PubMed for id: 766944350

Year	Number of Results
2007	1
2008	1
2012	1
2013	3
2014	1
2016	1
2019	1
2024	0

1

Exosomal FMR1-AS1 facilitates maintaining cancer stem-like cell dynamic equilibrium via TLR7/NFκB/c-Myc signaling in female esophageal carcinoma.

Li W, Zhang L, Guo B, Deng J, Wu S, Li F, Wang Y, Lu J, Zhou Y. Li W, et al. Mol Cancer. 2019 Feb 8;18(1):22. doi: 10.1186/s12943-019-0949-7. Mol Cancer. 2019. PMID: 30736860 Free PMC article.

2

The long non-coding RNA FMR4 promotes proliferation of human neural precursor cells and epigenetic regulation of gene expression in trans.

Peschansky VJ, Pastori C, Zeier Z, Wentzel K, Velmeshev D, Magistri M, Silva JP, Wahlestedt C. Peschansky VJ, et al. Mol Cell Neurosci. 2016 Jul;74:49-57. doi: 10.1016/j.mcn.2016.03.008. Epub 2016 Mar 19. Mol Cell Neurosci. 2016. PMID: 27001315 Free article.

3

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. Pastori C, et al. Hum Genet. 2014 Jan;133(1):59-67. doi: 10.1007/s00439-013-1356-6. Epub 2013 Sep 5. Hum Genet. 2014. PMID: 24005575 Free PMC article.

4

Role of CTCF protein in regulating FMR1 locus transcription.

Lanni S, Goracci M, Borrelli L, Mancano G, Chiurazzi P, Moscato U, Ferrè F, Helmer-Citterich M, Tabolacci E, Neri G. Lanni S, et al. PLoS Genet. 2013;9(7):e1003601. doi: 10.1371/journal.pgen.1003601. Epub 2013 Jul 18. PLoS Genet. 2013. PMID: 23874213 Free PMC article.

5

Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French families.

Huc-Chabrolle M, Charon C, Guilmatre A, Vourc'h P, Tripi G, Barthez MA, Sizaret E, Thepault RA, Le Gallic S, Hager J, Toutain A, Raynaud M, Andres C, Campion D, Laumonnier F, Bonnet-Brilhault F. Huc-Chabrolle M, et al. Behav Genet. 2013 Mar;43(2):132-40. doi: 10.1007/s10519-012-9575-5. Epub 2013 Jan 11. Behav Genet. 2013. PMID: 23307483 Free article.

6

De novo microduplication of the FMR1 gene in a patient with developmental delay, epilepsy and hyperactivity.

Vengoechea J, Parikh AS, Zhang S, Tassone F. Vengoechea J, et al. Eur J Hum Genet. 2012 Nov;20(11):1197-200. doi: 10.1038/ejhg.2012.78. Epub 2012 May 2. Eur J Hum Genet. 2012. PMID: 22549406 Free PMC article.

7

A novel RNA transcript with antiapoptotic function is silenced in fragile X syndrome.

Khalil AM, Faghihi MA, Modarresi F, Brothers SP, Wahlestedt C. Khalil AM, et al. PLoS One. 2008 Jan 23;3(1):e1486. doi: 10.1371/journal.pone.0001486. PLoS One. 2008. PMID: 18213394 Free PMC article.

8

An antisense transcript spanning the CGG repeat region of FMR1 is upregulated in premutation carriers but silenced in full mutation individuals.

Ladd PD, Smith LE, Rabaia NA, Moore JM, Georges SA, Hansen RS, Hagerman RJ, Tassone F, Tapscott SJ, Filippova GN. Ladd PD, et al. Hum Mol Genet. 2007 Dec 15;16(24):3174-87. doi: 10.1093/hmg/ddm293. Epub 2007 Oct 6. Hum Mol Genet. 2007. PMID: 17921506

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