[cite web | title = Entrez Gene: FOXL2 forkhead box L2| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=668| accessdate = ] ] PBB_Summary
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ee also
* FOX proteins
References
Further reading
PBB_Further_reading
citations =
*cite journal | author=de Die-Smulders CE, Engelen JJ, Donk JM, Fryns JP |title=Further evidence for the location of the BPES gene at 3q2. |journal=J. Med. Genet. |volume=28 |issue= 10 |pages= 725 |year= 1991 |pmid= 1941972 |doi=
*cite journal | author=Vaiman D, Schibler L, Oustry-Vaiman A, "et al." |title=High-resolution human/goat comparative map of the goat polled/intersex syndrome (PIS): the human homologue is contained in a human YAC from HSA3q23. |journal=Genomics |volume=56 |issue= 1 |pages= 31–9 |year= 1999 |pmid= 10036183 |doi= 10.1006/geno.1998.5691
*cite journal | author=Kaestner KH, Knochel W, Martinez DE |title=Unified nomenclature for the winged helix/forkhead transcription factors. |journal=Genes Dev. |volume=14 |issue= 2 |pages= 142–6 |year= 2000 |pmid= 10702024 |doi=
*cite journal | author=Crisponi L, Deiana M, Loi A, "et al." |title=The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome. |journal=Nat. Genet. |volume=27 |issue= 2 |pages= 159–66 |year= 2001 |pmid= 11175783 |doi= 10.1038/84781
*cite journal | author=De Baere E, Dixon MJ, Small KW, "et al." |title=Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlation. |journal=Hum. Mol. Genet. |volume=10 |issue= 15 |pages= 1591–600 |year= 2001 |pmid= 11468277 |doi=
*cite journal | author=Dollfus H, Kumaramanickavel G, Biswas P, "et al." |title=Identification of a new TWIST mutation (7p21) with variable eyelid manifestations supports locus homogeneity of BPES at 3q22. |journal=J. Med. Genet. |volume=38 |issue= 7 |pages= 470–2 |year= 2001 |pmid= 11474656 |doi=
*cite journal | author=Yamada T, Hayasaka S, Matsumoto M, "et al." |title=Heterozygous 17-bp deletion in the forkhead transcription factor gene, FOXL2, in a Japanese family with blepharophimosis-ptosis-epicanthus inversus syndrome. |journal=J. Hum. Genet. |volume=46 |issue= 12 |pages= 733–6 |year= 2002 |pmid= 11776388 |doi=
*cite journal | author=Kosaki K, Ogata T, Kosaki R, "et al." |title=A novel mutation in the FOXL2 gene in a patient with blepharophimosis syndrome: differential role of the polyalanine tract in the development of the ovary and the eyelid. |journal=Ophthalmic Genet. |volume=23 |issue= 1 |pages= 43–7 |year= 2002 |pmid= 11910558 |doi=
*cite journal | author=Bell R, Murday VA, Patton MA, Jeffery S |title=Two families with blepharophimosis/ptosis/epicanthus inversus syndrome have mutations in the putative forkhead transcription factor FOXL2. |journal=Genet. Test. |volume=5 |issue= 4 |pages= 335–8 |year= 2002 |pmid= 11960581 |doi= 10.1089/109065701753617499
*cite journal | author=Harris SE, Chand AL, Winship IM, "et al." |title=Identification of novel mutations in FOXL2 associated with premature ovarian failure. |journal=Mol. Hum. Reprod. |volume=8 |issue= 8 |pages= 729–33 |year= 2003 |pmid= 12149404 |doi=
*cite journal | author=De Baere E, Lemercier B, Christin-Maitre S, "et al." |title=FOXL2 mutation screening in a large panel of POF patients and XX males. |journal=J. Med. Genet. |volume=39 |issue= 8 |pages= e43 |year= 2002 |pmid= 12161610 |doi=
*cite journal | author=Ramírez-Castro JL, Pineda-Trujillo N, Valencia AV, "et al." |title=Mutations in FOXL2 underlying BPES (types 1 and 2) in Colombian families. |journal=Am. J. Med. Genet. |volume=113 |issue= 1 |pages= 47–51 |year= 2003 |pmid= 12400065 |doi= 10.1002/ajmg.10741
*cite journal | author=Cocquet J, Pailhoux E, Jaubert F, "et al." |title=Evolution and expression of FOXL2. |journal=J. Med. Genet. |volume=39 |issue= 12 |pages= 916–21 |year= 2003 |pmid= 12471206 |doi=
*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=De Baere E, Beysen D, Oley C, "et al." |title=FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation. |journal=Am. J. Hum. Genet. |volume=72 |issue= 2 |pages= 478–87 |year= 2003 |pmid= 12529855 |doi=
*cite journal | author=Mazumdar A, Kumar R |title=Estrogen regulation of Pak1 and FKHR pathways in breast cancer cells. |journal=FEBS Lett. |volume=535 |issue= 1-3 |pages= 6–10 |year= 2003 |pmid= 12560069 |doi=
*cite journal | author=Fokstuen S, Antonarakis SE, Blouin JL |title=FOXL2-mutations in blepharophimosis-ptosis-epicanthus inversus syndrome (BPES); challenges for genetic counseling in female patients. |journal=Am. J. Med. Genet. A |volume=117 |issue= 2 |pages= 143–6 |year= 2003 |pmid= 12567411 |doi= 10.1002/ajmg.a.10024
*cite journal | author=Dollfus H, Stoetzel C, Riehm S, "et al." |title=Sporadic and familial blepharophimosis -ptosis-epicanthus inversus syndrome: FOXL2 mutation screen and MRI study of the superior levator eyelid muscle. |journal=Clin. Genet. |volume=63 |issue= 2 |pages= 117–20 |year= 2003 |pmid= 12630957 |doi=
*cite journal | author=Udar N, Yellore V, Chalukya M, "et al." |title=Comparative analysis of the FOXL2 gene and characterization of mutations in BPES patients. |journal=Hum. Mutat. |volume=22 |issue= 3 |pages= 222–8 |year= 2003 |pmid= 12938087 |doi= 10.1002/humu.10251
*cite journal | author=Crisponi L, Uda M, Deiana M, "et al." |title=FOXL2 inactivation by a translocation 171 kb away: analysis of 500 kb of chromosome 3 for candidate long-range regulatory sequences. |journal=Genomics |volume=83 |issue= 5 |pages= 757–64 |year= 2004 |pmid= 15081106 |doi= 10.1016/j.ygeno.2003.11.010
External links
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