M
Marianna Kulka
Researcher at National Institute for Nanotechnology
Publications - 15
Citations - 1260
Marianna Kulka is an academic researcher from National Institute for Nanotechnology. The author has contributed to research in topics: Mast cell & Immunoglobulin E. The author has an hindex of 7, co-authored 15 publications receiving 955 citations.
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Journal ArticleDOI
Identification of a mast-cell-specific receptor crucial for pseudo-allergic drug reactions
Benjamin D. McNeil,Priyanka Pundir,Sonya Meeker,Liang Han,Bradley J. Undem,Marianna Kulka,Xinzhong Dong +6 more
TL;DR: In this paper, a mouse model was introduced to study mast cell activation by basic secretagogues and identify MRGPRX2 as a potential therapeutic target to reduce a subset of drug-induced adverse effects.
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Mast Cell Mediators: Their Differential Release and the Secretory Pathways Involved
TL;DR: This review summarizes the knowledge of MC mediators and will focus on what is known about the discriminatory release of these mediators dependent upon diverse stimuli, MC phenotypes, and species of origin, as well as on the intracellular synthesis, storage, and secretory processes involved.
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Cross-Talk Between Human Mast Cells and Epithelial Cells By IgE-Mediated Periostin Production in Eosinophilic Nasal Polyps
Dae Woo Kim,Marianna Kulka,Ara Jo,Kyoung Mi Eun,Narcy Arizmendi,Brian P. Tancowny,Seung No Hong,Jung Pyo Lee,Hong Ryul Jin,Richard F. Lockey,Dong-Kyu Kim,Seong H. Cho +11 more
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American cranberry (Vaccinium macrocarpon) extract affects human prostate cancer cell growth via cell cycle arrest by modulating expression of cell cycle regulators.
Bob A. Deziel,James MacPhee,Kunal Patel,Adriana Catalli,Marianna Kulka,Catherine C. Neto,Katherine Gottschall-Pass,Robert A. R. Hurta +7 more
TL;DR: It is demonstrated that phytochemical extracts from the American cranberry (Vaccinium macrocarpon) can affect the behaviour of human prostate cancer cells in vitro and further support the potential health benefits associated with cranberries.
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n-3 Polyunsaturated fatty acids inhibit Fc ε receptor I-mediated mast cell activation
TL;DR: N-3 PUFA suppress FcεRI-mediated activation of mast cells, which results in reduced mediator release and a decrease in LAT and Lyn expression as well as abnormal shuttling of Fc ε receptor I to lipid rafts.