Zobrazeno 1 - 10
of 95
pro vyhledávání: '"Mehmet Uzunel"'
Autor:
Karin E. Lundin, Qing Wang, Abdulrahman Hamasy, Per Marits, Mehmet Uzunel, Valtteri Wirta, Ann-Charlotte Wikström, Anders Fasth, Olov Ekwall, C.I. Edvard Smith
Publikováno v:
BMC Pediatrics, Vol 18, Iss 1, Pp 1-8 (2018)
Abstract Background A novel immunodeficiency, frequently accompanied by high serum-IgE, and caused by mutations in the PGM3 gene was described in 2014. To date there are no unique phenotype characteristics for PGM3 deficiency. PGM3 encodes a carbohyd
Externí odkaz:
https://doaj.org/article/a6e1df9a6703422893cc377f144f1b9d
Autor:
Arwen Stikvoort, Mikael Sundin, Mehmet Uzunel, Jens Gertow, Berit Sundberg, Marie Schaffer, Jonas Mattsson, Michael Uhlin
Publikováno v:
PLoS ONE, Vol 11, Iss 5, p e0154737 (2016)
Long-term stable mixed chimerism is a rare and poorly understood phenomenon post hematopoietic stem cell transplantation. This study aims to shed light on whether the two hematopoietic systems in patients with mixed chimerism remain functional. Addit
Externí odkaz:
https://doaj.org/article/9ce91c58026c43a6a4e6506d609411ab
Autor:
Anna Maria Jonsson Kanold, Elisabet Svenungsson, Iva Gunnarsson, Cecilia Götherström, Leonid Padyukov, Nikos Papadogiannakis, Mehmet Uzunel, Magnus Westgren
Publikováno v:
PLoS ONE, Vol 8, Iss 9, p e74534 (2013)
BackgroundNaturally acquired microchimerism may arise in the mother and her child during pregnancy when bidirectional trafficking of cells occurs through the placental barrier. The occurrence of maternal microchimerism (maternal cells in the offsprin
Externí odkaz:
https://doaj.org/article/ffc739b0757c4eacb5b9e78708bbf883
Autor:
Ahmed Gaballa, Mikael Sundin, Arwen Stikvoort, Muhamed Abumaree, Mehmet Uzunel, Darius Sairafi, Michael Uhlin
Publikováno v:
International Journal of Molecular Sciences, Vol 17, Iss 10, p 1705 (2016)
Allogeneic hematopoietic stem cell transplantation (HSCT) is a well-established treatment modality for a variety of malignant diseases as well as for inborn errors of the metabolism or immune system. Regardless of disease origin, good clinical effect
Externí odkaz:
https://doaj.org/article/b0bacfb3011646c699ae5003ea2fda43
Publikováno v:
Vox Sanguinis. 117:1296-1301
Anti-D prophylaxis, administered to RhD-negative women, has significantly reduced the incidence of RhD immunization. Non-invasive fetal RHD screening has been used in Stockholm for more than 10 years to identify women who will benefit from prophylaxi
Autor:
Abdulrahman Hamasy, Olov Ekwall, Qing Wang, C. I. Edvard Smith, Valtteri Wirta, Ann-Charlotte Wikström, Mehmet Uzunel, Karin E. Lundin, Anders Fasth, Per Marits
Publikováno v:
BMC Pediatrics, Vol 18, Iss 1, Pp 1-8 (2018)
BMC Pediatrics
BMC Pediatrics
Background A novel immunodeficiency, frequently accompanied by high serum-IgE, and caused by mutations in the PGM3 gene was described in 2014. To date there are no unique phenotype characteristics for PGM3 deficiency. PGM3 encodes a carbohydrate-modi
Autor:
Mehmet Uzunel, Bita Khoein, Yaser Heshmati, Helen Kaipe, Julian Walfridsson, Olle Ringdén, Behnam Sadeghi
Publikováno v:
Cytotherapy. 17:1732-1745
Background aims Human decidual stromal cells ( h DSCs) may cure acute graft-versus-host disease (GVHD) in humans. We evaluated immunosuppression by xenogenic h DSCs in mice, both in vitro and in vivo . Methods h DSCs inhibited mouse lymphocyte prolif
Autor:
Mehmet Uzunel, Olle Ringdén, P. Svenberg, Tengyu Wang, Michael Uhlin, Jonas Mattsson, Emma Watz, Mats Remberger
Publikováno v:
Clinical transplantation. 33(6)
Background Graft-versus-host disease (GVHD) and relapse remain majobstacles ftreatment success in allogeneic hematopoietic stem cell transplantation (HSCT). In the present study, we evaluated the immune cell profile of the graft to outcome after HSCT
Publikováno v:
Immunology. 144:687-703
Antigen recognition reduces T-cell motility, and induces prolonged contact with antigen-presenting cells and activation through mechanisms that remain unclear. Here we show that the T-cell receptor (TCR) and CD28 regulate T-cell motility, contact wit
Autor:
Brigitta Omazic, Mehmet Uzunel, Jacek Winiarski, Berit Sundberg, Henric Lindqvist, Mikael Sundin, M. Remberger
Publikováno v:
Pediatric Blood & Cancer. 62:890-896
Background Hypogammaglobulinemia (hypo-IgG) is common early post-HSCT in children, occasionally necessitating long-term immunoglobulin (Ig) G replacement therapy. IgG replacement may not reduce mortality, although infectious complications are decreas