The Endoplasmic Reticulum Enzyme DGAT2 Is Found in Mitochondria-associated Membranes and Has a Mitochondrial Targeting Signal That Promotes Its Association with Mitochondria

Improved monomeric red, orange and yellow fluorescent proteins derived from Discosoma sp. red fluorescent protein

Shaner, N. C., Campbell, R. E., Steinbach, P. A., Giepmans, B. N. G., Palmer, A. E., & Tsien, R. Y. (2004) · Nature Biotechnology · doi:10.1038/nbt1037 · Cited by 4,619

A monomeric red fluorescent protein

Campbell, R. E., Tour, O., Palmer, A. E., Steinbach, P. A., Baird, G. S., Zacharias, D. A., & Tsien, R. Y. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.082243699 · Cited by 2,346

Biochemistry of Lipids, Lipoproteins and Membranes

(2021) · Elsevier eBooks · doi:10.1016/c2020-0-00089-7 · Cited by 1,402

Phospholipid synthesis in a membrane fraction associated with mitochondria.

Vance, J. E. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)39106-9 · Cited by 1,153

Identification of a gene encoding an acyl CoA:diacylglycerol acyltransferase, a key enzyme in triacylglycerol synthesis

Cases, S., Smith, S. J., Zheng, Y.-W., Myers, H. M., Lear, S. R., Sande, E., Novak, S., Collins, C. C., Welch, C. L., Lusis, A. J., et al. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.22.13018 · Cited by 1,138

Thematic review series: Glycerolipids. DGAT enzymes and triacylglycerol biosynthesis

Yen, C.-L. E., Stone, S. J., Koliwad, S., Harris, C., & Farese, R. V. (2008) · Journal of Lipid Research · doi:10.1194/jlr.r800018-jlr200 · Cited by 1,105

Enzymes of triacylglycerol synthesis and their regulation

Coleman, R. (2003) · Progress in Lipid Research · doi:10.1016/s0163-7827(03)00051-1 · Cited by 985

The lipid handbook

Gunstone, F. D., Harwood, J. L., & Padley, F. B. (1994) · Cited by 972

Integrated analysis of protein composition, tissue diversity, and gene regulation in mouse mitochondria.

Mootha, V. K., Bunkenborg, J., Olsen, J. V., Hjerrild, M., Wisniewski, J. R., Stahl, E., Bolouri, M. S., Ray, H. N., Sihag, S., Kamal, M., et al. (2003) · Cell · doi:10.1016/s0092-8674(03)00926-7 · Cited by 889

Cloning of DGAT2, a Second Mammalian Diacylglycerol Acyltransferase, and Related Family Members

Cases, S., Stone, S. J., Zhou, P., Yen, E., Tow, B., Lardizabal, K. D., Voelker, T., & Farese, R. V. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m106219200 · Cited by 818

Mind the gap: Methods to study membrane contact sites

Sarhadi, T. R., Panse, J. S., & Nagotu, S. (2023) · Experimental Cell Research · doi:10.1016/j.yexcr.2023.113756 · Cited by 9

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Yadav, A., Ouyang, X., Barkley, M., Watson, J. C., Madhamanchi, K., Kramer, J., Zhang, J., & Melkani, G. C. (2026) · Aging Cell · doi:10.1111/acel.70439 · Cited by 9

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Kumar, V. K., Lackey, A. I., Snyder, J. E., Karhadkar, S. S., Rao, A. D., DiCarlo, A., & Sato, P. Y. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.609241 · Cited by 8

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Reza, A. H. M. M., Zhou, Y., Qin, J., & Tang, Y. (2021) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2021.06.009 · Cited by 8

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McFie, P. J., Ambilwade, P. P., Vu, H., & Stone, S. J. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.07.040 · Cited by 8

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Makio, T., & Simmen, T. (2024) · Contact · doi:10.1177/25152564241261228 · Cited by 8

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Li, Y., Ye, L., Cui, Y.-Z., Xu, F., Chen, X., Zhang, F.-F., Lü, Y., Zheng, Y.-X., & Man, X. (2025) · JCI Insight · doi:10.1172/jci.insight.192507 · Cited by 7

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Tehran, D. A., & Pizzo, P. (2025) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-025-05830-6 · Cited by 8

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Roy, R., Adhikary, A., De, R., & Ghosh, S. (2026) · APOPTOSIS · doi:10.1007/s10495-025-02252-4 · Cited by 7

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Irshad, Z., Lund, J., Sillars, A., Løvsletten, N. G., Gharanei, S., Salt, I. P., Freeman, D. J., Gill, J. M. R., Thoresen, G. H., Rustan, A. C., et al. (2023) · The FASEB Journal · doi:10.1096/fj.202300960rr · Cited by 6

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Kwiatkowska, M., Polit, J. T., Popłońska, K., Stępiński, D., & Wojtczak, A. (2013) · Acta Physiologiae Plantarum · doi:10.1007/s11738-013-1235-8 · Cited by 7

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Mak, H. Y. (2013) · Methods in cell biology · doi:10.1016/b978-0-12-408051-5.00003-6 · Cited by 7

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Green, D. R. (2020) · Science · doi:10.1126/science.abe7891 · Cited by 7

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Litvinova, L. S., Vulf, M. A., Yurova, K. A., Хазиахматова, О. Г., Malashchenko, V. V., Bograya, M., Kozlov, I. G., & Тодосенко, Н. М. (2024) · Current Medicinal Chemistry · doi:10.2174/0109298673309247240610050423 · Cited by 6

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Wang, J., Wang, M., Zeng, X., Li, Y., Lei, L., Chen, C., Lin, X., Fang, P., Guo, Y., Jiang, X., et al. (2025) · Cell Communication and Signaling · doi:10.1186/s12964-025-02089-z · Cited by 6

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Lupette, J., & Maréchal, É. (2020) · Results and problems in cell differentiation · doi:10.1007/978-3-030-51849-3_11 · Cited by 6

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Wei, M., Huang, X., Bian, C., Sun, J. H., & Ji, H. (2021) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2021.104197 · Cited by 6

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Mansbach, C. M., & Abumrad, N. A. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-382026-6.00060-9 · Cited by 6

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Kamisaka, Y., Rie, G. O. T. O., Shibakami, M., Yoshioka, K., & Sato, Y. (2011) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.110034 · Cited by 6

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Lin, Y.-M., Chong, W. M., Huang, C., Chang, H.-J., Cheung, C. H. Y., & Liao, J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.24.626799 · Cited by 6

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Bassot, A., Violy, L., Gorka, L., Cigalotto, L., Namasivayam, B., Mikaélian, I., Johnston, E. S., Han, C., Gadet, R., Alpha‐Bazin, B., et al. (2026) · Nature Cell Biology · doi:10.1038/s41556-026-01980-2 · Cited by 5

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Cao, Z., Wang, X., Huang, X., & Mak, H. Y. (2020) · BioEssays · doi:10.1002/bies.202000199 · Cited by 5

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McFie, P. J., Izzard, S., Vu, H., Jin, Y., Beauchamp, E., Berthiaume, L. G., & Stone, S. J. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2016.06.021 · Cited by 5

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Luo, X.-A., Zhu, Y.-M., Liu, T., Wang, X., Zhou, P.-P., Bao, Z., & Yu, L. (2017) · Biotechnology Letters · doi:10.1007/s10529-017-2306-5 · Cited by 5

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Siloto, R. M. P., Liu, Q., Weselake, R. J., He, X., & McKeon, T. A. (2010) · doi:10.1002/9780470608524.ch1 · Cited by 5

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Idi, W., Sheta, R., & Oueslati, A. (2025) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2025.1681039 · Cited by 6

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Fernàndez‐Bernal, A., Mota‐Martorell, N., Pamplona, R., Área-Gómez, E., & Portero‐Otín, M. (2025) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2025.168021 · Cited by 4

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Hernandez‐Corbacho, M. J., & Canals, D. (2023) · Molecular Pharmacology · doi:10.1124/molpharm.123.000763 · Cited by 4

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Liesa, M. (2022) · The EMBO Journal · doi:10.15252/embj.2022111238 · Cited by 4

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Kimura, H., Arasaki, K., Iitsuka, M., & Tagaya, M. (2019) · Contact · doi:10.1177/2515256419838719 · Cited by 4

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Shahzad, Q., Xu, H., Pu, L., Waqas, M., Wadood, A. A., Xie, L., Ke-huan, L., Liang, X., & Lu, Y. (2020) · Theriogenology · doi:10.1016/j.theriogenology.2020.03.013 · Cited by 4

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Yang, Z., Zhang, Z., Zhao, Y., Ye, Q., Li, X., Meng, L., Long, J., Zhang, S., & Zhang, L. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.935898 · Cited by 5

CES1 Increases Hepatic Triacylglycerol Synthesis Through Activation of PPARγ, LXR and SREBP1c

Rajakumar, S., Lian, J., Watts, R., Nelson, R., Saikali, M. F., Cummins, C. L., & Lehner, R. S. (2025) · Cells · doi:10.3390/cells14191548 · Cited by 5

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Fu, L., Lu, H., Li, R., Liu, P., & Liang, B. (2026) · Protein & Cell · doi:10.1093/procel/pwag048 · Cited by 3

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Fuwa, M., Kajita, K., Mori, I., Asano, M., Kajita, T., Senda, T., Inagaki, T., & Morita, H. (2024) · FEBS Letters · doi:10.1002/1873-3468.14877 · Cited by 3

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Gross, D. A., & Silver, D. L. (2013) · Methods in cell biology · doi:10.1016/b978-0-12-408051-5.00010-3 · Cited by 3

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Eckhardt, M. (2025) · Lipidology · doi:10.3390/lipidology2030016 · Cited by 3

Comprehensive bioinformatics analysis and experimental verification identify mitochondrial gene Dgat2 as a novel therapeutic biomarker for myocardial ischemia-reperfusion

Li, H., Zhou, Y., Xue, W., Yin, P., Liu, L., Wu, S., Zhao, Y., An, Q., & Sun, Y. (2025) · Frontiers in Endocrinology · doi:10.3389/fendo.2025.1539646 · Cited by 2

Proteomic mapping and optogenetic manipulation of membrane contact sites

Lin, G., Shi, W., Zhang, N., Lee, Y., Wang, Y., & Ji, J. (2022) · Biochemical Journal · doi:10.1042/bcj20220382 · Cited by 2

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Kawelke, S. (2016) · doi:10.53846/goediss-5298 · Cited by 2

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Wang, F., Huynh, P. M., & An, Y. (2024) · Comprehensive physiology · doi:10.1002/cphy.c230009 · Cited by 10

Lipid droplets as stress-buffering organelles in cancer cell homeostasis

Wei, R., & Petritsch, C. K. (2026) · Communications Biology · doi:10.1038/s42003-026-10566-5 · Cited by 2

A Bayesian hierarchically structured prior for gene‐based association testing with multiple traits in genome‐wide association studies

Yang, Y. A., Basu, S., & Zhang, L. (2021) · Genetic Epidemiology · doi:10.1002/gepi.22437 · Cited by 1

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Shahzad, Q., Waqas, M., & Lu, Y. (2023) · Sustainable agriculture reviews · doi:10.1007/978-3-031-21630-5_7 · Cited by 1

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ChuanRen, Q. U., & Lei, L. I. U. (2024) · Scientia Sinica Vitae · doi:10.1360/ssv-2024-0103 · Cited by 1

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Li, J., Lin, Q., Ren, C., Li, X., Li, X., Li, H., & Li, S. (2025) · International Journal of Surgery · doi:10.1097/js9.0000000000002362 · Cited by 1

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Olofsson, S., Andersson, L. K., Perman, J., Rutberg, M., Haversen, L., Lu, L., Lu, E., Mobini, R., Ståhlman, M., Myhre, S., et al. (2011) · InTech eBooks · doi:10.5772/21559 · Cited by 1

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Larson, A. M., & Hauswald, M. (2013) · Springer eBooks · doi:10.1007/978-1-4614-9005-0_2 · Cited by 1

Genetically targeted fluorescent probes reveal dynamic calcium responses to adrenergic signaling in multiple cardiomyocyte compartments

Luptak, I., Morgan, R. J., Baka, T., Croteau, D., Moverman, D. J., Sarnak, H., Kirber, M. T., Bachschmid, M. M., Colucci, W. S., & Pimentel, D. R. (2019) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2019.105569 · Cited by 1

Regulation of Acyl-CoA:Diacylglycerol Acyltransferase-1 by Protein Phosphorylation

Han, J. (2011) · University Library - University of Saskatchewan (University of Saskatchewan) · Cited by 1

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Rieck, A., Günther, G., Hengstler, J. G., & Vartak, N. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.11.531838 · Cited by 1

Identification of Proteins That Interact with Acyl CoA:Diacylglycerol Acyltransferase (DGAT) Enzymes

Jin, Y. (2011) · University Library - University of Saskatchewan (University of Saskatchewan)

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Tarifa, E. (2012) · UVaDOC UVaDOC University of Valladolid Documentary Repository (University of Valladolid) · doi:10.35376/10324/1423

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Bosma, M., Minnaard, R., Sparks, L. M., Schaart, G., Losen, M. H., Baets, M. H. D., Duimel, H., Kersten, S., Bickel, P. E., Schrauwen, P., et al. (2011) · Nederlands Tijdschrift voor Diabetologie · doi:10.1007/s12467-011-0097-1

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Shi, X. (2010) · The Journal of the American Medical Association (JAMA) Network (American Medical Association) · doi:10.13028/zv35-6223

Biochemical Characterization of a Type II Diacylglycerol Acyltransferase from Claviceps purpurea

Mavraganis, I. (2009) · University Library - University of Saskatchewan (University of Saskatchewan)

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Voyias, P. D. (2026) · Warwick Research Archive Portal (University of Warwick) · doi:10.82444/warw.33705232

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Chaudhari, A. (2016) · Gothenburg University Publications Electronic Archive (Gothenburg University)

Role and regulation of Gp78 E3 ubiquitin ligase and its ligand autocrine motility factor in mitochondrial dynamics and mitochondria-endoplasmic reticulum association

Wang, P. T. C. (2015) · cIRcle (University of British Columbia) · doi:10.14288/1.0166455

REVIEWS Intracellular Signal for Skeletal Muscle Adaptation Lipid metabolism in skeletal muscle: generation of adaptive and maladaptive intracellular signals for cellular function

Watt, M. J., & Hoy, A. J. (2012)

The Implications of CD36 Alteration on Rodent Skeletal Muscle Lipid Metabolism

Stuart, J. D., & Lally, V. E. (2012)

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Tran, T. N. T. (2017) · K-State Research Exchange (Kansas State University)

Regulation and Functions of Cardiac Lipins

Kok, B. P. (2012) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r30b09

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Whytock, K. L. (2021) · Liverpool John Moores University · doi:10.24377/ljmu.t.00009962

Prohibitin depletion extends lifespan of a TORC2/SGK-1 mutant through autophagyPreprint

Hernando‐Rodríguez, B., Pérez‐Jiménez, M. M., Rodríguez‐Palero, M. J., Pla, A., Martínez‐Bueno, M. D., Ruiz, P. D. L. C., Gatsi, R., & Artal‐Sanz, M. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/792465

Recruitment of Peroxin14 to lipid droplets affects triglyceride storage in DrosophilaPreprint

Anderson‐Baron, M., Ueda, K., Haskins, J., Hughes, S. C., & Simmonds, A. J. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.02.450950

Mitochondria-associated membranes in the maintenance of cell homeostasis

Camougrand, N. M., & Manon, S. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-821562-3.00043-5

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Ketz, J. S. (2013) · The Research Repository @ WVU (West Virginia University) · doi:10.33915/etd.3613

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Rehling, P., & Callegari, S. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.732960734.793549254

AI-guided screen identifies probucol-mediated mitophagy enhancement through modulation of lipid dropletsPreprint

Moskal, N., Visanji, N. P., Gorbenko, O., Narasimhan, V., Tyrrell, H., Nash, J., Lewis, P. N., & McQuibban, G. A. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.18.492560

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Lees, R. N., How, S., Quilez, S., Landers, S., Rodriguez, S. A., Bernasconi, A. E., Ostler, J. J., & Pham, A. H. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-19116-9.00005-1

Lipid Droplet Remodeling Safeguards Redox Balance through the DGAT1–PANK2–NRF2 Axis in Mammalian Oocytes and Drives Age-Associated DeclinePreprint

Birajdar, P., Kumar, A., Kumari, A., Mohanty, A., Athar, M., Kumar, A., Kiran Kumar, P., Abhilasha, S., Sabnam, S., Silambresan, Y., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.28.691261

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Thazar-Poulot, N. (2011) · theses.fr (ABES) · doi:10.70675/356023f4z2c31z4f83z9b1cz7abbc911ce52

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Blond, E. (2012) · theses.fr (ABES) · doi:10.70675/189ac795z9e7az4eb1z9b88z991750b0b668

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Bassot, A. (2019) · theses.fr (ABES) · doi:10.70675/bf11117az778az470az8feczf040df41bbd1

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Ajjaji, D. (2019) · theses.fr (ABES) · doi:10.70675/f97a4676za9baz4e62zb3dfzf2ae4234d574

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Chorlay, A. (2019) · theses.fr (ABES) · doi:10.70675/0fed6361z7fe2z4048z8d79zfb32b8fdf7fc

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Liu, D. (2019) · theses.fr (ABES) · doi:10.70675/da9fa152zdcc0z498dz9194z563d22d0b77c

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Kieu, T. (2021) · theses.fr (ABES) · doi:10.70675/09ffad1dzef26z436ez94eezf8f77c83e342

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Guyard, V. (2024) · doi:10.70675/42360da9zcedfz4d36zb416z3c80e620bdac

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Cheng, J.-Y., Gu, H.-X., He, C.-H., Gong, W., Yang, K.-J., Liu, Y.-Y., Chen, Z., Jiao, Q.-B., Zhang, X.-W., & Luo, H. (2026) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2026.179145

Lipid droplet–mitochondria mismatch in atherosclerosis: From disrupted lipid routing to persistent inflammation and necrotic core expansion

Gu, M., Qiu, Y., Wang, Y., Xu, J., Liao, Z., Li, R., & Wu, W. (2026) · International Immunopharmacology · doi:10.1016/j.intimp.2026.117327

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Gao, Y., Shao, M., Fang, Y., Zeng, J., & Sun, H. Q. (2026) · Bioscience Reports · doi:10.1042/bsr20260413

Mapping Mitochondrial Architecture in the Brain: Methods and Insights

Miller, E. K., & Nahirney, P. C. (2026) · Neuromethods · doi:10.1007/978-1-0716-5456-9_5

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Zhang, S., Cedillo, L., & Villanueva, C. J. (2026) · Journal of Lipid Research · doi:10.1016/j.jlr.2026.101150

Artificial Endoplasmic Reticulum-Lipid Droplet Tethers Facilitate Lipid Incorporation Into Lipid Droplets

Williams, V. H., Miner, G. E., & Cohen, S. (2026) · Contact · doi:10.1177/25152564261494192

Murine Diacylglycerol Acyltransferase-2 (DGAT2) Can Catalyze Triacylglycerol Synthesis and Promote Lipid Droplet Formation Independent of Its Localization to the Endoplasmic Reticulum

McFie, P. J., Banman, S. L., Kary, S., & Stone, S. J. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.256008 · Cited by 149

J. Biol. Chem.

Stone, S., Levin, M., Zhou, P., Han, J., Walther, T. C., & Farese, R. (2008) · MPG.PuRe (Max Planck Society)

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McFie, P. J., Jin, Y., Banman, S. L., Beauchamp, E., Berthiaume, L. G., & Stone, S. J. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2014.06.004 · Cited by 20

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