Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Alexandra Löfstedt"'
Autor:
Esther Lörinc, Peter Priftakis, Jacek Winiarski, Samuel C. C. Chiang, Bianca Tesi, Nikolaos Kartalis, Yenan T. Bryceson, Fredrik Lindgren, Jan-Inge Henter, Marie Meeths, Alexandra Löfstedt
Publikováno v:
Journal of Clinical Immunology. 36:480-489
Autosomal recessive mutations in LRBA, encoding for LPS-responsive beige-like anchor protein, were described in patients with a common variable immunodeficiency (CVID)-like disease characterized by hypogammaglobulinemia, autoimmune cytopenias, and en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb9c130228e01d2185cc5e3b446ce914
https://doi.org/10.1007/s10875-016-0289-y
https://doi.org/10.1007/s10875-016-0289-y
Autor:
Samuel C. C. Chiang, Alexandra Löfstedt, Yenan T. Bryceson, Marie Meeths, Jan-Inge Henter, Martha-Lena Müller, Bianca Tesi
Publikováno v:
Experimental Cell Research
In experimental settings, lymphocyte cytotoxicity has been recognized as a central mechanism for immune defense against infected and neoplastic cells. More recently, molecular determinants of lymphocyte cytotoxicity have been identified through studi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f1ae4f1686661df98d8805d2a5fbf36
https://doi.org/10.1016/j.yexcr.2014.03.014
https://doi.org/10.1016/j.yexcr.2014.03.014
Autor:
Yenan T. Bryceson, Samuel C. C. Chiang, Ruta Samaitiene, Audrone Muleviciene, Sigita Stankeviciene, Carsten Speckmann, Birute Burnyte, Miriam Heizmann, Sandra Juozapaite, Nerija Vaiciene-Magistris, Valdone Miseviciene, Marie Meeths, Jan-Inge Henter, Vytautas Zekas, Matthias Voss, Stephan Ehl, Alexandra Löfstedt, Reda Matuzeviciene, Jelena Rascon, Egle Kvedaraite, Bianca Tesi, Anders Fasth, Martha-Lena Müller, Rosita Kiudeliene, Magnus Nordenskjöld
Publikováno v:
The Journal of Allergy and Clinical Immunology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77beda991beb1f2c11b33a6d3a354ee3
https://doi.org/10.1016/j.jaci.2018.02.031
https://doi.org/10.1016/j.jaci.2018.02.031
Autor:
Jan-Inge Henter, Yenan T. Bryceson, Marie Meeths, Erik Onelöv, Samuel C. C. Chiang, Alexandra Löfstedt
Publikováno v:
The Lancet. Haematology. 2(12)
Mutations in genes for perforin-dependent lymphocyte cytotoxicity are associated with haemophagocytic lymphohistiocytosis, a rare disease of severe hyperinflammation that typically becomes evident in early childhood. It has been suggested that indivi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df52d93f9bbdf873c9e79d1820f278bd
https://pubmed.ncbi.nlm.nih.gov/26686402
https://pubmed.ncbi.nlm.nih.gov/26686402