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Atg37 regulates the assembly of the pexophagic receptor protein complex
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inferred← citeshttps://doi.org/10.2139/ssrn.4793027openalex-extracted
Intricacies of Lipid Supply in Autophagic Membrane Expansion
inferred← citeshttps://doi.org/10.1002/1873-3468.14412openalex-snapshot
Cargo receptors and adaptors for selective autophagy in plant cells
inferred← citeshttps://doi.org/10.1007/s00418-018-1724-3openalex-snapshot
Pexophagy in yeast and mammals: an update on mysteries
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2024.119742openalex-snapshot
The Hansenula polymorpha mitochondrial carrier family protein Mir1 is dually localized at peroxisomes and mitochondria
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.09.153openalex-snapshot
Pexophagy is induced by increasing peroxisomal reactive oxygen species in 1′10-phenanthroline-treated cells
inferred← citeshttps://doi.org/10.1016/j.fmre.2023.04.016openalex-snapshot
Peroxisome and pexophagy in neurological diseases
inferred← citeshttps://doi.org/10.1016/j.jmb.2024.168691openalex-snapshot
Phospholipid Supply for Autophagosome Biogenesis
inferred← citeshttps://doi.org/10.1016/j.plipres.2015.04.001openalex-snapshot
Long-chain acyl-CoA esters in metabolism and signaling: Role of acyl-CoA binding proteins
inferred← citeshttps://doi.org/10.1016/j.semcdb.2016.03.022openalex-snapshot
Autophagy in plant pathogenic fungi
inferred← citeshttps://doi.org/10.1038/nrm.2016.74openalex-snapshot
Mechanistic insights into selective autophagy pathways: lessons from yeast
inferred← citeshttps://doi.org/10.1042/bst20150268openalex-snapshot
Autophagic degradation of peroxisomes in mammals
inferred← citeshttps://doi.org/10.1042/ns20180134openalex-snapshot
Autophagy in the mammalian nervous system: a primer for neuroscientists
inferred← citeshttps://doi.org/10.1074/jbc.m116.760090openalex-snapshot
Deficiency of a Retinal Dystrophy Protein, Acyl-CoA Binding Domain-containing 5 (ACBD5), Impairs Peroxisomal β-Oxidation of Very-long-chain Fatty Acids
inferred← citeshttps://doi.org/10.1080/15548627.2015.1100356openalex-snapshot
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
inferred← citeshttps://doi.org/10.1080/15548627.2017.1413521openalex-snapshot
Pex3 and Atg37 compete to regulate the interaction between the pexophagy receptor, Atg30, and the Hrr25 kinase
inferred← citeshttps://doi.org/10.1080/15548627.2018.1507440openalex-snapshot
NBR1 is involved in selective pexophagy in filamentous ascomycetes and can be functionally replaced by a tagged version of its human homolog
inferred← citeshttps://doi.org/10.1080/15548627.2020.1797280openalex-snapshot
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 1
inferred← citeshttps://doi.org/10.1093/femsyr/fow038openalex-snapshot
Yeast peroxisomes: structure, functions and biotechnological opportunities
inferred← citeshttps://doi.org/10.1098/rsob.240291openalex-snapshot
Whole organism and tissue-specific analysis of pexophagy in Drosophila
inferred← citeshttps://doi.org/10.1101/2023.11.15.567167openalex-snapshot
The Hansenula polymorpha Mitochondrial Carrier Family proteins Mir1 and Aac2 are dually localized at peroxisomes and mitochondria
inferred← citeshttps://doi.org/10.1111/imr.12864openalex-snapshot
Age‐related factors that affect B cell responses to vaccination in mice and humans
inferred← citeshttps://doi.org/10.1152/physrev.00033.2016openalex-snapshot
Redox Regulation of Homeostasis and Proteostasis in Peroxisomes
inferred← citeshttps://doi.org/10.1161/circresaha.116.303790openalex-snapshot
Molecular Mechanisms of Mitochondrial Autophagy/Mitophagy in the Heart
inferred← citeshttps://doi.org/10.1186/s12943-024-01934-yopenalex-snapshot
Selective autophagy in cancer: mechanisms, therapeutic implications, and future perspectives
inferred← citeshttps://doi.org/10.14348/molcells.2018.2245openalex-snapshot
Pexophagy: Molecular Mechanisms and Implications for Health and Diseases.
inferred← citeshttps://doi.org/10.15407/visn2016.12.048openalex-snapshot
Механізми автофагії, або самопоїдання – постійної деградації клітинного матеріалу, без якої життя неможливе
inferred← citeshttps://doi.org/10.18632/oncotarget.7958openalex-snapshot
Age-related changes in the transcriptome of antibody-secreting cells
inferred← citeshttps://doi.org/10.3389/fcell.2015.00056openalex-snapshot
The different facets of organelle interplay—an overview of organelle interactions
inferred← citeshttps://doi.org/10.3389/fnmol.2025.1602343openalex-snapshot
The neurological pathology of peroxisomal ACBD5 deficiency – lessons from patients and mouse models
inferred← citeshttps://doi.org/10.3390/cells10010017openalex-snapshot
Sorting Nexins in Protein Homeostasis
inferred← citeshttps://doi.org/10.3390/cells11020215openalex-snapshot
Komagataella phaffii Cue5 Piggybacks on Lipid Droplets for Its Vacuolar Degradation during Stationary Phase Lipophagy
inferred← citeshttps://doi.org/10.3390/ijms21020578openalex-snapshot
Pexophagy: A Model for Selective Autophagy
inferred← citeshttps://doi.org/10.5167/uzh-131237openalex-snapshot
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
inferred← citeshttps://doi.org/10.53846/goediss-6798openalex-snapshot
The interplay of SmNBR1 and SmATG8 in selective autophagy of the filamentous fungus Sordaria macrospora
inferred← citeshttps://doi.org/10.7150/thno.49860openalex-snapshot
Selective autophagy of intracellular organelles: Recent research advances
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