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Results by year

Year	Number of Results
1990	2
1991	3
1992	1
1993	10
1994	9
1995	20
1996	16
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1998	20
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2000	15
2001	34
2002	31
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2004	32
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2020	2
2023	3
2024	0

675 results

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Mutations of fibroblast growth factor receptor 3 gene (FGFR3) in transitional cell carcinoma of urinary bladder in Thai patients [Revision-2a].

Jantip J, Tanthanuch M, Kanngurn S, Karnchanawanichkul W, Pripatnanont C, Sangkhathat S, Thongsuksai P. Jantip J, et al. J Med Assoc Thai. 2013 Aug;96(8):976-83. J Med Assoc Thai. 2013. PMID: 23991606

FGFR3 has tumor suppressor properties in cells with epithelial phenotype.

Lafitte M, Moranvillier I, Garcia S, Peuchant E, Iovanna J, Rousseau B, Dubus P, Guyonnet-Dupérat V, Belleannée G, Ramos J, Bedel A, de Verneuil H, Moreau-Gaudry F, Dabernat S. Lafitte M, et al. Mol Cancer. 2013 Jul 31;12:83. doi: 10.1186/1476-4598-12-83. Mol Cancer. 2013. PMID: 23902722 Free PMC article.

Synapse location during growth depends on glia location.

Shao Z, Watanabe S, Christensen R, Jorgensen EM, Colón-Ramos DA. Shao Z, et al. Cell. 2013 Jul 18;154(2):337-50. doi: 10.1016/j.cell.2013.06.028. Cell. 2013. PMID: 23870123 Free PMC article.

FGFR3 transmembrane domain interactions persist in the presence of its extracellular domain.

Sarabipour S, Hristova K. Sarabipour S, et al. Biophys J. 2013 Jul 2;105(1):165-71. doi: 10.1016/j.bpj.2013.05.053. Biophys J. 2013. PMID: 23823235 Free PMC article.

The pathogenic A391E mutation in FGFR3 induces a structural change in the transmembrane domain dimer.

Mudumbi KC, Julius A, Herrmann J, Li E. Mudumbi KC, et al. J Membr Biol. 2013 Jun;246(6):487-93. doi: 10.1007/s00232-013-9563-6. Epub 2013 Jun 1. J Membr Biol. 2013. PMID: 23727984

A novel missense mutation of FGFR3 in a Chinese female and her fetus with Hypochondroplasia by next-generation sequencing.

Wang H, Sun Y, Wu W, Wei X, Lan Z, Xie J. Wang H, et al. Clin Chim Acta. 2013 Aug 23;423:62-5. doi: 10.1016/j.cca.2013.04.015. Epub 2013 Apr 24. Clin Chim Acta. 2013. PMID: 23726269

Expression of FGFR3 and FGFR4 and clinical risk factors associated with progression-free survival in synovial sarcoma.

Charbonneau B, Vogel RI, Manivel JC, Rizzardi A, Schmechel SC, Ognjanovic S, Subramanian S, Largaespada D, Weigel B. Charbonneau B, et al. Hum Pathol. 2013 Sep;44(9):1918-26. doi: 10.1016/j.humpath.2013.03.001. Epub 2013 May 10. Hum Pathol. 2013. PMID: 23664540 Free PMC article.

Temporal and occipital lobe features in children with hypochondroplasia/FGFR3 gene mutation.

Philpott CM, Widjaja E, Raybaud C, Branson HM, Kannu P, Blaser S. Philpott CM, et al. Pediatr Radiol. 2013 Sep;43(9):1190-5. doi: 10.1007/s00247-013-2684-3. Epub 2013 May 7. Pediatr Radiol. 2013. PMID: 23649205

Autosomal recessive isolated familial acanthosis nigricans in a Pakistani family due to a homozygous mutation in the insulin receptor gene.

Ahmad S, Mahmoudi H, Naeem M, Betz RC. Ahmad S, et al. Br J Dermatol. 2013 Aug;169(2):476-8. doi: 10.1111/bjd.12293. Br J Dermatol. 2013. PMID: 23448340 No abstract available.

Multiple consequences of a single amino acid pathogenic RTK mutation: the A391E mutation in FGFR3.

Chen F, Sarabipour S, Hristova K. Chen F, et al. PLoS One. 2013;8(2):e56521. doi: 10.1371/journal.pone.0056521. Epub 2013 Feb 20. PLoS One. 2013. PMID: 23437153 Free PMC article.

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