[cite web | title = Entrez Gene: AFF2 AF4/FMR2 family, member 2| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2334| accessdate = ] ] PBB_Summary
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References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Mulley JC, Yu S, Loesch DZ, "et al." |title=FRAXE and mental retardation. |journal=J. Med. Genet. |volume=32 |issue= 3 |pages= 162–9 |year= 1995 |pmid= 7783162 |doi=
*cite journal | author=Gecz J, Gedeon AK, Sutherland GR, Mulley JC |title=Identification of the gene FMR2, associated with FRAXE mental retardation. |journal=Nat. Genet. |volume=13 |issue= 1 |pages= 105–8 |year= 1996 |pmid= 8673085 |doi= 10.1038/ng0596-105
*cite journal | author=Gu Y, Shen Y, Gibbs RA, Nelson DL |title=Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island. |journal=Nat. Genet. |volume=13 |issue= 1 |pages= 109–13 |year= 1996 |pmid= 8673086 |doi= 10.1038/ng0596-109
*cite journal | author=Chakrabarti L, Knight SJ, Flannery AV, Davies KE |title=A candidate gene for mild mental handicap at the FRAXE fragile site. |journal=Hum. Mol. Genet. |volume=5 |issue= 2 |pages= 275–82 |year= 1996 |pmid= 8824884 |doi=
*cite journal | author=Gécz J, Oostra BA, Hockey A, "et al." |title=FMR2 expression in families with FRAXE mental retardation. |journal=Hum. Mol. Genet. |volume=6 |issue= 3 |pages= 435–41 |year= 1997 |pmid= 9147647 |doi=
*cite journal | author=Gecz J, Bielby S, Sutherland GR, Mulley JC |title=Gene structure and subcellular localization of FMR2, a member of a new family of putative transcription activators. |journal=Genomics |volume=44 |issue= 2 |pages= 201–13 |year= 1997 |pmid= 9299237 |doi= 10.1006/geno.1997.4867
*cite journal | author=Chakrabarti L, Bristulf J, Foss GS, Davies KE |title=Expression of the murine homologue of FMR2 in mouse brain and during development. |journal=Hum. Mol. Genet. |volume=7 |issue= 3 |pages= 441–8 |year= 1998 |pmid= 9467002 |doi=
*cite journal | author=Gecz J, Mulley JC |title=Characterisation and expression of a large, 13.7 kb FMR2 isoform. |journal=Eur. J. Hum. Genet. |volume=7 |issue= 2 |pages= 157–62 |year= 1999 |pmid= 10196698 |doi= 10.1038/sj.ejhg.5200279
*cite journal | author=Murray A, Webb J, Dennis N, "et al." |title=Microdeletions in FMR2 may be a significant cause of premature ovarian failure. |journal=J. Med. Genet. |volume=36 |issue= 10 |pages= 767–70 |year= 1999 |pmid= 10528856 |doi=
*cite journal | author=Dias Neto E, Correa RG, Verjovski-Almeida S, "et al." |title=Shotgun sequencing of the human transcriptome with ORF expressed sequence tags. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=97 |issue= 7 |pages= 3491–6 |year= 2000 |pmid= 10737800 |doi=
*cite journal | author=Lo Nigro C, Faravelli F, Cavani S, "et al." |title=FRAXE mutation in a mentally retarded subject and in his phenotypically normal twin brother. |journal=Eur. J. Hum. Genet. |volume=8 |issue= 3 |pages= 157–62 |year= 2000 |pmid= 10780779 |doi= 10.1038/sj.ejhg.5200425
*cite journal | author=Tzeng CC, Tzeng PY, Sun HS, "et al." |title=Implication of screening for FMR1 and FMR2 gene mutation in individuals with nonspecific mental retardation in Taiwan. |journal=Diagn. Mol. Pathol. |volume=9 |issue= 2 |pages= 75–80 |year= 2000 |pmid= 10850542 |doi=
*cite journal | author=Musumeci SA, Scuderi C, Ferri R, "et al." |title=Does a peculiar EEG pattern exist also for FRAXE mental retardation? |journal=Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology |volume=111 |issue= 9 |pages= 1632–6 |year= 2000 |pmid= 10964075 |doi=
*cite journal | author=Hillman MA, Gecz J |title=Fragile XE-associated familial mental retardation protein 2 (FMR2) acts as a potent transcription activator. |journal=J. Hum. Genet. |volume=46 |issue= 5 |pages= 251–9 |year= 2001 |pmid= 11355014 |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=Kitano T, Schwarz C, Nickel B, Pääbo S |title=Gene diversity patterns at 10 X-chromosomal loci in humans and chimpanzees. |journal=Mol. Biol. Evol. |volume=20 |issue= 8 |pages= 1281–9 |year= 2004 |pmid= 12777533 |doi= 10.1093/molbev/msg134
*cite journal | author=Ross MT, Grafham DV, Coffey AJ, "et al." |title=The DNA sequence of the human X chromosome. |journal=Nature |volume=434 |issue= 7031 |pages= 325–37 |year= 2005 |pmid= 15772651 |doi= 10.1038/nature03440
*cite journal | author=Brylawski BP, Chastain PD, Cohen SM, "et al." |title=Mapping of an origin of DNA replication in the promoter of fragile X gene FMR1. |journal=Exp. Mol. Pathol. |volume=82 |issue= 2 |pages= 190–6 |year= 2007 |pmid= 17196195 |doi= 10.1016/j.yexmp.2006.10.004
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