Menten B - Search Results

1

TEAD4 regulates trophectoderm differentiation upstream of CDX2 in a GATA3-independent manner in the human preimplantation embryo.

Stamatiadis P, Cosemans G, Boel A, Menten B, De Sutter P, Stoop D, Chuva de Sousa Lopes SM, Lluis F, Coucke P, Heindryckx B. Stamatiadis P, et al. Among authors: menten b. Hum Reprod. 2022 Jul 30;37(8):1760-1773. doi: 10.1093/humrep/deac138. Hum Reprod. 2022. PMID: 35700449

2

Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis.

Hellemans J, Preobrazhenska O, Willaert A, Debeer P, Verdonk PC, Costa T, Janssens K, Menten B, Van Roy N, Vermeulen SJ, Savarirayan R, Van Hul W, Vanhoenacker F, Huylebroeck D, De Paepe A, Naeyaert JM, Vandesompele J, Speleman F, Verschueren K, Coucke PJ, Mortier GR. Hellemans J, et al. Among authors: menten b. Nat Genet. 2004 Nov;36(11):1213-8. doi: 10.1038/ng1453. Epub 2004 Oct 17. Nat Genet. 2004. PMID: 15489854

3

The influence of early embryo traits on human embryonic stem cell derivation efficiency.

O'Leary T, Heindryckx B, Lierman S, Van der Jeught M, Menten B, Deforce D, Cornelissen R, de Sousa Lopes SC, De Sutter P. O'Leary T, et al. Among authors: menten b. Stem Cells Dev. 2011 May;20(5):785-93. doi: 10.1089/scd.2010.0338. Epub 2010 Oct 17. Stem Cells Dev. 2011. PMID: 20809773

4

Applying massive parallel sequencing to molecular diagnosis of Marfan and Loeys-Dietz syndromes.

Baetens M, Van Laer L, De Leeneer K, Hellemans J, De Schrijver J, Van De Voorde H, Renard M, Dietz H, Lacro RV, Menten B, Van Criekinge W, De Backer J, De Paepe A, Loeys B, Coucke PJ. Baetens M, et al. Among authors: menten b. Hum Mutat. 2011 Sep;32(9):1053-62. doi: 10.1002/humu.21525. Epub 2011 Jul 20. Hum Mutat. 2011. PMID: 21542060

5

Alternative Routes to Induce Naïve Pluripotency in Human Embryonic Stem Cells.

Duggal G, Warrier S, Ghimire S, Broekaert D, Van der Jeught M, Lierman S, Deroo T, Peelman L, Van Soom A, Cornelissen R, Menten B, Mestdagh P, Vandesompele J, Roost M, Slieker RC, Heijmans BT, Deforce D, De Sutter P, De Sousa Lopes SC, Heindryckx B. Duggal G, et al. Among authors: menten b. Stem Cells. 2015 Sep;33(9):2686-98. doi: 10.1002/stem.2071. Epub 2015 Jun 24. Stem Cells. 2015. PMID: 26108678

6

Whole genome amplification with SurePlex results in better copy number alteration detection using sequencing data compared to the MALBAC method.

Deleye L, De Coninck D, Christodoulou C, Sante T, Dheedene A, Heindryckx B, Van den Abbeel E, De Sutter P, Menten B, Deforce D, Van Nieuwerburgh F. Deleye L, et al. Among authors: menten b. Sci Rep. 2015 Jun 30;5:11711. doi: 10.1038/srep11711. Sci Rep. 2015. PMID: 26122179 Free PMC article.

7

Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts.

Deleye L, Dheedene A, De Coninck D, Sante T, Christodoulou C, Heindryckx B, Van den Abbeel E, De Sutter P, Deforce D, Menten B, Van Nieuwerburgh F. Deleye L, et al. Among authors: menten b. Fertil Steril. 2015 Nov;104(5):1276-85.e1. doi: 10.1016/j.fertnstert.2015.07.1144. Epub 2015 Aug 14. Fertil Steril. 2015. PMID: 26282994 Free article.

8

Zebrafish Collagen Type I: Molecular and Biochemical Characterization of the Major Structural Protein in Bone and Skin.

Gistelinck C, Gioia R, Gagliardi A, Tonelli F, Marchese L, Bianchi L, Landi C, Bini L, Huysseune A, Witten PE, Staes A, Gevaert K, De Rocker N, Menten B, Malfait F, Leikin S, Carra S, Tenni R, Rossi A, De Paepe A, Coucke P, Willaert A, Forlino A. Gistelinck C, et al. Among authors: menten b. Sci Rep. 2016 Feb 15;6:21540. doi: 10.1038/srep21540. Sci Rep. 2016. PMID: 26876635 Free PMC article.

9

BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessment.

Boel A, Steyaert W, De Rocker N, Menten B, Callewaert B, De Paepe A, Coucke P, Willaert A. Boel A, et al. Among authors: menten b. Sci Rep. 2016 Jul 27;6:30330. doi: 10.1038/srep30330. Sci Rep. 2016. PMID: 27461955 Free PMC article.

10

Performance of a TthPrimPol-based whole genome amplification kit for copy number alteration detection using massively parallel sequencing.

Deleye L, De Coninck D, Dheedene A, De Sutter P, Menten B, Deforce D, Van Nieuwerburgh F. Deleye L, et al. Among authors: menten b. Sci Rep. 2016 Aug 22;6:31825. doi: 10.1038/srep31825. Sci Rep. 2016. PMID: 27546482 Free PMC article.

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