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Mohamed Trebak

Researcher at Pennsylvania State University

Publications -  173
Citations -  9538

Mohamed Trebak is an academic researcher from Pennsylvania State University. The author has contributed to research in topics: ORAI1 & STIM1. The author has an hindex of 50, co-authored 157 publications receiving 7984 citations. Previous affiliations of Mohamed Trebak include State University of New York System & Assiut University.

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Guidelines for the use of flow cytometry and cell sorting in immunological studies (second edition)

Andrea Cossarizza, +462 more
TL;DR: These guidelines are a consensus work of a considerable number of members of the immunology and flow cytometry community providing the theory and key practical aspects offlow cytometry enabling immunologists to avoid the common errors that often undermine immunological data.
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Stim1 and Orai1 Mediate CRAC Currents and Store-Operated Calcium Entry Important for Endothelial Cell Proliferation

TL;DR: It is shown that passive store depletion by thapsigargin or receptor activation by either thrombin or the vascular endothelial growth factor activates the same pathway in primary ECs with classical SOCE pharmacological features, and the requirement of Stim1/Orai1 in the endothelial SOCE pathway is established.
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The mammalian TRPC cation channels

TL;DR: This review summarizes recent findings on the structure, regulation and function of the apparently ubiquitous TRPC cation channels.
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A Novel Native Store-operated Calcium Channel Encoded by Orai3 SELECTIVE REQUIREMENT OF Orai3 VERSUS Orai1 IN ESTROGEN RECEPTOR-POSITIVE VERSUS ESTROGEN RECEPTOR-NEGATIVE BREAST CANCER CELLS

TL;DR: Ca2+ imaging, pharmacology, patch clamp electrophysiology, and molecular knockdown are used to show that native SOCE and ICRAC in estrogen receptor-positive (ER+) breast cancer cell lines are mediated by STIM1/2 and Orai3 while estrogen receptors-negative (ER−) breast cancer cells use the canonical STIM 1/Orai1 pathway.
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Calcium signalling in T cells

TL;DR: The expression and function of various Ca2+-permeable channels in the plasma membrane, endoplasmic reticulum, mitochondria and endolysosomes of T cells are reviewed and their role in shaping immunity and the pathogenesis of immune-mediated diseases is reviewed.