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Page 1
Knockout mouse model for Fxr2: a model for mental retardation.
Bontekoe CJ, McIlwain KL, Nieuwenhuizen IM, Yuva-Paylor LA, Nellis A, Willemsen R, Fang Z, Kirkpatrick L, Bakker CE, McAninch R, Cheng NC, Merriweather M, Hoogeveen AT, Nelson D, Paylor R, Oostra BA. Bontekoe CJ, et al. Among authors: hoogeveen at. Hum Mol Genet. 2002 Mar 1;11(5):487-98. doi: 10.1093/hmg/11.5.487. Hum Mol Genet. 2002. PMID: 11875043
The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome.
Willemsen R, Hoogeveen-Westerveld M, Reis S, Holstege J, Severijnen LA, Nieuwenhuizen IM, Schrier M, van Unen L, Tassone F, Hoogeveen AT, Hagerman PJ, Mientjes EJ, Oostra BA. Willemsen R, et al. Among authors: hoogeveen at. Hum Mol Genet. 2003 May 1;12(9):949-59. doi: 10.1093/hmg/ddg114. Hum Mol Genet. 2003. PMID: 12700164 Free article.
Loss of FMR1 hypermethylation in somatic cell heterokaryons.
Stoyanova V, Rossetti S, VAN Unen L, Oostra BA, Hoogeveen AT. Stoyanova V, et al. Among authors: hoogeveen at. FASEB J. 2004 Dec;18(15):1964-6. doi: 10.1096/fj.04-2499fje. Epub 2004 Sep 17. FASEB J. 2004. PMID: 15377638
The fragile X syndrome.
Hoogeveen AT, Oostra BA. Hoogeveen AT, et al. J Inherit Metab Dis. 1997 Jun;20(2):139-51. doi: 10.1023/a:1005392319533. J Inherit Metab Dis. 1997. PMID: 9211186 Review.
Animal model for fragile X syndrome.
Oostra BA, Hoogeveen AT. Oostra BA, et al. Among authors: hoogeveen at. Ann Med. 1997 Dec;29(6):563-7. doi: 10.3109/07853899709007483. Ann Med. 1997. PMID: 9562525 Free article. Review.
93 results