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The Function of Lipin in the Wing Development of Drosophila melanogaster
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Cytometry of cyclin proteins
inferredcites →https://doi.org/10.1002/bies.950170603openalex-snapshot
Cyclin‐dependent protein kinases: Key regulators of the eukaryotic cell cycle
inferredcites →https://doi.org/10.1002/dvdy.23942openalex-snapshot
Expression and function of scalloped during Drosophila development
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Evidence for post‐transcriptional regulation of cyclin B1 mRNA in the cell cycle and following irradiation in HeLa cells.
inferredcites →https://doi.org/10.1006/dbio.1999.9459openalex-snapshot
Tissue-Specific Regulation of Vein/EGF Receptor Signaling in Drosophila
inferredcites →https://doi.org/10.1007/978-1-61779-998-3_40openalex-snapshot
Histone H2AX Phosphorylation: A Marker for DNA Damage
inferredcites →https://doi.org/10.1016/0092-8674(89)90183-9openalex-snapshot
Genetic control of cell division patterns in the Drosophila embryo
inferredcites →https://doi.org/10.1016/0167-4781(89)90130-9openalex-snapshot
Interaction of DNA polymerases with phospholipids
inferredcites →https://doi.org/10.1016/j.cell.2011.06.034openalex-snapshot
mTOR Complex 1 Regulates Lipin 1 Localization to Control the SREBP Pathway
inferredcites →https://doi.org/10.1016/j.cmet.2004.12.002openalex-snapshot
Lipin, a lipodystrophy and obesity gene
inferredcites →https://doi.org/10.1016/j.cmet.2005.05.004openalex-snapshot
Metabolic control through the PGC-1 family of transcription coactivators
inferredcites →https://doi.org/10.1016/j.cmet.2006.08.005openalex-snapshot
Lipin 1 is an inducible amplifier of the hepatic PGC-1α/PPARα regulatory pathway
inferredcites →https://doi.org/10.1016/j.jbior.2017.08.001openalex-snapshot
Phosphatidate phosphatase regulates membrane phospholipid synthesis via phosphatidylserine synthase
inferredcites →https://doi.org/10.1016/j.molcel.2007.11.015openalex-snapshot
The DNA Damage Response: Ten Years After
inferredcites →https://doi.org/10.1016/j.tem.2011.02.006openalex-snapshot
Dual function lipin proteins and glycerolipid metabolism
inferredcites →https://doi.org/10.1016/s0021-9258(17)41939-9openalex-snapshot
Coordination of membrane phospholipid synthesis with the cell cycle.
inferredcites →https://doi.org/10.1016/s0065-3233(04)69004-8openalex-snapshot
Coordination of Repair, Checkpoint, and Cell Death Responses to DNA Damage
inferredcites →https://doi.org/10.1016/s0079-6603(00)65010-9openalex-snapshot
Regulation of mammalian cell membrane biosynthesis
inferredcites →https://doi.org/10.1016/s0092-8674(00)00034-9openalex-snapshot
Mitotic Phosphorylation of Histone H3 Is Governed by Ipl1/aurora Kinase and Glc7/PP1 Phosphatase in Budding Yeast and Nematodes
inferredcites →https://doi.org/10.1016/s0092-8674(00)80718-7openalex-snapshot
Phosphorylation of Histone H3 Is Required for Proper Chromosome Condensation and Segregation
inferredcites →https://doi.org/10.1016/s0092-8674(00)81519-6openalex-snapshot
Cdk Phosphorylation Triggers Sequential Intramolecular Interactions that Progressively Block Rb Functions as Cells Move through G1
inferredcites →https://doi.org/10.1016/s0163-7827(03)00051-1openalex-snapshot
Enzymes of triacylglycerol synthesis and their regulation
inferredcites →https://doi.org/10.1016/s0300-483x(02)00460-2openalex-snapshot
Cell cycle checkpoint signaling:
inferredcites →https://doi.org/10.1016/s1016-8478(23)13152-9openalex-snapshot
Drosophila melanogaster: a Model for the Study of DNA Damage Checkpoint Response
inferredcites →https://doi.org/10.1038/35044005openalex-snapshot
The DNA damage response: putting checkpoints in perspective
inferredcites →https://doi.org/10.1038/83685openalex-snapshot
Lipodystrophy in the fld mouse results from mutation of a new gene encoding a nuclear protein, lipin
inferredcites →https://doi.org/10.1038/nature03097openalex-snapshot
Cell-cycle checkpoints and cancer
inferredcites →https://doi.org/10.1038/nrm2330openalex-snapshot
Membrane lipids: where they are and how they behave
inferredcites →https://doi.org/10.1038/sj.emboj.7600672openalex-snapshot
The yeast lipin Smp2 couples phospholipid biosynthesis to nuclear membrane growth
inferredcites →https://doi.org/10.1038/sj.onc.1208619openalex-snapshot
Pocket proteins and cell cycle control
inferredcites →https://doi.org/10.1042/bsr20171270openalex-snapshot
SREBP-1c as a molecular bridge between lipogenesis and cell cycle progression of clear cell renal carcinoma
inferredcites →https://doi.org/10.1046/j.1432-1327.1999.00822.xopenalex-snapshot
Phosphatidic acid, a key intermediate in lipid metabolism
inferredcites →https://doi.org/10.1073/pnas.0712168105openalex-snapshot
A chemical method for fast and sensitive detection of DNA synthesis in vivo
inferredcites →https://doi.org/10.1073/pnas.1205221109openalex-snapshot
Mouse lipin-1 and lipin-2 cooperate to maintain glycerolipid homeostasis in liver and aging cerebellum
inferredcites →https://doi.org/10.1074/jbc.m609537200openalex-snapshot
Insulin Controls Subcellular Localization and Multisite Phosphorylation of the Phosphatidic Acid Phosphatase, Lipin 1
inferredcites →https://doi.org/10.1074/jbc.m610745200openalex-snapshot
Three Mammalian Lipins Act as Phosphatidate Phosphatases with Distinct Tissue Expression Patterns
inferredcites →https://doi.org/10.1074/jbc.m804278200openalex-snapshot
Temporal and Spatial Regulation of the Phosphatidate Phosphatases Lipin 1 and 2
inferredcites →https://doi.org/10.1074/jbc.m807882200openalex-snapshot
Lipin 2 Is a Liver-enriched Phosphatidate Phosphohydrolase Enzyme That Is Dynamically Regulated by Fasting and Obesity in Mice
inferredcites →https://doi.org/10.1083/jcb.200812045openalex-snapshot
The decision to enter mitosis: feedback and redundancy in the mitotic entry network
inferredcites →https://doi.org/10.1093/jnci/92.5.376openalex-snapshot
Preclinical and Clinical Development of Cyclin-Dependent Kinase Modulators
inferredcites →https://doi.org/10.1093/nar/gkf496openalex-snapshot
DNA double-strand break-induced phosphorylation of Drosophila histone variant H2Av helps prevent radiation-induced apoptosis
inferredcites →https://doi.org/10.1093/oxfordjournals.jbchem.a124812openalex-snapshot
Selective Inhibition of DNA Polymerase ε by Phosphatidylinositol
inferredcites →https://doi.org/10.1097/mol.0b013e32832adee5openalex-snapshot
The lipin family: mutations and metabolism
inferredcites →https://doi.org/10.1111/j.1440-169x.2011.01289.xopenalex-snapshot
Negative modulation of bone morphogenetic protein signaling by Dullard during wing vein formation in Drosophila
inferredcites →https://doi.org/10.1126/science.274.5293.1664openalex-snapshot
Cell Cycle Checkpoints: Preventing an Identity Crisis
inferredcites →https://doi.org/10.1128/jb.169.8.3701-3706.1987openalex-snapshot
DNA replication initiation, doubling of rate of phospholipid synthesis, and cell division in Escherichia coli
inferredcites →https://doi.org/10.1128/mcb.01335-10openalex-snapshot
Lipin Is a Central Regulator of Adipose Tissue Development and Function in Drosophila melanogaster
inferredcites →https://doi.org/10.1128/mcb.16.12.7173openalex-snapshot
The Rb Family Contains a Conserved Cyclin-Dependent-Kinase-Regulated Transcriptional Repressor Motif
inferredcites →https://doi.org/10.1146/annurev.biochem.73.011303.073723openalex-snapshot
Molecular Mechanisms of Mammalian DNA Repair and the DNA Damage Checkpoints
inferredcites →https://doi.org/10.1146/annurev.cellbio.13.1.261openalex-snapshot
CYCLIN-DEPENDENT KINASES: Engines, Clocks, and Microprocessors
inferredcites →https://doi.org/10.1152/ajpendo.90958.2008openalex-snapshot
Biochemistry, physiology, and genetics of GPAT, AGPAT, and lipin enzymes in triglyceride synthesis
inferredcites →https://doi.org/10.1194/jlr.r800019-jlr200openalex-snapshot
Thematic Review Series: Glycerolipids. Multiple roles for lipins/phosphatidate phosphatase enzymes in lipid metabolism
inferredcites →https://doi.org/10.1242/dev.118.2.401openalex-snapshot
Targeted gene expression as a means of altering cell fates and generating dominant phenotypes
inferredcites →https://doi.org/10.1242/dev.120.11.3131openalex-snapshot
Transcriptional regulation of string (cdc25): a link between developmental programming and the cell cycle
inferredcites →https://doi.org/10.1242/jcs.00135openalex-snapshot
An evolutionarily conserved fission yeast protein, Ned1, implicated in normal nuclear morphology and chromosome stability, interacts with Dis3, Pim1/RCC1 and an essential nucleoporin
inferredcites →https://doi.org/10.1242/jcs.173740openalex-snapshot
Drosophila lipin interacts with insulin and TOR signaling pathways in the control of growth and lipid metabolism
inferredcites →https://doi.org/10.1371/journal.pgen.1000435openalex-snapshot
Heterochromatic Genome Stability Requires Regulators of Histone H3 K9 Methylation
inferredcites →https://doi.org/10.1371/journal.pone.0042587openalex-snapshot
Role of High-Fat Diet in Stress Response of Drosophila
inferredcites →https://doi.org/10.2217/17460875.2.2.229openalex-snapshot
Triacylglycerol Metabolism In Adipose Tissue
inferredcites →https://doi.org/10.3390/ijms17050648openalex-snapshot
Function of Lipid Storage Droplet 1 (Lsd1) in Wing Development of Drosophila melanogaster
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.3945342openalex-extracted
The Insecticidal Capacity of Ethanol Extract from Cascabela Peruviana (L.) Lippold Against Fruit Fly
inferred← citeshttps://doi.org/10.1002/fsn3.4223openalex-snapshot
Drosophila models of the anti‐inflammatory and anti‐obesity mechanisms of kombucha tea produced by Camellia sinensis leaf fermentation
inferred← citeshttps://doi.org/10.1016/j.heliyon.2022.e09313openalex-snapshot
The insecticidal capacity of ethanol extract from Cascabela peruviana (L.) Lippold against fruit fly
inferred← citeshttps://doi.org/10.1016/j.ibmb.2020.103469openalex-snapshot
Diverse roles of phosphatidate phosphatases in insect development and metabolism
inferred← citeshttps://doi.org/10.1016/j.ibmb.2021.103668openalex-snapshot
Lipin modulates lipid metabolism during reproduction in the cabbage beetle
inferred← citeshttps://doi.org/10.1038/s41598-022-08299-6openalex-snapshot
Dysfunction of lipid storage droplet-2 suppresses endoreplication and induces JNK pathway-mediated apoptotic cell death in Drosophila salivary glands
inferred← citeshttps://doi.org/10.1134/s1990519x21040076openalex-snapshot
Lipin Family Proteins: Structure, Functions, and Related Diseases
inferred← citeshttps://doi.org/10.22144/ctu.jvn.2022.114openalex-snapshot
Khả năng gây độc của cỏ sữa lá nhỏ (Euphorbia thymifolia L.) trên mô hình ruồi giấm (Drosophila melanogaster)
inferred← citeshttps://doi.org/10.31893/jabb.22018openalex-snapshot
Evaluation of the insecticidal activity of Solanum mammosum (L.) fruit extract against Drosophila melanogaster
inferred← citeshttps://doi.org/10.3390/ijms21114086openalex-snapshot
Role of Serotonin Transporter in Eye Development of Drosophila melanogaster
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