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Maya Schuldiner

Researcher at Weizmann Institute of Science

Publications -  179
Citations -  14192

Maya Schuldiner is an academic researcher from Weizmann Institute of Science. The author has contributed to research in topics: Endoplasmic reticulum & Gene. The author has an hindex of 48, co-authored 159 publications receiving 12233 citations. Previous affiliations of Maya Schuldiner include Hebrew University of Jerusalem & Massachusetts Institute of Technology.

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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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Effects of eight growth factors on the differentiation of cells derived from human embryonic stem cells

TL;DR: This analysis sets the stage for directing differentiation of human ES cells in culture and indicates that multiple human cell types may be enriched in vitro by specific factors.
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An ER-Mitochondria Tethering Complex Revealed by a Synthetic Biology Screen

TL;DR: In this article, the authors identified the Mmm1/Mdm10/mdm12/mdr34 complex as a molecular tether between the endoplasmic reticulum (ER) and mitochondria.
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Comprehensive characterization of genes required for protein folding in the endoplasmic reticulum

TL;DR: This strategy revealed multiple conserved factors critical for endoplasmic reticulum folding, including an intimate dependence on the later secretory pathway, a previously uncharacterized six-protein transmembrane complex, and a co-chaperone complex that delivers tail-anchored proteins to their membrane insertion machinery.
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Characterization of the expression of MHC proteins in human embryonic stem cells

TL;DR: The results demonstrate that human ES cells can express high levels of MHC-I proteins and thus may be rejected on transplantation, and isotyped several of the published ES cell lines for their human leukocyte antigens.