| scholarly article | Q13442814 |
| P2093 | author name string | R. Kageyama | |
| S. Yamada | |||
| S. Komatsu | |||
| K. Shiota | |||
| Y. Bessho | |||
| R. Sakata | |||
| P2860 | cites work | Hes7: a bHLH-type repressor gene regulated by Notch and expressed in the presomitic mesoderm | Q24290956 |
| The bHLH regulator pMesogenin1 is required for maturation and segmentation of paraxial mesoderm | Q28505459 | ||
| Targeted disruption of mammalian hairy and Enhancer of split homolog-1 (HES-1) leads to up-regulation of neural helix-loop-helix factors, premature neurogenesis, and severe neural tube defects | Q28507755 | ||
| Mice lacking both presenilin genes exhibit early embryonic patterning defects | Q28508946 | ||
| Requirement of the paraxis gene for somite formation and musculoskeletal patterning | Q28510545 | ||
| Oscillating expression of c-Hey2 in the presomitic mesoderm suggests that the segmentation clock may use combinatorial signaling through multiple interacting bHLH factors | Q28510928 | ||
| Notch1 is required for the coordinate segmentation of somites | Q28513676 | ||
| Presenilin 1 is required for Notch1 and DII1 expression in the paraxial mesoderm | Q28585594 | ||
| Uncx4.1 is required for the formation of the pedicles and proximal ribs and acts upstream of Pax9 | Q28585821 | ||
| Mammalian achaete-scute and atonal homologs regulate neuronal versus glial fate determination in the central nervous system | Q28591759 | ||
| Notch signalling is required for cyclic expression of the hairy-like gene HES1 in the presomitic mesoderm | Q28594325 | ||
| The role of presenilin 1 during somite segmentation | Q28594372 | ||
| Disruption of the mouse RBP-J kappa gene results in early embryonic death | Q28610816 | ||
| A clock-work somite | Q33825400 | ||
| Notch signalling and the synchronization of the somite segmentation clock | Q33926876 | ||
| Maintenance of somite borders in mice requires the Delta homologue DII1. | Q34422203 | ||
| Control of her1 expression during zebrafish somitogenesis by a delta-dependent oscillator and an independent wave-front activity | Q40443832 | ||
| A gene that resuscitates a theory--somitogenesis and a molecular oscillator | Q41737710 | ||
| Induction of c-fos gene and protein by growth factors precedes activation of c-myc | Q44887897 | ||
| Embryonic lethality in mice homozygous for a processing-deficient allele of Notch1. | Q45345845 | ||
| Zebrafish Mesp family genes, mesp-a and mesp-b are segmentally expressed in the presomitic mesoderm, and Mesp-b confers the anterior identity to the developing somites. | Q47073326 | ||
| lunatic fringe is an essential mediator of somite segmentation and patterning | Q47741550 | ||
| Defects in somite formation in lunatic fringe-deficient mice | Q47741558 | ||
| The mouse pudgy mutation disrupts Delta homologue Dll3 and initiation of early somite boundaries | Q47852383 | ||
| Avian hairy gene expression identifies a molecular clock linked to vertebrate segmentation and somitogenesis | Q48041941 | ||
| Mesp2: a novel mouse gene expressed in the presegmented mesoderm and essential for segmentation initiation | Q48047260 | ||
| Dynamic expression of lunatic fringe suggests a link between notch signaling and an autonomous cellular oscillator driving somite segmentation. | Q52179113 | ||
| The lunatic fringe gene is a target of the molecular clock linked to somite segmentation in avian embryos. | Q52184463 | ||
| Waves of mouse Lunatic fringe expression, in four-hour cycles at two-hour intervals, precede somite boundary formation. | Q52184506 | ||
| Notch1 is essential for postimplantation development in mice. | Q52512097 | ||
| Interaction between Notch signalling and Lunatic fringe during somite boundary formation in the mouse | Q57315074 | ||
| Interactions between somite cells: the formation and maintenance of segment boundaries in the chick embryo | Q69396944 | ||
| P433 | issue | 20 | |
| P921 | main subject | Hes family bHLH transcription factor 7 | Q21495819 |
| P304 | page(s) | 2642–2647 | |
| P577 | publication date | 2001-10-15 | |
| P1433 | published in | Genes & Development | Q1524533 |
| P1476 | title | Dynamic expression and essential functions of Hes7 in somite segmentation | |
| P478 | volume | 15 |
| Q44096560 | 3'-UTR-dependent regulation of mRNA turnover is critical for differential distribution patterns of cyclic gene mRNAs. |
| Q35617198 | A Notch feeling of somite segmentation and beyond |
| Q39888155 | A Wnt oscillator model for somitogenesis |
| Q37902096 | A fluorescence spotlight on the clockwork development and metabolism of bone. |
| Q35897471 | A transgenic Tbx6;CreERT2 line for inducible gene manipulation in the presomitic mesoderm |
| Q92957605 | An In Vitro Human Segmentation Clock Model Derived from Embryonic Stem Cells |
| Q92923798 | Analysing diffusion and flow-driven instability using semidefinite programming |
| Q28587304 | Analysis of Ripply1/2-deficient mouse embryos reveals a mechanism underlying the rostro-caudal patterning within a somite |
| Q34314148 | Analysis of her1 and her7 mutants reveals a spatio temporal separation of the somite clock module |
| Q51994121 | Appropriate suppression of Notch signaling by Mesp factors is essential for stripe pattern formation leading to segment boundary formation. |
| Q52010517 | Autoinhibition with transcriptional delay: a simple mechanism for the zebrafish somitogenesis oscillator. |
| Q37141071 | Building the spine: the vertebrate segmentation clock. |
| Q35058303 | Canine disorder mirrors human disease: exonic deletion in HES7 causes autosomal recessive spondylocostal dysostosis in miniature Schnauzer dogs. |
| Q35018076 | Catching a wave: the oscillator and wavefront that create the zebrafish somite |
| Q28593449 | Cdx regulates Dll1 in multiple lineages |
| Q46524965 | Cell cycle-dependent expression of a hairy and Enhancer of split (hes) homolog during cleavage and segmentation in leech embryos |
| Q78588722 | Cellular clockwork |
| Q33290478 | Chick Hairy1 protein interacts with Sap18, a component of the Sin3/HDAC transcriptional repressor complex. |
| Q42401022 | Churchill and Sip1a repress fibroblast growth factor signaling during zebrafish somitogenesis |
| Q34137887 | Clock regulatory elements control cyclic expression of Lunatic fringe during somitogenesis |
| Q48796148 | Cloning, characterization and promoter analysis of common carp hairy/Enhancer-of-split-related gene, her6. |
| Q33612536 | Combined GWAS and 'guilt by association'-based prioritization analysis identifies functional candidate genes for body size in sheep |
| Q38200068 | Coming together is a beginning: the making of an intervertebral disc |
| Q52023087 | Comparative analysis of her genes during fish somitogenesis suggests a mouse/chick-like mode of oscillation in medaka. |
| Q24801572 | Comparative analysis of somitogenesis related genes of the hairy/Enhancer of split class in Fugu and zebrafish |
| Q34342220 | Comparative and evolutionary analysis of the HES/HEY gene family reveal exon/intron loss and teleost specific duplication events |
| Q40245530 | Completing the set of h/E(spl) cyclic genes in zebrafish: her12 and her15 reveal novel modes of expression and contribute to the segmentation clock. |
| Q34568331 | Cooperative Mesp activity is required for normal somitogenesis along the anterior-posterior axis |
| Q42055406 | Cooperative function of deltaC and her7 in anterior segment formation |
| Q47073624 | Coordination of symmetric cyclic gene expression during somitogenesis by Suppressor of Hairless involves regulation of retinoic acid catabolism |
| Q92503844 | Coupling delay controls synchronized oscillation in the segmentation clock |
| Q37592411 | Cyclic Nrarp mRNA expression is regulated by the somitic oscillator but Nrarp protein levels do not oscillate. |
| Q37229838 | Cyclical expression of the Notch/Wnt regulator Nrarp requires modulation by Dll3 in somitogenesis |
| Q46636227 | Dact1 presomitic mesoderm expression oscillates in phase with Axin2 in the somitogenesis clock of mice |
| Q28069407 | Delta-Notch signalling in segmentation |
| Q36857288 | Delta-Notch--and then? Protein interactions and proposed modes of repression by Hes and Hey bHLH factors |
| Q39532078 | Different types of oscillations in Notch and Fgf signaling regulate the spatiotemporal periodicity of somitogenesis |
| Q30945648 | Differential axial requirements for lunatic fringe and Hes7 transcription during mouse somitogenesis |
| Q50353951 | Differential regulation of Hes/Hey genes during inner ear development |
| Q33518475 | Discovery of candidate disease genes in ENU-induced mouse mutants by large-scale sequencing, including a splice-site mutation in nucleoredoxin |
| Q28589511 | Dll3 pudgy mutation differentially disrupts dynamic expression of somite genes |
| Q36895542 | Dynamic CREB family activity drives segmentation and posterior polarity specification in mammalian somitogenesis |
| Q35635073 | Dynamics of the slowing segmentation clock reveal alternating two-segment periodicity. |
| Q50043698 | ES cell-derived presomitic mesoderm-like tissues for analysis of synchronized oscillations in the segmentation clock |
| Q28731907 | Evidence for intron length conservation in a set of mammalian genes associated with embryonic development |
| Q36794463 | Evolutionary conservation and divergence of the segmentation process in arthropods |
| Q34145324 | Expression of the oscillating gene her1 is directly regulated by Hairy/Enhancer of Split, T-box, and Suppressor of Hairless proteins in the zebrafish segmentation clock |
| Q28591828 | Fbxw8 is essential for Cul1-Cul7 complex formation and for placental development |
| Q21090160 | From dynamic expression patterns to boundary formation in the presomitic mesoderm |
| Q55492743 | Geminin Orchestrates Somite Formation by Regulating Fgf8 and Notch Signaling. |
| Q36318161 | Genetic association analysis between polymorphisms of HAIRY-AND-ENHANCER-OF SPLIT-7 and congenital scoliosis |
| Q35697802 | Genetic reevaluation of the role of F-box proteins in cyclin D1 degradation |
| Q34234902 | Hes7 3'UTR is required for somite segmentation function |
| Q42738593 | Identification of oscillatory genes in somitogenesis from functional genomic analysis of a human mesenchymal stem cell model |
| Q50762926 | In vivo analysis of mRNA stability using the Tet-Off system in the chicken embryo. |
| Q36665547 | In vivo consequences of deleting EGF repeats 8-12 including the ligand binding domain of mouse Notch1. |
| Q28505422 | Instability of Hes7 protein is crucial for the somite segmentation clock |
| Q46091969 | Interactions between muscle fibers and segment boundaries in zebrafish |
| Q34602627 | Intronic delay is essential for oscillatory expression in the segmentation clock |
| Q42601930 | Involvement of Notch and Delta genes in spider segmentation |
| Q52040762 | Involvement of SIP1 in positioning of somite boundaries in the mouse embryo. |
| Q33784419 | Left-right function of dmrt2 genes is not conserved between zebrafish and mouse |
| Q28510335 | Lfng regulates the synchronized oscillation of the mouse segmentation clock via trans-repression of Notch signalling |
| Q26865201 | Life rhythm as a symphony of oscillatory patterns: electromagnetic energy and sound vibration modulates gene expression for biological signaling and healing |
| Q35524555 | MBTPS1/SKI-1/S1P proprotein convertase is required for ECM signaling and axial elongation during somitogenesis and vertebral development†. |
| Q28511004 | Mash1 and Math3 are required for development of branchiomotor neurons and maintenance of neural progenitors |
| Q42828942 | MicroRNA9 regulates neural stem cell differentiation by controlling Hes1 expression dynamics in the developing brain. |
| Q33779631 | Modeling the zebrafish segmentation clock's gene regulatory network constrained by expression data suggests evolutionary transitions between oscillating and nonoscillating transcription |
| Q35238701 | Modelling coupled oscillations in the Notch, Wnt, and FGF signaling pathways during somitogenesis: a comprehensive mathematical model |
| Q46419557 | Modulation of Notch Signaling During Somitogenesis |
| Q50422140 | Modulation of Phase Shift between Wnt and Notch Signaling Oscillations Controls Mesoderm Segmentation. |
| Q38671655 | Molecular mechanism for cyclic generation of somites: Lessons from mice and zebrafish. |
| Q51975063 | Mouse Ripply2 is downstream of Wnt3a and is dynamically expressed during somitogenesis. |
| Q53096591 | Mutation of HES7 in a large extended family with spondylocostal dysostosis and dextrocardia with situs inversus. |
| Q24323154 | Mutation of the fucose-specific beta1,3 N-acetylglucosaminyltransferase LFNG results in abnormal formation of the spine |
| Q21710714 | Mutations in the MESP2 gene cause spondylothoracic dysostosis/Jarcho-Levin syndrome |
| Q37396888 | NOTCH signaling in Sertoli cells regulates gonocyte fate |
| Q32874834 | Negative feedback loop formed by Lunatic fringe and Hes7 controls their oscillatory expression during somitogenesis |
| Q39295423 | Neurogenin2 expression together with NeuroM regulates GDNF family neurotrophic factor receptor α1 (GFRα1) expression in the embryonic spinal cord |
| Q61800422 | Noise-resistant developmental reproducibility in vertebrate somite formation |
| Q34809773 | Noncyclic Notch activity in the presomitic mesoderm demonstrates uncoupling of somite compartmentalization and boundary formation |
| Q36960089 | Notch Signaling and the Skeleton |
| Q46795621 | Notch Signaling in Development, Tissue Homeostasis, and Disease |
| Q89860460 | Notch Signaling in Skeletal Development, Homeostasis and Pathogenesis |
| Q33627230 | Notch and the skeleton |
| Q28590793 | Notch is a critical component of the mouse somitogenesis oscillator and is essential for the formation of the somites |
| Q27021132 | Notch regulation of bone development and remodeling and related skeletal disorders |
| Q28258962 | Notch signaling in human development and disease |
| Q35848797 | Notch signaling in skeletal health and disease |
| Q37503775 | Notch signaling, the segmentation clock, and the patterning of vertebrate somites |
| Q28504465 | Notch signalling in the paraxial mesoderm is most sensitive to reduced Pofut1 levels during early mouse development |
| Q25255507 | Number of active transcription factor binding sites is essential for the Hes7 oscillator |
| Q30845466 | Optogenetic perturbation and bioluminescence imaging to analyze cell-to-cell transfer of oscillatory information |
| Q36762222 | Oscillator mechanism of Notch pathway in the segmentation clock |
| Q27322653 | Oscillatory control of Delta-like1 in cell interactions regulates dynamic gene expression and tissue morphogenesis. |
| Q38116917 | Oscillatory gene expression and somitogenesis. |
| Q89771836 | Overview of Basic Mechanisms of Notch Signaling in Development and Disease |
| Q48140686 | Patterning spinal nerves and vertebral bones. |
| Q48294316 | Periodic Lunatic fringe expression is controlled during segmentation by a cyclic transcriptional enhancer responsive to notch signaling. |
| Q28585491 | Periodic repression by the bHLH factor Hes7 is an essential mechanism for the somite segmentation clock |
| Q46713018 | Pnrc2 regulates 3'UTR-mediated decay of segmentation clock-associated transcripts during zebrafish segmentation |
| Q40286298 | Posterior-anterior gradient of zebrafish hes6 expression in the presomitic mesoderm is established by the combinatorial functions of the downstream enhancer and 3'UTR. |
| Q42579695 | Practical lessons from theoretical models about the somitogenesis |
| Q89081045 | Presomitic mesoderm-specific expression of the transcriptional repressor Hes7 is controlled by E-box, T-box, and Notch signaling pathways |
| Q51989566 | Priming, initiation and synchronization of the segmentation clock by deltaD and deltaC. |
| Q24677654 | Protein O -fucosyltransferase 1 is an essential component of Notch signaling pathways |
| Q91562404 | Pumilio response and AU-rich elements drive rapid decay of Pnrc2-regulated cyclic gene transcripts |
| Q30476642 | Real-time imaging of the somite segmentation clock: revelation of unstable oscillators in the individual presomitic mesoderm cells |
| Q90836297 | Recapitulating the human segmentation clock with pluripotent stem cells |
| Q42416456 | Resolving early mesoderm diversification through single-cell expression profiling |
| Q38667929 | Revisiting the involvement of signaling gradients in somitogenesis |
| Q28509532 | Ripply2 is essential for precise somite formation during mouse early development |
| Q64105061 | Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate |
| Q34353557 | Scoliosis and segmentation defects of the vertebrae |
| Q34770048 | Segmental patterning of the vertebrate embryonic axis |
| Q28512351 | Segmentation defects of Notch pathway mutants and absence of a synergistic phenotype in lunatic fringe/radical fringe double mutant mice |
| Q52602912 | Segmentation of the zebrafish axial skeleton relies on notochord sheath cells and not on the segmentation clock. |
| Q33286066 | Setting the tempo in development: an investigation of the zebrafish somite clock mechanism |
| Q37778384 | Signaling Pathways in Human Skeletal Dysplasias |
| Q42629116 | Somitogenesis in the anole lizard and alligator reveals evolutionary convergence and divergence in the amniote segmentation clock. |
| Q35550763 | Somitogenesis: breaking new boundaries. |
| Q42174470 | Sprouty4, an FGF inhibitor, displays cyclic gene expression under the control of the notch segmentation clock in the mouse PSM. |
| Q27318039 | Stochastic Regulation of her1/7 Gene Expression Is the Source of Noise in the Zebrafish Somite Clock Counteracted by Notch Signalling |
| Q36127626 | Sumoylation of Hes6 Regulates Protein Degradation and Hes1-Mediated Transcription |
| Q50473575 | Supt20 is required for development of the axial skeleton. |
| Q47824382 | Tbx18 and boundary formation in chick somite and wing development. |
| Q35741905 | The Her7 node modulates the network topology of the zebrafish segmentation clock via sequestration of the Hes6 hub. |
| Q28505901 | The Mesp2 transcription factor establishes segmental borders by suppressing Notch activity |
| Q42004851 | The WHHERE coactivator complex is required for retinoic acid-dependent regulation of embryonic symmetry. |
| Q28511944 | The Wnt3a/β-catenin target gene Mesogenin1 controls the segmentation clock by activating a Notch signalling program |
| Q47074205 | The characterization of zebrafish antimorphic mib alleles reveals that Mib and Mind bomb-2 (Mib2) function redundantly |
| Q90836265 | The clock that controls spine development modelled in a dish |
| Q92472109 | The gene encoding the ketogenic enzyme HMGCS2 displays a unique expression during gonad development in mice |
| Q63433298 | The generation of vertebral segmental patterning in the chick embryo |
| Q36814549 | The genetics and embryology of zebrafish metamerism |
| Q36488814 | The long and short of it: somite formation in mice |
| Q34160267 | The microRNA-processing enzyme Dicer is dispensable for somite segmentation but essential for limb bud positioning |
| Q37888532 | The mouse notches up another success: understanding the causes of human vertebral malformation. |
| Q28506772 | The period of the somite segmentation clock is sensitive to Notch activity |
| Q43010260 | The precise timeline of transcriptional regulation reveals causation in mouse somitogenesis network |
| Q28591870 | The protocadherin papc is involved in the organization of the epithelium along the segmental border during mouse somitogenesis |
| Q35853789 | The synchrony and cyclicity of developmental events |
| Q30410818 | The transcriptome of utricle hair cell regeneration in the avian inner ear. |
| Q54967467 | Time-lapse observation of stepwise regression of Erk activity in zebrafish presomitic mesoderm. |
| Q33660946 | Timing embryo segmentation: dynamics and regulatory mechanisms of the vertebrate segmentation clock |
| Q28481517 | Topology and dynamics of the zebrafish segmentation clock core circuit |
| Q24672577 | Transcriptional oscillation of lunatic fringe is essential for somitogenesis |
| Q33364683 | Turn It Down a Notch |
| Q34329197 | Two novel missense mutations in HAIRY-AND-ENHANCER-OF-SPLIT-7 in a family with spondylocostal dysostosis |
| Q37785200 | Ultradian Oscillations in Notch Signaling Regulate Dynamic Biological Events |
| Q34341432 | Ultradian oscillations and pulses: coordinating cellular responses and cell fate decisions |
| Q35854990 | Ultradian oscillations of Stat, Smad, and Hes1 expression in response to serum. |
| Q37141076 | Ultradian oscillators in somite segmentation and other biological events |
| Q41492486 | Unraveling the nature of the segmentation clock: Intrinsic disorder of clock proteins and their interaction map. |
| Q60492563 | Vertebrate Segmentation: Lunatic Transcriptional Regulation |
| Q34538497 | Whole Genome Sequencing Identifies a Missense Mutation in HES7 Associated with Short Tails in Asian Domestic Cats |
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| Q35974724 | Whole genome sequencing in cats, identifies new models for blindness in AIPL1 and somite segmentation in HES7. |
| Q38349987 | Xenopus Rnd1 and Rnd3 GTP-binding proteins are expressed under the control of segmentation clock and required for somite formation |
| Q33826911 | Zebrafish hairy/enhancer of split protein links FGF signaling to cyclic gene expression in the periodic segmentation of somites. |
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