018)

Role of NKG2D, DNAM-1 and natural cytotoxicity receptors in cytotoxicity toward rhabdomyosarcoma cell lines mediated by resting and IL-15-activated human natural killer cells

por Boerman, Gerharda H., van Ostaijen-ten Dam, Monique M., Kraal, Kathelijne C. J. M., Santos, Susy J., Ball, Lynne M., Lankester, Arjan C., Schilham, Marco W., Egeler, R. Maarten, van Tol, Maarten J. D.
Publicado no Cancer Immunol Immunother (2015)

Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects

por Weemaes, Corry MR, van Tol, Maarten JD, Wang, Jun, van Ostaijen-ten Dam, Monique M, van Eggermond, Marja CJA, Thijssen, Peter E, Aytekin, Caner, Brunetti-Pierri, Nicola, van der Burg, Mirjam, Graham Davies, E, Ferster, Alina, Furthner, Dieter, Gimelli, Giorgio, Gennery, Andy, Kloeckener-Gruissem, Barbara, Meyn, Stephan, Powell, Cynthia, Reisli, Ismail, Schuetz, Catharina, Schulz, Ansgar, Shugar, Andrea, van den Elsen, Peter J, van der Maarel, Silvère M
Publicado em 2013

Mutations in CDCA7 and HELLS cause immunodeficiency–centromeric instability–facial anomalies syndrome

por Thijssen, Peter E., Ito, Yuya, Grillo, Giacomo, Wang, Jun, Velasco, Guillaume, Nitta, Hirohisa, Unoki, Motoko, Yoshihara, Minako, Suyama, Mikita, Sun, Yu, Lemmers, Richard J. L. F., de Greef, Jessica C., Gennery, Andrew, Picco, Paolo, Kloeckener-Gruissem, Barbara, Güngör, Tayfun, Reisli, Ismail, Picard, Capucine, Kebaili, Kamila, Roquelaure, Bertrand, Iwai, Tsuyako, Kondo, Ikuko, Kubota, Takeo, van Ostaijen-Ten Dam, Monique M., van Tol, Maarten J. D., Weemaes, Corry, Francastel, Claire, van der Maarel, Silvère M., Sasaki, Hiroyuki
Publicado no Nat Commun (2015)

Corrigendum: Mutations in CDCA7 and HELLS cause immunodeficiency–centromeric instability–facial anomalies syndrome

por Thijssen, Peter E., Ito, Yuya, Grillo, Giacomo, Wang, Jun, Velasco, Guillaume, Nitta, Hirohisa, Unoki, Motoko, Yoshihara, Minako, Suyama, Mikita, Sun, Yu, Lemmers, Richard J. L. F., de Greef, Jessica C., Gennery, Andrew, Picco, Paolo, Kloeckener-Gruissem, Barbara, Güngör, Tayfun, Reisli, Ismail, Picard, Capucine, Kebaili, Kamila, Roquelaure, Bertrand, Iwai, Tsuyako, Kondo, Ikuko, Kubota, Takeo, van Ostaijen-Ten Dam, Monique M., van Tol, Maarten J. D., Weemaes, Corry, Francastel, Claire, van der Maarel, Silvère M., Sasaki, Hiroyuki
Publicado no Nat Commun (2016)

Loss of ZBTB24 impairs nonhomologous end-joining and class-switch recombination in patients with ICF syndrome

por Helfricht, Angela, Thijssen, Peter E., Rother, Magdalena B., Shah, Rashmi G., Du, Likun, Takada, Sanami, Rogier, Mélanie, Moritz, Jacques, IJspeert, Hanna, Stoepker, Chantal, van Ostaijen-ten Dam, Monique M., Heyer, Vincent, Luijsterburg, Martijn S., de Groot, Anton, Jak, Rianca, Grootaers, Gwendolynn, Wang, Jun, Rao, Pooja, Vertegaal, Alfred C.O., van Tol, Maarten J.D., Pan-Hammarström, Qiang, Reina-San-Martin, Bernardo, Shah, Girish M., van der Burg, Mirjam, van der Maarel, Silvère M., van Attikum, Haico
Publicado no J Exp Med (2020)

Mutations in ZBTB24 Are Associated with Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome Type 2

por de Greef, Jessica C., Wang, Jun, Balog, Judit, den Dunnen, Johan T., Frants, Rune R., Straasheijm, Kirsten R., Aytekin, Caner, van der Burg, Mirjam, Duprez, Laurence, Ferster, Alina, Gennery, Andrew R., Gimelli, Giorgio, Reisli, Ismail, Schuetz, Catharina, Schulz, Ansgar, Smeets, Dominique F.C.M., Sznajer, Yves, Wijmenga, Cisca, van Eggermond, Marja C., van Ostaijen-ten Dam, Monique M., Lankester, Arjan C., van Tol, Maarten J.D., van den Elsen, Peter J., Weemaes, Corry M., van der Maarel, Silvère M.
Publicado em 2011

Mutations in DNMT3B Modify Epigenetic Repression of the D4Z4 Repeat and the Penetrance of Facioscapulohumeral Dystrophy

por van den Boogaard, Marlinde L., Lemmers, Richard J.L.F., Balog, Judit, Wohlgemuth, Mariëlle, Auranen, Mari, Mitsuhashi, Satomi, van der Vliet, Patrick J., Straasheijm, Kirsten R., van den Akker, Rob F.P., Kriek, Marjolein, Laurense-Bik, Marlies E.Y., Raz, Vered, van Ostaijen-ten Dam, Monique M., Hansson, Kerstin B.M., van der Kooi, Elly L., Kiuru-Enari, Sari, Udd, Bjarne, van Tol, Maarten J.D., Nishino, Ichizo, Tawil, Rabi, Tapscott, Stephen J., van Engelen, Baziel G.M., van der Maarel, Silvère M.
Publicado no Am J Hum Genet (2016)