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Normal phenotype in two brothers with a full FMR1 mutation.
Smeets HJ, Smits AP, Verheij CE, Theelen JP, Willemsen R, van de Burgt I, Hoogeveen AT, Oosterwijk JC, Oostra BA. Smeets HJ, et al. Among authors: hoogeveen at. Hum Mol Genet. 1995 Nov;4(11):2103-8. doi: 10.1093/hmg/4.11.2103. Hum Mol Genet. 1995. PMID: 8589687
Fxr1 knockout mice show a striated muscle phenotype: implications for Fxr1p function in vivo.
Mientjes EJ, Willemsen R, Kirkpatrick LL, Nieuwenhuizen IM, Hoogeveen-Westerveld M, Verweij M, Reis S, Bardoni B, Hoogeveen AT, Oostra BA, Nelson DL. Mientjes EJ, et al. Among authors: hoogeveen at, hoogeveen westerveld m. Hum Mol Genet. 2004 Jul 1;13(13):1291-302. doi: 10.1093/hmg/ddh150. Epub 2004 May 5. Hum Mol Genet. 2004. PMID: 15128702
FMRP is associated to the ribosomes via RNA.
Tamanini F, Meijer N, Verheij C, Willems PJ, Galjaard H, Oostra BA, Hoogeveen AT. Tamanini F, et al. Among authors: hoogeveen at. Hum Mol Genet. 1996 Jun;5(6):809-13. doi: 10.1093/hmg/5.6.809. Hum Mol Genet. 1996. PMID: 8776596
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, hoogeveen westerveld m. Hum Mol Genet. 2003 May 1;12(9):949-59. doi: 10.1093/hmg/ddg114. Hum Mol Genet. 2003. PMID: 12700164 Free article.
142 results