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Items: 1 to 20 of 54

1.

Genetic variants in RBFOX3 are associated with sleep latency.

Amin N, Allebrandt KV, van der Spek A, Müller-Myhsok B, Hek K, Teder-Laving M, Hayward C, Esko T, van Mill JG, Mbarek H, Watson NF, Melville SA, Del Greco FM, Byrne EM, Oole E, Kolcic I, Chen TH, Evans DS, Coresh J, Vogelzangs N, Karjalainen J, Willemsen G, Gharib SA, Zgaga L, Mihailov E, Stone KL, Campbell H, Brouwer RW, Demirkan A, Isaacs A, Dogas Z, Marciante KD, Campbell S, Borovecki F, Luik AI, Li M, Hottenga JJ, Huffman JE, van den Hout MC, Cummings SR, Aulchenko YS, Gehrman PR, Uitterlinden AG, Wichmann HE, Müller-Nurasyid M, Fehrmann RS, Montgomery GW, Hofman A, Kao WH, Oostra BA, Wright AF, Vink JM, Wilson JF, Pramstaller PP, Hicks AA, Polasek O, Punjabi NM, Redline S, Psaty BM, Heath AC, Merrow M, Tranah GJ, Gottlieb DJ, Boomsma DI, Martin NG, Rudan I, Tiemeier H, van IJcken WF, Penninx BW, Metspalu A, Meitinger T, Franke L, Roenneberg T, van Duijn CM.

Eur J Hum Genet. 2016 Oct;24(10):1488-95. doi: 10.1038/ejhg.2016.31. Epub 2016 May 4.

2.

Chronic HIV-1 Tat and HIV reduce Rbfox3/NeuN: evidence for sex-related effects.

Hahn YK, Masvekar RR, Xu R, Hauser KF, Knapp PE.

Curr HIV Res. 2015;13(1):10-20.

3.

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.

4.

Common genetic variants in ARNTL and NPAS2 and at chromosome 12p13 are associated with objectively measured sleep traits in the elderly.

Evans DS, Parimi N, Nievergelt CM, Blackwell T, Redline S, Ancoli-Israel S, Orwoll ES, Cummings SR, Stone KL, Tranah GJ; Study of Osteoporotic Fractures (SOF); Osteoporotic Fractures in Men (MrOS) Study Group.

Sleep. 2013 Mar 1;36(3):431-46. doi: 10.5665/sleep.2466.

5.

Altered subcellular localization of the NeuN/Rbfox3 RNA splicing factor in HIV-associated neurocognitive disorders (HAND).

Lucas CH, Calvez M, Babu R, Brown A.

Neurosci Lett. 2014 Jan 13;558:97-102. doi: 10.1016/j.neulet.2013.10.037. Epub 2013 Nov 8.

6.

A genome-wide association study of sleep habits and insomnia.

Byrne EM, Gehrman PR, Medland SE, Nyholt DR, Heath AC, Madden PA, Hickie IB, Van Duijn CM, Henders AK, Montgomery GW, Martin NG, Wray NR; Chronogen Consortium.

Am J Med Genet B Neuropsychiatr Genet. 2013 Jul;162B(5):439-51. doi: 10.1002/ajmg.b.32168. Epub 2013 May 31.

7.

Genome-wide association analysis of actigraphic sleep phenotypes in the LIFE Adult Study.

Spada J, Scholz M, Kirsten H, Hensch T, Horn K, Jawinski P, Ulke C, Burkhardt R, Wirkner K, Loeffler M, Hegerl U, Sander C.

J Sleep Res. 2016 Dec;25(6):690-701. doi: 10.1111/jsr.12421. Epub 2016 Apr 29.

8.

RBFOX3/NeuN is Required for Hippocampal Circuit Balance and Function.

Wang HY, Hsieh PF, Huang DF, Chin PS, Chou CH, Tung CC, Chen SY, Lee LJ, Gau SS, Huang HS.

Sci Rep. 2015 Dec 1;5:17383. doi: 10.1038/srep17383.

9.

A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor.

Byrne EM, Johnson J, McRae AF, Nyholt DR, Medland SE, Gehrman PR, Heath AC, Madden PA, Montgomery GW, Chenevix-Trench G, Martin NG.

Sleep. 2012 Jul 1;35(7):967-75. doi: 10.5665/sleep.1962.

10.

Endometrial vezatin and its association with endometriosis risk.

Holdsworth-Carson SJ, Fung JN, Luong HT, Sapkota Y, Bowdler LM, Wallace L, Teh WT, Powell JE, Girling JE, Healey M, Montgomery GW, Rogers PA.

Hum Reprod. 2016 May;31(5):999-1013. doi: 10.1093/humrep/dew047. Epub 2016 Mar 22.

PMID:
27005890
11.

NeuN/Rbfox3 nuclear and cytoplasmic isoforms differentially regulate alternative splicing and nonsense-mediated decay of Rbfox2.

Dredge BK, Jensen KB.

PLoS One. 2011;6(6):e21585. doi: 10.1371/journal.pone.0021585. Epub 2011 Jun 29.

12.

RBFOX3 regulates Claudin-1 expression in human lung tissue via attenuation of proteasomal degradation.

Kim YE, Choi S, Kim JO, Kim KK.

Biosci Rep. 2017 Feb 23;37(1). pii: BSR20160623. doi: 10.1042/BSR20160623. Print 2017 Feb 28.

13.

Neuronal Splicing Regulator RBFOX3 (NeuN) Regulates Adult Hippocampal Neurogenesis and Synaptogenesis.

Lin YS, Wang HY, Huang DF, Hsieh PF, Lin MY, Chou CH, Wu IJ, Huang GJ, Gau SS, Huang HS.

PLoS One. 2016 Oct 4;11(10):e0164164. doi: 10.1371/journal.pone.0164164. eCollection 2016.

14.

A comprehensive family-based replication study of schizophrenia genes.

Aberg KA, Liu Y, Bukszár J, McClay JL, Khachane AN, Andreassen OA, Blackwood D, Corvin A, Djurovic S, Gurling H, Ophoff R, Pato CN, Pato MT, Riley B, Webb T, Kendler K, O'Donovan M, Craddock N, Kirov G, Owen M, Rujescu D, St Clair D, Werge T, Hultman CM, Delisi LE, Sullivan P, van den Oord EJ.

JAMA Psychiatry. 2013 Jun;70(6):573-81.

15.

Replication of Genome-Wide Association Studies (GWAS) loci for sleep in the British G1219 cohort.

Parsons MJ, Lester KJ, Barclay NL, Nolan PM, Eley TC, Gregory AM.

Am J Med Genet B Neuropsychiatr Genet. 2013 Jul;162B(5):431-8. doi: 10.1002/ajmg.b.32106.

PMID:
23780892
16.

Identification and characterization of the RNA-binding protein Rbfox3 in zebrafish embryo.

Won M, Lee S, Choi S, Ro H, Kim KJ, Kim JH, Kim KE, Kim KK.

Biochem Biophys Res Commun. 2016 Apr 1;472(2):373-8. doi: 10.1016/j.bbrc.2016.03.005. Epub 2016 Mar 4.

PMID:
26952657
17.

BET1L and TNRC6B associate with uterine fibroid risk among European Americans.

Edwards TL, Michels KA, Hartmann KE, Velez Edwards DR.

Hum Genet. 2013 Aug;132(8):943-53. doi: 10.1007/s00439-013-1306-3. Epub 2013 Apr 19.

18.

Variants in calcium voltage-gated channel subunit Alpha1 C-gene (CACNA1C) are associated with sleep latency in infants.

Kantojärvi K, Liuhanen J, Saarenpää-Heikkilä O, Satomaa AL, Kylliäinen A, Pölkki P, Jaatela J, Toivola A, Milani L, Himanen SL, Porkka-Heiskanen T, Paavonen J, Paunio T.

PLoS One. 2017 Aug 9;12(8):e0180652. doi: 10.1371/journal.pone.0180652. eCollection 2017.

19.

Meta-analysis of genome-wide association for migraine in six population-based European cohorts.

Ligthart L, de Vries B, Smith AV, Ikram MA, Amin N, Hottenga JJ, Koelewijn SC, Kattenberg VM, de Moor MH, Janssens AC, Aulchenko YS, Oostra BA, de Geus EJ, Smit JH, Zitman FG, Uitterlinden AG, Hofman A, Willemsen G, Nyholt DR, Montgomery GW, Terwindt GM, Gudnason V, Penninx BW, Breteler M, Ferrari MD, Launer LJ, van Duijn CM, van den Maagdenberg AM, Boomsma DI.

Eur J Hum Genet. 2011 Aug;19(8):901-7. doi: 10.1038/ejhg.2011.48. Epub 2011 Mar 30.

20.

Glutamate Networks Implicate Cognitive Impairments in Schizophrenia: Genome-Wide Association Studies of 52 Cognitive Phenotypes.

Ohi K, Hashimoto R, Ikeda M, Yamamori H, Yasuda Y, Fujimoto M, Umeda-Yano S, Fukunaga M, Fujino H, Watanabe Y, Iwase M, Kazui H, Iwata N, Weinberger DR, Takeda M.

Schizophr Bull. 2015 Jul;41(4):909-18. doi: 10.1093/schbul/sbu171. Epub 2014 Dec 22.

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