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CDK1 and CDK2 regulate phosphorylation-dependent NICD1 turnover and the periodicity of the segmentation clock
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/jez.b.21305openalex-snapshot
Developmental control of segment numbers in vertebrates
inferredcites →https://doi.org/10.1007/978-1-62703-444-9_10openalex-snapshot
DNA Transfection: Calcium Phosphate Method
inferredcites →https://doi.org/10.1007/s10059-009-0001-7openalex-snapshot
Regulation of Notch1/NICD and Hes1 Expressions by GSK-3α/β
inferredcites →https://doi.org/10.1007/s11538-017-0356-4openalex-snapshot
A Multi-stage Representation of Cell Proliferation as a Markov Process
inferredcites →https://doi.org/10.1016/j.asd.2016.11.007openalex-snapshot
Delta-Notch signalling in segmentation
inferredcites →https://doi.org/10.1016/j.ccell.2014.09.013openalex-snapshot
Tumor Suppression by the Fbw7 Ubiquitin Ligase: Mechanisms and Opportunities
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.cell.2011.05.011openalex-snapshot
Vertebrate Segmentation: From Cyclic Gene Networks to Scoliosis
inferredcites →https://doi.org/10.1016/j.cell.2012.02.054openalex-snapshot
A Mechanism for Gene-Environment Interaction in the Etiology of Congenital Scoliosis
inferredcites →https://doi.org/10.1016/j.cell.2016.11.034openalex-snapshot
CDK Substrate Phosphorylation and Ordering the Cell Cycle
inferredcites →https://doi.org/10.1016/j.cell.2017.08.043openalex-snapshot
Excitable Dynamics and Yap-Dependent Mechanical Cues Drive the Segmentation Clock
inferredcites →https://doi.org/10.1016/j.celrep.2012.11.012openalex-snapshot
Accelerating the Tempo of the Segmentation Clock by Reducing the Number of Introns in the Hes7 Gene
inferredcites →https://doi.org/10.1016/j.cub.2003.09.024openalex-snapshot
Cdk2 Knockout Mice Are Viable
inferredcites →https://doi.org/10.1016/j.cub.2010.05.071openalex-snapshot
Segment Number and Axial Identity in a Segmentation Clock Period Mutant
inferredcites →https://doi.org/10.1016/j.cub.2010.06.034openalex-snapshot
Intercellular Coupling Regulates the Period of the Segmentation Clock
inferredcites →https://doi.org/10.1016/j.devcel.2006.02.011openalex-snapshot
Oscillations of the Snail Genes in the Presomitic Mesoderm Coordinate Segmental Patterning and Morphogenesis in Vertebrate Somitogenesis
inferredcites →https://doi.org/10.1016/j.devcel.2012.09.009openalex-snapshot
Single-Cell-Resolution Imaging of the Impact of Notch Signaling and Mitosis on Segmentation Clock Dynamics
inferredcites →https://doi.org/10.1016/j.devcel.2017.04.001openalex-snapshot
The Canonical Notch Signaling Pathway: Structural and Biochemical Insights into Shape, Sugar, and Force
inferredcites →https://doi.org/10.1016/j.gde.2006.12.001openalex-snapshot
The multifaceted role of Notch in cancer
inferredcites →https://doi.org/10.1016/j.jtbi.2011.05.004openalex-snapshot
The clock and wavefront model revisited
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.molcel.2007.02.022openalex-snapshot
Structure of a Fbw7-Skp1-Cyclin E Complex: Multisite-Phosphorylated Substrate Recognition by SCF Ubiquitin Ligases
inferredcites →https://doi.org/10.1016/j.molcel.2011.08.025openalex-snapshot
Systematic and Quantitative Assessment of the Ubiquitin-Modified Proteome
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.tcb.2010.07.001openalex-snapshot
The segmentation clock mechanism moves up a notch
inferredcites →https://doi.org/10.1016/j.ydbio.2009.02.035openalex-snapshot
Interfering with Wnt signalling alters the periodicity of the segmentation clock
inferredcites →https://doi.org/10.1016/j.ydbio.2012.10.014openalex-snapshot
Modelling Delta-Notch perturbations during zebrafish somitogenesis
inferredcites →https://doi.org/10.1016/s0092-8674(03)00034-5openalex-snapshot
Structural Basis for Phosphodependent Substrate Selection and Orientation by the SCFCdc4 Ubiquitin Ligase
inferredcites →https://doi.org/10.1016/s0960-9822(03)00494-9openalex-snapshot
Oscillatory Expression of Hes1, p53, and NF-κB Driven by Transcriptional Time Delays
inferredcites →https://doi.org/10.1016/s0960-9822(03)00534-7openalex-snapshot
Autoinhibition with Transcriptional Delay
inferredcites →https://doi.org/10.1038/35044091openalex-snapshot
Notch signalling and the synchronization of the somite segmentation clock
inferredcites →https://doi.org/10.1038/nature06046openalex-snapshot
Cdk1 is sufficient to drive the mammalian cell cycle
inferredcites →https://doi.org/10.1038/nature08356openalex-snapshot
Tankyrase inhibition stabilizes axin and antagonizes Wnt signalling
inferredcites →https://doi.org/10.1038/ncb0805-779openalex-snapshot
Cdk1: the dominant sibling of Cdk2
inferredcites →https://doi.org/10.1038/ncb3046openalex-snapshot
Cyclin C is a haploinsufficient tumour suppressor
inferredcites →https://doi.org/10.1038/ncomms11861openalex-snapshot
Faster embryonic segmentation through elevated Delta-Notch signalling
inferredcites →https://doi.org/10.1038/nrm3582openalex-snapshot
Mechanisms and function of substrate recruitment by F-box proteins
inferredcites →https://doi.org/10.1038/nrm3891openalex-snapshot
Signalling dynamics in vertebrate segmentation
inferredcites →https://doi.org/10.1038/onc.2009.170openalex-snapshot
Mammalian cell-cycle regulation: several Cdks, numerous cyclins and diverse compensatory mechanisms
inferredcites →https://doi.org/10.1038/onc.2010.222openalex-snapshot
The ubiquitous nature of cancer: the role of the SCFFbw7 complex in development and transformation
inferredcites →https://doi.org/10.1042/bcj20160557openalex-snapshot
Phos-tag analysis of Rab10 phosphorylation by LRRK2: a powerful assay for assessing kinase function and inhibitors
inferredcites →https://doi.org/10.1073/pnas.0600447103openalex-snapshot
Selective small-molecule inhibitor reveals critical mitotic functions of human CDK1
inferredcites →https://doi.org/10.1073/pnas.1115201109openalex-snapshot
Cyclin-dependent kinase 1 (Cdk1) is essential for cell division and suppression of DNA re-replication but not for liver regeneration
inferredcites →https://doi.org/10.1074/jbc.270.41.23922openalex-snapshot
The Transcriptional Elongation Inhibitor 5,6-Dichloro-1-β-D-ribofuranosylbenzimidazole Inhibits Transcription Factor IIH-associated Protein Kinase
inferredcites →https://doi.org/10.1074/jbc.m101343200openalex-snapshot
Functional Interaction between SEL-10, an F-box Protein, and the Nuclear Form of Activated Notch1 Receptor
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.m304001200openalex-snapshot
Phosphorylation by Glycogen Synthase Kinase-3β Down-regulates Notch Activity, a Link for Notch and Wnt Pathways
inferredcites →https://doi.org/10.1074/mcp.m112.017905openalex-snapshot
Proteomic Analyses Reveal Divergent Ubiquitylation Site Patterns in Murine Tissues
inferredcites →https://doi.org/10.1074/mcp.t500024-mcp200openalex-snapshot
Phosphate-binding Tag, a New Tool to Visualize Phosphorylated Proteins
inferredcites →https://doi.org/10.1084/jem.20050559openalex-snapshot
Notch1 modulates timing of G1-S progression by inducing SKP2 transcription and p27Kip1 degradation
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.20070876openalex-snapshot
FBW7 mutations in leukemic cells mediate NOTCH pathway activation and resistance to γ-secretase inhibitors
inferredcites →https://doi.org/10.1091/mbc.e11-02-0139openalex-snapshot
The period of the somite segmentation clock is sensitive to Notch activity
inferredcites →https://doi.org/10.1101/cshperspect.a017772openalex-snapshot
Cutaneous Notch Signaling in Health and Disease
inferredcites →https://doi.org/10.1124/jpet.103.060715openalex-snapshot
Studies of Aβ Pharmacodynamics in the Brain, Cerebrospinal Fluid, and Plasma in Young (Plaque-Free) Tg2576 Mice Using the γ-Secretase Inhibitor N2-[(2 S)-2-(3,5-Difluorophenyl)-2-hydroxyethanoyl]-N1-[(7 S)-5-methyl-6-oxo-6,7-dihydro-5 H-dibenzo[b,d]azepin-7-yl]-L-alaninamide (LY-411575)
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.1133141openalex-snapshot
A Complex Oscillating Network of Signaling Genes Underlies the Mouse Segmentation Clock
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/10.1128/mcb.02478-05openalex-snapshot
Identification of a Conserved Negative Regulatory Sequence That Influences the Leukemogenic Activity of NOTCH1
inferredcites →https://doi.org/10.1128/mcb.21.21.7403-7415.2001openalex-snapshot
SEL-10 Is an Inhibitor of Notch Signaling That Targets Notch for Ubiquitin-Mediated Protein Degradation
inferredcites →https://doi.org/10.1128/mcb.24.20.8813-8822.2004openalex-snapshot
Notch Activation Induces Endothelial Cell Cycle Arrest and Participates in Contact Inhibition: Role of p21 Cip1 Repression
inferredcites →https://doi.org/10.1158/0008-5472.can-05-0233openalex-snapshot
Seliciclib (CYC202, R-Roscovitine) Induces Cell Death in Multiple Myeloma Cells by Inhibition of RNA Polymerase II–Dependent Transcription and Down-regulation of Mcl-1
inferredcites →https://doi.org/10.1158/0008-5472.can-09-1843openalex-snapshot
Preclinical Profile of a Potent γ-Secretase Inhibitor Targeting Notch Signaling with In vivo Efficacy and Pharmacodynamic Properties
inferredcites →https://doi.org/10.1158/1078-0432.ccr-14-1348openalex-snapshot
PEST Domain Mutations in Notch Receptors Comprise an Oncogenic Driver Segment in Triple-Negative Breast Cancer Sensitive to a γ-Secretase Inhibitor
inferredcites →https://doi.org/10.1182/blood-2008-03-147967openalex-snapshot
Notch signaling mediates G1/S cell-cycle progression in T cells via cyclin D3 and its dependent kinases
inferredcites →https://doi.org/10.1186/1471-2407-9-281openalex-snapshot
The cyclin-dependent kinase inhibitor 5, 6-dichloro-1-beta-D-ribofuranosylbenzimidazole induces nongenotoxic, DNA replication-independent apoptosis of normal and leukemic cells, regardless of their p53 status
inferredcites →https://doi.org/10.1186/bcr3447openalex-snapshot
Notch activation stimulates migration of breast cancer cells and promotes tumor growth
inferredcites →https://doi.org/10.1186/gb-2008-9-10-r149openalex-snapshot
Identification of CDK2 substrates in human cell lysates
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.024919openalex-snapshot
Genetic substitution of Cdk1 by Cdk2 leads to embryonic lethality and loss of meiotic function of Cdk2
inferredcites →https://doi.org/10.1242/dev.077230openalex-snapshot
The elongation rate of RNA polymerase II in zebrafish and its significance in the somite segmentation clock
inferredcites →https://doi.org/10.1242/dev.091744openalex-snapshot
Cdks, cyclins and CKIs: roles beyond cell cycle regulation
inferredcites →https://doi.org/10.1242/dev.093278openalex-snapshot
Short-lived Her proteins drive robust synchronized oscillations in the zebrafish segmentation clock
inferredcites →https://doi.org/10.1371/journal.pbio.0040121openalex-snapshot
Notch Promotes Neural Lineage Entry by Pluripotent Embryonic Stem Cells
inferredcites →https://doi.org/10.1371/journal.pgen.1000662openalex-snapshot
Notch Is a Critical Component of the Mouse Somitogenesis Oscillator and Is Essential for the Formation of the Somites
inferredcites →https://doi.org/10.1371/journal.pone.0050645openalex-snapshot
The Transcription Factor YY1 Is a Novel Substrate for Aurora B Kinase at G2/M Transition of the Cell Cycle
inferredcites →https://doi.org/10.1517/13543784.2012.707192openalex-snapshot
MLN4924: a novel first-in-class inhibitor of NEDD8-activating enzyme for cancer therapy
inferredcites →https://doi.org/10.2976/1.3027088openalex-snapshot
Delayed coupling theory of vertebrate segmentation
inferredcites →https://doi.org/10.3390/ijms14036359openalex-snapshot
Ubiquitinations in the Notch Signaling Pathway
inferredcites →https://doi.org/10.3978/j.issn.2305-5839.2015.03.61openalex-snapshot
Roscovitine in cancer and other diseases.
inferredcites →https://doi.org/10.7554/elife.05842openalex-snapshot
A balance of positive and negative regulators determines the pace of the segmentation clock
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1038/s41467-021-26605-0openalex-snapshot
Cell cycle arrest determines adult neural stem cell ontogeny by an embryonic Notch-nonoscillatory Hey1 module
inferred← citeshttps://doi.org/10.1101/789446openalex-snapshot
The effect of Rosovitine on mPSM explants: a real time analysis
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