Kater-Baats E - Search Results

1

Next-generation cytogenetics: Comprehensive assessment of 52 hematological malignancy genomes by optical genome mapping.

Neveling K, Mantere T, Vermeulen S, Oorsprong M, van Beek R, Kater-Baats E, Pauper M, van der Zande G, Smeets D, Weghuis DO, Stevens-Kroef MJPL, Hoischen A. Neveling K, et al. Among authors: kater baats e. Am J Hum Genet. 2021 Aug 5;108(8):1423-1435. doi: 10.1016/j.ajhg.2021.06.001. Epub 2021 Jul 7. Am J Hum Genet. 2021. PMID: 34237281 Free PMC article.

2

Optical genome mapping enables constitutional chromosomal aberration detection.

Mantere T, Neveling K, Pebrel-Richard C, Benoist M, van der Zande G, Kater-Baats E, Baatout I, van Beek R, Yammine T, Oorsprong M, Hsoumi F, Olde-Weghuis D, Majdali W, Vermeulen S, Pauper M, Lebbar A, Stevens-Kroef M, Sanlaville D, Dupont JM, Smeets D, Hoischen A, Schluth-Bolard C, El Khattabi L. Mantere T, et al. Among authors: kater baats e. Am J Hum Genet. 2021 Aug 5;108(8):1409-1422. doi: 10.1016/j.ajhg.2021.05.012. Epub 2021 Jul 7. Am J Hum Genet. 2021. PMID: 34237280 Free PMC article.

3

Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations.

Neveling K, Tjwan Thung D, Beulen L, van Rens-Buijsman W, Gomes I, van den Heuvel S, Mieloo H, Derks-Prinsen I, Kater-Baats E, Faas BH. Neveling K, et al. Among authors: kater baats e. Prenat Diagn. 2016 Mar;36(3):216-23. doi: 10.1002/pd.4777. Epub 2016 Feb 15. Prenat Diagn. 2016. PMID: 26774010

4

Disruption of a novel MFS transporter gene, DIRC2, by a familial renal cell carcinoma-associated t(2;3)(q35;q21).

Bodmer D, Eleveld M, Kater-Baats E, Janssen I, Janssen B, Weterman M, Schoenmakers E, Nickerson M, Linehan M, Zbar B, van Kessel AG. Bodmer D, et al. Among authors: kater baats e. Hum Mol Genet. 2002 Mar 15;11(6):641-9. doi: 10.1093/hmg/11.6.641. Hum Mol Genet. 2002. PMID: 11912179

5

Multiplex ligation-dependent probe amplification (MLPA) as a stand-alone test for rapid aneuploidy detection in amniotic fluid cells.

Kooper AJ, Faas BH, Kater-Baats E, Feuth T, Janssen JC, van der Burgt I, Lotgering FK, van Kessel AG, Smits AP. Kooper AJ, et al. Among authors: kater baats e. Prenat Diagn. 2008 Nov;28(11):1004-10. doi: 10.1002/pd.2111. Prenat Diagn. 2008. PMID: 18925610

6

Mapping and characterization of the mouse and human SS18 genes, two human SS18-like genes and a mouse Ss18 pseudogene.

de Bruijn DR, Kater-Baats E, Eleveld M, Merkx G, Geurts Van Kessel A. de Bruijn DR, et al. Among authors: kater baats e. Cytogenet Cell Genet. 2001;92(3-4):310-9. doi: 10.1159/000056920. Cytogenet Cell Genet. 2001. PMID: 11435705

7

de Bruijn DR, dos Santos NR, Kater-Baats E, Thijssen J, van den Berk L, Stap J, Balemans M, Schepens M, Merkx G, van Kessel AG. de Bruijn DR, et al. Among authors: kater baats e. Genes Chromosomes Cancer. 2002 Jul;34(3):285-98. doi: 10.1002/gcc.10073. Genes Chromosomes Cancer. 2002. PMID: 12007189

8

Delineation of the protein domains responsible for SYT, SSX, and SYT-SSX nuclear localization.

dos Santos NR, de Bruijn DR, Kater-Baats E, Otte AP, van Kessel AG. dos Santos NR, et al. Among authors: kater baats e. Exp Cell Res. 2000 Apr 10;256(1):192-202. doi: 10.1006/excr.2000.4813. Exp Cell Res. 2000. PMID: 10739666

9

Heterogeneous expression of the SSX cancer/testis antigens in human melanoma lesions and cell lines.

dos Santos NR, Torensma R, de Vries TJ, Schreurs MW, de Bruijn DR, Kater-Baats E, Ruiter DJ, Adema GJ, van Muijen GN, van Kessel AG. dos Santos NR, et al. Among authors: kater baats e. Cancer Res. 2000 Mar 15;60(6):1654-62. Cancer Res. 2000. PMID: 10749136

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