Citations for
1ATXN10, SCA10
Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instability.
McFarland KN, Liu J, Landrian I, Gao R, Sarkar PS, Raskin S, Moscovich M, Gatto EM, Teive HA, Ochoa A, Rasmussen A, Ashizawa T.
Eur J Hum Genet 21(11):1272-6. doi: 10.1038/ejhg.2013.32. Epub 2013 Feb 27. 2013
2ATXN10, IQCB1, JBTS24, MKS1, NPHP17, TCTN2
Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways.
Sang L, Miller JJ, Corbit KC, Giles RH, Brauer MJ, Otto EA, Baye LM, Wen X, Scales SJ, Kwong M, Huntzicker EG, Sfakianos MK, Sandoval W, Bazan JF, Kulkarni P, Garcia-Gonzalo FR, Seol AD, O'Toole JF, Held S, Reutter HM, Lane WS, Rafiq MA, Noor A, Ansar M, Devi AR, Sheffield VC, Slusarski DC, Vincent JB, Doherty DA, Hildebrandt F, Reiter JF, Jackson PK.
Cell 145(4):513-28. 2011
3ATXN10, PLK1
Phosphorylation of Ataxin-10 by polo-like kinase 1 is required for cytokinesis.
Li J, Wang J, Hou W, Jing Z, Tian C, Han Y, Liao J, Dong MQ, Xu X.
Cell Cycle 10(17):2946-58. Epub 2011 Sep 1. 2011
4ATXN10, SCA10
The ATTCT repeats of spinocerebellar ataxia type 10 display strong nucleosome assembly which is enhanced by repeat interruptions.
Hagerman KA, Ruan H, Edamura KN, Matsuura T, Pearson CE, Wang YH.
Gene 434(1-2):29-34. Epub 2008 Dec 25. 2009
5ATXN10, SCA10
Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10).
Almeida T, Alonso I, Martins S, Ramos EM, Azevedo L, Ohno K, Amorim A, Saraiva-Pereira ML, Jardim LB, Matsuura T, Sequeiros J, Silveira I.
PLoS One 4(2):e4553. Epub 2009 Feb 23. 2009
6ATXN10, SCA10
Unstable spinocerebellar ataxia type 10 (ATTCT*(AGAAT) repeats are associated with aberrant replication at the ATX10 locus and replication origin-dependent expansion at an ectopic site in human cells.
Liu G, Bissler JJ, Sinden RR, Leffak M.
Mol Cell Biol 27(22):7828-38. Epub 2007 Sep 10. 2007
7SCA10, ATXN10
Interruptions in the Expanded ATTCT Repeat of Spinocerebellar Ataxia Type 10: Repeat Purity as a Disease Modifier?
Matsuura T, Fang P, Pearson CE, Jayakar P, Ashizawa T, Roa BB, Nelson DL.
Am J Hum Genet 78(1):125-9. Epub 2005 Nov 15. 2006
8ATXN10,GNB2
Ataxin 10 induces neuritogenesis via interaction with G-protein beta2 subunit..
Waragai M, Nagamitsu S, Xu W, Li YJ, Lin X, Ashizawa T.
Neurosci Res 83:1170-8 2006
9ATXN10, GNB2
Ataxin 10 induces neuritogenesis via interaction with G-protein beta2 subunit.
Waragai M, Nagamitsu S, Xu W, Li YJ, Lin X, Ashizawa T.
J Neurosci Res 83(7):1170-8. 2006
10SCA10, ATXN10
The role of ataxin 10 in the pathogenesis of spinocerebellar ataxia type 10.
Wakamiya M, Matsuura T, Liu Y, Schuster GC, Gao R, Xu W, Sarkar PS, Lin X, Ashizawa T.
Neurology 67(4):607-13. 2006
11FXN, FRDA, FRAXA, FMR1, FRAXE, ATXN1, SCA1, ATXN2, SCA2, ATXN3, MJD, ATXN7, SCA7, SCA6, CACNA1A, SCA17, TBP, DRPLA, ATN1, AR, SBMA, DM1, DMPK, DM2, CNBP, SCA10, ATXN10, SCA12, PPP2R2B, SCA8, ATXN8OS
Diseases of unstable repeat expansion: mechanisms and common principles.
Gatchel JR, Zoghbi HY.
Nat Rev Genet 6(10):743-55. Review. 2005
12SCA10, ATXN10
The AUUCU repeats responsible for spinocerebellar ataxia type 10 form unusual RNA hairpins.
Handa V, Yeh HJ, McPhie P, Usdin K.
J Biol Chem 280(32):29340-5. Epub 2005 Jun 20. 2005
13ATXN10
Ataxin-10 interacts with O-GlcNAc transferase OGT in pancreatic beta cells.
Andrali SS, Marz P, Ozcan S.
Biochem Biophys Res Commun 337(1):149-53. 2005
14ATXN10, SCA10
Ataxin-10, the spinocerebellar ataxia type 10 neurodegenerative disorder protein, is essential for survival of cerebellar neurons.
Marz P, Probst A, Lang S, Schwager M, Rose-John S, Otten U, Ozbek S.
J Biol Chem 279(34):35542-50. Epub 2004 Jun 16. 2004
15SCA10, ATXN10
SCA10 and ATTCT repeat expansion: clinical features and molecular aspects.
Lin X, Ashizawa T.
Cytogenet Genome Res 100(1-4):184-8. No abstract available. 2003
16AIF1L, ANKHD1, ANKRD20A1, ANKRD27, ANKRD32, APH1B, APOLD1, ARMC4, ATXN10, C10orf10, C10orf10, C10orf118, C2orf14, C2orf16, C6orf60, C6orf62, C8orf71, CALCOCO1, CAMKK1, CCDC113, CCDC135, CCDC9, CCDC90B, CCNB2, CD99L2, CHPF, CLIC4, CLPB, CRELD1, CYBRD1, DDX47, DHRS7B, ESPN, FIP1L1, FLYWCH1, FYTTD1, GABARAPL1, GOLT1B, GPS2, GRIPAP1, HIGD1A, IER3IP1, KIF18A, KIRREL2, KLC2, LHX6, LMAN2L, MAF1, MED23, MIS12, MOB4, MYCBPAP, NCALD, NELF, NELFB, NRBF2, NRIP2, NRIP2, NRSN2, NUDT12, PCBD2, PMFBP1, PRPF31, PRSS23, QRSL1, RGMA, RGMB, RNF123, RNF146, RWDD3, SAMHD1, SECISBP2, SEMA4F, SERBP1, SERP1, SH3BP5L, SLC25A24, SLC25A39, SLC37A3, SLC41A2, SLC6A16, SMC6, SPEF1, STMN2, TARDBP, TBC1D3, TBL2, TFIP11, TIGD6, TIMMDC1, TMEM117, TMEM186, TNB, TRAF7, TRAPPC8, TSC22D3, TSPAN14, TWF2, UBA5, UNC50, WDR24, WDR37, WDR91, WSB1, YIPF3, ZC3H13, ZMYND12, ZMYND15, ZRANB3
Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs.
Wiemann S, Weil B, Wellenreuther R, Gassenhuber J, Glassl S, Ansorge W, Bocher M, Blocker H, Bauersachs S, Blum H, Lauber J, Dusterhoft A, Beyer A, Kohrer K, Strack N, Mewes HW, Ottenwalder B, Obermaier B, Tampe J, Heubner D, Wambutt R, Korn B, Klein M, Poustka A.
Genome Res 11(3):422-35. 2001
17SCA10, ATXN10
Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.
Matsuura T, Yamagata T, Burgess DL, Rasmussen A, Grewal RP, Watase K, Khajavi M, McCall AE, Davis CF, Zu L, Achari M, Pulst SM, Alonso E, Noebels JL, Nelson DL, Zoghbi HY, Ashizawa T.
Nat Genet 26(2):191-4. 2000
18ADIPOR1, AIG1, AMDHD2, ANKHD1, ANKRD20A1, ANKRD27, ANKRD32, APH1A, APH1B, APIP, APOLD1, ARS2, ASCC1, ATXN10, BOLA1, C10orf10, C14orf166, C19orf56, C20orf109, C20orf4, C2orf14, C2orf16, C6orf60, C6orf62, CALCOCO1, CAMKK1, CCDC113, CCDC53, CCDC9, CCNB2, CD99L2, CDK5RAP1, CDK5RAP1, CGI-96, CHMP5, CHPF, CIAO2B, CLIC4, CLPB, COPZ1, COQ4, COQ6, CRELD1, CUTC, CYBRD1, DDX47, DERA, DHRS7, DHRS7B, DHRS7B, DPH5, DTNB, DYNC1LI2, EEF1AKNMT, ELOVL1, EMC9, ERGIC3, ESPN, EXOSC1, EXOSC3, FAHD2A, FAM108B1, FAM18B, FAM32A, FAM82B, FCF1, FIP1L1, FLYWCH1, FYTTD1, GABARAPL1, GET4, GLOD4, GLRX2, GOLT1B, GOLT1B, GPR89A, GPS2, GRIPAP1, HDDC2, HDGFRP3, HIGD1A, IER3IP1, IFT52, ISOC1, KIF18A, KIF20B, KIRREL2, KL3, KLC2, LACTB2, LHX6, LMAN2L, LUC7L2, MAF1, MAGMAS, MECR, MED23, MED31, MEMO, METTL9, MIS12, MOABHD5, MOB4, MPC1, MRPL11, MRPL2, MRPL4, MRPL48, MRPS15, MRPS16, MRPS16P2, MRPS18C, MRPS23, MRPS33, MTCH1, MTERF3, MTO1, MYCBPAP, NCALD, NCIE2, NDUFAF1, NELF, NELFB, NFU1, NMD3, NOSIP, NRBF2, NRIP2, NRIP2, NRSN2, NUDT12, OTUD6B, PARVB, PCBD2, PHF20L1, PIGT, PMFBP1, PNAS-4, PRPF31, PRSS23, PTRH2, QRSL1, RBMX2, RGMA, RGMB, RNF103-CHMP3, RNF123, RNF146, RRNAD1, RRP15, RWDD1, RWDD3, SAMHD1, SAMM50, SCCPDH, SECISBP2, SEMA4F, SERBP1, SERBP1, SERP1, SH3BP5L, SIDT2, SLC25A24, SLC25A39, SLC35C2, SLC37A3, SLC41A2, SLC6A16, SLMO2, SMC6, SPEF1, SQRDL, STARD10, STMN2, SYF2, TARDBP, TBC1D3, TBL2, TFB1M, TFIP11, THAP4, THAP4, TIGD6, TIMMDC1, TMED5, TMED7, TMEM47, TPPP3, TRAF7, TRAPPC12, TRAPPC4, TRMT6, TRNT1, TSC22D3, TSPAN14, TWF2, UBE1DC1, UBE2J1, UCHL5, UNC50, USP39, UTP11L, VPS36, WDR37, WDR50, WDR91, WSB1, YARS2, YIPF3, YPEL5, ZC2HC1A, ZC3H13, ZDHHC9, ZMYND12, ZMYND15, ZRANB3
Identification of novel human genes evolutionarily conserved in Caenorhabditis elegans by comparative proteomics.
Lai CH, Chou CY, Ch'ang LY, Liu CS, Lin W.
Genome Res 10(5):703-13. 2000
19SCA10, ATXN10
Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22.
Zu L, et al.
Am J Hum Genet 64(2):594-9. 1999
20SCA10, ATXN10
Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy.
Matsuura T, et al.
Ann Neurol 45(3):407-11. 1999