Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 86

1.

Developmental expression of Xenopus fragile X mental retardation-1 gene.

Lim JH, Luo T, Sargent TD, Fallon JR.

Int J Dev Biol. 2005;49(8):981-4.

2.

Two members of the Fxr gene family, Fmr1 and Fxr1, are differentially expressed in Xenopus tropicalis.

Blonden L, van 't Padje S, Severijnen LA, Destree O, Oostra BA, Willemsen R.

Int J Dev Biol. 2005;49(4):437-41.

3.

Expression of fragile X mental retardation protein within the vocal control system of developing and adult male zebra finches.

Winograd C, Clayton D, Ceman S.

Neuroscience. 2008 Nov 11;157(1):132-42. doi: 10.1016/j.neuroscience.2008.09.005. Epub 2008 Sep 9.

4.

Characterisation of Fmrp in zebrafish: evolutionary dynamics of the fmr1 gene.

van 't Padje S, Engels B, Blonden L, Severijnen LA, Verheijen F, Oostra BA, Willemsen R.

Dev Genes Evol. 2005 Apr;215(4):198-206. Epub 2005 Jan 27.

PMID:
15818485
5.

AP-2alpha selectively regulates fragile X mental retardation-1 gene transcription during embryonic development.

Lim JH, Booker AB, Luo T, Williams T, Furuta Y, Lagutin O, Oliver G, Sargent TD, Fallon JR.

Hum Mol Genet. 2005 Jul 15;14(14):2027-34. Epub 2005 Jun 1.

6.

FXR1, an autosomal homolog of the fragile X mental retardation gene.

Siomi MC, Siomi H, Sauer WH, Srinivasan S, Nussbaum RL, Dreyfuss G.

EMBO J. 1995 Jun 1;14(11):2401-8.

7.

Epigenetic characterization of the FMR1 gene and aberrant neurodevelopment in human induced pluripotent stem cell models of fragile X syndrome.

Sheridan SD, Theriault KM, Reis SA, Zhou F, Madison JM, Daheron L, Loring JF, Haggarty SJ.

PLoS One. 2011;6(10):e26203. doi: 10.1371/journal.pone.0026203. Epub 2011 Oct 12.

8.

Characterization of dFMR1, a Drosophila melanogaster homolog of the fragile X mental retardation protein.

Wan L, Dockendorff TC, Jongens TA, Dreyfuss G.

Mol Cell Biol. 2000 Nov;20(22):8536-47.

9.

FMR1 transcript isoforms: association with polyribosomes; regional and developmental expression in mouse brain.

Brackett DM, Qing F, Amieux PS, Sellers DL, Horner PJ, Morris DR.

PLoS One. 2013;8(3):e58296. doi: 10.1371/journal.pone.0058296. Epub 2013 Mar 7.

10.

BDNF in fragile X syndrome.

Castrén ML, Castrén E.

Neuropharmacology. 2014 Jan;76 Pt C:729-36. doi: 10.1016/j.neuropharm.2013.05.018. Epub 2013 May 29. Review.

PMID:
23727436
11.

Unstable mutations in the FMR1 gene and the phenotypes.

Loesch D, Hagerman R.

Adv Exp Med Biol. 2012;769:78-114. Review.

12.

Protective effects of melatonin against oxidative stress in Fmr1 knockout mice: a therapeutic research model for the fragile X syndrome.

Romero-Zerbo Y, Decara J, el Bekay R, Sanchez-Salido L, Del Arco-Herrera I, de Fonseca FR, de Diego-Otero Y.

J Pineal Res. 2009 Mar;46(2):224-34. doi: 10.1111/j.1600-079X.2008.00653.x. Epub 2008 Dec 23.

PMID:
19141086
13.

Comprehensive analysis of the transcriptional landscape of the human FMR1 gene reveals two new long noncoding RNAs differentially expressed in Fragile X syndrome and Fragile X-associated tremor/ataxia syndrome.

Pastori C, Peschansky VJ, Barbouth D, Mehta A, Silva JP, Wahlestedt C.

Hum Genet. 2014 Jan;133(1):59-67. doi: 10.1007/s00439-013-1356-6. Epub 2013 Sep 5.

14.

Enhanced markers of oxidative stress, altered antioxidants and NADPH-oxidase activation in brains from Fragile X mental retardation 1-deficient mice, a pathological model for Fragile X syndrome.

el Bekay R, Romero-Zerbo Y, Decara J, Sanchez-Salido L, Del Arco-Herrera I, Rodríguez-de Fonseca F, de Diego-Otero Y.

Eur J Neurosci. 2007 Dec;26(11):3169-80. Epub 2007 Nov 14.

PMID:
18005058
15.

Expression of fragile X mental retardation protein and Fmr1 mRNA during folliculogenesis in the rat.

Ferder I, Parborell F, Sundblad V, Chiauzzi V, Gómez K, Charreau EH, Tesone M, Dain L.

Reproduction. 2013 Apr 15;145(4):335-43. doi: 10.1530/REP-12-0305. Print 2013 Apr.

16.
17.

Fragile-X syndrome and fragile X-associated tremor/ataxia syndrome: two faces of FMR1.

Jacquemont S, Hagerman RJ, Hagerman PJ, Leehey MA.

Lancet Neurol. 2007 Jan;6(1):45-55.

PMID:
17166801
19.

Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.

Coffee B, Keith K, Albizua I, Malone T, Mowrey J, Sherman SL, Warren ST.

Am J Hum Genet. 2009 Oct;85(4):503-14. doi: 10.1016/j.ajhg.2009.09.007.

20.

Delayed myelination in a mouse model of fragile X syndrome.

Pacey LK, Xuan IC, Guan S, Sussman D, Henkelman RM, Chen Y, Thomsen C, Hampson DR.

Hum Mol Genet. 2013 Oct 1;22(19):3920-30. doi: 10.1093/hmg/ddt246. Epub 2013 Jun 4.

Items per page

Supplemental Content

Write to the Help Desk