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Items: 1 to 20 of 48

1.

Fox-3 and PSF interact to activate neural cell-specific alternative splicing.

Kim KK, Kim YC, Adelstein RS, Kawamoto S.

Nucleic Acids Res. 2011 Apr;39(8):3064-78. doi: 10.1093/nar/gkq1221. Epub 2010 Dec 21.

2.

iCLIP reveals the function of hnRNP particles in splicing at individual nucleotide resolution.

König J, Zarnack K, Rot G, Curk T, Kayikci M, Zupan B, Turner DJ, Luscombe NM, Ule J.

Nat Struct Mol Biol. 2010 Jul;17(7):909-15. doi: 10.1038/nsmb.1838. Epub 2010 Jul 4.

3.

Integrative modeling defines the Nova splicing-regulatory network and its combinatorial controls.

Zhang C, Frias MA, Mele A, Ruggiu M, Eom T, Marney CB, Wang H, Licatalosi DD, Fak JJ, Darnell RB.

Science. 2010 Jul 23;329(5990):439-43. doi: 10.1126/science.1191150. Epub 2010 Jun 17.

4.

Autoregulation of Fox protein expression to produce dominant negative splicing factors.

Damianov A, Black DL.

RNA. 2010 Feb;16(2):405-16. doi: 10.1261/rna.1838210. Epub 2009 Dec 30.

5.

An inducible change in Fox-1/A2BP1 splicing modulates the alternative splicing of downstream neuronal target exons.

Lee JA, Tang ZZ, Black DL.

Genes Dev. 2009 Oct 1;23(19):2284-93. doi: 10.1101/gad.1837009. Epub 2009 Sep 17.

6.

Identification of neuronal nuclei (NeuN) as Fox-3, a new member of the Fox-1 gene family of splicing factors.

Kim KK, Adelstein RS, Kawamoto S.

J Biol Chem. 2009 Nov 6;284(45):31052-61. doi: 10.1074/jbc.M109.052969. Epub 2009 Aug 27.

7.

Fox-1 family of RNA-binding proteins.

Kuroyanagi H.

Cell Mol Life Sci. 2009 Dec;66(24):3895-907. doi: 10.1007/s00018-009-0120-5. Review.

8.

Excitability changes related to GABAA receptor plasticity during pregnancy.

Maguire J, Ferando I, Simonsen C, Mody I.

J Neurosci. 2009 Jul 29;29(30):9592-601. doi: 10.1523/JNEUROSCI.2162-09.2009.

9.

Developmental control of CaV1.2 L-type calcium channel splicing by Fox proteins.

Tang ZZ, Zheng S, Nikolic J, Black DL.

Mol Cell Biol. 2009 Sep;29(17):4757-65. doi: 10.1128/MCB.00608-09. Epub 2009 Jun 29.

10.

Ultrafast and memory-efficient alignment of short DNA sequences to the human genome.

Langmead B, Trapnell C, Pop M, Salzberg SL.

Genome Biol. 2009;10(3):R25. doi: 10.1186/gb-2009-10-3-r25. Epub 2009 Mar 4.

11.

Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice.

Papale LA, Beyer B, Jones JM, Sharkey LM, Tufik S, Epstein M, Letts VA, Meisler MH, Frankel WN, Escayg A.

Hum Mol Genet. 2009 May 1;18(9):1633-41. doi: 10.1093/hmg/ddp081. Epub 2009 Mar 2.

12.

SNAP-25 in neuropsychiatric disorders.

Corradini I, Verderio C, Sala M, Wilson MC, Matteoli M.

Ann N Y Acad Sci. 2009 Jan;1152:93-9. doi: 10.1111/j.1749-6632.2008.03995.x.

13.

An RNA code for the FOX2 splicing regulator revealed by mapping RNA-protein interactions in stem cells.

Yeo GW, Coufal NG, Liang TY, Peng GE, Fu XD, Gage FH.

Nat Struct Mol Biol. 2009 Feb;16(2):130-7. doi: 10.1038/nsmb.1545. Epub 2009 Jan 11.

14.

An ancient duplication of exon 5 in the Snap25 gene is required for complex neuronal development/function.

Johansson JU, Ericsson J, Janson J, Beraki S, Stanić D, Mandic SA, Wikström MA, Hökfelt T, Ogren SO, Rozell B, Berggren PO, Bark C.

PLoS Genet. 2008 Nov;4(11):e1000278. doi: 10.1371/journal.pgen.1000278. Epub 2008 Nov 28.

15.

Temporal lobe epilepsy: where do the seizures really begin?

Bertram EH.

Epilepsy Behav. 2009 Jan;14 Suppl 1:32-7. doi: 10.1016/j.yebeh.2008.09.017. Epub 2008 Oct 31. Review.

16.

Defining the regulatory network of the tissue-specific splicing factors Fox-1 and Fox-2.

Zhang C, Zhang Z, Castle J, Sun S, Johnson J, Krainer AR, Zhang MQ.

Genes Dev. 2008 Sep 15;22(18):2550-63. doi: 10.1101/gad.1703108. Erratum in: Genes Dev. 2008 Oct 15;22(20):2902.

17.

Alternative splicing events identified in human embryonic stem cells and neural progenitors.

Yeo GW, Xu X, Liang TY, Muotri AR, Carson CT, Coufal NG, Gage FH.

PLoS Comput Biol. 2007 Oct;3(10):1951-67. Epub 2007 Aug 24.

18.

Neuronal regulation of alternative pre-mRNA splicing.

Li Q, Lee JA, Black DL.

Nat Rev Neurosci. 2007 Nov;8(11):819-31. Review.

PMID:
17895907
19.

Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autism.

Martin CL, Duvall JA, Ilkin Y, Simon JS, Arreaza MG, Wilkes K, Alvarez-Retuerto A, Whichello A, Powell CM, Rao K, Cook E, Geschwind DH.

Am J Med Genet B Neuropsychiatr Genet. 2007 Oct 5;144B(7):869-76.

PMID:
17503474
20.

Strong association of de novo copy number mutations with autism.

Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T, Yamrom B, Yoon S, Krasnitz A, Kendall J, Leotta A, Pai D, Zhang R, Lee YH, Hicks J, Spence SJ, Lee AT, Puura K, Lehtimäki T, Ledbetter D, Gregersen PK, Bregman J, Sutcliffe JS, Jobanputra V, Chung W, Warburton D, King MC, Skuse D, Geschwind DH, Gilliam TC, Ye K, Wigler M.

Science. 2007 Apr 20;316(5823):445-9. Epub 2007 Mar 15.

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