On the public citation graph
Notch signaling and Notch signaling modifiers
0 signed · 227 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bies.10300openalex-snapshot
The pleiotropic functions of the Y‐box‐binding protein, YB‐1
inferredcites →https://doi.org/10.1002/jcp.10208openalex-snapshot
HES and HERP families: Multiple effectors of the notch signaling pathway
inferredcites →https://doi.org/10.1002/jnr.20625openalex-snapshot
Amyloid precursor protein interacts with notch receptors
inferredcites →https://doi.org/10.1006/dbio.1997.8723openalex-snapshot
Requirement for Dynamin during Notch Signaling inDrosophilaNeurogenesis
inferredcites →https://doi.org/10.1006/dbio.2001.0482openalex-snapshot
scabrous Modifies Epithelial Cell Adhesion and Extends the Range of Lateral Signalling during Development of the Spaced Bristle Pattern in Drosophila
inferredcites →https://doi.org/10.1016/0092-8674(85)90229-6openalex-snapshot
Nucleotide sequence from the neurogenic locus Notch implies a gene product that shares homology with proteins containing EGF-like repeats
inferredcites →https://doi.org/10.1016/0092-8674(89)90060-3openalex-snapshot
Cell autonomy of lin-12 function in a cell fate decision in C. elegans
inferredcites →https://doi.org/10.1016/j.bbamcr.2011.03.004openalex-snapshot
The EGF-like proteins DLK1 and DLK2 function as inhibitory non-canonical ligands of NOTCH1 receptor that modulate each other's activities
inferredcites →https://doi.org/10.1016/j.bbrc.2008.02.010openalex-snapshot
Inhibitory effect of CT domain of CCN3/NOV on proliferation and differentiation of osteogenic mesenchymal stem cells, Kusa-A1
inferredcites →https://doi.org/10.1016/j.cell.2009.03.045openalex-snapshot
The Canonical Notch Signaling Pathway: Unfolding the Activation Mechanism
inferredcites →https://doi.org/10.1016/j.devcel.2009.03.010openalex-snapshot
Notch Signaling: The Core Pathway and Its Posttranslational Regulation
inferredcites →https://doi.org/10.1016/j.eururo.2008.03.006openalex-snapshot
Delta-Like 1 (Dlk-1), a Novel Marker of Prostate Basal and Candidate Epithelial Stem Cells, Is Downregulated by Notch Signalling in Intermediate/Transit Amplifying Cells of the Human Prostate
inferredcites →https://doi.org/10.1016/j.jmb.2006.09.071openalex-snapshot
Quantitative Dissection of the Notch:CSL Interaction: Insights into the Notch-mediated Transcriptional Switch
inferredcites →https://doi.org/10.1016/j.jmb.2006.10.043openalex-snapshot
The EGF-like Protein dlk1 Inhibits Notch Signaling and Potentiates Adipogenesis of Mesenchymal Cells
inferredcites →https://doi.org/10.1016/j.molcel.2004.10.014openalex-snapshot
Mastermind Recruits CycC:CDK8 to Phosphorylate the Notch ICD and Coordinate Activation with Turnover
inferredcites →https://doi.org/10.1016/j.mvr.2008.01.001openalex-snapshot
Microfibril-associate glycoprotein-2 (MAGP-2) promotes angiogenic cell sprouting by blocking notch signaling in endothelial cells
inferredcites →https://doi.org/10.1016/j.neuron.2011.02.031openalex-snapshot
Notch in the Vertebrate Nervous System: An Old Dog with New Tricks
inferredcites →https://doi.org/10.1016/j.tibs.2008.07.006openalex-snapshot
The CCN family of proteins: structure–function relationships
inferredcites →https://doi.org/10.1016/j.yexcr.2004.10.001openalex-snapshot
dlk acts as a negative regulator of Notch1 activation through interactions with specific EGF-like repeats
inferredcites →https://doi.org/10.1016/s0070-2153(10)92003-6openalex-snapshot
Canonical and Non-Canonical Notch Ligands
inferredcites →https://doi.org/10.1016/s0092-8674(03)00810-9openalex-snapshot
F3/Contactin Acts as a Functional Ligand for Notch during Oligodendrocyte Maturation
inferredcites →https://doi.org/10.1016/s0945-053x(98)90100-7openalex-snapshot
Two-hybrid analysis reveals multiple direct interactions for thrombospondin 1
inferredcites →https://doi.org/10.1016/s0960-9822(00)00577-7openalex-snapshot
Mastermind is a putative activator for Notch
inferredcites →https://doi.org/10.1016/s0960-9822(01)00527-9openalex-snapshot
Neuralized functions as an E3 ubiquitin ligase during Drosophila development
inferredcites →https://doi.org/10.1016/s1097-2765(00)80417-7openalex-snapshot
A Novel Proteolytic Cleavage Involved in Notch Signaling
inferredcites →https://doi.org/10.1016/s1097-2765(04)00120-0openalex-snapshot
Anchoring Notch Genetics and Biochemistry
inferredcites →https://doi.org/10.1016/s1534-5807(01)00091-0openalex-snapshot
Xenopus Neuralized Is a Ubiquitin Ligase that Interacts with XDelta1 and Regulates Notch Signaling
inferredcites →https://doi.org/10.1016/s1534-5807(01)00092-2openalex-snapshot
Drosophila Neuralized Is a Ubiquitin Ligase that Promotes the Internalization and Degradation of Delta
inferredcites →https://doi.org/10.1016/s1534-5807(01)00093-4openalex-snapshot
neuralized Encodes a Peripheral Membrane Protein Involved in Delta Signaling and Endocytosis
inferredcites →https://doi.org/10.1016/s1534-5807(02)00409-4openalex-snapshot
Mind Bomb Is a Ubiquitin Ligase that Is Essential for Efficient Activation of Notch Signaling by Delta
inferredcites →https://doi.org/10.1038/368150a0openalex-snapshot
Sequence of C. elegans lag-2 reveals a cell-signalling domain shared with Delta and Serrate of Drosophila
inferredcites →https://doi.org/10.1038/383707a0openalex-snapshot
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
inferredcites →https://doi.org/10.1038/74307openalex-snapshot
Mutations in the human Delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis
inferredcites →https://doi.org/10.1038/82644openalex-snapshot
MAML1, a human homologue of Drosophila Mastermind, is a transcriptional co-activator for NOTCH receptors
inferredcites →https://doi.org/10.1038/embor.2009.81openalex-snapshot
Y‐box protein‐1 is actively secreted through a non‐classical pathway and acts as an extracellular mitogen
inferredcites →https://doi.org/10.1038/nature02157openalex-snapshot
Delta-promoted filopodia mediate long-range lateral inhibition in Drosophila
inferredcites →https://doi.org/10.1038/nature02190openalex-snapshot
Notch activity acts as a sensor for extracellular calcium during vertebrate left–right determination
inferredcites →https://doi.org/10.1038/nature03940openalex-snapshot
Mutations in NOTCH1 cause aortic valve disease
inferredcites →https://doi.org/10.1038/nature05313openalex-snapshot
Inhibition of Dll4 signalling inhibits tumour growth by deregulating angiogenesis
inferredcites →https://doi.org/10.1038/nature05355openalex-snapshot
Blockade of Dll4 inhibits tumour growth by promoting non-productive angiogenesis
inferredcites →https://doi.org/10.1038/ncb1896openalex-snapshot
Epidermal growth factor-like domain 7 (EGFL7) modulates Notch signalling and affects neural stem cell renewal
inferredcites →https://doi.org/10.1038/ng0797-235openalex-snapshot
Mutations in the human Jagged1 gene are responsible for Alagille syndrome
inferredcites →https://doi.org/10.1038/ng0797-243openalex-snapshot
Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1
inferredcites →https://doi.org/10.1038/nn1492openalex-snapshot
DNER acts as a neuron-specific Notch ligand during Bergmann glial development
inferredcites →https://doi.org/10.1038/nsmb1227openalex-snapshot
Structural basis for autoinhibition of Notch
inferredcites →https://doi.org/10.1073/pnas.0407290101openalex-snapshot
Haploinsufficiency of delta-like 4 ligand results in embryonic lethality due to major defects in arterial and vascular development
inferredcites →https://doi.org/10.1073/pnas.091584598openalex-snapshot
Vascular patterning defects associated with expression of activated Notch4 in embryonic endothelium
inferredcites →https://doi.org/10.1073/pnas.95.14.8108openalex-snapshot
The Notch1 receptor is cleaved constitutively by a furin-like convertase
inferredcites →https://doi.org/10.1074/jbc.274.46.32961openalex-snapshot
Mouse Jagged1 Physically Interacts with Notch2 and Other Notch Receptors
inferredcites →https://doi.org/10.1074/jbc.m008925200openalex-snapshot
Extracellular Matrix Metalloproteinase 2 Levels Are Regulated by the Low Density Lipoprotein-related Scavenger Receptor and Thrombospondin 2
inferredcites →https://doi.org/10.1074/jbc.m104533200openalex-snapshot
Protein Interaction Studies of MAGP-1 with Tropoelastin and Fibrillin-1
inferredcites →https://doi.org/10.1074/jbc.m107234200openalex-snapshot
Murine Notch Homologs (N1–4) Undergo Presenilin-dependent Proteolysis
inferredcites →https://doi.org/10.1074/jbc.m109.046599openalex-snapshot
YB-1 Acts as a Ligand for Notch-3 Receptors and Modulates Receptor Activation
inferredcites →https://doi.org/10.1074/jbc.m110.144634openalex-snapshot
Low Density Lipoprotein Receptor-related Protein-1 (LRP1) Regulates Thrombospondin-2 (TSP2) Enhancement of Notch3 Signaling
inferredcites →https://doi.org/10.1074/jbc.m203727200openalex-snapshot
The Nephroblastoma Overexpressed Gene (NOV/ccn3) Protein Associates with Notch1 Extracellular Domain and Inhibits Myoblast Differentiation via Notch Signaling Pathway
inferredcites →https://doi.org/10.1074/jbc.m206363200openalex-snapshot
Microfibril-associated Glycoprotein-2 Interacts with Fibrillin-1 and Fibrillin-2 Suggesting a Role for MAGP-2 in Elastic Fiber Assembly
inferredcites →https://doi.org/10.1074/jbc.m312337200openalex-snapshot
Mouse Fbw7/Sel-10/Cdc4 Is Required for Notch Degradation during Vascular Development
inferredcites →https://doi.org/10.1074/jbc.m313505200openalex-snapshot
NB-3/Notch1 Pathway via Deltex1 Promotes Neural Progenitor Cell Differentiation into Oligodendrocytes
inferredcites →https://doi.org/10.1074/jbc.m500273200openalex-snapshot
The Extracellular Matrix Protein MAGP-2 Interacts with Jagged1 and Induces Its Shedding from the Cell Surface
inferredcites →https://doi.org/10.1074/jbc.m600298200openalex-snapshot
Microfibrillar Proteins MAGP-1 and MAGP-2 Induce Notch1 Extracellular Domain Dissociation and Receptor Activation
inferredcites →https://doi.org/10.1074/jbc.m708424200openalex-snapshot
Localization of the Delta-like-1-binding Site in Human Notch-1 and Its Modulation by Calcium Affinity
inferredcites →https://doi.org/10.1074/jbc.m803650200openalex-snapshot
Thrombospondin 2 Potentiates Notch3/Jagged1 Signaling
inferredcites →https://doi.org/10.1083/jcb.200407100openalex-snapshot
The adhesion force of Notch with Delta and the rate of Notch signaling
inferredcites →https://doi.org/10.1083/jcb.200609014openalex-snapshot
DSL ligand endocytosis physically dissociates Notch1 heterodimers before activating proteolysis can occur
inferredcites →https://doi.org/10.1086/505332openalex-snapshot
NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway
inferredcites →https://doi.org/10.1091/mbc.8.9.1751openalex-snapshot
Functional domains of LAG-2, a putative signaling ligand for LIN-12 and GLP-1 receptors in Caenorhabditis elegans.
inferredcites →https://doi.org/10.1093/emboj/cdf541openalex-snapshot
Presenilins mediate a dual intramembranous γ‐secretase cleavage of Notch‐1
inferredcites →https://doi.org/10.1093/hmg/10.2.163openalex-snapshot
Familial Tetralogy of Fallot caused by mutation in the jagged1 gene
inferredcites →https://doi.org/10.1093/hmg/8.5.723openalex-snapshot
Embryonic Lethality and Vascular Defects in Mice Lacking the Notch Ligand Jagged1
inferredcites →https://doi.org/10.1093/hmg/ddp211openalex-snapshot
CADASIL mutations enhance spontaneous multimerization of NOTCH3
inferredcites →https://doi.org/10.1093/hmg/ddp468openalex-snapshot
Mutations in NOTCH3 cause the formation and retention of aggregates in the endoplasmic reticulum, leading to impaired cell proliferation
inferredcites →https://doi.org/10.1093/jn/136.12.2953openalex-snapshot
Pref-1, a Preadipocyte Secreted Factor That Inhibits Adipogenesis
inferredcites →https://doi.org/10.1101/gad.14.11.1343openalex-snapshot
Notch signaling is essential for vascular morphogenesis in mice
inferredcites →https://doi.org/10.1101/gad.3.8.1099openalex-snapshot
Notch is required for successive cell decisions in the developing Drosophila retina.
inferredcites →https://doi.org/10.1101/gad.308904openalex-snapshot
Notch3 is required for arterial identity and maturation of vascular smooth muscle cells
inferredcites →https://doi.org/10.1111/j.1538-7836.2005.01371.xopenalex-snapshot
Beyond endocytosis: LRP function in cell migration, proliferation and vascular permeability
inferredcites →https://doi.org/10.1126/science.1102160openalex-snapshot
Activating Mutations of NOTCH1 in Human T Cell Acute Lymphoblastic Leukemia
inferredcites →https://doi.org/10.1126/science.1136031openalex-snapshot
NOV (CCN3) Functions as a Regulator of Human Hematopoietic Stem or Progenitor Cells
inferredcites →https://doi.org/10.1128/mcb.20.5.1825-1835.2000openalex-snapshot
Calcium Depletion Dissociates and Activates Heterodimeric Notch Receptors
inferredcites →https://doi.org/10.1128/mcb.24.8.3505-3513.2004openalex-snapshot
Dual Roles for the Notch Target Gene Hes-1 in the Differentiation of 3T3-L1 Preadipocytes
inferredcites →https://doi.org/10.1128/mcb.6.9.3094openalex-snapshot
Sequence of the notch locus of Drosophila melanogaster: relationship of the encoded protein to mammalian clotting and growth factors.
inferredcites →https://doi.org/10.1152/physiolgenomics.00078.2009openalex-snapshot
Lack of periostin leads to suppression of Notch1 signaling and calcific aortic valve disease
inferredcites →https://doi.org/10.1158/0008-5472.can-07-0969openalex-snapshot
Delta-like 4 Notch Ligand Regulates Tumor Angiogenesis, Improves Tumor Vascular Function, and Promotes Tumor Growth In vivo
inferredcites →https://doi.org/10.1159/000324209openalex-snapshot
Extracellular YB-1 Blockade in Experimental Nephritis Upregulates Notch-3 Receptor Expression and Signaling
inferredcites →https://doi.org/10.1161/01.cir.0000160870.93058.ddopenalex-snapshot
Essential Role of Endothelial Notch1 in Angiogenesis
inferredcites →https://doi.org/10.1161/atvbaha.110.203356openalex-snapshot
CCN3 Inhibits Neointimal Hyperplasia Through Modulation of Smooth Muscle Cell Growth and Migration
inferredcites →https://doi.org/10.1161/circresaha.109.213785openalex-snapshot
Gene Deletion Screen for Cardiomyopathy in Adult Drosophila Identifies a New Notch Ligand
inferredcites →https://doi.org/10.1172/jci15924openalex-snapshot
Inhibition of adipogenesis and development of glucose intolerance by soluble preadipocyte factor–1 (Pref-1)
inferredcites →https://doi.org/10.1172/jci30070openalex-snapshot
An essential role for Notch in neural crest during cardiovascular development and smooth muscle differentiation
inferredcites →https://doi.org/10.1182/blood-2010-03-274860openalex-snapshot
Impaired angiogenesis and altered Notch signaling in mice overexpressing endothelial Egfl7
inferredcites →https://doi.org/10.1186/1471-213x-8-11openalex-snapshot
The atypical mammalian ligand Delta-like homologue 1 (Dlk1) can regulate Notch signalling in Drosophila
inferredcites →https://doi.org/10.1186/1471-213x-8-18openalex-snapshot
Abnormal skeletal and cardiac development, cardiomyopathy, muscle atrophy and cataracts in mice with a targeted disruption of the Nov (Ccn3) gene
inferredcites →https://doi.org/10.1186/1745-6150-2-19openalex-snapshot
The intracellular region of Notch ligands: does the tail make the difference?
inferredcites →https://doi.org/10.1242/dev.01413openalex-snapshot
Drosophila Epsin mediates a select endocytic pathway that DSL ligands must enter to activate Notch
inferredcites →https://doi.org/10.1242/dev.01434openalex-snapshot
Fat facets and Liquid facets promote Delta endocytosis and Delta signaling in the signaling cells
inferredcites →https://doi.org/10.1242/dev.01459openalex-snapshot
Epsin potentiatesNotchpathway activity inDrosophilaandC. elegans
inferredcites →https://doi.org/10.1242/dev.01789openalex-snapshot
The roles of receptor and ligand endocytosis in regulating Notch signaling
inferredcites →https://doi.org/10.1242/dev.01922openalex-snapshot
Mind bomb 1 is essential for generating functional Notch ligands to activate Notch
inferredcites →https://doi.org/10.1242/dev.120.10.2913openalex-snapshot
lag-2 may encode a signaling ligand for the GLP-1 and LIN-12 receptors of C. elegans
inferredcites →https://doi.org/10.1242/dev.121.12.4275openalex-snapshot
Interchangeability of Caenorhabditis elegans DSL proteins and intrinsic signalling activity of their extracellular domains in vivo
inferredcites →https://doi.org/10.1242/dev.127.7.1373openalex-snapshot
Ligand endocytosis drives receptor dissociation and activation in the Notch pathway
inferredcites →https://doi.org/10.1242/dev.128.4.491openalex-snapshot
Defects in development of the kidney, heart and eye vasculature in mice homozygous for a hypomorphic Notch2 mutation
inferredcites →https://doi.org/10.1242/jcs.112.19.3289openalex-snapshot
Ligand-receptor interactions and trans-endocytosis of Delta, Serrate and Notch: members of the Notch signalling pathway in Drosophila
inferredcites →https://doi.org/10.1371/journal.pbio.0060196openalex-snapshot
OSM-11 Facilitates LIN-12 Notch Signaling during Caenorhabditis elegans Vulval Development
inferredcites →https://doi.org/10.1371/journal.pone.0012234openalex-snapshot
Periostin Associates with Notch1 Precursor to Maintain Notch1 Expression under a Stress Condition in Mouse Cells
inferredcites →https://doi.org/10.1634/stemcells.2007-0106openalex-snapshot
Morphological and Functional Characterization of Predifferentiation of Myelinating Glia-Like Cells from Human Bone Marrow Stromal Cells Through Activation of F3/Notch Signaling in Mouse Retina
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.4768258openalex-extracted
Microenvironmental Entropy Dynamics Analysis Reveals Novel Insights In Notch-Delta-Jagged Decision-Making Mechanism
inferred← citeshttps://doi.org/10.1002/bdr2.2183openalex-snapshot
Molecular insights of KMT2D and clinical aspects of Kabuki syndrome type 1
inferred← citeshttps://doi.org/10.1002/cnm.3323openalex-snapshot
Lateral induction limits the impact of cell connectivity on Notch signaling in arterial walls
inferred← citeshttps://doi.org/10.1002/dvdy.24386openalex-snapshot
Proper notch activity is necessary for the establishment of proximal cells and differentiation of intermediate, distal, and connecting tubule in Xenopus pronephros development
inferred← citeshttps://doi.org/10.1002/mc.23937openalex-snapshot
Reduced JAG1 Expression Through miR‐200 Overexpression or Crispr‐Cas Mediated Knockout Impairs TNBC Growth and Metastasis
inferred← citeshttps://doi.org/10.1002/mgg3.921openalex-snapshot
Gene expression profiles and bioinformatics analysis of insulin‐like growth factor‐1 promotion of osteogenic differentiation
inferred← citeshttps://doi.org/10.1002/path.4101openalex-snapshot
Notch3 and kidney injury: never two without three
inferred← citeshttps://doi.org/10.1002/rco2.70052openalex-snapshot
A Possible Association of Elevated Delta‐Like Protein 4 Concentration With Low Walking Speed and Low Handgrip Strength in Japanese Older Adults
inferred← citeshttps://doi.org/10.1007/82_2012_229openalex-snapshot
The Notch Pathway in Hematopoietic Stem Cells
inferred← citeshttps://doi.org/10.1007/978-3-030-48457-6_9openalex-snapshot
Tenascin-C Function in Glioma: Immunomodulation and Beyond
inferred← citeshttps://doi.org/10.1007/978-3-030-80962-1_273-1openalex-snapshot
Vascular Modulation of Antitumor Immunity: A Crosstalk Between Immune Cells and the Tumor Vasculature
inferred← citeshttps://doi.org/10.1007/978-3-032-00761-2_273openalex-snapshot
Vascular Modulation of Antitumor Immunity: A Crosstalk Between Immune Cells and the Tumor Vasculature
inferred← citeshttps://doi.org/10.1007/s00432-013-1534-xopenalex-snapshot
Dll4-Notch signaling in regulation of tumor angiogenesis
inferred← citeshttps://doi.org/10.1007/s00432-021-03604-8openalex-snapshot
A review: hippo signaling pathway promotes tumor invasion and metastasis by regulating target gene expression
inferred← citeshttps://doi.org/10.1007/s10072-024-07908-8openalex-snapshot
NOTCH3 variants of unknown significance underpin vascular dysfunction in neurodegenerative disease: a case series of three nfvPPA-FTD patients
inferred← citeshttps://doi.org/10.1007/s10495-015-1188-zopenalex-snapshot
Role of CSL-dependent and independent Notch signaling pathways in cell apoptosis
inferred← citeshttps://doi.org/10.1007/s11864-021-00834-3openalex-snapshot
Drug Development in Neuroendocrine Tumors: What Is on the Horizon?
inferred← citeshttps://doi.org/10.1007/s12035-019-01706-6openalex-snapshot
μ Opioid Receptor-Triggered Notch-1 Activation Contributes to Morphine Tolerance: Role of Neuron–Glia Communication
inferred← citeshttps://doi.org/10.1007/s12185-026-04263-6openalex-snapshot
Pediatric T-cell lymphoblastic lymphoma with t(9;17)(q34;q23)-associated N-terminally truncated NOTCH1 activation: a case report
inferred← citeshttps://doi.org/10.1007/s12195-021-00694-9openalex-snapshot
Epithelial-to-Mesenchymal Transition Signaling Pathways Responsible for Breast Cancer Metastasis
inferred← citeshttps://doi.org/10.1007/s12975-021-00908-2openalex-snapshot
Electrophilic and Drug-Induced Stimulation of NOTCH3 N-terminal Fragment Oligomerization in Cerebrovascular Pathology
inferred← citeshttps://doi.org/10.1016/bs.pbr.2016.03.005openalex-snapshot
Mechanisms of cellular plasticity in cerebral perivascular region
inferred← citeshttps://doi.org/10.1016/j.ajpath.2020.11.015openalex-snapshot
Overlapping Protein Accumulation Profiles of CADASIL and CAA
inferred← citeshttps://doi.org/10.1016/j.aqrep.2023.101537openalex-snapshot
Cloning of notch1 and its role in the growth and development of Exopalaemon carinicauda
inferred← citeshttps://doi.org/10.1016/j.bcp.2012.05.013openalex-snapshot
β,β-Dimethylacrylshikonin exerts antitumor activity via Notch-1 signaling pathway in vitro and in vivo
inferred← citeshttps://doi.org/10.1016/j.biocel.2013.03.020openalex-snapshot
Collagen represses canonical Notch signaling and binds to Notch ectodomain
inferred← citeshttps://doi.org/10.1016/j.biochi.2018.04.020openalex-snapshot
Notch3 is involved in adipogenesis of human adipose-derived stromal/stem cells
inferred← citeshttps://doi.org/10.1016/j.biopha.2020.110416openalex-snapshot
The oncogenic role of Jagged1/Notch signaling in cancer
inferred← citeshttps://doi.org/10.1016/j.canlet.2017.11.033openalex-snapshot
Stanniocalcin-1 augments stem-like traits of glioblastoma cells through binding and activating NOTCH1
inferred← citeshttps://doi.org/10.1016/j.ccmp.2023.100114openalex-snapshot
Phytochemical Loaded Nanovehicles of Biopolymer for Breast Cancer: A Systemic Review
inferred← citeshttps://doi.org/10.1016/j.clindermatol.2012.08.014openalex-snapshot
Melanocytes, melanocyte stem cells, and melanoma stem cells
inferred← citeshttps://doi.org/10.1016/j.cpt.2024.01.001openalex-snapshot
Despicable role of epithelial–mesenchymal transition in breast cancer metastasis: Exhibiting de novo restorative regimens
inferred← citeshttps://doi.org/10.1016/j.cub.2014.07.054openalex-snapshot
Uninflatable and Notch Control the Targeting of Sara Endosomes during Asymmetric Division
inferred← citeshttps://doi.org/10.1016/j.cub.2015.02.053openalex-snapshot
Uninflatable and Notch Control the Targeting of Sara Endosomes during Asymmetric Division
inferred← citeshttps://doi.org/10.1016/j.ejphar.2018.02.051openalex-snapshot
Novel Insights on Notch signaling pathways in liver fibrosis
inferred← citeshttps://doi.org/10.1016/j.htct.2024.02.016openalex-snapshot
Exploring novel protein biomarkers for early-stage diagnosis and prognosis of T-acute lymphoblastic leukemia (T-ALL)
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2017.01.067openalex-snapshot
The non-canonical NOTCH1 ligand Delta-like 1 homolog (DLK1) self interacts in mammals
inferred← citeshttps://doi.org/10.1016/j.isci.2024.110569openalex-snapshot
Microenvironmental entropy dynamics analysis reveals novel insights into Notch-Delta-Jagged decision-making mechanism
inferred← citeshttps://doi.org/10.1016/j.jmbbm.2022.105325openalex-snapshot
Computational analysis of the role of mechanosensitive Notch signaling in arterial adaptation to hypertension
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2016.12.003openalex-snapshot
The bad seed gardener: Deubiquitinases in the cancer stem-cell signaling network and therapeutic resistance
inferred← citeshttps://doi.org/10.1016/j.semcdb.2023.06.007openalex-snapshot
Pathophysiological roles of thrombospondin-4 in disease development
inferred← citeshttps://doi.org/10.1016/j.ydbio.2012.01.017openalex-snapshot
A comprehensive analysis of Delta signaling in pre-gastrular sea urchin embryos
inferred← citeshttps://doi.org/10.1016/j.yjmcc.2012.03.007openalex-snapshot
Notch signaling and cardiac repair
inferred← citeshttps://doi.org/10.1021/pr501174popenalex-snapshot
Glycomic Analysis of Membrane Glycoproteins with Bisecting Glycosylation from Ovarian Cancer Tissues Reveals Novel Structures and Functions
inferred← citeshttps://doi.org/10.1038/s41598-024-71634-6openalex-snapshot
Notch1 Phase Separation Coupled Percolation facilitates target gene expression and enhancer looping
inferred← citeshttps://doi.org/10.1038/srep27985openalex-snapshot
A humanized anti-DLL4 antibody promotes dysfunctional angiogenesis and inhibits breast tumor growth
inferred← citeshttps://doi.org/10.1073/pnas.1416287112openalex-snapshot
Jagged–Delta asymmetry in Notch signaling can give rise to a Sender/Receiver hybrid phenotype
inferred← citeshttps://doi.org/10.1080/19336918.2015.1008333openalex-snapshot
Transcriptional regulation of tenascin genes
inferred← citeshttps://doi.org/10.1088/1367-2630/17/5/055021openalex-snapshot
Operating principles of Notch–Delta–Jagged module of cell–cell communication
inferred← citeshttps://doi.org/10.1089/dna.2018.4478openalex-snapshot
BMP9 Promotes the Extracellular Matrix of Nucleus Pulposus Cells via Inhibition of the Notch Signaling Pathway
inferred← citeshttps://doi.org/10.1096/fj.14-252379openalex-snapshot
Factor‐inhibiting HIF‐1 (FIH‐1) is required for human vascular endothelial cell survival
inferred← citeshttps://doi.org/10.1096/fj.202302014rrropenalex-snapshot
Acute exposure to electronic cigarette components alters mRNA expression of pre‐osteoblasts
inferred← citeshttps://doi.org/10.1096/fj.202402545ropenalex-snapshot
Notch signaling pathway in osteogenesis, bone development, metabolism, and diseases
inferred← citeshttps://doi.org/10.1097/wnr.0000000000000725openalex-snapshot
Crosstalk between Notch and Sonic hedgehog signaling in a mouse model of amyotrophic lateral sclerosis
inferred← citeshttps://doi.org/10.1101/2025.02.11.637745openalex-snapshot
Cell-Cell Communication and Gene Regulation of Stem Cell-Parenchymal Cell Fusion
inferred← citeshttps://doi.org/10.1111/ajt.15141openalex-snapshot
Circulating delta-like Notch ligand 1 is correlated with cardiac allograft vasculopathy and suppressed in heart transplant recipients on everolimus-based immunosuppression
inferred← citeshttps://doi.org/10.1111/cga.12039openalex-snapshot
Molecular and cellular mechanisms of development underlying congenital diseases
inferred← citeshttps://doi.org/10.1111/exd.13856openalex-snapshot
Regulation of melanocyte stem cells in the pigmentation of skin and its appendages: Biological patterning and therapeutic potentials
inferred← citeshttps://doi.org/10.1111/jne.12172openalex-snapshot
Activity‐Dependent Notch Signalling in the Hypothalamic‐Neurohypophysial System of Adult Mouse Brains
inferred← citeshttps://doi.org/10.1111/joa.12232openalex-snapshot
Cell and matrix modulation in prenatal and postnatal equine growth cartilage, zones of Ranvier and articular cartilage
inferred← citeshttps://doi.org/10.1128/mbio.00076-22openalex-snapshot
Ehrlichia SLiM Ligand Mimetic Activates Notch Signaling in Human Monocytes
inferred← citeshttps://doi.org/10.1159/000369069openalex-snapshot
Delta-Like 1 Homologue (DLK1) Protein in Neurons of the Arcuate Nucleus That Control Weight Homeostasis and Effect of Fasting on Hypothalamic DLK1 mRNA
inferred← citeshttps://doi.org/10.11606/t.43.2015.tde-07042015-151144openalex-snapshot
Tópicos em sinalização celular e bioinformática: Princípios de funcionamento do circuito de sinalização Notch e aprendizagem supervisionada variacional de relevância
inferred← citeshttps://doi.org/10.1177/1010428317694320openalex-snapshot
Crocodile choline from Crocodylus siamensis induces apoptosis of human gastric cancer
inferred← citeshttps://doi.org/10.1186/s12861-019-0199-3openalex-snapshot
A modifier in the 129S2/SvPasCrl genome is responsible for the viability of Notch1[12f/12f] mice
inferred← citeshttps://doi.org/10.1186/s12964-025-02190-3openalex-snapshot
Regulation of Notch signaling by multiple Ankyrin repeat containing protein Mask
inferred← citeshttps://doi.org/10.1186/s13046-020-01669-wopenalex-snapshot
Aspartate β-hydroxylase as a target for cancer therapy
inferred← citeshttps://doi.org/10.1186/s13058-014-0513-8openalex-snapshot
Loss of periostin/OSF-2 in ErbB2/Neu-driven tumors results in androgen receptor-positive molecular apocrine-like tumors with reduced Notch1 activity
inferred← citeshttps://doi.org/10.1186/s13072-021-00412-9openalex-snapshot
SUMOylated non-canonical polycomb PRC1.6 complex as a prerequisite for recruitment of transcription factor RBPJ
inferred← citeshttps://doi.org/10.1186/s40001-025-02626-zopenalex-snapshot
Current research of the Notch pathway in hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1210/er.2014-1101openalex-snapshot
The Mammalian Blood-Testis Barrier: Its Biology and Regulation
inferred← citeshttps://doi.org/10.1242/dev.141762openalex-snapshot
Drosophila Crumbs prevents ectopic Notch activation in developing wings by inhibiting ligand-independent endocytosis
inferred← citeshttps://doi.org/10.12775/jehs.2022.12.08.074openalex-snapshot
Molecular biology of the cell
inferred← citeshttps://doi.org/10.12998/wjcc.v10.i18.6277openalex-snapshot
De novo brain arteriovenous malformation formation and development: A case report
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1010169openalex-snapshot
A new model of Notch signalling: Control of Notch receptor cis-inhibition via Notch ligand dimers
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1012825openalex-snapshot
A model of Notch signalling control of angiogenesis: Evidence of a role for Notch ligand heterodimerization
inferred← citeshttps://doi.org/10.1371/journal.pgen.1007153openalex-snapshot
AKAP200 promotes Notch stability by protecting it from Cbl/lysosome-mediated degradation in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1371/journal.pone.0095744openalex-snapshot
Competition in Notch Signaling with Cis Enriches Cell Fate Decisions
inferred← citeshttps://doi.org/10.1371/journal.pone.0157540openalex-snapshot
Genomic Characteristics of Genetic Creutzfeldt-Jakob Disease Patients with V180I Mutation and Associations with Other Neurodegenerative Disorders
inferred← citeshttps://doi.org/10.1371/journal.pone.0224941openalex-snapshot
Altered expression of Notch1 in Alzheimer's disease
inferred← citeshttps://doi.org/10.1387/ijdb.170202sbopenalex-snapshot
Developmental cell-cell communication pathways in the cephalochordate amphioxus: actors and functions
inferred← citeshttps://doi.org/10.1530/rep-13-0474openalex-snapshot
Fetal–maternal communication: the role of Notch signalling in embryo implantation
inferred← citeshttps://doi.org/10.1530/rep-18-0239openalex-snapshot
Regulation of GDNF expression in Sertoli cells
inferred← citeshttps://doi.org/10.1590/1414-431x20133177openalex-snapshot
Role of Notch signaling in the mammalian heart
inferred← citeshttps://doi.org/10.2147/ott.s224465openalex-snapshot
Self-Renewal Signalling Pathway Inhibitors: Perspectives on Therapeutic Approaches for Cancer Stem Cells
inferred← citeshttps://doi.org/10.2147/ott.s244860openalex-snapshot
The Role of DLLs in Cancer: A Novel Therapeutic Target
inferred← citeshttps://doi.org/10.2217/epi-2023-0270openalex-snapshot
The Epigenetics Orchestra of Notch Signaling: A Symphony for Cancer Therapy
inferred← citeshttps://doi.org/10.26442/00403660.2018.12.000014openalex-snapshot
Notch signal pathway - therapeutic target for regulation of reparative processes in the heart
inferred← citeshttps://doi.org/10.3389/fbioe.2023.1217211openalex-snapshot
Biomedical engineering approaches for the delivery of JAGGED1 as a potential tissue regenerative therapy
inferred← citeshttps://doi.org/10.3389/fcell.2019.00119openalex-snapshot
Modulation of Nerve Cell Differentiation: Role of Polyphenols and of Contactin Family Components
inferred← citeshttps://doi.org/10.3389/fonc.2013.00273openalex-snapshot
Disruption of Prostate Epithelial Differentiation Pathways and Prostate Cancer Development
inferred← citeshttps://doi.org/10.3389/fonc.2022.971462openalex-snapshot
Matricellular protein tenascin C: Implications in glioma progression, gliomagenesis, and treatment
inferred← citeshttps://doi.org/10.3389/fonc.2024.1431418openalex-snapshot
Targeted therapy approaches for epithelial-mesenchymal transition in triple negative breast cancer
inferred← citeshttps://doi.org/10.3390/app16073403openalex-snapshot
Effects of Physical Stimulation and Bioactive Agents in Bone Regenerative Medicine: Recent Advances and Synergistic Approaches
inferred← citeshttps://doi.org/10.3390/biom14040480openalex-snapshot
Mechanism of Notch Signaling Pathway in Malignant Progression of Glioblastoma and Targeted Therapy
inferred← citeshttps://doi.org/10.3390/cancers11030292openalex-snapshot
Role of Notch Signaling Pathway in Glioblastoma Pathogenesis
inferred← citeshttps://doi.org/10.3390/cancers12113253openalex-snapshot
Deubiquitinating Enzyme-Mediated Signaling Networks in Cancer Stem Cells
inferred← citeshttps://doi.org/10.3390/cancers14040976openalex-snapshot
Dissecting Tumor Growth: The Role of Cancer Stem Cells in Drug Resistance and Recurrence
inferred← citeshttps://doi.org/10.3390/cancers14153786openalex-snapshot
The Role of PTEN in Epithelial–Mesenchymal Transition
inferred← citeshttps://doi.org/10.3390/cells14181428openalex-snapshot
The Colonic Crypt: Cellular Dynamics and Signaling Pathways in Homeostasis and Cancer
inferred← citeshttps://doi.org/10.3390/ijms22031325openalex-snapshot
Relevance of Notch Signaling for Bone Metabolism and Regeneration
inferred← citeshttps://doi.org/10.3390/jpm12121969openalex-snapshot
Overview on Common Genes Involved in the Onset of Glioma and on the Role of Migraine as Risk Factor: Predictive Biomarkers or Therapeutic Targets?
inferred← citeshttps://doi.org/10.3390/microorganisms10050846openalex-snapshot
Relationship between the Chromosome Structural Dynamics and Gene Expression—A Chicken and Egg Dilemma?
inferred← citeshttps://doi.org/10.3390/neurolint15040078openalex-snapshot
Headache and NOTCH3 Gene Variants in Patients with CADASIL
inferred← citeshttps://doi.org/10.3760/cma.j.issn.0366-6999.20130721openalex-snapshot
Activated Notch1 reduces myocardial ischemia reperfusion injury in vitro during ischemic postconditioning by crosstalk with the RISK signaling pathway
inferred← citeshttps://doi.org/10.4103/1673-5374.130083openalex-snapshot
Increased expression of Notch1 in temporal lobe epilepsy: animal models and clinical evidence
inferred← citeshttps://doi.org/10.4161/cc.23121openalex-snapshot
Stacking the DEK: From chromatin topology to cancer stem cells
inferred← citeshttps://doi.org/10.4172/2168-9431.1000147openalex-snapshot
Duchenne Muscular Dystrophy (DMD): Should it be Considered a Systemic Disease?
inferred← citeshttps://doi.org/10.52155/ijpsat.v34.1.4557openalex-snapshot
Updates of Role of Stem Cells in Cancer Therapy
inferred← citeshttps://doi.org/10.54289/jcrmh2300135openalex-snapshot
The Special Role of JAK/STAT, and Notch Signaling Pathways in Cancer Pathogenesis
inferred← citeshttps://doi.org/10.6084/m9.figshare.15087482openalex-snapshot
Additional file 2 of SUMOylated non-canonical polycomb PRC1.6 complex as a prerequisite for recruitment of transcription factor RBPJ
inferred← citeshttps://doi.org/10.70675/8e4b1cfdzd2c7z4197zbda8z76e7ad8f87f5openalex-snapshot
Impact d'une exposition prénatale à l'alcool sur le développement de la rétine.
inferred← citeshttps://doi.org/10.70675/d4f13688z5749z4813zbab0ze3e1c13a644copenalex-snapshot
Dynamique du chromosome bactérien et expression génique chez la bactérie phytopathogène Dickeya dadantii
inferred← citeshttps://doi.org/10.70675/f9c5e21cz2cf8z424dz8a35z45035aaef298openalex-snapshot
Les effets des lipides exosomaux sur les cellules tumorales pancréatiques humaines : entre apoptose et survie
inferred← citeshttps://doi.org/10.7243/2052-7896-1-4openalex-snapshot
NOTCH2 expression is decreased in epithelial ovarian cancer and is related to the tumor histological subtype
inferred← citeshttps://doi.org/10.7275/7602425.0openalex-snapshot
The Role of NOTCH3 Signaling in T Helper Cell Differentiation and Induction of EAE
inferred← citeshttps://doi.org/10.7554/elife.07343openalex-snapshot
Logics and properties of a genetic regulatory program that drives embryonic muscle development in an echinoderm
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.