Zobrazeno 1 - 10
of 151
pro vyhledávání: '"J, Out"'
Autor:
John Charles A. Lacson, Shawn A. Zamani, Luis Alberto Ribeiro Froes, Nandita Mitra, Lu Qian, Scarlet H. Doyle, Esther Azizi, Claudia Balestrini, D. Timothy Bishop, William Bruno, Blanca Carlos-Ortega, Francisco Cuellar, Anne E. Cust, David E. Elder, Anne-Marie Gerdes, Paola Ghiorzo, Thais C. Grazziotin, Nelleke A. Gruis, Johan Hansson, Marko Hočevar, Veronica Höiom, Elizabeth A. Holland, Christian Ingvar, Gilles Landman, Alejandra Larre-Borges, Graham J. Mann, Montserrat Molgo, Luciana Facure Moredo, Håkan Olsson, Jacoba J. Out-Luiting, Barbara Perić, Dace Pjanova, Susana Puig, Julio Salas-Alanis, Helen Schmid, Karin A. W. Wadt, Julia A. Newton-Bishop, Peter A. Kanetsky, on behalf of the GenoMEL Study Group
Publikováno v:
BMC Public Health, Vol 21, Iss 1, Pp 1-16 (2021)
Abstract Background Individuals from melanoma-prone families have similar or reduced sun-protective behaviors compared to the general population. Studies on trends in sun-related behaviors have been temporally and geographically limited. Methods Indi
Externí odkaz:
https://doaj.org/article/294d462bfbc04eba8673cab873afcf12
Autor:
Armando N. Bastidas Torres, Rutger C. Melchers, Liana van Grieken, Jacoba J. Out-Luiting, Hailiang Mei, Cedrick Agaser, Thomas B. Kuipers, Koen D. Quint, Rein Willemze, Maarten H. Vermeer, Cornelis P. Tensen
Publikováno v:
Haematologica, Vol 107, Iss 7 (2021)
Primary cutaneous anaplastic large cell lymphoma (pcALCL), a hematological neoplasm caused by skin-homing CD30+ malignant T cells, is part of the spectrum of primary cutaneous CD30+ lymphoproliferative disorders. To date, only a small number of molec
Externí odkaz:
https://doaj.org/article/fce423f6d3854a1bb5656e0fe65ff376
Autor:
Armando N. Bastidas Torres, Davy Cats, Jacoba J. Out-Luiting, Daniele Fanoni, Hailiang Mei, Luigia Venegoni, Rein Willemze, Maarten H. Vermeer, Emilio Berti, Cornelis P. Tensen
Publikováno v:
Haematologica, Vol 107, Iss 3 (2021)
Primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma (pcAECyTCL) is a rare variant of cutaneous T-cell lymphoma with an aggressive clinical course and a very poor prognosis. Until now, neither a systematic characterization of ge
Externí odkaz:
https://doaj.org/article/0329258aee024b59b90918c65373cba9
Publikováno v:
Biochemistry and Biophysics Reports, Vol 24, Iss , Pp 100832- (2020)
Cutaneous T-cell lymphomas and leukemias (CTCLs) are a heterogeneous group of extranodal non-Hodgkin's lymphomas. These are characterized by an accumulation of malignant CD4+ T-lymphocytes in the skin, lymph nodes, and peripheral blood. Novel treatme
Externí odkaz:
https://doaj.org/article/8dcd113a6b02481897ba7c6f10c06145
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:
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
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 Figure 1 from Novel and Highly Recurrent Chromosomal Alterations in Sézary Syndrome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0984f7a43a55f5d9267bf5866cadd76a
https://doi.org/10.1158/0008-5472.22376198
https://doi.org/10.1158/0008-5472.22376198
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 1 from Novel and Highly Recurrent Chromosomal Alterations in Sézary Syndrome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d72b41385f4d41dac5fe4240a05b20f0
https://doi.org/10.1158/0008-5472.22376195.v1
https://doi.org/10.1158/0008-5472.22376195.v1
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 3 from Novel and Highly Recurrent Chromosomal Alterations in Sézary Syndrome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::196cfa3b998bb7a2ae730c8a9fa30452
https://doi.org/10.1158/0008-5472.22376189.v1
https://doi.org/10.1158/0008-5472.22376189.v1