scholarly article | Q13442814 |
P356 | DOI | 10.1002/GENE.10081 |
P698 | PubMed publication ID | 12001066 |
P2093 | author name string | Nian Zhang | |
Thomas Gridley | |||
Christine R. Norton | |||
P2860 | cites work | Fringe boundaries coincide with Notch-dependent patterning centres in mammals and alter Notch-dependent development in Drosophila | Q28115115 |
Fringe is a glycosyltransferase that modifies Notch | Q28143123 | ||
Manic fringe and lunatic fringe modify different sites of the Notch2 extracellular region, resulting in different signaling modulation | Q28188343 | ||
Oscillating expression of c-Hey2 in the presomitic mesoderm suggests that the segmentation clock may use combinatorial signaling through multiple interacting bHLH factors | Q28510928 | ||
Presenilin 1 is required for Notch1 and DII1 expression in the paraxial mesoderm | Q28585594 | ||
Defects in limb, craniofacial, and thymic development in Jagged2 mutant mice | Q28586431 | ||
Embryonic lethality and vascular defects in mice lacking the Notch ligand Jagged1 | Q28589104 | ||
Dynamic expression and essential functions of Hes7 in somite segmentation | Q28593057 | ||
The notch signalling regulator fringe acts in the Golgi apparatus and requires the glycosyltransferase signature motif DXD. | Q33909902 | ||
Somite formation and patterning | Q33914527 | ||
Notch signalling and the synchronization of the somite segmentation clock | Q33926876 | ||
Fringe modulation of Jagged1-induced Notch signaling requires the action of beta 4galactosyltransferase-1 | Q33949989 | ||
A molecular clock involved in somite segmentation. | Q34173684 | ||
Perinatal lethality and defects in hindbrain development in mice homozygous for a targeted mutation of the zinc finger gene Krox20. | Q34343668 | ||
Maintenance of somite borders in mice requires the Delta homologue DII1. | Q34422203 | ||
Fringe differentially modulates Jagged1 and Delta1 signalling through Notch1 and Notch2. | Q40862987 | ||
Mammalian Notch1 is modified with two unusual forms of O-linked glycosylation found on epidermal growth factor-like modules | Q40891320 | ||
Glycosyltransferase activity of Fringe modulates Notch-Delta interactions. | Q45345395 | ||
A mouse gene of the paired-related homeobox class expressed in the caudal somite compartment and in the developing vertebral column, kidney and nervous system | Q47681842 | ||
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 | ||
Homologues of c-hairy1 (her9) and lunatic fringe in zebrafish are expressed in the developing central nervous system, but not in the presomitic mesoderm | Q48333698 | ||
Zebrafish lunatic fringe demarcates segmental boundaries. | Q52133312 | ||
Mesp2 initiates somite segmentation through the Notch signalling pathway. | Q52166230 | ||
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 | ||
Fringe modulates Notch-ligand interactions. | Q52194027 | ||
Notch1 is essential for postimplantation development in mice. | Q52512097 | ||
Interaction between Notch signalling and Lunatic fringe during somite boundary formation in the mouse | Q57315074 | ||
Galaxy clusters: Well of darkness | Q57746408 | ||
A mutation in the Lunatic fringe gene suppresses the effects of a Jagged2 mutation on inner hair cell development in the cochlea | Q73849637 | ||
P433 | issue | 1 | |
P921 | main subject | phenotype | Q104053 |
Delta like canonical Notch ligand 1 | Q21982911 | ||
Delta like canonical Notch ligand 3 | Q21982924 | ||
LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Q21986096 | ||
Notch 1 | Q21986193 | ||
P304 | page(s) | 21–28 | |
P577 | publication date | 2002-05-01 | |
P1433 | published in | Genesis | Q5532784 |
P1476 | title | Segmentation defects of Notch pathway mutants and absence of a synergistic phenotype in lunatic fringe/radical fringe double mutant mice | |
P478 | volume | 33 |
Q37405136 | A Notch updated |
Q28742953 | A survey of small RNAs in human sperm |
Q36821431 | Anabolic actions of Notch on mature bone |
Q51946283 | Bile duct proliferation in Jag1/fringe heterozygous mice identifies candidate modifiers of the Alagille syndrome hepatic phenotype. |
Q28589511 | Dll3 pudgy mutation differentially disrupts dynamic expression of somite genes |
Q35101893 | Fine-tuning Notch1 activation by endocytosis and glycosylation |
Q28509366 | Fringe glycosyltransferases differentially modulate Notch1 proteolysis induced by Delta1 and Jagged1 |
Q34492882 | Lipid phosphate phosphatase-2 activity regulates S-phase entry of the cell cycle in Rat2 fibroblasts |
Q46749922 | Lunatic fringe, manic fringe, and radical fringe recognize similar specificity determinants in O-fucosylated epidermal growth factor-like repeats |
Q36389083 | Lunatic, Manic, and Radical Fringe Each Promote T and B Cell Development |
Q37145399 | MFng is dispensable for mouse pancreas development and function |
Q37421674 | Manic fringe is not required for embryonic development, and fringe family members do not exhibit redundant functions in the axial skeleton, limb, or hindbrain |
Q46419557 | Modulation of Notch Signaling During Somitogenesis |
Q24540500 | Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype |
Q24323154 | Mutation of the fucose-specific beta1,3 N-acetylglucosaminyltransferase LFNG results in abnormal formation of the spine |
Q32874834 | Negative feedback loop formed by Lunatic fringe and Hes7 controls their oscillatory expression during somitogenesis |
Q46795621 | Notch Signaling in Development, Tissue Homeostasis, and Disease |
Q35858248 | Notch signaling in mammary development and oncogenesis |
Q36140085 | Notch signaling in the mammalian central nervous system: insights from mouse mutants |
Q28587727 | Notch signaling regulates left-right asymmetry determination by inducing Nodal expression |
Q28504465 | Notch signalling in the paraxial mesoderm is most sensitive to reduced Pofut1 levels during early mouse development |
Q28512806 | Notch1 and 2 cooperate in limb ectoderm to receive an early Jagged2 signal regulating interdigital apoptosis |
Q28545998 | O-fucosylation of DLL3 is required for its function during somitogenesis |
Q24677654 | Protein O -fucosyltransferase 1 is an essential component of Notch signaling pathways |
Q36382727 | Regulation of intrathymic T-cell development by Lunatic Fringe- Notch1 interactions |
Q33969519 | Role of glycosylation of Notch in development |
Q37308624 | Role of unusual O-glycans in intercellular signaling |
Q34023789 | Roles of Glycosylation in Notch Signaling |
Q34585462 | Roles of O-fucose glycans in notch signaling revealed by mutant mice. |
Q41773509 | Structural and mechanistic insights into lunatic fringe from a kinetic analysis of enzyme mutants |
Q28584296 | The divergent DSL ligand Dll3 does not activate Notch signaling but cell autonomously attenuates signaling induced by other DSL ligands |
Q52009415 | The fringe molecules induce endocrine differentiation in embryonic endoderm by activating cMyt1/cMyt3. |
Q36488814 | The long and short of it: somite formation in mice |
Q37256458 | The many facets of Notch ligands |
Q37888532 | The mouse notches up another success: understanding the causes of human vertebral malformation. |
Q62555277 | The mouse rib-vertebrae mutation is a hypomorphic Tbx6 allele |
Q38547337 | The multiple roles of epidermal growth factor repeat O-glycans in animal development |
Q34116042 | The search for glycan function: fucosylation of the TGF-beta1 receptor is required for receptor activation |
Q24672577 | Transcriptional oscillation of lunatic fringe is essential for somitogenesis |
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