Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sietse J. Luk"'
Autor:
Juliette Krop, Anita van der Zwan, Marieke E. Ijsselsteijn, Hanneke Kapsenberg, Sietse J. Luk, Sanne H. Hendriks, Carin van der Keur, Lotte J. Verleng, Antonis Somarakis, Lotte van der Meeren, Geert Haasnoot, Manon Bos, Noel F.C.C. de Miranda, Susana M. Chuva de Sousa Lopes, Marie-Louise P. van der Hoorn, Frits Koning, Frans H.J. Claas, Sebastiaan Heidt, Michael Eikmans
Publikováno v:
iScience, Vol 25, Iss 7, Pp 104648- (2022)
Summary: Although the immunological complexity of the maternal-fetal interface is well appreciated, the actual interaction of maternal immune cells and fetal trophoblasts is insufficiently understood. To comprehend the composition and spatial orienta
Externí odkaz:
https://doaj.org/article/2f915b7656e34a9eb9b7e0a3202223f6
Autor:
Sietse J Luk, Dirk M van der Steen, Renate S Hagedoorn, Ekaterina S Jordanova, Marco W Schilham, Judith VMG Bovée, Arjen HG Cleven, JH Frederik Falkenburg, Karoly Szuhai, Mirjam HM Heemskerk
Publikováno v:
OncoImmunology, Vol 7, Iss 12 (2018)
Synovial sarcoma expresses multiple cancer testis antigens that could potentially be targeted by T-cell receptor (TCR) gene therapy. In this study we investigated whether PRAME-TCR-gene therapy could be an effective treatment for synovial sarcoma by
Externí odkaz:
https://doaj.org/article/65c69a122ffc47aebe923affccb2dc4b
Autor:
Boyd Kenkhuis, Marieke E. Ijsselsteijn, Thomas Höllt, Noel F C C de Miranda, Boudewijn P. F. Lelieveldt, Antonios Somarakis, Sietse J. Luk
Publikováno v:
IEEE Transactions on Visualization and Computer Graphics, 27(2), 733-743. IEEE COMPUTER SOC
IEEE Transactions on Visualization and Computer Graphics
IEEE Transactions on Visualization and Computer Graphics, 27(2)
IEEE Transactions on Visualization and Computer Graphics
IEEE Transactions on Visualization and Computer Graphics, 27(2)
Spatially-resolved omics-data enable researchers to precisely distinguish cell types in tissue and explore their spatial interactions, enabling deep understanding of tissue functionality. To understand what causes or deteriorates a disease and identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83dedd042ee6a560110f8f0057e9d9fc
http://hdl.handle.net/1887/3264160
http://hdl.handle.net/1887/3264160
Autor:
Juliette Krop, Anita van der Zwan, Marieke E. Ijsselsteijn, Hanneke Kapsenberg, Sietse J. Luk, Sanne H. Hendriks, Carin van der Keur, Lotte J. Verleng, Antonis Somarakis, Lotte van der Meeren, Geert W. Haasnoot, Manon Bos, Noel F. C. C. de Miranda, Susana M. Chuva de Sousa Lopes, Marie-Louise P. van der Hoorn, Frits Koning, Frans HJ Claas, Sebastiaan Heidt, Michael Eikmans
Publikováno v:
SSRN Electronic Journal.
Autor:
Pieter A. van der Velden, Martine J. Jager, Daniëlle Krijgsman, Dirk M. van der Steen, Renate S. Hagedoorn, Gregorius P M Luyten, Mehmet Dogrusöz, J. William Harbour, Mirjam H.M. Heemskerk, Gülçin Gezgin, Jinfeng Cao, Matthew G. Field, Karoly Szuhai, Ekaterina S. Jordanova, Sietse J. Luk
Publikováno v:
JAMA Ophthalmology, 135(6)
Gezgin, G, Luk, S J, Cao, J, Dogrusoz, M, van der Steen, D M, Hagedoorn, R S, Krijgsman, D, van der Velden, P A, Field, M G, Luyten, G P M, Szuhai, K, Harbour, J W, Jordanova, E S, Heemskerk, M H M & Jager, M J 2017, ' PRAME as a Potential Target for Immunotherapy in Metastatic Uveal Melanoma ', Jama ophthalmology, vol. 135, no. 6, pp. 541-549 . https://doi.org/10.1001/jamaophthalmol.2017.0729
Jama ophthalmology, 135(6), 541-549. American Medical Association
Gezgin, G, Luk, S J, Cao, J, Dogrusoz, M, van der Steen, D M, Hagedoorn, R S, Krijgsman, D, van der Velden, P A, Field, M G, Luyten, G P M, Szuhai, K, Harbour, J W, Jordanova, E S, Heemskerk, M H M & Jager, M J 2017, ' PRAME as a Potential Target for Immunotherapy in Metastatic Uveal Melanoma ', Jama ophthalmology, vol. 135, no. 6, pp. 541-549 . https://doi.org/10.1001/jamaophthalmol.2017.0729
Jama ophthalmology, 135(6), 541-549. American Medical Association
Importance Uveal melanoma (UM) is an intraocular primary malignant neoplasm that often gives rise to metastatic disease for which there are no effective therapies. A substantial proportion of UMs express the cancer-testis antigen PRAME (preferentiall
Autor:
Judith V.M.G. Bovée, Mirjam H.M. Heemskerk, Marco W. Schilham, Ekaterina S. Jordanova, J.H. Frederik Falkenburg, Arjen H.G. Cleven, Karoly Szuhai, Dirk M. van der Steen, Renate S. Hagedoorn, Sietse J. Luk
Publikováno v:
OncoImmunology, 7(12). Landes Bioscience
Luk, S J, Steen, D M V D, Hagedoorn, R S, Jordanova, E S, Schilham, M W, Bovée, J V MG, Cleven, A H G, Falkenburg, J H F, Szuhai, K & Heemskerk, M H M 2018, ' PRAME and HLA Class I expression patterns make synovial sarcoma a suitable target for PRAME specific T-cell receptor gene therapy ', OncoImmunology, vol. 7, no. 12 . https://doi.org/10.1080/2162402X.2018.1507600
Oncoimmunology
OncoImmunology, Vol 7, Iss 12 (2018)
OncoImmunology, 7(12)
OncoImmunology
Luk, S J, Steen, D M V D, Hagedoorn, R S, Jordanova, E S, Schilham, M W, Bovée, J V MG, Cleven, A H G, Falkenburg, J H F, Szuhai, K & Heemskerk, M H M 2018, ' PRAME and HLA Class I expression patterns make synovial sarcoma a suitable target for PRAME specific T-cell receptor gene therapy ', OncoImmunology, vol. 7, no. 12 . https://doi.org/10.1080/2162402X.2018.1507600
Oncoimmunology
OncoImmunology, Vol 7, Iss 12 (2018)
OncoImmunology, 7(12)
OncoImmunology
Synovial sarcoma expresses multiple cancer testis antigens that could potentially be targeted by T-cell receptor (TCR) gene therapy. In this study we investigated whether PRAME-TCR-gene therapy could be an effective treatment for synovial sarcoma by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62d59316e6a2ddefbdf086681278966c
https://research.vumc.nl/en/publications/d441dc61-b512-4089-9b4a-e053c6406d6c
https://research.vumc.nl/en/publications/d441dc61-b512-4089-9b4a-e053c6406d6c
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.
Review on NFATC2 (nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 2), with data on DNA, on the protein encoded, and where the gene is implicated.