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Perk-Dependent Translational Regulation Promotes Tumor Cell Adaptation and Angiogenesis in Response to Hypoxic Stress

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Five-year experience with combined operative and radiotherapeutic treatment of recurrent gynecologic tumors infiltrating the pelvic wall

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Long-term engraftment of hepatocytes transplanted on biodegradable polymer sponges

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Matrix metalloproteinase 13 (collagenase 3) in human rheumatoid synovium

inferredcites →https://doi.org/10.1002/jbt.20116openalex-snapshot

Superinduction of metallothionein I by inhibition of protein synthesis: Role of a labile repressor in MTF-1 mediated gene transcription

inferredcites →https://doi.org/10.1002/path.1778openalex-snapshot

Up‐regulation of gene expression by hypoxia is mediated predominantly by hypoxia‐inducible factor 1 (HIF‐1)

inferredcites →https://doi.org/10.1006/bbrc.1999.1674openalex-snapshot

Hypoxia Regulates the Expression of the Adrenomedullin and HIF-1 Genes in Cultured HL-1 Cardiomyocytes

inferredcites →https://doi.org/10.1006/jmbi.2001.5315openalex-snapshot

Suppression of 15-lipoxygenase synthesis by hnRNP E1 is dependent on repetitive nature of LOX mRNA 3′-UTR control element DICE

inferredcites →https://doi.org/10.1007/978-1-4615-0067-4_13openalex-snapshot

Tissue Inhibitor of Metalloproteinases-3 and Sorsby Fundus Dystrophy

inferredcites →https://doi.org/10.1007/978-1-4615-0081-0_9openalex-snapshot

Matrix Metalloproteinases and Tumor Progression

inferredcites →https://doi.org/10.1016/j.bbrc.2005.07.157openalex-snapshot

Murine lipid phosphate phosphohydrolase-3 acts as a cell-associated integrin ligand

inferredcites →https://doi.org/10.1016/j.biochi.2004.12.009openalex-snapshot

Collagenases in cancer

inferredcites →https://doi.org/10.1016/j.brainres.2003.11.065openalex-snapshot

Nuclear localization of the hypoxia-regulated pro-apoptotic protein BNIP3 after global brain ischemia in the rat hippocampus

inferredcites →https://doi.org/10.1016/j.molcel.2006.01.010openalex-snapshot

Hypoxia-Induced Energy Stress Regulates mRNA Translation and Cell Growth

inferredcites →https://doi.org/10.1016/j.yexcr.2004.01.013openalex-snapshot

Human neuroblastoma cells exposed to hypoxia: induction of genes associated with growth, survival, and aggressive behavior

inferredcites →https://doi.org/10.1016/s0009-2797(00)00267-2openalex-snapshot

Aldehyde dehydrogenase 3 gene regulation: studies on constitutive and hypoxia-modulated expression

inferredcites →https://doi.org/10.1016/s0014-5793(98)01025-4openalex-snapshot

The vascular endothelial growth factor mRNA contains an internal ribosome entry site

inferredcites →https://doi.org/10.1016/s0014-5793(99)00185-4openalex-snapshot

Hypoxia increases the association of 4E‐binding protein 1 with the initiation factor 4E in isolated rat hepatocytes

inferredcites →https://doi.org/10.1016/s0021-9258(19)55717-9openalex-snapshot

Coordinated Up-regulation by Hypoxia of Adrenomedullin and One of Its Putative Receptors (RDC-1) in Cells of the Rat Blood-Brain Barrier

inferredcites →https://doi.org/10.1016/s0021-9258(19)89457-7openalex-snapshot

Molecular cloning and expression of collagenase-3, a novel human matrix metalloproteinase produced by breast carcinomas

inferredcites →https://doi.org/10.1016/s0168-8278(03)00503-8openalex-snapshot

Hexokinase II and VEGF expression in liver tumors: correlation with hypoxia-inducible factor-1α and its significance

inferredcites →https://doi.org/10.1016/s0168-9525(00)02106-5openalex-snapshot

Internal ribosome initiation of translation and the control of cell death

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(00)80240-3openalex-snapshot

A Cell Cycle–Dependent Internal Ribosome Entry Site

inferredcites →https://doi.org/10.1016/s1097-2765(00)80330-5openalex-snapshot

Perk Is Essential for Translational Regulation and Cell Survival during the Unfolded Protein Response

inferredcites →https://doi.org/10.1016/s1097-2765(01)00264-7openalex-snapshot

Diabetes Mellitus and Exocrine Pancreatic Dysfunction in Perk−/− Mice Reveals a Role for Translational Control in Secretory Cell Survival

inferredcites →https://doi.org/10.1016/s1097-2765(01)00265-9openalex-snapshot

Translational Control Is Required for the Unfolded Protein Response and In Vivo Glucose Homeostasis

inferredcites →https://doi.org/10.1016/s1097-2765(03)00105-9openalex-snapshot

An Integrated Stress Response Regulates Amino Acid Metabolism and Resistance to Oxidative Stress

inferredcites →https://doi.org/10.1016/s1097-2765(03)00395-2openalex-snapshot

Oncogenic Ras and Akt Signaling Contribute to Glioblastoma Formation by Differential Recruitment of Existing mRNAs to Polysomes

inferredcites →https://doi.org/10.1016/s1471-4914(01)02102-5openalex-snapshot

Thrombospondins and tumor angiogenesis

inferredcites →https://doi.org/10.1016/s1535-6108(03)00058-8openalex-snapshot

Remodeling of the extracellular matrix through overexpression of collagen VI contributes to cisplatin resistance in ovarian cancer cells

inferredcites →https://doi.org/10.1023/a:1006332011207openalex-snapshot

Overexpression of the glucose-regulated stress gene GRP78 in malignant but not benign human breast lesions

inferredcites →https://doi.org/10.1038/11109openalex-snapshot

A new internal-ribosome-entry-site motif potentiates XIAP- mediated cytoprotection

inferredcites →https://doi.org/10.1038/16729openalex-snapshot

Protein translation and folding are coupled by an endoplasmic-reticulum-resident kinase

inferredcites →https://doi.org/10.1038/35014014openalex-snapshot

Dynamic interaction of BiP and ER stress transducers in the unfolded-protein response

inferredcites →https://doi.org/10.1038/353090a0openalex-snapshot

Internal initiation of translation mediated by the 5′ leader of a cellular mRNA

inferredcites →https://doi.org/10.1038/359843a0openalex-snapshot

Vascular endothelial growth factor induced by hypoxia may mediate hypoxia-initiated angiogenesis

inferredcites →https://doi.org/10.1038/36285openalex-snapshot

Mutation of the mouse klotho gene leads to a syndrome resembling ageing.

inferredcites →https://doi.org/10.1038/379088a0openalex-snapshot

Hypoxia-mediated selection of cells with diminished apoptotic potential in solid tumours

inferredcites →https://doi.org/10.1038/labinvest.3780253openalex-snapshot

Engineering and Characterization of Functional Human Microvessels in Immunodeficient Mice

inferredcites →https://doi.org/10.1038/nm0603-685openalex-snapshot

Molecular regulation of vessel maturation

inferredcites →https://doi.org/10.1038/sj.bjc.6602864openalex-snapshot

In vitro hypoxia-conditioned colon cancer cell lines derived from HCT116 and HT29 exhibit altered apoptosis susceptibility and a more angiogenic profile in vivo

inferredcites →https://doi.org/10.1038/sj.emboj.7600030openalex-snapshot

Cytoprotection by pre‐emptive conditional phosphorylation of translation initiation factor 2

inferredcites →https://doi.org/10.1038/sj.emboj.7600777openalex-snapshot

ER stress‐regulated translation increases tolerance to extreme hypoxia and promotes tumor growth

inferredcites →https://doi.org/10.1038/sj.emboj.7600998openalex-snapshot

Gene expression during acute and prolonged hypoxia is regulated by distinct mechanisms of translational control

inferredcites →https://doi.org/10.1038/sj.onc.1202237openalex-snapshot

Nrf2 and Nrf1 in association with Jun proteins regulate antioxidant response element-mediated expression and coordinated induction of genes encoding detoxifying enzymes

inferredcites →https://doi.org/10.1038/sj.onc.1209781openalex-snapshot

Induction of activating transcription factor 3 by anoxia is independent of p53 and the hypoxic HIF signalling pathway

inferredcites →https://doi.org/10.1046/j.1087-0024.2000.00005.xopenalex-snapshot

Thrombospondin 2 Modulates Collagen Fibrillogenesis and Angiogenesis

inferredcites →https://doi.org/10.1046/j.1432-1033.2002.02974.xopenalex-snapshot

Phosphorylation of initiation factor‐2α is required for activation of internal translation initiation during cell differentiation

inferredcites →https://doi.org/10.1046/j.1471-4159.1998.71062477.xopenalex-snapshot

Excitatory Amino Acid Synthesis in Hypoxic Brain Slices: Does Alanine Act as a Substrate for Glutamate Production in Hypoxia?

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.91.14.6496openalex-snapshot

Oxygen-regulated control elements in the phosphoglycerate kinase 1 and lactate dehydrogenase A genes: similarities with the erythropoietin 3' enhancer.

inferredcites →https://doi.org/10.1073/pnas.93.18.9493openalex-snapshot

Unifying theory of hypoxia tolerance: molecular/metabolic defense and rescue mechanisms for surviving oxygen lack.

inferredcites →https://doi.org/10.1073/pnas.93.25.14960openalex-snapshot

Nrf1 and Nrf2 positively and c-Fos and Fra1 negatively regulate the human antioxidant response element-mediated expression of NAD(P)H:quinone oxidoreductase 1 gene

inferredcites →https://doi.org/10.1073/pnas.96.23.13118openalex-snapshot

Identification of eukaryotic mRNAs that are translated at reduced cap binding complex eIF4F concentrations using a cDNA microarray

inferredcites →https://doi.org/10.1073/pnas.97.16.9082openalex-snapshot

Expression of the gene encoding the proapoptotic Nip3 protein is induced by hypoxia

inferredcites →https://doi.org/10.1074/jbc.272.14.9356openalex-snapshot

PDGF2/c-sis mRNA Leader Contains a Differentiation-linked Internal Ribosomal Entry Site (D-IRES)

inferredcites →https://doi.org/10.1074/jbc.272.31.19253openalex-snapshot

Transactivation and Inhibitory Domains of Hypoxia-inducible Factor 1α

inferredcites →https://doi.org/10.1074/jbc.272.9.5375openalex-snapshot

Hypoxia-inducible Factor-1 Mediates Transcriptional Activation of the Heme Oxygenase-1 Gene in Response to Hypoxia

inferredcites →https://doi.org/10.1074/jbc.m108181200openalex-snapshot

Glucose Catabolism in Cancer Cells

inferredcites →https://doi.org/10.1074/jbc.m206521200openalex-snapshot

Distribution of PG-M/Versican Variants in Human Tissues andde Novo Expression of Isoform V3 upon Endothelial Cell Activation, Migration, and Neoangiogenesis in Vitro

inferredcites →https://doi.org/10.1074/jbc.m212770200openalex-snapshot

A Novel Hypoxia-inducible Factor-independent Hypoxic Response Regulating Mammalian Target of Rapamycin and Its Targets

inferredcites →https://doi.org/10.1074/jbc.m308737200openalex-snapshot

Translational Induction of the Inhibitor of Apoptosis Protein HIAP2 during Endoplasmic Reticulum Stress Attenuates Cell Death and Is Mediated via an Inducible Internal Ribosome Entry Site Element

inferredcites →https://doi.org/10.1074/jbc.m311802200openalex-snapshot

Grb10 Prevents Nedd4-mediated Vascular Endothelial Growth Factor Receptor-2 Degradation

inferredcites →https://doi.org/10.1074/jbc.m403026200openalex-snapshot

Tissue Inhibitor of Metalloproteinases-3 (TIMP-3) Is a Binding Partner of Epithelial Growth Factor-containing Fibulin-like Extracellular Matrix Protein 1 (EFEMP1)

inferredcites →https://doi.org/10.1074/jbc.m412744200openalex-snapshot

Internal Translation Initiation Mediated by the Angiogenic Factor Tie2

inferredcites →https://doi.org/10.1080/15216540500138337openalex-snapshot

Eph-modulated Cell Morphology, Adhesion and Motility in Carcinogenesis

inferredcites →https://doi.org/10.1083/jcb.200408003openalex-snapshot

Translation reinitiation at alternative open reading frames regulates gene expression in an integrated stress response

inferredcites →https://doi.org/10.1091/mbc.02-02-0017openalex-snapshot

Hypoxia-inducible Factor-1α mRNA Contains an Internal Ribosome Entry Site That Allows Efficient Translation during Normoxia and Hypoxia

inferredcites →https://doi.org/10.1093/emboj/cdg165openalex-snapshot

Regulation of cell–cell interactions by phosphatidic acid phosphatase 2b/VCIP

inferredcites →https://doi.org/10.1096/fj.02-0340fjeopenalex-snapshot

Pericyte‐specific expression of Rgs5: implications for PDGF and EDG receptor signaling during vascular maturation

inferredcites →https://doi.org/10.1096/fj.04-1918fjeopenalex-snapshot

Cyclic exposure to hypoxia and reoxygenation selects for tumor cells with defects in mitochondrial apoptotic pathways

inferredcites →https://doi.org/10.1096/fj.04-3647fjeopenalex-snapshot

Hypoxia up‐regulates expression of Eph receptors and ephrins in mouse skin

inferredcites →https://doi.org/10.1096/fj.14.11.1641openalex-snapshot

Isolation of translationally controlled mRNAs by differential screening

inferredcites →https://doi.org/10.1101/gad.12.2.149openalex-snapshot

Cellular and developmental control of O 2 homeostasis by hypoxia-inducible factor 1α

inferredcites →https://doi.org/10.1101/gad.8.16.1875openalex-snapshot

Mice deficient for PDGF B show renal, cardiovascular, and hematological abnormalities.

inferredcites →https://doi.org/10.1101/gad.8.16.1888openalex-snapshot

Abnormal kidney development and hematological disorders in PDGF beta-receptor mutant mice.

inferredcites →https://doi.org/10.1111/j.1432-1033.1996.00403.xopenalex-snapshot

Identification of Hypoxically Inducible mRNAs in HeLa Cells Using Differential‐Display PCR

inferredcites →https://doi.org/10.1126/science.277.5323.242openalex-snapshot

Pericyte Loss and Microaneurysm Formation in PDGF-B-Deficient Mice

inferredcites →https://doi.org/10.1128/cdli.10.2.308-314.2003openalex-snapshot

Elevated Levels of Matrix Metalloproteinase 9 and Tissue Inhibitor of Metalloproteinase 1 during the Acute Phase of Kawasaki Disease

inferredcites →https://doi.org/10.1128/mcb.18.6.3112openalex-snapshot

Translation of Vascular Endothelial Growth Factor mRNA by Internal Ribosome Entry: Implications for Translation under Hypoxia

inferredcites →https://doi.org/10.1128/mcb.22.11.3864-3874.2002openalex-snapshot

The PERK Eukaryotic Initiation Factor 2α Kinase Is Required for the Development of the Skeletal System, Postnatal Growth, and the Function and Viability of the Pancreas

inferredcites →https://doi.org/10.1128/mcb.22.21.7405-7416.2002openalex-snapshot

Regulation of Protein Synthesis by Hypoxia via Activation of the Endoplasmic Reticulum Kinase PERK and Phosphorylation of the Translation Initiation Factor eIF2α

inferredcites →https://doi.org/10.1128/mcb.23.20.7198-7209.2003openalex-snapshot

Nrf2 Is a Direct PERK Substrate and Effector of PERK-Dependent Cell Survival

inferredcites →https://doi.org/10.1128/mcb.23.7.2316-2328.2003openalex-snapshot

von Hippel-Lindau Protein-Mediated Repression of Tumor Necrosis Factor Alpha Translation Revealed through Use of cDNA Arrays

inferredcites →https://doi.org/10.1128/mcb.24.17.7469-7482.2004openalex-snapshot

Activating Transcription Factor 4 Is Translationally Regulated by Hypoxic Stress

inferredcites →https://doi.org/10.1128/mcb.24.3.1365-1377.2004openalex-snapshot

Activating Transcription Factor 3 Is Integral to the Eukaryotic Initiation Factor 2 Kinase Stress Response

inferredcites →https://doi.org/10.1128/mcb.26.10.3955-3965.2006openalex-snapshot

Hypoxia Inhibits Protein Synthesis through a 4E-BP1 and Elongation Factor 2 Kinase Pathway Controlled by mTOR and Uncoupled in Breast Cancer Cells

inferredcites →https://doi.org/10.1158/0008-5472.can-04-1606openalex-snapshot

XBP1 Is Essential for Survival under Hypoxic Conditions and Is Required for Tumor Growth

inferredcites →https://doi.org/10.1158/1541-7786.mcr-06-0150openalex-snapshot

“Translating” Tumor Hypoxia: Unfolded Protein Response (UPR)–Dependent and UPR-Independent Pathways

inferredcites →https://doi.org/10.1182/blood-2003-06-1859openalex-snapshot

Anoxic induction of ATF-4 through HIF-1–independent pathways of protein stabilization in human cancer cells

inferredcites →https://doi.org/10.1186/1478-811x-3-9openalex-snapshot

Anti-lipid phosphate phosphohydrolase-3 (LPP3) antibody inhibits bFGF- and VEGF-induced capillary morphogenesis of endothelial cells

inferredcites →https://doi.org/10.1210/en.2005-0467openalex-snapshot

Insulin-Like Growth Factor Binding Protein-2 Binding to Extracellular Matrix Plays a Critical Role in Neuroblastoma Cell Proliferation, Migration, and Invasion

inferredcites →https://doi.org/10.1242/dev.00635openalex-snapshot

The lipid phosphatase LPP3 regulates extra-embryonic vasculogenesis and axis patterning

inferredcites →https://doi.org/10.1242/dev.126.14.3047openalex-snapshot

Role of PDGF-B and PDGFR-β in recruitment of vascular smooth muscle cells and pericytes during embryonic blood vessel formation in the mouse

inferredcites →https://doi.org/10.1261/rna.2158605openalex-snapshot

Spurious splicing within the XIAP 5′ UTR occurs in the Rluc/Fluc but not the βgal/CAT bicistronic reporter system

inferredcites →https://doi.org/10.1385/0-89603-178-0:217openalex-snapshot

Use of E. coli lacZ (β-Galactosidase) as a Reporter Gene

inferredcites →https://doi.org/10.1387/ijdb.041811afopenalex-snapshot

Matrix metalloproteinases in cancer: from new functions to improved inhibition strategies

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Protein-Rich Foods, Sea Foods, and Gut Microbiota Amplify Immune Responses in Chronic Diseases and Cancers – Targeting Perk as a Novel Therapeutic Strategy for Cancer

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Regulation of the Unfolded Protein Response in Cancer

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Lipid Mediated Regulation of Protein Kinases

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Hypoxia‐Activated Prodrugs of PERK Inhibitors

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Optogenetic Control of the Integrated Stress Response Limits Glioblastoma Invasion

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Dual Activators of Protein Kinase R (PKR) and Protein Kinase R‐Like Kinase (PERK) Identify Common and Divergent Catalytic Targets

inferred← citeshttps://doi.org/10.1002/ccs3.12054openalex-snapshot

Exploring the dual role of endoplasmic reticulum stress in urological cancers: Implications for tumor progression and cell death interactions

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Hypoxic regulation of the PERK/ATF4/LAMP3‐arm of the unfolded protein response in head and neck squamous cell carcinoma

inferred← citeshttps://doi.org/10.1002/jcb.30247openalex-snapshot

Endoplasmic reticulum stress in nonalcoholic (metabolic associated) fatty liver disease (NAFLD/MAFLD)

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PERK Integrates Oncogenic Signaling and Cell Survival During Cancer Development

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Dysregulation of protein synthesis and disease

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Function and mutual interaction of BiP‐, PERK‐, and IRE1α‐dependent signalling pathways in vascular tumours

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Misfolded Proteins and Retinal Dystrophies

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Genome-Wide Analysis of Translational Control

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The Regulation of the Unfolded Protein Response and Its Roles in Tumorigenesis and Cancer Therapy

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ATF4, Hypoxia and Treatment Resistance in Cancer

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Role of Protein Translation in Unfolded Protein Response

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The Unfolded Protein Response in Triple-Negative Breast Cancer

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Alternative Mechanisms of mRNA Translation Initiation in Cellular Stress Response and Cancer

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Role of Endoplasmic Reticulum ER Stress-Induced Cell Death Mechanisms

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Malattia Leventinese (Autosomal Dominant Drusen)

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Signaling the Unfolded Protein Response in cancer

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UPR Activation in Cancer Cells: A Double-Edged Sword

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The eIF2 Complex and eIF2α

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Cell-Nonautonomous ER Stress-Mediated Dysregulation of Immunity by Cancer Cells

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Intersection of the unfolded protein response and hepatic lipid metabolism

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More than just scanning: the importance of cap-independent mRNA translation initiation for cellular stress response and cancer

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Expression vector cassette engineering for recombinant therapeutic production in mammalian cell systems

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Endoplasmic reticulum stress regulates tumor growth and anti-tumor immunity: a promising opportunity for cancer immunotherapy

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Potential for therapeutic manipulation of the UPR in disease

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4-phenylbutyric acid attenuates endoplasmic reticulum stress-mediated apoptosis and protects the hepatocytes from intermittent hypoxia-induced injury

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Endoplasmic reticulum Metallo protease 1, a triggering factor for unfolded protein response and promising target in colorectal cancer

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Endoplasmic reticulum stress-induced cell death mechanism

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Type I interferons and endoplasmic reticulum stress in health and disease

inferred← citeshttps://doi.org/10.1016/j.addr.2007.06.002openalex-snapshot

Visiting the ER: The endoplasmic reticulum as a target for therapeutics in traffic related diseases☆

inferred← citeshttps://doi.org/10.1016/j.bbagrm.2010.08.006openalex-snapshot

Massive translational repression of gene expression during mouse erythroid differentiation

inferred← citeshttps://doi.org/10.1016/j.bbagrm.2014.11.002openalex-snapshot

Stress-mediated translational control in cancer cells

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2011.06.011openalex-snapshot

Urban planning of the endoplasmic reticulum (ER): How diverse mechanisms segregate the many functions of the ER

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2014.01.012openalex-snapshot

Endoplasmic reticulum stress associated responses in cancer

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2014.09.016openalex-snapshot

Thermotolerance induced at a mild temperature of 40°C alleviates heat shock-induced ER stress and apoptosis in HeLa cells

inferred← citeshttps://doi.org/10.1016/j.bbcan.2026.189686openalex-snapshot

Targeting the integrated stress response to overcome cancer therapy resistance: From mechanisms to therapeutic opportunities

inferred← citeshttps://doi.org/10.1016/j.bbrc.2012.11.105openalex-snapshot

Dimerization of pro-oncogenic protein Anterior Gradient 2 is required for the interaction with BiP/GRP78

inferred← citeshttps://doi.org/10.1016/j.bbrc.2013.09.129openalex-snapshot

Down-regulation of PERK enhances resistance to ionizing radiation

inferred← citeshttps://doi.org/10.1016/j.bbrc.2014.06.091openalex-snapshot

Chemical chaperones reduce ionizing radiation-induced endoplasmic reticulum stress and cell death in IEC-6 cells

inferred← citeshttps://doi.org/10.1016/j.biochi.2022.01.017openalex-snapshot

The unfolded protein response and the biology of uveal melanoma

inferred← citeshttps://doi.org/10.1016/j.brainres.2016.03.015openalex-snapshot

Signaling the Unfolded Protein Response in primary brain cancers

inferred← citeshttps://doi.org/10.1016/j.brainres.2016.06.021openalex-snapshot

Reprint of: Signaling the Unfolded Protein Response in primary brain cancers

inferred← citeshttps://doi.org/10.1016/j.canlet.2010.07.016openalex-snapshot

Targeting ER stress induced apoptosis and inflammation in cancer

inferred← citeshttps://doi.org/10.1016/j.ccr.2014.03.015openalex-snapshot

Endoplasmic Reticulum Stress in Malignancy

inferred← citeshttps://doi.org/10.1016/j.ceb.2011.01.003openalex-snapshot

Protein folding stress in neurodegenerative diseases: a glimpse into the ER

inferred← citeshttps://doi.org/10.1016/j.cell.2016.12.004openalex-snapshot

Tumorigenic and Immunosuppressive Effects of Endoplasmic Reticulum Stress in Cancer

inferred← citeshttps://doi.org/10.1016/j.cellsig.2012.09.012openalex-snapshot

Ursolic acid induces ER stress response to activate ASK1–JNK signaling and induce apoptosis in human bladder cancer T24 cells

inferred← citeshttps://doi.org/10.1016/j.cellsig.2013.11.026openalex-snapshot

HDAC4 protects cells from ER stress induced apoptosis through interaction with ATF4

inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116318openalex-snapshot

ER stress tolerance is regulated by copper-dependent PERK kinase activity

inferred← citeshttps://doi.org/10.1016/j.cmet.2015.07.010openalex-snapshot

ER Stress and Angiogenesis

inferred← citeshttps://doi.org/10.1016/j.critrevonc.2017.04.005openalex-snapshot

Aberrant cancer metabolism in epithelial–mesenchymal transition and cancer metastasis: Mechanisms in cancer progression

inferred← citeshttps://doi.org/10.1016/j.critrevonc.2018.05.003openalex-snapshot

The unfolded protein response as a target for anticancer therapeutics

inferred← citeshttps://doi.org/10.1016/j.drup.2007.05.001openalex-snapshot

Autophagy signaling in cancer and its potential as novel target to improve anticancer therapy

inferred← citeshttps://doi.org/10.1016/j.ejphar.2009.06.064openalex-snapshot

Targeting the endoplasmic reticulum-stress response as an anticancer strategy

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2017.03.031openalex-snapshot

The endoplasmic reticulum: A hub of protein quality control in health and disease

inferred← citeshttps://doi.org/10.1016/j.jbc.2025.110976openalex-snapshot

4E-BP1 differentially regulates translation of a subset of human mRNAs

inferred← citeshttps://doi.org/10.1016/j.jhep.2018.06.008openalex-snapshot

Endoplasmic reticulum stress signalling and the pathogenesis of non-alcoholic fatty liver disease

inferred← citeshttps://doi.org/10.1016/j.jmb.2010.09.016openalex-snapshot

The Roles of Stress-Activated Sty1 and Gcn2 Kinases and of the Protooncoprotein Homologue Int6/eIF3e in Responses to Endogenous Oxidative Stress during Histidine Starvation

inferred← citeshttps://doi.org/10.1016/j.lfs.2020.118186openalex-snapshot

Antioxidants with two faces toward cancer

inferred← citeshttps://doi.org/10.1016/j.mce.2017.05.027openalex-snapshot

ER stress and cancer: The FOXO forkhead transcription factor link

inferred← citeshttps://doi.org/10.1016/j.neo.2018.03.005openalex-snapshot

Role of Mitochondria-Associated ER Membranes in Calcium Regulation in Cancer-Specific Settings

inferred← citeshttps://doi.org/10.1016/j.pharmthera.2016.07.007openalex-snapshot

Targeting the angio-proteostasis network: Combining the forces against cancer

inferred← citeshttps://doi.org/10.1016/j.pharmthera.2024.108604openalex-snapshot

Protein-rich foods, sea foods, and gut microbiota amplify immune responses in chronic diseases and cancers – Targeting PERK as a novel therapeutic strategy for chronic inflammatory diseases, neurodegenerative disorders, and cancer

inferred← citeshttps://doi.org/10.1016/j.preteyeres.2014.12.001openalex-snapshot

The unfolded protein response in retinal vascular diseases: Implications and therapeutic potential beyond protein folding

inferred← citeshttps://doi.org/10.1016/j.prp.2023.154706openalex-snapshot

Role of the ER-induced UPR pathway, apoptosis, and autophagy in colorectal cancer

inferred← citeshttps://doi.org/10.1016/j.radonc.2009.08.017openalex-snapshot

Hypoxic activation of the unfolded protein response (UPR) induces expression of the metastasis-associated gene LAMP3

inferred← citeshttps://doi.org/10.1016/j.radonc.2011.05.058openalex-snapshot

Translational control is a major contributor to hypoxia induced gene expression

inferred← citeshttps://doi.org/10.1016/j.radonc.2013.06.037openalex-snapshot

The PERK/ATF4/LAMP3-arm of the unfolded protein response affects radioresistance by interfering with the DNA damage response

inferred← citeshttps://doi.org/10.1016/j.semcancer.2015.03.003openalex-snapshot

Controlling the unfolded protein response-mediated life and death decisions in cancer

inferred← citeshttps://doi.org/10.1016/j.semcancer.2015.03.010openalex-snapshot

The PERKs of damage-associated molecular patterns mediating cancer immunogenicity: From sensor to the plasma membrane and beyond

inferred← citeshttps://doi.org/10.1016/j.semcancer.2015.04.002openalex-snapshot

Cell intrinsic and extrinsic activators of the unfolded protein response in cancer: Mechanisms and targets for therapy

inferred← citeshttps://doi.org/10.1016/j.semcancer.2015.04.003openalex-snapshot

ER proteostasis addiction in cancer biology: Novel concepts

inferred← citeshttps://doi.org/10.1016/j.semcancer.2018.01.011openalex-snapshot

Homeostatic interplay between FoxO proteins and ER proteostasis in cancer and other diseases

inferred← citeshttps://doi.org/10.1016/j.semcancer.2023.11.001openalex-snapshot

Hypoxia signaling and metastatic progression

inferred← citeshttps://doi.org/10.1016/j.tcb.2016.06.005openalex-snapshot

Translation Initiation Factors: Reprogramming Protein Synthesis in Cancer

inferred← citeshttps://doi.org/10.1016/j.tibs.2007.06.005openalex-snapshot

Gene regulation under low oxygen: holding your breath for transcription

inferred← citeshttps://doi.org/10.1016/j.trecan.2016.03.007openalex-snapshot

Endoplasmic Reticulum Stress and the Hallmarks of Cancer

inferred← citeshttps://doi.org/10.1016/j.trecan.2019.12.001openalex-snapshot

Targeting the Unfolded Protein Response in Hormone-Regulated Cancers

inferred← citeshttps://doi.org/10.1016/j.trecan.2020.09.005openalex-snapshot

Cancer Plasticity: The Role of mRNA Translation

inferred← citeshttps://doi.org/10.1016/j.ygyno.2011.11.045openalex-snapshot

Endoplasmic reticulum stress is activated in endometrial adenocarcinoma

inferred← citeshttps://doi.org/10.1016/s0076-6879(07)35014-3openalex-snapshot

Hypoxia and the Unfolded Protein Response

inferred← citeshttps://doi.org/10.1021/jm300713sopenalex-snapshot

Discovery of 7-Methyl-5-(1-{[3-(trifluoromethyl)phenyl]acetyl}-2,3-dihydro-1 H -indol-5-yl)-7 H -pyrrolo[2,3- d ]pyrimidin-4-amine (GSK2606414), a Potent and Selective First-in-Class Inhibitor of Protein Kinase R (PKR)-like Endoplasmic Reticulum Kinase (PERK)

inferred← citeshttps://doi.org/10.1021/ml400228eopenalex-snapshot

Discovery of GSK2656157: An Optimized PERK Inhibitor Selected for Preclinical Development

inferred← citeshttps://doi.org/10.1038/cdd.2009.164openalex-snapshot

NF45 functions as an IRES trans-acting factor that is required for translation of cIAP1 during the unfolded protein response

inferred← citeshttps://doi.org/10.1038/cdd.2016.74openalex-snapshot

Decreased MORF leads to prolonged endoplasmic reticulum stress in periodontitis-associated chronic inflammation

inferred← citeshttps://doi.org/10.1038/emboj.2010.110openalex-snapshot

How do tumours adapt to nutrient stress?

inferred← citeshttps://doi.org/10.1038/gt.2011.11openalex-snapshot

In vitro and in vivo comparison of viral and cellular internal ribosome entry sites for bicistronic vector expression

inferred← citeshttps://doi.org/10.1038/nrc2344openalex-snapshot

Hypoxia, DNA repair and genetic instability

inferred← citeshttps://doi.org/10.1038/nrc2501openalex-snapshot

Hypoxia signalling through mTOR and the unfolded protein response in cancer

inferred← citeshttps://doi.org/10.1038/nrc3800openalex-snapshot

The impact of the endoplasmic reticulum protein-folding environment on cancer development

inferred← citeshttps://doi.org/10.1038/nrd3976openalex-snapshot

Targeting the unfolded protein response in disease

inferred← citeshttps://doi.org/10.1038/nri.2016.62openalex-snapshot

The unfolded protein response in immunity and inflammation

inferred← citeshttps://doi.org/10.1038/nrm2199openalex-snapshot

Signal integration in the endoplasmic reticulum unfolded protein response

inferred← citeshttps://doi.org/10.1038/onc.2010.153openalex-snapshot

PERK promotes cancer cell proliferation and tumor growth by limiting oxidative DNA damage

inferred← citeshttps://doi.org/10.1038/onc.2010.191openalex-snapshot

Regulation of autophagy by ATF4 in response to severe hypoxia

inferred← citeshttps://doi.org/10.1038/onc.2011.522openalex-snapshot

The unfolded protein response controls induction and activation of ADAM17/TACE by severe hypoxia and ER stress

inferred← citeshttps://doi.org/10.1038/onc.2012.130openalex-snapshot

The critical roles of endoplasmic reticulum chaperones and unfolded protein response in tumorigenesis and anticancer therapies

inferred← citeshttps://doi.org/10.1038/onc.2013.554openalex-snapshot

Stress signaling and the shaping of the mammary tissue in development and cancer

inferred← citeshttps://doi.org/10.1038/onc.2015.108openalex-snapshot

The evolving paradigm of cell-nonautonomous UPR-based regulation of immunity by cancer cells

inferred← citeshttps://doi.org/10.1038/onc.2015.495openalex-snapshot

CHK2 stability is regulated by the E3 ubiquitin ligase SIAH2

inferred← citeshttps://doi.org/10.1038/onc.2016.121openalex-snapshot

NCOA3 coactivator is a transcriptional target of XBP1 and regulates PERK–eIF2α–ATF4 signalling in breast cancer

inferred← citeshttps://doi.org/10.1038/oncsis.2017.72openalex-snapshot

Endoplasmic reticulum stress signaling and chemotherapy resistance in solid cancers

inferred← citeshttps://doi.org/10.1038/s41389-020-0201-8openalex-snapshot

PERK-mediated expression of peptidylglycine α-amidating monooxygenase supports angiogenesis in glioblastoma

inferred← citeshttps://doi.org/10.1038/s41413-025-00457-6openalex-snapshot

The role of the unfolded protein response pathway in bone homeostasis and potential therapeutic target in cancer-associated bone disease

inferred← citeshttps://doi.org/10.1038/s41467-017-01052-yopenalex-snapshot

Cancer-specific PERK signaling drives invasion and metastasis through CREB3L1

inferred← citeshttps://doi.org/10.1038/s41580-020-0227-yopenalex-snapshot

Cellular adaptation to hypoxia through hypoxia inducible factors and beyond

inferred← citeshttps://doi.org/10.1038/s41585-022-00649-3openalex-snapshot

The endoplasmic reticulum stress response in prostate cancer

inferred← citeshttps://doi.org/10.1038/srep11781openalex-snapshot

Signaling through alternative Integrated Stress Response pathways compensates for GCN2 loss in a mouse model of soft tissue sarcoma

inferred← citeshttps://doi.org/10.1039/b708867aopenalex-snapshot

Cap-independent regulation of gene expression in apoptosis

inferred← citeshttps://doi.org/10.1042/bc20070098openalex-snapshot

Re‐programming of translation following cell stress allows IRES‐mediated translation to predominate

inferred← citeshttps://doi.org/10.1073/pnas.1516362112openalex-snapshot

Type I interferons mediate pancreatic toxicities of PERK inhibition

inferred← citeshttps://doi.org/10.1074/jbc.m109.006510openalex-snapshot

Hypoxia-induced Expression of Carbonic Anhydrase 9 Is Dependent on the Unfolded Protein Response

inferred← citeshttps://doi.org/10.1074/jbc.m113.507194openalex-snapshot

Endoplasmic Reticulum (ER) Stress and Hypoxia Response Pathways Interact to Potentiate Hypoxia-inducible Factor 1 (HIF-1) Transcriptional Activity on Targets Like Vascular Endothelial Growth Factor (VEGF)

inferred← citeshttps://doi.org/10.1074/jbc.m708285200openalex-snapshot

Translational Control of C-terminal Src Kinase (Csk) Expression by PRL3 Phosphatase

inferred← citeshttps://doi.org/10.1074/jbc.m805056200openalex-snapshot

Hypoxic Reactive Oxygen Species Regulate the Integrated Stress Response and Cell Survival

inferred← citeshttps://doi.org/10.1080/13543776.2017.1238072openalex-snapshot

Protein kinase R(PKR)–like endoplasmic reticulum kinase (PERK) inhibitors: a patent review (2010-2015)

inferred← citeshttps://doi.org/10.1080/15476286.2015.1017236openalex-snapshot

Stabilization of the G-quadruplex at the VEGF IRES represses cap-independent translation

inferred← citeshttps://doi.org/10.1080/15476286.2015.1086866openalex-snapshot

Elaborate uORF/IRES features control expression and localization of human glycyl-tRNA synthetase

inferred← citeshttps://doi.org/10.1083/jcb.201307185openalex-snapshot

Two phases of disulfide bond formation have differing requirements for oxygen

inferred← citeshttps://doi.org/10.1089/ars.2007.1764openalex-snapshot

Translational Control and the Unfolded Protein Response

inferred← citeshttps://doi.org/10.1089/ars.2009.2991openalex-snapshot

Amyotrophic Lateral Sclerosis Pathogenesis: A Journey Through the Secretory Pathway

inferred← citeshttps://doi.org/10.1089/ars.2013.5648openalex-snapshot

MicroRNA Target Identification: Lessons from HypoxamiRs

inferred← citeshttps://doi.org/10.1089/ars.2014.5851openalex-snapshot

Endoplasmic Reticulum Stress and Oxidative Stress in Cell Fate Decision and Human Disease

inferred← citeshttps://doi.org/10.1089/cbr.2017.2309openalex-snapshot

An Overview of Unfolded Protein Response Signaling and Its Role in Cancer

inferred← citeshttps://doi.org/10.1093/abbs/gmab131openalex-snapshot

Targeting UPR branches, a potential strategy for enhancing efficacy of cancer chemotherapy

inferred← citeshttps://doi.org/10.1093/abbs/gmt014openalex-snapshot

Molecular mechanisms of neurodegeneration mediated by dysfunctional subcellular organelles in transmissible spongiform encephalopathies

inferred← citeshttps://doi.org/10.1093/cvr/cvw090openalex-snapshot

Endothelial lipid phosphate phosphatase-3 deficiency that disrupts the endothelial barrier function is a modifier of cardiovascular development

inferred← citeshttps://doi.org/10.1093/nar/gkm1007openalex-snapshot

The eIF4G homolog DAP5/p97 supports the translation of select mRNAs during endoplasmic reticulum stress

inferred← citeshttps://doi.org/10.1093/nar/gkm483openalex-snapshot

A search for structurally similar cellular internal ribosome entry sites

inferred← citeshttps://doi.org/10.1093/nar/gkw1117openalex-snapshot

An mRNA-specific tRNAicarrier eIF2A plays a pivotal role in cell proliferation under stress conditions: stress-resistant translation of c-Src mRNA is mediated by eIF2A

inferred← citeshttps://doi.org/10.1093/oxfordhb/9780190686307.013.9openalex-snapshot

Internal Ribosome Entry Site-Mediated Translation in Neuronal Protein Synthesis

inferred← citeshttps://doi.org/10.1101/2020.06.26.174615openalex-snapshot

Recombinant Helicobacter pylori CagA protein induces endoplasmic reticulum stress and autophagy in human cells

inferred← citeshttps://doi.org/10.1101/2023.09.25.559258openalex-snapshot

ATE1 activates ER-stress and UPR pathways in glioblastoma

inferred← citeshttps://doi.org/10.1101/cshperspect.a012302openalex-snapshot

Toward a Genome-Wide Landscape of Translational Control

inferred← citeshttps://doi.org/10.1111/boc.201800050openalex-snapshot

The role of the unfolded protein response in cancer progression: From oncogenesis to chemoresistance

inferred← citeshttps://doi.org/10.1111/febs.14359openalex-snapshot

Regulation of tumor–stroma interactions by the unfolded protein response

inferred← citeshttps://doi.org/10.1111/j.1349-7006.2007.00551.xopenalex-snapshot

Stress signaling in cancer

inferred← citeshttps://doi.org/10.1111/j.1747-0285.2010.01048.xopenalex-snapshot

Structural Determinants of PERK Inhibitor Potency and Selectivity

inferred← citeshttps://doi.org/10.1111/j.1748-1716.2008.01894.xopenalex-snapshot

Cellular oxygen sensing, signalling and how to survive translational arrest in hypoxia

inferred← citeshttps://doi.org/10.1111/j.1749-6632.2012.06739.xopenalex-snapshot

Unfolded protein response to autophagy as a promising druggable target for anticancer therapy

inferred← citeshttps://doi.org/10.1111/wrr.12603openalex-snapshot

Inhibition of IRE1 results in decreased scar formation

inferred← citeshttps://doi.org/10.1126/scisignal.aaf2753openalex-snapshot

PERK mediates the IRES-dependent translational activation of mRNAs encoding angiogenic growth factors after ischemic stress

inferred← citeshttps://doi.org/10.1128/mcb.00063-12openalex-snapshot

PERK Utilizes Intrinsic Lipid Kinase Activity To Generate Phosphatidic Acid, Mediate Akt Activation, and Promote Adipocyte Differentiation

inferred← citeshttps://doi.org/10.1128/mcb.01009-12openalex-snapshot

PERK Is Required in the Adult Pancreas and Is Essential for Maintenance of Glucose Homeostasis

inferred← citeshttps://doi.org/10.1128/mcb.02284-07openalex-snapshot

Hypoxic Inhibition of Nonsense-Mediated RNA Decay Regulates Gene Expression and the Integrated Stress Response

inferred← citeshttps://doi.org/10.1128/mcb.05164-11openalex-snapshot

PERK Integrates Autophagy and Oxidative Stress Responses To Promote Survival during Extracellular Matrix Detachment

inferred← citeshttps://doi.org/10.1146/annurev.pathmechdis.3.121806.151434openalex-snapshot

Endoplasmic Reticulum Stress in Disease Pathogenesis

inferred← citeshttps://doi.org/10.1146/annurev.pathol.3.121806.151434openalex-snapshot

Endoplasmic Reticulum Stress in Disease Pathogenesis

inferred← citeshttps://doi.org/10.1146/annurev.physiol.70.113006.100526openalex-snapshot

Hypoxia-Induced Signaling in the Cardiovascular System

inferred← citeshttps://doi.org/10.1152/ajpcell.00239.2021openalex-snapshot

Adaptive and maladaptive roles of lipid droplets in health and disease

inferred← citeshttps://doi.org/10.1152/ajpcell.00292.2014openalex-snapshot

Cellular Mechanisms of Endoplasmic Reticulum Stress Signaling in Health and Disease. 3. Orchestrating the unfolded protein response in oncogenesis: an update

inferred← citeshttps://doi.org/10.1152/ajprenal.00683.2016openalex-snapshot

MIF-2/D-DT enhances proximal tubular cell regeneration through SLPI- and ATF4-dependent mechanisms

inferred← citeshttps://doi.org/10.1155/2014/513787openalex-snapshot

New Insights into the Pathogenesis of Alcohol-Induced ER Stress and Liver Diseases

inferred← citeshttps://doi.org/10.1155/2015/417281openalex-snapshot

Cancer Microenvironment and Endoplasmic Reticulum Stress Response

inferred← citeshttps://doi.org/10.1155/2017/2969271openalex-snapshot

Unfolded Protein Response of the Endoplasmic Reticulum in Tumor Progression and Immunogenicity

inferred← citeshttps://doi.org/10.1155/2019/5729710openalex-snapshot

The Role of the ER-Induced UPR Pathway and the Efficacy of Its Inhibitors and Inducers in the Inhibition of Tumor Progression

inferred← citeshttps://doi.org/10.1158/0008-5472.c.6498146openalex-snapshot

Data from Dual Function of Pancreatic Endoplasmic Reticulum Kinase in Tumor Cell Growth Arrest and Survival

inferred← citeshttps://doi.org/10.1158/0008-5472.c.6498146.v1openalex-snapshot

Data from Dual Function of Pancreatic Endoplasmic Reticulum Kinase in Tumor Cell Growth Arrest and Survival

inferred← citeshttps://doi.org/10.1158/0008-5472.can-07-2950openalex-snapshot

Critical Role of the Stress Chaperone GRP78/BiP in Tumor Proliferation, Survival, and Tumor Angiogenesis in Transgene-Induced Mammary Tumor Development

inferred← citeshttps://doi.org/10.1158/0008-5472.can-07-6215openalex-snapshot

Dual Function of Pancreatic Endoplasmic Reticulum Kinase in Tumor Cell Growth Arrest and Survival

inferred← citeshttps://doi.org/10.1158/0008-5472.can-12-0474openalex-snapshot

The Unfolded Protein Response Induces the Angiogenic Switch in Human Tumor Cells through the PERK/ATF4 Pathway

inferred← citeshttps://doi.org/10.1158/0008-5472.can-12-3109openalex-snapshot

Characterization of a Novel PERK Kinase Inhibitor with Antitumor and Antiangiogenic Activity

inferred← citeshttps://doi.org/10.1158/1078-0432.ccr-13-0526openalex-snapshot

Hypoxic Activation of the PERK/eIF2α Arm of the Unfolded Protein Response Promotes Metastasis through Induction of LAMP3

inferred← citeshttps://doi.org/10.1158/1078-0432.ccr-23-1182openalex-snapshot

PERK Inhibition by HC-5404 Sensitizes Renal Cell Carcinoma Tumor Models to Antiangiogenic Tyrosine Kinase Inhibitors

inferred← citeshttps://doi.org/10.1158/1541-7786.mcr-09-0502openalex-snapshot

Nonsense-Mediated RNA Decay Regulation by Cellular Stress: Implications for Tumorigenesis

inferred← citeshttps://doi.org/10.1158/2159-8290.cd-14-1490openalex-snapshot

Endoplasmic Reticulum Stress–Activated Cell Reprogramming in Oncogenesis

inferred← citeshttps://doi.org/10.1172/jci62973openalex-snapshot

ER stress–mediated autophagy promotes Myc-dependent transformation and tumor growth

inferred← citeshttps://doi.org/10.1177/09636897221083549openalex-snapshot

The Endoplasmic Reticulum-Stressed Head and Neck Squamous Cell Carcinoma Cells Induced Exosomal miR-424-5p Inhibits Angiogenesis and Migration of Humanumbilical Vein Endothelial Cells Through LAMC1-Mediated Wnt/β-Catenin Signaling Pathway

inferred← citeshttps://doi.org/10.1177/1947601910383011openalex-snapshot

The Unfolded Protein Response, Degradation from the Endoplasmic Reticulum, and Cancer

inferred← citeshttps://doi.org/10.1179/1973947815y.0000000006openalex-snapshot

X-box binding protein 1 (XBP-1) enhances colorectal cancer cell invasion

inferred← citeshttps://doi.org/10.1183/16000617.0184-2020openalex-snapshot

The integrated stress response in pulmonary disease

inferred← citeshttps://doi.org/10.1186/1476-4598-10-51openalex-snapshot

Lipid phosphate phosphatase-3 regulates tumor growth via β-catenin and Cyclin-D1 signaling

inferred← citeshttps://doi.org/10.1186/s40364-025-00813-yopenalex-snapshot

Targeting the unfolded protein response for cancer therapy: mitigating tumor adaptation and immune suppression

inferred← citeshttps://doi.org/10.1189/jlb.0313153openalex-snapshot

Cellular stress response and innate immune signaling: integrating pathways in host defense and inflammation

inferred← citeshttps://doi.org/10.1248/bpb.b17-00342openalex-snapshot

ER Stress and Disease: Toward Prevention and Treatment

inferred← citeshttps://doi.org/10.1261/rna.534807openalex-snapshot

Identification of mRNAs that continue to associate with polysomes during hypoxia

inferred← citeshttps://doi.org/10.1261/rna.857308openalex-snapshot

Translational repression during chronic hypoxia is dependent on glucose levels

inferred← citeshttps://doi.org/10.13025/17487openalex-snapshot

The role of microRNAs during endoplasmic reticulum stress induced cell death

inferred← citeshttps://doi.org/10.13028/0dfp-kp70openalex-snapshot

Transcriptional Regulation of VEGFA by Unfolded Protein Response Signaling Pathway

inferred← citeshttps://doi.org/10.13028/m2v30xopenalex-snapshot

Exploiting DNA Repair and ER Stress Response Pathways to Induce Apoptosis in Glioblastoma Multiforme: A Dissertation

inferred← citeshttps://doi.org/10.13130/tagliavacca-luigina_phd2010-12-16openalex-snapshot

THE PROTEOSTASIS OF THE ENDOPLASMIC RETICULUM AND THE ACTIVATION OF THE UNFOLDED PROTEIN RESPONSE PATHWAY IN VIVO

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