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Absence of common somatic alterations in genes on 1p and 19q in oligodendrogliomas.
Bralten LB, Nouwens S, Kockx C, Erdem L, Hoogenraad CC, Kros JM, Moorhouse MJ, Sillevis Smitt PA, van der Spek P, van Ijcken W, Stubbs A, French PJ. Bralten LB, et al. Among authors: kockx c. PLoS One. 2011;6(7):e22000. doi: 10.1371/journal.pone.0022000. Epub 2011 Jul 7. PLoS One. 2011. PMID: 21760942 Free PMC article.
Targeted Next Generation Sequencing reveals previously unidentified TSC1 and TSC2 mutations.
Nellist M, Brouwer RW, Kockx CE, van Veghel-Plandsoen M, Withagen-Hermans C, Prins-Bakker L, Hoogeveen-Westerveld M, Mrsic A, van den Berg MM, Koopmans AE, de Wit MC, Jansen FE, Maat-Kievit AJ, van den Ouweland A, Halley D, de Klein A, van IJcken WF. Nellist M, et al. Among authors: kockx ce. BMC Med Genet. 2015 Feb 25;16:10. doi: 10.1186/s12881-015-0155-4. BMC Med Genet. 2015. PMID: 25927202 Free PMC article.
UGT1A1 Genetic Variations and a Haplotype Associated with Neonatal Hyperbilirubinemia in Indonesian Population.
Wisnumurti DA, Sribudiani Y, Porsch RM, Maskoen AM, Abdulhamied LI, Rahayuningsih SE, Asni EK, Sleutels F, Kockx CEM, van Ijcken WFJ, Sukadi A, Achmad TH. Wisnumurti DA, et al. Among authors: kockx cem. Biomed Res Int. 2018 Jan 23;2018:9425843. doi: 10.1155/2018/9425843. eCollection 2018. Biomed Res Int. 2018. PMID: 29607327 Free PMC article. Clinical Trial.
Identification of microRNAs in human plasma.
van der Eerden BC, Alves RD, Kockx CE, Ozgur Z, Schreuders-Koedam M, van de Peppel J, van Ijcken WF, van Leeuwen JP. van der Eerden BC, et al. Among authors: kockx ce. Methods Mol Biol. 2015;1226:71-85. doi: 10.1007/978-1-4939-1619-1_7. Methods Mol Biol. 2015. PMID: 25331044
Deciphering the RNA landscape by RNAome sequencing.
Derks KW, Misovic B, van den Hout MC, Kockx CE, Gomez CP, Brouwer RW, Vrieling H, Hoeijmakers JH, van IJcken WF, Pothof J. Derks KW, et al. Among authors: kockx ce. RNA Biol. 2015;12(1):30-42. doi: 10.1080/15476286.2015.1017202. RNA Biol. 2015. PMID: 25826412 Free PMC article.
29 results