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Items: 10

1.
2.

Multipotent versus differentiated cell fate selection in the developing Drosophila airways.

Matsuda R, Hosono C, Samakovlis C, Saigo K.

Elife. 2015 Dec 2;4. pii: e09646. doi: 10.7554/eLife.09646.

3.

The archipelago ubiquitin ligase subunit acts in target tissue to restrict tracheal terminal cell branching and hypoxic-induced gene expression.

Mortimer NT, Moberg KH.

PLoS Genet. 2013;9(2):e1003314. doi: 10.1371/journal.pgen.1003314. Epub 2013 Feb 14.

4.

Liquid facets-related (lqfR) is required for egg chamber morphogenesis during Drosophila oogenesis.

Leventis PA, Da Sylva TR, Rajwans N, Wasiak S, McPherson PS, Boulianne GL.

PLoS One. 2011;6(10):e25466. doi: 10.1371/journal.pone.0025466. Epub 2011 Oct 17.

5.

Regulation of the Drosophila hypoxia-inducible factor alpha Sima by CRM1-dependent nuclear export.

Romero NM, Irisarri M, Roth P, Cauerhff A, Samakovlis C, Wappner P.

Mol Cell Biol. 2008 May;28(10):3410-23. doi: 10.1128/MCB.01027-07. Epub 2008 Mar 10.

6.
7.

From fate to function: the Drosophila trachea and salivary gland as models for tubulogenesis.

Kerman BE, Cheshire AM, Andrew DJ.

Differentiation. 2006 Sep;74(7):326-48. Review.

8.

dAkt kinase controls follicle cell size during Drosophila oogenesis.

Cavaliere V, Donati A, Hsouna A, Hsu T, Gargiulo G.

Dev Dyn. 2005 Mar;232(3):845-54.

9.

Coordinated functions of Akt/PKB and ETS1 in tubule formation.

Lavenburg KR, Ivey J, Hsu T, Muise-Helmericks RC.

FASEB J. 2003 Dec;17(15):2278-80. Epub 2003 Oct 2.

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