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Results: 1 to 20 of 24

Cited In for PubMed (Select 21271641)

1.

Neuropilins define distinct populations of neural crest cells.

Lumb R, Wiszniak S, Kabbara S, Scherer M, Harvey N, Schwarz Q.

Neural Dev. 2014 Nov 3;9(1):24. doi: 10.1186/1749-8104-9-24.

2.

Sox2 acts as a rheostat of epithelial to mesenchymal transition during neural crest development.

Mandalos N, Rhinn M, Granchi Z, Karampelas I, Mitsiadis T, Economides AN, Dollé P, Remboutsika E.

Front Physiol. 2014 Sep 12;5:345. doi: 10.3389/fphys.2014.00345. eCollection 2014.

3.

Identification of a face enhancer reveals direct regulation of LIM homeobox 8 (Lhx8) by wingless-int (WNT)/β-catenin signaling.

Landin Malt A, Cesario JM, Tang Z, Brown S, Jeong J.

J Biol Chem. 2014 Oct 31;289(44):30289-301. doi: 10.1074/jbc.M114.592014. Epub 2014 Sep 4.

PMID:
25190800
4.

A neuron autonomous role for the familial dysautonomia gene ELP1 in sympathetic and sensory target tissue innervation.

Jackson MZ, Gruner KA, Qin C, Tourtellotte WG.

Development. 2014 Jun;141(12):2452-61. doi: 10.1242/dev.107797.

5.

Human stem cells for craniomaxillofacial reconstruction.

Jalali M, Kirkpatrick WN, Cameron MG, Pauklin S, Vallier L.

Stem Cells Dev. 2014 Jul 1;23(13):1437-51. doi: 10.1089/scd.2013.0576. Epub 2014 Apr 2.

6.

The neural crest cell cycle is related to phases of migration in the head.

Ridenour DA, McLennan R, Teddy JM, Semerad CL, Haug JS, Kulesa PM.

Development. 2014 Mar;141(5):1095-103. doi: 10.1242/dev.098855.

7.

Tissue specific roles for the ribosome biogenesis factor Wdr43 in zebrafish development.

Zhao C, Andreeva V, Gibert Y, LaBonty M, Lattanzi V, Prabhudesai S, Zhou Y, Zon L, McCann KL, Baserga S, Yelick PC.

PLoS Genet. 2014 Jan 30;10(1):e1004074. doi: 10.1371/journal.pgen.1004074. eCollection 2014 Jan.

8.

Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears.

Gordon CT, Petit F, Kroisel PM, Jakobsen L, Zechi-Ceide RM, Oufadem M, Bole-Feysot C, Pruvost S, Masson C, Tores F, Hieu T, Nitschké P, Lindholm P, Pellerin P, Guion-Almeida ML, Kokitsu-Nakata NM, Vendramini-Pittoli S, Munnich A, Lyonnet S, Holder-Espinasse M, Amiel J.

Am J Hum Genet. 2013 Dec 5;93(6):1118-25. doi: 10.1016/j.ajhg.2013.10.023. Epub 2013 Nov 21.

9.

A critical role for PDGFRα signaling in medial nasal process development.

He F, Soriano P.

PLoS Genet. 2013;9(9):e1003851. doi: 10.1371/journal.pgen.1003851. Epub 2013 Sep 26.

10.

Susceptibility to DNA damage as a molecular mechanism for non-syndromic cleft lip and palate.

Kobayashi GS, Alvizi L, Sunaga DY, Francis-West P, Kuta A, Almada BV, Ferreira SG, de Andrade-Lima LC, Bueno DF, Raposo-Amaral CE, Menck CF, Passos-Bueno MR.

PLoS One. 2013 Jun 12;8(6):e65677. doi: 10.1371/journal.pone.0065677. Print 2013.

11.

Zebrafish Zic2a and Zic2b regulate neural crest and craniofacial development.

Teslaa JJ, Keller AN, Nyholm MK, Grinblat Y.

Dev Biol. 2013 Aug 1;380(1):73-86. doi: 10.1016/j.ydbio.2013.04.033. Epub 2013 May 8.

12.

Human genetic variation within neural crest enhancers: molecular and phenotypic implications.

Rada-Iglesias A, Prescott SL, Wysocka J.

Philos Trans R Soc Lond B Biol Sci. 2013 May 6;368(1620):20120360. doi: 10.1098/rstb.2012.0360. Print 2013. Review.

13.

Hand in glove: brain and skull in development and dysmorphogenesis.

Richtsmeier JT, Flaherty K.

Acta Neuropathol. 2013 Apr;125(4):469-89. doi: 10.1007/s00401-013-1104-y. Epub 2013 Mar 23. Review.

14.

Trisomy 21 and facial developmental instability.

Starbuck JM, Cole TM 3rd, Reeves RH, Richtsmeier JT.

Am J Phys Anthropol. 2013 May;151(1):49-57. doi: 10.1002/ajpa.22255. Epub 2013 Mar 15.

15.

Ground-state transcriptional requirements for skin-derived precursors.

Suflita MT, Pfaltzgraff ER, Mundell NA, Pevny LH, Labosky PA.

Stem Cells Dev. 2013 Jun 15;22(12):1779-88. doi: 10.1089/scd.2012.0501. Epub 2013 Feb 27.

16.

Regenerative strategies for craniofacial disorders.

Garland CB, Pomerantz JH.

Front Physiol. 2012 Dec 14;3:453. doi: 10.3389/fphys.2012.00453. eCollection 2012.

17.

Recurrent de novo mutations in PACS1 cause defective cranial-neural-crest migration and define a recognizable intellectual-disability syndrome.

Schuurs-Hoeijmakers JH, Oh EC, Vissers LE, Swinkels ME, Gilissen C, Willemsen MA, Holvoet M, Steehouwer M, Veltman JA, de Vries BB, van Bokhoven H, de Brouwer AP, Katsanis N, Devriendt K, Brunner HG.

Am J Hum Genet. 2012 Dec 7;91(6):1122-7. doi: 10.1016/j.ajhg.2012.10.013. Epub 2012 Nov 15.

18.

Atypical face shape and genomic structural variants in epilepsy.

Chinthapalli K, Bartolini E, Novy J, Suttie M, Marini C, Falchi M, Fox Z, Clayton LM, Sander JW, Guerrini R, Depondt C, Hennekam R, Hammond P, Sisodiya SM.

Brain. 2012 Oct;135(Pt 10):3101-14. doi: 10.1093/brain/aws232. Epub 2012 Sep 13.

19.

Stem cells in the face: tooth regeneration and beyond.

Mao JJ, Prockop DJ.

Cell Stem Cell. 2012 Sep 7;11(3):291-301. doi: 10.1016/j.stem.2012.08.010. Review. Erratum in: Cell Stem Cell. 2012 Oct 5;11(4):579. Robey, Pamela G [removed].

20.

A stable cranial neural crest cell line from mouse.

Ishii M, Arias AC, Liu L, Chen YB, Bronner ME, Maxson RE.

Stem Cells Dev. 2012 Nov 20;21(17):3069-80. doi: 10.1089/scd.2012.0155. Epub 2012 Oct 4.

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