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Items: 1 to 20 of 24

1.

Stall in Canonical Autophagy-Lysosome Pathways Prompts Nucleophagy-Based Nuclear Breakdown in Neurodegeneration.

Baron O, Boudi A, Dias C, Schilling M, Nölle A, Vizcay-Barrena G, Rattray I, Jungbluth H, Scheper W, Fleck RA, Bates GP, Fanto M.

Curr Biol. 2017 Dec 4;27(23):3626-3642.e6. doi: 10.1016/j.cub.2017.10.054. Epub 2017 Nov 22.

2.

Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera.

Hirvonen EAM, Pitkänen E, Hemminki K, Aaltonen LA, Kilpivaara O.

Hum Genomics. 2017 Apr 20;11(1):6. doi: 10.1186/s40246-017-0102-x.

3.

New insights into transcriptional and leukemogenic mechanisms of AML1-ETO and E2A fusion proteins.

Li J, Guo C, Steinauer N, Zhang J.

Front Biol (Beijing). 2016 Aug;11(4):285-304. doi: 10.1007/s11515-016-1415-1. Epub 2016 Sep 3.

4.

The promise and perils of HDAC inhibitors in neurodegeneration.

Didonna A, Opal P.

Ann Clin Transl Neurol. 2015 Jan;2(1):79-101. doi: 10.1002/acn3.147. Epub 2014 Dec 3. Review.

5.

The expanding role for chromatin and transcription in polyglutamine disease.

Mohan RD, Abmayr SM, Workman JL.

Curr Opin Genet Dev. 2014 Jun;26:96-104. doi: 10.1016/j.gde.2014.06.008. Epub 2014 Aug 11. Review.

6.

Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxias.

Matilla-Dueñas A, Ashizawa T, Brice A, Magri S, McFarland KN, Pandolfo M, Pulst SM, Riess O, Rubinsztein DC, Schmidt J, Schmidt T, Scoles DR, Stevanin G, Taroni F, Underwood BR, Sánchez I.

Cerebellum. 2014 Apr;13(2):269-302. doi: 10.1007/s12311-013-0539-y.

7.

A multidimensional approach to an in-depth proteomics analysis of transcriptional regulators in neuroblastoma cells.

Li Q, Jain MR, Chen W, Li H.

J Neurosci Methods. 2013 Jun 15;216(2):118-27. doi: 10.1016/j.jneumeth.2013.03.016. Epub 2013 Apr 1.

8.

LANP mediates neuritic pathology in Spinocerebellar ataxia type 1.

Cvetanovic M, Kular RK, Opal P.

Neurobiol Dis. 2012 Dec;48(3):526-32. doi: 10.1016/j.nbd.2012.07.024. Epub 2012 Aug 4.

9.

Polyglutamine expansion alters the dynamics and molecular architecture of aggregates in dentatorubropallidoluysian atrophy.

Hinz J, Lehnhardt L, Zakrzewski S, Zhang G, Ignatova Z.

J Biol Chem. 2012 Jan 13;287(3):2068-78. doi: 10.1074/jbc.M111.318915. Epub 2011 Dec 1.

10.

Polyglutamine Atrophin provokes neurodegeneration in Drosophila by repressing fat.

Napoletano F, Occhi S, Calamita P, Volpi V, Blanc E, Charroux B, Royet J, Fanto M.

EMBO J. 2011 Mar 2;30(5):945-58. doi: 10.1038/emboj.2011.1. Epub 2011 Jan 28.

11.

Characterization of a t(5;8)(q31;q21) translocation in a patient with mental retardation and congenital heart disease: implications for involvement of RUNX1T1 in human brain and heart development.

Zhang L, Tümer Z, Møllgård K, Barbi G, Rossier E, Bendsen E, Møller RS, Ullmann R, He J, Papadopoulos N, Tommerup N, Larsen LA.

Eur J Hum Genet. 2009 Aug;17(8):1010-8. doi: 10.1038/ejhg.2008.269. Epub 2009 Jan 28.

12.

Atrophin proteins interact with the Fat1 cadherin and regulate migration and orientation in vascular smooth muscle cells.

Hou R, Sibinga NE.

J Biol Chem. 2009 Mar 13;284(11):6955-65. doi: 10.1074/jbc.M809333200. Epub 2009 Jan 7.

13.

Atrophin proteins: an overview of a new class of nuclear receptor corepressors.

Wang L, Tsai CC.

Nucl Recept Signal. 2008;6:e009. doi: 10.1621/nrs.06009. Epub 2008 Oct 31. Review.

14.

Atrophin recruits HDAC1/2 and G9a to modify histone H3K9 and to determine cell fates.

Wang L, Charroux B, Kerridge S, Tsai CC.

EMBO Rep. 2008 Jun;9(6):555-62. doi: 10.1038/embor.2008.67. Epub 2008 May 2.

15.

Myeloid translocation gene family members associate with T-cell factors (TCFs) and influence TCF-dependent transcription.

Moore AC, Amann JM, Williams CS, Tahinci E, Farmer TE, Martinez JA, Yang G, Luce KS, Lee E, Hiebert SW.

Mol Cell Biol. 2008 Feb;28(3):977-87. Epub 2007 Nov 26.

16.

Drosophila brakeless interacts with atrophin and is required for tailless-mediated transcriptional repression in early embryos.

Haecker A, Qi D, Lilja T, Moussian B, Andrioli LP, Luschnig S, Mannervik M.

PLoS Biol. 2007 Jun;5(6):e145.

17.

Nuclear receptor TLX prevents retinal dystrophy and recruits the corepressor atrophin1.

Zhang CL, Zou Y, Yu RT, Gage FH, Evans RM.

Genes Dev. 2006 May 15;20(10):1308-20.

18.

Histone deacetylase-associating Atrophin proteins are nuclear receptor corepressors.

Wang L, Rajan H, Pitman JL, McKeown M, Tsai CC.

Genes Dev. 2006 Mar 1;20(5):525-30. Epub 2006 Feb 15.

19.

ETO-2 associates with SCL in erythroid cells and megakaryocytes and provides repressor functions in erythropoiesis.

Schuh AH, Tipping AJ, Clark AJ, Hamlett I, Guyot B, Iborra FJ, Rodriguez P, Strouboulis J, Enver T, Vyas P, Porcher C.

Mol Cell Biol. 2005 Dec;25(23):10235-50.

20.

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