Zobrazeno 1 - 10
of 112
pro vyhledávání: '"Remco, Van Doorn"'
Autor:
Roderick C. Slieker, Daniël O. Warmerdam, Maarten H. Vermeer, Remco van Doorn, Mirjam H. M. Heemskerk, Ferenc A. Scheeren
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-7 (2024)
Abstract The Major Histocompatibility Complex class I (MHC-I) system plays a vital role in immune responses by presenting antigens to T cells. Allele specific technologies, including recombinant MHC-I technologies, have been extensively used in T cel
Externí odkaz:
https://doaj.org/article/db6bb0c4084a42c19c01bc85581e798a
Autor:
Gido Gravesteijn, Remco J. Hack, Aat A. Mulder, Minne N. Cerfontaine, Remco van Doorn, Ingrid M. Hegeman, Carolina R. Jost, Julie W. Rutten, Saskia A.J. Lesnik Oberstein
Publikováno v:
Cerebral Circulation - Cognition and Behavior, Vol 6, Iss , Pp 100107- (2024)
Externí odkaz:
https://doaj.org/article/ded8e4caaa614d8fa6b31004e0b12348
Publikováno v:
Acta Dermato-Venereologica, Vol 103 (2023)
Abstract is missing (Short communication)
Externí odkaz:
https://doaj.org/article/c5ecc17e78a54622a935f989062912b1
Autor:
Eliza Mari Kwesi-Maliepaard, Muddassir Malik, Tibor van Welsem, Remco van Doorn, Maarten H. Vermeer, Hanneke Vlaming, Heinz Jacobs, Fred van Leeuwen
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Cutaneous T-cell lymphomas (CTCLs) are a subset of T-cell malignancies presenting in the skin. The treatment options for CTCL, in particular in advanced stages, are limited. One of the emerging therapies for CTCL is treatment with histone deacetylase
Externí odkaz:
https://doaj.org/article/b241d9f6d9584cc68a04b26f8668305b
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-9 (2021)
Abstract Background Macrophage activation syndrome (MAS) is a life-threatening hyperinflammatory syndrome and is caused by a severely dysregulated immune response. It has rarely been associated with neonatal lupus. Case presentation We present a fema
Externí odkaz:
https://doaj.org/article/1d4b0b2ce3d44f16a643d51fa105b8c0
Autor:
Rajiv S Raktoe, Marion H Rietveld, Jacoba J Out-Luiting, Marianna Kruithof-de Julio, Paul PM van Zuijlen, Remco van Doorn, Abdoelwaheb El Ghalbzouri
Publikováno v:
Scars, Burns & Healing, Vol 6 (2020)
Background: In burn patients, wound healing is often accompanied by hypertrophic scar (HS) development, resulting in both functional and aesthetic problems. HSs are characterised by abundant presence of myofibroblasts that contribute to overproductio
Externí odkaz:
https://doaj.org/article/4953c9c3c9d64ef4aadc4cd441c4ed64
Autor:
Catarina Salgado, Celine Roelse, Rogier Nell, Nelleke Gruis, Remco van Doorn, Pieter van der Velden
Publikováno v:
PLoS ONE, Vol 15, Iss 4, p e0231418 (2020)
The telomerase reverse transcriptase (TERT) gene is responsible for telomere maintenance in germline and stem cells, and is re-expressed in 90% of human cancers. CpG methylation in the TERT promoter (TERTp) was correlated with TERT mRNA expression. F
Externí odkaz:
https://doaj.org/article/d122cb4569974013b8507b8bce875a18
Publikováno v:
Acta Dermato-Venereologica, Vol 98, Iss 7, Pp 667-670 (2018)
Approximately 10% of all melanomas occur in subjects with a family history of melanoma. This retrospective follow-up study investigated the characteristics of patients with familial melanoma who made unscheduled visits to our pigmented lesions clinic
Externí odkaz:
https://doaj.org/article/61528ee4a0d846379d3d362b5e2e4d5c
Autor:
Cornelis P. Tensen, Rein Willemze, Karoly Szuhai, Marije IJszenga, Jeroen Knijnenburg, Jacoba J. Out-Luiting, Ulf Landegren, Karl-Johan Leuchowius, Ola Söderberg, Sylke Gellrich, Marie-Louise Geerts, Marie-Jeanne P. Gerritsen, Pieter C. van Voorst Vader, Sean Whittaker, Xin Mao, Remco Dijkman, Remco van Doorn, Maarten H. Vermeer
Supplementary Table 4 from Novel and Highly Recurrent Chromosomal Alterations in Sézary Syndrome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cab9a9e190142539a89d6dab66f48e4
https://doi.org/10.1158/0008-5472.22376186
https://doi.org/10.1158/0008-5472.22376186
Autor:
Cornelis P. Tensen, Rein Willemze, Karoly Szuhai, Marije IJszenga, Jeroen Knijnenburg, Jacoba J. Out-Luiting, Ulf Landegren, Karl-Johan Leuchowius, Ola Söderberg, Sylke Gellrich, Marie-Louise Geerts, Marie-Jeanne P. Gerritsen, Pieter C. van Voorst Vader, Sean Whittaker, Xin Mao, Remco Dijkman, Remco van Doorn, Maarten H. Vermeer
Supplementary Table 2 from Novel and Highly Recurrent Chromosomal Alterations in Sézary Syndrome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c019720b072ef1a7656554e6a439231
https://doi.org/10.1158/0008-5472.22376192
https://doi.org/10.1158/0008-5472.22376192