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Items: 1 to 20 of 80

1.

RBFOX1, encoding a splicing regulator, is a candidate gene for aggressive behavior.

Fernàndez-Castillo N, Gan G, van Donkelaar MMJ, Vaht M, Weber H, Retz W, Meyer-Lindenberg A, Franke B, Harro J, Reif A, Faraone SV, Cormand B.

Eur Neuropsychopharmacol. 2017 Nov 23. pii: S0924-977X(17)32003-5. doi: 10.1016/j.euroneuro.2017.11.012. [Epub ahead of print]

PMID:
29174947
2.

Orchestration of neurodevelopmental programs by RBFOX1: implications for autism spectrum disorder.

Bill BR, Lowe JK, Dybuncio CT, Fogel BL.

Int Rev Neurobiol. 2013;113:251-67. doi: 10.1016/B978-0-12-418700-9.00008-3. Review.

3.

Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy.

Lal D, Pernhorst K, Klein KM, Reif P, Tozzi R, Toliat MR, Winterer G, Neubauer B, Nürnberg P, Rosenow F, Becker F, Lerche H, Kunz WS, Kurki MI, Hoffmann P, Becker AJ, Perucca E, Zara F, Sander T, Weber YG.

Epilepsia. 2015 Sep;56(9):e129-33. doi: 10.1111/epi.13076. Epub 2015 Jul 15.

4.

RBFOX1 regulates both splicing and transcriptional networks in human neuronal development.

Fogel BL, Wexler E, Wahnich A, Friedrich T, Vijayendran C, Gao F, Parikshak N, Konopka G, Geschwind DH.

Hum Mol Genet. 2012 Oct 1;21(19):4171-86. doi: 10.1093/hmg/dds240. Epub 2012 Jun 23.

5.

Essential role of the nuclear isoform of RBFOX1, a candidate gene for autism spectrum disorders, in the brain development.

Hamada N, Ito H, Nishijo T, Iwamoto I, Morishita R, Tabata H, Momiyama T, Nagata K.

Sci Rep. 2016 Aug 2;6:30805. doi: 10.1038/srep30805.

6.

Outfoxed by RBFOX1-a caution about ascertainment bias.

Kamien B, Lionel AC, Bain N, Scherer SW, Hunter M.

Am J Med Genet A. 2014 Jun;164A(6):1411-8. doi: 10.1002/ajmg.a.36458. Epub 2014 Mar 24.

PMID:
24664471
7.

Role of the cytoplasmic isoform of RBFOX1/A2BP1 in establishing the architecture of the developing cerebral cortex.

Hamada N, Ito H, Iwamoto I, Morishita R, Tabata H, Nagata K.

Mol Autism. 2015 Oct 20;6:56. doi: 10.1186/s13229-015-0049-5. eCollection 2015.

8.

Aggressive behavior in humans: Genes and pathways identified through association studies.

Fernàndez-Castillo N, Cormand B.

Am J Med Genet B Neuropsychiatr Genet. 2016 Jul;171(5):676-96. doi: 10.1002/ajmg.b.32419. Epub 2016 Jan 15. Review.

PMID:
26773414
9.

Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy.

Lal D, Trucks H, Møller RS, Hjalgrim H, Koeleman BP, de Kovel CG, Visscher F, Weber YG, Lerche H, Becker F, Schankin CJ, Neubauer BA, Surges R, Kunz WS, Zimprich F, Franke A, Illig T, Ried JS, Leu C, Nürnberg P, Sander T; EMINet Consortium; EPICURE Consortium.

Epilepsia. 2013 Feb;54(2):265-71. doi: 10.1111/epi.12084. Epub 2013 Jan 25.

10.

Cytoplasmic Rbfox1 Regulates the Expression of Synaptic and Autism-Related Genes.

Lee JA, Damianov A, Lin CH, Fontes M, Parikshak NN, Anderson ES, Geschwind DH, Black DL, Martin KC.

Neuron. 2016 Jan 6;89(1):113-28. doi: 10.1016/j.neuron.2015.11.025. Epub 2015 Dec 10.

11.

The splicing regulator Rbfox1 (A2BP1) controls neuronal excitation in the mammalian brain.

Gehman LT, Stoilov P, Maguire J, Damianov A, Lin CH, Shiue L, Ares M Jr, Mody I, Black DL.

Nat Genet. 2011 May 29;43(7):706-11. doi: 10.1038/ng.841.

12.

The RNA-binding protein Rbfox1 regulates splicing required for skeletal muscle structure and function.

Pedrotti S, Giudice J, Dagnino-Acosta A, Knoblauch M, Singh RK, Hanna A, Mo Q, Hicks J, Hamilton S, Cooper TA.

Hum Mol Genet. 2015 Apr 15;24(8):2360-74. doi: 10.1093/hmg/ddv003. Epub 2015 Jan 9.

13.

RBFox1-mediated RNA splicing regulates cardiac hypertrophy and heart failure.

Gao C, Ren S, Lee JH, Qiu J, Chapski DJ, Rau CD, Zhou Y, Abdellatif M, Nakano A, Vondriska TM, Xiao X, Fu XD, Chen JN, Wang Y.

J Clin Invest. 2016 Jan;126(1):195-206. doi: 10.1172/JCI84015. Epub 2015 Nov 30.

15.

RBFOX1 and RBFOX3 mutations in rolandic epilepsy.

Lal D, Reinthaler EM, Altmüller J, Toliat MR, Thiele H, Nürnberg P, Lerche H, Hahn A, Møller RS, Muhle H, Sander T, Zimprich F, Neubauer BA.

PLoS One. 2013 Sep 6;8(9):e73323. doi: 10.1371/journal.pone.0073323. eCollection 2013.

16.

Upregulation of RBFOX1 in the malformed cortex of patients with intractable epilepsy and in cultured rat neurons.

Wen M, Yan Y, Yan N, Chen XS, Liu SY, Feng ZH.

Int J Mol Med. 2015 Mar;35(3):597-606. doi: 10.3892/ijmm.2015.2061. Epub 2015 Jan 5.

17.

Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD).

Pistoni M, Shiue L, Cline MS, Bortolanza S, Neguembor MV, Xynos A, Ares M Jr, Gabellini D.

PLoS Genet. 2013;9(1):e1003186. doi: 10.1371/journal.pgen.1003186. Epub 2013 Jan 3.

18.

A transcriptional network associated with natural variation in Drosophila aggressive behavior.

Edwards AC, Ayroles JF, Stone EA, Carbone MA, Lyman RF, Mackay TF.

Genome Biol. 2009;10(7):R76. doi: 10.1186/gb-2009-10-7-r76. Epub 2009 Jul 16.

19.

Genetics of aggressive behavior: An overview.

Veroude K, Zhang-James Y, Fernàndez-Castillo N, Bakker MJ, Cormand B, Faraone SV.

Am J Med Genet B Neuropsychiatr Genet. 2016 Jan;171B(1):3-43. doi: 10.1002/ajmg.b.32364. Epub 2015 Sep 8. Review.

PMID:
26345359
20.

Analysis of RBFOX1 gene expression in lymphoblastoid cell lines of Italian discordant autism spectrum disorders sib-pairs.

Prandini P, Zusi C, Malerba G, Itan, Pignatti PF, Trabetti E.

Mol Cell Probes. 2014 Oct-Dec;28(5-6):242-5. doi: 10.1016/j.mcp.2014.05.001. Epub 2014 Jun 3.

PMID:
24938762

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