PubMed for id: 3841

Year	Number of Results
1984	3
1986	4
1987	2
1988	6
1989	5
1990	8
1991	8
1992	13
1993	16
1994	7
1995	9
1996	9
1997	4
1998	4
1999	10
2000	5
2001	12
2002	21
2003	14
2004	25
2005	17
2006	23
2007	20
2008	28
2009	23
2010	17
2011	22
2012	18
2013	15
2019	1
2024	0

1

FGF signaling sustains the odontogenic fate of dental mesenchyme by suppressing β-catenin signaling.

Liu C, Gu S, Sun C, Ye W, Song Z, Zhang Y, Chen Y. Liu C, et al. Development. 2013 Nov;140(21):4375-85. doi: 10.1242/dev.097733. Epub 2013 Sep 25. Development. 2013. PMID: 24067353 Free PMC article.

2

Congenital Deafness with Labyrinthine Aplasia, Microtia, and Microdontia.

Ordonez J, Tekin M. Ordonez J, et al. 2012 Sep 20 [updated 2019 Apr 4]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2012 Sep 20 [updated 2019 Apr 4]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 22993869 Free Books & Documents. Review.

3

Ectopic expression of Fgf3 leads to aberrant lineage segregation in the mouse parthenote preimplantation embryos.

Chen YH, Yu J. Chen YH, et al. Dev Dyn. 2012 Nov;241(11):1651-64. doi: 10.1002/dvdy.23851. Epub 2012 Sep 4. Dev Dyn. 2012. PMID: 22930543 Free article.

4

LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutations.

Sensi A, Ceruti S, Trevisi P, Gualandi F, Busi M, Donati I, Neri M, Ferlini A, Martini A. Sensi A, et al. Am J Med Genet A. 2011 May;155A(5):1096-101. doi: 10.1002/ajmg.a.33962. Epub 2011 Apr 7. Am J Med Genet A. 2011. PMID: 21480479

5

Elevated FGF 23 and phosphorus are associated with coronary calcification in hemodialysis patients.

Srivaths PR, Goldstein SL, Silverstein DM, Krishnamurthy R, Brewer ED. Srivaths PR, et al. Pediatr Nephrol. 2011 Jun;26(6):945-51. doi: 10.1007/s00467-011-1822-0. Epub 2011 Feb 27. Pediatr Nephrol. 2011. PMID: 21359960

6

Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome.

Riazuddin S, Ahmed ZM, Hegde RS, Khan SN, Nasir I, Shaukat U, Riazuddin S, Butman JA, Griffith AJ, Friedman TB, Choi BY. Riazuddin S, et al. BMC Med Genet. 2011 Feb 9;12:21. doi: 10.1186/1471-2350-12-21. BMC Med Genet. 2011. PMID: 21306635 Free PMC article.

7

FGF signaling controls caudal hindbrain specification through Ras-ERK1/2 pathway.

Aragon F, Pujades C. Aragon F, et al. BMC Dev Biol. 2009 Dec 3;9:61. doi: 10.1186/1471-213X-9-61. BMC Dev Biol. 2009. PMID: 19958530 Free PMC article.

8

A FGF3 mutation associated with differential inner ear malformation, microtia, and microdontia.

Ramsebner R, Ludwig M, Parzefall T, Lucas T, Baumgartner WD, Bodamer O, Cengiz FB, Schoefer C, Tekin M, Frei K. Ramsebner R, et al. Laryngoscope. 2010 Feb;120(2):359-64. doi: 10.1002/lary.20689. Laryngoscope. 2010. PMID: 19950373

9

Boundary cells regulate a switch in the expression of FGF3 in hindbrain rhombomeres.

Sela-Donenfeld D, Kayam G, Wilkinson DG. Sela-Donenfeld D, et al. BMC Dev Biol. 2009 Feb 20;9:16. doi: 10.1186/1471-213X-9-16. BMC Dev Biol. 2009. PMID: 19232109 Free PMC article.

10

Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3).

Alsmadi O, Meyer BF, Alkuraya F, Wakil S, Alkayal F, Al-Saud H, Ramzan K, Al-Sayed M. Alsmadi O, et al. Eur J Hum Genet. 2009 Jan;17(1):14-21. doi: 10.1038/ejhg.2008.141. Epub 2008 Aug 13. Eur J Hum Genet. 2009. PMID: 18701883 Free PMC article.

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