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Items: 1 to 20 of 35

1.

CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy.

Qiu XB, Qu XK, Li RG, Liu H, Xu YJ, Zhang M, Shi HY, Hou XM, Liu X, Yuan F, Sun YM, Wang J, Huang RT, Xue S, Yang YQ.

Clin Chem Lab Med. 2017 Aug 28;55(9):1417-1425. doi: 10.1515/cclm-2016-0612.

PMID:
28099117
2.

Identification of CASZ1 NES reveals potential mechanisms for loss of CASZ1 tumor suppressor activity in neuroblastoma.

Liu Z, Lam N, Wang E, Virden RA, Pawel B, Attiyeh EF, Maris JM, Thiele CJ.

Oncogene. 2017 Jan 5;36(1):97-109. doi: 10.1038/onc.2016.179. Epub 2016 Jun 6.

3.
4.

Characterization of critical domains within the tumor suppressor CASZ1 required for transcriptional regulation and growth suppression.

Virden RA, Thiele CJ, Liu Z.

Mol Cell Biol. 2012 Apr;32(8):1518-28. doi: 10.1128/MCB.06039-11. Epub 2012 Feb 13.

5.

CASZ1b, the short isoform of CASZ1 gene, coexpresses with CASZ1a during neurogenesis and suppresses neuroblastoma cell growth.

Liu Z, Naranjo A, Thiele CJ.

PLoS One. 2011 Apr 7;6(4):e18557. doi: 10.1371/journal.pone.0018557.

6.

CASZ1, a candidate tumor-suppressor gene, suppresses neuroblastoma tumor growth through reprogramming gene expression.

Liu Z, Yang X, Li Z, McMahon C, Sizer C, Barenboim-Stapleton L, Bliskovsky V, Mock B, Ried T, London WB, Maris J, Khan J, Thiele CJ.

Cell Death Differ. 2011 Jul;18(7):1174-83. doi: 10.1038/cdd.2010.187. Epub 2011 Jan 21.

7.

Quantitative analysis of human tissue-specific differences in methylation.

Igarashi J, Muroi S, Kawashima H, Wang X, Shinojima Y, Kitamura E, Oinuma T, Nemoto N, Song F, Ghosh S, Held WA, Nagase H.

Biochem Biophys Res Commun. 2008 Nov 28;376(4):658-64. doi: 10.1016/j.bbrc.2008.09.044. Epub 2008 Sep 19.

8.

Genetic and epigenetic changes in the common 1p36 deletion in neuroblastoma tumours.

Carén H, Fransson S, Ejeskär K, Kogner P, Martinsson T.

Br J Cancer. 2007 Nov 19;97(10):1416-24. Epub 2007 Oct 16.

9.

Neuroblastoma tumors with favorable and unfavorable outcomes: Significant differences in mRNA expression of genes mapped at 1p36.2.

Fransson S, Martinsson T, Ejeskär K.

Genes Chromosomes Cancer. 2007 Jan;46(1):45-52.

PMID:
17044048
10.

Molecular cloning and characterization of human Castor, a novel human gene upregulated during cell differentiation.

Liu Z, Yang X, Tan F, Cullion K, Thiele CJ.

Biochem Biophys Res Commun. 2006 Jun 9;344(3):834-44. Epub 2006 Apr 19.

PMID:
16631614
11.

Identification and characterization of survival-related gene, a novel cell survival gene controlling apoptosis and tumorigenesis.

Yuan ZR, Wang R, Solomon J, Luo X, Sun H, Zhang L, Shi Y.

Cancer Res. 2005 Dec 1;65(23):10716-24.

12.

CASZ1 loss-of-function mutation associated with congenital heart disease.

Huang RT, Xue S, Wang J, Gu JY, Xu JH, Li YJ, Li N, Yang XX, Liu H, Zhang XD, Qu XK, Xu YJ, Qiu XB, Li RG, Yang YQ.

Gene. 2016 Dec 20;595(1):62-68. doi: 10.1016/j.gene.2016.09.044. Epub 2016 Sep 28.

PMID:
27693370
13.

CASZ1 inhibits cell cycle progression in neuroblastoma by restoring pRb activity.

Liu Z, Rader J, He S, Phung T, Thiele CJ.

Cell Cycle. 2013 Jul 15;12(14):2210-8. doi: 10.4161/cc.25265.

14.

Loss of gene function as a consequence of human papillomavirus DNA integration.

Schmitz M, Driesch C, Beer-Grondke K, Jansen L, Runnebaum IB, Dürst M.

Int J Cancer. 2012 Sep 1;131(5):E593-602. doi: 10.1002/ijc.27433. Epub 2012 Feb 22.

15.

Formation of a TBX20-CASZ1 protein complex is protective against dilated cardiomyopathy and critical for cardiac homeostasis.

Kennedy L, Kaltenbrun E, Greco TM, Temple B, Herring LE, Cristea IM, Conlon FL.

PLoS Genet. 2017 Sep 25;13(9):e1007011. doi: 10.1371/journal.pgen.1007011. eCollection 2017 Sep.

16.

EZH2 Mediates epigenetic silencing of neuroblastoma suppressor genes CASZ1, CLU, RUNX3, and NGFR.

Wang C, Liu Z, Woo CW, Li Z, Wang L, Wei JS, Marquez VE, Bates SE, Jin Q, Khan J, Ge K, Thiele CJ.

Cancer Res. 2012 Jan 1;72(1):315-24. doi: 10.1158/0008-5472.CAN-11-0961. Epub 2011 Nov 8.

17.

Association analysis of chromosome 1 migraine candidate genes.

Fernandez F, Curtain RP, Colson NJ, Ovcaric M, MacMillan J, Griffiths LR.

BMC Med Genet. 2007 Aug 29;8:57.

18.

Blood pressure and hypertension are associated with 7 loci in the Japanese population.

Takeuchi F, Isono M, Katsuya T, Yamamoto K, Yokota M, Sugiyama T, Nabika T, Fujioka A, Ohnaka K, Asano H, Yamori Y, Yamaguchi S, Kobayashi S, Takayanagi R, Ogihara T, Kato N.

Circulation. 2010 Jun 1;121(21):2302-9. doi: 10.1161/CIRCULATIONAHA.109.904664. Epub 2010 May 17.

PMID:
20479155
19.

Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians.

Kato N, Takeuchi F, Tabara Y, Kelly TN, Go MJ, Sim X, Tay WT, Chen CH, Zhang Y, Yamamoto K, Katsuya T, Yokota M, Kim YJ, Ong RT, Nabika T, Gu D, Chang LC, Kokubo Y, Huang W, Ohnaka K, Yamori Y, Nakashima E, Jaquish CE, Lee JY, Seielstad M, Isono M, Hixson JE, Chen YT, Miki T, Zhou X, Sugiyama T, Jeon JP, Liu JJ, Takayanagi R, Kim SS, Aung T, Sung YJ, Zhang X, Wong TY, Han BG, Kobayashi S, Ogihara T, Zhu D, Iwai N, Wu JY, Teo YY, Tai ES, Cho YS, He J.

Nat Genet. 2011 Jun;43(6):531-8. doi: 10.1038/ng.834. Epub 2011 May 15.

20.

Genome-wide association study of blood pressure and hypertension.

Levy D, Ehret GB, Rice K, Verwoert GC, Launer LJ, Dehghan A, Glazer NL, Morrison AC, Johnson AD, Aspelund T, Aulchenko Y, Lumley T, Köttgen A, Vasan RS, Rivadeneira F, Eiriksdottir G, Guo X, Arking DE, Mitchell GF, Mattace-Raso FU, Smith AV, Taylor K, Scharpf RB, Hwang SJ, Sijbrands EJ, Bis J, Harris TB, Ganesh SK, O'Donnell CJ, Hofman A, Rotter JI, Coresh J, Benjamin EJ, Uitterlinden AG, Heiss G, Fox CS, Witteman JC, Boerwinkle E, Wang TJ, Gudnason V, Larson MG, Chakravarti A, Psaty BM, van Duijn CM.

Nat Genet. 2009 Jun;41(6):677-87. doi: 10.1038/ng.384. Epub 2009 May 10.

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