Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Susan M. Schlenner"'
Autor:
Sabine Tejpar, Abhishek D Garg, Louis Boon, Massimiliano Mazzone, Jenny Sprooten, Isaure Vanmeerbeek, Stefan Naulaerts, Raquel Salvador, Jannes Govaerts, Rosa Trotta, Samantha Pretto, Shikang Zhao, Sarah Trusso Cafarello, Joren Verelst, Maarten Jacquemyn, Martyna Pociupany, Susan M Schlenner, Dirk Daelemans
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 11, Iss Suppl 1 (2023)
Externí odkaz:
https://doaj.org/article/4d74b171dccc4687ac58e89d21d9fc32
Autor:
Vanshika Malviya, Lidia Yshii, Steffie Junius, Abhishek D Garg, Stephanie Humblet‐Baron, Susan M Schlenner
Publikováno v:
Immunology and cell biology.
FOXP3-expressing regulatory T cells (T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e60936c59c4c7e7215eb7dd790e7daf
https://pubmed.ncbi.nlm.nih.gov/36479949
https://pubmed.ncbi.nlm.nih.gov/36479949
Autor:
Jeroen Raes, Pierre Lemaitre, Margaux Gerbaux, Steffie Junius, Kailash Singh, Václav Gergelits, Vanshika Malviya, Oliver T. Burton, Frederik Staels, Adrian Liston, Adamantios V. Mavrogiannis, Stephanie Humblet-Baron, Raul Yhossef Tito Tadeo, Susan M. Schlenner
Publikováno v:
Science Immunology. 6
Regulatory T cells (Tregs) are indispensable for the control of immune homeostasis and have clinical potential as a cell therapy for treating autoimmunity. Tregs can lose expression of the lineage-defining Foxp3 transcription factor and acquire effec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::133306e499aff16dc10d01aad4f61acf
https://doi.org/10.1126/sciimmunol.abe4723
https://doi.org/10.1126/sciimmunol.abe4723
Autor:
Kelly Hilven, Bénédicte Dubois, Satu Mustjoki, Lies Van Horebeek, Susan M. Schlenner, Adrian Liston, Klara Mallants, An Goris, Annemarie van Nieuwenhuijze, Paula Savola, Tiina Kelkka
Publikováno v:
Human Molecular Genetics
The role of somatic variants in diseases beyond cancer is increasingly being recognized, with potential roles in autoinflammatory and autoimmune diseases. However, as mutation rates and allele fractions are lower, studies in these diseases are substa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e77cd9331fa625846dcfd2121bc1f00b
https://doi.org/10.1093/hmg/ddy425
https://doi.org/10.1093/hmg/ddy425
Autor:
Oliver T. Burton, Tino Hochepied, Carlos P. Roca, Félix Lombard-Vadnais, Adrian Liston, Kailash Singh, Alena Moudra, Meryem Aloulou, Francisco J. Naranjo, James Dooley, Timotheus Y.F. Halim, Sylvie Lesage, Carly E. Whyte, Lubna Kouser, Susan M. Schlenner
Interleukin 2 (IL-2) is a key homeostatic cytokine, with potential therapeutic applications in both immunogenic and tolerogenic immune modulation. Clinical application has been hampered by pleiotropic functionality and wide-spread receptor expression
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4132ed651c3551b982dd32fb50756a98
https://doi.org/10.1101/2020.12.18.423431
https://doi.org/10.1101/2020.12.18.423431
Autor:
Steffie, Junius, Adamantios V, Mavrogiannis, Pierre, Lemaitre, Margaux, Gerbaux, Frederik, Staels, Vanshika, Malviya, Oliver, Burton, Václav, Gergelits, Kailash, Singh, Raul Yhossef, Tito Tadeo, Jeroen, Raes, Stephanie, Humblet-Baron, Adrian, Liston, Susan M, Schlenner
Publikováno v:
Science immunology. 6(61)
Regulatory T cells (T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4fb10982bd5c2cf2beca929fb8a76a00
https://pubmed.ncbi.nlm.nih.gov/34301799
https://pubmed.ncbi.nlm.nih.gov/34301799
Autor:
Margareta Nikolic, Mathieu Bollen, Raphael Rouget, Marloes C. M. Jonkhout, Mónica Ferreira, Shannah Boens, Aleyde Van Eynde, Kifayathullah Liakath-Ali, Kathelijne Szekér, Susan M. Schlenner, Iris Verbinnen
Publikováno v:
J Invest Dermatol
Nuclear inhibitor of protein phosphatase 1 (NIPP1) is a ubiquitously expressed nuclear protein that regulates functions of protein serine/threonine phosphatase-1 in cell proliferation and lineage specification. The role of NIPP1 in tissue homeostasis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72e3630612c4effcc8c41def4dcb0afe
https://lirias.kuleuven.be/handle/123456789/649048
https://lirias.kuleuven.be/handle/123456789/649048
Autor:
Isaure Vanmeerbeek, Geert Bultynck, Susan M. Schlenner, Shaun Martin, Pieter De Wijngaert, Peter Vangheluwe, Dmitri V. Krysko, Jenny Sprooten, Abhishek D. Garg, Jan B. Parys, Peter Vandenabeele
Publikováno v:
CELLS
Cells
Cells, Vol 9, Iss 1823, p 1823 (2020)
Cells
Cells, Vol 9, Iss 1823, p 1823 (2020)
Immune-checkpoint blockers (ICBs) have revolutionized oncology and firmly established the subfield of immuno-oncology. Despite this renaissance, a subset of cancer patients remain unresponsive to ICBs due to widespread immuno-resistance. To "break" c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f9614c7549b3952d6661f28a2faee66
https://hdl.handle.net/1854/LU-8675048
https://hdl.handle.net/1854/LU-8675048
Autor:
Mieke Metzemaekers, Susan M. Schlenner, Emanuela Pasciuto, Patrick Matthys, Stephanie Humblet-Baron, Elien Smeets, Adrian Liston, Axelle Kerstens, Joost Schymkowitz, Laura Seldeslachts, Paul Proost, Sarah Haßdenteufel, Carine Wouters, Frank Claessens, Julika Neumann, Teresa Prezzemolo, Nancy Boeckx, Vasiliki Lagou, John S. Barber, Frederic Rousseau, Bert Malengier-Devlies, Rob van der Kant, Erika Van Nieuwenhove, Christine Devalck, Isabelle Meyts, Sven Lang, Richard Zimmermann, Daniele Di Marino, Sebastian Munck, Mathijs Willemsen
Publikováno v:
Journal of allergy and clinical immunology
The Journal of Allergy and Clinical Immunology
Journal of Allergy and Clinical Immunology
The Journal of Allergy and Clinical Immunology
Journal of Allergy and Clinical Immunology
Background: The molecular cause of severe congenital neutropenia (SCN) is unknown in 30% to 50% of patients. SEC61A1 encodes the α-subunit of the Sec61 complex, which governs endoplasmic reticulum protein transport and passive calcium leakage. Recen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b4167ed5c5db874f50ba44ce06bf3f6
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/307196
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/307196
Autor:
Kathleen Stirrups, Chris Van Geet, Stephanie Humblet-Baron, Ernest Turro, Daniel Greene, Isabelle Meyts, Erika Van Nieuwenhove, Roxanne Collin, Patrick Matthys, Karen Put, Sylvie Lesage, Jessica Heremans, Adrian Liston, Josselyn E. Garcia-Perez, Christopher J. Penkett, Ingele Casteels, Francis de Zegher, Chantal Thys, Kathleen Freson, Susan M. Schlenner, Carine Wouters
Publikováno v:
Journal of Allergy and Clinical Immunology. 142:630-646
BACKGROUND: Roifman syndrome is a rare inherited disorder characterized by spondyloepiphyseal dysplasia, growth retardation, cognitive delay, hypogammaglobulinemia, and, in some patients, thrombocytopenia. Compound heterozygous variants in the small
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdada06f12b6b129608753fed95333e0
https://doi.org/10.1016/j.jaci.2017.11.061
https://doi.org/10.1016/j.jaci.2017.11.061