Author
E. Weiss
Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.
Biology Disciplines
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2016-2024 · peak 3/yrCo-Author Collaboration Network
10 top collaborators · 7 mutual co-author links11 papers
Recent·Most cited
Facile detection of peptide-protein interactions using an electrophoretic crosslinking shift assay
The paper introduces ECSA, an electrophoretic crosslinking shift assay, to detect low-affinity peptide-protein interactions, demonstrating its effectiveness with MAP kinase and D-motif peptides.
bioRxiv · Apr 22, 2024Biochemistry
CD56-mediated activation of human natural killer cells is triggered by Aspergillus fumigatus galactosaminogalactan
L. Heilg, F. Natasha, N. Trinks, V. K. AIMANIANDA BOPAIAH, S. Sze Wah Wong, T. Fontaine, U. Terpitz, L. Strobel, F. Le Mauff, D. Sheppard, S. Schaeuble, O. Kurzai, K. Huenniger, E. Weiss, M. Vargas, , J. Loeffler
This study identifies galactosaminogalactan as the fungal ligand for CD56 on human NK cells, triggering antifungal responses and immune cell activation.
bioRxiv · Aug 18, 2023 · PreprintMicrobiology
Unprecedented yet gradual nature of first millennium CE intercontinental crop plant dispersal revealed in ancient Negev desert refuse
D. Fuks, Y. Melamed, D. Langgut, T. Erickson-Gini, Y. Tepper, G. Bar-Oz, E. Weiss
The paper analyzes ancient Negev desert refuse to show that the first millennium CE was a significant period for crop dispersal, supporting a gradualist model over abrupt changes.
bioRxiv · Dec 1, 2022Ecology
Rapid differentiation of regulatory CD4+ T cells in the infarcted myocardium blunts in situ inflammation
M. Delgobo, E. Weiss, D. E. Ashour, L. Popiolkowski, P. Arampatzi, V. Stangl, P. Arias-Loza, P. Rainer, A.-E. Saliba, B. Ludewig, U. Hofmann, S. Frantz, G. C. Ramos
This study shows that CD4+ T cells in the infarcted heart rapidly become regulatory, reducing inflammation, and identifies mechanisms of their differentiation and function.
bioRxiv · Mar 25, 2022Immunology
Trade-Offs Between Hepatic Host Defense and Metabolic Programs Underlie Sex-Biased Diseases
J. Nikkanen, Y. A. Leong, W. C. Krause, D. Dermadi, J. A. Maschek, T. Van Ry, J. Cox, E. Weiss, O. Gokcumen, A. Chawla, H. Ingraham
This study identifies a sex-dependent trade-off between hepatic host defense and metabolic programs in mice, showing that BCL6 protects males from infection but increases metabolic disease risk under dietary excess.
bioRxiv · Jan 7, 2022Physiology
4 β-hydroxycholesterol is a pro-lipogenic factor that promotes SREBP1c expression and activity through Liver X-receptor.
O. Moldavski, P.-J. H. Zushin, C. A. Berdan, R. J. van Eijkeren, X. Jiang, M. Qian, D. S. Ory, D. F. Covey, D. Nomura, A. Stahl, E. Weiss, R. Zoncu
This study identifies 4β-hydroxycholesterol as a pro-lipogenic factor that activates SREBP1c via LXR to promote de novo lipogenesis.
bioRxiv · Aug 20, 2020Biochemistry
On the origin of photoperiod non-responsiveness in barley
R. Sharma, S. Shaaf, K. Neumann, Y. Guo, M. Mascher, M. David, A. Al-Yassin, H. Özkan, T. Blake, S. Hübner, N. P. Castaneda-Alvarez, S. Grando, S. Ceccarelli, M. Baum, A. Graner, , B. Kilian
This study identifies the origin of photoperiod non-responsiveness in barley by analyzing genetic variation and haplotype relationships in wild and domesticated barleys.
bioRxiv · Jul 2, 2020 · PreprintPlant Biology
Ndr/Lats kinases bind specific Mob-family coactivators through a conserved and modular interface
B. Parker, G. Gogl, M. Balint, C. Hetenyi, A. Remenyi, E. Weiss
The paper determines the crystal structures of Ndr/Lats kinase NTR-Mob complexes and identifies conserved residues involved in kinase-coactivator binding and activation.
bioRxiv · Mar 19, 2019Biochemistry
LiF-MS: Mapping unstructured peptide-protein interactions using Ligand-Footprinting Mass Spectrometry
B. Parker, E. Goncz, D. T. Krist, A. Statsyuk, A. I. Nesvizhskii, E. Weiss
This paper introduces LiF-MS, a method to map peptide-protein interactions by detecting binding sites and dynamic disorder using mass spectrometry.
bioRxiv · Jul 3, 2018 · PreprintBiochemistry
Adipocyte Jak2 Mediates Growth Hormone-Induced Hepatic Insulin Resistance
K. Corbit, J. P. G. Camporez, J. L. Tran, C. G. Wilson, D. Lowe, S. Nordstrom, K. Ganeshan, R. J. Perry, G. Schulman, M. J. Jurczak, E. Weiss
This study shows that adipocyte Jak2 mediates GH-induced hepatic insulin resistance through an adipose-dependent mechanism.
bioRxiv · Sep 20, 2016Physiology