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Regulation of Notch signaling by E3 ubiquitin ligases
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ajmg.a.32401openalex-snapshot
Johanson–Blizzard syndrome: Report of a novel mutation and severe liver involvement
inferredcites →https://doi.org/10.1002/ajmg.a.32566openalex-snapshot
Johanson–Blizzard syndrome caused by identicalUBR1mutations in two unrelated girls, one with a cardiomyopathy
inferredcites →https://doi.org/10.1002/cbin.11089openalex-snapshot
Synergistic interaction of Deltex and Hrp48 leads to JNK activation
inferredcites →https://doi.org/10.1002/cbin.11521openalex-snapshot
Deltex cooperates with TRAF6 to promote apoptosis and cell migration through Eiger‐independent JNK activation in Drosophila
inferredcites →https://doi.org/10.1007/978-3-030-36422-9_7openalex-snapshot
Regulation of Notch Signaling in Drosophila melanogaster: The Role of the Heterogeneous Nuclear Ribonucleoprotein Hrp48 and Deltex
inferredcites →https://doi.org/10.1007/978-3-319-89512-3_8openalex-snapshot
Integration of Drosophila and Human Genetics to Understand Notch Signaling Related Diseases
inferredcites →https://doi.org/10.1007/s00018-012-1084-4openalex-snapshot
Balanced ubiquitination determines cellular responsiveness to extracellular stimuli
inferredcites →https://doi.org/10.1007/s00223-015-9967-7openalex-snapshot
Ubiquitin E3 Ligase LNX2 is Critical for Osteoclastogenesis In Vitro by Regulating M-CSF/RANKL Signaling and Notch2
inferredcites →https://doi.org/10.1007/s00438-005-0087-3openalex-snapshot
The first deltex null mutant indicates tissue-specific deltex-dependent Notch signaling in Drosophila
inferredcites →https://doi.org/10.1007/s004390000431openalex-snapshot
Chromosomal localization, genomic characterization, and mapping to the Noonan syndrome critical region of the human Deltex (DTX1) gene
inferredcites →https://doi.org/10.1016/j.ajhg.2010.01.028openalex-snapshot
Human ITCH E3 Ubiquitin Ligase Deficiency Causes Syndromic Multisystem Autoimmune Disease
inferredcites →https://doi.org/10.1016/j.ajhg.2020.11.018openalex-snapshot
UBR7 functions with UBR5 in the Notch signaling pathway and is involved in a neurodevelopmental syndrome with epilepsy, ptosis, and hypothyroidism
inferredcites →https://doi.org/10.1016/j.bbrc.2009.10.093openalex-snapshot
Alzheimer’s disease and Notch signaling
inferredcites →https://doi.org/10.1016/j.ccr.2014.02.018openalex-snapshot
From Fly Wings to Targeted Cancer Therapies: A Centennial for Notch Signaling
inferredcites →https://doi.org/10.1016/j.ceb.2006.06.009openalex-snapshot
Endosome dynamics during development
inferredcites →https://doi.org/10.1016/j.cell.2005.08.017openalex-snapshot
Asymmetric Rab11 Endosomes Regulate Delta Recycling and Specify Cell Fate in the Drosophila Nervous System
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.cellsig.2014.09.016openalex-snapshot
TRAF6 is a novel regulator of Notch signaling in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.cellsig.2018.05.003openalex-snapshot
Deltex interacts with Eiger and consequently influences the cell death in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/j.cub.2004.11.030openalex-snapshot
Regulation of Notch Endosomal Sorting and Signaling by Drosophila Nedd4 Family Proteins
inferredcites →https://doi.org/10.1016/j.cub.2004.12.028openalex-snapshot
Drosophila Nedd4 Regulates Endocytosis of Notch and Suppresses Its Ligand-Independent Activation
inferredcites →https://doi.org/10.1016/j.cub.2010.10.034openalex-snapshot
Mechanism and Significance of cis-Inhibition in Notch Signalling
inferredcites →https://doi.org/10.1016/j.devcel.2005.09.019openalex-snapshot
The Drosophila Tumor Suppressor vps25 Prevents Nonautonomous Overproliferation by Regulating Notch Trafficking
inferredcites →https://doi.org/10.1016/j.devcel.2005.09.020openalex-snapshot
Tumor Suppressor Properties of the ESCRT-II Complex Component Vps25 in Drosophila
inferredcites →https://doi.org/10.1016/j.devcel.2008.09.002openalex-snapshot
Drosophila HOPS and AP-3 Complex Genes Are Required for a Deltex-Regulated Activation of Notch in the Endosomal Trafficking Pathway
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.devcel.2012.04.005openalex-snapshot
Notch Ligand Endocytosis Generates Mechanical Pulling Force Dependent on Dynamin, Epsins, and Actin
inferredcites →https://doi.org/10.1016/j.devcel.2012.04.007openalex-snapshot
Optical Tweezers Studies on Notch: Single-Molecule Interaction Strength Is Independent of Ligand Endocytosis
inferredcites →https://doi.org/10.1016/j.gde.2009.04.005openalex-snapshot
Endocytic regulation of Notch signaling
inferredcites →https://doi.org/10.1016/j.mod.2011.02.002openalex-snapshot
Numb regulates Notch1, but not Notch3, during myogenesis
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.semcdb.2012.01.008openalex-snapshot
Endocytic routes to Notch activation
inferredcites →https://doi.org/10.1016/j.semcdb.2012.01.010openalex-snapshot
Notch signaling in human development and disease
inferredcites →https://doi.org/10.1016/j.ydbio.2005.10.008openalex-snapshot
Regulation of expression of Vg and establishment of the dorsoventral compartment boundary in the wing imaginal disc by Suppressor of Hairless
inferredcites →https://doi.org/10.1016/j.ydbio.2012.01.004openalex-snapshot
Drosophila Epsin's role in Notch ligand cells requires three Epsin protein functions: The lipid binding function of the ENTH domain, a single Ubiquitin interaction motif, and a subset of the C-terminal protein binding modules
inferredcites →https://doi.org/10.1016/s0070-2153(10)92005-xopenalex-snapshot
Endocytosis and Intracellular Trafficking of Notch and Its Ligands
inferredcites →https://doi.org/10.1016/s0070-2153(10)92008-5openalex-snapshot
Notch Targets and Their Regulation
inferredcites →https://doi.org/10.1016/s0092-8674(00)80335-9openalex-snapshot
Kuzbanian Controls Proteolytic Processing of Notch and Mediates Lateral Inhibition during Drosophila and Vertebrate Neurogenesis
inferredcites →https://doi.org/10.1016/s0092-8674(00)81368-9openalex-snapshot
An Activated Form of Notch Influences the Choice between CD4 and CD8 T Cell Lineages
inferredcites →https://doi.org/10.1016/s0092-8674(03)01074-2openalex-snapshot
Back to the Future with Ubiquitin
inferredcites →https://doi.org/10.1016/s0960-9822(01)00562-0openalex-snapshot
Novel Notch alleles reveal a Deltex-dependent pathway repressing neural fate
inferredcites →https://doi.org/10.1016/s0960-9822(01)00679-0openalex-snapshot
Protein Degradation: Four E3s For The Notch Pathway
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/10.1034/j.1601-5223.2002.1360201.xopenalex-snapshot
General outlines of the molecular genetics of the Notch signalling pathway in Drosophila melanogaster: a review
inferredcites →https://doi.org/10.1038/19083openalex-snapshot
A presenilin-1-dependent γ-secretase-like protease mediates release of Notch intracellular domain
inferredcites →https://doi.org/10.1038/19091openalex-snapshot
Presenilin is required for activity and nuclear access of Notch in Drosophila
inferredcites →https://doi.org/10.1038/19096openalex-snapshot
Neurogenic phenotypes and altered Notch processing in Drosophila Presenilin mutants
inferredcites →https://doi.org/10.1038/embor.2012.18openalex-snapshot
Cargo ubiquitination is essential for multivesicular body intralumenal vesicle formation
inferredcites →https://doi.org/10.1038/ncb1327openalex-snapshot
Regulation of Notch signalling by non-visual β-arrestin
inferredcites →https://doi.org/10.1038/ng0298-143openalex-snapshot
The itchy locus encodes a novel ubiquitin protein ligase that is disrupted in a18H mice
inferredcites →https://doi.org/10.1038/ng1681openalex-snapshot
Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome)
inferredcites →https://doi.org/10.1038/nm.3046openalex-snapshot
Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy
inferredcites →https://doi.org/10.1038/nrm2009openalex-snapshot
Notch signalling: a simple pathway becomes complex
inferredcites →https://doi.org/10.1038/onc.2010.62openalex-snapshot
Regulation of NOTCH signaling by reciprocal inhibition of HES1 and Deltex 1 and its role in osteosarcoma invasiveness
inferredcites →https://doi.org/10.1038/s41375-019-0653-zopenalex-snapshot
Therapeutic targeting of the E3 ubiquitin ligase SKP2 in T-ALL
inferredcites →https://doi.org/10.1038/s41418-018-0164-xopenalex-snapshot
M1-linked ubiquitination by LUBEL is required for inflammatory responses to oral infection in Drosophila
inferredcites →https://doi.org/10.1038/sj.emboj.7601360openalex-snapshot
A ubiquitin ligase complex assembles linear polyubiquitin chains
inferredcites →https://doi.org/10.1038/sj.onc.1201618openalex-snapshot
Identification of a human homolog of the Drosophila neuralized gene within the 10q25.1 malignant astrocytoma deletion region
inferredcites →https://doi.org/10.1042/bj20121249openalex-snapshot
Non-degradative ubiquitination of the Notch1 receptor by the E3 ligase MDM2 activates the Notch signalling pathway
inferredcites →https://doi.org/10.1042/bst20160227openalex-snapshot
Molecular basis for specificity of the Met1-linked polyubiquitin signal
inferredcites →https://doi.org/10.1073/pnas.011530298openalex-snapshot
Presenilin-mediated transmembrane cleavage is required for Notch signal transduction in Drosophila
inferredcites →https://doi.org/10.1073/pnas.0601700103openalex-snapshot
Impaired neurogenesis and cardiovascular development in mice lacking the E3 ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway
inferredcites →https://doi.org/10.1073/pnas.0800695105openalex-snapshot
The intracellular region of Notch ligands Dll1 and Dll3 regulates their trafficking and signaling activity
inferredcites →https://doi.org/10.1073/pnas.1517033112openalex-snapshot
Lnx2 ubiquitin ligase is essential for exocrine cell differentiation in the early zebrafish pancreas
inferredcites →https://doi.org/10.1073/pnas.1601537113openalex-snapshot
Oncogenic mutations in the FBXW7 gene of adult T-cell leukemia patients
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/10.1073/pnas.98.1.229openalex-snapshot
Presenilin-mediated transmembrane cleavage is required for Notch signal transduction in Drosophila
inferredcites →https://doi.org/10.1074/jbc.m007300200openalex-snapshot
Recognition and Ubiquitination of Notch by Itch, a Hect-type E3 Ubiquitin Ligase
inferredcites →https://doi.org/10.1074/jbc.m103992200openalex-snapshot
The Notch Intracellular Domain Is Ubiquitinated and Negatively Regulated by the Mammalian Sel-10 Homolog
inferredcites →https://doi.org/10.1074/jbc.m108552200openalex-snapshot
c-Cbl Binding and Ubiquitin-dependent Lysosomal Degradation of Membrane-associated Notch1
inferredcites →https://doi.org/10.1074/jbc.m109.014845openalex-snapshot
Numb Regulates Post-endocytic Trafficking and Degradation of Notch1
inferredcites →https://doi.org/10.1074/jbc.m111.303875openalex-snapshot
MDM2 Protein-mediated Ubiquitination of NUMB Protein
inferredcites →https://doi.org/10.1074/jbc.m112.398263openalex-snapshot
The E3 Ligase Mind Bomb-1 (Mib1) Modulates Delta-Notch Signaling to Control Neurogenesis and Gliogenesis in the Developing Spinal Cord
inferredcites →https://doi.org/10.1074/jbc.m302827200openalex-snapshot
Mammalian Numb Proteins Promote Notch1 Receptor Ubiquitination and Degradation of the Notch1 Intracellular Domain
inferredcites →https://doi.org/10.1074/jbc.m606601200openalex-snapshot
Neuralized-2 Regulates a Notch Ligand in Cooperation with Mind Bomb-1
inferredcites →https://doi.org/10.1074/jbc.m706974200openalex-snapshot
Neuralized-like 1 (Neurl1) Targeted to the Plasma Membrane by N-Myristoylation Regulates the Notch Ligand Jagged1
inferredcites →https://doi.org/10.1074/jbc.r300018200openalex-snapshot
Non-traditional Functions of Ubiquitin and Ubiquitin-binding Proteins
inferredcites →https://doi.org/10.1080/09687860500129778openalex-snapshot
Endocytic regulation of Notch activation and down-regulation (Review)
inferredcites →https://doi.org/10.1080/2162402x.2015.1022308openalex-snapshot
Fbxw7 suppresses cancer metastasis by inhibiting niche formation
inferredcites →https://doi.org/10.1083/jcb.200310098openalex-snapshot
Monoubiquitination and endocytosis direct γ-secretase cleavage of activated Notch receptor
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/10.1083/jcb.200708127openalex-snapshot
Endosomal entry regulates Notch receptor activation in Drosophila melanogaster
inferredcites →https://doi.org/10.1083/jcb.201104146openalex-snapshot
Synergy between the ESCRT-III complex and Deltex defines a ligand-independent Notch signal
inferredcites →https://doi.org/10.1084/jem.20070872openalex-snapshot
The SCFFBW7 ubiquitin ligase complex as a tumor suppressor in T cell leukemia
inferredcites →https://doi.org/10.1084/jem.20141130openalex-snapshot
Human HOIP and LUBAC deficiency underlies autoinflammation, immunodeficiency, amylopectinosis, and lymphangiectasia
inferredcites →https://doi.org/10.1091/mbc.e09-11-0926openalex-snapshot
Neuralized Promotes Basal to Apical Transcytosis of Delta in Epithelial Cells
inferredcites →https://doi.org/10.1091/mbc.e13-01-0042openalex-snapshot
The E3 ubiquitin ligase mind bomb 1 ubiquitinates and promotes the degradation of survival of motor neuron protein
inferredcites →https://doi.org/10.1093/emboj/21.1.93openalex-snapshot
LNX functions as a RING type E3 ubiquitin ligase that targets the cell fate determinant Numb for ubiquitin‐dependent degradation
inferredcites →https://doi.org/10.1093/genetics/126.3.665openalex-snapshot
deltex, a locus interacting with the neurogenic genes, Notch, Delta and mastermind in Drosophila melanogaster.
inferredcites →https://doi.org/10.1093/genetics/131.1.99openalex-snapshot
A genetic analysis of deltex and its interaction with the Notch locus in Drosophila melanogaster.
inferredcites →https://doi.org/10.1093/genetics/136.2.585openalex-snapshot
A member of the Notch group of interacting loci, deltex encodes a cytoplasmic basic protein.
inferredcites →https://doi.org/10.1093/genetics/150.4.1477openalex-snapshot
Genetic Characterization of the Drosophila melanogaster Suppressor of deltex Gene: A Regulator of Notch Signaling
inferredcites →https://doi.org/10.1093/genetics/152.2.567openalex-snapshot
The Drosophila melanogaster Suppressor of deltex Gene, a Regulator of the Notch Receptor Signaling Pathway, Is an E3 Class Ubiquitin Ligase
inferredcites →https://doi.org/10.1093/hmg/ddl425openalex-snapshot
Itch genetically interacts with Notch1 in a mouse autoimmune disease model
inferredcites →https://doi.org/10.1093/hmg/ddw365openalex-snapshot
MIB2variants altering NOTCH signalling result in left ventricle hypertrabeculation/non-compaction and are associated with Ménétrier-like gastropathy
inferredcites →https://doi.org/10.1093/hmg/ddx030openalex-snapshot
LRRK2(I2020T) functional genetic interactors that modify eye degeneration and dopaminergic cell loss in Drosophila
inferredcites →https://doi.org/10.1093/hmg/ddz135openalex-snapshot
The fruit fly at the interface of diagnosis and pathogenic mechanisms of rare and common human diseases
inferredcites →https://doi.org/10.1093/jnci/djt337openalex-snapshot
Final Overall Survival: Fulvestrant 500 mg vs 250 mg in the Randomized CONFIRM Trial
inferredcites →https://doi.org/10.1093/jnci/dju107openalex-snapshot
FBXW7 Mutations in Melanoma and a New Therapeutic Paradigm
inferredcites →https://doi.org/10.1101/gad.942302openalex-snapshot
kuzbanian-mediated cleavage of Drosophila Notch
inferredcites →https://doi.org/10.1111/cas.14288openalex-snapshot
Ubiquitination of NOTCH2 by DTX3 suppresses the proliferation and migration of human esophageal carcinoma
inferredcites →https://doi.org/10.1111/dgd.12640openalex-snapshot
Making sense out of missense mutations: Mechanistic dissection of Notch receptors through structure‐function studies inDrosophila
inferredcites →https://doi.org/10.1111/imr.12307openalex-snapshot
The multifaceted role of the E3 ubiquitin ligase HOIL ‐1: beyond linear ubiquitination
inferredcites →https://doi.org/10.1111/j.1365-2443.2011.01488.xopenalex-snapshot
Roles of Drosophila Deltex in Notch receptor endocytic trafficking and activation
inferredcites →https://doi.org/10.1111/j.1600-0854.2010.01126.xopenalex-snapshot
The Multiple Facets of Ubiquitination in the Regulation of Notch Signaling Pathway
inferredcites →https://doi.org/10.1126/science.14.345.225openalex-snapshot
JESSE WILLIAM LAZEAR MEMORIAL
inferredcites →https://doi.org/10.1126/science.284.5415.770openalex-snapshot
Notch Signaling: Cell Fate Control and Signal Integration in Development
inferredcites →https://doi.org/10.1146/annurev.neuro.25.030702.130823openalex-snapshot
The Role of Notch in Promoting Glial and Neural Stem Cell Fates
inferredcites →https://doi.org/10.1172/jci120401openalex-snapshot
Ubiquitin ligase RNF8 suppresses Notch signaling to regulate mammary development and tumorigenesis
inferredcites →https://doi.org/10.1172/jci78782openalex-snapshot
F-box protein FBXW7 inhibits cancer metastasis in a non-cell-autonomous manner
inferredcites →https://doi.org/10.1186/1750-2187-8-7openalex-snapshot
TRAF molecules in cell signaling and in human diseases
inferredcites →https://doi.org/10.1186/s12929-020-00655-wopenalex-snapshot
N6-methyladenosine methyltransferase METTL3 affects the phenotype of cerebral arteriovenous malformation via modulating Notch signaling pathway
inferredcites →https://doi.org/10.1186/s13046-019-1382-xopenalex-snapshot
An essential role of RNF187 in Notch1 mediated metastasis of hepatocellular carcinoma
inferredcites →https://doi.org/10.1242/dev.01074openalex-snapshot
Notch signaling: control of cell communication and cell fate
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.01448openalex-snapshot
Drosophila Deltex mediates Suppressor of Hairless-independent and late-endosomal activation of Notch signaling
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.01825openalex-snapshot
The ubiquitin ligaseDrosophilaMind bomb promotes Notch signaling by regulating the localization and activity of Serrate and Delta
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.02686openalex-snapshot
LobeandSerrateare required for cell survival during early eye development inDrosophila
inferredcites →https://doi.org/10.1242/dev.063610openalex-snapshot
Notch signaling: simplicity in design, versatility in function
inferredcites →https://doi.org/10.1242/dev.120.3.473openalex-snapshot
Cytosolic interaction between deltex and Notch ankyrin repeats implicates deltex in the Notch signaling pathway
inferredcites →https://doi.org/10.1242/dev.120.9.2385openalex-snapshot
The intracellular domain of mouse Notch: a constitutively activated repressor of myogenesis directed at the basic helix-loop-helix region of MyoD
inferredcites →https://doi.org/10.1242/dev.121.8.2633openalex-snapshot
Deltex acts as a positive regulator of Notch signaling through interactions with the Notch ankyrin repeats
inferredcites →https://doi.org/10.1242/dev.121855openalex-snapshot
Inhibition of Daughterless by Extramacrochaetae mediates Notch-induced cell proliferation
inferredcites →https://doi.org/10.1242/dev.127.2.291openalex-snapshot
Antagonism of Notch signaling activity by members of a novel protein family encoded by the Bearded and Enhancer of split gene complexes
inferredcites →https://doi.org/10.1242/dev.128.1.107openalex-snapshot
Notch signalling acts in postmitotic avian myogenic cells to control MyoD activation
inferredcites →https://doi.org/10.1242/dev.170837openalex-snapshot
Regulation of Notch signaling by the chromatin-modeling protein Hat-trick
inferredcites →https://doi.org/10.1242/dmm.010660openalex-snapshot
Elevated expression of the V-ATPase C subunit triggers JNK-dependent cell invasion and overgrowth in a Drosophila epithelium
inferredcites →https://doi.org/10.1242/jcs.068965openalex-snapshot
Trp53 regulates Notch 4 signaling through Mdm2
inferredcites →https://doi.org/10.1242/jcs.091777openalex-snapshot
HECT and RING finger families of E3 ubiquitin ligases at a glance
inferredcites →https://doi.org/10.1371/journal.pgen.1005503openalex-snapshot
The Parkinson’s Disease-Associated Protein Kinase LRRK2 Modulates Notch Signaling through the Endosomal Pathway
inferredcites →https://doi.org/10.1371/journal.pgen.1006634openalex-snapshot
Epilepsy-associated gene Nedd4-2 mediates neuronal activity and seizure susceptibility through AMPA receptors
inferredcites →https://doi.org/10.1371/journal.pone.0001221openalex-snapshot
An Obligatory Role of Mind Bomb-1 in Notch Signaling of Mammalian Development
inferredcites →https://doi.org/10.1371/journal.pone.0002735openalex-snapshot
AIP4/Itch Regulates Notch Receptor Degradation in the Absence of Ligand
inferredcites →https://doi.org/10.1371/journal.pone.0057793openalex-snapshot
Deltex-1 Activates Mitotic Signaling and Proliferation and Increases the Clonogenic and Invasive Potential of U373 and LN18 Glioblastoma Cells and Correlates with Patient Survival
inferredcites →https://doi.org/10.1371/journal.pone.0068247openalex-snapshot
The Drosophila Importin-α3 Is Required for Nuclear Import of Notch In Vivo and It Displays Synergistic Effects with Notch Receptor on Cell Proliferation
inferredcites →https://doi.org/10.1371/journal.pone.0187571openalex-snapshot
A screen for E3 ubiquitination ligases that genetically interact with the adaptor protein Cindr during Drosophila eye patterning
inferredcites →https://doi.org/10.15252/embr.201642378openalex-snapshot
Linear ubiquitination by LUBEL has a role in Drosophila heat stress response
inferredcites →https://doi.org/10.1534/genetics.116.198879openalex-snapshot
Regulation of Notch Signaling by the Heterogeneous Nuclear Ribonucleoprotein Hrp48 and Deltex in Drosophila melanogaster
inferredcites →https://doi.org/10.1534/genetics.117.201624openalex-snapshot
William Friedman, Geneticist Turned Cryptographer
inferredcites →https://doi.org/10.1677/joe-07-0242openalex-snapshot
Cell and molecular biology of Notch
inferredcites →https://doi.org/10.18632/oncotarget.15446openalex-snapshot
The E3 ubiquitin ligase NEDD4 is translationally upregulated and facilitates pancreatic cancer
inferredcites →https://doi.org/10.18632/oncotarget.3742openalex-snapshot
Deltex-3-like (DTX3L) stimulates metastasis of melanoma through FAK/PI3K/AKT but not MEK/ERK pathway
inferredcites →https://doi.org/10.3324/haematol.2016.157495openalex-snapshot
Deltex-1 mutations predict poor survival in diffuse large B-cell lymphoma
inferredcites →https://doi.org/10.3389/fimmu.2019.00479openalex-snapshot
Second Case of HOIP Deficiency Expands Clinical Features and Defines Inflammatory Transcriptome Regulated by LUBAC
inferredcites →https://doi.org/10.3390/ijms14036359openalex-snapshot
Ubiquitinations in the Notch Signaling Pathway
inferredcites →https://doi.org/10.3892/ol.2020.12298openalex-snapshot
Expression levels of FBXW7 and MDM2 E3 ubiquitin ligases and their c‑Myc and p53 substrates in patients with dysplastic nevi or melanoma
inferredcites →https://doi.org/10.3892/or.2017.5572openalex-snapshot
Regulation of glioma migration and invasion via modification of Rap2a activity by the ubiquitin ligase Nedd4-1
inferredcites →https://doi.org/10.4049/jimmunol.1202469openalex-snapshot
Role of Recycling, Mindbomb1 Association, and Exclusion from Lipid Rafts of Delta-like 4 for Effective Notch Signaling To Drive T Cell Development
inferredcites →https://doi.org/10.4161/cib.19995openalex-snapshot
Regulation of ligand-independent Notch signal through intracellular trafficking
inferredcites →https://doi.org/10.7150/jca.38286openalex-snapshot
TRIM67 Promotes the Proliferation, Migration, and Invasion of Non-Small-Cell Lung Cancer by Positively Regulating the Notch Pathway
inferredcites →https://doi.org/10.7554/elife.04415openalex-snapshot
Cis-interactions between Notch and its ligands block ligand-independent Notch activity
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1186/s12885-022-10383-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s12964-025-02190-3openalex-snapshot
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