Merrill AE - Search Results

1

Ribosome biogenesis in skeletal development and the pathogenesis of skeletal disorders.

Trainor PA, Merrill AE. Trainor PA, et al. Among authors: merrill ae. Biochim Biophys Acta. 2014 Jun;1842(6):769-78. doi: 10.1016/j.bbadis.2013.11.010. Epub 2013 Nov 16. Biochim Biophys Acta. 2014. PMID: 24252615 Free PMC article. Review.

2

Signaling Pathways in Craniofacial Development: Insights from Rare Skeletal Disorders.

Neben CL, Merrill AE. Neben CL, et al. Among authors: merrill ae. Curr Top Dev Biol. 2015;115:493-542. doi: 10.1016/bs.ctdb.2015.09.005. Epub 2015 Oct 23. Curr Top Dev Biol. 2015. PMID: 26589936 Review.

3

The Roles of RNA Polymerase I and III Subunits Polr1c and Polr1d in Craniofacial Development and in Zebrafish Models of Treacher Collins Syndrome.

Noack Watt KE, Achilleos A, Neben CL, Merrill AE, Trainor PA. Noack Watt KE, et al. Among authors: merrill ae. PLoS Genet. 2016 Jul 22;12(7):e1006187. doi: 10.1371/journal.pgen.1006187. eCollection 2016 Jul. PLoS Genet. 2016. PMID: 27448281 Free PMC article.

4

Ribosome biogenesis is dynamically regulated during osteoblast differentiation.

Neben CL, Lay FD, Mao X, Tuzon CT, Merrill AE. Neben CL, et al. Among authors: merrill ae. Gene. 2017 May 15;612:29-35. doi: 10.1016/j.gene.2016.11.010. Epub 2016 Nov 12. Gene. 2017. PMID: 27847259 Free PMC article.

5

tp53-dependent and independent signaling underlies the pathogenesis and possible prevention of Acrofacial Dysostosis-Cincinnati type.

Watt KEN, Neben CL, Hall S, Merrill AE, Trainor PA. Watt KEN, et al. Among authors: merrill ae. Hum Mol Genet. 2018 Aug 1;27(15):2628-2643. doi: 10.1093/hmg/ddy172. Hum Mol Genet. 2018. PMID: 29750247 Free PMC article.

6

Bent bone dysplasia-FGFR2 type, a distinct skeletal disorder, has deficient canonical FGF signaling.

Merrill AE, Sarukhanov A, Krejci P, Idoni B, Camacho N, Estrada KD, Lyons KM, Deixler H, Robinson H, Chitayat D, Curry CJ, Lachman RS, Wilcox WR, Krakow D. Merrill AE, et al. Am J Hum Genet. 2012 Mar 9;90(3):550-7. doi: 10.1016/j.ajhg.2012.02.005. Epub 2012 Mar 1. Am J Hum Genet. 2012. PMID: 22387015 Free PMC article.

7

A requirement for Fgfr2 in middle ear development.

Rigueur D, Roberts RR, Bobzin L, Merrill AE. Rigueur D, et al. Among authors: merrill ae. Genesis. 2019 Jan;57(1):e23252. doi: 10.1002/dvg.23252. Epub 2018 Oct 4. Genesis. 2019. PMID: 30253032 Free PMC article.

8

Nuclear Fibroblast Growth Factor Receptor Signaling in Skeletal Development and Disease.

Tuzon CT, Rigueur D, Merrill AE. Tuzon CT, et al. Among authors: merrill ae. Curr Osteoporos Rep. 2019 Jun;17(3):138-146. doi: 10.1007/s11914-019-00512-2. Curr Osteoporos Rep. 2019. PMID: 30982184 Free PMC article. Review.

9

FGFR2 mutations in bent bone dysplasia syndrome activate nucleolar stress and perturb cell fate determination.

Neben CL, Tuzon CT, Mao X, Lay FD, Merrill AE. Neben CL, et al. Among authors: merrill ae. Hum Mol Genet. 2017 Sep 1;26(17):3253-3270. doi: 10.1093/hmg/ddx209. Hum Mol Genet. 2017. PMID: 28595297 Free PMC article.

10

Nuclear FGFR2 regulates musculoskeletal integration within the developing limb.

Salva JE, Roberts RR, Stucky TS, Merrill AE. Salva JE, et al. Among authors: merrill ae. Dev Dyn. 2019 Mar;248(3):233-246. doi: 10.1002/dvdy.9. Epub 2019 Jan 28. Dev Dyn. 2019. PMID: 30620790 Free PMC article.

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