Susceptibility genes in the pathogenesis of murine lupus

por Nguyen, Charles, Limaye, Nisha, Wakeland, Edward K
Publicado 2002

Liquid Biopsy to Detect Minimal Residual Disease: Methodology and Impact

por Honoré, Natasha, Galot, Rachel, van Marcke, Cédric, Limaye, Nisha, Machiels, Jean-Pascal
Publicado 2021

High p16(INK4a), a marker of cellular senescence, is associated with renal injury, impairment and outcome in lupus nephritis

por Tilman, Gaëlle, Bouzin, Caroline, Aydin, Selda, Tamirou, Farah, Galant, Christine, Coulie, Pierre G, Houssiau, Frédéric, Lauwerys, Bernard, Limaye, Nisha
Publicado 2021

Somatic Mutations in the Angiopoietin-Receptor TIE2 Can Cause Both Solitary and Multiple Sporadic Venous Malformations

por Limaye, Nisha, Wouters, Vinciane, Uebelhoer, Melanie, Tuominen, Marjut, Wirkkala, Riikka, Mulliken, John B., Eklund, Lauri, Boon, Laurence M., Vikkula, Miikka
Publicado 2008

Suppressed NFAT-dependent VEGFR1 expression and constitutive VEGFR2 signaling in infantile hemangioma

por Jinnin, Masatoshi, Medici, Damian, Park, Lucy, Limaye, Nisha, Liu, Yanqiu, Boscolo, Elisa, Bischoff, Joyce, Vikkula, Miikka, Boye, Eileen, Olsen, Bjorn R.
Publicado 2008

Common Transcriptomic Effects of Abatacept and Other DMARDs on Rheumatoid Arthritis Synovial Tissue

por Triaille, Clement, Durez, Patrick, Sokolova, Tatiana, Tilman, Gaëlle, Méric de Bellefon, Laurent, Galant, Christine, Coulie, Pierre, Lauwerys, Bernard R., Limaye, Nisha
Publicado 2021

p16(Ink4a), a marker of cellular senescence, is associated with renal disease in the B6.NZMSle1/Sle2/Sle3 mouse model of lupus

por Tilman, Gaëlle, Dupré, Emilie, Watteyne, Laura, Baert, Charlotte Anne, Nolf, Delphine, Benhaddi, Fatima, Lambert, Fanny, Daumerie, Aurélie, Bouzin, Caroline, Lucas, Sophie, Limaye, Nisha
Publicado 2023

Development of SARS-CoV2 humoral response including neutralizing antibodies is not sufficient to protect patients against fatal infection

por Choteau, Mathilde, Scohy, Anaïs, Messe, Stéphane, Luyckx, Mathieu, Dechamps, Mélanie, Montiel, Virginie, Yombi, Jean Cyr, Gruson, Damien, Limaye, Nisha, Michiels, Thomas, Dumoutier, Laure
Publicado 2022

CCNF (Cyclin F) as a Candidate Gene for Familial Hodgkin Lymphoma: Additional Evidence for the Importance of Mitotic Checkpoint Defects in Tumorigenesis

por Khoury, Elsa, Maalouf, Hiba, Mendola, Antonella, Boutry, Simon, Camboni, Alessandra, D’Angiolella, Vincenzo, Choquet, Sylvain, Landman-Parker, Judith, Besson, Caroline, Poirel, Hélène A., Limaye, Nisha
Publicado 2023

Disease activity drives transcriptomic heterogeneity in early untreated rheumatoid synovitis

por Triaille, Clément, Tilman, Gaëlle, Sokolova, Tatiana, Loriot, Axelle, Marchandise, Joelle, De Montjoye, Stéphanie, Nzeusseu-Toukap, Adrien, Méric de Bellefon, Laurent, Bouzin, Caroline, Galant, Christine, Durez, Patrick, Lauwerys, Bernard R, Limaye, Nisha
Publicado 2023

Tumor sequencing is useful to refine the analysis of germline variants in unexplained high-risk breast cancer families

por Van Marcke, Cédric, Helaers, Raphaël, De Leener, Anne, Merhi, Ahmad, Schoonjans, Céline A., Ambroise, Jérôme, Galant, Christine, Delrée, Paul, Rothé, Françoise, Bar, Isabelle, Khoury, Elsa, Brouillard, Pascal, Canon, Jean-Luc, Vuylsteke, Peter, Machiels, Jean-Pascal, Berlière, Martine, Limaye, Nisha, Vikkula, Miikka, Duhoux, François P.
Publicado 2020

Somatic mosaic IDH1 or IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome

por Pansuriya, Twinkal C., van Eijk, Ronald, Adamo, Pio d', van Ruler, Maayke A.J.H., Kuijjer, Marieke L., Oosting, Jan, Cleton-Jansen, Anne-Marie, van Oosterwijk, Jolieke G., Verbeke, Sofie L.J., Meijer, Daniëlle, van Wezel, Tom, Nord, Karolin H., Sangiorgi, Luca, Toker, Berkin, Liegl-Atzwanger, Bernadette, San-Julian, Mikel, Sciot, Raf, Limaye, Nisha, Kindblom, Lars-Gunnar, Daugaard, Soeren, Godfraind, Catherine, Boon, Laurence M., Vikkula, Miikka, Kurek, Kyle C., Szuhai, Karoly, French, Pim J., Bovée, Judith V.M.G.
Publicado 2011