The DOI matches its Crossref record; 12 of the 12 references it cites were found in a registry or an index.
The ins and outs of endoplasmic reticulum‐controlled lipid biosynthesis
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Donnelly, K. L., Smith, C. I., Schwarzenberg, S. J., Jessurun, J., Boldt, M. D., & Parks, E. J. (2005) · Journal of Clinical Investigation · doi:10.1172/jci23621 · Cited by 3,604
Activation of a metabolic gene regulatory network downstream of mTOR complex 1
Düvel, K., Yecies, J. L., Menon, S., Raman, P., Lipovsky, A. I., Souza, A. L., Triantafellow, E., Ma, Q., Gorski, R., Cleaver, S., et al. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.06.022 · Cited by 2,020
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Lipid landscapes and pipelines in membrane homeostasis
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Signaling functions of phosphatidic acid
WANG, X., DEVAIAH, S., ZHANG, W., & WELTI, R. (2006) · Progress in Lipid Research · doi:10.1016/j.plipres.2006.01.005 · Cited by 757
Sriburi, R., Jackowski, S., Mori, K., & Brewer, J. W. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200406136 · Cited by 653
Rhee, E. P., Cheng, S., Larson, M. G., Walford, G. A., Lewis, G. D., McCabe, E., Yang, E., Farrell, L., Fox, C. S., O’Donnell, C. J., et al. (2011) · Journal of Clinical Investigation · doi:10.1172/jci44442 · Cited by 647 · cited 1×
“…parallel with restoring normal hepatic ER membrane composition [120], clinical data correlate specific acyl chain TAG profiles with type 2 diabetes [127], and genetically reducing lipin degradation in mice (thereby allowing SREBP suppression) reduces high-fat-diet liver pathology and circulating…”
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The SREBP Pathway in Drosophila
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Cited by
Endoplasmic reticulum stress and unfolded protein response in cardiovascular diseases
Ren, J., Bi, Y., Sowers, J. R., Hetz, C., & Zhang, Y. (2021) · Nature Reviews Cardiology · doi:10.1038/s41569-021-00511-w · Cited by 708
Structural and mechanistic basis of the EMC-dependent biogenesis of distinct transmembrane clients
Miller-Vedam, L. E., Bräuning, B., Popova, K. D., Schirle Oakdale, N. T., Bonnar, J. L., Prabu, J. R., Boydston, E. A., Sevillano, N., Shurtleff, M. J., Stroud, R. M., et al. (2020) · eLife · doi:10.7554/elife.62611 · Cited by 87
“Notably, several other membrane proteins involved in ER homeostasis, including Opi1 and Ire1, also contain amphipathic helices that have been proposed to sense the properties of the lipid bilayer (Volmer et al., 2013; Jacquemyn et al., 2017; Halbleib et al., 2017; Hofbauer et al., 2018; Cho et al., 2019).”
BackgroundThe YAP-TEAD complex promotes senescent cell survival by lowering endoplasmic reticulum stress
Anerillas, C., Mazan-Mamczarz, K., Herman, A. B., Munk, R., Lam, K.-W. G., Calvo-Rubio, M., Garrido, A., Tsitsipatis, D., Martindale, J. L., Altés, G., et al. (2023) · Nature Aging · doi:10.1038/s43587-023-00480-4 · Cited by 76
Axonal Organelles as Molecular Platforms for Axon Growth and Regeneration after Injury
Petrova, V., Nieuwenhuis, B., Fawcett, J. W., & Eva, R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22041798 · Cited by 32
Ferrero, E., Vaz, F. M., Cheillan, D., Brusco, A., & Marelli, C. (2025) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2025.109050 · Cited by 24
Metadata
- Authors
- Jacquemyn, J., Cascalho, A., & Goodchild, R. E.
- Venue
- EMBO reports
- Published
- 2017-10-26
- Volume
- 18
- Issue
- 11
- Pages
- 1905-1921
- ISSN
- 1469-221X (ISSN-L)
- 1469-3178
- OpenAlex
- W2766477555
- Cited by
- 286
- References
- 12
- FWCI
- 6.44
- Type
- journal article
- Language
- en
- Open access
- green
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- Jacquemyn, J., Cascalho, A., & Goodchild, R. E. (2017). The ins and outs of endoplasmic reticulum‐controlled lipid biosynthesis. EMBO reports. https://doi.org/10.15252/embr.201643426
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
