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Nutrient sensing and TOR signaling in yeast and mammals

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inferredcites →https://doi.org/10.1006/mcne.2002.1184openalex-snapshot
Tsc2 Null Murine Neuroepithelial Cells Are a Model for Human Tuber Giant Cells, and Show Activation of an mTOR Pathway
inferredcites →https://doi.org/10.1007/s00109-015-1326-7openalex-snapshot
mTOR in health and in sickness
inferredcites →https://doi.org/10.1016/0092-8674(92)90193-gopenalex-snapshot
Phosphorylation of initiation factor 2α by protein kinase GCN2 mediates gene-specific translational control of GCN4 in yeast
inferredcites →https://doi.org/10.1016/0092-8674(93)90144-fopenalex-snapshot
Target of rapamycin in yeast, TOR2, is an essential phosphatidylinositol kinase homolog required for G1 progression
inferredcites →https://doi.org/10.1016/0092-8674(94)90570-3openalex-snapshot
RAFT1: A mammalian protein that binds to FKBP12 in a rapamycin-dependent fashion and is homologous to yeast TORs
inferredcites →https://doi.org/10.1016/0378-1119(94)90599-1openalex-snapshot
Genetic and biochemical evidence for yeast GCN2 protein kinase polymerization
inferredcites →https://doi.org/10.1016/j.ccell.2014.09.008openalex-snapshot
Rab1A Is an mTORC1 Activator and a Colorectal Oncogene
inferredcites →https://doi.org/10.1016/j.cell.2006.01.016openalex-snapshot
TOR Signaling in Growth and Metabolism
inferredcites →https://doi.org/10.1016/j.cell.2008.06.028openalex-snapshot
p53 Target Genes Sestrin1 and Sestrin2 Connect Genotoxic Stress and mTOR Signaling
inferredcites →https://doi.org/10.1016/j.cell.2008.11.044openalex-snapshot
Bidirectional Transport of Amino Acids Regulates mTOR and Autophagy
inferredcites →https://doi.org/10.1016/j.cell.2010.02.024openalex-snapshot
Ragulator-Rag Complex Targets mTORC1 to the Lysosomal Surface and Is Necessary for Its Activation by Amino Acids
inferredcites →https://doi.org/10.1016/j.cell.2012.02.044openalex-snapshot
Leucyl-tRNA Synthetase Is an Intracellular Leucine Sensor for the mTORC1-Signaling Pathway
inferredcites →https://doi.org/10.1016/j.cell.2012.03.017openalex-snapshot
mTOR Signaling in Growth Control and Disease
inferredcites →https://doi.org/10.1016/j.cell.2012.07.032openalex-snapshot
Ragulator Is a GEF for the Rag GTPases that Signal Amino Acid Levels to mTORC1
inferredcites →https://doi.org/10.1016/j.cell.2013.06.041openalex-snapshot
Methionine Inhibits Autophagy and Promotes Growth by Inducing the SAM-Responsive Methylation of PP2A
inferredcites →https://doi.org/10.1016/j.cell.2013.11.049openalex-snapshot
Spatial Control of the TSC Complex Integrates Insulin and Nutrient Regulation of mTORC1 at the Lysosome
inferredcites →https://doi.org/10.1016/j.cell.2014.01.024openalex-snapshot
Regulation of TORC1 in Response to Amino Acid Starvation via Lysosomal Recruitment of TSC2
inferredcites →https://doi.org/10.1016/j.cell.2014.08.038openalex-snapshot
Sestrins Function as Guanine Nucleotide Dissociation Inhibitors for Rag GTPases to Control mTORC1 Signaling
inferredcites →https://doi.org/10.1016/j.cell.2016.02.035openalex-snapshot
The CASTOR Proteins Are Arginine Sensors for the mTORC1 Pathway
inferredcites →https://doi.org/10.1016/j.celrep.2014.09.014openalex-snapshot
The Sestrins Interact with GATOR2 to Negatively Regulate the Amino-Acid-Sensing Pathway Upstream of mTORC1
inferredcites →https://doi.org/10.1016/j.celrep.2014.10.019openalex-snapshot
Sestrins Inhibit mTORC1 Kinase Activation through the GATOR Complex
inferredcites →https://doi.org/10.1016/j.celrep.2015.08.059openalex-snapshot
Amino Acids Stimulate TORC1 through Lst4-Lst7, a GTPase-Activating Protein Complex for the Rag Family GTPase Gtr2
inferredcites →https://doi.org/10.1016/j.celrep.2016.07.008openalex-snapshot
Leucyl-tRNA Synthetase Activates Vps34 in Amino Acid-Sensing mTORC1 Signaling
inferredcites →https://doi.org/10.1016/j.cmet.2013.08.018openalex-snapshot
Sestrins Orchestrate Cellular Metabolism to Attenuate Aging
inferredcites →https://doi.org/10.1016/j.cmet.2013.09.005openalex-snapshot
AMP as a Low-Energy Charge Signal Autonomously Initiates Assembly of AXIN-AMPK-LKB1 Complex for AMPK Activation
inferredcites →https://doi.org/10.1016/j.cmet.2014.06.014openalex-snapshot
The Lysosomal v-ATPase-Ragulator Complex Is a Common Activator for AMPK and mTORC1, Acting as a Switch between Catabolism and Anabolism
inferredcites →https://doi.org/10.1016/j.cmet.2014.09.013openalex-snapshot
AMPK—Sensing Energy while Talking to Other Signaling Pathways
inferredcites →https://doi.org/10.1016/j.cub.2005.02.053openalex-snapshot
Rheb Binds and Regulates the mTOR Kinase
inferredcites →https://doi.org/10.1016/j.devcel.2014.03.017openalex-snapshot
RagA, but Not RagB, Is Essential for Embryonic Development and Adult Mice
inferredcites →https://doi.org/10.1016/j.devcel.2015.02.010openalex-snapshot
MCRS1 Binds and Couples Rheb to Amino Acid-Dependent mTORC1 Activation
inferredcites →https://doi.org/10.1016/j.immuni.2014.08.011openalex-snapshot
The Histidine Transporter SLC15A4 Coordinates mTOR-Dependent Inflammatory Responses and Pathogenic Antibody Production
inferredcites →https://doi.org/10.1016/j.jmb.2010.07.034openalex-snapshot
Structural Conservation of Components in the Amino Acid Sensing Branch of the TOR Pathway in Yeast and Mammals
inferredcites →https://doi.org/10.1016/j.molcel.2008.03.003openalex-snapshot
AMPK Phosphorylation of Raptor Mediates a Metabolic Checkpoint
inferredcites →https://doi.org/10.1016/j.molcel.2009.06.033openalex-snapshot
The Vam6 GEF Controls TORC1 by Activating the EGO Complex
inferredcites →https://doi.org/10.1016/j.molcel.2012.02.009openalex-snapshot
Leucyl-tRNA Synthetase Controls TORC1 via the EGO Complex
inferredcites →https://doi.org/10.1016/j.molcel.2012.05.043openalex-snapshot
Glutaminolysis Activates Rag-mTORC1 Signaling
inferredcites →https://doi.org/10.1016/j.molcel.2012.06.009openalex-snapshot
TBC1D7 Is a Third Subunit of the TSC1-TSC2 Complex Upstream of mTORC1
inferredcites →https://doi.org/10.1016/j.molcel.2012.08.001openalex-snapshot
The G Protein-Coupled Taste Receptor T1R1/T1R3 Regulates mTORC1 and Autophagy
inferredcites →https://doi.org/10.1016/j.molcel.2013.09.016openalex-snapshot
The Folliculin Tumor Suppressor Is a GAP for the RagC/D GTPases That Signal Amino Acid Levels to mTORC1
inferredcites →https://doi.org/10.1016/j.molcel.2015.03.033openalex-snapshot
The Ubiquitination of RagA GTPase by RNF152 Negatively Regulates mTORC1 Activation
inferredcites →https://doi.org/10.1016/j.molcel.2015.05.010openalex-snapshot
Skp2-Mediated RagA Ubiquitination Elicits a Negative Feedback to Prevent Amino-Acid-Dependent mTORC1 Hyperactivation by Recruiting GATOR1
inferredcites →https://doi.org/10.1016/j.molmed.2012.05.007openalex-snapshot
Amino acids and mTORC1: from lysosomes to disease
inferredcites →https://doi.org/10.1016/j.str.2012.09.019openalex-snapshot
Ego3 Functions as a Homodimer to Mediate the Interaction between Gtr1-Gtr2 and Ego1 in the EGO Complex to Activate TORC1
inferredcites →https://doi.org/10.1016/j.tcb.2014.03.003openalex-snapshot
Regulation of mTORC1 by amino acids
inferredcites →https://doi.org/10.1016/j.tcb.2015.06.002openalex-snapshot
Regulation of mTORC1 by PI3K signaling
inferredcites →https://doi.org/10.1016/j.tem.2009.05.008openalex-snapshot
ATF4-dependent transcription mediates signaling of amino acid limitation
inferredcites →https://doi.org/10.1016/s0092-8674(00)80324-4openalex-snapshot
The Mouse Locus Encodes Axin, an Inhibitor of the Wnt Signaling Pathway That Regulates Embryonic Axis Formation
inferredcites →https://doi.org/10.1016/s0092-8674(02)00808-5openalex-snapshot
mTOR Interacts with Raptor to Form a Nutrient-Sensitive Complex that Signals to the Cell Growth Machinery
inferredcites →https://doi.org/10.1016/s0092-8674(02)00833-4openalex-snapshot
Raptor, a Binding Partner of Target of Rapamycin (TOR), Mediates TOR Action
inferredcites →https://doi.org/10.1016/s0092-8674(03)00929-2openalex-snapshot
TSC2 Mediates Cellular Energy Response to Control Cell Growth and Survival
inferredcites →https://doi.org/10.1016/s1097-2765(00)00028-9openalex-snapshot
Uncharged tRNA Activates GCN2 by Displacing the Protein Kinase Moiety from a Bipartite tRNA-Binding Domain
inferredcites →https://doi.org/10.1016/s1097-2765(00)00108-8openalex-snapshot
Regulated Translation Initiation Controls Stress-Induced Gene Expression in Mammalian Cells
inferredcites →https://doi.org/10.1016/s1097-2765(02)00568-3openalex-snapshot
Identification of the Tuberous Sclerosis Complex-2 Tumor Suppressor Gene Product Tuberin as a Target of the Phosphoinositide 3-Kinase/Akt Pathway
inferredcites →https://doi.org/10.1016/s1097-2765(02)00636-6openalex-snapshot
Two TOR Complexes, Only One of which Is Rapamycin Sensitive, Have Distinct Roles in Cell Growth Control
inferredcites →https://doi.org/10.1016/s1097-2765(03)00220-xopenalex-snapshot
Insulin Activation of Rheb, a Mediator of mTOR/S6K/4E-BP Signaling, Is Inhibited by TSC1 and 2
inferredcites →https://doi.org/10.1038/35007072openalex-snapshot
A family of candidate taste receptors in human and mouse
inferredcites →https://doi.org/10.1038/369756a0openalex-snapshot
A mammalian protein targeted by G1-arresting rapamycin–receptor complex
inferredcites →https://doi.org/10.1038/celldisc.2015.49openalex-snapshot
Conserved regulators of Rag GTPases orchestrate amino acid-dependent TORC1 signaling
inferredcites →https://doi.org/10.1038/celldisc.2016.35openalex-snapshot
Structural insight into the arginine-binding specificity of CASTOR1 in amino acid-dependent mTORC1 signaling
inferredcites →https://doi.org/10.1038/cr.2015.146openalex-snapshot
Multiple amino acid sensing inputs to mTORC1
inferredcites →https://doi.org/10.1038/cr.2015.86openalex-snapshot
Crystal structure of the Ego1-Ego2-Ego3 complex and its role in promoting Rag GTPase-dependent TORC1 signaling
inferredcites →https://doi.org/10.1038/nature14107openalex-snapshot
SLC38A9 is a component of the lysosomal amino acid sensing machinery that controls mTORC1
inferredcites →https://doi.org/10.1038/nature19079openalex-snapshot
Mechanism of arginine sensing by CASTOR1 upstream of mTORC1
inferredcites →https://doi.org/10.1038/nature726openalex-snapshot
An amino-acid taste receptor
inferredcites →https://doi.org/10.1038/ncb1753openalex-snapshot
Regulation of TORC1 by Rag GTPases in nutrient response
inferredcites →https://doi.org/10.1038/ncb839openalex-snapshot
TSC2 is phosphorylated and inhibited by Akt and suppresses mTOR signalling
inferredcites →https://doi.org/10.1038/ncb847openalex-snapshot
Tsc tumour suppressor proteins antagonize amino-acid–TOR signalling
inferredcites →https://doi.org/10.1038/ncomms10025openalex-snapshot
Janus-faced Sestrin2 controls ROS and mTOR signalling through two separate functional domains
inferredcites →https://doi.org/10.1038/ncomms10662openalex-snapshot
Lysosomal recruitment of TSC2 is a universal response to cellular stress
inferredcites →https://doi.org/10.1038/ncomms8250openalex-snapshot
LAPTM4b recruits the LAT1-4F2hc Leu transporter to lysosomes and promotes mTORC1 activation
inferredcites →https://doi.org/10.1038/nrm2249openalex-snapshot
AMP-activated/SNF1 protein kinases: conserved guardians of cellular energy
inferredcites →https://doi.org/10.1038/nrm2822openalex-snapshot
The nuts and bolts of AGC protein kinases
inferredcites →https://doi.org/10.1038/nrm3311openalex-snapshot
AMPK: a nutrient and energy sensor that maintains energy homeostasis
inferredcites →https://doi.org/10.1038/nrm3522openalex-snapshot
Amino acid signalling upstream of mTOR
inferredcites →https://doi.org/10.1038/nrm3757openalex-snapshot
Making new contacts: the mTOR network in metabolism and signalling crosstalk
inferredcites →https://doi.org/10.1038/onc.2010.177openalex-snapshot
Proton-assisted amino-acid transporters are conserved regulators of proliferation and amino-acid-dependent mTORC1 activation
inferredcites →https://doi.org/10.1038/onc.2012.465openalex-snapshot
HIF-independent role of prolyl hydroxylases in the cellular response to amino acids
inferredcites →https://doi.org/10.1038/onc.2015.363openalex-snapshot
PAT4 levels control amino-acid sensitivity of rapamycin-resistant mTORC1 from the Golgi and affect clinical outcome in colorectal cancer
inferredcites →https://doi.org/10.1038/onc.2015.381openalex-snapshot
ASCT2/SLC1A5 controls glutamine uptake and tumour growth in triple-negative basal-like breast cancer
inferredcites →https://doi.org/10.1038/srep09502openalex-snapshot
Sestrin2 inhibits mTORC1 through modulation of GATOR complexes
inferredcites →https://doi.org/10.1038/srep13828openalex-snapshot
TSC2 mediates hyperosmotic stress-induced inactivation of mTORC1
inferredcites →https://doi.org/10.1038/srep27698openalex-snapshot
GCN2 contributes to mTORC1 inhibition by leucine deprivation through an ATF4 independent mechanism
inferredcites →https://doi.org/10.1042/bst0370242openalex-snapshot
Amino-acid-induced signalling via the SPS-sensing pathway in yeast
inferredcites →https://doi.org/10.1042/bst20130041openalex-snapshot
A growing role for mTOR in promoting anabolic metabolism
inferredcites →https://doi.org/10.1046/j.1365-2958.1998.00714.xopenalex-snapshot
The permease homologue Ssy1p controls the expression of amino acid and peptide transporter genes in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1073/pnas.0400541101openalex-snapshot
Reinitiation involving upstream ORFs regulates ATF4 mRNA translation in mammalian cells
inferredcites →https://doi.org/10.1073/pnas.202476899openalex-snapshot
Tuberous sclerosis complex-1 and -2 gene products function together to inhibit mammalian target of rapamycin (mTOR)-mediated downstream signaling
inferredcites →https://doi.org/10.1073/pnas.81.20.6442openalex-snapshot
Evidence for translational regulation of the activator of general amino acid control in yeast.
inferredcites →https://doi.org/10.1073/pnas.86.12.4579openalex-snapshot
Juxtaposition of domains homologous to protein kinases and histidyl-tRNA synthetases in GCN2 protein suggests a mechanism for coupling GCN4 expression to amino acid availability.
inferredcites →https://doi.org/10.1073/pnas.91.26.12574openalex-snapshot
RAPT1, a mammalian homolog of yeast Tor, interacts with the FKBP12/rapamycin complex.
inferredcites →https://doi.org/10.1074/jbc.270.2.815openalex-snapshot
Isolation of a Protein Target of the FKBP12-Rapamycin Complex in Mammalian Cells
inferredcites →https://doi.org/10.1074/jbc.270.48.28982openalex-snapshot
Cloning of a Novel Family of Mammalian GTP-binding Proteins (RagA, RagBs, RagB1) with Remote Similarity to the Ras-related GTPases
inferredcites →https://doi.org/10.1074/jbc.273.23.14484openalex-snapshot
Amino Acid Sufficiency and mTOR Regulate p70 S6 Kinase and eIF-4E BP1 through a Common Effector Mechanism
inferredcites →https://doi.org/10.1074/jbc.275.15.11198openalex-snapshot
The Saccharomyces cerevisiae Rheb G-protein Is Involved in Regulating Canavanine Resistance and Arginine Uptake
inferredcites →https://doi.org/10.1074/jbc.c300133200openalex-snapshot
Rapamycin-induced Translational Derepression of GCN4 mRNA Involves a Novel Mechanism for Activation of the eIF2α Kinase GCN2
inferredcites →https://doi.org/10.1074/jbc.m004389200openalex-snapshot
Novel G Proteins, Rag C and Rag D, Interact with GTP-binding Proteins, Rag A and Rag B
inferredcites →https://doi.org/10.1074/jbc.m008028200openalex-snapshot
A Family of Yeast Proteins Mediating Bidirectional Vacuolar Amino Acid Transport
inferredcites →https://doi.org/10.1074/jbc.m110.106864openalex-snapshot
Structural and Functional Insights into Saccharomyces cerevisiae Tpa1, a Putative Prolylhydroxylase Influencing Translation Termination and Transcription
inferredcites →https://doi.org/10.1074/jbc.m110.121947openalex-snapshot
Integration of General Amino Acid Control and Target of Rapamycin (TOR) Regulatory Pathways in Nitrogen Assimilation in Yeast
inferredcites →https://doi.org/10.1074/jbc.m114.574335openalex-snapshot
Nitrogen Source Activates TOR (Target of Rapamycin) Complex 1 via Glutamine and Independently of Gtr/Rag Proteins
inferredcites →https://doi.org/10.1074/jbc.m201959200openalex-snapshot
ATF4 Is a Mediator of the Nutrient-sensing Response Pathway That Activates the Human Asparagine Synthetase Gene
inferredcites →https://doi.org/10.1074/jbc.m311862200openalex-snapshot
Induction of CHOP Expression by Amino Acid Limitation Requires Both ATF4 Expression and ATF2 Phosphorylation
inferredcites →https://doi.org/10.1074/jbc.m402228200openalex-snapshot
Dimerization Is Required for Activation of eIF2 Kinase Gcn2 in Response to Diverse Environmental Stress Conditions
inferredcites →https://doi.org/10.1074/jbc.m404559200openalex-snapshot
Preservation of Liver Protein Synthesis during Dietary Leucine Deprivation Occurs at the Expense of Skeletal Muscle Mass in Mice Deleted for eIF2 Kinase GCN2
inferredcites →https://doi.org/10.1080/21541248.2016.1211070openalex-snapshot
Unsolved mysteries of Rag GTPase signaling in yeast
inferredcites →https://doi.org/10.1083/jcb.201107033openalex-snapshot
Class III PI-3-kinase activates phospholipase D in an amino acid–sensing mTORC1 pathway
inferredcites →https://doi.org/10.1083/jcb.201307084openalex-snapshot
Recruitment of folliculin to lysosomes supports the amino acid–dependent activation of Rag GTPases
inferredcites →https://doi.org/10.1091/mbc.7.1.25openalex-snapshot
TOR controls translation initiation and early G1 progression in yeast.
inferredcites →https://doi.org/10.1091/mbc.e11-04-0282openalex-snapshot
A phosphodegron controls nutrient-induced proteasomal activation of the signaling protease Ssy5
inferredcites →https://doi.org/10.1091/mbc.e15-07-0470openalex-snapshot
Dynamic relocation of the TORC1–Gtr1/2–Ego1/2/3 complex is regulated by Gtr1 and Gtr2
inferredcites →https://doi.org/10.1091/mbc.e15-08-0581openalex-snapshot
A LAPF/phafin1-like protein regulates TORC1 and lysosomal membrane permeabilization in response to endoplasmic reticulum membrane stress
inferredcites →https://doi.org/10.1093/genetics/152.3.853openalex-snapshot
Saccharomyces cerevisiae Putative G Protein, Gtr1p, Which Forms Complexes With Itself and a Novel Protein Designated as Gtr2p, Negatively Regulates the Ran/Gsp1p G Protein Cycle Through Gtr2p
inferredcites →https://doi.org/10.1093/hmg/11.5.525openalex-snapshot
A mouse model of TSC1 reveals sex-dependent lethality from liver hemangiomas, and up-regulation of p70S6 kinase activity in Tsc1 null cells
inferredcites →https://doi.org/10.1093/nar/gkt563openalex-snapshot
The eIF2α/ATF4 pathway is essential for stress-induced autophagy gene expression
inferredcites →https://doi.org/10.1101/cshperspect.a019141openalex-snapshot
The Opposing Actions of Target of Rapamycin and AMP-Activated Protein Kinase in Cell Growth Control
inferredcites →https://doi.org/10.1101/gad.1069003openalex-snapshot
Translational control by TOR and TAP42 through dephosphorylation of eIF2α kinase GCN2
inferredcites →https://doi.org/10.1101/gad.1110003openalex-snapshot
Rheb GTPase is a direct target of TSC2 GAP activity and regulates mTOR signaling
inferredcites →https://doi.org/10.1101/gad.239202openalex-snapshot
Receptor-mediated endoproteolytic activation of two transcription factors in yeast
inferredcites →https://doi.org/10.1101/gad.269324.115openalex-snapshot
GCN2 sustains mTORC1 suppression upon amino acid deprivation by inducing Sestrin2
inferredcites →https://doi.org/10.1101/gad.374206openalex-snapshot
Regulation of transcription factor latency by receptor-activated proteolysis
inferredcites →https://doi.org/10.1126/science.1157535openalex-snapshot
The Rag GTPases Bind Raptor and Mediate Amino Acid Signaling to mTORC1
inferredcites →https://doi.org/10.1126/science.1207056openalex-snapshot
mTORC1 Senses Lysosomal Amino Acids Through an Inside-Out Mechanism That Requires the Vacuolar H + -ATPase
inferredcites →https://doi.org/10.1126/science.1232044openalex-snapshot
A Tumor Suppressor Complex with GAP Activity for the Rag GTPases That Signal Amino Acid Sufficiency to mTORC1
inferredcites →https://doi.org/10.1126/science.1257132openalex-snapshot
Lysosomal amino acid transporter SLC38A9 signals arginine sufficiency to mTORC1
inferredcites →https://doi.org/10.1126/science.1259472openalex-snapshot
Differential regulation of mTORC1 by leucine and glutamine
inferredcites →https://doi.org/10.1126/science.1715094openalex-snapshot
Targets for Cell Cycle Arrest by the Immunosuppressant Rapamycin in Yeast
inferredcites →https://doi.org/10.1126/science.aab2674openalex-snapshot
Sestrin2 is a leucine sensor for the mTORC1 pathway
inferredcites →https://doi.org/10.1126/science.aad0489openalex-snapshot
mTORC1 induces purine synthesis through control of the mitochondrial tetrahydrofolate cycle
inferredcites →https://doi.org/10.1126/science.aad2087openalex-snapshot
Structural basis for leucine sensing by the Sestrin2-mTORC1 pathway
inferredcites →https://doi.org/10.1126/scisignal.2004112openalex-snapshot
Amino Acid Deprivation Inhibits TORC1 Through a GTPase-Activating Protein Complex for the Rag Family GTPase Gtr1
inferredcites →https://doi.org/10.1126/scisignal.aaf2885openalex-snapshot
Sestrin regulation of TORC1: Is Sestrin a leucine sensor?
inferredcites →https://doi.org/10.1126/scisignal.aah4497openalex-snapshot
The apo-structure of the leucine sensor Sestrin2 is still elusive
inferredcites →https://doi.org/10.1128/ec.01.1.22-32.2002openalex-snapshot
Gcn4p, a Master Regulator of Gene Expression, Is Controlled at Multiple Levels by Diverse Signals of Starvation and Stress
inferredcites →https://doi.org/10.1128/ec.5.3.601-608.2006openalex-snapshot
Mapping of an Internal Protease Cleavage Site in the Ssy5p Component of the Amino Acid Sensor of Saccharomyces cerevisiae and Functional Characterization of the Resulting Pro- and Protease Domains by Gain-of-Function Genetics
inferredcites →https://doi.org/10.1128/mcb.00125-15openalex-snapshot
Amino Acid-Dependent mTORC1 Regulation by the Lysosomal Membrane Protein SLC38A9
inferredcites →https://doi.org/10.1128/mcb.00323-10openalex-snapshot
The Prodomain of Ssy5 Protease Controls Receptor-Activated Proteolysis of Transcription Factor Stp1
inferredcites →https://doi.org/10.1128/mcb.01084-06openalex-snapshot
Effect of 21 Different Nitrogen Sources on Global Gene Expression in the Yeast Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1128/mcb.15.8.4497openalex-snapshot
The Histidyl-tRNA Synthetase-Related Sequence in the eIF-2α Protein Kinase GCN2 Interacts with tRNA and Is Required for Activation in Response to Starvation for Different Amino Acids
inferredcites →https://doi.org/10.1128/mcb.19.2.989openalex-snapshot
Amino Acid Signaling in Saccharomyces cerevisiae : a Permease-Like Sensor of External Amino Acids and F-Box Protein Grr1p Are Required for Transcriptional Induction of the AGP1 Gene, Which Encodes a Broad-Specificity Amino Acid Permease
inferredcites →https://doi.org/10.1128/mcb.19.8.5405openalex-snapshot
Ssy1p and Ptr3p Are Plasma Membrane Components of a Yeast System That Senses Extracellular Amino Acids
inferredcites →https://doi.org/10.1128/mcb.21.3.814-826.2001openalex-snapshot
Genetic and Biochemical Analysis of the Yeast Plasma Membrane Ssy1p-Ptr3p-Ssy5p Sensor of Extracellular Amino Acids
inferredcites →https://doi.org/10.1128/mcb.24.22.9771-9785.2004openalex-snapshot
Amino Acid Signaling in Yeast: Casein Kinase I and the Ssy5 Endoprotease Are Key Determinants of Endoproteolytic Activation of the Membrane-Bound Stp1 Transcription Factor
inferredcites →https://doi.org/10.1128/mcb.25.21.9435-9446.2005openalex-snapshot
Divergence of Stp1 and Stp2 Transcription Factors in Candida albicans Places Virulence Factors Required for Proper Nutrient Acquisition under Amino Acid Control
inferredcites →https://doi.org/10.1146/annurev.micro.59.031805.133833openalex-snapshot
TRANSLATIONAL REGULATION OFGCN4AND THE GENERAL AMINO ACID CONTROL OF YEAST
inferredcites →https://doi.org/10.1242/jcs.047191openalex-snapshot
TORC1 controls degradation of the transcription factor Stp1, a key effector of the SPS amino-acid-sensing pathway in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1242/jcs.111.1.11openalex-snapshot
RagA is a functional homologue of S. cerevisiae Gtr1p involved in the Ran/Gsp1-GTPase pathway
inferredcites →https://doi.org/10.1242/jcs.168922openalex-snapshot
SEA you later alli-GATOR – a dynamic regulator of the TORC1 stress response pathway
inferredcites →https://doi.org/10.1371/journal.pone.0036616openalex-snapshot
Proton-Assisted Amino Acid Transporter PAT1 Complexes with Rag GTPases and Activates TORC1 on Late Endosomal and Lysosomal Membranes
inferredcites →https://doi.org/10.1534/genetics.107.075077openalex-snapshot
Dal81 Enhances Stp1- and Stp2-Dependent Transcription Necessitating Negative Modulation by Inner Nuclear Membrane Protein Asi1 in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1534/genetics.111.133306openalex-snapshot
Regulation of Amino Acid, Nucleotide, and Phosphate Metabolism in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1534/genetics.111.133363openalex-snapshot
Target of Rapamycin (TOR) in Nutrient Signaling and Growth Control
inferredcites →https://doi.org/10.1534/genetics.114.168369openalex-snapshot
State Transitions in the TORC1 Signaling Pathway and Information Processing in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1534/genetics.166.4.1727openalex-snapshot
The External Amino Acid Signaling Pathway Promotes Activation of Stp1 and Uga35/Dal81 Transcription Factors for Induction of the AGP1 Gene in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.2337/db10-1246openalex-snapshot
Leucine Deprivation Increases Hepatic Insulin Sensitivity via GCN2/mTOR/S6K1 and AMPK Pathways
inferredcites →https://doi.org/10.3945/ajcn.113.070086openalex-snapshot
Role of amino acid transporters in amino acid sensing
inferredcites →https://doi.org/10.4161/auto.29397openalex-snapshot
Reciprocal conversion of Gtr1 and Gtr2 nucleotide-binding states by Npr2-Npr3 inactivates TORC1 and induces autophagy
inferredcites →https://doi.org/10.4161/cc.26000openalex-snapshot
SEACing the GAP that nEGOCiates TORC1 activation
inferredcites →https://doi.org/10.4161/sgtp.24262openalex-snapshot
Discovery of new Longin and Roadblock domains that form platforms for small GTPases in Ragulator and TRAPP-II
inferredcites →https://doi.org/10.7554/elife.09181openalex-snapshot
Snf1/AMPK promotes the formation of Kog1/Raptor-bodies to increase the activation threshold of TORC1 in budding yeast
inferredcites →https://doi.org/10.7554/elife.11058openalex-snapshot
Control of TSC2-Rheb signaling axis by arginine regulates mTORC1 activity

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.3917161openalex-extracted
A Sphingolipid-mTORC1 Nutrient-Sensing Machinery Enables Animal Development by Suppression of the Intestinal Peroxisome Relocation, Hormone Secretion and the Gut-Brain Crosstalk
inferred← citeshttps://doi.org/10.1002/1873-3468.12882openalex-snapshot
Ecm33 is a novel factor involved in efficient glucose uptake for nutrition‐responsive TORC 1 signaling in yeast
inferred← citeshttps://doi.org/10.1002/1873-3468.13661openalex-snapshot
The activation mechanism of plant S6 kinase (S6K), a substrate of TOR kinase, is different from that of mammalian S6K
inferred← citeshttps://doi.org/10.1002/1873-3468.13722openalex-snapshot
Mitotic cyclin Clb4 is required for the intracellular adaptation to glucose starvation in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1002/1873-3468.13888openalex-snapshot
TOR kinase activity in Chlamydomonas reinhardtii is modulated by cellular metabolic states
inferred← citeshttps://doi.org/10.1002/1873-3468.14741openalex-snapshot
Nutrient‐dependent signaling pathways that control autophagy in yeast
inferred← citeshttps://doi.org/10.1002/1873-3468.14980openalex-snapshot
Fission yeast Pib2 localizes to vacuolar membranes and regulates TOR complex 1 through evolutionarily conserved domains
inferred← citeshttps://doi.org/10.1002/aac2.12044openalex-snapshot
The critical function of metabolic reprogramming in cancer metastasis
inferred← citeshttps://doi.org/10.1002/advs.202414496openalex-snapshot
Pupylation‐Based Proximity Labeling Unravels a Comprehensive Protein and Phosphoprotein Interactome of the Arabidopsis TOR Complex
inferred← citeshttps://doi.org/10.1002/ana.25351openalex-snapshot
KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy‐lysosome defect
inferred← citeshttps://doi.org/10.1002/bies.201900194openalex-snapshot
Nutrient Sensing and Response Drive Developmental Progression in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1002/bies.202300243openalex-snapshot
The molecular mechanisms regulating the assembly of the autophagy initiation complex
inferred← citeshttps://doi.org/10.1002/bit.70381openalex-snapshot
Transcriptomics‐Driven Identification and Engineering of a Novel Lactone Esterase ( Sr LE) for Efficient Sophorolipid Lactonization in the Yeast Starmerella riodocensis
inferred← citeshttps://doi.org/10.1002/jobm.202400658openalex-snapshot
AMPK Activates Cellulase Secretion in Penicillium funiculosum by Downregulating P‐HOG1 MAPK Levels
inferred← citeshttps://doi.org/10.1002/mbo3.1176openalex-snapshot
Magnesium depletion extends fission yeast lifespan via general amino acid control activation
inferred← citeshttps://doi.org/10.1002/mbo3.730openalex-snapshot
Yeast transformation efficiency is enhanced by TORC 1‐ and eisosome‐dependent signaling
inferred← citeshttps://doi.org/10.1002/pld3.184openalex-snapshot
Reciprocal regulation of photosynthesis and mitochondrial respiration by TOR kinase in Chlamydomonas reinhardtii
inferred← citeshttps://doi.org/10.1002/wrna.1480openalex-snapshot
LARP1 on TOP of ribosome production
inferred← citeshttps://doi.org/10.1002/yea.3351openalex-snapshot
Indirect monitoring of TORC1 signalling pathway reveals molecular diversity among different yeast strains
inferred← citeshttps://doi.org/10.1002/yea.3849openalex-snapshot
TorC1 and nitrogen catabolite repression control of integrated GABA shunt and retrograde pathway gene expression
inferred← citeshttps://doi.org/10.1002/yea.3911openalex-snapshot
High nitrogen concentration causes G2/M arrest in Hanseniaspora vineae
inferred← citeshttps://doi.org/10.1002/yea.3939openalex-snapshot
Yeast Crf1p is an activator with different roles in regulation of target genes
inferred← citeshttps://doi.org/10.1002/yea.70008openalex-snapshot
From Yeast to Therapeutics: Modeling Neurodegenerative Diseases in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1007/978-1-0716-4284-9_7openalex-snapshot
Visualization of Subcellular mTOR Complex 1 Activity with a FRET-Based Sensor (TORCAR)
inferred← citeshttps://doi.org/10.1007/978-1-0716-5304-3_17openalex-snapshot
Quantitative Coarse-Grained Modeling of Microbial Metabolism: Uncovering Growth Laws, Environmental Responses, and Host-Circuit Coupling
inferred← citeshttps://doi.org/10.1007/978-3-030-00737-9_8openalex-snapshot
The Yeast Prefoldin Bud27
inferred← citeshttps://doi.org/10.1007/978-3-030-49924-2_8openalex-snapshot
8 Coordination of Fungal Secondary Metabolism and Development
inferred← citeshttps://doi.org/10.1007/978-3-030-94004-1_8openalex-snapshot
Signaling Pathways that Regulate Macropinocytosis in Mammalian Cells
inferred← citeshttps://doi.org/10.1007/978-3-319-89315-0_5openalex-snapshot
Hyperlipidemias and Obesity
inferred← citeshttps://doi.org/10.1007/978-981-16-2830-6_15openalex-snapshot
Autophagy in Drosophila and Zebrafish
inferred← citeshttps://doi.org/10.1007/s00018-019-03122-4openalex-snapshot
Autophagy in hypoxic ovary
inferred← citeshttps://doi.org/10.1007/s00248-026-02782-7openalex-snapshot
Anhydrobiosis as a Model of Aging and Longevity: The Role of Autophagy and Metabolism in Yeast Cells
inferred← citeshttps://doi.org/10.1007/s00281-021-00860-1openalex-snapshot
Regulation of eosinophil functions by autophagy
inferred← citeshttps://doi.org/10.1007/s00294-017-0738-zopenalex-snapshot
Control of RNA polymerase II-transcribed genes by direct binding of TOR kinase
inferred← citeshttps://doi.org/10.1007/s00294-018-00929-9openalex-snapshot
Whi2: a new player in amino acid sensing
inferred← citeshttps://doi.org/10.1007/s00294-019-01045-yopenalex-snapshot
tRNA wobble-uridine modifications as amino acid sensors and regulators of cellular metabolic state
inferred← citeshttps://doi.org/10.1007/s00294-021-01180-5openalex-snapshot
Ccr4-Not as a mediator of environmental signaling: a jack of all trades and master of all
inferred← citeshttps://doi.org/10.1007/s00294-025-01321-0openalex-snapshot
Possible regulatory network and associated pathways governing the expression of ADH2 in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1007/s00438-019-01592-6openalex-snapshot
Leucine depletion extends the lifespans of leucine-auxotrophic fission yeast by inducing Ecl1 family genes via the transcription factor Fil1
inferred← citeshttps://doi.org/10.1007/s00535-026-02437-xopenalex-snapshot
S-adenosylhomocysteine hydrolase-like protein 1 deficiency resulted in stronger inflammation reaction in acute pancreatitis
inferred← citeshttps://doi.org/10.1007/s10565-021-09625-wopenalex-snapshot
Neuroprotective properties of queen bee acid by autophagy induction
inferred← citeshttps://doi.org/10.1007/s11274-026-04947-5openalex-snapshot
Molecular frontiers of fungal autophagy: from molecular mechanisms to potential targets for antifungal drug discovery
inferred← citeshttps://doi.org/10.1007/s11357-022-00598-0openalex-snapshot
The PICLS high-throughput screening method for agents extending cellular longevity identifies 2,5-anhydro-D-mannitol as novel anti-aging compound
inferred← citeshttps://doi.org/10.1007/s11357-026-02527-xopenalex-snapshot
Copper and iron engage distinct metabolic programs for cellular survival
inferred← citeshttps://doi.org/10.1007/s11626-022-00682-xopenalex-snapshot
14-3-3β is essential for milk composition stimulated by Leu/IGF-1 via IGF1R signaling pathway in BMECs
inferred← citeshttps://doi.org/10.1007/s12268-020-1481-4openalex-snapshot
Die Rolle von mTORC1 in der Verstoffwechslung extrazellulärer Proteine
inferred← citeshttps://doi.org/10.1007/s12672-024-01525-9openalex-snapshot
MicroRNA-mediated autophagy and drug resistance in cancer: mechanisms and therapeutic strategies
inferred← citeshttps://doi.org/10.1007/s13402-022-00716-2openalex-snapshot
OSW-1 induces apoptosis and cyto-protective autophagy, and synergizes with chemotherapy on triple negative breast cancer metastasis
inferred← citeshttps://doi.org/10.1016/b978-0-12-815962-0.00008-1openalex-snapshot
Yeast as a model organism for aging research
inferred← citeshttps://doi.org/10.1016/b978-0-12-819460-7.00001-3openalex-snapshot
Regulation | mTOR and its Substrates
inferred← citeshttps://doi.org/10.1016/b978-0-12-820528-0.00015-6openalex-snapshot
Retrograde signaling: A novel antifungal drug target
inferred← citeshttps://doi.org/10.1016/b978-0-12-821618-7.00106-1openalex-snapshot
The Late Endosome
inferred← citeshttps://doi.org/10.1016/b978-0-12-822003-0.00024-3openalex-snapshot
Autophagy in cell plasticity with particular focus on paligenosis
inferred← citeshttps://doi.org/10.1016/b978-0-323-95424-2.00011-xopenalex-snapshot
Carbohydrate and protein metabolism
inferred← citeshttps://doi.org/10.1016/b978-0-323-99606-8.00019-5openalex-snapshot
Advances in metabolic engineering of yeasts
inferred← citeshttps://doi.org/10.1016/bs.mie.2022.07.007openalex-snapshot
Purification and biochemical characterization of the Rag GTPase heterodimer
inferred← citeshttps://doi.org/10.1016/j.algal.2024.103848openalex-snapshot
Dissecting nitrogen starvation signaling in Chlamydomonas: Insights from arginine-fed transcriptome profiling
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2024.741473openalex-snapshot
Fasting time after feeding affects the evaluation of metabolic response in abalone Haliotis discus hannai to nutrients using dietary methionine as an example
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2024.741849openalex-snapshot
A comprehensive analysis of metabolomics and transcriptomics revealed the mTOR-autophagy pathway is involved in ammonia metabolism of yellow catfish Pelteobagrus fulvidraco
inferred← citeshttps://doi.org/10.1016/j.bbagen.2018.12.011openalex-snapshot
The regulation of TORC1 pathway by the yeast chaperones Hsp31 is mediated by SFP1 and affects proteasomal activity
inferred← citeshttps://doi.org/10.1016/j.bbagen.2025.130810openalex-snapshot
G-quadruplex in cancer energy metabolism: A potential therapeutic target
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2019.194414openalex-snapshot
A genome-wide transcriptional study reveals that iron deficiency inhibits the yeast TORC1 pathway
inferred← citeshttps://doi.org/10.1016/j.bbalip.2019.03.005openalex-snapshot
ER platforms mediating autophagosome generation
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2018.12.008openalex-snapshot
The emerging interrelation between ROCO and related kinases, intracellular Ca2+ signaling, and autophagy
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2020.118926openalex-snapshot
Autophagy and the Wnt signaling pathway: A focus on Wnt/β-catenin signaling
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2021.119061openalex-snapshot
Cell death as a result of calcium signaling modulation: A cancer-centric prospective
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2025.119957openalex-snapshot
POLR1D, a shared subunit of RNA polymerase I and III, modulates mTORC1 activity
inferred← citeshttps://doi.org/10.1016/j.bbcan.2023.189006openalex-snapshot
Role of stress granules in tumorigenesis and cancer therapy
inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.05.123openalex-snapshot
The TORC1 signaling pathway regulates respiration-induced mitophagy in yeast
inferred← citeshttps://doi.org/10.1016/j.bbrc.2021.10.015openalex-snapshot
Carbon starvation-induced synthesis of GDH2 and PEPCK is essential for the survival of Pichia pastoris
inferred← citeshttps://doi.org/10.1016/j.bbrc.2023.02.063openalex-snapshot
FPR1 is essential for rapamycin-induced lifespan extension in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/j.bbrc.2024.149499openalex-snapshot
Interaction between Gtr2p and ribosomal Rps31p affects the incorporation of Rps31p into ribosomes of Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/j.bbrc.2024.150639openalex-snapshot
TOR2 plays the central role in rapamycin-induced lifespan extension in budding yeast
inferred← citeshttps://doi.org/10.1016/j.bcp.2024.116115openalex-snapshot
Potential role of modulating autophagy levels in sensorineural hearing loss
inferred← citeshttps://doi.org/10.1016/j.biochi.2019.06.016openalex-snapshot
Targeting TOR signaling for enhanced lipid productivity in algae
inferred← citeshttps://doi.org/10.1016/j.biochi.2022.10.004openalex-snapshot
Autophagy: Dual roles and perspective for clinical treatment of colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.biopha.2020.110799openalex-snapshot
microRNA-based autophagy inhibition as targeted therapy in pancreatic cancer
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2021.107740openalex-snapshot
Cultivation processes to select microorganisms with high accumulation ability
inferred← citeshttps://doi.org/10.1016/j.canlet.2023.216178openalex-snapshot
m6A-modification of cyclin D1 and c-myc IRESs in glioblastoma controls ITAF activity and resistance to mTOR inhibition
inferred← citeshttps://doi.org/10.1016/j.cbpa.2024.111799openalex-snapshot
Salinity stress impairs disease resistance in white shrimp, Penaeus vannamei through AMPK pathway, ameliorated by dietary glucose-mediated energy homeostasis
inferred← citeshttps://doi.org/10.1016/j.ceb.2017.10.006openalex-snapshot
Upstairs, downstairs: spatial regulation of Hippo signalling
inferred← citeshttps://doi.org/10.1016/j.cell.2019.10.036openalex-snapshot
Cryo-EM Structure of the Human FLCN-FNIP2-Rag-Ragulator Complex
inferred← citeshttps://doi.org/10.1016/j.cell.2020.10.016openalex-snapshot
Neurons Release Serine to Support mRNA Translation in Pancreatic Cancer
inferred← citeshttps://doi.org/10.1016/j.celrep.2017.10.029openalex-snapshot
The mTORC1 Signaling Network Senses Changes in Cellular Purine Nucleotide Levels
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.03.022openalex-snapshot
Mitochondrial Protein Synthesis and mtDNA Levels Coordinated through an Aminoacyl-tRNA Synthetase Subunit
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.02.058openalex-snapshot
The GATA Transcription Factor Gaf1 Represses tRNAs, Inhibits Growth, and Extends Chronological Lifespan Downstream of Fission Yeast TORC1
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.108024openalex-snapshot
Phosphoproteomic Analysis across the Yeast Life Cycle Reveals Control of Fatty Acyl Chain Length by Phosphorylation of the Fatty Acid Synthase Complex
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.108830openalex-snapshot
Amino acids-Rab1A-mTORC1 signaling controls whole-body glucose homeostasis
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.109490openalex-snapshot
Inhibition of PHLPP1/2 phosphatases rescues pancreatic β-cells in diabetes
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.110149openalex-snapshot
Phosphoproteomic responses of TORC1 target kinases reveal discrete and convergent mechanisms that orchestrate the quiescence program in yeast
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110534openalex-snapshot
The mTOR chromatin-bound interactome in prostate cancer
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110554openalex-snapshot
Cdc48 influence on separase levels is independent of mitosis and suggests translational sensitivity of separase
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110631openalex-snapshot
A negative feedback loop of TOR signaling balances growth and stress-response trade-offs in plants
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111140openalex-snapshot
A sphingolipid-mTORC1 nutrient-sensing pathway regulates animal development by an intestinal peroxisome relocation-based gut-brain crosstalk
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.113205openalex-snapshot
Metabolism of glucose activates TORC1 through multiple mechanisms in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114281openalex-snapshot
Sch9S6K controls DNA repair and DNA damage response efficiency in aging cells
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115282openalex-snapshot
Selective clearance of aberrant membrane proteins by TORC1-mediated micro-ER-phagy
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115683openalex-snapshot
TORC1 autonomously controls its spatial partitioning via the Rag GTPase tether Tco89
inferred← citeshttps://doi.org/10.1016/j.cels.2018.08.001openalex-snapshot
Machine Learning Predicts the Yeast Metabolome from the Quantitative Proteome of Kinase Knockouts
inferred← citeshttps://doi.org/10.1016/j.chembiol.2019.05.009openalex-snapshot
Discovery of Small-Molecule Selective mTORC1 Inhibitors via Direct Inhibition of Glucose Transporters
inferred← citeshttps://doi.org/10.1016/j.clindermatol.2017.09.006openalex-snapshot
Acne vulgaris: The metabolic syndrome of the pilosebaceous follicle
inferred← citeshttps://doi.org/10.1016/j.cmet.2018.04.009openalex-snapshot
Arginase 2 Suppresses Renal Carcinoma Progression via Biosynthetic Cofactor Pyridoxal Phosphate Depletion and Increased Polyamine Toxicity
inferred← citeshttps://doi.org/10.1016/j.cmet.2019.05.002openalex-snapshot
Nutrient Sensing in CD11c Cells Alters the Gut Microbiota to Regulate Food Intake and Body Mass
inferred← citeshttps://doi.org/10.1016/j.cmet.2020.01.015openalex-snapshot
AMPK and TOR: The Yin and Yang of Cellular Nutrient Sensing and Growth Control
inferred← citeshttps://doi.org/10.1016/j.cmet.2023.10.016openalex-snapshot
The tRNA-GCN2-FBXO22-axis-mediated mTOR ubiquitination senses amino acid insufficiency
inferred← citeshttps://doi.org/10.1016/j.compbiolchem.2023.107875openalex-snapshot
Investigation of Macrocyclic mTOR Modulators of Rapamycin Binding Site via Pharmacoinformatics Approaches
inferred← citeshttps://doi.org/10.1016/j.copbio.2019.11.021openalex-snapshot
Yeast systems biology in understanding principles of physiology underlying complex human diseases
inferred← citeshttps://doi.org/10.1016/j.csbj.2021.12.003openalex-snapshot
Yeast Crf1p: An activator in need is an activator indeed
inferred← citeshttps://doi.org/10.1016/j.ctmp.2024.200174openalex-snapshot
Targeting STAT3-mediated autophagy with small molecules in cancer treatment – A comprehensive review
inferred← citeshttps://doi.org/10.1016/j.cub.2017.11.069openalex-snapshot
Cell Size and Growth Rate Are Modulated by TORC2-Dependent Signals
inferred← citeshttps://doi.org/10.1016/j.cub.2019.07.039openalex-snapshot
Leucine-Rich Repeat Extensin Proteins and Their Role in Cell Wall Sensing
inferred← citeshttps://doi.org/10.1016/j.devcel.2020.02.015openalex-snapshot
Glycolysis-Independent Glucose Metabolism Distinguishes TE from ICM Fate during Mammalian Embryogenesis
inferred← citeshttps://doi.org/10.1016/j.engmic.2023.100079openalex-snapshot
Profiling proteomic responses to hexokinase-II depletion in terpene-producing Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/j.envpol.2023.121670openalex-snapshot
Nickel nanoparticles induce autophagy and apoptosis via HIF-1α/mTOR signaling in human bronchial epithelial cells
inferred← citeshttps://doi.org/10.1016/j.envpol.2023.123090openalex-snapshot
Inulin alleviates perfluorooctanoic acid-induced intestinal injury in mice by modulating the PI3K/AKT/mTOR signaling pathway
inferred← citeshttps://doi.org/10.1016/j.fbio.2026.110090openalex-snapshot
Fungal nitrogen overflow-driven cross-feeding alleviates bacterial growth limitations and promotes γ-aminobutyric acid and ethyl ester biosynthesis
inferred← citeshttps://doi.org/10.1016/j.fct.2024.114510openalex-snapshot
Rapamycin protects Sertoli cells against BPA-induced autophagy disorders
inferred← citeshttps://doi.org/10.1016/j.foodres.2026.120882openalex-snapshot
Amino acid cross-feeding by Debaryomyces hansenii promotes bacterial growth and flavor metabolite formation in fermented sausages
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2024.10.288openalex-snapshot
A critical role for microglia in regulating metabolic homeostasis and neural repair after spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.funbio.2020.10.009openalex-snapshot
Carbamoyl phosphate synthetase subunit Cpa1 interacting with Dut1, controls development, arginine biosynthesis, and pathogenicity of Colletotrichum gloeosporioides
inferred← citeshttps://doi.org/10.1016/j.hnm.2023.200210openalex-snapshot
Visceral fat: A key mediator of NAFLD development and progression
inferred← citeshttps://doi.org/10.1016/j.ibmb.2021.103667openalex-snapshot
Halofuginone triggers a transcriptional program centered on ribosome biogenesis and function in honey bees
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.09.211openalex-snapshot
Insights into intracellular signaling network in Fusarium species
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.141730openalex-snapshot
The role of the poly(A) binding protein-binding protein MoPbp1 as a regulator of the TOR signaling pathway in growth, autophagy, and pathogenicity of the rice blast fungus
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.149944openalex-snapshot
TSC2 is a positive master regulator of cellulase production by affecting protein secretion in Trichoderma reesei
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2026.111813openalex-snapshot
Effect of nitrogen status on competitive abilities between indigenous and commercial wine strains in alcoholic fermentation
inferred← citeshttps://doi.org/10.1016/j.immuni.2025.06.010openalex-snapshot
More TOR: The expanding role of mTOR in regulating immune responses
inferred← citeshttps://doi.org/10.1016/j.immuni.2026.04.004openalex-snapshot
Metabolic and transcriptional plasticity supports CD8+ T cell resilience and anti-tumor immunity under nutrient stress
inferred← citeshttps://doi.org/10.1016/j.intimp.2026.116902openalex-snapshot
Targeting macrophage metabolism: Ghrelin regulates macrophage polarization via dual modulation of the AMPK/mTOR axis in immune-mediated diseases
inferred← citeshttps://doi.org/10.1016/j.isci.2019.08.002openalex-snapshot
Eukaryotic Adaptation to Years-Long Starvation Resembles that of Bacteria
inferred← citeshttps://doi.org/10.1016/j.isci.2019.09.025openalex-snapshot
Pib2-Dependent Feedback Control of the TORC1 Signaling Network by the Npr1 Kinase
inferred← citeshttps://doi.org/10.1016/j.isci.2020.100858openalex-snapshot
Exposure of Pancreatic β-Cells to Excess Glucose Results in Bimodal Activation of mTORC1 and mTOR-Dependent Metabolic Acceleration
inferred← citeshttps://doi.org/10.1016/j.isci.2021.102778openalex-snapshot
A novel amino acid signaling process governs glucose-6-phosphatase transcription
inferred← citeshttps://doi.org/10.1016/j.isci.2022.104186openalex-snapshot
The TORC1 phosphoproteome in C. elegans reveals roles in transcription and autophagy
inferred← citeshttps://doi.org/10.1016/j.isci.2022.104238openalex-snapshot
Plasma membrane H+-ATPases promote TORC1 activation in plant suspension cells
inferred← citeshttps://doi.org/10.1016/j.isci.2023.108777openalex-snapshot
Rapamycin-sensitive mechanisms confine the growth of fission yeast below the temperatures detrimental to cell physiology
inferred← citeshttps://doi.org/10.1016/j.isci.2024.110814openalex-snapshot
FYVE1/FREE1 is involved in glutamine-responsive TORC1 activation in plants
inferred← citeshttps://doi.org/10.1016/j.jare.2021.10.014openalex-snapshot
Salicylic acid fights against Fusarium wilt by inhibiting target of rapamycin signaling pathway in Fusarium oxysporum
inferred← citeshttps://doi.org/10.1016/j.jbc.2021.100891openalex-snapshot
Regulation of inorganic polyphosphate is required for proper vacuolar proteolysis in fission yeast
inferred← citeshttps://doi.org/10.1016/j.jbc.2021.101100openalex-snapshot
Alkaline intracellular pH (pHi) activates AMPK–mTORC2 signaling to promote cell survival during growth factor limitation
inferred← citeshttps://doi.org/10.1016/j.jbc.2021.101103openalex-snapshot
The yoga of Rag GTPases: Dynamic structural poses confer amino acid sensing by mTORC1
inferred← citeshttps://doi.org/10.1016/j.jbc.2022.102030openalex-snapshot
Prolonged deprivation of arginine or leucine induces PI3K/Akt-dependent reactivation of mTORC1
inferred← citeshttps://doi.org/10.1016/j.jbc.2023.104644openalex-snapshot
An affinity tool for the isolation of endogenous active mTORC1 from various cellular sources
inferred← citeshttps://doi.org/10.1016/j.jbc.2025.110329openalex-snapshot
Perturbations in L-serine metabolism regulate protein quality control through the sensor of the retrograde response pathway RTG2 in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/j.jbc.2025.110700openalex-snapshot
TOR signaling regulates GPCR levels on the plasma membrane and suppresses the Saccharomyces cerevisiae mating pathway
inferred← citeshttps://doi.org/10.1016/j.jbc.2026.113107openalex-snapshot
An intricate functional relationship between NuA4 and Sfp1 regulates ribosome biogenesis in response to nutrient availability
inferred← citeshttps://doi.org/10.1016/j.jbc.2026.113228openalex-snapshot
Leucyl-tRNA synthetase as a molecular target of isobutanol-mediated growth inhibition in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/j.jbc.2026.113580openalex-snapshot
Medulloblastoma-associated mutations in the RNA helicase DDX3X/DED1 cause defects in the translational response to TORC1 inhibition
inferred← citeshttps://doi.org/10.1016/j.jbior.2017.11.001openalex-snapshot
Dysregulation of mRNA translation and energy metabolism in cancer
inferred← citeshttps://doi.org/10.1016/j.jbior.2017.12.002openalex-snapshot
Disrupting the ‘Warburg effect’ re-routes cancer cells to OXPHOS offering a vulnerability point via ‘ferroptosis’-induced cell death
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2025.05.015openalex-snapshot
Control of alcoholic fermentation through modulation of nitrogen metabolism in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/j.jgg.2022.05.006openalex-snapshot
Fecal microbiota transplantation from young donor mice improves ovarian function in aged mice
inferred← citeshttps://doi.org/10.1016/j.jgg.2026.01.007openalex-snapshot
Transcriptional, epigenetic, and post-translational regulation of plant autophagy
inferred← citeshttps://doi.org/10.1016/j.jgg.2026.06.002openalex-snapshot
Divergent roles of the Rag GTPases MoGtr1 and MoGtr2 in TOR signaling, autophagy, and pathogenicity of Magnaporthe oryzae
inferred← citeshttps://doi.org/10.1016/j.jmb.2018.10.008openalex-snapshot
Transcriptional and Epigenetic Regulation by the Mechanistic Target of Rapamycin Complex 1 Pathway
inferred← citeshttps://doi.org/10.1016/j.jmb.2019.09.005openalex-snapshot
Mechanisms of Autophagy in Metabolic Stress Response
inferred← citeshttps://doi.org/10.1016/j.jmb.2020.01.017openalex-snapshot
Autophagy as a Cellular Stress Response Mechanism in the Nervous System
inferred← citeshttps://doi.org/10.1016/j.jmb.2020.166743openalex-snapshot
Architecture of the Tuberous Sclerosis Protein Complex
inferred← citeshttps://doi.org/10.1016/j.jnutbio.2024.109592openalex-snapshot
Nutrient-epigenome interactions: Implications for personalized nutrition against aging-associated diseases
inferred← citeshttps://doi.org/10.1016/j.jplph.2022.153716openalex-snapshot
Roles of TOR signaling in nutrient deprivation and abiotic stress
inferred← citeshttps://doi.org/10.1016/j.jplph.2024.154186openalex-snapshot
TOR in plants: Multidimensional regulators of plant growth and signaling pathways
inferred← citeshttps://doi.org/10.1016/j.lfs.2021.119312openalex-snapshot
Piperine protects against pancreatic β-cell dysfunction by alleviating macrophage inflammation in obese mice
inferred← citeshttps://doi.org/10.1016/j.livres.2020.02.004openalex-snapshot
Nutrient mTORC1 signaling contributes to hepatic lipid metabolism in the pathogenesis of non-alcoholic fatty liver disease
inferred← citeshttps://doi.org/10.1016/j.lwt.2024.115732openalex-snapshot
Protective effect of wheat gluten peptides against ethanol-stress damage in yeast cell and identification of anti-ethanol peptides
inferred← citeshttps://doi.org/10.1016/j.mce.2017.09.008openalex-snapshot
Endocrine and physiological regulation of neutral fat storage in Drosophila
inferred← citeshttps://doi.org/10.1016/j.mib.2017.12.012openalex-snapshot
How yeast coordinates metabolism, growth and division
inferred← citeshttps://doi.org/10.1016/j.mib.2021.09.003openalex-snapshot
Arginine sensing in intracellular parasitism of Leishmania
inferred← citeshttps://doi.org/10.1016/j.micres.2023.127361openalex-snapshot
Components of TOR and MAP kinase signaling control chemotropism and pathogenicity in the fungal pathogen Verticillium dahliae
inferred← citeshttps://doi.org/10.1016/j.molcel.2017.09.026openalex-snapshot
Intersubunit Crosstalk in the Rag GTPase Heterodimer Enables mTORC1 to Respond Rapidly to Amino Acid Availability
inferred← citeshttps://doi.org/10.1016/j.molcel.2019.10.009openalex-snapshot
Interconversion between Anticipatory and Active GID E3 Ubiquitin Ligase Conformations via Metabolically Driven Substrate Receptor Assembly
inferred← citeshttps://doi.org/10.1016/j.molcel.2021.03.031openalex-snapshot
The dynamic mechanism of 4E-BP1 recognition and phosphorylation by mTORC1
inferred← citeshttps://doi.org/10.1016/j.molcel.2021.04.020openalex-snapshot
More writing: mTORC1 promotes m6A mRNA methylation
inferred← citeshttps://doi.org/10.1016/j.molcel.2021.06.017openalex-snapshot
An mTORC1-GRASP55 signaling axis controls unconventional secretion to reshape the extracellular proteome upon stress
inferred← citeshttps://doi.org/10.1016/j.molcel.2022.12.011openalex-snapshot
GATOR2 rings GATOR1 to speak to mTORC1
inferred← citeshttps://doi.org/10.1016/j.molcel.2023.08.016openalex-snapshot
Regulation of nucleo-cytosolic 26S proteasome translocation by aromatic amino acids via mTOR is essential for cell survival under stress
inferred← citeshttps://doi.org/10.1016/j.molcel.2024.04.016openalex-snapshot
eIF4F complex dynamics are important for the activation of the integrated stress response
inferred← citeshttps://doi.org/10.1016/j.molcel.2024.10.008openalex-snapshot
mTORC1 activity licenses its own release from the lysosomal surface
inferred← citeshttps://doi.org/10.1016/j.molcel.2025.09.001openalex-snapshot
A network of P-body and Whi3 condensates adjusts cell fate decisions to cellular context
inferred← citeshttps://doi.org/10.1016/j.molcel.2025.12.018openalex-snapshot
EGO complex at 20: The Rag GTPase-TORC1 nutrient-sensing blueprint
inferred← citeshttps://doi.org/10.1016/j.molcel.2026.06.014openalex-snapshot
LRRC58 defines an E3 ubiquitin ligase complex sensitive to cysteine abundance
inferred← citeshttps://doi.org/10.1016/j.molp.2026.08.018openalex-snapshot
The TORC–SnRK axis: An integrative signaling framework balancing growth and stress responses in plants
inferred← citeshttps://doi.org/10.1016/j.mycmed.2023.101363openalex-snapshot
In silico-chemogenomic repurposing of new chemical scaffolds for histoplasmosis treatment
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2021.108012openalex-snapshot
Mapping of mTOR drug targets: Featured platforms for anti-cancer drug discovery
inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.110220openalex-snapshot
TOR and SnRK1 signaling pathways in plant response to abiotic stresses: Do they always act according to the “yin-yang” model?
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112577openalex-snapshot
Research progress on the autophagy gene ATG6 in planta
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.107641openalex-snapshot
Phosphoproteomics analysis of the effect of target of rapamycin kinase inhibition on Cucumis sativus in response to Podosphaera xanthii
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2017.05.001openalex-snapshot
Augmenting brain metabolism to increase macro- and chaperone-mediated autophagy for decreasing neuronal proteotoxicity and aging
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2024.112904openalex-snapshot
Plumbagin controls fungal postharvest pathogens by affecting metabolism and inducing autophagy
inferred← citeshttps://doi.org/10.1016/j.semcancer.2019.08.020openalex-snapshot
Pro-survival autophagy: An emerging candidate of tumor progression through maintaining hallmarks of cancer
inferred← citeshttps://doi.org/10.1016/j.semcancer.2021.06.019openalex-snapshot
Attacking the PI3K/Akt/mTOR signaling pathway for targeted therapeutic treatment in human cancer
inferred← citeshttps://doi.org/10.1016/j.semcdb.2026.103690openalex-snapshot
Nutrient-sensing pathways in adult stem cells: Orchestrating homeostasis, aging, and disease
inferred← citeshttps://doi.org/10.1016/j.tcb.2019.12.006openalex-snapshot
Relevance and Regulation of Cell Density
inferred← citeshttps://doi.org/10.1016/j.tcb.2020.12.003openalex-snapshot
Expanding the View of IKK: New Substrates and New Biology
inferred← citeshttps://doi.org/10.1016/j.tcb.2022.06.008openalex-snapshot
Nutrient availability as an arbiter of cell size
inferred← citeshttps://doi.org/10.1016/j.tem.2023.01.004openalex-snapshot
Regulation of mTOR by phosphatidic acid
inferred← citeshttps://doi.org/10.1016/j.tibs.2020.04.010openalex-snapshot
Coupling of Ribosome Synthesis and Translational Capacity with Cell Growth
inferred← citeshttps://doi.org/10.1016/j.tibs.2020.11.004openalex-snapshot
A Tour of TOR Complex Signaling in Plants
inferred← citeshttps://doi.org/10.1016/j.tim.2021.08.002openalex-snapshot
The phosphate language of fungi
inferred← citeshttps://doi.org/10.1016/j.tips.2017.09.003openalex-snapshot
Leveraging Chemotype-Specific Resistance for Drug Target Identification and Chemical Biology
inferred← citeshttps://doi.org/10.1016/j.tplants.2018.03.010openalex-snapshot
The Plant Target of Rapamycin Kinase: A connecTOR between Sulfur and Growth
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