Cox TC - Search Results

1

Solution structure of the MID1 B-box2 CHC(D/C)C(2)H(2) zinc-binding domain: insights into an evolutionarily conserved RING fold.

Massiah MA, Matts JA, Short KM, Simmons BN, Singireddy S, Yi Z, Cox TC. Massiah MA, et al. Among authors: cox tc. J Mol Biol. 2007 May 25;369(1):1-10. doi: 10.1016/j.jmb.2007.03.017. Epub 2007 Mar 15. J Mol Biol. 2007. PMID: 17428496

2

MID1 and MID2 homo- and heterodimerise to tether the rapamycin-sensitive PP2A regulatory subunit, alpha 4, to microtubules: implications for the clinical variability of X-linked Opitz GBBB syndrome and other developmental disorders.

Short KM, Hopwood B, Yi Z, Cox TC. Short KM, et al. Among authors: cox tc. BMC Cell Biol. 2002;3:1. doi: 10.1186/1471-2121-3-1. Epub 2002 Jan 4. BMC Cell Biol. 2002. PMID: 11806752 Free PMC article.

3

A new X-linked syndrome with agenesis of the corpus callosum, mental retardation, coloboma, micrognathia, and a mutation in the Alpha 4 gene at Xq13.

Graham JM Jr, Wheeler P, Tackels-Horne D, Lin AE, Hall BD, May M, Short KM, Schwartz CE, Cox TC. Graham JM Jr, et al. Among authors: cox tc. Am J Med Genet A. 2003 Nov 15;123A(1):37-44. doi: 10.1002/ajmg.a.20504. Am J Med Genet A. 2003. PMID: 14556245

4

Subclassification of the RBCC/TRIM superfamily reveals a novel motif necessary for microtubule binding.

Short KM, Cox TC. Short KM, et al. Among authors: cox tc. J Biol Chem. 2006 Mar 31;281(13):8970-80. doi: 10.1074/jbc.M512755200. Epub 2006 Jan 23. J Biol Chem. 2006. PMID: 16434393 Free article.

5

Solution structure of the RBCC/TRIM B-box1 domain of human MID1: B-box with a RING.

Massiah MA, Simmons BN, Short KM, Cox TC. Massiah MA, et al. Among authors: cox tc. J Mol Biol. 2006 Apr 28;358(2):532-45. doi: 10.1016/j.jmb.2006.02.009. Epub 2006 Feb 20. J Mol Biol. 2006. PMID: 16529770

6

Structure of the MID1 tandem B-boxes reveals an interaction reminiscent of intermolecular ring heterodimers.

Tao H, Simmons BN, Singireddy S, Jakkidi M, Short KM, Cox TC, Massiah MA. Tao H, et al. Among authors: cox tc. Biochemistry. 2008 Feb 26;47(8):2450-7. doi: 10.1021/bi7018496. Epub 2008 Jan 26. Biochemistry. 2008. PMID: 18220417

7

Purifying natively folded proteins from inclusion bodies using sarkosyl, Triton X-100, and CHAPS.

Tao H, Liu W, Simmons BN, Harris HK, Cox TC, Massiah MA. Tao H, et al. Among authors: cox tc. Biotechniques. 2010 Jan;48(1):61-4. doi: 10.2144/000113304. Biotechniques. 2010. PMID: 20078429 Free article.

8

The MID1 E3 ligase catalyzes the polyubiquitination of Alpha4 (α4), a regulatory subunit of protein phosphatase 2A (PP2A): novel insights into MID1-mediated regulation of PP2A.

Du H, Huang Y, Zaghlula M, Walters E, Cox TC, Massiah MA. Du H, et al. Among authors: cox tc. J Biol Chem. 2013 Jul 19;288(29):21341-21350. doi: 10.1074/jbc.M113.481093. Epub 2013 Jun 5. J Biol Chem. 2013. PMID: 23740247 Free PMC article.

9

Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1.

Slavotinek AM, Baranzini SE, Schanze D, Labelle-Dumais C, Short KM, Chao R, Yahyavi M, Bijlsma EK, Chu C, Musone S, Wheatley A, Kwok PY, Marles S, Fryns JP, Maga AM, Hassan MG, Gould DB, Madireddy L, Li C, Cox TC, Smyth I, Chudley AE, Zenker M. Slavotinek AM, et al. Among authors: cox tc. J Med Genet. 2011 Jun;48(6):375-82. doi: 10.1136/jmg.2011.089631. Epub 2011 Apr 20. J Med Genet. 2011. PMID: 21507892 Free PMC article.

10

Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice.

Vissers LE, Cox TC, Maga AM, Short KM, Wiradjaja F, Janssen IM, Jehee F, Bertola D, Liu J, Yagnik G, Sekiguchi K, Kiyozumi D, van Bokhoven H, Marcelis C, Cunningham ML, Anderson PJ, Boyadjiev SA, Passos-Bueno MR, Veltman JA, Smyth I, Buckley MF, Roscioli T. Vissers LE, et al. Among authors: cox tc. PLoS Genet. 2011 Sep;7(9):e1002278. doi: 10.1371/journal.pgen.1002278. Epub 2011 Sep 8. PLoS Genet. 2011. PMID: 21931569 Free PMC article.

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