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A Dynamic Interface between Vacuoles and Mitochondria in Yeast
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A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION
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Systematic Genetic Analysis with Ordered Arrays of Yeast Deletion Mutants
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Mitochondrial Dynamics in the Regulation of Nutrient Utilization and Energy Expenditure
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An ER-Mitochondria Tethering Complex Revealed by a Synthetic Biology Screen
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Self-citationThe role of mitochondria in aging
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Structure and function of ER membrane contact sites with other organelles
Phillips, M. J., & Voeltz, G. K. (2016) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2015.8 · Cited by 933
The lysosome as a cellular centre for signalling, metabolism and quality control
Lawrence, R. E., & Zoncu, R. (2019) · Nature Cell Biology · doi:10.1038/s41556-018-0244-7 · Cited by 920
MCOLN1 is a ROS sensor in lysosomes that regulates autophagy
Zhang, X., Cheng, X., Yu, L., Yang, J., Calvo, R., Patnaik, S., Hu, X., Gao, Q., Yang, M., Lawas, M., et al. (2016) · Nature Communications · doi:10.1038/ncomms12109 · Cited by 558
Mechanisms of autophagy–lysosome dysfunction in neurodegenerative diseases
Nixon, R. A., & Rubinsztein, D. C. (2024) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-024-00757-5 · Cited by 435
Shai, N., Yifrach, E., van Roermund, C. W. T., Cohen, N., Bibi, C., IJlst, L., Cavellini, L., Meurisse, J., Schuster, R., Zada, L., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-03957-8 · Cited by 320
Self-citationNPC1 regulates ER contacts with endocytic organelles to mediate cholesterol egress
Höglinger, D., Burgoyne, T., Sanchez-Heras, E., Hartwig, P., Colaco, A., Newton, J., Futter, C. E., Spiegel, S., Platt, F. M., & Eden, E. R. (2019) · Nature Communications · doi:10.1038/s41467-019-12152-2 · Cited by 299
The aging lysosome: An essential catalyst for late-onset neurodegenerative diseases
Nixon, R. A. (2020) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2020.140443 · Cited by 149
Structure–Function Insights into Direct Lipid Transfer between Membranes by Mmm1–Mdm12 of ERMES
Kawano, S., Tamura, Y., Kojima, R., Bala, S., Asai, E., Michel, A. H., Kornmann, B., Riezman, I., Riezman, H., Sakae, Y., et al. (2018) · Journal of Cell Biology · doi:10.1083/jcb.201704119 · Cited by 148
“However, the recent identification of direct physical contacts between the membranes of two organelles (Kornmann et al., 2009; Elbaz-Alon et al., 2014; Hönscher et al., 2014; Lahiri et al., 2014; Murley et al., 2015) highlights the need for coordinated functions of distinct organelles through direct exchange of metabo…”
BackgroundSystem-level impact of mitochondria on fungal virulence: to metabolism and beyond
Calderone, R., Li, D., & Traven, A. (2015) · FEMS Yeast Research · doi:10.1093/femsyr/fov027 · Cited by 101
A Phospholipid Transfer Function of ER-Mitochondria Encounter Structure Revealed in Vitro
Kojima, R., Endo, T., & Tamura, Y. (2016) · Scientific Reports · doi:10.1038/srep30777 · Cited by 91
Structure of the HOPS tethering complex, a lysosomal membrane fusion machinery
Shvarev, D., Schoppe, J., König, C., Perz, A., Füllbrunn, N., Kiontke, S., Langemeyer, L., Januliene, D., Schnelle, K., Kümmel, D., et al. (2022) · eLife · doi:10.7554/elife.80901 · Cited by 85
Phosphatidylserine transport by Ups2–Mdm35 in respiration-active mitochondria
Miyata, N., Watanabe, Y., Tamura, Y., Endo, T., & Kuge, O. (2016) · Journal of Cell Biology · doi:10.1083/jcb.201601082 · Cited by 83
Preserving Lysosomal Function in the Aging Brain: Insights from Neurodegeneration
Peng, W., Minakaki, G., Nguyen, M., & Krainc, D. (2019) · Neurotherapeutics · doi:10.1007/s13311-019-00742-3 · Cited by 79
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Koch, B., & Traven, A. (2019) · Current Genetics · doi:10.1007/s00294-019-00942-6 · Cited by 26
Mitochondrial Control of Fungal Cell Walls: Models and Relevance in Fungal Pathogens
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DIP2 is a unique regulator of diacylglycerol lipid homeostasis in eukaryotes
Mondal, S., Kinatukara, P., Singh, S., Shambhavi, S., Patil, G. S., Dubey, N., Singh, S. H., Pal, B., Shekar, P. C., Kamat, S. S., et al. (2022) · eLife · doi:10.7554/elife.77665 · Cited by 19
Loss of Num1-mediated cortical dynein anchoring negatively impacts respiratory growth
White, A. J., Harper, C. S., Rosario, E. M., Dietz, J. V., Addis, H. G., Fox, J. L., Khalimonchuk, O., & Lackner, L. L. (2022) · Journal of Cell Science · doi:10.1242/jcs.259980 · Cited by 6
Membrane contact sites regulate vacuolar fission via sphingolipid metabolism
Hanaoka, K., Nishikawa, K., Ikeda, A., Schlarmann, P., Sasaki, S., Fujii, S., Yamashita, S., Nakaji, A., & Funato, K. (2024) · eLife · doi:10.7554/elife.89938 · Cited by 6
Membrane contact sites regulate vacuolar fission via sphingolipid metabolism
Hanaoka, K., Nishikawa, K., Ikeda, A., Schlarmann, P., Yamashita, S., Nakaji, A., Fujii, S., & Funato, K. (2023) · doi:10.1101/2023.06.21.546015
Metadata
- Authors
- Elbaz-Alon, Y., Rosenfeld-Gur, E., Shinder, V., Futerman, A. H., Geiger, T., & Schuldiner, M.
- Venue
- Developmental Cell
- Publisher
- Elsevier BV
- Published
- 2014-07
- Volume
- 30
- Issue
- 1
- Pages
- 95-102
- ISSN
- 1534-5807 (ISSN-L)
- OpenAlex
- W2066029883
- Cited by
- 380
- References
- 7
- FWCI
- 19.01
- Type
- journal article
- Language
- en
- Open access
- bronze
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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.