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Hermona Soreq

Researcher at Hebrew University of Jerusalem

Publications -  521
Citations -  27215

Hermona Soreq is an academic researcher from Hebrew University of Jerusalem. The author has contributed to research in topics: Acetylcholinesterase & Cholinergic. The author has an hindex of 80, co-authored 503 publications receiving 25411 citations. Previous affiliations of Hermona Soreq include Tel Aviv Sourasky Medical Center & Life Sciences Institute.

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Differentiation of human embryonic stem cells into embryoid bodies compromising the three embryonic germ layers.

TL;DR: The ability to induce formation of human embryoid bodies that contain cells of neuronal, hematopoietic and cardiac origins will be useful in studying early human embryonic development as well as in transplantation medicine.
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Amplification, enhanced expression and possible rearrangement of EGF receptor gene in primary human brain tumours of glial origin

TL;DR: 4 of 10 primary brain tumours of glial origin which express levels of EGF receptors that are higher than normal also have amplified EGF receptor genes, suggesting that such altered expression and amplification is a particular feature of certain human tumours.
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Function of alternative splicing.

TL;DR: Evidence is now accumulating that alternative splicing coordinates physiologically meaningful changes in protein isoform expression and is a key mechanism to generate the complex proteome of multicellular organisms.
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Acetylcholinesterase New roles for an old actor

TL;DR: The time is ripe to summarize the evidence on a remarkable diversity of acetylcholinesterase functions, as well as some of the long-suspected 'non-classical' actions of this enzyme, which have more recently driven a profound revolution in research.
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Acute stress facilitates long-lasting changes in cholinergic gene expression

TL;DR: The results suggest a model in which robust cholinergic stimulation triggers rapid induction of the gene encoding the transcription factor c-Fos, which mediates selective regulatory effects on the long-lasting activities of genes involved in acetylcholine metabolism.