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Items: 1 to 20 of 103


fgf20 is essential for initiating zebrafish fin regeneration.

Whitehead GG, Makino S, Lien CL, Keating MT.

Science. 2005 Dec 23;310(5756):1957-60.


Bentho-pelagic divergence of cichlid feeding architecture was prodigious and consistent during multiple adaptive radiations within African rift-lakes.

Cooper WJ, Parsons K, McIntyre A, Kern B, McGee-Moore A, Albertson RC.

PLoS One. 2010 Mar 8;5(3):e9551. doi: 10.1371/journal.pone.0009551.


FishFace: interactive atlas of zebrafish craniofacial development at cellular resolution.

Eames BF, DeLaurier A, Ullmann B, Huycke TR, Nichols JT, Dowd J, McFadden M, Sasaki MM, Kimmel CB.

BMC Dev Biol. 2013 May 28;13:23. doi: 10.1186/1471-213X-13-23.


Fgf8 haploinsufficiency results in distinct craniofacial defects in adult zebrafish.

Albertson RC, Yelick PC.

Dev Biol. 2007 Jun 15;306(2):505-15. Epub 2007 Mar 24.


Zebrafish Craniofacial Development: A Window into Early Patterning.

Mork L, Crump G.

Curr Top Dev Biol. 2015;115:235-69. doi: 10.1016/bs.ctdb.2015.07.001. Epub 2015 Oct 6. Review.


Further analysis of the Crouzon mouse: effects of the FGFR2(C342Y) mutation are cranial bone-dependent.

Liu J, Nam HK, Wang E, Hatch NE.

Calcif Tissue Int. 2013 May;92(5):451-66. doi: 10.1007/s00223-013-9701-2. Epub 2013 Jan 29.


Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice.

Motch Perrine SM, Cole TM 3rd, Martínez-Abadías N, Aldridge K, Jabs EW, Richtsmeier JT.

BMC Dev Biol. 2014 Feb 28;14:8. doi: 10.1186/1471-213X-14-8.


Cell adhesion molecule cadherin-6 function in zebrafish cranial and lateral line ganglia development.

Liu Q, Dalman MR, Sarmah S, Chen S, Chen Y, Hurlbut AK, Spencer MA, Pancoe L, Marrs JA.

Dev Dyn. 2011 Jul;240(7):1716-26. doi: 10.1002/dvdy.22665. Epub 2011 May 16.


Divergent requirements for fibroblast growth factor signaling in zebrafish maxillary barbel and caudal fin regeneration.

Duszynski RJ, Topczewski J, LeClair EE.

Dev Growth Differ. 2013 Feb;55(2):282-300. doi: 10.1111/dgd.12035. Epub 2013 Jan 28.


Fgf20b is required for the ectomesenchymal fate establishment of cranial neural crest cells in zebrafish.

Yamauchi H, Goto M, Katayama M, Miyake A, Itoh N.

Biochem Biophys Res Commun. 2011 Jun 17;409(4):705-10. doi: 10.1016/j.bbrc.2011.05.069. Epub 2011 May 20.


The feelgood mutation in zebrafish dysregulates COPII-dependent secretion of select extracellular matrix proteins in skeletal morphogenesis.

Melville DB, Montero-Balaguer M, Levic DS, Bradley K, Smith JR, Hatzopoulos AK, Knapik EW.

Dis Model Mech. 2011 Nov;4(6):763-76. doi: 10.1242/dmm.007625. Epub 2011 Jul 4.


The craniofacial phenotype of the Crouzon mouse: analysis of a model for syndromic craniosynostosis using three-dimensional MicroCT.

Perlyn CA, DeLeon VB, Babbs C, Govier D, Burell L, Darvann T, Kreiborg S, Morriss-Kay G.

Cleft Palate Craniofac J. 2006 Nov;43(6):740-8.


lessen encodes a zebrafish trap100 required for enteric nervous system development.

Pietsch J, Delalande JM, Jakaitis B, Stensby JD, Dohle S, Talbot WS, Raible DW, Shepherd IT.

Development. 2006 Feb;133(3):395-406. Epub 2006 Jan 5.


Tissue-specific responses to aberrant FGF signaling in complex head phenotypes.

Martínez-Abadías N, Motch SM, Pankratz TL, Wang Y, Aldridge K, Jabs EW, Richtsmeier JT.

Dev Dyn. 2013 Jan;242(1):80-94. doi: 10.1002/dvdy.23903. Epub 2012 Dec 5.


Craniofacial skeletal defects of adult zebrafish Glypican 4 (knypek) mutants.

LeClair EE, Mui SR, Huang A, Topczewska JM, Topczewski J.

Dev Dyn. 2009 Oct;238(10):2550-63. doi: 10.1002/dvdy.22086.


Prdm1a is necessary for posterior pharyngeal arch development in zebrafish.

Birkholz DA, Olesnicky Killian EC, George KM, Artinger KB.

Dev Dyn. 2009 Oct;238(10):2575-87. doi: 10.1002/dvdy.22090.

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