254 related articles for article (PubMed ID: 17937396)
1. Mouse Ripply2 is downstream of Wnt3a and is dynamically expressed during somitogenesis.
Biris KK; Dunty WC; Yamaguchi TP
Dev Dyn; 2007 Nov; 236(11):3167-72. PubMed ID: 17937396
[TBL] [Abstract][Full Text] [Related]
2. Wnt3a/beta-catenin signaling controls posterior body development by coordinating mesoderm formation and segmentation.
Dunty WC; Biris KK; Chalamalasetty RB; Taketo MM; Lewandoski M; Yamaguchi TP
Development; 2008 Jan; 135(1):85-94. PubMed ID: 18045842
[TBL] [Abstract][Full Text] [Related]
3. Segmental border is defined by Ripply2-mediated Tbx6 repression independent of Mesp2.
Zhao W; Ajima R; Ninomiya Y; Saga Y
Dev Biol; 2015 Apr; 400(1):105-17. PubMed ID: 25641698
[TBL] [Abstract][Full Text] [Related]
4. Presomitic mesoderm-specific expression of the transcriptional repressor
Hayashi S; Nakahata Y; Kohno K; Matsui T; Bessho Y
J Biol Chem; 2018 Aug; 293(31):12167-12176. PubMed ID: 29895619
[TBL] [Abstract][Full Text] [Related]
5. Notch is a critical component of the mouse somitogenesis oscillator and is essential for the formation of the somites.
Ferjentsik Z; Hayashi S; Dale JK; Bessho Y; Herreman A; De Strooper B; del Monte G; de la Pompa JL; Maroto M
PLoS Genet; 2009 Sep; 5(9):e1000662. PubMed ID: 19779553
[TBL] [Abstract][Full Text] [Related]
6. The oscillation of Notch activation, but not its boundary, is required for somite border formation and rostral-caudal patterning within a somite.
Oginuma M; Takahashi Y; Kitajima S; Kiso M; Kanno J; Kimura A; Saga Y
Development; 2010 May; 137(9):1515-22. PubMed ID: 20335362
[TBL] [Abstract][Full Text] [Related]
7. Oscillating expression of c-Hey2 in the presomitic mesoderm suggests that the segmentation clock may use combinatorial signaling through multiple interacting bHLH factors.
Leimeister C; Dale K; Fischer A; Klamt B; Hrabe de Angelis M; Radtke F; McGrew MJ; Pourquié O; Gessler M
Dev Biol; 2000 Nov; 227(1):91-103. PubMed ID: 11076679
[TBL] [Abstract][Full Text] [Related]
8. From dynamic expression patterns to boundary formation in the presomitic mesoderm.
Tiedemann HB; Schneltzer E; Zeiser S; Hoesel B; Beckers J; Przemeck GK; de Angelis MH
PLoS Comput Biol; 2012; 8(6):e1002586. PubMed ID: 22761566
[TBL] [Abstract][Full Text] [Related]
9. Wnt3a plays a major role in the segmentation clock controlling somitogenesis.
Aulehla A; Wehrle C; Brand-Saberi B; Kemler R; Gossler A; Kanzler B; Herrmann BG
Dev Cell; 2003 Mar; 4(3):395-406. PubMed ID: 12636920
[TBL] [Abstract][Full Text] [Related]
10. Mouse Nkd1, a Wnt antagonist, exhibits oscillatory gene expression in the PSM under the control of Notch signaling.
Ishikawa A; Kitajima S; Takahashi Y; Kokubo H; Kanno J; Inoue T; Saga Y
Mech Dev; 2004 Dec; 121(12):1443-53. PubMed ID: 15511637
[TBL] [Abstract][Full Text] [Related]
11. Mesp2 and Tbx6 cooperatively create periodic patterns coupled with the clock machinery during mouse somitogenesis.
Oginuma M; Niwa Y; Chapman DL; Saga Y
Development; 2008 Aug; 135(15):2555-62. PubMed ID: 18579680
[TBL] [Abstract][Full Text] [Related]
12. Posterior-anterior gradient of zebrafish hes6 expression in the presomitic mesoderm is established by the combinatorial functions of the downstream enhancer and 3'UTR.
Kawamura A; Ovara H; Ooka Y; Kinoshita H; Hoshikawa M; Nakajo K; Yokota D; Fujino Y; Higashijima S; Takada S; Yamasu K
Dev Biol; 2016 Jan; 409(2):543-54. PubMed ID: 26596999
[TBL] [Abstract][Full Text] [Related]
13. Dact1 presomitic mesoderm expression oscillates in phase with Axin2 in the somitogenesis clock of mice.
Suriben R; Fisher DA; Cheyette BN
Dev Dyn; 2006 Nov; 235(11):3177-83. PubMed ID: 17013874
[TBL] [Abstract][Full Text] [Related]
14. Somitogenesis in the anole lizard and alligator reveals evolutionary convergence and divergence in the amniote segmentation clock.
Eckalbar WL; Lasku E; Infante CR; Elsey RM; Markov GJ; Allen AN; Corneveaux JJ; Losos JB; DeNardo DF; Huentelman MJ; Wilson-Rawls J; Rawls A; Kusumi K
Dev Biol; 2012 Mar; 363(1):308-19. PubMed ID: 22178152
[TBL] [Abstract][Full Text] [Related]
15. Dynamic CREB family activity drives segmentation and posterior polarity specification in mammalian somitogenesis.
Lopez TP; Fan CM
Proc Natl Acad Sci U S A; 2013 May; 110(22):E2019-27. PubMed ID: 23671110
[TBL] [Abstract][Full Text] [Related]
16. Dynamic expression of lunatic fringe suggests a link between notch signaling and an autonomous cellular oscillator driving somite segmentation.
Aulehla A; Johnson RL
Dev Biol; 1999 Mar; 207(1):49-61. PubMed ID: 10049564
[TBL] [Abstract][Full Text] [Related]
17. Sprouty4, an FGF inhibitor, displays cyclic gene expression under the control of the notch segmentation clock in the mouse PSM.
Hayashi S; Shimoda T; Nakajima M; Tsukada Y; Sakumura Y; Dale JK; Maroto M; Kohno K; Matsui T; Bessho Y
PLoS One; 2009; 4(5):e5603. PubMed ID: 19440349
[TBL] [Abstract][Full Text] [Related]
18. Oscillatory gene expression and somitogenesis.
Kageyama R; Niwa Y; Isomura A; González A; Harima Y
Wiley Interdiscip Rev Dev Biol; 2012; 1(5):629-41. PubMed ID: 23799565
[TBL] [Abstract][Full Text] [Related]
19. Scanning electron microscopic evidence for physical segmental boundaries in the anterior presomitic mesoderm.
Pu Q; Patel K; Berger J; Christ B; Huang R
Ann Anat; 2013 Oct; 195(5):484-7. PubMed ID: 23742979
[TBL] [Abstract][Full Text] [Related]
20. Ripply2 is essential for precise somite formation during mouse early development.
Chan T; Kondow A; Hosoya A; Hitachi K; Yukita A; Okabayashi K; Nakamura H; Ozawa H; Kiyonari H; Michiue T; Ito Y; Asashima M
FEBS Lett; 2007 Jun; 581(14):2691-6. PubMed ID: 17531978
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]