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Items: 1 to 20 of 122

1.
2.

Retinoic Acid Activity in Undifferentiated Neural Progenitors Is Sufficient to Fulfill Its Role in Restricting Fgf8 Expression for Somitogenesis.

Cunningham TJ, Brade T, Sandell LL, Lewandoski M, Trainor PA, Colas A, Mercola M, Duester G.

PLoS One. 2015 Sep 14;10(9):e0137894. doi: 10.1371/journal.pone.0137894. eCollection 2015.

3.

Requirement of mesodermal retinoic acid generated by Raldh2 for posterior neural transformation.

Molotkova N, Molotkov A, Sirbu IO, Duester G.

Mech Dev. 2005 Feb;122(2):145-55.

4.

Retinoic acid regulation of the somitogenesis clock.

Duester G.

Birth Defects Res C Embryo Today. 2007 Jun;81(2):84-92. Review.

5.

Modelling asymmetric somitogenesis: Deciphering the mechanisms behind species differences.

Vroomans RMA, Ten Tusscher KHWJ.

Dev Biol. 2017 Jul 1;427(1):21-34. doi: 10.1016/j.ydbio.2017.05.010. Epub 2017 May 12.

PMID:
28506615
6.

Retinoic acid controls the bilateral symmetry of somite formation in the mouse embryo.

Vermot J, Gallego Llamas J, Fraulob V, Niederreither K, Chambon P, Dollé P.

Science. 2005 Apr 22;308(5721):563-6. Epub 2005 Feb 24.

7.

Uncoupling of retinoic acid signaling from tailbud development before termination of body axis extension.

Cunningham TJ, Zhao X, Duester G.

Genesis. 2011 Oct;49(10):776-83. doi: 10.1002/dvg.20763. Epub 2011 Aug 24.

8.

The zebrafish neckless mutation reveals a requirement for raldh2 in mesodermal signals that pattern the hindbrain.

Begemann G, Schilling TF, Rauch GJ, Geisler R, Ingham PW.

Development. 2001 Aug;128(16):3081-94.

9.

Rere controls retinoic acid signalling and somite bilateral symmetry.

Vilhais-Neto GC, Maruhashi M, Smith KT, Vasseur-Cognet M, Peterson AS, Workman JL, Pourquié O.

Nature. 2010 Feb 18;463(7283):953-7. doi: 10.1038/nature08763.

PMID:
20164929
10.

Retinoic acid signalling in the zebrafish embryo is necessary during pre-segmentation stages to pattern the anterior-posterior axis of the CNS and to induce a pectoral fin bud.

Grandel H, Lun K, Rauch GJ, Rhinn M, Piotrowski T, Houart C, Sordino P, Küchler AM, Schulte-Merker S, Geisler R, Holder N, Wilson SW, Brand M.

Development. 2002 Jun;129(12):2851-65.

11.

Retinoic acid controls body axis extension by directly repressing Fgf8 transcription.

Kumar S, Duester G.

Development. 2014 Aug;141(15):2972-7. doi: 10.1242/dev.112367.

12.
14.

Retinoic acid signalling links left-right asymmetric patterning and bilaterally symmetric somitogenesis in the zebrafish embryo.

Kawakami Y, Raya A, Raya RM, Rodríguez-Esteban C, Izpisúa Belmonte JC.

Nature. 2005 May 12;435(7039):165-71.

15.
16.

Retinoic acid promotes limb induction through effects on body axis extension but is unnecessary for limb patterning.

Zhao X, Sirbu IO, Mic FA, Molotkova N, Molotkov A, Kumar S, Duester G.

Curr Biol. 2009 Jun 23;19(12):1050-7. doi: 10.1016/j.cub.2009.04.059. Epub 2009 May 21.

17.
18.
19.

Retinoic acid activates myogenesis in vivo through Fgf8 signalling.

Hamade A, Deries M, Begemann G, Bally-Cuif L, Genêt C, Sabatier F, Bonnieu A, Cousin X.

Dev Biol. 2006 Jan 1;289(1):127-40. Epub 2005 Nov 28.

20.

Surface ectoderm is necessary for the morphogenesis of somites.

Correia KM, Conlon RA.

Mech Dev. 2000 Mar 1;91(1-2):19-30.

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