FGF14

Fibroblast growth factor 14, also known as FGF14, is a human gene.cite web | title = Entrez Gene: FGF14 fibroblast growth factor 14| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2259| accessdate = ]

PBB_Summary
section_title =
summary_text = The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. A mutation in this gene is associated with autosomal dominant cerebral ataxia. Alternatively spliced transcript variants have been found for this gene.cite web | title = Entrez Gene: FGF14 fibroblast growth factor 14| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2259| accessdate = ]

References

Further reading

PBB_Further_reading
citations =
*cite journal | author=Smallwood PM, Munoz-Sanjuan I, Tong P, "et al." |title=Fibroblast growth factor (FGF) homologous factors: new members of the FGF family implicated in nervous system development. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=93 |issue= 18 |pages= 9850–7 |year= 1996 |pmid= 8790420 |doi=
*cite journal | author=Wang Q, Bardgett ME, Wong M, "et al." |title=Ataxia and paroxysmal dyskinesia in mice lacking axonally transported FGF14. |journal=Neuron |volume=35 |issue= 1 |pages= 25–38 |year= 2002 |pmid= 12123606 |doi=
*cite journal | author=Chumakov I, Blumenfeld M, Guerassimenko O, "et al." |title=Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 21 |pages= 13675–80 |year= 2002 |pmid= 12364586 |doi= 10.1073/pnas.182412499
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=van Swieten JC, Brusse E, de Graaf BM, "et al." |title=A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected] . |journal=Am. J. Hum. Genet. |volume=72 |issue= 1 |pages= 191–9 |year= 2003 |pmid= 12489043 |doi=
*cite journal | author=Dunham A, Matthews LH, Burton J, "et al." |title=The DNA sequence and analysis of human chromosome 13. |journal=Nature |volume=428 |issue= 6982 |pages= 522–8 |year= 2004 |pmid= 15057823 |doi= 10.1038/nature02379
*cite journal | author=Popovici C, Conchonaud F, Birnbaum D, Roubin R |title=Functional phylogeny relates LET-756 to fibroblast growth factor 9. |journal=J. Biol. Chem. |volume=279 |issue= 38 |pages= 40146–52 |year= 2004 |pmid= 15199049 |doi= 10.1074/jbc.M405795200
*cite journal | author=Stevanin G, Durr A, Dussert C, "et al." |title=Mutations in the FGF14 gene are not a major cause of spinocerebellar ataxia in Caucasians. |journal=Neurology |volume=63 |issue= 5 |pages= 936 |year= 2005 |pmid= 15365159 |doi=
*cite journal | author=Dalski A, Atici J, Kreuz FR, "et al." |title=Mutation analysis in the fibroblast growth factor 14 gene: frameshift mutation and polymorphisms in patients with inherited ataxias. |journal=Eur. J. Hum. Genet. |volume=13 |issue= 1 |pages= 118–20 |year= 2005 |pmid= 15470364 |doi= 10.1038/sj.ejhg.5201286
*cite journal | author=Lou JY, Laezza F, Gerber BR, "et al." |title=Fibroblast growth factor 14 is an intracellular modulator of voltage-gated sodium channels. |journal=J. Physiol. (Lond.) |volume=569 |issue= Pt 1 |pages= 179–93 |year= 2006 |pmid= 16166153 |doi= 10.1113/jphysiol.2005.097220
*cite journal | author=Brusse E, de Koning I, Maat-Kievit A, "et al." |title=Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene (SCA27): A new phenotype. |journal=Mov. Disord. |volume=21 |issue= 3 |pages= 396–401 |year= 2006 |pmid= 16211615 |doi= 10.1002/mds.20708
*cite journal | author=Zhao Y, Lim SW, Tan EK |title=Genetic analysis of SCA 27 in ataxia and childhood onset postural tremor. |journal=Am. J. Med. Genet. B Neuropsychiatr. Genet. |volume=144 |issue= 3 |pages= 395–6 |year= 2007 |pmid= 17221845 |doi= 10.1002/ajmg.b.30472
*cite journal | author=Wozniak DF, Xiao M, Xu L, "et al." |title=Impaired spatial learning and defective theta burst induced LTP in mice lacking fibroblast growth factor 14. |journal=Neurobiol. Dis. |volume=26 |issue= 1 |pages= 14–26 |year= 2007 |pmid= 17236779 |doi= 10.1016/j.nbd.2006.11.014

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