Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2015 | 1 |
2016 | 2 |
2017 | 3 |
2018 | 1 |
2024 | 0 |
Search Results
7 results
Results by year
Filters applied: . Clear all
Page 1
Osteogenesis of Crouzon-Mutated Cells in an Experimental Model.
J Craniofac Surg. 2018 Jan;29(1):237-242. doi: 10.1097/SCS.0000000000004056.
J Craniofac Surg. 2018.
PMID: 29065044
Free PMC article.
FGFR2c-mediated ERK-MAPK activity regulates coronal suture development.
Pfaff MJ, Xue K, Li L, Horowitz MC, Steinbacher DM, Eswarakumar JVP.
Pfaff MJ, et al.
Dev Biol. 2016 Jul 15;415(2):242-250. doi: 10.1016/j.ydbio.2016.03.026. Epub 2016 Mar 28.
Dev Biol. 2016.
PMID: 27034231
Free PMC article.
Item in Clipboard
Testis Determination Requires a Specific FGFR2 Isoform to Repress FOXL2.
Bagheri-Fam S, Bird AD, Zhao L, Ryan JM, Yong M, Wilhelm D, Koopman P, Eswarakumar VP, Harley VR.
Bagheri-Fam S, et al.
Endocrinology. 2017 Nov 1;158(11):3832-3843. doi: 10.1210/en.2017-00674.
Endocrinology. 2017.
PMID: 28938467
Free PMC article.
Item in Clipboard
Molecular analysis of FGFR 2 and associated clinical observations in two Chinese families with Crouzon syndrome.
Lin Y, Gao H, Ai S, Eswarakumar JV, Li T, Liu B, Jiang H, Liu Y, Liu X, Li Y, Ni Y, Chen J, Lin Z, Liang X, Jin C, Huang X, Lu L, Liu Y.
Lin Y, et al.
Mol Med Rep. 2016 Sep;14(3):1941-6. doi: 10.3892/mmr.2016.5497. Epub 2016 Jul 11.
Mol Med Rep. 2016.
PMID: 27430617
Free PMC article.
Item in Clipboard
FGFR2 mutations and associated clinical observations in two Chinese patients with Crouzon syndrome.
Lin Y, Gao H, Ai S, Eswarakumar JVP, Zhu Y, Chen C, Li T, Liu B, Jiang H, Liu Y, Li Y, Wu Q, Li H, Liang X, Jin C, Huang X, Lu L.
Lin Y, et al.
Mol Med Rep. 2017 Nov;16(5):5841-5846. doi: 10.3892/mmr.2017.7397. Epub 2017 Aug 29.
Mol Med Rep. 2017.
PMID: 28901406
Free PMC article.
Item in Clipboard
FGFR2 mutation in 46,XY sex reversal with craniosynostosis.
Bagheri-Fam S, Ono M, Li L, Zhao L, Ryan J, Lai R, Katsura Y, Rossello FJ, Koopman P, Scherer G, Bartsch O, Eswarakumar JV, Harley VR.
Bagheri-Fam S, et al.
Hum Mol Genet. 2015 Dec 1;24(23):6699-710. doi: 10.1093/hmg/ddv374. Epub 2015 Sep 11.
Hum Mol Genet. 2015.
PMID: 26362256
Free PMC article.
Item in Clipboard
C278F mutation in FGFR2 gene causes two different types of syndromic craniosynostosis in two Chinese patients.
Lin Y, Gao H, Ai S, Eswarakumar JVP, Chen C, Zhu Y, Li T, Liu B, Liu X, Luo L, Jiang H, Li Y, Liang X, Jin C, Huang X, Lu L.
Lin Y, et al.
Mol Med Rep. 2017 Oct;16(4):5333-5337. doi: 10.3892/mmr.2017.7248. Epub 2017 Aug 14.
Mol Med Rep. 2017.
PMID: 28849010
Free PMC article.
Item in Clipboard
Cite
Cite