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991.
The discovery that NK cells are able to specifically recognize cells lacking the expression of self‐MHC class I molecules provided the first insight into NK cell recognition of tumour cells. It started a flourishing field of NK cell research aimed at exploring the molecular nature of NK cell receptors involved in tumour cell recognition. While much of the important early work was conducted in murine experimental model systems, studies of human NK cells rapidly followed. Over the years, human NK cell research has swiftly progressed, aided by new detailed molecular information on human NK cell development, differentiation, molecular specificity, tissue heterogeneity and functional capacity. NK cells have also been studied in many different diseases aside from cancer, including viral diseases, autoimmunity, allergy and primary immunodeficiencies. These fields of research have all, indirectly or directly, provided further insights into NK cell‐mediated recognition of target cells and paved the way for the development of NK cell‐based immunotherapies for human cancer. Excitingly, NK cell‐based immunotherapy now opens up for novel strategies aimed towards treating malignant diseases, either alone or in combination with other drugs. Reviewed here are some personal reflections of select contributions leading up to the current state‐of‐the‐art in the field, with a particular emphasis on contributions from our own laboratory. This review is part of a series of articles on immunology in Scandinavia, published in conjunction with the 50th anniversary of the Scandinavian Society for Immunology. 相似文献
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Looking towards objective quality evaluation in colonoscopy: Analysis of visual gaze patterns 下载免费PDF全文
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Rhabdomyosarcoma and rhabdomyoma associated with nevoid basal cell carcinoma syndrome: Local treatment strategy 下载免费PDF全文
Adeline Kerbrat MS Aurelie Beaufrere MS Cecilia Neiva‐Vaz MD Louis Galmiche MD PhD Kahina Belhous MD Daniel Orbach MD Marion Gauthier‐Villars MD Arnaud Picard MD PhD Natacha Kadlub MD PhD 《Pediatric dermatology》2018,35(4):e245-e247
This article presents the case of a child presenting with a rhabdomyosarcoma associated with a fetal rhabdomyoma in the setting of nevoid basal cell carcinoma syndrome. Oncologic strategy is discussed. 相似文献
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Subcategorization of atypia of undetermined significance/follicular lesion of undetermined significance (AUS/FLUS): a study applying Thyroid Imaging Reporting and Data System (TIRADS) 下载免费PDF全文
Jung Hyun Yoon Hyeong Ju Kwon Eun‐Kyung Kim Hee Jung Moon Jin Young Kwak 《Clinical endocrinology》2016,85(2):275-282
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Efficacy and Safety of Transthoracic Echocardiography Alone in Transcatheter Closure of Secundum‐Type Atrial Septal Defects in Adults 下载免费PDF全文
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Targeted ultradeep next‐generation sequencing as a method for KIT D816V mutation analysis in mastocytosis 下载免费PDF全文
Thomas Kristensen Sigurd Broesby‐Olsen Hanne Vestergaard Carsten Bindslev‐Jensen Michael Boe Mller 《European journal of haematology》2016,96(4):381-388
Next‐generation sequencing (NGS) is becoming increasingly used for diagnostic mutation analysis in myeloid neoplasms and may also represent a feasible technique in mastocytosis. However, detection of the KIT D816V mutation requires a highly sensitive method in most patients due to the typically low mutation levels. In this study, we established an NGS‐based KIT mutation analysis and analyzed the sensitivity of D816V detection using the Ion Torrent platform. Eighty‐two individual NGS analyses were included in the study. All samples were also analyzed using highly sensitive KIT D816V mutation‐specific qPCR. Measurements of the background level in D816V‐negative samples supported a cutoff for positivity of 0.2% in three different NGS panels. Clinical samples from patients with SM that tested positive using qPCR with a D816V allele burden >0.2% also tested positive using NGS. Samples that tested positive using qPCR with an allele burden <0.2% tested negative using NGS. We thereby demonstrate that caution should be taken when using the potentially very sensitive NGS technique for KIT D816V mutation analysis in mastocytosis, as many patients with SM have D816V mutation levels below the detection limit of NGS. A dedicated and highly sensitive KIT D816V mutation analysis therefore remains important in mastocytosis diagnostics. 相似文献