On the public citation graph

Molecular mechanisms of caspase regulation during apoptosis

0 signed · 1913 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/cbic.200300614openalex-snapshot
Worms, Life, and Death (Nobel Lecture)
inferredcites →https://doi.org/10.1002/jmr.615openalex-snapshot
Conformational restrictions in the active site of unliganded human caspase‐3
inferredcites →https://doi.org/10.1002/prot.340110407openalex-snapshot
Protein folding and association: Insights from the interfacial and thermodynamic properties of hydrocarbons
inferredcites →https://doi.org/10.1007/978-1-4757-9217-1_1openalex-snapshot
Genetic Control of Programmed Cell Death in the Nematode Caenorhabditis Elegans
inferredcites →https://doi.org/10.1016/0092-8674(93)90485-9openalex-snapshot
The C. elegans cell death gene ced-3 encodes a protein similar to mammalian interleukin-1β-converting enzyme
inferredcites →https://doi.org/10.1016/0092-8674(94)90303-4openalex-snapshot
Crystal structure of the cysteine protease interleukin-1β-converting enzyme: A (p20/p10)2 homodimer
inferredcites →https://doi.org/10.1016/0092-8674(94)90506-1openalex-snapshot
C. elegans cell survival gene ced-9 encodes a functional homolog of the mammalian proto-oncogene bcl-2
inferredcites →https://doi.org/10.1016/j.ceb.2003.10.009openalex-snapshot
Mechanisms of caspase activation
inferredcites →https://doi.org/10.1016/j.cell.2004.06.007openalex-snapshot
Caspase Activation
inferredcites →https://doi.org/10.1016/s0014-5793(01)02366-3openalex-snapshot
Two splicing variants of a new inhibitor of apoptosis gene with different biological properties and tissue distribution pattern
inferredcites →https://doi.org/10.1016/s0021-9258(19)61483-3openalex-snapshot
The Drosophila Caspase DRONC Cleaves following Glutamate or Aspartate and Is Regulated by DIAP1, HID, and GRIM
inferredcites →https://doi.org/10.1016/s0092-8674(00)00008-8openalex-snapshot
Smac, a Mitochondrial Protein that Promotes Cytochrome c–Dependent Caspase Activation by Eliminating IAP Inhibition
inferredcites →https://doi.org/10.1016/s0092-8674(00)00009-xopenalex-snapshot
Identification of DIABLO, a Mammalian Protein that Promotes Apoptosis by Binding to and Antagonizing IAP Proteins
inferredcites →https://doi.org/10.1016/s0092-8674(00)00119-7openalex-snapshot
Insights into Programmed Cell Death through Structural Biology
inferredcites →https://doi.org/10.1016/s0092-8674(00)80434-1openalex-snapshot
Cytochrome c and dATP-Dependent Formation of Apaf-1/Caspase-9 Complex Initiates an Apoptotic Protease Cascade
inferredcites →https://doi.org/10.1016/s0092-8674(00)80605-4openalex-snapshot
Inherited Human Caspase 10 Mutations Underlie Defective Lymphocyte and Dendritic Cell Apoptosis in Autoimmune Lymphoproliferative Syndrome Type II
inferredcites →https://doi.org/10.1016/s0092-8674(00)81182-4openalex-snapshot
The C. elegans Protein EGL-1 Is Required for Programmed Cell Death and Interacts with the Bcl-2–like Protein CED-9
inferredcites →https://doi.org/10.1016/s0092-8674(00)81334-3openalex-snapshot
Human ICE/CED-3 Protease Nomenclature
inferredcites →https://doi.org/10.1016/s0092-8674(00)81589-5openalex-snapshot
Bid, a Bcl2 Interacting Protein, Mediates Cytochrome c Release from Mitochondria in Response to Activation of Cell Surface Death Receptors
inferredcites →https://doi.org/10.1016/s0092-8674(00)81590-1openalex-snapshot
Cleavage of BID by Caspase 8 Mediates the Mitochondrial Damage in the Fas Pathway of Apoptosis
inferredcites →https://doi.org/10.1016/s0092-8674(00)81683-9openalex-snapshot
The Hallmarks of Cancer
inferredcites →https://doi.org/10.1016/s0092-8674(00)81873-5openalex-snapshot
Programmed Cell Death in Animal Development
inferredcites →https://doi.org/10.1016/s0092-8674(00)81974-1openalex-snapshot
The Drosophila Caspase Inhibitor DIAP1 Is Essential for Cell Survival and Is Negatively Regulated by HID
inferredcites →https://doi.org/10.1016/s0092-8674(01)00272-0openalex-snapshot
Structural Basis of Caspase-7 Inhibition by XIAP
inferredcites →https://doi.org/10.1016/s0092-8674(01)00273-2openalex-snapshot
Structural Basis of Caspase Inhibition by XIAP
inferredcites →https://doi.org/10.1016/s0092-8674(01)00274-4openalex-snapshot
Structural Basis for the Inhibition of Caspase-3 by XIAP
inferredcites →https://doi.org/10.1016/s0092-8674(01)00544-xopenalex-snapshot
Crystal Structure of a Procaspase-7 Zymogen
inferredcites →https://doi.org/10.1016/s0092-8674(04)00046-7openalex-snapshot
Cell Death
inferredcites →https://doi.org/10.1016/s0952-7915(00)00168-0openalex-snapshot
Apoptosis genes and autoimmunity
inferredcites →https://doi.org/10.1016/s0955-0674(02)00381-2openalex-snapshot
Apoptosomes: engines for caspase activation
inferredcites →https://doi.org/10.1016/s0959-437x(96)90007-6openalex-snapshot
Programmed cell death in invertebrates
inferredcites →https://doi.org/10.1016/s0960-9822(00)00781-8openalex-snapshot
ML-IAP, a novel inhibitor of apoptosis that is preferentially expressed in human melanomas
inferredcites →https://doi.org/10.1016/s0962-8924(99)01609-8openalex-snapshot
An exegesis of IAPs: salvation and surprises from BIR motifs
inferredcites →https://doi.org/10.1016/s0962-8924(99)01646-3openalex-snapshot
An emerging blueprint for apoptosis in Drosophila
inferredcites →https://doi.org/10.1016/s0969-2126(02)00732-3openalex-snapshot
Apoptosome
inferredcites →https://doi.org/10.1016/s0969-2126(99)80179-8openalex-snapshot
The three-dimensional structure of caspase-8: an initiator enzyme in apoptosis
inferredcites →https://doi.org/10.1016/s0969-2126(99)80180-4openalex-snapshot
The atomic-resolution structure of human caspase-8, a key activator of apoptosis
inferredcites →https://doi.org/10.1016/s1074-5521(00)00123-xopenalex-snapshot
The structures of caspases-1, -3, -7 and -8 reveal the basis for substrate and inhibitor selectivity
inferredcites →https://doi.org/10.1016/s1097-2765(00)80032-5openalex-snapshot
Autoproteolytic Activation of Pro-Caspases by Oligomerization
inferredcites →https://doi.org/10.1016/s1097-2765(00)80095-7openalex-snapshot
Autoactivation of Procaspase-9 by Apaf-1-Mediated Oligomerization
inferredcites →https://doi.org/10.1016/s1097-2765(00)80222-1openalex-snapshot
The Engagement of Sec61p in the ER Dislocation Process
inferredcites →https://doi.org/10.1016/s1097-2765(00)80385-8openalex-snapshot
HAC-1, a Drosophila Homolog of APAF-1 and CED-4, Functions in Developmental and Radiation-Induced Apoptosis
inferredcites →https://doi.org/10.1016/s1097-2765(00)80386-xopenalex-snapshot
Control of the Cell Death Pathway by Dapaf-1, a Drosophila Apaf-1/CED-4-Related Caspase Activator
inferredcites →https://doi.org/10.1016/s1097-2765(01)00282-9openalex-snapshot
Structural Analysis of a Functional DIAP1 Fragment Bound to Grim and Hid Peptides
inferredcites →https://doi.org/10.1016/s1097-2765(01)00341-0openalex-snapshot
A Serine Protease, HtrA2, Is Released from the Mitochondria and Interacts with XIAP, Inducing Cell Death
inferredcites →https://doi.org/10.1016/s1097-2765(02)00482-3openalex-snapshot
Mechanisms of Caspase Activation and Inhibition during Apoptosis
inferredcites →https://doi.org/10.1016/s1097-2765(02)00501-4openalex-snapshot
A Caspase-Related Protease Regulates Apoptosis in Yeast
inferredcites →https://doi.org/10.1016/s1097-2765(03)00051-0openalex-snapshot
A Unified Model for Apical Caspase Activation
inferredcites →https://doi.org/10.1016/s1097-2765(03)00054-6openalex-snapshot
Mechanism of XIAP-Mediated Inhibition of Caspase-9
inferredcites →https://doi.org/10.1016/s1097-2765(03)00059-5openalex-snapshot
Insights into the Regulatory Mechanism for Caspase-8 Activation
inferredcites →https://doi.org/10.1016/s1535-6108(02)00024-7openalex-snapshot
A matter of life and death
inferredcites →https://doi.org/10.1021/bi010574wopenalex-snapshot
Mechanism-Based Inactivation of Caspases by the Apoptotic Suppressor p35
inferredcites →https://doi.org/10.1021/bi980893wopenalex-snapshot
Interaction of the Baculovirus Anti-apoptotic Protein p35 with Caspases. Specificity, Kinetics, and Characterization of the Caspase/p35 Complex
inferredcites →https://doi.org/10.1038/10701openalex-snapshot
Solution structure of a baculoviral inhibitor of apoptosis (IAP) repeat.
inferredcites →https://doi.org/10.1038/12984openalex-snapshot
Dark is a Drosophila homologue of Apaf-1/CED-4 and functions in an evolutionarily conserved death pathway
inferredcites →https://doi.org/10.1038/35022514openalex-snapshot
Structural and biochemical basis of apoptotic activation by Smac/DIABLO
inferredcites →https://doi.org/10.1038/35037739openalex-snapshot
Apoptosis in the nervous system
inferredcites →https://doi.org/10.1038/35038119openalex-snapshot
Structure of a serpin–protease complex shows inhibition by deformation
inferredcites →https://doi.org/10.1038/35050006openalex-snapshot
Structural basis for binding of Smac/DIABLO to the XIAP BIR3 domain
inferredcites →https://doi.org/10.1038/35050012openalex-snapshot
Structural basis of IAP recognition by Smac/DIABLO
inferredcites →https://doi.org/10.1038/35065125openalex-snapshot
A conserved XIAP-interaction motif in caspase-9 and Smac/DIABLO regulates caspase activity and apoptosis
inferredcites →https://doi.org/10.1038/35068604openalex-snapshot
Covalent inhibition revealed by the crystal structure of the caspase-8/p35 complex
inferredcites →https://doi.org/10.1038/356768a0openalex-snapshot
A novel heterodimeric cysteine protease is required for interleukin-1βprocessing in monocytes
inferredcites →https://doi.org/10.1038/370270a0openalex-snapshot
Structure and mechanism of interleukin-lβ converting enzyme
inferredcites →https://doi.org/10.1038/44617openalex-snapshot
NMR structure and mutagenesis of the inhibitor-of-apoptosis protein XIAP
inferredcites →https://doi.org/10.1038/87548openalex-snapshot
A structural view of mitochondria-mediated apoptosis.
inferredcites →https://doi.org/10.1038/bjc.1972.33openalex-snapshot
Apoptosis: A Basic Biological Phenomenon with Wideranging Implications in Tissue Kinetics
inferredcites →https://doi.org/10.1038/ncb793openalex-snapshot
Hid, Rpr and Grim negatively regulate DIAP1 levels through distinct mechanisms
inferredcites →https://doi.org/10.1038/ncb795openalex-snapshot
Regulation of Drosophila IAP1 degradation and apoptosis by reaper and ubcD1
inferredcites →https://doi.org/10.1038/ncb798openalex-snapshot
Reaper eliminates IAP proteins through stimulated IAP degradation and generalized translational inhibition
inferredcites →https://doi.org/10.1038/ncb799openalex-snapshot
The DIAP1 RING finger mediates ubiquitination of Dronc and is indispensable for regulating apoptosis
inferredcites →https://doi.org/10.1038/ncb984openalex-snapshot
Degradation of DIAP1 by the N-end rule pathway is essential for regulating apoptosis
inferredcites →https://doi.org/10.1038/nm0897-917openalex-snapshot
A novel anti-apoptosis gene, survivin, expressed in cancer and lymphoma
inferredcites →https://doi.org/10.1038/nrc883openalex-snapshot
The Bcl2 family: regulators of the cellular life-or-death switch
inferredcites →https://doi.org/10.1038/nrm830openalex-snapshot
IAP proteins: blocking the road to death's door
inferredcites →https://doi.org/10.1038/nsb0796-619openalex-snapshot
The three-dimensional structure of apopain/CPP32, a key mediator of apoptosis
inferredcites →https://doi.org/10.1038/nsb795openalex-snapshot
Structural insights into the pro-apoptotic function of mitochondrial serine protease HtrA2/Omi
inferredcites →https://doi.org/10.1038/nsb989openalex-snapshot
Molecular mechanism of Reaper-Grim-Hid-mediated suppression of DIAP1-dependent Dronc ubiquitination
inferredcites →https://doi.org/10.1038/nsmb764openalex-snapshot
Molecular mechanisms of DrICE inhibition by DIAP1 and removal of inhibition by Reaper, Hid and Grim
inferredcites →https://doi.org/10.1038/sj.cdd.4400756openalex-snapshot
The fly caspases
inferredcites →https://doi.org/10.1038/sj.cdd.4400765openalex-snapshot
Understanding IAP function and regulation: a view from Drosophila
inferredcites →https://doi.org/10.1038/sj.cdd.4400957openalex-snapshot
A conserved tetrapeptide motif: potentiating apoptosis through IAP-binding
inferredcites →https://doi.org/10.1038/sj.cdd.4400970openalex-snapshot
The serine protease Omi/HtrA2 is released from mitochondria during apoptosis. Omi interacts with caspase-inhibitor XIAP and induces enhanced caspase activity
inferredcites →https://doi.org/10.1038/sj.cdd.4401135openalex-snapshot
The p35 relative, p49, inhibits mammalian and Drosophila caspases including DRONC and protects against apoptosis
inferredcites →https://doi.org/10.1038/sj.cdd.4401186openalex-snapshot
The CD95(APO-1/Fas) DISC and beyond
inferredcites →https://doi.org/10.1038/sj.emboj.7594736openalex-snapshot
Baculovirus apoptotic suppressor P49 is a substrate inhibitor of initiator caspases resistant to P35 in vivo
inferredcites →https://doi.org/10.1073/pnas.221580098openalex-snapshot
Structural basis for the activation of human procaspase-7
inferredcites →https://doi.org/10.1073/pnas.231465798openalex-snapshot
Dimer formation drives the activation of the cell death protease caspase 9
inferredcites →https://doi.org/10.1073/pnas.95.7.3655openalex-snapshot
Synthetic activation of caspases: Artificial death switches
inferredcites →https://doi.org/10.1073/pnas.96.20.10964openalex-snapshot
Caspase activation: The induced-proximity model
inferredcites →https://doi.org/10.1074/jbc.272.10.6539openalex-snapshot
Structure of Recombinant Human CPP32 in Complex with the Tetrapeptide Acetyl-Asp-Val-Ala-Asp Fluoromethyl Ketone
inferredcites →https://doi.org/10.1074/jbc.272.29.17907openalex-snapshot
A Combinatorial Approach Defines Specificities of Members of the Caspase Family and Granzyme B
inferredcites →https://doi.org/10.1074/jbc.272.3.1421openalex-snapshot
Spodoptera frugiperda Caspase-1, a Novel Insect Death Protease That Cleaves the Nuclear Immunophilin FKBP46, Is the Target of the Baculovirus Antiapoptotic Protein p35
inferredcites →https://doi.org/10.1074/jbc.273.17.10107openalex-snapshot
Generation of Constitutively Active Recombinant Caspases-3 and -6 by Rearrangement of Their Subunits
inferredcites →https://doi.org/10.1074/jbc.273.5.2926openalex-snapshot
An Induced Proximity Model for Caspase-8 Activation
inferredcites →https://doi.org/10.1074/jbc.274.17.11549openalex-snapshot
An APAF-1·Cytochrome c Multimeric Complex Is a Functional Apoptosome That Activates Procaspase-9
inferredcites →https://doi.org/10.1074/jbc.274.25.17941openalex-snapshot
Cytochrome c and dATP-mediated Oligomerization of Apaf-1 Is a Prerequisite for Procaspase-9 Activation
inferredcites →https://doi.org/10.1074/jbc.c000405200openalex-snapshot
Cytochrome c Promotes Caspase-9 Activation by Inducing Nucleotide Binding to Apaf-1
inferredcites →https://doi.org/10.1074/jbc.m000869200openalex-snapshot
The Drosophila caspase DRONC is a glutamate/aspartate protease whose activity is regulated by DIAP1, HID and GRIM
inferredcites →https://doi.org/10.1074/jbc.m003670200openalex-snapshot
Livin, a Novel Inhibitor of Apoptosis Protein Family Member
inferredcites →https://doi.org/10.1074/jbc.m006226200openalex-snapshot
NMR Structure and Mutagenesis of the Third Bir Domain of the Inhibitor of Apoptosis Protein XIAP
inferredcites →https://doi.org/10.1074/jbc.m109721200openalex-snapshot
Identification of Omi/HtrA2 as a Mitochondrial Apoptotic Serine Protease That Disrupts Inhibitor of Apoptosis Protein-Caspase Interaction
inferredcites →https://doi.org/10.1074/jbc.m109784200openalex-snapshot
The Serine Protease Omi/HtrA2 Regulates Apoptosis by Binding XIAP through a Reaper-like Motif
inferredcites →https://doi.org/10.1074/jbc.m109891200openalex-snapshot
HtrA2 Promotes Cell Death through Its Serine Protease Activity and Its Ability to Antagonize Inhibitor of Apoptosis Proteins
inferredcites →https://doi.org/10.1074/jbc.m203464200openalex-snapshot
The Drosophila DIAP1 Protein Is Required to Prevent Accumulation of a Continuously Generated, Processed Form of the Apical Caspase DRONC
inferredcites →https://doi.org/10.1074/jbc.m208810200openalex-snapshot
Characterization of the Apoptosis Suppressor Protein P49 from the Spodoptera littoralisNucleopolyhedrovirus
inferredcites →https://doi.org/10.1074/jbc.m304895200openalex-snapshot
Crystal Structure of Caspase-2, Apical Initiator of the Intrinsic Apoptotic Pathway
inferredcites →https://doi.org/10.1074/jbc.m310061200openalex-snapshot
Requirement of Both the Second and Third BIR Domains for the Relief of X-linked Inhibitor of Apoptosis Protein (XIAP)-mediated Caspase Inhibition by Smac
inferredcites →https://doi.org/10.1074/jbc.m312472200openalex-snapshot
Crystal Structure of an Invertebrate Caspase
inferredcites →https://doi.org/10.1093/emboj/19.4.589openalex-snapshot
Induction of apoptosis by Drosophila reaper, hid and grim through inhibition of IAP function
inferredcites →https://doi.org/10.1093/emboj/19.4.598openalex-snapshot
The Drosophila caspase DRONC is regulated by DIAP1
inferredcites →https://doi.org/10.1093/emboj/21.9.2189openalex-snapshot
Unrestrained caspase‐dependent cell death caused by loss of Diap1 function requires the Drosophila Apaf‐1 homolog, Dark
inferredcites →https://doi.org/10.1093/emboj/cdf530openalex-snapshot
Jafrac2 is an IAP antagonist that promotes cell death by liberating Dronc from DIAP1
inferredcites →https://doi.org/10.1101/gad.10.9.1073openalex-snapshot
The Caenorhabditis elegans cell-death protein CED-3 is a cysteine protease with substrate specificities similar to those of the human CPP32 protease.
inferredcites →https://doi.org/10.1101/gad.13.24.3179openalex-snapshot
Caspase-9 and APAF-1 form an active holoenzyme
inferredcites →https://doi.org/10.1101/gad.13.3.239openalex-snapshot
IAP family proteins---suppressors of apoptosis
inferredcites →https://doi.org/10.1107/s0021889891004399openalex-snapshot
MOLSCRIPT: a program to produce both detailed and schematic plots of protein structures
inferredcites →https://doi.org/10.1111/j.1768-322x.1996.tb00978.xopenalex-snapshot
Phosphorus distribution in perichromatin granules and surrounding nucleoplasm as visualized by electron spectroscopic imaging
inferredcites →https://doi.org/10.1126/science.1062236openalex-snapshot
Controlling the Caspases
inferredcites →https://doi.org/10.1126/science.1373520openalex-snapshot
Molecular Cloning of the Interleukin-1β Converting Enzyme
inferredcites →https://doi.org/10.1126/science.281.5381.1312openalex-snapshot
Caspases: Enemies Within
inferredcites →https://doi.org/10.1126/science.281.5381.1355openalex-snapshot
Essential Role of CED-4 Oligomerization in CED-3 Activation and Apoptosis
inferredcites →https://doi.org/10.1126/science.7569933openalex-snapshot
Inhibition of ICE Family Proteases by Baculovirus Antiapoptotic Protein p35
inferredcites →https://doi.org/10.1126/science.7878464openalex-snapshot
Apoptosis in the Pathogenesis and Treatment of Disease
inferredcites →https://doi.org/10.1146/annurev.biochem.68.1.383openalex-snapshot
Mammalian Caspases: Structure, Activation, Substrates, and Functions During Apoptosis
inferredcites →https://doi.org/10.1146/annurev.cellbio.15.1.269openalex-snapshot
Biochemical Pathways of Caspase Activation During Apoptosis
inferredcites →https://doi.org/10.1146/annurev.genet.33.1.29openalex-snapshot
Fas Ligand-Induced Apoptosis
inferredcites →https://doi.org/10.1523/jneurosci.22-06-02035.2002openalex-snapshot
The Neuronal Apoptosis Inhibitory Protein Is a Direct Inhibitor of Caspases 3 and 7

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.4681762openalex-extracted
Multimodal Measurement of Apoptosis -- Integration of Biosensing, Imaging, and Analysis
inferred← citeshttps://doi.org/10.1002/0471266949.bmc029.pub2openalex-snapshot
Receptor Targets in Drug Discovery
inferred← citeshttps://doi.org/10.1002/1873-3468.13689openalex-snapshot
Multiple system‐level feedback loops control life‐and‐death decisions in endoplasmic reticulum stress
inferred← citeshttps://doi.org/10.1002/3527600906.mcb.201200012openalex-snapshot
RNA Regulation in Apoptosis
inferred← citeshttps://doi.org/10.1002/9780470015902.a0021576openalex-snapshot
Mitochondrial Outer Membrane Permeabilization
inferred← citeshttps://doi.org/10.1002/9780470015902.a0021579openalex-snapshot
Structures, Domains and Functions in Cell Death ( DD , DED , CARD , PYD )
inferred← citeshttps://doi.org/10.1002/9780470015902.a0021983openalex-snapshot
Structure and Function of IAP and Bcl‐2 Proteins
inferred← citeshttps://doi.org/10.1002/9780470048672.wecb467openalex-snapshot
Post‐Translational Modifications to Regulate Protein Function
inferred← citeshttps://doi.org/10.1002/9780470910108.ch10openalex-snapshot
Tradition and Perspectives of Greco‐Arab and Islamic Herbal Medicine
inferred← citeshttps://doi.org/10.1002/9780470944363.ch12openalex-snapshot
Arab Medicinal Plants: From Traditional Uses to Scientific Knowledge
inferred← citeshttps://doi.org/10.1002/9780470995983.ch6openalex-snapshot
Mechanisms of Defence to Pathogens: Biochemistry and Physiology
inferred← citeshttps://doi.org/10.1002/9781118735183.ch29openalex-snapshot
Specific Light-Up Bioprobes with Aggregation-Induced Emission Characteristics for Protein Sensing
inferred← citeshttps://doi.org/10.1002/9781119432463.ch2openalex-snapshot
Mitochondria in Focus: Targeting the Cell‐Death Mechanism
inferred← citeshttps://doi.org/10.1002/9781119643098.ch54openalex-snapshot
AIE‐active Fluorescence Probes for Enzymes and Their Applications in Disease Theranostics
inferred← citeshttps://doi.org/10.1002/9781119865452.ch6openalex-snapshot
Biomedical Applications of Carrageenan
inferred← citeshttps://doi.org/10.1002/9783527619665.ch9openalex-snapshot
Caspases: Agents of Defense and Destruction
inferred← citeshttps://doi.org/10.1002/9783527621071.ch17openalex-snapshot
Combinatorial Synthesis of Alkaloid‐like Compounds In Search of Chemical Probes of Protein‐Protein Interactions
inferred← citeshttps://doi.org/10.1002/9783527630332.ch12openalex-snapshot
A Systems Biology Approach to Construct a Cancer‐Perturbed Protein–Protein Interaction Network for Apoptosis by Means of Microarray and Database Mining
inferred← citeshttps://doi.org/10.1002/9783527682423.ch38openalex-snapshot
mAbs Targeting Apoptosis, Angiogenesis Inhibitors, and Other mAbs in Phase 1 and 2 Clinical Studies for Immunological Disorders
inferred← citeshttps://doi.org/10.1002/adfm.201502728openalex-snapshot
Light‐Up Probe for Targeted and Activatable Photodynamic Therapy with Real‐Time In Situ Reporting of Sensitizer Activation and Therapeutic Responses
inferred← citeshttps://doi.org/10.1002/age.70214openalex-snapshot
FBLN1 Regulates Embryonic Myoblast Proliferation and Differentiation in Geese: Functional Characterization of a Meat Quality‐Associated Candidate Gene From Prior Multi‐Omics Screening
inferred← citeshttps://doi.org/10.1002/ange.201107795openalex-snapshot
Multiplex Imaging of an Intracellular Proteolytic Cascade by using a Broad‐Spectrum Nanoquencher
inferred← citeshttps://doi.org/10.1002/ange.201208239openalex-snapshot
Supramolecular Control of Enzyme Activity through Cucurbit[8]uril‐Mediated Dimerization
inferred← citeshttps://doi.org/10.1002/ange.201411594openalex-snapshot
Intracellular Delivery of Peptidyl Ligands by Reversible Cyclization: Discovery of a PDZ Domain Inhibitor that Rescues CFTR Activity
inferred← citeshttps://doi.org/10.1002/ange.202102160openalex-snapshot
Dynamic Protease Activation on a Multimeric Synthetic Protein Scaffold via Adaptable DNA‐Based Recruitment Domains
inferred← citeshttps://doi.org/10.1002/anie.201107795openalex-snapshot
Multiplex Imaging of an Intracellular Proteolytic Cascade by using a Broad‐Spectrum Nanoquencher
inferred← citeshttps://doi.org/10.1002/anie.201208239openalex-snapshot
Supramolecular Control of Enzyme Activity through Cucurbit[8]uril‐Mediated Dimerization
inferred← citeshttps://doi.org/10.1002/anie.201411594openalex-snapshot
Intracellular Delivery of Peptidyl Ligands by Reversible Cyclization: Discovery of a PDZ Domain Inhibitor that Rescues CFTR Activity
inferred← citeshttps://doi.org/10.1002/anie.202102160openalex-snapshot
Dynamic Protease Activation on a Multimeric Synthetic Protein Scaffold via Adaptable DNA‐Based Recruitment Domains
inferred← citeshttps://doi.org/10.1002/arch.21106openalex-snapshot
THE Spodoptera frugiperda EFFECTOR CASPASE SF‐CASPASE‐1 BECOMES UNSTABLE FOLLOWING ITS ACTIVATION
inferred← citeshttps://doi.org/10.1002/ardp.201300180openalex-snapshot
Discovery of 2‐ P henyl‐ N ‐(5‐(trifluoromethyl)‐1,3,4‐thiadiazol‐2‐yl)acetamide Derivatives as Apoptosis Inducers via the Caspase Pathway with Potential Anticancer Activity
inferred← citeshttps://doi.org/10.1002/bdra.20274openalex-snapshot
Differential teratogenic response of TNFα+/+and TNFα−/−mice to cyclophosphamide: The possible role of NF‐κB
inferred← citeshttps://doi.org/10.1002/bdrc.20052openalex-snapshot
Teratogen-induced apoptotic cell death: Does the apoptotic machinery act as a protector of embryos exposed to teratogens?
inferred← citeshttps://doi.org/10.1002/bies.201300052openalex-snapshot
Cell death proteins: An evolutionary role in cellular adaptation before the advent of apoptosis
inferred← citeshttps://doi.org/10.1002/bit.20871openalex-snapshot
Targeting early apoptotic genes in batch and fed‐batch CHO cell cultures
inferred← citeshttps://doi.org/10.1002/bit.27204openalex-snapshot
Engineered Fn3 protein has targeted therapeutic effect on mesothelin‐expressing cancer cells and increases tumor cell sensitivity to chemotherapy
inferred← citeshttps://doi.org/10.1002/btpr.1763openalex-snapshot
Use of an anti‐apoptotic CHO cell line for transient gene expression
inferred← citeshttps://doi.org/10.1002/btpr.3211openalex-snapshot
Characterization of cell cycle and apoptosis in Chinese hamster ovary cell culture using flow cytometry for bioprocess monitoring
inferred← citeshttps://doi.org/10.1002/cbdv.200800340openalex-snapshot
Platinum–DNA Interactions and Subsequent Cellular Processes Controlling Sensitivity to Anticancer Platinum Complexes
inferred← citeshttps://doi.org/10.1002/cbf.1774openalex-snapshot
Apoptosis: why and how does it occur in biology?
inferred← citeshttps://doi.org/10.1002/cbic.200800528openalex-snapshot
Allosteric Regulation of Proteases
inferred← citeshttps://doi.org/10.1002/cbic.201300315openalex-snapshot
Small‐Molecule Procaspase Activators Identified Using Fluorescence Polarization
inferred← citeshttps://doi.org/10.1002/cbic.201400073openalex-snapshot
Genetic Encoding of Caged Cysteine and Caged Homocysteine in Bacterial and Mammalian Cells
inferred← citeshttps://doi.org/10.1002/cbin.10034openalex-snapshot
Propofol induces apoptosis of hepatocellular carcinoma cells by upregulation of microRNA‐199a expression
inferred← citeshttps://doi.org/10.1002/chem.200900766openalex-snapshot
Cell‐Permeable [99mTc(CO3)]‐Labeled Fluorogenic Caspase 3 Substrate for Dual‐Modality Detection of Apoptosis
inferred← citeshttps://doi.org/10.1002/chem.201300814openalex-snapshot
Histone‐Deacetylase‐Targeted Fluorescent Ruthenium(II) Polypyridyl Complexes as Potent Anticancer Agents
inferred← citeshttps://doi.org/10.1002/chem.201404749openalex-snapshot
Anti‐Cancer Iron(II) Complexes of Pentadentate N‐Donor Ligands: Cytotoxicity, Transcriptomics Analyses, and Mechanisms of Action
inferred← citeshttps://doi.org/10.1002/chem.201505160openalex-snapshot
Mono‐ and Dinuclear Phosphorescent Rhenium(I) Complexes: Impact of Subcellular Localization on Anticancer Mechanisms
inferred← citeshttps://doi.org/10.1002/cm.20391openalex-snapshot
Mechanical dynamics of single cells during early apoptosis
inferred← citeshttps://doi.org/10.1002/cmdc.200900245openalex-snapshot
α‐Bromoacrylamido N‐Substituted Isatin Derivatives as Potent Inducers of Apoptosis in Human Myeloid Leukemia Cells
inferred← citeshttps://doi.org/10.1002/cmdc.201100232openalex-snapshot
Synthesis and in vitro Anticancer Activity of Ruthenium–Cymene Complexes with Cyclohexyl‐Functionalized Ethylenediamine‐N,N′‐diacetate‐Type Ligands
inferred← citeshttps://doi.org/10.1002/cmdc.201300379openalex-snapshot
Mitochondrial Fragmentation Is an Important Cellular Event Induced by Ruthenium(II) Polypyridyl Complexes in Osteosarcoma Cells
inferred← citeshttps://doi.org/10.1002/cmdc.201900410openalex-snapshot
Bivalent SMAC Mimetics for Treating Cancer by Antagonizing Inhibitor of Apoptosis Proteins
inferred← citeshttps://doi.org/10.1002/dc.21095openalex-snapshot
Cell survival and apoptosis‐related molecules in cancer cells in effusions: A comprehensive review
inferred← citeshttps://doi.org/10.1002/dc.22809openalex-snapshot
The diagnostic and research applications of flow cytometry in cytopathology
inferred← citeshttps://doi.org/10.1002/dvdy.21599openalex-snapshot
Palatal seam disintegration: To die or not to die? that is no longer the question
inferred← citeshttps://doi.org/10.1002/hep4.1971openalex-snapshot
A new detection system for serum fragmented cytokeratin 18 as a biomarker reflecting histologic activities of human nonalcoholic steatohepatitis
inferred← citeshttps://doi.org/10.1002/ijc.31965openalex-snapshot
Therapeutic value of steroidal alkaloids in cancer: Current trends and future perspectives
inferred← citeshttps://doi.org/10.1002/jbio.201500258openalex-snapshot
Visualising apoptosis in live zebrafish using fluorescence lifetime imaging with optical projection tomography to map FRET biosensor activity in space and time
inferred← citeshttps://doi.org/10.1002/jbm.a.36002openalex-snapshot
Caspase mediated beclin‐1 dependent autophagy tuning activity and apoptosis promotion by surface modified hausmannite nanoparticle
inferred← citeshttps://doi.org/10.1002/jbt.21541openalex-snapshot
A Comparative Study of In Vitro Cytotoxic, Antioxidant, and Antimicrobial Activity of Pt(II), Zn(II), Cu(II), and Co(III) Complexes with N‐heteroaromatic Schiff Base (E)‐2‐[N′‐(1‐pyridin‐2‐yl‐ethylidene)hydrazino]acetate
inferred← citeshttps://doi.org/10.1002/jcb.20409openalex-snapshot
Discovery, regulation, and action of the major apoptotic nucleases DFF40/CAD and endonuclease G
inferred← citeshttps://doi.org/10.1002/jcb.20839openalex-snapshot
Effects of PPARγ agonists on cell survival and focal adhesions in a Chinese thyroid carcinoma cell line
inferred← citeshttps://doi.org/10.1002/jcb.22196openalex-snapshot
Reactive oxygen species‐induced cell death of rat primary astrocytes through mitochondria‐mediated mechanism
inferred← citeshttps://doi.org/10.1002/jcb.28205openalex-snapshot
Smac mimetics as novel promising modulators of apoptosis in the treatment of breast cancer
inferred← citeshttps://doi.org/10.1002/jcb.29065openalex-snapshot
Green synthesized‐zinc oxide nanoparticles, the strong apoptosis inducer as an exclusive antitumor agent in murine breast tumor model and human breast cancer cell lines (MCF7)
inferred← citeshttps://doi.org/10.1002/jcp.21350openalex-snapshot
Bcl‐xL prevents staurosporine‐induced hepatocyte apoptosis by restoring protein kinase B/mitogen‐activated protein kinase activity and mitochondria integrity
inferred← citeshttps://doi.org/10.1002/jcp.24318openalex-snapshot
Galectin‐3 deficiency protects pancreatic islet cells from cytokine‐triggered apoptosis in vitro
inferred← citeshttps://doi.org/10.1002/jcp.24863openalex-snapshot
The Synergistic Effect of SAHA and Parthenolide in MDA‐MB231 Breast Cancer Cells
inferred← citeshttps://doi.org/10.1002/jemt.20774openalex-snapshot
The toxic effect of ketamine on SH‐SY5Y neuroblastoma cell line and human neuron
inferred← citeshttps://doi.org/10.1002/jgm.1390openalex-snapshot
Efficient gene delivery into mammalian cells by recombinant baculovirus containing a hybrid cytomegalovirus promoter/Semliki Forest virus replicon
inferred← citeshttps://doi.org/10.1002/jhet.4573openalex-snapshot
Diastereomerically pure (S)‐ verbenone‐isoxazoline hybrids: Synthesis, molecular structure, Hirshfeld surface analysis, density functional theory, cytotoxic effect, and apoptosis induction
inferred← citeshttps://doi.org/10.1002/jnr.22007openalex-snapshot
Neuropathy‐induced apoptosis: Protective effect of physostigmine
inferred← citeshttps://doi.org/10.1002/jsp2.1292openalex-snapshot
Targeted screening of inflammatory mediators in spontaneous degenerative disc disease in dogs reveals an upregulation of the tumor necrosis superfamily
inferred← citeshttps://doi.org/10.1002/mabi.200700008openalex-snapshot
Chondroitin‐4‐Sulfate: A Bioactive Macromolecule to Foster Vascular Healing around Stent‐Grafts after Endovascular Aneurysm Repair
inferred← citeshttps://doi.org/10.1002/mc.21990openalex-snapshot
IL‐32γ enhances TNF‐α‐induced cell death in colon cancer
inferred← citeshttps://doi.org/10.1002/mco2.70268openalex-snapshot
Oxidative Stress: Signaling Pathways, Biological Functions, and Disease
inferred← citeshttps://doi.org/10.1002/mrd.20561openalex-snapshot
Comparative analysis of apoptotic pathways in rat, mouse, and hamster spermatozoa
inferred← citeshttps://doi.org/10.1002/mrd.20822openalex-snapshot
Relevance of caspase activity during apoptosis in pubertal rat spermatogenesis
inferred← citeshttps://doi.org/10.1002/mrd.22938openalex-snapshot
Lysophosphatidic acid accelerates development of porcine embryos by activating formation of the blastocoel
inferred← citeshttps://doi.org/10.1002/path.1885openalex-snapshot
Regulation and interplay of apoptotic and non‐apoptotic cell death
inferred← citeshttps://doi.org/10.1002/pbc.20805openalex-snapshot
Survivin: An inhibitor of apoptosis in pediatric cancer
inferred← citeshttps://doi.org/10.1002/pmic.200700114openalex-snapshot
A la carte proteomics with an emphasis on gel‐free techniques
inferred← citeshttps://doi.org/10.1002/pmic.200800031openalex-snapshot
NDRG1 is down‐regulated in the early apoptotic event induced by camptothecin analogs: The potential role in proteolytic activation of PKCδ and apoptosis
inferred← citeshttps://doi.org/10.1002/pmic.201100353openalex-snapshot
Dissecting cell death with proteomic scalpels
inferred← citeshttps://doi.org/10.1002/pmic.201400002openalex-snapshot
ScreenCap3: Improving prediction of caspase‐3 cleavage sites using experimentally verified noncleavage sites
inferred← citeshttps://doi.org/10.1002/ppap.201400102openalex-snapshot
Dielectric Barrier Discharge Plasma Efficiently Delivers an Apoptotic Response in Human Monocytic Lymphoma
inferred← citeshttps://doi.org/10.1002/pro.70320openalex-snapshot
Ligand binding Pro ‐miscuity of acylpeptide hydrolase, structural analysis of a detoxifying serine hydrolase
inferred← citeshttps://doi.org/10.1002/pros.22960openalex-snapshot
γ‐oryzanol reduces caveolin‐1 and PCGEM1 expression, markers of aggressiveness in prostate cancer cell lines
inferred← citeshttps://doi.org/10.1002/prp2.125openalex-snapshot
Metformin protects primary rat hepatocytes against oxidative stress‐induced apoptosis
inferred← citeshttps://doi.org/10.1002/ptr.7356openalex-snapshot
Cardioprotective effects of alpha‐mangostin on doxorubicin‐induced cardiotoxicity in rats
inferred← citeshttps://doi.org/10.1002/ptr.8316openalex-snapshot
Exploring the therapeutic implications of natural compounds modulating apoptosis in vascular dementia
inferred← citeshttps://doi.org/10.1002/sita.200600117openalex-snapshot
Avian influenza virus signaling: implications for the disease severity of H5N1 infection
inferred← citeshttps://doi.org/10.1002/slct.202301955openalex-snapshot
Synthesis, Characterization and Apoptosis Capabilities of a Novel Naphthoquinone‐Derived Compound in Triple‐Negative Breast Cancer
inferred← citeshttps://doi.org/10.1002/smll.201902485openalex-snapshot
Bioinspired Peptoid Nanotubes for Targeted Tumor Cell Imaging and Chemo‐Photodynamic Therapy
inferred← citeshttps://doi.org/10.1002/tox.22582openalex-snapshot
GMI, a fungal immunomodulatory protein from Ganoderma microsporum, induce apoptosis via β‐catenin suppression in lung cancer cells
inferred← citeshttps://doi.org/10.1002/tox.22737openalex-snapshot
Antioxidant and anti‐apoptotic effects of royal jelly against nicotine‐induced testicular injury in mice
inferred← citeshttps://doi.org/10.1002/tox.22924openalex-snapshot
Betulin inhibits mTOR and induces autophagy to promote apoptosis in human osteosarcoma cell lines
inferred← citeshttps://doi.org/10.1002/tox.22986openalex-snapshot
Antimycin A shows selective antiproliferation to oral cancer cells by oxidative stress‐mediated apoptosis and DNA damage
inferred← citeshttps://doi.org/10.1002/vms3.684openalex-snapshot
Anti‐cancer potentials of Gynura procumbens leaves extract against two canine mammary cancer cell lines
inferred← citeshttps://doi.org/10.1007/16833_2024_488openalex-snapshot
Composition of Proapoptotic Montmorillonite-Cytochrome c Nanoplates with High Anticancer Cytotoxicity: Monolayer Adsorption Approach
inferred← citeshttps://doi.org/10.1007/3-540-28516-4_6openalex-snapshot
Signals and Targets Triggered by Self-Incompatibility in Plants: Recognition of “Self” Can Be Deadly
inferred← citeshttps://doi.org/10.1007/3-540-30328-6_23openalex-snapshot
Cell Death and Acute Lung Injury
inferred← citeshttps://doi.org/10.1007/82_2015_467openalex-snapshot
Prix Fixe: Efferocytosis as a Four-Course Meal
inferred← citeshttps://doi.org/10.1007/978-0-387-39954-6_5openalex-snapshot
Heat Shock Proteins and the Regulation of Apoptosis
inferred← citeshttps://doi.org/10.1007/978-0-387-68113-9_3openalex-snapshot
Cell Structure, Function, and Genetics
inferred← citeshttps://doi.org/10.1007/978-0-387-69945-5_12openalex-snapshot
The Apoptotic Mitochondrial Pathway – Modulators, Interventions and Clinical Implications
inferred← citeshttps://doi.org/10.1007/978-0-387-73226-8_1openalex-snapshot
Introduction
inferred← citeshttps://doi.org/10.1007/978-0-387-77383-4_35openalex-snapshot
Apoptosis in Critical Illness: A Primer for the Intensivist
inferred← citeshttps://doi.org/10.1007/978-1-4020-5129-6_8openalex-snapshot
CELL ADHESION-MEDIATED RADIATION RESISTANCE: THE ROLE OF INTEGRINS AND INTEGRIN PROXIMAL PROTEIN
inferred← citeshttps://doi.org/10.1007/978-1-4020-6554-5_10openalex-snapshot
Regulation of Programmed Cell Death by the P53 Pathway
inferred← citeshttps://doi.org/10.1007/978-1-4020-8696-0openalex-snapshot
Targeted Radionuclide Tumor Therapy
inferred← citeshttps://doi.org/10.1007/978-1-4020-8696-0_12openalex-snapshot
Radiation Induced Cell Deaths
inferred← citeshttps://doi.org/10.1007/978-1-4020-9873-4_2openalex-snapshot
Apoptosis
inferred← citeshttps://doi.org/10.1007/978-1-4419-0131-6_5openalex-snapshot
Targeting of Apoptosis Signaling Pathways and Their Mediators for Cancer Therapy
inferred← citeshttps://doi.org/10.1007/978-1-4419-1145-2_7openalex-snapshot
The Adenomatous Polyposis Coli Tumor Suppressor and Wnt Signaling in the Regulation of Apoptosis
inferred← citeshttps://doi.org/10.1007/978-1-4419-5797-9_24openalex-snapshot
Construction of Cancer-Perturbed Protein–Protein Interaction Network of Apoptosis for Drug Target Discovery
inferred← citeshttps://doi.org/10.1007/978-1-4419-9533-9_4openalex-snapshot
Mast Cell Apoptosis and Survival
inferred← citeshttps://doi.org/10.1007/978-1-4614-3335-4_31openalex-snapshot
Apoptosis and Male Infertility
inferred← citeshttps://doi.org/10.1007/978-1-4614-5847-0_1openalex-snapshot
Defective Apoptosis Signaling in Cancer
inferred← citeshttps://doi.org/10.1007/978-1-4614-5847-0_10openalex-snapshot
SMAC IAP Addiction in Cancer
inferred← citeshttps://doi.org/10.1007/978-1-4614-5947-7_12openalex-snapshot
Therapeutic Induction of Apoptosis in Nasopharyngeal Carcinoma
inferred← citeshttps://doi.org/10.1007/978-1-4614-6280-4_11openalex-snapshot
Stress Induced Mutagenesis, Genetic Diversification, and Cell Survival via Anastasis, the Reversal of Late Stage Apoptosis
inferred← citeshttps://doi.org/10.1007/978-1-4614-9158-3_12openalex-snapshot
Apoptosis and Male Infertility
inferred← citeshttps://doi.org/10.1007/978-1-4939-0894-3_24openalex-snapshot
Applications of Small-Animal Molecular Imaging in Drug Development
inferred← citeshttps://doi.org/10.1007/978-1-4939-3581-9_4openalex-snapshot
Detection of Initiator Caspase Induced Proximity in Single Cells by Caspase Bimolecular Fluorescence Complementation
inferred← citeshttps://doi.org/10.1007/978-1-4939-3588-8_2openalex-snapshot
Detection of Apoptosis: From Bench Side to Clinical Practice
inferred← citeshttps://doi.org/10.1007/978-1-59745-199-4_13openalex-snapshot
The Role of Proteasome in Apoptosis
inferred← citeshttps://doi.org/10.1007/978-1-59745-199-4_17openalex-snapshot
The Biology of Caspases
inferred← citeshttps://doi.org/10.1007/978-1-59745-199-4_2openalex-snapshot
Protein Kinase C and Apoptosis
inferred← citeshttps://doi.org/10.1007/978-1-59745-204-5_19openalex-snapshot
Modulation of Caspase Activation by Toxoplasma gondii
inferred← citeshttps://doi.org/10.1007/978-1-59745-435-3openalex-snapshot
Cellular Respiration and Carcinogenesis
inferred← citeshttps://doi.org/10.1007/978-1-59745-435-3_12openalex-snapshot
How Cancer Cells Escape Death
inferred← citeshttps://doi.org/10.1007/978-1-60327-017-5_1openalex-snapshot
Analysing Caspase Activation and Caspase Activity in Apoptotic Cells
inferred← citeshttps://doi.org/10.1007/978-1-60327-381-7_1openalex-snapshot
Caspases: Activation, Regulation, and Function
inferred← citeshttps://doi.org/10.1007/978-1-60761-543-9_9openalex-snapshot
PKC and the Control of Apoptosis
inferred← citeshttps://doi.org/10.1007/978-1-61779-527-5_5openalex-snapshot
Analyzing Cell Death Events in Cultured Leukocytes
inferred← citeshttps://doi.org/10.1007/978-3-030-32300-4_37openalex-snapshot
Apoptosis and Male Infertility
inferred← citeshttps://doi.org/10.1007/978-3-030-74330-7_1openalex-snapshot
Targeted Nanotheranostic Systems in Cancer Therapy
inferred← citeshttps://doi.org/10.1007/978-3-030-79871-0_7openalex-snapshot
Next-Generation Cell Engineering Platform for Improving Recombinant Protein Production in Mammalian Cells
inferred← citeshttps://doi.org/10.1007/978-3-319-30079-5_5openalex-snapshot
What Is the Pathobiology of Inflammation to Cell Death? Apoptosis, Necrosis, Necroptosis, Autophagic Cell Death, Pyroptosis, and NETosis
inferred← citeshttps://doi.org/10.1007/978-3-540-68486-2_11openalex-snapshot
Self-Incompatibility in Papaver Rhoeas: Progress in Understanding Mechanisms Involved in Regulating Self-Incompatibility in Papaver
inferred← citeshttps://doi.org/10.1007/978-3-540-69414-4_8openalex-snapshot
Molekulare Grundlagen der Apoptose
inferred← citeshttps://doi.org/10.1007/978-3-540-77290-3_35openalex-snapshot
Apoptosis in Critical Illness: A Primer for the Intensivist
inferred← citeshttps://doi.org/10.1007/978-3-7091-0885-7_3openalex-snapshot
Compartmentalization of Proteolysis
inferred← citeshttps://doi.org/10.1007/978-4-431-54965-9_19openalex-snapshot
Neuroprotection for Retinal Detachment
inferred← citeshttps://doi.org/10.1007/978-4-431-54965-9_8openalex-snapshot
RIP Kinase-Mediated Programmed Necrosis
inferred← citeshttps://doi.org/10.1007/978-4-431-87704-2_11openalex-snapshot
The Apoptotic Signaling Network Dynamically Interprets the Outputs of Individual Signaling Pathways in an Early Analog and Late Digital Manner
inferred← citeshttps://doi.org/10.1007/978-88-470-0571-6_18openalex-snapshot
The cell in shock
inferred← citeshttps://doi.org/10.1007/978-94-007-2019-0_3openalex-snapshot
Astrocytic Tumors: Role of Antiapoptotic Proteins
inferred← citeshttps://doi.org/10.1007/978-981-13-8367-0_9openalex-snapshot
Investigating the Role of Mitochondria in Type 2 Diabetes – Lessons from Lipidomics and Proteomics Studies of Skeletal Muscle and Liver
inferred← citeshttps://doi.org/10.1007/978-981-19-2944-1_11openalex-snapshot
Genetic Study of Kawasaki Disease
inferred← citeshttps://doi.org/10.1007/978-981-287-846-5_12openalex-snapshot
The Optic Nerve
inferred← citeshttps://doi.org/10.1007/978-981-97-7905-5_18openalex-snapshot
Apoptosis: Natural Product-Derived Small Molecules as Therapeutics
inferred← citeshttps://doi.org/10.1007/s00018-006-6091-xopenalex-snapshot
The function of apolipoproteins L
inferred← citeshttps://doi.org/10.1007/s00018-008-7564-xopenalex-snapshot
The imidazoline RX871024 induces death of proliferating insulin-secreting cells by activation of c-jun N-terminal kinase
inferred← citeshttps://doi.org/10.1007/s00018-008-8329-2openalex-snapshot
Selenocystine induces apoptosis of A375 human melanoma cells by activating ROS-mediated mitochondrial pathway and p53 phosphorylation
inferred← citeshttps://doi.org/10.1007/s00018-008-8472-9openalex-snapshot
Roles of the Major Apoptotic Nuclease-DNA Fragmentation Factor-in Biology and Disease
inferred← citeshttps://doi.org/10.1007/s00018-009-0151-yopenalex-snapshot
Suppressor of cytokine signaling-1 inhibits caspase activation and protects from cytokine-induced beta cell death
inferred← citeshttps://doi.org/10.1007/s00018-010-0287-9openalex-snapshot
Non-caspase proteases: triggers or amplifiers of apoptosis?
inferred← citeshttps://doi.org/10.1007/s00018-012-1165-4openalex-snapshot
Heat stress response of male germ cells
inferred← citeshttps://doi.org/10.1007/s00109-019-01851-4openalex-snapshot
Traumatic brain injury-induced downregulation of Nrf2 activates inflammatory response and apoptotic cell death
inferred← citeshttps://doi.org/10.1007/s00125-011-2277-3openalex-snapshot
An siRNA screen identifies transmembrane 7 superfamily member 3 (TM7SF3), a seven transmembrane orphan receptor, as an inhibitor of cytokine-induced death of pancreatic beta cells
inferred← citeshttps://doi.org/10.1007/s00204-013-1110-9openalex-snapshot
Cadmium and cellular signaling cascades: interactions between cell death and survival pathways
inferred← citeshttps://doi.org/10.1007/s00210-018-1531-3openalex-snapshot
Sodium valproate ameliorates memory impairment and reduces the elevated levels of apoptotic caspases in the hippocampus of diabetic mice
inferred← citeshttps://doi.org/10.1007/s00210-023-02419-3openalex-snapshot
Effect of isolated grandivittin from Ferulago trifida Boiss. (Apiaceae) on the proliferation and apoptosis of human lung cancer A549 cells
inferred← citeshttps://doi.org/10.1007/s00210-025-03875-9openalex-snapshot
Research progress on the bioactivity of platycodin D from Platycodon grandifloras
inferred← citeshttps://doi.org/10.1007/s00343-026-5044-5openalex-snapshot
Characterization of jellyfish (Aurelia coerulea) caspases: reciprocal regulations and their effects on apoptosis activation and GSDME cleavage
inferred← citeshttps://doi.org/10.1007/s00395-012-0314-0openalex-snapshot
Remote ischemic preconditioning regulates HIF-1α levels, apoptosis and inflammation in heart tissue of cardiosurgical patients: a pilot experimental study
inferred← citeshttps://doi.org/10.1007/s00418-016-1508-6openalex-snapshot
Expression of Fas, FasL, caspase-8 and other factors of the extrinsic apoptotic pathway during the onset of interdigital tissue elimination
inferred← citeshttps://doi.org/10.1007/s00430-005-0239-4openalex-snapshot
Apoptosis in infectious disease: how bacteria interfere with the apoptotic apparatus
inferred← citeshttps://doi.org/10.1007/s00432-008-0444-9openalex-snapshot
Pathogenesis of malignant pleural mesothelioma and the role of environmental and genetic factors
inferred← citeshttps://doi.org/10.1007/s00705-014-2232-yopenalex-snapshot
Bursal transcriptome of chickens protected by DNA vaccination versus those challenged with infectious bursal disease virus
inferred← citeshttps://doi.org/10.1007/s10103-019-02794-5openalex-snapshot
The study of killing effect and inducing apoptosis of 630-nm laser on lung adenocarcinoma A549 cells mediated by hematoporphyrin derivatives in vitro
inferred← citeshttps://doi.org/10.1007/s10238-017-0482-1openalex-snapshot
Resistance to apoptosis in Leishmania infantum-infected human macrophages: a critical role for anti-apoptotic Bcl-2 protein and cellular IAP1/2
inferred← citeshttps://doi.org/10.1007/s10269-005-0246-5openalex-snapshot
Biologie de la transition vers l’hormonorésistance des cancers de la prostate
inferred← citeshttps://doi.org/10.1007/s10495-005-0887-2openalex-snapshot
Motexafin gadolinium induces mitochondriallymediated caspase-dependent apoptosis
inferred← citeshttps://doi.org/10.1007/s10495-006-0012-1openalex-snapshot
Up-regulation of CD95 (Apo-1/Fas) is associated with spermatocyte apoptosis during the first round of spermatogenesis in the rat
inferred← citeshttps://doi.org/10.1007/s10495-009-0343-9openalex-snapshot
Nuclear translocation of dihydrofolate reductase is not a pre-requisite for DNA damage induced apoptosis
inferred← citeshttps://doi.org/10.1007/s10495-009-0346-6openalex-snapshot
Can’t live without them, can live with them: roles of caspases during vital cellular processes
inferred← citeshttps://doi.org/10.1007/s10495-009-0358-2openalex-snapshot
Inhibitor of apoptosis proteins in Drosophila: gatekeepers of death
inferred← citeshttps://doi.org/10.1007/s10495-011-0610-4openalex-snapshot
Pro-apoptotic cell death genes, hid and reaper, from the tephritid pest species, Anastrepha suspensa
inferred← citeshttps://doi.org/10.1007/s10495-011-0614-0openalex-snapshot
Insulin receptor signaling activated by penta-O-galloyl-α-d-glucopyranose induces p53 and apoptosis in cancer cells
inferred← citeshttps://doi.org/10.1007/s10495-011-0684-zopenalex-snapshot
RNase MC2: a new Momordica charantia ribonuclease that induces apoptosis in breast cancer cells associated with activation of MAPKs and induction of caspase pathways
inferred← citeshttps://doi.org/10.1007/s10495-012-0709-2openalex-snapshot
Apoptosis, necrosis and autophagy are influenced by metabolic energy sources in cultured rat spermatocytes
inferred← citeshttps://doi.org/10.1007/s10495-013-0927-2openalex-snapshot
Targeting elongation factor-2 kinase (eEF-2K) induces apoptosis in human pancreatic cancer cells
inferred← citeshttps://doi.org/10.1007/s10495-014-0978-zopenalex-snapshot
Hydrogen sulfide improves left ventricular function in smoking rats via regulation of apoptosis and autophagy
inferred← citeshttps://doi.org/10.1007/s10495-014-1054-4openalex-snapshot
Tandem DEDs and CARDs suggest novel mechanisms of signaling complex assembly
inferred← citeshttps://doi.org/10.1007/s10495-014-1062-4openalex-snapshot
The versatile roles of CARDs in regulating apoptosis, inflammation, and NF-κB signaling
inferred← citeshttps://doi.org/10.1007/s10499-025-02301-4openalex-snapshot
Modulatory effects of dietary jackfruit peel waste on haematology, immune, genes responses during ammonia toxicity in Nile tilapia
inferred← citeshttps://doi.org/10.1007/s10534-014-9819-3openalex-snapshot
Roles of oxidative stress and endoplasmic reticulum stress in selenium deficiency-induced apoptosis in chicken liver
inferred← citeshttps://doi.org/10.1007/s10534-017-0051-9openalex-snapshot
The ability of silver(I) thiocyanate 4-methoxyphenyl phosphine to induce apoptotic cell death in esophageal cancer cells is correlated to mitochondrial perturbations
inferred← citeshttps://doi.org/10.1007/s10555-018-9736-yopenalex-snapshot
Novel roles of apoptotic caspases in tumor repopulation, epigenetic reprogramming, carcinogenesis, and beyond
inferred← citeshttps://doi.org/10.1007/s10571-009-9348-8openalex-snapshot
Differential PARP Cleavage: An Indication of Heterogeneous Forms of Cell Death and Involvement of Multiple Proteases in the Infarct of Focal Cerebral Ischemia in Rat
inferred← citeshttps://doi.org/10.1007/s10571-014-0142-xopenalex-snapshot
Administration of Antagomir-223 Inhibits Apoptosis, Promotes Angiogenesis and Functional Recovery in Rats with Spinal Cord Injury
inferred← citeshttps://doi.org/10.1007/s10616-012-9481-yopenalex-snapshot
Beyond annexin V: fluorescence response of cellular membranes to apoptosis
inferred← citeshttps://doi.org/10.1007/s10637-017-0489-1openalex-snapshot
Synthesis, characterization, and evaluation of Cd[L-proline]2, a novel histone deacetylase inhibitor that induces epigenetic modification of histone deacetylase isoforms in A549 cells
inferred← citeshttps://doi.org/10.1007/s10646-012-0977-1openalex-snapshot
Pyrosequencing-based transcriptomic resources in the pond snail Lymnaea stagnalis, with a focus on genes involved in molecular response to diquat-induced stress
inferred← citeshttps://doi.org/10.1007/s10753-014-0012-1openalex-snapshot
Proapoptotic Activity of a Monomeric Smac Mimetic on Human Fibroblast-Like Synoviocytes from Patients with Rheumatoid Arthritis
inferred← citeshttps://doi.org/10.1007/s10815-018-1319-xopenalex-snapshot
Magnetic-activated cell sorting is not completely effective at reducing sperm DNA fragmentation
showing the first 200 of 1785 · page through all 1785
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.