Citations for
1RERE, RERED
De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 Deletions.
Fregeau B, Kim BJ, Hernández-García A, Jordan VK, Cho MT, Schnur RE, Monaghan KG, Juusola J, Rosenfeld JA, Bhoj E, Zackai EH, Sacharow S, Barañano K, Bosch DG, de Vries BB, Lindstrom K, Schroeder A, James P, Kulch P, Lalani SR, van Haelst MM, van Gassen KL, van Binsbergen E, Barkovich AJ, Scott DA, Sherr EH.
Am J Hum Genet 98(5):963-70. doi: 10.1016/j.ajhg.2016.03.002. Epub 2016 Apr 14. 2016
2RERE
Mouse model reveals the role of RERE in cerebellar foliation and the migration and maturation of Purkinje cells.
Kim BJ, Scott DA.
PLoS One 9(1):e87518. doi: 10.1371/journal.pone.0087518. eCollection 2014. 2014
3RERE
An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions.
Kim BJ, Zaveri HP, Shchelochkov OA, Yu Z, Hernández-García A, Seymour ML, Oghalai JS, Pereira FA, Stockton DW, Justice MJ, Lee B, Scott DA.
PLoS One 8(2):e57460. doi: 10.1371/journal.pone.0057460. Epub 2013 Feb 25. 2013
4RERE
Rere controls retinoic acid signalling and somite bilateral symmetry.
Vilhais-Neto GC, Maruhashi M, Smith KT, Vasseur-Cognet M, Peterson AS, Workman JL, Pourquié O.
Nature 463(7283):953-7. 2010
5ATN1, FAT1, RERE
Atrophin proteins interact with the Fat1 cadherin and regulate migration and orientation in vascular smooth muscle cells.
Hou R, Sibinga NE.
J Biol Chem 284(11):6955-65. Epub 2009 Jan 7. 2009
6ATN1, RERE
Atrophin proteins: an overview of a new class of nuclear receptor corepressors.
Wang L, Tsai CC.
Nucl Recept Signal 6:e009. Epub 2008 Oct 31. Review. 2008
7RERE
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 9(6):555-62. Epub 2008 May 2. 2008
8RERE
REREa/Atrophin-2 interacts with histone deacetylase and Fgf8 signaling to regulate multiple processes of zebrafish development.
Plaster N, Sonntag C, Schilling TF, Hammerschmidt M.
Dev Dyn 236(7):1891-904. Erratum in: Dev Dyn. 2007 Oct;236(10):2971. 2007
9ATN1, RERE
Functional architecture of atrophins.
Shen Y, Lee G, Choe Y, Zoltewicz JS, Peterson AS.
J Biol Chem 282(7):5037-44. Epub 2006 Dec 6. 2007
10RERE, TSPAN8, HHIP, CHI3L1
Novel differential gene expression in human cirrhosis detected by suppression subtractive hybridization.
Shackel NA, McGuinness PH, Abbott CA, Gorrell MD, McCaughan GW.
Hepatology 38(3):577-88. 2003
11RERE
Human RERE is localized to nuclear promyelocytic leukemia oncogenic domains and enhances apoptosis.
Waerner T, Gardellin P, Pfizenmaier K, Weith A, Kraut N.
Cell Growth Differ 12(4):201-10. 2001
12RERE, SLC45A1
Identification and characterization of novel genes located at the t(1;15)(p36.2;q24) translocation breakpoint in the neuroblastoma cell line NGP.
Amler LC, Bauer A, Corvi R, Dihlmann S, Praml C, Cavenee WK, Schwab M, Hampton GM.
Genomics 64(2):195-202. 2000
13C1orf34, CDC42BPA, CEP170, CROCC, CROCC, CYHR1, DENND4B, DISC1, DNAJC6, FAM20B, FAM91A2, HS2ST1, IPP, KIF21B, MACF1, NMNAT2, NOS1AP, PDE4DIP, PLCH2, POGZ, RABGAP1L, RERE, RPRD2, SDC3, SLC35E2, SNX27, SRGAP2, SZT2, TMCC2, UBR4, ZBTB40
Characterization of cDNA clones in size-fractionated cDNA libraries from human brain.
Seki N, Ohira M, Nagase T, Ishikawa K, Miyajima N, Nakajima D, Nomura N,Ohara O.
DNA Res 4(5):345-9. 1997
14RERE
Cloning and expression of the rat atrophin-I (DRPLA disease gene) homologue.
Loev SJ, Margolis RL, Young WS, Li SH, Schilling G, Ashworth RG, Ross CA.
Neurobiol Dis 2(3):129-38. 1995