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Items: 18


Widely tunable GaAs bandgap via strain engineering in core/shell nanowires with large lattice mismatch.

Balaghi L, Bussone G, Grifone R, Hübner R, Grenzer J, Ghorbani-Asl M, Krasheninnikov AV, Schneider H, Helm M, Dimakis E.

Nat Commun. 2019 Jun 26;10(1):2793. doi: 10.1038/s41467-019-10654-7.


Expression patterns of Rbm24 in lens, nasal epithelium, and inner ear during mouse embryonic development.

Grifone R, Saquet A, Xu Z, Shi DL.

Dev Dyn. 2018 Oct;247(10):1160-1169. doi: 10.1002/dvdy.24666. Epub 2018 Oct 7.


Strain distribution in single, suspended germanium nanowires studied using nanofocused x-rays.

Keplinger M, Grifone R, Greil J, Kriegner D, Persson J, Lugstein A, Schülli T, Stangl J.

Nanotechnology. 2016 Feb 5;27(5):055705. doi: 10.1088/0957-4484/27/5/055705. Epub 2016 Jan 12.


The RNA-binding protein Rbm24 is transiently expressed in myoblasts and is required for myogenic differentiation during vertebrate development.

Grifone R, Xie X, Bourgeois A, Saquet A, Duprez D, Shi DL.

Mech Dev. 2014 Nov;134:1-15. doi: 10.1016/j.mod.2014.08.003. Epub 2014 Sep 16.


Compact ultrahigh vacuum sample environments for x-ray nanobeam diffraction and imaging.

Evans PG, Chahine G, Grifone R, Jacques VL, Spalenka JW, Schülli TU.

Rev Sci Instrum. 2013 Nov;84(11):113903. doi: 10.1063/1.4829629.


Six1 regulates stem cell repair potential and self-renewal during skeletal muscle regeneration.

Le Grand F, Grifone R, Mourikis P, Houbron C, Gigaud C, Pujol J, Maillet M, Pagès G, Rudnicki M, Tajbakhsh S, Maire P.

J Cell Biol. 2012 Sep 3;198(5):815-32. doi: 10.1083/jcb.201201050.


In situ three-dimensional reciprocal-space mapping during mechanical deformation.

Cornelius TW, Davydok A, Jacques VL, Grifone R, Schülli T, Richard MI, Beutier G, Verdier M, Metzger TH, Pietsch U, Thomas O.

J Synchrotron Radiat. 2012 Sep;19(Pt 5):688-94. doi: 10.1107/S0909049512023758. Epub 2012 Jul 7.


Inactivation of Six2 in mouse identifies a novel genetic mechanism controlling development and growth of the cranial base.

He G, Tavella S, Hanley KP, Self M, Oliver G, Grifone R, Hanley N, Ward C, Bobola N.

Dev Biol. 2010 Aug 15;344(2):720-30. doi: 10.1016/j.ydbio.2010.05.509. Epub 2010 May 31.


Relationship between neural crest cells and cranial mesoderm during head muscle development.

Grenier J, Teillet MA, Grifone R, Kelly RG, Duprez D.

PLoS One. 2009;4(2):e4381. doi: 10.1371/journal.pone.0004381. Epub 2009 Feb 9.


Properties of branchiomeric and somite-derived muscle development in Tbx1 mutant embryos.

Grifone R, Jarry T, Dandonneau M, Grenier J, Duprez D, Kelly RG.

Dev Dyn. 2008 Oct;237(10):3071-8. doi: 10.1002/dvdy.21718.


Heartening news for head muscle development.

Grifone R, Kelly RG.

Trends Genet. 2007 Aug;23(8):365-9. Epub 2007 May 23.


Eya1 and Eya2 proteins are required for hypaxial somitic myogenesis in the mouse embryo.

Grifone R, Demignon J, Giordani J, Niro C, Souil E, Bertin F, Laclef C, Xu PX, Maire P.

Dev Biol. 2007 Feb 15;302(2):602-16. Epub 2006 Sep 1.


Apoptotic neutrophils release macrophage migration inhibitory factor upon stimulation with tumor necrosis factor-alpha.

Daryadel A, Grifone RF, Simon HU, Yousefi S.

J Biol Chem. 2006 Sep 15;281(37):27653-61. Epub 2006 Jul 21.


Patterning of the third pharyngeal pouch into thymus/parathyroid by Six and Eya1.

Zou D, Silvius D, Davenport J, Grifone R, Maire P, Xu PX.

Dev Biol. 2006 May 15;293(2):499-512. Epub 2006 Mar 10.


Six1 and Six4 homeoproteins are required for Pax3 and Mrf expression during myogenesis in the mouse embryo.

Grifone R, Demignon J, Houbron C, Souil E, Niro C, Seller MJ, Hamard G, Maire P.

Development. 2005 May;132(9):2235-49. Epub 2005 Mar 23.


Six1 and Eya1 expression can reprogram adult muscle from the slow-twitch phenotype into the fast-twitch phenotype.

Grifone R, Laclef C, Spitz F, Lopez S, Demignon J, Guidotti JE, Kawakami K, Xu PX, Kelly R, Petrof BJ, Daegelen D, Concordet JP, Maire P.

Mol Cell Biol. 2004 Jul;24(14):6253-67.


Delineation of a 2.8 megabases region harboring a potential tumor suppressor gene involved in renal cell carcinoma, that is commonly deleted from chromosome 14.

Gallou C, Méjean A, Bouvier R, Lucien F, Perennou M, Zindy PJ, Grifone R, Chrétien Y, Junien C, Béroud C.

Anticancer Res. 2003 Nov-Dec;23(6C):4865-70.


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